Colin Ross

BSc, PhD, MSc

Investigator, BC Children's Hospital
Associate Dean, Research, Faculty of Pharmaceutical Sciences

The goal of my research is to develop new treatments for patients with rare diseases. One strategy that we are working on is to develop new gene therapies. Another approach that we are working on is to understand why certain patients respond positively to a medication, while others receive no benefit, or worse, develop debilitating or life-threatening adverse drug reactions (ADRs) to the same dose of medication. We work collaboratively with clinicians and researchers from across Canada and around the world.

1. We successfully developed the first gene therapy to achieve regulatory approval. That work has led to many new gene therapies coming onto the market and many more in development. We are now working on several approaches to reduce the high costs of gene therapies by developing more efficient products and improved manufacturing.

2. We are developing new approaches for gene therapy that utilize genome editing for improved effectiveness and reduced costs.

3. We have recruited patients that have suffered specific serious ADRs, as well as control patients that have recived the same drugs without ADRs. We use high-throughput genomics and next-generation DNA sequencing technologies to identify the genetic factors of severe ADRs of key clinical importance.

The research involves many approaches from statistical, computational and molecular genetics, to molecular biology, and cell biology. The program’s mission is to translate these findings into new diagnostics and therapeutics that will improve the quality of lives of patients and families.

Academic Affiliations

  • Professor, , , Faculty of Pharmaceutical Sciences, University of British Columbia
  • Research Theme: Evidence to Innovation
  • Research Group(s): Childhood Cancer and Blood Research; Clinical Pharmacology; Rare Diseases

Contact Information

Location

950 West 28th Ave, Vancouver, BC, Canada, V5Z 4H4

Oral morphine pharmacokinetics in healthy children and the effect of genetic polymorphisms: An exploratory study

Paediatrics & Child Health

Lauren Faught and Abdelbaset A Elzagallaai and Nicholas Tonial and Samina Ali and Natasha Lepore and Jaime Reardon and Brad Urquhart and Colin Ross and Michael J Rieder and Naveen Poonai

DOI: 10.1093/pch/pxaf084

02 / 2026

Pathway-Informed Machine Learning Identifies Genetic Predictors of High-Dose Methotrexate-Induced Mucositis in Pediatric Acute Lymphoblastic Leukemia

Clinical Pharmacology & Therapeutics

Xiao Yu Cindy Zhang and Erika N. Scott and Hedy Maagdenberg and Alice Man and Kathy H. Li and S. Rod Rassekh and Bruce C. Carleton and Colin J. D. Ross and Wyeth W. Wasserman and Catrina M. Loucks

DOI: 10.1002/cpt.70135

02 / 2026

Supplementary Fig. 1 from Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin J.D. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.30706748

11 / 2025

Supplementary Fig. 5 from Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin J.D. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.30706736

11 / 2025

Supplementary Fig. 2 from Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin J.D. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.30706745

11 / 2025

Supplementary Data 1 from Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin J.D. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.30706751

11 / 2025

Supplementary Fig. 4 from Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin J.D. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.30706739

11 / 2025

Supplementary Fig. 3 from Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin J.D. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.30706742

11 / 2025

Machine learning model identifies genetic predictors of cisplatin-induced ototoxicity in CERS6 and TLR4

Computers in Biology and Medicine

Ali Arab and Bahareh Kashani and Miguel Cordova-Delgado and Erika N. Scott and Kaveh Alemi and Jessica Trueman and Gabriella Groeneweg and Wan-Chun Chang and Catrina M. Loucks and Colin J.D. Ross and Bruce C. Carleton and Martin Ester

DOI: 10.1016/j.compbiomed.2024.109324

12 / 2024

Genomic variations associated with risk and protection against vincristine-induced peripheral neuropathy in pediatric cancer patients

npj Genomic Medicine

Kheireddin Mufti and Miguel Cordova and Erika N. Scott and Jessica N. Trueman and Jessica M. Lovnicki and Catrina M. Loucks and Shahrad R. Rassekh and Colin J. D. Ross and Bruce C. Carleton and Gabriella S. S. Groeneweg and Michelle Higginson and Wan-Chun Chang and Kathy Li and Fudan Miao and Derek Yau and Lucie Pecheux and Bina Gyawali and Amanda Perreault and Fatema Abbasi and Gregory Guilcher and Gesche Riabowol and Geert t Jong and Michelle Staub and Geoff Cuvelier and Kathleen Felton and Sara Khalaj and Michael Rieder and Awatif Abuzgaia and Tamorah Lewis and Himal Ghimire and Paul Nathan and Donna Johnston and Mounira Ibrahim and Jean-Franois Bussires and Thana-Rafi Jean-Baptiste and Denis Lebel and Maja Krajinovic and Thai Hoa Tran and Kerry Goralski and Zara Forbrigger and Ketan Kulkarni

DOI: 10.1038/s41525-024-00443-7

11 / 2024

Supplementary Fig. 1 from INTRAVENOUS N-ACETYLCYSTEINE TO PREVENT CISPLATIN-INDUCED HEARING LOSS IN CHILDREN: A NONRANDOMIZED CONTROLLED PHASE 1 TRIAL

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin JD. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.27031420

09 / 2024

Supplementary Fig. 5 from INTRAVENOUS N-ACETYLCYSTEINE TO PREVENT CISPLATIN-INDUCED HEARING LOSS IN CHILDREN: A NONRANDOMIZED CONTROLLED PHASE 1 TRIAL

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin JD. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.27031408.v1

09 / 2024

Supplementary Fig. 4 from INTRAVENOUS N-ACETYLCYSTEINE TO PREVENT CISPLATIN-INDUCED HEARING LOSS IN CHILDREN: A NONRANDOMIZED CONTROLLED PHASE 1 TRIAL

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin JD. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.27031411

09 / 2024

Data from INTRAVENOUS N-ACETYLCYSTEINE TO PREVENT CISPLATIN-INDUCED HEARING LOSS IN CHILDREN: A NONRANDOMIZED CONTROLLED PHASE 1 TRIAL

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin JD. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.c.6664582.v3

09 / 2024

Supplementary Data 1 from INTRAVENOUS N-ACETYLCYSTEINE TO PREVENT CISPLATIN-INDUCED HEARING LOSS IN CHILDREN: A NONRANDOMIZED CONTROLLED PHASE 1 TRIAL

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin JD. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.27031423

09 / 2024

Supplementary Fig. 3 from INTRAVENOUS N-ACETYLCYSTEINE TO PREVENT CISPLATIN-INDUCED HEARING LOSS IN CHILDREN: A NONRANDOMIZED CONTROLLED PHASE 1 TRIAL

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin JD. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.27031414

09 / 2024

Supplementary Fig. 2 from INTRAVENOUS N-ACETYLCYSTEINE TO PREVENT CISPLATIN-INDUCED HEARING LOSS IN CHILDREN: A NONRANDOMIZED CONTROLLED PHASE 1 TRIAL

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin JD. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.27031417

09 / 2024

The Role of Pharmacogenomics in Rare Diseases

Drug Safety

Man, A. and Groeneweg, G.S.S. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.1007/s40264-024-01416-6

Urinary TIMP-2*IGFBP-7 to diagnose acute kidney injury in children receiving cisplatin

Pediatric Nephrology

Chui, H. and McMahon, K.R. and Rassekh, S.R. and Schultz, K.R. and Blydt-Hansen, T.D. and Mammen, C. and Pinsk, M. and Cuvelier, G.D.E. and Carleton, B.C. and Tsuyuki, R.T. and Ross, C.J.D. and Devarajan, P. and Huynh, L. and Yordanova, M. and Crpeau-Hubert, F. and Wang, S. and Cockovski, V. and Palijan, A. and Zappitelli, M.

DOI: 10.1007/s00467-023-06007-8

Systemic delivery of proteins using novel peptides via the sublingual route

Journal of Controlled Release

Wu, J. and Jones, N. and Hohenwarter, L. and Zhao, F. and Chan, V. and Tan, Z. and Carlaw, T. and Morin, T. and Li, J. and Kaur, T. and Andrew, L.J. and Ross, C.J.D. and Hedtrich, S. and Li, S.-D.

DOI: 10.1016/j.jconrel.2024.02.042

CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disorders

Genetics in Medicine

van Karnebeek, C.D.M. and Tarailo-Graovac, M. and Leen, R. and Meinsma, R. and Correard, S. and Jansen-Meijer, J. and Prykhozhij, S.V. and Pena, I.A. and Ban, K. and Schock, S. and Saxena, V. and Pras-Raves, M.L. and Drgemller, B.I. and Grootemaat, A.E. and van der Wel, N.N. and Dobritzsch, D. and Roseboom, W. and Schomakers, B.V. and Jaspers, Y.R.J. and Zoetekouw, L. and Roelofsen, J. and Ferreira, C.R. and van der Lee, R. and Ross, C.J. and Kochan, J. and McIntyre, R.L. and van Klinken, J.B. and van Weeghel, M. and Kramer, G. and Weschke, B. and Labrune, P. and Willemsen, M.A. and Riva, D. and Garavaglia, B. and Moeschler, J.B. and Filiano, J.J. and Ekker, M. and Berman, J.N. and Dyment, D. and Vaz, F.M. and Wassermann, W.W. and Houtkooper, R.H. and van Kuilenburg, A.B.P.

DOI: 10.1016/j.gim.2024.101104

Data from Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Etan Orgel and Kristin R. Knight and Yueh-Yun Chi and Jemily Malvar and Teresa Rushing and Victoria Mena and Laurie S. Eisenberg and Shahrad R. Rassekh and Colin J.D. Ross and Erika N. Scott and Michael Neely and Edward A. Neuwelt and Leslie L. Muldoon and David R. Freyer

DOI: 10.1158/1078-0432.c.6664582.v2

07 / 2023

Implementation of pharmacogenetic testing in oncology: DPYD-guided dosing to prevent fluoropyrimidine toxicity in British Columbia

Frontiers in Pharmacology

Wu, A. and Anderson, H. and Hughesman, C. and Young, S. and Lohrisch, C. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.3389/fphar.2023.1257745

RBL2 Regulates Cardiac Sensitivity to Anthracycline Chemotherapy

JACC: CardioOncology

Xia, P. and Chen, J. and Sapkota, Y. and Scott, E.N. and Liu, Y. and Hudson, M.M. and Rassekh, S.R. and Carleton, B.C. and Ross, C.J.D. and Chow, E.J. and Cheng, Z.

DOI: 10.1016/j.jaccao.2022.10.017

A luciferase reporter mouse model to optimize in vivo gene editing validated by lipid nanoparticle delivery of adenine base editors

Molecular Therapy

Yu, S.-Y. and Carlaw, T. and Thomson, T. and Birkenshaw, A. and Basha, G. and Kurek, D. and Huang, C. and Kulkarni, J. and Zhang, L.-H. and Ross, C.J.D.

DOI: 10.1016/j.ymthe.2023.02.009

Development of a Dose-Adjusted Polygenic Risk Model for Anthracycline-Induced Cardiotoxicity

Therapeutic Drug Monitoring

Siemens, A. and Rassekh, S.R. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.1097/FTD.0000000000001077

Acute kidney injury during cisplatin therapy and associations with kidney outcomes 2 to 6months post-cisplatin in children: a multi-centre, prospective observational study

Pediatric Nephrology

McMahon, K.R. and Lebel, A. and Rassekh, S.R. and Schultz, K.R. and Blydt-Hansen, T.D. and Cuvelier, G.D.E. and Mammen, C. and Pinsk, M. and Carleton, B.C. and Tsuyuki, R.T. and Ross, C.J.D. and Huynh, L. and Yordanova, M. and Crpeau-Hubert, F. and Wang, S. and Palijan, A. and Lee, J. and Boyko, D. and Zappitelli, M.

DOI: 10.1007/s00467-022-05745-5

Systematic Critical Review of Genetic Factors Associated with Cisplatin-induced Ototoxicity: Canadian Pharmacogenomics Network for Drug Safety 2022 Update

Therapeutic Drug Monitoring

Scott, E.N. and Joseph, A.A. and Dhanda, A. and Tanoshima, R. and Brooks, B. and Rod Rassekh, S. and Ross, C.J.D. and Carleton, B.C. and Loucks, C.M.

DOI: 10.1097/FTD.0000000000001113

Preclinical Development and Characterization of Novel Adeno-Associated Viral Vectors for the Treatment of Lipoprotein Lipase Deficiency

Human Gene Therapy

Mehta, N. and Gilbert, R. and Chahal, P.S. and Moreno, M.J. and Nassoury, N. and Coulombe, N. and Lytvyn, V. and Mercier, M. and Fatehi, D. and Lin, W. and Harvey, E.M. and Zhang, L.-H. and Nazemi-Moghaddam, N. and Elahi, S.M. and Ross, C.J.D. and Stanimirovic, D.B. and Hayden, M.R.

DOI: 10.1089/hum.2023.075

Effects of pharmacogenetic profiles on pediatric pain relief and adverse events with ibuprofen and oxycodone

Pain Reports

Ali, S. and Yukseloglu, A. and Ross, C.J. and Rosychuk, R.J. and Drendel, A.L. and Manaloor, R. and Johnson, D.W. and Le May, S. and Carleton, B.

DOI: 10.1097/PR9.0000000000001113

Generation of a human induced pluripotent stem cell line from a patient with hypomyelinating leukodystrophy 22 (HLD22)

Stem Cell Research

Ozgoren, O.K. and Sequiera, G.L. and Ferrari Bardile, C. and Gjervan, S.C. and Salman, A. and Lehman, A. and Turvey, S.E. and Ross, C.J.D. and Stockler, S. and Pouladi, M.A.

DOI: 10.1016/j.scr.2023.103174

Association Between HLA"DPB1 and Antineutrophil Cytoplasmic Antibody"Associated Vasculitis in Children

Arthritis and Rheumatology

Gibson, K.M. and Drgemller, B.I. and Foell, D. and Benseler, S.M. and Graham, J. and Hancock, R.E.W. and Luqmani, R.A. and Cabral, D.A. and Brown, K.L. and Ross, C.J.

DOI: 10.1002/art.42423

Noninvasive testing for mycophenolate exposure in children with renal transplant using urinary metabolomics

Pediatric Transplantation

Taha, K. and Sharma, A. and Kroeker, K. and Ross, C. and Carleton, B. and Wishart, D. and Medeiros, M. and Blydt-Hansen, T.D.

DOI: 10.1111/petr.14460

Lipid Nanoparticle-Mediated Hit-and-Run Approaches Yield Efficient and Safe In Situ Gene Editing in Human Skin

ACS Nano

Bolsoni, J. and Liu, D. and Mohabatpour, F. and Ebner, R. and Sadhnani, G. and Tafech, B. and Leung, J. and Shanta, S. and An, K. and Morin, T. and Chen, Y. and Arguello, A. and Choate, K. and Jan, E. and Ross, C.J. and Brambilla, D. and Witzigmann, D. and Kulkarni, J. and Cullis, P.R. and Hedtrich, S.

DOI: 10.1021/acsnano.3c08644

Human ASXL1 Deficiency Causes Epigenetic Dysfunction, Combined Immunodeficiency and EBV"Associated Hodgkin Lymphoma

medRxiv

Fu, M.P. and Sharma, M. and Merrill, S.M. and Yousefi, P. and Tan, R. and Modi, B.P. and Bel, K.D. and Deyell, R.J. and Rozmus, J. and Rehmus, W. and Hildebrand, K.J. and James, E. and Blanchard-Rohner, G. and Lin, S. and Shopsowitz, K.E. and Setiadi, A. and Terry, J. and Lee, A.F. and Drgemller, B.I. and Matthews, A. and Tarailo-Graovac, M. and Sauv, L. and Mitchell, H. and Prendiville, J.S. and MacIsaac, J.L. and Dever, K. and Lin, D.T.S. and Meijer, M. and Ross, C.J.D. and Dobson, S.R.M. and Vercauteren, S.M. and Wasserman, W.W. and van Karnebeek, C.D.M. and McKinnon, M.L. and Kobor, M.S. and Turvey, S.E. and Biggs, C.M.

DOI: 10.1101/2023.12.20.23300096

Role of Cisplatin Dose Intensity and TPMT Variation in the Development of Hearing Loss in Children

Therapeutic Drug Monitoring

Siemens, A. and Brooks, B. and Rassekh, S.R. and Meijer, A.J.M. and Van Den Heuvel-Eibrink, M.M. and Xu, W. and Loucks, C.M. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.1097/FTD.0000000000001085

Intravenous N-Acetylcysteine to Prevent Cisplatin-Induced Hearing Loss in Children: A Nonrandomized Controlled Phase I Trial

Clinical cancer research : an official journal of the American Association for Cancer Research

Orgel, E. and Knight, K.R. and Chi, Y.-Y. and Malvar, J. and Rushing, T. and Mena, V. and Eisenberg, L.S. and Rassekh, S.R. and Ross, C.J.D. and Scott, E.N. and Neely, M. and Neuwelt, E.A. and Muldoon, L.L. and Freyer, D.R.

DOI: 10.1158/1078-0432.CCR-23-0252

Lipid-Nanoparticle-Based Delivery of CRISPR/Cas9 Genome-Editing Components

Molecular Pharmaceutics

Kazemian, P. and Yu, S.-Y. and Thomson, S.B. and Birkenshaw, A. and Leavitt, B.R. and Ross, C.J.D.

DOI: 10.1021/acs.molpharmaceut.1c00916

Identification of Drug Transporter Genomic Variants and Inhibitors That Protect Against Doxorubicin-Induced Cardiotoxicity

Circulation

Magdy, T. and Jouni, M. and Kuo, H.-H. and Weddle, C.J. and Lyra-Leite, D. and Fonoudi, H. and Romero-Tejeda, M. and Gharib, M. and Javed, H. and Fajardo, G. and Ross, C.J.D. and Carleton, B.C. and Bernstein, D. and Burridge, P.W.

DOI: 10.1161/CIRCULATIONAHA.121.055801

A pharmacogenomic investigation of the cardiac safety profile of ondansetron in children and pregnant women

Biomedicine and Pharmacotherapy

Drgemller, B.I. and Wright, G.E.B. and Trueman, J. and Shaw, K. and Staub, M. and Chaudhry, S. and Miao, F. and Higginson, M. and Groeneweg, G.S.S. and Brown, J. and Magee, L.A. and Whyte, S.D. and West, N. and Brodie, S.M. and Jong, G.?. and Israels, S. and Berger, H. and Ito, S. and Rassekh, S.R. and Sanatani, S. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.1016/j.biopha.2022.112684

Urine Neutrophil Gelatinase-Associated Lipocalin and Kidney Injury Molecule-1 to Detect Pediatric Cisplatin-Associated Acute Kidney Injury

Kidney360

Mcmahon, K.R. and Chui, H. and Rassekh, S.R. and Schultz, K.R. and Blydt-Hansen, T.D. and Mammen, C. and Pinsk, M. and Cuvelier, G.D.E. and Carleton, B.C. and Tsuyuki, R.T. and Ross, C.J.D. and Devarajan, P. and Huynh, L. and Yordanova, M. and Crpeau-Hubert, F. and Wang, S. and Cockovski, V. and Palijan, A. and Zappitelli, M.

DOI: 10.34067/KID.0004802021

The cumulative incidence of cisplatin-induced hearing loss in young children is higher and develops at an early stage during therapy compared with older children based on 2052 audiological assessments

Cancer

Meijer, A.J.M. and Li, K.H. and Brooks, B. and Clemens, E. and Ross, C.J. and Rassekh, S.R. and Hoetink, A.E. and van Grotel, M. and van den Heuvel-Eibrink, M.M. and Carleton, B.C.

DOI: 10.1002/cncr.33848

Experiences with Genetic Counseling, Testing, and Diagnosis among Adolescents with a Genetic Condition: A Scoping Review

JAMA Pediatrics

Wainstein, T. and Marshall, S.K. and Ross, C.J.D. and Virani, A.K. and Austin, J.C. and Elliott, A.M.

DOI: 10.1001/jamapediatrics.2021.4290

Assessing the role of adolescent hormonal contraceptive use on risk for depression: a 3-year longitudinal study protocol

BMC Women's Health

Zareian, B. and Anderl, C. and LeMoult, J. and Galea, L.A.M. and Prior, J.C. and Rights, J.D. and Ross, C.J. and Ge, S. and Hayward, A.C. and Chen, F.S.

DOI: 10.1186/s12905-022-01623-2

All-trans retinoic acid (ATRA) regulates key genes in the RARG-TOP2B pathway and reduces anthracycline-induced cardiotoxicity

PLoS ONE

Hasbullah, J.S. and Scott, E.N. and Bhavsar, A.P. and Gunaretnam, E.P. and Miao, F. and Soliman, H. and Carleton, B.C. and Ross, C.J.D.

DOI: 10.1371/journal.pone.0276541

Pharmacogenomic study of anthracycline-induced cardiotoxicity in Mexican pediatric patients

Pharmacogenomics

Vargas-Neri, J.L. and Carleton, B. and Ross, C.J. and Medeiros, M. and Castaeda-Hernndez, G. and Clark, P.

DOI: 10.2217/pgs-2021-0144

Patient-specific genetic factors predict treatment failure in sofosbuvir-treated patients with chronic hepatitis C

Liver International

Loucks, C.M. and Lin, J.J. and Trueman, J.N. and Drgemller, B.I. and Wright, G.E.B. and Chang, W.-C. and Li, K.H. and Yoshida, E.M. and Ford, J.-A. and Lee, S.S. and Crotty, P. and Kim, R.B. and Al-Judaibi, B. and Schwarz, U.I. and Ramji, A. and Farivar, J.F. and Tam, E. and Walston, L.L. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.1111/liv.15175

Increasing the Targeting Scope of CRISPR Base Editing System beyond NGG

CRISPR Journal

Yu, S.-Y. and Birkenshaw, A. and Thomson, T. and Carlaw, T. and Zhang, L.-H. and Ross, C.J.D.

DOI: 10.1089/crispr.2021.0109

A Systematic Review of Polygenic Models for Predicting Drug Outcomes

Journal of Personalized Medicine

Siemens, A. and Anderson, S.J. and Rassekh, S.R. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.3390/jpm12091394

A cross-sectional study of the relationship between CYP2D6 and CYP2C19 variations and depression symptoms, for women taking SSRIs during pregnancy

Archives of Women's Mental Health

Hippman, C. and Slomp, C. and Morris, E. and Batallones, R. and Inglis, A. and Carrion, P. and Brain, U. and Higginson, M. and Wright, G.E.B. and Balneaves, L.G. and Ryan, D. and Nislow, C. and Ross, C.J.D. and Gaedigk, A. and Oberlander, T.F. and Austin, J.

DOI: 10.1007/s00737-021-01149-w

Pharmacogenetic testing to guide therapeutic decision-making and improve outcomes for children undergoing anthracycline-based chemotherapy

Basic and Clinical Pharmacology and Toxicology

Loucks, C.M. and Yan, K. and Tanoshima, R. and Ross, C.J.D. and Rassekh, S.R. and Carleton, B.C.

DOI: 10.1111/bcpt.13593

Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation Study

Journal of Personalized Medicine

Zazuli, Z. and de Jong, C. and Xu, W. and Vijverberg, S.J.H. and Masereeuw, R. and Patel, D. and Mirshams, M. and Khan, K. and Cheng, D. and Ordonez-Perez, B. and Huang, S.H. and Spreafico, A. and Hansen, A.R. and Goldstein, D.P. and de Almeida, J.R. and Bratman, S.V. and Hope, A. and Knox, J.J. and Wong, R.K.S. and Darling, G.E. and Kitchlu, A. and van Haarlem, S.W.A. and van der Meer, F. and van Lindert, A.S.R. and Heuvel, A.T. and Brouwer, J. and Ross, C.J.D. and Carleton, B.C. and Egberts, T.C.G. and Herder, G.J.M. and Deneer, V.H.M. and Maitland-Van der Zee, A.H. and Liu, G.

DOI: 10.3390/JPM11111233

TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study

npj Precision Oncology

Meijer, A.J.M. and Diepstraten, F.A. and Langer, T. and Broer, L. and Domingo, I.K. and Clemens, E. and Uitterlinden, A.G. and de Vries, A.C.H. and van Grotel, M. and Vermeij, W.P. and Ozinga, R.A. and Binder, H. and Byrne, J. and van Dulmen-den Broeder, E. and Garr, M.L. and Grabow, D. and Kaatsch, P. and Kaiser, M. and Kenborg, L. and Winther, J.F. and Rechnitzer, C. and Hasle, H. and Kepak, T. and Kepakova, K. and Tissing, W.J.E. and van der Kooi, A.L.F. and Kremer, L.C.M. and Kruseova, J. and Pluijm, S.M.F. and Kuehni, C.E. and van der Pal, H.J.H. and Parfitt, R. and Spix, C. and Tillmanns, A. and Deuster, D. and Matulat, P. and Calaminus, G. and Hoetink, A.E. and Elsner, S. and Gebauer, J. and Haupt, R. and Lackner, H. and Blattmann, C. and Neggers, S.J.C.M.M. and Rassekh, S.R. and Wright, G.E.B. and Brooks, B. and Nagtegaal, A.P. and Drgemller, B.I. and Ross, C.J.D. and Bhavsar, A.P. and am Zehnhoff-Dinnesen, A.G. and Carleton, B.C. and Zolk, O. and van den Heuvel-Eibrink, M.M. and de Vries, A.C.H. and van Grotel, M. and van Dulmen-den Broeder, E. and van der Kooi, A.L.F. and Kremer, L.C.M. and van der Pal, H.J.H. and Calaminus, G.

DOI: 10.1038/s41698-021-00178-z

Secondary biogenic amine deficiencies: genetic etiology, therapeutic interventions, and clinical effects

Neurogenetics

van Karnebeek, C.D. and Blydt-Hansen, I. and Matthews, A.M. and Avramovic, V. and Price, M. and Drogemoller, B. and Shyr, C. and Lee, J. and Mwenifumbo, J. and Ghani, A. and Stockler, S. and Friedman, J.M. and Lehman, A. and Ross, C.J. and Wasserman, W.W. and Tarailo-Graovac, M. and Horvath, G.A.

DOI: 10.1007/s10048-021-00652-7

Integrating disease and drug-related phenotypes for improved identification of pharmacogenomic variants

Pharmacogenomics

Ouellette, T.W. and Wright, G.E.B. and Drgemller, B.I. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.2217/pgs-2020-0130

Transcriptome-wide association study uncovers the role of essential genes in anthracycline-induced cardiotoxicity

npj Genomic Medicine

Scott, E.N. and Wright, G.E.B. and Drgemller, B.I. and Hasbullah, J.S. and Gunaretnam, E.P. and Miao, F. and Bhavsar, A.P. and Shen, F. and Schneider, B.P. and Carleton, B.C. and Ross, C.J.D.

DOI: 10.1038/s41525-021-00199-4

RARG variant predictive of doxorubicin-induced cardiotoxicity identifies a cardioprotective therapy

Cell Stem Cell

Magdy, T. and Jiang, Z. and Jouni, M. and Fonoudi, H. and Lyra-Leite, D. and Jung, G. and Romero-Tejeda, M. and Kuo, H.-H. and Fetterman, K.A. and Gharib, M. and Burmeister, B.T. and Zhao, M. and Sapkota, Y. and Ross, C.J. and Carleton, B.C. and Bernstein, D. and Burridge, P.W.

DOI: 10.1016/j.stem.2021.08.006

Prevalence and risk factors for cisplatin-induced hearing loss in children, adolescents, and young adults: a multi-institutional North American cohort study

The Lancet Child and Adolescent Health

Moke, D.J. and Luo, C. and Millstein, J. and Knight, K.R. and Rassekh, S.R. and Brooks, B. and Ross, C.J.D. and Wright, M. and Mena, V. and Rushing, T. and Esbenshade, A.J. and Carleton, B.C. and Orgel, E.

DOI: 10.1016/S2352-4642(21)00020-1

Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatment

Biomedicine and Pharmacotherapy

Lin, J.J. and Loucks, C.M. and Trueman, J.N. and Drgemller, B.I. and Wright, G.E.B. and Yoshida, E.M. and Ford, J.-A. and Lee, S.S. and Kim, R.B. and Al-Judaibi, B. and Schwarz, U.I. and Ramji, A. and Tam, E. and Ross, C.J. and Carleton, B.C.

DOI: 10.1016/j.biopha.2021.112195

Autoantibodies Against Lysosome Associated Membrane Protein-2 (LAMP-2) in Pediatric Chronic Primary Systemic Vasculitis

Frontiers in Immunology

Gibson, K.M. and Kain, R. and Luqmani, R.A. and Ross, C.J. and Cabral, D.A. and Brown, K.L.

DOI: 10.3389/fimmu.2020.624758

Challenges and Opportunities in Implementing Pharmacogenetic Testing in Clinical Settings

Annual Review of Pharmacology and Toxicology

Chang, W.-C. and Tanoshima, R. and Ross, C.J.D. and Carleton, B.C.

DOI: 10.1146/annurev-pharmtox-030920-025745

Neonatal T Helper 17 Responses Are Skewed Towards an Immunoregulatory Interleukin-22 Phenotype

Frontiers in Immunology

Razzaghian, H.R. and Sharafian, Z. and Sharma, A.A. and Boyce, G.K. and Lee, K. and Da Silva, R. and Orban, P.C. and Sekaly, R.-P. and Ross, C.J. and Lavoie, P.M.

DOI: 10.3389/fimmu.2021.655027

Different Disease Endotypes in Phenotypically Similar Vasculitides Affecting Small-to-Medium Sized Blood Vessels

Frontiers in Immunology

Gill, E.E. and Smith, M.L. and Gibson, K.M. and Morishita, K.A. and Lee, A.H.Y. and Falsafi, R. and Graham, J. and Foell, D. and Benseler, S.M. and Ross, C.J. and Luqmani, R.A. and Cabral, D.A. and Hancock, R.E.W. and Brown, K.L.

DOI: 10.3389/fimmu.2021.638571

Adult GAMT deficiency: A literature review and report of two siblings

Molecular Genetics and Metabolism Reports

Modi, B.P. and Khan, H.N. and van der Lee, R. and Wasim, M. and Haaxma, C.A. and Richmond, P.A. and Drgemller, B. and Shah, S. and Salomons, G. and van der Kloet, F.M. and Vaz, F.M. and van der Crabben, S.N. and Ross, C.J. and Wasserman, W.W. and van Karnebeek, C.D.M. and Awan, F.R.

DOI: 10.1016/j.ymgmr.2021.100761

Economic Evidence on Potentially Curative Gene Therapy Products: A Systematic Literature Review

PharmacoEconomics

Ho, J.K. and Borle, K. and Dragojlovic, N. and Dhillon, M. and Kitchin, V. and Kopac, N. and Ross, C. and Lynd, L.D.

DOI: 10.1007/s40273-021-01051-4

Les tests pharmacognomiques: Amliorer le recours personnalis aux mdicaments pour les patients

Canadian family physician Medecin de famille canadien

Loucks, C.M. and Groeneweg, G. and Roy, C. and Lee, D.K. and Rieder, M.J. and Lebel, D. and Ito, S. and Ross, C.J. and Carleton, B.C.

Pharmacogenomic testing: Enhancing personalized medication use for patients

Canadian Family Physician

Loucks, C.M. and Groeneweg, G. and Roy, C. and Lee, D.K. and Rieder, M.J. and Lebel, D. and Ito, S. and Ross, C.J. and Carleton, B.C.

CRISPR/Cas9 Editing: Sparking Discussion on Safety in Light of the Need for New Therapeutics

Human Gene Therapy

Carlaw, T.M. and Zhang, L.-H. and Ross, C.J.D.

DOI: 10.1089/hum.2020.111

Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region

medRxiv

Ye, X. and Roslin, N.M. and Paterson, A.D. and Canada, C. and Lyons, C. and Pegado, V. and Richmond, P. and Shyr, C. and Fornes, O. and Han, X. and Higginson, M. and Ross, C.J. and Giaschi, D. and Gregory-Evans, C.Y. and Patel, M. and Wasserman, W.W.

DOI: 10.1101/2020.04.24.20077586

Epidemiologic Characteristics of Acute Kidney Injury during Cisplatin Infusions in Children Treated for Cancer

JAMA Network Open

McMahon, K.R. and Rassekh, S.R. and Schultz, K.R. and Blydt-Hansen, T. and Cuvelier, G.D.E. and Mammen, C. and Pinsk, M. and Carleton, B.C. and Tsuyuki, R.T. and Ross, C.J.D. and Palijan, A. and Huynh, L. and Yordanova, M. and Crpeau-Hubert, F. and Wang, S. and Boyko, D. and Zappitelli, M.

DOI: 10.1001/jamanetworkopen.2020.3639

A novel mouse model for pyridoxine-dependent epilepsy due to antiquitin deficiency

Human Molecular Genetics

Al-Shekaili, H.H. and Petkau, T.L. and Pena, I. and Lengyell, T.C. and Verhoeven-Duif, N.M. and Ciapaite, J. and Bosma, M. and Van Faassen, M. and Kema, I.P. and Horvath, G. and Ross, C. and Simpson, E.M. and Friedman, J.M. and Van Karnebeek, C. and Leavitt, B.R.

DOI: 10.1093/hmg/ddaa202

Prevention of adverse drug effects: A pharmacogenomic approach

Current Opinion in Pediatrics

Scott, E.N. and Hasbullah, J.S. and Carleton, B.C. and Ross, C.J.D.

DOI: 10.1097/MOP.0000000000000935

A prospective study to explore the relationship between MTHFR C677T genotype, physiological folate levels, and postpartum psychopathology in at-risk women

PLoS ONE

Morris, E. and Hippman, C. and Albert, A. and Slomp, C. and Inglis, A. and Carrion, P. and Batallones, R. and Andrighetti, H. and Ross, C. and Dyer, R. and Honer, W. and Austin, J.

DOI: 10.1371/journal.pone.0243936

Pharmacokinetic-Pharmacogenomic Model for Chinese Children Treated With Lamotrigine Also Applies for Mexican Children

Therapeutic Drug Monitoring

Jurez-Hernndez, J.E. and Gutirrez-Ceniceros, M. and Gonzlez-Ramrez, J.R. and Medeiros, M. and Carleton, B. and Ross, C. and Castaeda-Hernndez, G.

DOI: 10.1097/FTD.0000000000000792

Vincristine-induced peripheral neurotoxicity: A prospective cohort.

Pediatric hematology and oncology

Nama N and Barker MK and Kwan C and Sabarre C and Solimano V and Rankin A and Raabe J and Ross CJ and Carleton B and Zwicker JG and Rassekh SR

DOI: 10.1080/08880018.2019.1677832 PubMed: 31682156

11 / 2019

Identification of Novel Adenosine Deaminase 2 Gene Variants and Varied Clinical Phenotype in Pediatric Vasculitis.

Arthritis & rheumatology (Hoboken, N.J.)

Gibson KM and Morishita KA and Dancey P and Moorehead P and Drgemller B and Han X and Graham J and Hancock REW and Foell D and Benseler S and Luqmani R and Yeung RSM and Shenoi S and PedVas Investigators Network

DOI: 10.1002/art.40913 PubMed: 31008556

08 / 2019

Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy.

American journal of human genetics

van Karnebeek CDM and Ramos RJ and Wen XY and Tarailo-Graovac M and Gleeson JG and Skrypnyk C and Brand-Arzamendi K and Karbassi F and Issa MY and van der Lee R and Wevers RA

DOI: 10.1016/j.ajhg.2019.07.015 PubMed: 31422819

08 / 2019

An investigation of the glycosaminoglycan contribution to biaxial mechanical behaviours of porcine atrioventricular heart valve leaflets.

Journal of the Royal Society, Interface

Ross CJ and Laurence DW and Richardson J and Babu AR and Evans LE and Beyer EG and Childers RC and Wu Y and Towner RA and Fung KM and Mir A and Burkhart HM and Holzapfel GA and Lee CH

DOI: 10.1098/rsif.2019.0069 PubMed: 31266416

07 / 2019

Genome-Wide Association Studies of Drug-Induced Liver Injury Make Progress Beyond the HLA Region.

Gastroenterology

Wright GEB and Drgemller BI and Ross CJD and Carleton BC

DOI: 10.1053/j.gastro.2019.03.076 PubMed: 31348928

07 / 2019

Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease

Wright GE and Caron NS and Ng B and Casal L and Xu X and Ooi J and Pouladi MA and Mostafavi S and Ross CJ and Hayden MR

DOI: 10.1101/699033

07 / 2019

Pharmacogenomics of Cisplatin-Induced Ototoxicity: Successes, Shortcomings, and Future Avenues of Research.

Clinical pharmacology and therapeutics

Drgemller BI and Wright GEB and Lo C and Le T and Brooks B and Bhavsar AP and Rassekh SR and Ross CJD and Carleton BC

DOI: 10.1002/cpt.1483 PubMed: 31012503

06 / 2019

The influence of the noradrenergic/stress system on perceptual biases for reward.

Cognitive, affective & behavioral neuroscience

Ehlers MR and Ross CJD and Todd RM

DOI: 10.3758/s13415-018-00657-0 PubMed: 30357659

06 / 2019

Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease.

American journal of human genetics

Wright GEB and Collins JA and Kay C and McDonald C and Dolzhenko E and Xia Q and Becanovic K and Drgemller BI and Semaka A and Nguyen CM and Trost B and Richards F and Bijlsma EK and Hayden MR

DOI: 10.1016/j.ajhg.2019.04.007 PubMed: 31104771

05 / 2019

Outcome Definition Influences the Relationship Between Genetic Polymorphisms of ERCC1, ERCC2, SLC22A2 and Cisplatin Nephrotoxicity in Adult Testicular Cancer Patients.

Genes

Zazuli Z and Otten LS and Drgemller BI and Medeiros M and Monzon JG and Wright GEB and Kollmannsberger CK and Bedard PL and Chen Z and Gelmon KA and McGoldrick N and Kitchlu A and Maitland-van der Zee AH

DOI: 10.3390/genes10050364 PubMed: 31083486

05 / 2019

Common variants of the oxytocin receptor gene do not predict the positive mood benefits of prosocial spending.

Emotion (Washington, D.C.)

Whillans AV and Aknin LB and Ross CJ and Chen L and Chen FS

DOI: 10.1037/emo0000589 PubMed: 31021112

04 / 2019

Paediatric cardio-oncology: epidemiology, screening, prevention, and treatment.

Cardiovascular research

Chow EJ and Leger KJ and Bhatt NS and Mulrooney DA and Ross CJ and Aggarwal S and Bansal N and Ehrhardt MJ and Armenian SH and Scott JM and Hong B

DOI: 10.1093/cvr/cvz031 PubMed: 30768157

04 / 2019

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS.

The New England Journal of Medicine

van Kuilenburg ABP and Tarailo-Graovac M and Richmond PA and Drgemller BI and Pouladi MA and Leen R and Brand-Arzamendi K and Dobritzsch D and Dolzhenko E and Eberle MA and van Karnebeek CDM

DOI: 10.1056/nejmoa1806627 PubMed: 30970188

04 / 2019

PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights.

Brain : a journal of neurology

Johnstone DL and Al-Shekaili HH and Tarailo-Graovac M and Wolf NI and Ivy AS and Demarest S and Roussel Y and Ciapaite J and van Roermund CWT and Kernohan KD and Kosuta C and Ban K and van Karnebeek CDM

DOI: 10.1093/brain/awy346 PubMed: 30668673

03 / 2019

Deficiency of perforin and hCNT1, a novel inborn error of pyrimidine metabolism, associated with a rapidly developing lethal phenotype due to multi-organ failure.

Biochimica et biophysica acta. Molecular basis of disease

Prez-Torras S and Mata-Ventosa A and Drgemller B and Tarailo-Graovac M and Meijer J and Meinsma R and van Cruchten AG and Kulik W and Viel-Oliva A and Bidon-Chanal A and van Kuilenburg ABP

DOI: 10.1016/j.bbadis.2019.01.013 PubMed: 30658162

01 / 2019

Morphine biotransformation genes and neonatal clinical factors predicted behaviour problems in very preterm children at 18months.

EBioMedicine

Chau CMY and Ross CJD and Chau V and Synnes AR and Miller SP and Carleton B and Grunau RE

DOI: 10.1016/j.ebiom.2019.01.042 PubMed: 30709768

01 / 2019

Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function.

JCI insight

Wen XY and Tarailo-Graovac M and Brand-Arzamendi K and Willems A and Rakic B and Huijben K and Da Silva A and Pan X and El-Rass S and Ng R and Selby K and Philip AM and Yun J and Ye XC and Lefeber DJ

DOI: 10.1172/jci.insight.122373 PubMed: 30568043

12 / 2018

Atypical cerebral palsy: genomics analysis enables precision medicine.

Genetics in medicine : official journal of the American College of Medical Genetics

Matthews AM and Blydt-Hansen I and Al-Jabri B and Andersen J and Tarailo-Graovac M and Price M and Selby K and Demos M and Connolly M and Drgemoller B and Shyr C and Mwenifumbo J and United for Metabolic Diseases and the CAUSES Study

DOI: 10.1038/s41436-018-0376-y PubMed: 30542205

12 / 2018

HUME: large-scale detection of causal genetic factors of adverse drug reactions.

Bioinformatics (Oxford, England)

Mansouri M and Yuan B and Ross CJD and Carleton BC and Ester M

DOI: 10.1093/bioinformatics/bty475 PubMed: 29931042

12 / 2018

CYP2D6 as a treatment decision aid for ER-positive non-metastatic breast cancer patients: a systematic review with accompanying clinical practice guidelines.

Breast cancer research and treatment

Drgemller BI and Wright GEB and Shih J and Monzon JG and Gelmon KA and Ross CJD and Amstutz U and Carleton BC and CPNDS Clinical Recommendations Group

DOI: 10.1007/s10549-018-5027-0 PubMed: 30411242

11 / 2018

Cellular metabolism constrains innate immune responses in early human ontogeny.

Nature communications

Kan B and Michalski C and Fu H and Au HHT and Lee K and Marchant EA and Cheng MF and Anderson-Baucum E and Aharoni-Simon M and Tilley P and Mirmira RG and Ross CJ and Luciani DS and Jan E and Lavoie PM

DOI: 10.1038/s41467-018-07215-9 PubMed: 30446641

11 / 2018

Analyses of Adverse Drug Reactions-Nationwide Active Surveillance Network: Canadian Pharmacogenomics Network for Drug Safety Database.

Journal of clinical pharmacology

Tanoshima R and Khan A and Biala AK and Trueman JN and Drgemller BI and Wright GEB and Hasbullah JS and Groeneweg GSS and Ross CJD and Carleton BC and Canadian Pharmacogenomics Network for Drug Safety Consortium

DOI: 10.1002/jcph.1336 PubMed: 30452777

11 / 2018

S100A12 Serum Levels and PMN Counts Are Elevated in Childhood Systemic Vasculitides Especially Involving Proteinase 3 Specific Anti-neutrophil Cytoplasmic Antibodies.

Frontiers in pediatrics

Brown KL and Lubieniecka JM and Armaroli G and Kessel K and Gibson KM and Graham J and Liu D and Hancock REW and Ross CJ and Benseler SM and Luqmani RA and Cabral DA and Foell D and Kessel C

DOI: 10.3389/fped.2018.00341 PubMed: 30533405

11 / 2018

Affectively biased competition: sustained attention is tuned to rewarding expressions and is not modulated by norepinephrine receptor gene variant

Roberts KH and Manaligod MGM and Ross CJD and Mller DJ and Wieser MJ and Todd RM

DOI: 10.1101/442863

10 / 2018

Reducing anthracycline-induced cardiotoxicity through pharmacogenetics.

Pharmacogenomics

Scott E and Hasbullah JS and Ross CJ and Carleton BC

DOI: 10.2217/pgs-2018-0124 PubMed: 30213233

09 / 2018

Output from the CIHR Canadian HIV Trials Network international postdoctoral fellowship for capacity building in HIV clinical trials.

HIV/AIDS (Auckland, N.Z.)

Mbuagbaw L and Slogrove AL and Sas J and Lengwe Kunda J and Morfaw F and Mukonzo JK and Cao W and Ngomba-Kadima G and Zunza M and Ongolo-Zogo P and Nana PN and Cockcroft A and Anis AH

DOI: 10.2147/HIV.S150107 PubMed: 30147378

08 / 2018

Pharmacogenomics of Vincristine-Induced Peripheral Neuropathy Implicates Pharmacokinetic and Inherited Neuropathy Genes.

Clinical pharmacology and therapeutics

Wright GEB and Amstutz U and Drgemller BI and Shih J and Rassekh SR and Hayden MR and Carleton BC and Ross CJD and Canadian Pharmacogenomics Network for Drug Safety Consortium

DOI: 10.1002/cpt.1179 PubMed: 29999516

08 / 2018

A systematic review of the effects of CYP2D6 phenotypes on risperidone treatment in children and adolescents.

Child and Adolescent Psychiatry and Mental Health

Dodsworth T and Kim DD and Procyshyn RM and Ross CJ and Honer WG and Barr AM

DOI: 10.1186/s13034-018-0243-2 PubMed: 30026806

07 / 2018

Common variation near IRF6 is associated with IFN--induced liver injury in multiple sclerosis.

Nature genetics

Kowalec K and Wright GEB and Drgemller BI and Aminkeng F and Bhavsar AP and Kingwell E and Yoshida EM and Traboulsee A and Marrie RA and Kremenchutzky M and Campbell TL and Carleton BC

DOI: 10.1038/s41588-018-0168-y PubMed: 30013178

07 / 2018

Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder Phenotype.

Neuroscience

Horvath GA and Zhao Y and Tarailo-Graovac M and Boelman C and Gill H and Shyr C and Lee J and Blydt-Hansen I and Drgemller BI and Moreland J and Ross CJ and Wasserman WW and van Karnebeek CDM

DOI: 10.1016/j.neuroscience.2018.05.031 PubMed: 29852244

05 / 2018

Genome sequencing reveals a novel genetic mechanism underlying dihydropyrimidine dehydrogenase deficiency: A novel missense variant c.1700G>A and a large intragenic inversion in DPYD spanning intron 8 to intron 12.

Human mutation

van Kuilenburg ABP and Tarailo-Graovac M and Meijer J and Drogemoller B and Vockley J and Maurer D and Dobritzsch D and Ross CJ and Wasserman W and Meinsma R and Zoetekouw L and van Karnebeek CDM

DOI: 10.1002/humu.23538 PubMed: 29691939

04 / 2018

Further Investigation of the Role of ACYP2 and WFS1 Pharmacogenomic Variants in the Development of Cisplatin-Induced Ototoxicity in Testicular Cancer Patients.

Clinical cancer research : an official journal of the American Association for Cancer Research

Drgemller BI and Brooks B and Critchley C and Monzon JG and Wright GEB and Liu G and Renouf DJ and Kollmannsberger CK and Bedard PL and Hayden MR and Gelmon KA and Carleton BC and Ross CJD

DOI: 10.1158/1078-0432.ccr-17-2810 PubMed: 29358504

04 / 2018

Pharmacogenomic Variability of Oral Baclofen Clearance and Clinical Response in Children With Cerebral Palsy.

PM & R : the journal of injury, function, and rehabilitation

McLaughlin MJ and He Y and Brunstrom-Hernandez J and Thio LL and Carleton BC and Ross CJD and Gaedigk A and Lewandowski A and Dai H and Jusko WJ and Leeder JS

DOI: 10.1016/j.pmrj.2017.08.441 PubMed: 28867665

03 / 2018

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.

Neurology

McCormack M and Gui H and Ingason A and Speed D and Wright GEB and Zhang EJ and Secolin R and Yasuda C and Kwok M and Wolking S and Becker F and Rau S and Avbersek A and Heggeli K and Leu C and Cavalleri GL

DOI: 10.1212/wnl.0000000000004853 PubMed: 29288229

01 / 2018

The genotypic and phenotypic spectrum of MTO1 deficiency.

Molecular genetics and metabolism

O'Byrne JJ and Tarailo-Graovac M and Ghani A and Champion M and Deshpande C and Dursun A and Ozgul RK and Freisinger P and Garber I and Haack TB and Horvath R and Baric I and Husain RA and van Karnebeek CDM

DOI: 10.1016/j.ymgme.2017.11.003 PubMed: 29331171

01 / 2018

Improvement of Self-Injury With Dopamine and Serotonin Replacement Therapy in a Patient With a Hemizygous PAK3 Mutation: A New Therapeutic Strategy for Neuropsychiatric Features of an Intellectual Disability Syndrome.

Journal of child neurology

Horvath GA and Tarailo-Graovac M and Bartel T and Race S and Van Allen MI and Blydt-Hansen I and Ross CJ and Wasserman WW and Connolly MB and van Karnebeek CDM

DOI: 10.1177/0883073817740443 PubMed: 29246092

01 / 2018

An initial health economic evaluation of pharmacogenomic testing in patients treated for childhood cancer with anthracyclines.

Pediatric blood & cancer

Dionne F and Aminkeng F and Bhavsar AP and Groeneweg G and Smith A and Visscher H and Rassekh SR and Ross C and Carleton B

DOI: 10.1002/pbc.26887 PubMed: 29271558

12 / 2017

Association Between SLC16A5 Genetic Variation and Cisplatin-Induced Ototoxic Effects in Adult Patients With Testicular Cancer.

JAMA oncology

Drgemller BI and Monzon JG and Bhavsar AP and Borrie AE and Brooks B and Wright GEB and Liu G and Renouf DJ and Kollmannsberger CK and Bedard PL and Aminkeng F and Amstutz U and Carleton BC

DOI: 10.1001/jamaoncol.2017.0502 PubMed: 28448657

11 / 2017

A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder.

European journal of medical genetics

Matthews AM and Tarailo-Graovac M and Price EM and Blydt-Hansen I and Ghani A and Drgemller BI and Robinson WP and Ross CJ and Wasserman WW and Siden H and van Karnebeek CD

DOI: 10.1016/j.ejmg.2017.07.015 PubMed: 28778789

10 / 2017

Exploring genetic influences underlying acute aerobic exercise effects on motor learning.

Scientific reports

Mang CS and McEwen LM and MacIsaac JL and Snow NJ and Campbell KL and Kobor MS and Ross CJD and Boyd LA

DOI: 10.1038/s41598-017-12422-3 PubMed: 28935933

09 / 2017

Application of pharmacogenomics to investigate adverse drug reactions to the disease-modifying treatments for multiple sclerosis: a case-control study protocol for dimethyl fumarate-induced lymphopenia.

BMJ open

Kowalec K and Kingwell E and Carruthers R and Marrie RA and Bernatsky S and Traboulsee A and Ross CJD and Carleton B and Tremlett H

DOI: 10.1136/bmjopen-2017-016276 PubMed: 28576902

06 / 2017

A pharmacogenetic signature of high response to Copaxone in late-phase clinical-trial cohorts of multiple sclerosis.

Genome medicine

Ross CJ and Towfic F and Shankar J and Laifenfeld D and Thoma M and Davis M and Weiner B and Kusko R and Zeskind B and Knappertz V and Grossman I and Hayden MR

DOI: 10.1186/s13073-017-0436-y PubMed: 28569182

05 / 2017

Corrigendum: NANS-mediated synthesis of sialic acid is required for brain and skeletal development.

Nature genetics

van Karnebeek CDM and Bonaf L and Wen XY and Tarailo-Graovac M and Balzano S and Royer-Bertrand B and Ashikov A and Garavelli L and Mammi I and Turolla L and Breen C and Donnai D and Superti-Furga A

DOI: 10.1038/ng0617-969a PubMed: 28546570

05 / 2017

A case of splenomegaly in CBL syndrome.

Coe RR and McKinnon ML and Tarailo-Graovac M and Ross CJ and Wasserman WW and Friedman JM and Rogers PC and van Karnebeek CDM

DOI: 10.1016/j.ejmg.2017.04.009 PubMed: 28414188

04 / 2017

Pharmacogenomic screening for anthracycline-induced cardiotoxicity in childhood cancer.

Aminkeng F and Ross CJ and Rassekh SR and Rieder MJ and Bhavsar AP and Sanatani S and Bernstein D and Hayden MR and Amstutz U and Carleton BC

DOI: 10.1111/bcp.13218 PubMed: 28317142

03 / 2017

A girl with developmental delay, ataxia, cranial nerve palsies, severe respiratory problems in infancy-Expanding NDST1 syndrome.

Armstrong L and Tarailo-Graovac M and Sinclair G and Seath KI and Wasserman WW and Ross CJ and van Karnebeek CD

DOI: 10.1002/ajmg.a.37621 PubMed: 28211985

03 / 2017

The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.

Kay C and Tirado-Hurtado I and Cornejo-Olivas M and Collins JA and Wright G and Inca-Martinez M and Veliz-Otani D and Ketelaar ME and Slama RA and Ross CJ and Mazzetti P and Hayden MR

DOI: 10.1038/ejhg.2016.169 PubMed: 28000697

02 / 2017

Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease.

Tarailo-Graovac M and Drgemller BI and Wasserman WW and Ross CJ and van den Ouweland AM and Darin N and Kollberg G and van Karnebeek CD and Blomqvist M

DOI: 10.1186/s13023-017-0584-6 PubMed: 28187749

02 / 2017

Design and Methods of the Pan-Canadian Applying Biomarkers to Minimize Long-Term Effects of Childhood/Adolescent Cancer Treatment (ABLE) Nephrotoxicity Study: A Prospective Observational Cohort Study.

McMahon KR and Rod Rassekh S and Schultz KR and Pinsk M and Blydt-Hansen T and Mammen C and Tsuyuki RT and Devarajan P and Cuvelier GD and Mitchell LG and Baruchel S and Palijan A and Carleton BC and Ross CJ and Zappitelli M and Applying Biomarkers to Minimize Long-Term Effects of Childhood/Adolescent Cancer Treatment (ABLE) Research Group

DOI: 10.1177/2054358117690338 PubMed: 28270931

Pharmacogenetic variants in TPMT alter cellular responses to cisplatin in inner ear cell lines.

Bhavsar AP and Gunaretnam EP and Li Y and Hasbullah JS and Carleton BC and Ross CJ

DOI: 10.1371/journal.pone.0175711 PubMed: 28406961

Mitochondrial Complex III Deficiency with Ketoacidosis and Hyperglycemia Mimicking Neonatal Diabetes.

Anastasio N and Tarailo-Graovac M and Al-Khalifah R and Legault L and Drogemoller B and Ross CJ and Wasserman WW and van Karnebeek C and Buhas D

DOI: 10.1007/8904_2016_557 PubMed: 27074787

Editorial Note to:Nuclear Receptor NR1H3 in Familial Multiple Sclerosis.

Wang Z and Sadovnick AD and Traboulsee AL and Ross JP and Bernales CQ and Encarnacion M and Yee IM and de Lemos M and Greenwood T and Lee JD and Wright G and Ross CJ and Zhang S and Song W and Vilario-Gell C

DOI: 10.1016/j.neuron.2016.10.008 PubMed: 27764666

10 / 2016

The global spectrum of protein-coding pharmacogenomic diversity.

Wright GE and Carleton B and Hayden MR and Ross CJ

DOI: 10.1038/tpj.2016.77 PubMed: 27779249

10 / 2016

Case-Control Studies Are Not Familial Studies.

Wang Z and Sadovnick AD and Traboulsee AL and Ross JP and Bernales CQ and Encarnacion M and Yee IM and de Lemos M and Greenwood T and Lee JD and Wright G and Ross CJ and Zhang S and Song W and Vilario-Gell C

DOI: 10.1016/j.neuron.2016.09.053 PubMed: 27764669

10 / 2016

Recommendations for genetic testing to reduce the incidence of anthracycline-induced cardiotoxicity.

Aminkeng F and Ross CJ and Rassekh SR and Hwang S and Rieder MJ and Bhavsar AP and Smith A and Sanatani S and Gelmon KA and Bernstein D and Hayden MR and Amstutz U and Carleton BC and CPNDS Clinical Practice Recommendations Group

DOI: 10.1111/bcp.13008 PubMed: 27197003

09 / 2016

A Tetra-Primer Amplification Refractory System Technique for the Cost-Effective and Novel Genotyping of Eight Single-Nucleotide Polymorphisms of the Catechol-O-Methyltransferase Gene.

Wang CK and Aleksic A and Xu MS and Procyshyn RM and Ross CJ and Vila-Rodriguez F and Ramos-Miguel A and Yan R and Honer WG and Barr AM

DOI: 10.1089/gtmb.2015.0304 PubMed: 27228319

08 / 2016

Clinical Practice Recommendations for the Management and Prevention of Cisplatin-Induced Hearing Loss Using Pharmacogenetic Markers.

Lee JW and Pussegoda K and Rassekh SR and Monzon JG and Liu G and Hwang S and Bhavsar AP and Pritchard S and Ross CJ and Amstutz U and Carleton BC and CPNDS Clinical Recommendations Group

DOI: 10.1097/ftd.0000000000000298 PubMed: 26960170

08 / 2016

NANS-mediated synthesis of sialic acid is required for brain and skeletal development.

van Karnebeek CD and Bonaf L and Wen XY and Tarailo-Graovac M and Balzano S and Royer-Bertrand B and Ashikov A and Garavelli L and Mammi I and Turolla L and Breen C and Donnai D and Cormier V and Heron D and Nishimura G and Uchikawa S and Campos-Xavier B and Rossi A and Hennet T and Brand-Arzamendi K

DOI: 10.1038/ng.3578 PubMed: 27213289

07 / 2016

Nuclear Receptor NR1H3 in Familial Multiple Sclerosis.

Wang Z and Sadovnick AD and Traboulsee AL and Ross JP and Bernales CQ and Encarnacion M and Yee IM and de Lemos M and Greenwood T and Lee JD and Wright G and Ross CJ and Zhang S and Song W and Vilario-Gell C

DOI: 10.1016/j.neuron.2016.04.039 PubMed: 27253448

06 / 2016

Exome Sequencing and the Management of Neurometabolic Disorders.

Tarailo-Graovac M and Shyr C and Ross CJ and Horvath GA and Salvarinova R and Ye XC and Zhang LH and Bhavsar AP and Lee JJ and Drgemller BI and Abdelsayed M and Alfadhel M and Armstrong L and Baumgartner MR and Burda P and Connolly MB and Cameron J and Demos M and Dewan T and Dionne J

DOI: 10.1056/nejmoa1515792 PubMed: 27276562

06 / 2016

De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome.

Langlois S and Tarailo-Graovac M and Sayson B and Drgemller B and Swenerton A and Ross CJ and Wasserman WW and van Karnebeek CD

DOI: 10.1038/ejhg.2015.217 PubMed: 26486474

06 / 2016

Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis.

Santra S and Cameron JM and Shyr C and Zhang L and Drgemller B and Ross CJ and Wasserman WW and Wevers RA and Rodenburg RJ and Gupte G and Preece MA and van Karnebeek CD

DOI: 10.1016/j.ymgme.2016.03.001 PubMed: 26971250

05 / 2016

Pharmacogenomics strategies to optimize treatments for multiple sclerosis: Insights from clinical research.

Progress in neurobiology

Grossman I and Knappertz V and Laifenfeld D and Ross C and Zeskind B and Kolitz S and Ladkani D and Hayardeny L and Loupe P and Laufer R and Hayden M

DOI: 10.1016/j.pneurobio.2016.02.001 PubMed: 26952809

03 / 2016

Forensic Investigation of Methadone Concentrations in Deceased Breastfed Infants.

Madadi P and Kelly LE and Ross CJ and Kepron C and Edwards JN and Koren G

DOI: 10.1111/1556-4029.12972 PubMed: 26513313

03 / 2016

Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In Vitro.

Cohen AS and Yap DB and Lewis ME and Chijiwa C and Ramos-Arroyo MA and Tkachenko N and Milano V and Fradin M and McKinnon ML and Townsend KN and Xu J and Van Allen MI and Ross CJ and Dobyns WB and Weaver DD and Gibson WT

DOI: 10.1002/humu.22946 PubMed: 26694085

03 / 2016

Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?

Horvath GA and Demos M and Shyr C and Matthews A and Zhang L and Race S and Stockler-Ipsiroglu S and Van Allen MI and Mancarci O and Toker L and Pavlidis P and Ross CJ and Wasserman WW and Trump N and Heales S and Pope S and Cross JH and van Karnebeek CD

DOI: 10.1016/j.ymgme.2015.11.008 PubMed: 26647175

01 / 2016

Genetic diversity of variants involved in drug response and metabolism in Sri Lankan populations: implications for clinical implementation of pharmacogenomics.

Chan SL and Samaranayake N and Ross CJ and Toh MT and Carleton B and Hayden MR and Teo YY and Dissanayake VH and Brunham LR

DOI: 10.1097/fpc.0000000000000182 PubMed: 26444257

01 / 2016

Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy.

Child neurology open

Lee JJY and van Karnebeek CDM and Drgemoller B and Shyr C and Tarailo-Graovac M and Eydoux P and Ross CJ and Wasserman WW and Bjrnson B and Wu JK

DOI: 10.1177/2329048x16669912 PubMed: 28503617

Huntingtin Haplotypes Provide Prioritized Target Panels for Allele-specific Silencing in Huntington Disease Patients of European Ancestry.

Kay C and Collins JA and Skotte NH and Southwell AL and Warby SC and Caron NS and Doty CN and Nguyen B and Griguoli A and Ross CJ and Squitieri F and Hayden MR

DOI: 10.1038/mt.2015.128 PubMed: 26201449

11 / 2015

The pharmacogenetics of codeine pain relief in the postpartum period.

Baber M and Chaudhry S and Kelly L and Ross C and Carleton B and Berger H and Koren G

DOI: 10.1038/tpj.2015.3 PubMed: 25752520

10 / 2015

RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement.

Janer A and van Karnebeek CD and Sasarman F and Antonicka H and Al Ghamdi M and Shyr C and Dunbar M and Stockler-Ispiroglu S and Ross CJ and Vallance H and Dionne J and Wasserman WW and Shoubridge EA

DOI: 10.1038/ejhg.2014.293 PubMed: 25604853

10 / 2015

A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer.

Aminkeng F and Bhavsar AP and Visscher H and Rassekh SR and Li Y and Lee JW and Brunham LR and Caron HN and van Dalen EC and Kremer LC and van der Pal HJ and Amstutz U and Rieder MJ and Bernstein D and Carleton BC and Hayden MR and Ross CJ and Canadian Pharmacogenomics Network for Drug Safety Consortium

DOI: 10.1038/ng.3374 PubMed: 26237429

09 / 2015

Development of a cost-efficient novel method for rapid, concurrent genotyping of five common single nucleotide polymorphisms of the brain derived neurotrophic factor (BDNF) gene by tetra-primer amplification refractory mutation system.

Wang CK and Xu MS and Ross CJ and Lo R and Procyshyn RM and Vila-Rodriguez F and White RF and Honer WG and Barr AM

DOI: 10.1002/mpr.1475 PubMed: 26118823

09 / 2015

Cisplatin Nephrotoxicity and Longitudinal Growth in Children With Solid Tumors: A Retrospective Cohort Study.

Jimnez-Triana CA and Casteln-Martnez OD and Rivas-Ruiz R and Jimnez-Mndez R and Medina A and Clark P and Rassekh R and Castaeda-Hernndez G and Carleton B and Medeiros M and Canadian Pharmacogenomics Network for Drug Safety Consortium

DOI: 10.1097/md.0000000000001413 PubMed: 26313789

08 / 2015

Clinical Practice Recommendations on Genetic Testing of CYP2C9 and VKORC1 Variants in Warfarin Therapy.

Shaw K and Amstutz U and Kim RB and Lesko LJ and Turgeon J and Michaud V and Hwang S and Ito S and Ross C and Carleton BC and CPNDS Clinical Recommendation Group

DOI: 10.1097/ftd.0000000000000192 PubMed: 26186657

08 / 2015

Genetic determinants of cocaine-associated agranulocytosis.

Buxton JA and Omura J and Kuo M and Ross C and Tzemis D and Purssell R and Gardy J and Carleton B

DOI: 10.1186/s13104-015-1219-4 PubMed: 26070312

06 / 2015

Association between regulatory advisories and codeine prescribing to postpartum women.

Smolina K and Weymann D and Morgan S and Ross C and Carleton B

DOI: 10.1001/jama.2015.3642 PubMed: 25965237

05 / 2015

Expansion of the QARS deficiency phenotype with report of a family with isolated supratentorial brain abnormalities.

Salvarinova R and Ye CX and Rossi A and Biancheri R and Roland EH and Pavlidis P and Ross CJ and Tarailo-Graovac M and Wasserman WW and van Karnebeek CD

DOI: 10.1007/s10048-014-0432-y PubMed: 25432320

04 / 2015

Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms.

Sirrs S and van Karnebeek CD and Peng X and Shyr C and Tarailo-Graovac M and Mandal R and Testa D and Dubin D and Carbonetti G and Glynn SE and Sayson B and Robinson WP and Han B and Wishart D and Ross CJ and Wasserman WW and Hurwitz TA and Sinclair G and Kaczocha M

DOI: 10.1186/s13023-015-0248-3 PubMed: 25885783

03 / 2015

Use of pharmacogenomics in pediatric renal transplant recipients.

Medeiros M and Castaeda-Hernndez G and Ross CJ and Carleton BC

DOI: 10.3389/fgene.2015.00041 PubMed: 25741362

Genetic variants in SLC22A17 and SLC22A7 are associated with anthracycline-induced cardiotoxicity in children.

Visscher H and Rassekh SR and Sandor GS and Caron HN and van Dalen EC and Kremer LC and van der Pal HJ and Rogers PC and Rieder MJ and Carleton BC and Hayden MR and Ross CJ and CPNDS consortium

DOI: 10.2217/pgs.15.61 PubMed: 26230641

The genotypic and phenotypic spectrum of PIGA deficiency.

Tarailo-Graovac M and Sinclair G and Stockler-Ipsiroglu S and Van Allen M and Rozmus J and Shyr C and Biancheri R and Oh T and Sayson B and Lafek M and Ross CJ and Robinson WP and Wasserman WW and Rossi A and van Karnebeek CD

DOI: 10.1186/s13023-015-0243-8 PubMed: 25885527

A single bout of high-intensity aerobic exercise facilitates response to paired associative stimulation and promotes sequence-specific implicit motor learning.

Mang CS and Snow NJ and Campbell KL and Ross CJ and Boyd LA

DOI: 10.1152/japplphysiol.00498.2014 PubMed: 25257866

12 / 2014

Pharmacogenomic diversity in Singaporean populations and Europeans.

Brunham LR and Chan SL and Li R and Aminkeng F and Liu X and Saw WY and Ong RT and Pillai EN and Carleton BC and Toh D and Tan SH and Koo SH and Lee EJ and Chia KS and Ross CJ and Hayden MR and Sung C and Teo YY

DOI: 10.1038/tpj.2014.22 PubMed: 24861855

12 / 2014

Hearing loss in Mexican children treated with cisplatin.

Casteln-Martnez OD and Jimnez-Mndez R and Rodrguez-Islas F and Fierro-Evans M and Vzquez-Gmez BE and Medina-Sansn A and Clark P and Carleton B and Ross C and Hildebrand C and Castaeda-Hernndez G and Rivas-Ruiz R

DOI: 10.1016/j.ijporl.2014.06.007 PubMed: 25037447

09 / 2014

Single point mutation in Rabenosyn-5 in a female with intractable seizures and evidence of defective endocytotic trafficking.

Stockler S and Corvera S and Lambright D and Fogarty K and Nosova E and Leonard D and Steinfeld R and Ackerley C and Shyr C and Au N and Selby K and van Allen M and Vallance H and Wevers R and Watkins D and Rosenblatt D and Ross CJ and Conibear E and Wasserman W and van Karnebeek C

DOI: 10.1186/s13023-014-0141-5 PubMed: 25233840

09 / 2014

Genetic markers of cisplatin-induced hearing loss in children.

Carleton BC and Ross CJ and Pussegoda K and Bhavsar AP and Visscher H and Lee JW and Brooks B and Rassekh SR and Dub MP and Hayden MR

DOI: 10.1038/clpt.2014.92 PubMed: 25141953

09 / 2014

Response to "evaluation of pharmacogenetic markers to predict the risk of Cisplatin-induced ototoxicity".

Carleton BC and Ross CJ and Bhavsar AP and Lee JW and Visscher H and Rassekh SR and Hayden MR

DOI: 10.1038/clpt.2014.90 PubMed: 24755913

08 / 2014

AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset.

Armstrong L and Biancheri R and Shyr C and Rossi A and Sinclair G and Ross CJ and Tarailo-Graovac M and Wasserman WW and van Karnebeek CD

DOI: 10.1007/s10048-014-0411-3 PubMed: 24958424

08 / 2014

The emerging era of pharmacogenomics: current successes, future potential, and challenges.

Lee JW and Aminkeng F and Bhavsar AP and Shaw K and Carleton BC and Hayden MR and Ross CJ

DOI: 10.1111/cge.12392 PubMed: 24684508

07 / 2014

VKORC1 and CYP2C9 genotypes are predictors of warfarin-related outcomes in children.

Shaw K and Amstutz U and Hildebrand C and Rassekh SR and Hosking M and Neville K and Leeder JS and Hayden MR and Ross CJ and Carleton BC

DOI: 10.1002/pbc.24932 PubMed: 24474498

06 / 2014

Codeine-related deaths: The role of pharmacogenetics and drug interactions.

Lam J and Woodall KL and Solbeck P and Ross CJ and Carleton BC and Hayden MR and Koren G and Madadi P

DOI: 10.1016/j.forsciint.2014.03.018 PubMed: 24747667

06 / 2014

Development of a broad-based ADME panel for use in pharmacogenomic studies.

Brown AM and Renaud Y and Ross C and Hansen M and Mongrain I and Valois D and Carleton BC and Hayden MR and Dub MP and Tardif JC and Phillips MS

DOI: 10.2217/pgs.14.81 PubMed: 25141894

06 / 2014

Higher frequency of genetic variants conferring increased risk for ADRs for commonly used drugs treating cancer, AIDS and tuberculosis in persons of African descent.

Aminkeng F and Ross CJ and Rassekh SR and Brunham LR and Sistonen J and Dube MP and Ibrahim M and Nyambo TB and Omar SA and Froment A and Bodo JM and Tishkoff S and Carleton BC and Hayden MR and Canadian Pharmacogenomics Network for Drug Safety Consortium

DOI: 10.1038/tpj.2013.13 PubMed: 23588107

04 / 2014

DNAJC13 mutations in Parkinson disease.

Vilario-Gell C and Rajput A and Milnerwood AJ and Shah B and Szu-Tu C and Trinh J and Yu I and Encarnacion M and Munsie LN and Tapia L and Gustavsson EK and Chou P and Tatarnikov I and Evans DM and Pishotta FT and Volta M and Beccano-Kelly D and Thompson C and Lin MK and Sherman HE

DOI: 10.1093/hmg/ddt570 PubMed: 24218364

04 / 2014

Role of TPMT and COMT genetic variation in cisplatin-induced ototoxicity.

Carleton BC and Ross CJ and Bhavsar AP and Amstutz U and Pussegoda K and Visscher H and Lee JW and Brooks B and Rassekh SR and Dub MP and Hayden MR

DOI: 10.1038/clpt.2013.219 PubMed: 24193170

03 / 2014

Mitochondrial carbonic anhydrase VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood.

van Karnebeek CD and Sly WS and Ross CJ and Salvarinova R and Yaplito-Lee J and Santra S and Shyr C and Horvath GA and Eydoux P and Lehman AM and Bernard V and Newlove T and Ukpeh H and Chakrapani A and Preece MA and Ball S and Pitt J and Vallance HD and Coulter-Mackie M and Nguyen H

DOI: 10.1016/j.ajhg.2014.01.006 PubMed: 24530203

03 / 2014

Pharmacogenetic-based efavirenz dose modification: suggestions for an African population and the different CYP2B6 genotypes.

PloS one

Mukonzo JK and Owen JS and Ogwal-Okeng J and Kuteesa RB and Nanzigu S and Sewankambo N and Thabane L and Gustafsson LL and Ross C and Aklillu E

DOI: 10.1371/journal.pone.0086919 PubMed: 24497997

01 / 2014

A novel recurrent mutation in ATP1A3 causes CAPOS syndrome.

Demos MK and van Karnebeek CD and Ross CJ and Adam S and Shen Y and Zhan SH and Shyr C and Horvath G and Suri M and Fryer A and Jones SJ and Friedman JM and FORGE Canada Consortium

DOI: 10.1186/1750-1172-9-15 PubMed: 24468074

01 / 2014

Exome sequencing pilot study in children with carbamazepine-induced serious skin reactions.

Amstutz U and Shyr C and Shear NH and Rieder MJ and Wasserman WW and Ross CJ and Carleton BC

DOI: 10.1186/2045-7022-4-s3-p119

Genetic markers of cisplatin-induced hearing loss in children

Clinical Advances in Hematology and Oncology

Carleton, B.C. and Ross, C.J. and Hayden, M.R.

Promoting neuroplasticity for motor rehabilitation after stroke: considering the effects of aerobic exercise and genetic variation on brain-derived neurotrophic factor.

Mang CS and Campbell KL and Ross CJ and Boyd LA

DOI: 10.2522/ptj.20130053 PubMed: 23907078

12 / 2013

Instructor comfort level in high-fidelity simulation.

Harder BN and Ross CJ and Paul P

DOI: 10.1016/j.nedt.2012.09.003 PubMed: 23025906

10 / 2013

Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children.

Pussegoda K and Ross CJ and Visscher H and Yazdanpanah M and Brooks B and Rassekh SR and Zada YF and Dub MP and Carleton BC and Hayden MR and CPNDS Consortium

DOI: 10.1038/clpt.2013.80 PubMed: 23588304

08 / 2013

Validation of variants in SLC28A3 and UGT1A6 as genetic markers predictive of anthracycline-induced cardiotoxicity in children.

Visscher H and Ross CJ and Rassekh SR and Sandor GS and Caron HN and van Dalen EC and Kremer LC and van der Pal HJ and Rogers PC and Rieder MJ and Carleton BC and Hayden MR and CPNDS Consortium

DOI: 10.1002/pbc.24505 PubMed: 23441093

08 / 2013

Putative association of ABCB1 2677G>T/A with oxycodone-induced central nervous system depression in breastfeeding mothers.

Lam J and Kelly L and Matok I and Ross CJ and Carleton BC and Hayden MR and Madadi P and Koren G

DOI: 10.1097/ftd.0b013e318288f158 PubMed: 23783165

08 / 2013

HLA-A 31:01 and HLA-B 15:02 as genetic markers for carbamazepine hypersensitivity in children.

Amstutz U and Ross CJ and Castro-Pastrana LI and Rieder MJ and Shear NH and Hayden MR and Carleton BC and CPNDS Consortium

DOI: 10.1038/clpt.2013.55 PubMed: 23588310

07 / 2013

From mutation identification to therapy: discovery and origins of the first approved gene therapy in the Western world.

Kastelein JJ and Ross CJ and Hayden MR

DOI: 10.1089/hum.2013.063 PubMed: 23578007

05 / 2013

Cancer pharmacogenomics in children: research initiatives and progress to date.

Rassekh SR and Ross CJ and Carleton BC and Hayden MR

DOI: 10.1007/s40272-013-0021-9 PubMed: 23529868

04 / 2013

Cancer Pharmacogenomics in Children

Cancer Genomics: From Bench to Personalized Medicine

Rassekh, S.R. and Ross, C.J.D.

DOI: 10.1016/B978-0-12-396967-5.00006-2

The Salmonella type III effector SspH2 specifically exploits the NLR co-chaperone activity of SGT1 to subvert immunity.

Bhavsar AP and Brown NF and Stoepel J and Wiermer M and Martin DD and Hsu KJ and Imami K and Ross CJ and Hayden MR and Foster LJ and Li X and Hieter P and Finlay BB

DOI: 10.1371/journal.ppat.1003518 PubMed: 23935490

A clinical tool for reducing central nervous system depression among neonates exposed to codeine through breast milk.

Kelly LE and Chaudhry SA and Rieder MJ and 't Jong G and Moretti ME and Lausman A and Ross C and Berger H and Carleton B and Hayden MR and Madadi P and Koren G

DOI: 10.1371/journal.pone.0070073 PubMed: 23922910

Clinical practice guideline: CYP2D6 genotyping for safe and efficacious codeine therapy

Journal of Population Therapeutics and Clinical Pharmacology

Madadi, P. and Amstutz, U. and Rieder, M. and Ito, S. and Fung, V. and Hwang, S. and Turgeon, J. and Michaud, V. and Koren, G. and Carleton, B.C. and Hayden, M.R. and Ross, C.J. and MacLeod, S. and Rassekh, R. and Lauder, G. and Smith, A. and Brunham, L. and Shear, N.H. and Liu, G. and Kim, R. and Maher, M. and Flockhart, D.

Erratum: Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy (Nature Genetics (2009) 41 (1345-1349))

Nature Genetics

Ross, C.J.D. and Katzov-Eckert, H. and Dub, M.-P. and Brooks, B. and Rassekh, S.R. and Barhdadi, A. and Feroz-Zada, Y. and Visscher, H. and Brown, A.M.K. and Rieder, M.J. and Rogers, P.C. and Phillips, M.S. and Carleton, B.C. and Hayden, M.R.

DOI: 10.1038/ng.0513-578

Pharmacogenomic investigation of adverse drug reactions(ADRs): the ADR prioritization tool, APT.

Shaw K and Amstutz U and Castro-Pastrana L and Loo TT and Ross CJ and Ito S and Reider MJ and Maher M and Macleod S and Koren G and Hayden MR and Carleton BC

PubMed: 23824325

Pharmacogenomic investigation of adverse drug reactions (ADRS): The ADR prioritization tool, APT

Journal of Population Therapeutics and Clinical Pharmacology

Shaw, K. and Amstutz, U. and Castro-Pastrana, L. and Loo, T.T. and Ross, C.J. and Ito, S. and Rieder, M.J. and Maher, M. and MacLeod, S. and Koren, G. and Hayden, M.R. and Carleton, B.C.

Life-threatening adverse events following therapeutic opioid administration in adults: is pharmacogenetic analysis useful?

Madadi P and Sistonen J and Silverman G and Gladdy R and Ross CJ and Carleton BC and Carvalho JC and Hayden MR and Koren G

DOI: 10.1155/2013/518012 PubMed: 23748253

Clinical practice guideline: CYP2D6 genotyping for safe and efficacious codeine therapy.

Madadi P and Amstutz U and Rieder M and Ito S and Fung V and Hwang S and Turgeon J and Michaud V and Koren G and Carleton BC and CPNDS Clinical Recommendations Group

PubMed: 24214521

Apnea and oxygen desaturations in children treated with opioids after adenotonsillectomy for obstructive sleep apnea syndrome: a prospective pilot study.

Khetani JD and Madadi P and Sommer DD and Reddy D and Sistonen J and Ross CJ and Carleton BC and Hayden MR and Koren G

DOI: 10.1007/bf03262421 PubMed: 23013460

12 / 2012

Postpartum maternal codeine therapy and the risk of adverse neonatal outcomes: the devil is in the details.

Lam J and Matlow JN and Ross CJ and Hayden MR and Carleton BC and Madadi P

DOI: 10.1097/ftd.0b013e31825da19f PubMed: 22777151

08 / 2012

Economic impact of a genetic test for cisplatin-induced ototoxicity.

Dionne F and Mitton C and Rassekh R and Brooks B and Ross C and Hayden M and Carleton B

DOI: 10.1038/tpj.2011.15 PubMed: 21502965

06 / 2012

Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin.

Brunham LR and Lansberg PJ and Zhang L and Miao F and Carter C and Hovingh GK and Visscher H and Jukema JW and Stalenhoef AF and Ross CJ and Carleton BC and Kastelein JJ and Hayden MR

DOI: 10.1038/tpj.2010.92 PubMed: 21243006

06 / 2012

More codeine fatalities after tonsillectomy in North American children.

Kelly LE and Rieder M and van den Anker J and Malkin B and Ross C and Neely MN and Carleton B and Hayden MR and Madadi P and Koren G

DOI: 10.1542/peds.2011-2538 PubMed: 22492761

05 / 2012

Pharmacogenomic prediction of anthracycline-induced cardiotoxicity in children.

Visscher H and Ross CJ and Rassekh SR and Barhdadi A and Dub MP and Al-Saloos H and Sandor GS and Caron HN and van Dalen EC and Kremer LC and van der Pal HJ and Brown AM and Rogers PC and Phillips MS and Rieder MJ and Carleton BC and Hayden MR and Canadian Pharmacogenomics Network for Drug Safety Consortium

DOI: 10.1200/jco.2010.34.3467 PubMed: 21900104

05 / 2012

Prediction of codeine toxicity in infants and their mothers using a novel combination of maternal genetic markers.

Sistonen J and Madadi P and Ross CJ and Yazdanpanah M and Lee JW and Landsmeer ML and Nauta M and Carleton BC and Koren G and Hayden MR

DOI: 10.1038/clpt.2011.280 PubMed: 22398969

04 / 2012

Suspected opioid overdose case resolved by CYP2D6 genotyping.

Shaw KD and Amstutz U and Jimenez-Mendez R and Ross CJ and Carleton BC

DOI: 10.1097/ftd.0b013e31824a1e21 PubMed: 22406651

04 / 2012

Apnea and oxygen desaturations in children treated with opioids after adenotonsillectomy for obstructive sleep apnea syndrome: A prospective pilot study

Pediatric Drugs

Khetani, J.D. and Madadi, P. and Sommer, D.D. and Reddy, D. and Sistonen, J. and Ross, C.J.D. and Carleton, B.C. and Hayden, M.R. and Koren, G.

DOI: 10.2165/11633570

Erratum: Economic impact of a genetic test for cisplatin-induced ototoxicity (The Pharmacogenomics Journal (2012) 12 (205-213) DOI: 10.1038/tpj.2011.15)

Pharmacogenomics Journal

Dionne, F. and Mitton, C. and Rassekh, R. and Brooks, B. and Ross, C. and Hayden, M. and Carleton, B.

DOI: 10.1038/tpj.2011.21

Pharmacogenomics of cardiovascular drugs and adverse effects in pediatrics.

Visscher H and Amstutz U and Sistonen J and Ross CJ and Hayden MR and Carleton BC

DOI: 10.1097/fjc.0b013e3182163b82 PubMed: 21386709

09 / 2011

CYP2D6 polymorphisms and codeine analgesia in postpartum pain management: a pilot study.

VanderVaart S and Berger H and Sistonen J and Madadi P and Matok I and Gijsen VM and de Wildt SN and Taddio A and Ross CJ and Carleton BC and Hayden MR and Koren G

DOI: 10.1097/ftd.0b013e3182272b10 PubMed: 21743374

08 / 2011

HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia.

Warby SC and Visscher H and Collins JA and Doty CN and Carter C and Butland SL and Hayden AR and Kanazawa I and Ross CJ and Hayden MR

DOI: 10.1038/ejhg.2010.229 PubMed: 21248742

05 / 2011

Pharmacogenomics of serious adverse drug reactions in pediatric oncology

Journal of Population Therapeutics and Clinical Pharmacology

Ross, C.J.D. and Visscher, H. and Rod Rassekh, S. and Castro-Pastrana, L.I. and Shereck, E. and Carleton, B. and Hayden, M.R.

Amelioration of hypertriglyceridemia with hypo-alpha-cholesterolemia in LPL deficient mice by hematopoietic cell-derived LPL.

Ding Y and Zhang L and Wang Y and Huang W and Tang Y and Bai L and Ross CJ and Hayden MR and Liu G

DOI: 10.1371/journal.pone.0025620 PubMed: 21980507

Pharmacogenomics of serious adverse drug reactions in pediatric oncology.

Ross CJ and Visscher H and Rassekh SR and Castro-Pastrana LI and Shereck E and Carleton B and Hayden MR

PubMed: 21467604

The communication of pharmacogenetic research results: Participants weigh in on their informational needs in a pilot study

Journal of Population Therapeutics and Clinical Pharmacology

Madadi, P. and Joly, Y. and Avard, D. and Chitayat, D.C. and Smith, M.A. and Ross, C.J.D. and Carleton, B.C. and Hayden, M.R. and Koren, G.

Communicating pharmacogenetic research results to breastfeeding mothers taking codeine: a pilot study of perceptions and benefits.

Madadi P and Joly Y and Avard D and Chitayat DC and Smith MA and Ross CJ and Carleton BC and Hayden MR and Koren G

DOI: 10.1038/clpt.2010.125 PubMed: 20739920

12 / 2010

Fatal hydrocodone overdose in a child: pharmacogenetics and drug interactions.

Madadi P and Hildebrandt D and Gong IY and Schwarz UI and Ciszkowski C and Ross CJ and Sistonen J and Carleton BC and Hayden MR and Lauwers AE and Koren G

DOI: 10.1542/peds.2009-1907 PubMed: 20837591

10 / 2010

Pharmacogenomics and active surveillance for serious adverse drug reactions in children.

Loo TT and Ross CJ and Sistonen J and Visscher H and Madadi P and Koren G and Hayden MR and Carleton BC

DOI: 10.2217/pgs.10.111 PubMed: 20860467

09 / 2010

Ultrasound-guided sacroiliac joint injection in patients with established sacroiliitis: precise IA injection verified by MRI scanning does not predict clinical outcome.

Hartung W and Ross CJ and Straub R and Feuerbach S and Schlmerich J and Fleck M and Herold T

DOI: 10.1093/rheumatology/kep424 PubMed: 20019067

08 / 2010

The Canadian Pharmacogenomics Network for Drug Safety: a model for safety pharmacology.

Ross CJ and Visscher H and Sistonen J and Brunham LR and Pussegoda K and Loo TT and Rieder MJ and Koren G and Carleton BC and Hayden MR and CPNDS Consortium

DOI: 10.1089/thy.2010.1642 PubMed: 20578893

07 / 2010

Prenatal effects of selective serotonin reuptake inhibitor antidepressants, serotonin transporter promoter genotype (SLC6A4), and maternal mood on child behavior at 3 years of age.

Archives of pediatrics & adolescent medicine

Oberlander TF and Papsdorf M and Brain UM and Misri S and Ross C and Grunau RE

DOI: 10.1001/archpediatrics.2010.51 PubMed: 20439795

05 / 2010

The importance of XRCC2 in RAD51-related DNA damage repair.

Tambini CE and Spink KG and Ross CJ and Hill MA and Thacker J

DOI: 10.1016/j.dnarep.2010.01.016 PubMed: 20189471

05 / 2010

Perceptions about self-management among people with severe asthma.

Ross CJ and Williams BA and Low G and Vethanayagam D

DOI: 10.3109/02770901003611462 PubMed: 20394519

04 / 2010

Cases: Cocaine adulterant linked to neutropenia.

Wiens MO and Son WK and Ross C and Hayden M and Carleton B

DOI: 10.1503/cmaj.090286 PubMed: 19969562

01 / 2010

Glucose intolerance and decreased early insulin response in mice with severe hypertriglyceridemia.

Experimental biology and medicine (Maywood, N.J.)

Ding YL and Wang YH and Huang W and Liu G and Ross C and Hayden MR and Yang JK

DOI: 10.1258/ebm.2009.009100 PubMed: 20404017

01 / 2010

Characterization of microvascularization of liver tumor lesions with high resolution linear ultrasound and contrast enhanced ultrasound (CEUS) during surgery: First results.

Jung EM and Ross CJ and Rennert J and Scherer MN and Farkas S and von Breitenbuch P and Schnitzbauer AA and Piso P and Lamby P and Menzel C and Schreyer AG and Feuerbach S and Schlitt HJ and Loss M

DOI: 10.3233/ch-2010-1336 PubMed: 21135485

Study of Heart and Renal Protection (SHARP): Randomized trial to assess the effects of lowering low-density lipoprotein cholesterol among 9,438 patients with chronic kidney disease

American Heart Journal

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and Langham, R. and Englebright, B. and Giang, M. and Lanteri, M. and Mullins, K. and Turner, C. and Collett, P. and Stokoe, S. and Sutherland, K. and Talafua, D. and Talaulikar, G. and Clarkson, A. and Rees, C. and Carney, G. and Falk, M. and Gracey, D. and Jadeer, A. and Johnson, P. and Karpe, K. and Singer, R. and Walters, G. and McDonald, S. and Burgess, J. and Fischer, K. and Gentgall, M. and Hockley, M. and Veitch, D. and De Jersey, P. and Gillam, A. and Hartig, V. and Holland, K. and McArdle, J. and Washington, W. and Rangan, G. and Mikaheal, M. and Murie, P. and Perez, N. and Punnoose, N. and Smolonogov, T. and Taler, N. and Williams, G. and Wen, C. and Kohlhagen, J. and Wessels, J. and Johnson, S. and Reid, A. and Ryan, J. and Taprell, D. and Auinger, M. and Eigner, M. and Kodras, K. and Leithner, C. and Magpantay, L. and Marterer, C. and Prager, R. and Prinz, C. and Seiringer, E. and Kramar, R. and Mitter, E. and Stummvoll, H. and Dieplinger, G. and Wenzel, R. and Stolz, G. 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DOI: 10.1016/j.ahj.2010.08.012

Application of principal component analysis to pharmacogenomic studies in Canada.

Visscher H and Ross CJ and Dub MP and Brown AM and Phillips MS and Carleton BC and Hayden MR

DOI: 10.1038/tpj.2009.36 PubMed: 19652663

12 / 2009

Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.

Ross CJ and Katzov-Eckert H and Dub MP and Brooks B and Rassekh SR and Barhdadi A and Feroz-Zada Y and Visscher H and Brown AM and Rieder MJ and Rogers PC and Phillips MS and Carleton BC and Hayden MR and CPNDS Consortium

DOI: 10.1038/ng.478 PubMed: 19898482

12 / 2009

Adverse drug reaction active surveillance: developing a national network in Canada's children's hospitals.

Carleton B and Poole R and Smith M and Leeder J and Ghannadan R and Ross C and Phillips M and Hayden M

DOI: 10.1002/pds.1772 PubMed: 19507171

08 / 2009

Enhanced atherothrombotic formation after oxidative injury by FeCl3 to the common carotid artery in severe combined hyperlipidemic mice.

Biochemical and biophysical research communications

Xian X and Ding Y and Zhang L and Wang Y and McNutt MA and Ross C and Hayden MR and Deng X and Liu G

DOI: 10.1016/j.bbrc.2009.05.101 PubMed: 19481534

05 / 2009

Plasma apolipoprotein AV levels in mice are positively associated with plasma triglyceride levels.

Vaessen SF and Dallinga-Thie GM and Ross CJ and Splint LJ and Castellani LW and Rensen PC and Hayden MR and Schaap FG and Kuivenhoven JA

DOI: 10.1194/jlr.m800551-jlr200 PubMed: 19141870

05 / 2009

Presynaptic defects underlying impaired learning and memory function in lipoprotein lipase-deficient mice.

Xian X and Liu T and Yu J and Wang Y and Miao Y and Zhang J and Yu Y and Ross C and Karasinska JM and Hayden MR and Liu G and Chui D

DOI: 10.1523/jneurosci.0297-09.2009 PubMed: 19357293

04 / 2009

Enhanced susceptibility to pancreatitis in severe hypertriglyceridaemic lipoprotein lipase-deficient mice and agonist-like function of pancreatic lipase in pancreatic cells.

Wang Y and Sternfeld L and Yang F and Rodriguez JA and Ross C and Hayden MR and Carriere F and Liu G and Hofer W and Schulz I

DOI: 10.1136/gut.2007.146258 PubMed: 18936103

03 / 2009

Acute hypertriglyceridemic pancreatitis during pregnancy due to homozygous lipoprotein lipase gene mutation.

Bartha I and Dinya T and Seres I and Paragh G and Ross C and Hayden MR and Bir S and Vargha G

DOI: 10.1016/j.cca.2008.10.016 PubMed: 19000906

02 / 2009

Pharmacogenetics of neonatal opioid toxicity following maternal use of codeine during breastfeeding: a case-control study.

Madadi P and Ross CJ and Hayden MR and Carleton BC and Gaedigk A and Leeder JS and Koren G

DOI: 10.1038/clpt.2008.157 PubMed: 18719619

01 / 2009

The role of free fatty acids, pancreatic lipase and Ca+ signalling in injury of isolated acinar cells and pancreatitis model in lipoprotein lipase-deficient mice.

Yang F and Wang Y and Sternfeld L and Rodriguez JA and Ross C and Hayden MR and Carriere F and Liu G and Schulz I

DOI: 10.1111/j.1748-1716.2008.01933.x PubMed: 18983441

01 / 2009

Genotypic Approaches to Therapy in Children (GATC): Using information technology to improve drug safety

Studies in Health Technology and Informatics

Wong, E. and Carleton, B.C. and Wright, D.F.B. and Smith, M.A. and Verbeek, L. and Hildebrand, C.A. and Stannard, P. and Vaillancourt, R. and Elliot-Miller, P. and Ross, C.J.D. and Hayden, M.R.

DOI: 10.3233/978-1-58603-979-0-209

Genotypic Approaches to Therapy in Children (GATC): using information technology to improve drug safety.

Wong E and Carleton BC and Wright DF and Smith MA and Verbeek L and Hildebrand CA and Stannard P and Vaillancourt R and Elliot-Miller P and Ross CJ and Hayden MR

PubMed: 19380938

Intramuscular administration of AAV1-lipoprotein lipase S447X lowers triglycerides in lipoprotein lipase-deficient patients.

Stroes ES and Nierman MC and Meulenberg JJ and Franssen R and Twisk J and Henny CP and Maas MM and Zwinderman AH and Ross C and Aronica E and High KA and Levi MM and Hayden MR and Kastelein JJ and Kuivenhoven JA

DOI: 10.1161/atvbaha.108.175620 PubMed: 18802015

12 / 2008

Spontaneous atherosclerosis in aged lipoprotein lipase-deficient mice with severe hypertriglyceridemia on a normal chow diet.

Zhang X and Qi R and Xian X and Yang F and Blackstein M and Deng X and Fan J and Ross C and Karasinska J and Hayden MR and Liu G

DOI: 10.1161/circresaha.107.156554 PubMed: 18032735

02 / 2008

Infant serotonin transporter (SLC6A4) promoter genotype is associated with adverse neonatal outcomes after prenatal exposure to serotonin reuptake inhibitor medications.

Oberlander TF and Bonaguro RJ and Misri S and Papsdorf M and Ross CJ and Simpson EM

DOI: 10.1038/sj.mp.4002007 PubMed: 17519929

01 / 2008

Genotypic approaches to therapy in children: a national active surveillance network (GATC) to study the pharmacogenomics of severe adverse drug reactions in children.

Ross CJ and Carleton B and Warn DG and Stenton SB and Rassekh SR and Hayden MR

DOI: 10.1196/annals.1423.020 PubMed: 17911433

09 / 2007

Screening and assessing adolescent asthmatics for anxiety disorders.

Ross CJ and Davis TM and Hogg DY

DOI: 10.1177/1054773806295235 PubMed: 17204805

02 / 2007

Expression of LPL in endothelial-intact artery results in lipid deposition and vascular cell adhesion molecule-1 upregulation in both LPL and ApoE-deficient mice.

Wang J and Xian X and Huang W and Chen L and Wu L and Zhu Y and Fan J and Ross C and Hayden MR and Liu G

DOI: 10.1161/01.atv.0000249683.80414.d9 PubMed: 17038632

01 / 2007

Pharmacogenomics and its implications for autoimmune disease.

Ross CJ and Katzov H and Carleton B and Hayden MR

DOI: 10.1016/j.jaut.2007.02.008 PubMed: 17418528

Volumetric cartilage measurements of porcine knee at 1.5-T and 3.0-T MR imaging: evaluation of precision and accuracy.

Bauer JS and Krause SJ and Ross CJ and Krug R and Carballido-Gamio J and Ozhinsky E and Majumdar S and Link TM

DOI: 10.1148/radiol.2412051330 PubMed: 17057067

11 / 2006

Elevated plasma triglyceride levels precede amyloid deposition in Alzheimer's disease mouse models with abundant A beta in plasma.

Burgess BL and McIsaac SA and Naus KE and Chan JY and Tansley GH and Yang J and Miao F and Ross CJ and van Eck M and Hayden MR and van Nostrand W and St George-Hyslop P and Westaway D and Wellington CL

DOI: 10.1016/j.nbd.2006.06.007 PubMed: 16899370

10 / 2006

Lipoprotein lipase S447X: a naturally occurring gain-of-function mutation.

Rip J and Nierman MC and Ross CJ and Jukema JW and Hayden MR and Kastelein JJ and Stroes ES and Kuivenhoven JA

DOI: 10.1161/01.atv.0000219283.10832.43 PubMed: 16574898

06 / 2006

Correction of feline lipoprotein lipase deficiency with adeno-associated virus serotype 1-mediated gene transfer of the lipoprotein lipase S447X beneficial mutation.

Ross CJ and Twisk J and Bakker AC and Miao F and Verbart D and Rip J and Godbey T and Dijkhuizen P and Hermens WT and Kastelein JJ and Kuivenhoven JA and Meulenberg JM and Hayden MR

DOI: 10.1089/hum.2006.17.487 PubMed: 16716106

05 / 2006

Hemorheological abnormalities in lipoprotein lipase deficient mice with severe hypertriglyceridemia.

Zhao T and Guo J and Li H and Huang W and Xian X and Ross CJ and Hayden MR and Wen Z and Liu G

DOI: 10.1016/j.bbrc.2006.01.067 PubMed: 16460682

03 / 2006

In response [5]

Arteriosclerosis, Thrombosis, and Vascular Biology

Ross, C.J.D. and Twisk, J. and Kuivenhoven, J.A. and Rip, J. and Kastelein, J.J. and Hayden, M.R.

DOI: 10.1161/01.ATV.0000203502.01793.8d

Gene therapy for lipoprotein lipase deficiency: working toward clinical application.

Rip J and Nierman MC and Sierts JA and Petersen W and Van den Oever K and Van Raalte D and Ross CJ and Hayden MR and Bakker AC and Dijkhuizen P and Hermens WT and Twisk J and Stroes E and Kastelein JJ and Kuivenhoven JA and Meulenberg JM

DOI: 10.1089/hum.2005.16.1276 PubMed: 16259561

11 / 2005

Complete rescue of lipoprotein lipase-deficient mice by somatic gene transfer of the naturally occurring LPLS447X beneficial mutation.

Ross CJ and Liu G and Kuivenhoven JA and Twisk J and Rip J and van Dop W and Excoffon KJ and Lewis SM and Kastelein JJ and Hayden MR

DOI: 10.1161/01.atv.0000176971.27302.b0 PubMed: 16002740

10 / 2005

Cognitive-behavioral treatment combined with asthma education for adults with asthma and coexisting panic disorder.

Ross CJ and Davis TM and MacDonald GF

DOI: 10.1177/1054773804273863 PubMed: 15793272

05 / 2005

Gene therapy provides hope for the treatment of arthritis

Clinical Genetics

Ross, C.J.D.

DOI: 10.1111/j.1399-0004.2005.0507b.x

Coagulating evidence for a new genetic link to drug responsiveness to warfarin therapy

Clinical Genetics

Ross, C.J.D.

DOI: 10.1111/j.1399-0004.2005.0507a.x

Long-term correction of murine lipoprotein lipase deficiency with AAV1-mediated gene transfer of the naturally occurring LPL(S447X) beneficial mutation.

Ross CJ and Twisk J and Meulenberg JM and Liu G and van den Oever K and Moraal E and Hermens WT and Rip J and Kastelein JJ and Kuivenhoven JA and Hayden MR

DOI: 10.1089/hum.2004.15.906 PubMed: 15353045

09 / 2004

Alterations of plasma lipids in mice via adenoviral-mediated hepatic overexpression of human ABCA1.

Wellington CL and Brunham LR and Zhou S and Singaraja RR and Visscher H and Gelfer A and Ross C and James E and Liu G and Huber MT and Yang YZ and Parks RJ and Groen A and Fruchart-Najib J and Hayden MR

DOI: 10.1194/jlr.m300110-jlr200 PubMed: 12730295

08 / 2003

Screening and assessing adult asthmatics for anxiety disorders.

Davis TM and Ross CJ and MacDonald GF

DOI: 10.1177/105477380201100206 PubMed: 11991171

05 / 2002

Treatment of hemophilia B in mice with nonautologous somatic gene therapeutics.

Van Raamsdonk JM and Ross CJ and Potter MA and Kurachi S and Kurachi K and Stafford DW and Chang PL

DOI: 10.1067/mlc.2002.120649 PubMed: 11873243

01 / 2002

Development of small alginate microcapsules for recombinant gene product delivery to the rodent brain.

Ross CJ and Chang PL

DOI: 10.1163/156856202320401988 PubMed: 12463513

Somatic gene therapy for a neurodegenerative disease using microencapsulated recombinant cells.

Ross CJ and Ralph M and Chang PL

DOI: 10.1006/exnr.2000.7531 PubMed: 11085893

12 / 2000

Treatment of a lysosomal storage disease, mucopolysaccharidosis VII, with microencapsulated recombinant cells.

Ross CJ and Bastedo L and Maier SA and Sands MS and Chang PL

DOI: 10.1089/104303400750001426 PubMed: 11044913

10 / 2000

Delivery of recombinant gene products to the central nervous system with nonautologous cells in alginate microcapsules.

Ross CJ and Ralph M and Chang PL

DOI: 10.1089/10430349950019183 PubMed: 10022530

01 / 1999

Encapsulation of various recombinant mammalian cell types in different alginate microcapsules.

Peirone M and Ross CJ and Hortelano G and Brash JL and Chang PL

DOI: 10.1002/(sici)1097-4636(19981215)42:4u003C587::aid-jbm15u003E3.0.co;2-x PubMed: 9827683

12 / 1998

A sequence-ready physical map of a region of 12q24.1.

Renault B and Hovnanian A and Bryce S and Chang JJ and Lau S and Sakuntabhai A and Monk S and Carter S and Ross CJ and Pang J and Twells R and Chamberlain S and Monaco AP and Strachan T and Kucherlapati R

DOI: 10.1006/geno.1997.4888 PubMed: 9344649

10 / 1997

Risk factors for nephropathy and cardiovascular disease in diabetic Northern Minnesota American Indians

Clinical Nephrology

Hirata-Dulas, C.A.I. and Rith-Najarian, S.J. and McIntyre, M.C. and Ross, C. and Dahl, D.C. and Keane, W.F. and Kasiske, B.L.

Canadian Pharmacogenomic Network for Drug Safety (CPNDS)

Canadian Institutes for Health Research (CIHR), Canada Foundation for Innovation (CFI), Genome British Columbia

The goal of CPNDS is to prevent adverse drug reactions (ADRs) in childhood by identifying predictive genomic markers for specific ADRs. Within five years, CPNDS intends to incorporate these markers into diagnostic tools that will be used to predict and prevent ADRs in children through specific dosing recommendations for commonly used drugs based on an individual's genetic make-up. The long-term goal for this project is to develop a user-friendly, and effective ADR monitoring tool and national database, to proactively prevent adverse drug reactions in susceptible children.

Specific projects seek to identify the key causal genetic factors of serious ADRs in children, including severe hearing loss caused by cisplatin chemotherapy; a lethal reaction to codeine in newborns and young children, anthracycline-induced heart failure, vincristine-induced peripheral neurotoxicity and drug-induced severe rash.

Grants

2020-2025 NRC gene therapy

2023-2028 CIHR Project Genome Editing

2022-2024 NMIN Gene Therapy Grand Challenge Award

2018-2024 Genome Canada Canadian Pharmacogenomics Network for Drug Safety ‘GO PGx’

Honours & Awards

New Investigator Award, Canadian Institutes of Health Research

Michael Smith Foundation Scholar Award

Gene Cure Foundation Champion of Genetics Award

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