Wendy Robinson

Characterizing placental dysfunction with DNA methylation profiling and placental histopathology

Placenta

Hannah J. Illing and Alexa A. Freedman and Ella O. Beraldo and Lauren Keenan-Devlin and Gregory E. Miller and Ann E. Borders and Wendy P. Robinson and Linda M. Ernst

03 / 2026

Exposure to prenatal maternal stress is associated with epigenetic age acceleration and altered cell composition in the placenta: The QF2011 Queensland Flood Study

Placenta

Ella O. Beraldo and Amy M. Inkster and Maria S. Peaherrera and E Magda Price and Johanna Schuetz and lodie Portales-Casamar and Sue Kildea and Cathy Vaillancourt and Suzanne King and Wendy P. Robinson

11 / 2025

Some lessons learned from genomic and epigenomic studies of the placenta

Placenta

Amy M. Inkster and Hannah J. Illing and Wendy P. Robinson

04 / 2025

eoPred: Predicting the placental phenotype of early-onset preeclampsia using DNA methylation

I. Fernndez-Boyano and A.M. Inkster and V. Yuan and W.P. Robinson

05 / 2023

Single-cell assessment of trophoblast stem cell-based organoids as human placenta-modeling platforms

Matthew J. Shannon and Gina L. McNeill and Burak Koksal and Jennet Baltayeva and Jasmin Wchter and Barbara Castellana and Maria S. Peaherrera and Wendy P. Robinson and Peter C. K. Leung and Alexander G. Beristain

11 / 2022

Sex-dependent placental mQTL provide insight into the prenatal origins of childhood-onset traits and conditions

William Casazza and Amy M. Inkster and Giulia F. Del Gobbo and Victor Yuan and Fabien Delahaye and Carmen Marsit and Yongjin P. Park and Wendy P. Robinson and Sara Mostafavi and Jessica K Dennis

10 / 2022

Are sex differences in cognitive impairment reflected in epigenetic age acceleration metrics?

Neurobiology of Aging

Amy M. Inkster and Paula Duarte-Guterman and Arianne Y. Albert and Cindy K. Barha and Liisa A.M. Galea and Wendy P. Robinson

01 / 2022

Genomic imbalances in the placenta are associated with poor fetal growth

Molecular Medicine

Giulia F. Del Gobbo and Yue Yin and Sanaa Choufani and Emma A. Butcher and John Wei and Evica Rajcan-Separovic and Hayley Bos and Peter von Dadelszen and Rosanna Weksberg and Wendy P. Robinson and Ryan K. C. Yuen

12 / 2021

A cross-cohort analysis of autosomal DNA methylation sex differences in the term placenta

Biology of Sex Differences

Amy M. Inkster and Victor Yuan and Chaini Konwar and Allison M. Matthews and Carolyn J. Brown and Wendy P. Robinson

12 / 2021

Cell-specific characterization of the placental methylome

BMC Genomics

Victor Yuan and Desmond Hui and Yifan Yin and Maria S. Peaherrera and Alexander G. Beristain and Wendy P. Robinson

12 / 2021

Mistakes Are Common; Should We Worry about Them?

Trends in Molecular Medicine

Wendy P. Robinson and Giulia F. Del Gobbo

08 / 2021

Sex Differences Are Here to Stay: Relevance to Prenatal Care

Journal of Clinical Medicine

Amy Inkster and Icar Fernndez-Boyano and Wendy Robinson

07 / 2021

Confined placental mosaicism involving multiple de novo copy number variants associated with fetal growth restriction: A case report

American Journal of Medical Genetics Part A

Giulia F. Del Gobbo and Victor Yuan and Wendy P. Robinson

06 / 2021

The significance of the placental genome and methylome in fetal and maternal health

Human Genetics

Giulia F. Del Gobbo and Chaini Konwar and Wendy P. Robinson

09 / 2020

Genomic Imbalances in the Placenta Contribute to Poor Fetal Growth

Giulia F. Del Gobbo and Yue Yin and Sanaa Choufani and Emma A. Butcher and John Wei and Evica Rajcan-Separovic and Hayley Bos and Peter von Dadelszen and Rosanna Weksberg and Wendy P Robinson and Ryan K.C. Yuen

07 / 2020

Low oxygen enhances trophoblast column growth by potentiating differentiation of the extravillous lineage and promoting LOX activity

Development

Jenna Treissman and Victor Yuan and Jennet Baltayeva and Hoa T. Le and Barbara Castellana and Wendy P. Robinson and Alexander G. Beristain

01 / 2020

Association of a placental Interleukin-6 genetic variant (rs1800796) with DNA methylation, gene expression and risk of acute chorioamnionitis

BMC Medical Genetics

Chaini Konwar and Giulia F. Del Gobbo and Jefferson Terry and Wendy P. Robinson

12 / 2019

Accurate ethnicity prediction from placental DNA methylation data

Epigenetics & Chromatin

Victor Yuan and E. Magda Price and Giulia Del Gobbo and Sara Mostafavi and Brian Cox and Alexandra M. Binder and Karin B. Michels and Carmen Marsit and Wendy P. Robinson

12 / 2019

Considerations when processing and interpreting genomics data of the placenta

Placenta

Chaini Konwar and Giulia Del Gobbo and Victor Yuan and Wendy P. Robinson

09 / 2019

Inflammation and epigenetic age in Alzheimers disease: do sex and APOE matter?

Paula Duarte-Guterman and Amy M. Inkster and Arianne Y. Albert and Cindy K. Barha and Wendy P. Robinson and Liisa A.M. Galea

08 / 2019

Altered levels of placental miR-338-3p and miR-518b are associated with acute chorioamnionitis and IL6 genotype

Placenta

Chaini Konwar and Irina Manokhina and Jefferson Terry and Amy M. Inkster and Wendy P. Robinson

07 / 2019

Low oxygen enhances trophoblast column growth by potentiating the extravillous lineage and promoting LOX activity

Jenna Treissman and Victor Yuan and Jennet Baltayeva and Hoa T. Le and Barbara Castellana and Wendy P. Robinson and Alexander G. Beristain

06 / 2019

Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication

European Journal of Medical Genetics

Ying Qiao and Hani Bagheri and Flamingo Tang and Chansonette Badduke and Sally Martell and Suzanne M.E. Lewis and Wendy Robinson and Mary B. Connolly and Laura Arbour and Evica Rajcan-Separovic

02 / 2019

DNA methylation profiling of acute chorioamnionitis-associated placentas and fetal membranes: insights into epigenetic variation in spontaneous preterm births

Epigenetics & Chromatin

Chaini Konwar and E. Magda Price and Li Qing Wang and Samantha L. Wilson and Jefferson Terry and Wendy P. Robinson

12 / 2018

Differences in DNA methylation of white blood cell types at birth and in adulthood reflect postnatal immune maturation and influence accuracy of cell type prediction

Jones M and Dinh L and Razzaghian HR and de Goede O and MacIsaac JL and Morin AM and Gervin K and Ng R and Duijts L and van Zelm MC and Moll HA and Lyle R and Robinson WP and Koestler DC and Kobor MS

08 / 2018

Utility of DNA methylation to assess placental health

Placenta

Wilson, Samantha L. and Robinson, Wendy P.

Mining DNA methylation alterations towards a classification of placental pathologies

Human Molecular Genetics

Wilson, Samantha L. and Leavey, Katherine and Cox, Brian J. and Robinson, Wendy P.

Adjusting for Batch Effects in DNA Methylation Microarray Data, a Lesson Learned

Frontiers in Genetics

Price, E. M. and Robinson, Wendy P.

Epigenetic regulation of placental gene expression in transcriptional subtypes of preeclampsia

Clinical Epigenetics

Leavey, Katherine and Wilson, Samantha L. and Bainbridge, Shannon A. and Robinson, Wendy P. and Cox, Brian J.

No evidence for association of MTHFR 677C > T and 1298A > C variants with placental DNA methylation

Clinical Epigenetics

Del Gobbo, Giulia F. and Price, E. Magda and Hanna, Courtney W. and Robinson, Wendy P.

Child mortality, hypothalamic-pituitaryadrenal axis activity and cellular aging in mothers

Plos One

Barha, Cindy K. and Salvante, Katrina G. and Hanna, Courtney W. and Wilson, Samantha L. and Robinson, Wendy P. and Altman, Rachel M. and Nepomnaschy, Pablo A.

Effect of Maternal Depression and Prenatal Antidepressant Exposure on Placental Serotoninergic and Glucocorticoids Systems Methylation

Birth Defects Research

Laurent, L. and Penaherrera, M. and Robinson, W. P. and Oberlander, T. F. and Vaillancourt, C.

An empirically driven data reduction method on the human 450K methylation array to remove tissue specific non-variable CpGs

Clinical Epigenetics

Edgar, Rachel D. and Jones, Meaghan J. and Robinson, Wendy P. and Kobor, Michael S.

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, A. M. and Tarailo-Graovac, M. and Price, E. M. and Blydt-Hansen, I. and Ghani, A. and Drogemoller, B. I. and Robinson, W. P. and Ross, C. J. and Wasserman, W. W. and Siden, H. and van Karnebeek, C. D.

Review: placental biomarkers for assessing fetal health

Human Molecular Genetics

Manokhina, Irina and Del Gobbo, Giulia F. and Konwar, Chaini and Wilson, Samantha L. and Robinson, Wendy P.

Cell-Free Placental DNA in Maternal Plasma in Relation to Placental Health and Function

Fetal Diagnosis and Therapy

Manokhina, Irina and Singh, Tanjot K. and Robinson, Wendy P.

Whole exome sequencing of families with 1q21.1 microdeletion or microduplication

American Journal of Medical Genetics Part a

Qiao, Ying and Badduke, Chansonette and Tang, Flamingo and Cowieson, David and Martell, Sally and Lewis, Suzanne M. E. and Penaherrera, Maria S. and Robinson, Wendy P. and Volchuk, Allen and Rajcan-Separovic, Evica

Cord blood hematopoietic cells from preterm infants display altered DNA methylation patterns

Clinical Epigenetics

de Goede, Olivia M. and Lavoie, Pascal M. and Robinson, Wendy P.

Characterizing the hypomethylated DNA methylation profile of nucleated red blood cells from cord blood

Epigenomics

de Goede, Olivia M. and Lavoie, Pascal M. and Robinson, Wendy P.

Pervasive polymorphic imprinted methylation in the human placenta

Genome Research

Hanna, Courtney W. and Penaherrera, Maria S. and Saadeh, Heba and Andrews, Simon and McFadden, Deborah E. and Kelsey, Gavin and Robinson, Wendy P.

Developmental transcription factor NFIB is a putative target of oncofetal miRNAs and is associated with tumour aggressiveness in lung adenocarcinoma

Journal of Pathology

Becker-Santos, Daiana D. and Thu, Kelsie L. and English, John C. and Pikor, Larissa A. and Martinez, Victor D. and Zhang, May and Vucic, Emily A. and Luk, Margaret T. Y. and Carraro, Anita and Korbelik, Jagoda and Piga, Daniela and Lhomme, Nicolas M. and Tsay, Mike J. and Yee, John and MacAulay, Calum E. and Lam, Stephen and Lockwood, William W. and Robinson, Wendy P. and Jurisica, Igor and Lam, Wan L.

Placental telomere length decline with gestational age differs by sex and TERT, DNMT1, and DNMT3A DNA methylation

Placenta

Wilson, Samantha L. and Liu, Yao and Robinson, Wendy P.

USING DNA METHYLATION SIGNATURES IN PLACENTAL TISSUE AND CELLS TO GAIN INSIGHT INTO CHORIOAMNIONITIS

Placenta

Konwar, Chaini and Price, E. Magda and Robinson, Wendy P.

TRANSCRIPTOMIC PROFILING OF SNCRNA IN PLACENTA BY RNASEQ

Placenta

Price, E. Magda and Martinez, Victor and Becker-Santos, Daiana and Manokhina, Irina and Lam, Wan L. and Robinson, Wendy P.

Profiling placental and fetal DNA methylation in human neural tube defects

Epigenetics & Chromatin

Price, E. Magda and Penaherrera, Maria S. and Portales-Casamar, Elodie and Pavlidis, Paul and Van Allen, Margot I. and McFadden, Deborah E. and Robinson, Wendy P.

Number of Children and Telomere Length in Women: A Prospective, Longitudinal Evaluation

Plos One

Barha, Cindy K. and Hanna, Courtney W. and Salvante, Katrina G. and Wilson, Samantha L. and Robinson, Wendy P. and Altman, Rachel M. and Nepomnaschy, Pablo A.

UNRAVELLING THE RELATIONSHIP BETWEEN EARLY AND LATE-ONSET PREECLAMPSIA. WHAT DOES THE PLACENTAL DNA METHYLATION PROFILE REVEAL?

Placenta

Wilson, Samantha L. and Leavey, Katherine and von Dadelszen, Peter and Cox, Brian and Robinson, Wendy P.

Stressful life events, the hypothalamic-pituitary-adrenal axis and cellular aging in women

American Journal of Human Biology

Nepomnaschy, P. A. and Barha, C. K. and Salvante, K. G. and Hanna, C. W. and Wilson, S. L. and Robinson, W. P. and Altman, R. M.

Molecular Aspects of Placental Development

Genetic Disorders and the Fetus

Wendy P. Robinson and Deborah E. McFadden

11 / 2015

Transient and placenta-specific imprinting in human development

Placenta

Courtney Hanna and Maria Penaherrera and Heba Saadeh and Deborah McFadden and Gavin Kelsey and Wendy Robinson

09 / 2015

An integrated transcriptional, epigenetic, and clinical analysis of preeclamptic placentas

Placenta

Katherine Leavey and Samantha Wilson and Shannon Bainbridge and Wendy Robinson and Brian Cox

09 / 2015

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

Orphanet journal of rare diseases

Sirrs, Sandra and van Karnebeek, Clara DM and Peng, Xiaoxue and Shyr, Casper and Tarailo-Graovac, Maja and Mandal, Rupasri and Testa, Daniel and Dubin, Devin and Carbonetti, Gregory and Glynn, Steven E and others

Genome-wide DNA methylation identifies trophoblast invasion-related genes: Claudin-4 and Fucosyltransferase IV control mobility via altering matrix metalloproteinase activity

Molecular human reproduction

Hu, Yuxiang and Blair, John D and Yuen, Ryan KC and Robinson, Wendy P and von Dadelszen, Peter

Functional consequences of copy number variants in miscarriage

Mol Cytogenet

Wen, Jiadi and Hanna, Courtney W and Martell, Sally and Leung, Peter CK and Lewis, Suzanne ME and Robinson, Wendy P and Stephenson, Mary D and Rajcan-Separovic, Evica

Defects in fatty acid amid hydrolase 2 associated with developmental and psychiatric disorders

MOLECULAR GENETICS AND METABOLISM

Sirrs, Sandra and Peng, Xiaoxue and Sinclair, Graham and Shyr, Casper and Mandal, Rupasri and Testa, Daniel and Dubin, Devin and Carbonetti, Gregory and Glynn, Steven E and Robinson, Wendy P and others

The human placental methylome

Cold Spring Harbor perspectives in medicine

Robinson, Wendy P and Price, E Magda

Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology

American Journal of Medical Genetics Part A

Uhlmann, Wendy R and Peaherrera, Maria S and Robinson, Wendy P and Milunsky, Jeff M and Nicholson, Jane M and Albin, Roger L

Placental DNA methylation at term reflects maternal serum levels of INHA and FN1, but not PAPPA, early in pregnancy

BMC medical genetics

Wilson, Samantha L and Blair, John D and Hogg, Kirsten and Langlois, Sylvie and von Dadelszen, Peter and Robinson, Wendy P

IFPA meeting 2014 workshop report: Animal models to study pregnancy pathologies; new approaches to study human placental exposure to xenobiotics; biomarkers of pregnancy pathologies; placental genetics and epigenetics; the placenta and stillbirth and fetal growth restriction

Placenta

Barbaux, S and Erwich, JJHM and Favaron, PO and Gil, S and Gallot, D and Golos, TG and Gonzalez-Bulnes, A and Guibourdenche, J and Heazell, AEP and Jansson, T and others

The genotypic and phenotypic spectrum of PIGA deficiency

Orphanet journal of rare diseases

Tarailo-Graovac, Maja and Sinclair, Graham and Stockler-Ipsiroglu, Sylvia and Van Allen, Margot and Rozmus, Jacob and Shyr, Casper and Biancheri, Roberta and Oh, Tracey and Sayson, Bryan and Lafek, Mirafe and others

Nucleated red blood cells impact DNA methylation and expression analyses of cord blood hematopoietic cells

Clinical epigenetics

de Goede, Olivia M and Razzaghian, Hamid R and Price, E Magda and Jones, Meaghan J and Kobor, Michael S and Robinson, Wendy P and Lavoie, Pascal M

Noninvasive nucleic acid--based approaches to monitor placental health and predict pregnancy-related complications

American journal of obstetrics and gynecology

Manokhina, Irina and Wilson, Samantha L and Robinson, Wendy P

ADAM12-directed ectodomain shedding of E-cadherin potentiates trophoblast fusion

Cell Death and Differentiation

Aghababaei, M. and Hogg, K. and Perdu, S. and Robinson, W. P. and Beristain, A. G.

Offspring mortality accelerates the aging process in mothers

AMERICAN JOURNAL OF HUMAN BIOLOGY

Barha, CK and Hanna, CW and Salvante, KG and Robinson, WP and Nepomnaschy, PA

Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsia

Placenta

Blair, JD and Langlois, S and McFadden, DE and Robinson, WP

Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes

Human mutation

Qiao, Ying and Mondal, Kajari and Trapani, Valentina and Wen, Jiadi and Carpenter, Gillian and Wildin, Robert and Price, E Magda and Gibbons, Richard J and Eichmeyer, Jennifer and Jiang, Ruby and others

Activation of endocrine-related gene expression in placental choriocarcinoma cell lines following DNA methylation knock-down

Molecular human reproduction

Hogg, K and Robinson, WP and Beristain, AG

A cryptic familial rearrangement of 11p15. 5, involving both imprinting centers, in a family with a history of short stature

American Journal of Medical Genetics Part A

Brown, Lindsay A and Rupps, Rosemarie and Peaherrera, Maria S and Robinson, Wendy P and Patel, Millan S and Eydoux, Patrice and Boerkoel, Cornelius F

IFPA Meeting 2013 Workshop Report II: Use of omics in understanding placental development, bioinformatics tools for gene expression analysis, planning and coordination of a placenta research network, placental imaging, evolutionary approaches to understanding pre-eclampsia

Placenta

Ackerman, WE and Adamson, L and Carter, Anthony Michael and Collins, S and Cox, B and Elliot, MG and Ermini, L and Gruslin, A and Hoodless, PA and Huang, J and others

Improved reporting of DNA methylation data derived from studies of the human placenta

epigenetics

Hogg, Kirsten and Price, E Magda and Robinson, Wendy P

Quantification of cell-free DNA in normal and complicated pregnancies: overcoming biological and technical issues

PloS one

Manokhina, Irina and Singh, Tanjot K and Peaherrera, Maria S and Robinson, Wendy P

Recurrent triploidy due to a failure to complete maternal Meiosis II: whole exome sequencing reveals candidate variants

Molecular human reproduction

Filges, I and Manokhina, I and Peaherrera, MS and McFadden, DE and Louie, K and Nosova, E and Friedman, JM and Robinson, WP

Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage

Molecular human reproduction

Manokhina, I and Hanna, CW and Stephenson, MD and McFadden, DE and Robinson, WP

Glucose as a fetal nutrient: dynamic regulation of several glucose transporter genes by DNA methylation in the human placenta across gestation

The Journal of nutritional biochemistry

Novakovic, Boris and Gordon, Lavinia and Robinson, Wendy P and Desoye, Gernot and Saffery, Richard

Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset preeclampsia

Molecular human reproduction

Blair, John D and Yuen, Ryan KC and Lim, Brendan K and McFadden, Deborah E and von Dadelszen, Peter and Robinson, Wendy P

miRNA expression in human lung cancer and fetal lung: a comparative study

BMC Proceedings

Becker-Santos, Daiana D and Thu, Kelsie L and Reis, Patricia P and Robinson, Wendy P and Lam, Stephen and Lam, Wan L

Hypoxia alters the epigenetic profile in cultured human placental trophoblasts

Epigenetics

Yuen, Ryan KC and Chen, Baosheng and Blair, John D and Robinson, Wendy P and Nelson, D Michael

Global analysis of DNA methylation changes during progression of oral cancer

Oral oncology

Towle, Rebecca and Truong, Danielle and Hogg, Kirsten and Robinson, Wendy P and Poh, Catherine F and Garnis, Cathie

DNA methylation profiling of placental villi from karyotypically normal miscarriage and recurrent miscarriage

The American journal of pathology

Hanna, Courtney W and McFadden, Deborah E and Robinson, Wendy P

X-Chromosome Inactivation

Epigenetics and Complex Traits

Robinson, Wendy P and Cotton, Allison M and Peaherrera, Maria S and Peeters, Samantha B and Brown, Carolyn J

The human placenta methylome

Proceedings of the national academy of sciences

Schroeder, Diane I and Blair, John D and Lott, Paul and Yu, Hung On Ken and Hong, Danna and Crary, Florence and Ashwood, Paul and Walker, Cheryl and Korf, Ian and Robinson, Wendy P and others

Hypomethylation of the LEP gene in placenta and elevated maternal leptin concentration in early onset pre-eclampsia

Molecular and cellular endocrinology

Hogg, Kirsten and Blair, John D and von Dadelszen, Peter and Robinson, Wendy P

Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array

Epigenetics & chromatin

Price, E Magda and Cotton, Allison M and Lam, Lucia L and Farr, Pau and Emberly, Eldon and Brown, Carolyn J and Robinson, Wendy P and Kobor, Michael S

Early onset pre-eclampsia is associated with altered DNA methylation of cortisol-signalling and steroidogenic genes in the placenta

PloS one

Hogg, Kirsten and Blair, John D and McFadden, Deborah E and von Dadelszen, Peter and Robinson, Wendy P

Beckwith--Wiedemann and Silver--Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth

Clinical genetics

Jacob, KJ and Robinson, WP and Lefebvre, L

Response to

Epigenetics

E. Magda Price and Wendy P. Robinson

08 / 2012

Beckwith--Wiedemann syndrome in sibs discordant for IC2 methylation

American Journal of Medical Genetics Part A

Niederhoffer, Karen Y and Peaherrera, Maria and Pugash, Denise and Rupps, Rosemarie and Arbour, Laura and Tessier, Francine and Choufani, Sanaa and Zhao, Chunhua and Manokhina, Irina and Shuman, Cheryl and others

Prenatal and perinatal environmental influences on the human fetal and placental epigenome

Clinical Pharmacology & Therapeutics

Hogg, K and Price, EM and Hanna, CW and Robinson, WP

IFPA Meeting 2011 workshop report III: Placental immunology; epigenetic and microRNA-dependent gene regulation; comparative placentation; trophoblast differentiation; stem cells

Placenta

Ackerman, WEt and Bulmer, JN and Carter, Anthony Michael and Chaillet, JR and Chamley, L and Chen, CP and Chuong, EB and Coleman, SJ and Collet, GP and Croy, BA and others

DNA methylation changes in whole blood is associated with exposure to the environmental contaminants, mercury, lead, cadmium and bisphenol A, in women undergoing ovarian stimulation for IVF

Human reproduction

Hanna, Courtney W and Bloom, Michael S and Robinson, Wendy P and Kim, Dongsul and Parsons, Patrick J and vom Saal, Frederick S and Taylor, Julia A and Steuerwald, Amy J and Fujimoto, Victor Y

Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage

Reproductive biomedicine online

Hanna, Courtney W and Blair, John D and Stephenson, Mary D and Robinson, Wendy P

Protein kinase profiling in miscarriage: implications for the pathogenesis of trisomic pregnancy.

Journal of obstetrics and gynaecology Canada: JOGC= Journal d'obstetrique et gynecologie du Canada: JOGC

Yong, PJ and McFadden, DE and Robinson, WP and others

Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation

Human reproduction

Peaherrera, MS and Jiang, R and Avila, L and Yuen, RKC and Brown, CJ and Robinson, WP

Different measures of genome-wide DNA methylation exhibit unique properties in placental and somatic tissues

Epigenetics

Price, E Magda and Cotton, Allison M and Peaherrera, Maria S and McFadden, Deborah E and Kobor, Michael S and Robinson, Wendy

Aneuploidy and Polyploidy

The Placenta: From Development to Disease, From Development to Disease

Diego-Alvarez, Dan and Robinson, Wendy P

TROPHOBLAST RESEARCH

Placenta

Carter, Anthony M and Staff, Anne Cathrine and Lash, Gendie E and Shiverick, Kathleen T and Miller, Richard K and Chamley, Larry and Clifton, Vicki and Harris, Lynda K and Katabuchi, Hidetaka and Keelan, Jeffrey and others

Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies

Epigenetics & chromatin

Yuen, Ryan KC and Jiang, Ruby and Peaherrera, Maria S and McFadden, Deborah E and Robinson, Wendy P

Extensive epigenetic reprogramming in human somatic tissues between fetus and adult

Epigenetics & chromatin

Yuen, Ryan KC and Neumann, Sarah MA and Fok, Alexandra K and Peaherrera, Maria S and McFadden, Deborah E and Robinson, Wendy P and Kobor, Michael S

Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors

BMC genomics

Novakovic, Boris and Yuen, Ryan K and Gordon, Lavinia and Penaherrera, Maria S and Sharkey, Andrew and Moffett, Ashley and Craig, Jeffrey M and Robinson, Wendy P and Saffery, Richard

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders

Clinical genetics

Bourque, DK and Peaherrera, MS and Yuen, RKC and Van Allen, MI and McFadden, DE and Robinson, WP

Review: a high capacity of the human placenta for genetic and epigenetic variation: implications for assessing pregnancy outcome

Placenta

Yuen, RKC and Robinson, WP

Placenta-specific expression of the interleukin-2 (IL-2) receptor $$ subunit from an endogenous retroviral promoter

Journal of Biological Chemistry

Cohen, Carla J and Rebollo, Rita and Babovic, Sonja and Dai, Elizabeth L and Robinson, Wendy P and Mager, Dixie L

Developmental origin of chorionic villus cultures from spontaneous abortion and chorionic villus sampling.

Journal of obstetrics and gynaecology Canada: JOGC= Journal d'obstetrique et gynecologie du Canada: JOGC

Yong, PJ and McFadden, DE and Robinson, WP

Are we ready for DNA methylation-based prenatal testing?

Epigenomics

Yuen, Ryan KC and Manokhina, Irina and Robinson, Wendy P

Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation

Human genetics

Cotton, Allison M and Lam, Lucia and Affleck, Joslynn G and Wilson, Ian M and Penaherrera, Maria S and McFadden, Deborah E and Kobor, Michael S and Lam, Wan L and Robinson, Wendy P and Brown, Carolyn J

DNA methylation at H19/IGF2 ICR1 in the placenta of pregnancies conceived by in vitro fertilization and intracytoplasmic sperm injection

Fertility and sterility

Wong, Edgar Chan and Hatakeyama, Chiho and Robinson, Wendy P and Ma, Sai

DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia

European Journal of Human Genetics

Yuen, Ryan KC and Peaherrera, Maria S and von Dadelszen, Peter and McFadden, Deborah E and Robinson, Wendy P

Evaluating DNA methylation and gene expression variability in the human term placenta

Placenta

Avila, L and Yuen, RK and Diego-Alvarez, D and Penaherrera, MS and Jiang, R and Robinson, WP

Pseudohypoparathyroidism type 1a and the GNAS p. R231H mutation: somatic mosaicism in a mother with two affected sons

American Journal of Medical Genetics Part A

Ngai, Ying Fai and Chijiwa, Chieko and Mercimek-Mahmutoglu, Saadet and Stewart, Laura and Yong, Siu-Li and Robinson, Wendy P and Gibson, William T

Genetic variation within the hypothalamus-pituitary-ovarian axis in women with recurrent miscarriage

Human reproduction

Hanna, Courtney W and Bretherick, Karla L and Liu, Chi-Chao and Stephenson, Mary D and Robinson, Wendy P

Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia

Placenta

Bourque, DK and Avila, L and Penaherrera, M and Von Dadelszen, P and Robinson, WP

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

Human reproduction

Rajcan-Separovic, E and Diego-Alvarez, D and Robinson, WP and Tyson, C and Qiao, Y and Harvard, C and Fawcett, C and Kalousek, D and Philipp, T and Somerville, MJ and others

Assessing the role of placental trisomy in preeclampsia and intrauterine growth restriction

Prenatal diagnosis

Robinson, Wendy P and Peaherrera, Maria S and Jiang, Ruby and Avila, Luana and Sloan, Jennifer and McFadden, Deborah E and Langlois, Sylvie and von Dadelszen, Peter

Methylation profiling in individuals with Russell--Silver syndrome

American Journal of Medical Genetics Part A

Peaherrera, Maria S and Weindler, Susanne and Van Allen, Margot I and Yong, Siu-Li and Metzger, Daniel L and McGillivray, Barbara and Boerkoel, Cornelius and Langlois, Sylvie and Robinson, Wendy P

Fertility and aging: do reproductive-aged Canadian women know what they need to know?

Fertility and sterility

Bretherick, Karla L and Fairbrother, Nichole and Avila, Luana and Harbord, Sara HA and Robinson, Wendy P

Inactive X chromosome-specific reduction in placental DNA methylation

Human molecular genetics

Cotton, Allison M and Avila, Luana and Penaherrera, Maria S and Affleck, Joslynn G and Robinson, Wendy P and Brown, Carolyn J

Telomere length and reproductive aging

Human Reproduction

Hanna, Courtney W and Bretherick, Karla L and Gair, Jane L and Fluker, Margo R and Stephenson, Mary D and Robinson, Wendy P

Placental weight in pregnancies with trisomy confined to the placenta

J Obstet Gynaecol Can

Yong, Paul J and von Dadelszen, Peter and McFadden, Deborah E and Barrett, IJ and Kalousek, DK and Robinson, WP

Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes

PloS one

Yuen, Ryan KC and Avila, Luana and Peaherrera, Maria S and von Dadelszen, Peter and Lefebvre, Louis and Kobor, Michael S and Robinson, Wendy P

A Genome-wide Search of Epigenetic Fetal DNA Markers for Non-invasive Prenatal Diagnosis of Aneuploidies

CHROMOSOME RESEARCH

Yuen, R and Penaherrera, M and von Dadelszen, P and Kobor, MS and Robinson, W

Telornere Length and Reproductive Aging EDITORIAL COMMENT

Hanna, Courtney W and Bretherick, Karla L and Gair, Jane L and Fluker, Margo R and Stephenson, Mary D and Robinson, Wendy P

Epigenetic alterations associated with premature ovarian failure

Fertility and Sterility

Ghahremani, Manda and Hanna, CW and Bretherick, KL and Penaherrera, MS and Fluker, Margo R and Robinson, Wendy P

MECP2 promoter methylation and X chromosome inactivation in autism

Autism Research

Nagarajan, Raman P and Patzel, Katherine A and Martin, Michelle and Yasui, Dag H and Swanberg, Susan E and Hertz-Picciotto, Irva and Hansen, Robin L and Van de Water, Judy and Pessah, Isaac N and Jiang, Ruby and others

Estrogen receptor $a$ gene polymorphisms are associated with idiopathic premature ovarian failure

Fertility and sterility

Bretherick, Karla L and Hanna, Courtney W and Currie, Lauren M and Fluker, Margo R and Hammond, Geoffrey L and Robinson, Wendy P

IGF2/H19 DMR methylation in placentas conceived by IVF or ICSI

Fertility and Sterility

Wong, E Chan and Hatakeyama, C and Robinson, WP and Ma, S

Origin and outcome of pregnancies affected by androgenetic/biparental chimerism

Human Reproduction

Robinson, Wendy P and Lauzon, Julie L and Innes, A Micheil and Lim, Ken and Arsovska, Snezana and McFadden, Deborah E

Toll-like receptor 4 polymorphisms and idiopathic chromosomally normal miscarriage

Human Reproduction

Hirschfeld, AF and Jiang, R and Robinson, WP and McFadden, DE and Turvey, SE

Skewed X-chromosome inactivation is associated with primary but not secondary ovarian failure

American Journal of Medical Genetics Part A

Bretherick, Karla L and Metzger, Daniel L and Chanoine, Jean-Pierre and Panagiotopoulos, Constadina and Watson, Spencer K and Lam, Wan L and Fluker, Margo R and Brown, Carolyn J and Robinson, Wendy P

Pregnancy and postnatal outcome of mosaic isochromosome 20q

Prenatal diagnosis

Robinson, WP and McGillivray, B and Friedman, JM

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15. 5

American Journal of Medical Genetics Part A

Robinson, WP and Slee, J and Smith, N and Murch, A and Watson, SK and Lam, WL and McFadden, DE

A skewed view of X chromosome inactivation

The Journal of clinical investigation

Minks, Jakub and Robinson, Wendy P and Brown, Carolyn J

334 PROTEIN KINASE EXPRESSION PROFILING IN HUMAN TRISOMY: GENE DOSAGE AND AMPLIFIED INSTABILITY.

Journal of Investigative Medicine

Yong, PJ and McFadden, DE and MacCalman, CD and Robinson, WP

Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism

Prenatal diagnosis

Langlois, Sylvie and Yong, Paul J and Yong, Siu Li and Barrett, Irene and Kalousek, Dagmar K and Miny, Peter and Exeler, Rita and Morris, Kathy and Robinson, Wendy P

Phenotype of triploid embryos

Journal of medical genetics

McFadden, Deborah E and Robinson, WP

The association between preeclampsia and placental trisomy 16 mosaicism

Prenatal diagnosis

Yong, Paul J and Langlois, Sylvie and Dadelszen, Peter von and Robinson, Wendy

P-159: Epigenetic analysis of H19/IGF2 in placentas from low birth weight (LBW) pregnancies following intracytoplasmic sperm injection (ICSI)

Fertility and Sterility

Hatakeyama, C and Robinson, WP and Ma, S

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia

Journal of medical genetics

Kaiser-Rogers, Kathleen A and Mcfadden, Deborah E and Livasy, Chad A and Dansereau, Jerome and Jiang, Ruby and Knops, Judith F and Lefebvre, Louis and Rao, Kathleen W and Robinson, Wendy P

5 Postnatal follow-up of newborns from CPM16 pregnancies1

Three Chromosomes and a Baby: Cytogenetic, Biological, and Clinical Aspects of the Trisomic Placenta

Kalousek, D and Langlois, S and Robinson, W

Frequency of chromosomal abnormalities in spontaneous abortions derived from intracytoplasmic sperm injection compared with those from in vitro fertilization

Fertility and sterility

Ma, Sai and Philipp, Tom and Zhao, Yulian and Stetten, Gail and Robinson, Wendy P and Kalousek, Dagmar

X-chromosome inactivation and telomere size in newborns resulting from intracytoplasmic sperm injection

American Journal of Medical Genetics Part A

Robinson, WP and Penaherrera, MS and Gair, J and Hatakeyama, C and Ma, S

The association of skewed X chromosome inactivation with aneuploidy in humans

Cytogenetic and genome research

Bretherick, K and Gair, J and Robinson, WP

FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure

Human genetics

Bretherick, Karla L and Fluker, Margo R and Robinson, Wendy P

Recurrent trisomy 21: four cases in three generations

Clinical genetics

Gair, JL and Arbour, L and Rupps, R and Jiang, R and Bruyere, H and Robinson, WP

18. Mosaicism

Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics

Robinson, Wendy P

Prenatally detected trisomy 20 mosaicism

Prenatal diagnosis

Robinson, WP and McGillivray, B and Lewis, MES and Arbour, L and Barrett, I and Kalousek, DK

X-Chromosome Inactivation (XCI) in Newborns Conceived Through Intracytoplasmic Sperm Injection (ICSI)

Fertility and Sterility

Hatakeyama, C and Penaherrera, M and Robinson, W and Ma, S

The dynamics of X-inactivation skewing as women age

Clinical genetics

Hatakeyama, C and Anderson, CL and Beever, CL and Penaherrera, MS and Brown, CJ and Robinson, WP

EXTRAVILLUS TROPHOBLAST DIFFERENTIATION IN MISCARRIAGE.: 523

Journal of Investigative Medicine

Yong, PJ and McFadden, DE and MacCalman, CD and Robinson, WP

An association between sex chromosomal aneuploidy in sperm and an abortus with 45, X of paternal origin: possible transmission of chromosomal abnormalities through ICSI

Human Reproduction

Tang, SS and Gao, H and Robinson, WP and Yuen, B Ho and Ma, S

A correlation between sex chromosomal aneuploidy in sperm and an abortus with 45, X of paternal origin: evidence of transmission of chromosomal abnormalities through ICSI

Fertility and Sterility

Tang, Steven S and Gao, HJ and Robinson, WP and Yuen, B Ho and Ma, SSY

Prenatally detected trisomy 4 and 6 mosaicism"cytogenetic results and clinical phenotype

Prenatal diagnosis

Wieczorek, Dagmar and Prott, Eva C and Robinson, Wendy P and Passarge, Eberhard and Gillessen-Kaesbach, Gabriele

Molecular Detection of Uniparental Disomy

Molecular Cytogenetics: Protocols and Applications

Robinson, Wendy P

Determination of birth weight in confined placental mosaicism.

JOURNAL OF INVESTIGATIVE MEDICINE

Yong, PJ and Kalousek, DK and Barrett, IJ and Robinson, WP

X inactivation skewing patterns change as women age.

AMERICAN JOURNAL OF HUMAN GENETICS

Anderson, CL and Hatakeyama, C and Beever, CL and Hayden, M and Casey, B and Brown, CJ and Robinson, WP

Frequency of chromosomal abnormalities in abortuses from ICSI and IVF

HUMAN REPRODUCTION

Ma, S and Zhao, Y and Philipp, T and Yuen, Ho B and Stetten, G and Garcia, J and Robinson, W and Kalousek, D

Is telomere length associated with trisomy risk in humans?

AMERICAN JOURNAL OF HUMAN GENETICS

Gair, J and Chavez, E and Stephenson, M and Langlois, S and Lansdorp, P and Robinson, W

ICSI and the transmission of X-autosomal translocation: a three-generation evaluation of X; 20 translocation: Case report

Human Reproduction

Ma, Sai and Yuen, Basil Ho and Penaherrera, Maria and Koehn, David and Ness, Larry and Robinson, Wendy

X chromosome inactivation patterns in Russell--Silver syndrome patients and their mothers

American Journal of Medical Genetics Part A

Beever, Christy L and Peaherrera, Maria S and Langlois, Sylvie and Robinson, Wendy R

Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies

The American Journal of Human Genetics

Beever, CL and Stephenson, MD and Penaherrera, MS and Jiang, RH and Kalousek, DK and Hayden, M and Field, L and Brown, CJ and Robinson, WP

Prenatally detected trisomy 4 and 6 mosaicism?cytogenetic results and clinical phenotype

Prenat. Diagn.

Dagmar Wieczorek and Eva C. Prott and Wendy P. Robinson and Eberhard Passarge and Gabriele Gillessen-Kaesbach

Does recurrent euploid and non-euploid miscarriage exist?

HUMAN REPRODUCTION

Graham, J and Robinson, W and Stephenson, M

Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism

Journal of medical genetics

Yong, PJ and Barrett, IJ and Kalousek, DK and Robinson, WP

Methylation of ZNF261 as an assay for determining X chromosome inactivation patterns

American Journal of Medical Genetics Part A

Beever, Christy and Lai, Betty PY and Baldry, Sarah EL and Peaherrera, Maria S and Jiang, Ruby and Robinson, Wendy P and Brown, Carolyn J

Developmental origin of cultured chorionic villi: implications for cytogenetics.

AMERICAN JOURNAL OF HUMAN GENETICS

Yong, PJ and McFadden, DE and MacCalman, CD and Robinson, WP

Skewed X-chromosome inactivation in premature ovarian failure.

AMERICAN JOURNAL OF HUMAN GENETICS

Bretherick, KL and Fluker, MR and Beever, CL and Anderson, CL and Brown, CJ and Robinson, WP

Cytogenetic and molecular study of a premature male infant with 46, XX derived from ICSI: case report

Human Reproduction

Ma, S and Tang, SS and Yuen, B Ho and Bruyere, H and Penaherrera, M and Robinson, WP

X-Chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t(X;20) case

Fertility and Sterility

Maria Penaherrea and Sai Ma and Basil Ho Yuen and Carolyn Brown and Wendy Robinson

09 / 2002

Brief Communication Dispermy"origin of diandric triploidy

Human Reproduction

McFadden, Deborah E and Jiang, Ruby and Langlois, Sylvie and Robinson, Wendy P

Skewed XCl in women experiencing a pregnancy with meiotic nondisjunction.

AMERICAN JOURNAL OF HUMAN GENETICS

Penaherrera, MS and Beever, CL and Jiang, RH and McFadden, DE and Hayden, MR and Field, LL and Kalousek, DK and Brown, CJ and Robinson, WP

Preeclampsia and confined placental mosaicism.

AMERICAN JOURNAL OF HUMAN GENETICS

Yong, PJ and Langlois, S and von Dadelszen, P and Barrett, IJ and Kalousek, DK and Robinson, WP

Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case--control study

Human Reproduction

Stephenson, MD and Awartani, KA and Robinson, WP

X-Chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t (X; 20) case

Fertility and Sterility

Penaherrea, Maria and Ma, Sai and Yuen, Basil Ho and Brown, Carolyn and Robinson, Wendy

Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies

American journal of medical genetics

Yong, PJ and Marion, SA and Barrett, IJ and Kalousek, DK and Robinson, WP

Dispermy"origin of diandric triploidy Brief Communication

Human Reproduction

McFadden, Deborah E and Jiang, Ruby and Langlois, Sylvie and Robinson, Wendy P

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism

Prenatal diagnosis

Robinson, Wendy P and McFadden, Deborah E and Barrett, Irene J and Kuchinka, Brian and Penaherrera, Maria S and Bruyre, Hlne and Best, Robert G and Pedreira, Denise AL and Langlois, Sylvie and Kalousek, Dagmar K

A rare case of mosaicism for paternal UPD 9 in a dizygotic twin pregnancy.

AMERICAN JOURNAL OF HUMAN GENETICS

Kaiser-Rogers, KA and Robinson, WP and Knops, JF and Vargo, D and Livasy, CA and Bailit, J and Rao, KW

Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters

American journal of medical genetics

Boyle, Jane and Sangha, Karan and Dill, Fred and Robinson, Wendy P and Yong, Siu-Li

Variability in DNA methylation assays of X chromosome inactivation (XCI).

AMERICAN JOURNAL OF HUMAN GENETICS

Beever, CL and Jiang, RH and Brown, CJ and Robinson, WP

Recurrent trisomy 15 in a female carrier of der (15) t (Y; 15)(q12; p13)

American journal of medical genetics

Rajcan-Separovic, Evica and Robinson, Wendy P and Stephenson, Mary and Pantzar, Tapio and Arbour, Laura and McFadden, Deborah and Guscott, Janet

Incomplete methylation of the inactivated X-chromosome in human chorionic villous samples.

AMERICAN JOURNAL OF HUMAN GENETICS

Penaherrera, MS and McDonald, HL and Brown, CJ and Robinson, WP

Cytogenetic investigation of fetuses and infants derived from intracytoplasmic sperm injection.

Fertility and Sterility

Ma, S and Lam, R and Robinson, WP and Chan, T and Yuen, B Ho

Cytogenetic investigation of fetuses and infants conceived through intracytoplasmic sperm injection

Fertility and sterility

Lam, Ryan and Ma, Sai and Robinson, Wendy P and Chan, Theresa and Yuen, Basil Ho

Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy

Prenatal diagnosis

Kuchinka, BD and Barrett, IJ and Moya, G and Sanchez, JM and Langlois, S and Yong, S-L and Kalousek, DK and Robinson, WP

The origin of abnormalities in recurrent aneuploidy.

AMERICAN JOURNAL OF HUMAN GENETICS

Robinson, WP and McFadden, DE and Stephenson, MS

The origin of abnormalities in recurrent aneuploidy/polyploidy

The American Journal of Human Genetics

Robinson, WP and McFadden, DE and Stephenson, MD

Prenatal diagnosis, outcome and imprinting in mosaic trisomy 16 pregnancies.

AMERICAN JOURNAL OF HUMAN GENETICS

Yong, PJ and Barrett, I and Kalousek, DK and Robinson, WP

Skewed X inactivation and recurrent spontaneous abortion.

Seminars in reproductive medicine

Robinson, WP and Beever, C and Brown, CJ and Stephenson, MD

Distribution of exchanges in chromosome 15 nondisjunction.

AMERICAN JOURNAL OF HUMAN GENETICS

Gair, JL and Kuchinka, BD and Robinson, WP

Cytogenetic analysis of miscarriages of couples with recurrent miscarriage: a case-control study.

Fertility and Sterility

Awartani, KA and Robinson, WP and Stephenson, MD

Statistical analysis of uniparental disomy data using hidden Markov models

Biometrics

Zhao, H and Li, J and Robinson, WP

Maternal origin of monosomy 21 derived from ICSI

Human Reproduction

Ma, Sai and Robinson, Wendy and Lam, Ryan and Yuen, Basil Ho

Clinical associations of women experiencing recurrent spontaneous abortion (RSA) and exhibiting skewed X chromosome inactivation (XCI).

AMERICAN JOURNAL OF HUMAN GENETICS

Beever, CL and Stephenson, MD and Popovska, V and Jiang, R and Sangha, KK and Ochnio, K and Brown, CJ and Robinson, WP

Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line

American journal of medical genetics

Bruyre, Hlne and Rupps, Rosemarie and Kuchinka, Brian D and Friedman, Jan M and Robinson, Wendy P

Multipoint genetic mapping with uniparental disomy data

The American Journal of Human Genetics

Zhao, Hongyu and Li, Jinming and Robinson, Wendy P

Mechanisms leading to uniparental disomy and their clinical consequences

Bioessays

Robinson, Wendy P

An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta

Clinical genetics

Penaherrera, MS and Barrett, IJ and Brown, CJ and Langlois, S and Yong, S-L and Lewis, S and Bruyere, H and Howard-Peebles, PN and Kalousek, DK and Robinson, WP

Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15

Clinical genetics

Robinson, Wendy P and Christian, Susan L and Kuchinka, Brian D and Peaherrera, Maria S and Das, Soma and Schuffenhauer, Simone and Malcolm, Susan and Schinzel, Albert A and Hassold, Terry J and Ledbetter, David H

The causes and consequences of random and non-random X chromosome inactivation in humans

Clinical genetics

Brown, CJ and Robinson, WP

Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assay

Journal of medical genetics

Kosaki, Kenjiro and KOSAKI, RIKA and ROBINSON, WENDY P and CRAIGEN, WILLIAM J and SHAFFER, LISA G and SATO, SEIJI and MATSUO, NOBUTAKE

Proximal deletion breakpoints in 15q11-q13 are sites of high homologous recombination.

AMERICAN JOURNAL OF HUMAN GENETICS

Gair, JL and Kuchinka, BD and Lalande, M and Ritchie, RJ and Robinson, WP

Gene conversion in the 15q imprinting center: Molecular evidence for homologous association of Imprinted chromosomal domains.

AMERICAN JOURNAL OF HUMAN GENETICS

Horsthemke, B and Gross, S and Robinson, W and Buiting, K

No association between an MTHFR polymorphism and occurrence of aneuploidy.

AMERICAN JOURNAL OF HUMAN GENETICS

Kuchinka, BD and Oppenheim, LN and Henderson, LJ and Stephenson, MD and Robinson, WP

Characteristics of Women with Recurrent Miscarriage (RM) and Skewed X-Chromosome Inactivation (XCI)

Fertility and Sterility

Stephenson, MD and Beever, CL and Robinson, WP

Statistical methods for human nondisjunction data.

AMERICAN JOURNAL OF HUMAN GENETICS

Li, J and Zhao, H and Sherman, SL and Robinson, WP

Diagnosis of maternal UPD 7 by methylation specific PCR.

AMERICAN JOURNAL OF HUMAN GENETICS

Kosaki, R and Kosaki, K and Robinson, W and Shaffer, L and Craigen, W and Matsuo, N

Report of the fourth international workshop on human chromosome 15 mapping 1997

Cytogenetic and Genome Research

Morton, Cynthia C and Christian, SL and Donlon, TA and Driscoll, DJ and Fink, JK and Gabriel, JM and Gotway, G and Greally, JM and Hitchins, MP and Howard, HC and others

Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7: Comparison with non-UPD7 cases

American journal of medical genetics

Bernard, LE and Penaherrera, MS and Van Allen, MI and Wang, MS and Yong, S-L and Gareis, F and Langlois, S and Robinson, WP

Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment

American journal of medical genetics

Robinson, WP and Bernasconi, F and Lau, A and McFadden, DE

Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion.

American journal of human genetics

Sangha, Karan K and Stephenson, Mary D and Brown, Carolyn J and Robinson, Wendy P

X chromosome inactivation studies in mosaic trisomies.

AMERICAN JOURNAL OF HUMAN GENETICS

Penaherrera, MS and Barrett, IJ and Brown, CJ and Kalousek, DK and Robinson, WP

Extremely skewed X chromosome inactivation is increased in women with recurrent spontaneous abortion.

AMERICAN JOURNAL OF HUMAN GENETICS

Robinson, WP and Sangha, KK and Stephenson, MD and Ochnio, K and Brown, CJ

Tissue specific involvement in fetal trisomy 16.

American Journal of Human Genetics

Bruyere, H and Barrett, IJ and Kalousek, DK and Robinson, WP

Sex chromosome complement of placental trophoblast in X chromosome aneuploid pregnancies.

AMERICAN JOURNAL OF HUMAN GENETICS

Barrett, IJ and Robinson, WP and Kalousek, DK

Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome

American journal of medical genetics

Wang, Michael S and Schinzel, Albert and Kotzot, Dieter and Balmer, Damina and Casey, Robin and Chodirker, Bernie N and Gyftodimou, Jolanda and Petersen, Michael B and Lopez-Rangel, Elana and Robinson, Wendy P

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination

Human molecular genetics

Robinson, WP and Kuchinka, BD and Bernasconi, F and Petersen, MB and Schulze, A and Br{\o}ndum-Nielsen, K and Christian, SL and Ledbetter, DH and Schinzel, AA and Horsthemke, B and others

The mechanisms involved in formation of deletions and duplications of 15q11-q13.

Journal of medical genetics

Robinson, WP and Dutly, F and Nicholls, RD and Bernasconi, F and Penaherrera, M and Michaelis, RC and Abeliovich, D and Schinzel, AA

Partial tetrasomy with triplication of chromosome (5)(p14-p15. 33) in a patient with severe multiple congenital anomalies

American journal of medical genetics

Harrison, Karen J and Teshima, Ikuko E and Silver, Meredith M and Jay, Venita and Unger, Sheila and Robinson, Wendy P and James, Andrew and Levin, Alex and Chitayat, David

Maternal uniparental disomy of chromosome 1 with no apparent phenotypic effects.

American journal of human genetics

Field, L Leigh and Tobias, Rose and Robinson, Wendy P and Paisey, Richard and Bain, Stephen

A meiotic origin of trisomy in pregnancies with confined placental mosaicism is correlated with increased risk of fetal intrauterine growth retardation and uniparental disomy

LABORATORY INVESTIGATION

Kalousek, DK and Robinson, WP and Barrett, I and Telenius, A and Wilson, RD and HowardPeebles, PN and Langlois, S

X chromosome inactivation patterns in human placenta.

AMERICAN JOURNAL OF HUMAN GENETICS

Penaherrera, MS and Lau, AW and Brown, CJ and Wilson, RD and Barrett, IJ and Kalousek, DK and Robinson, WP

Novel case of del (17)(q23. 1q23. 3) further highlights a recognizable phenotype involving deletions of chromosome (17)(q21q24)

American journal of medical genetics

Mickelson, Elizabeth CR and Robinson, Wendy P and Hrynchak, Monica A and Lewis, ME

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.

American journal of human genetics

Robinson, WP and Barrett, IJ and Bernard, L and Telenius, A and Bernasconi, F and Wilson, RD and Best, RG and Howard-Peebles, PN and Langlois, S and Kalousek, DK

XIST expression and X-chromosome inactivation in human preimplantation embryos.

American journal of human genetics

Brown, Carolyn J and Robinson, Wendy P

Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism

The American Journal of Human Genetics

Lau, Aster W and Brown, Carolyn J and Penaherrera, Maria and Langlois, Sylvie and Kalousek, Dagmar K and Robinson, Wendy P

Association of prenatally diagnosed confined placental mosaicism (CPM) and fetal gonadal mosaicism.

AMERICAN JOURNAL OF HUMAN GENETICS

Stavropoulos, DJ and Barrett, IJ and Lomax, BL and Bick, D and Bernasconi, F and Robinson, WP and Kalousek, DK

Mosaicism between maternal heterodisomy 16 and maternal heterodisomy 16p13-> qter combined with trisomy 16pter-> p13 associated with mental retardation and multiple anomalies.

CYTOGENETICS AND CELL GENETICS

Brecevic, L and Kotzot, D and Binkert, F and Robinson, W and Dutly, F and Ausserer, B and Schinzel, AA

Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios

Prenatal diagnosis

HANSEN, WENDY F and BERNARD, LYNN E and LANGLOIS, SYLVIE and RAO, KATHLEEN W and CHESCHEIR, NANCY C and AYLSWORTH, ARTHUR S and SMITH, D and ROBINSON, WENDY P and BARRETT, IRENE J and KALOUSEK, DAGMAR K

Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism.

AMERICAN JOURNAL OF HUMAN GENETICS

Robinson, WP and Lau, AW and Brown, CJ and Langlois, S and Kalousek, DK

Report of the third international workshop on human chromosome 15 mapping 1996

Cytogenetic and Genome Research

Robinson, Wendy and Knoll, Joan

Maternal age and recombination distribution associated with chromosome 15 nondisjunction.

AMERICAN JOURNAL OF HUMAN GENETICS

Kuchinka, BD and Hassold, TJ and Horsthemke, B and Langlois, S and Ledbetter, DH and Michaelis, RC and Schinzel, A and Schuffenhauer, S and Robinson, WP

Mosaicism most likely accounts for extended survival of trisomy 22

American journal of medical genetics

Robinson, Wendy P and Kalousek, Dagmar K

The extent, mechanism, and consequences of genetic variation, for recombination rate.

American journal of human genetics

Robinson, Wendy P

CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15

Prenatal diagnosis

Robinson, WP and Langlois, S and Schuffenhauer, S and Horsthemke, B and Michaelis, RC and Christian, S and Ledbetter, DH and Schinzel, A

Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.

European journal of human genetics: EJHG

Schinzel, A and Kotzot, D and Brecevic, L and Robinson, WP and Dutly, F and Dauwerse, H and Binkert, F and Baumer, A and Ausserer, B

Analysis of nine pregnancies with confined placental mosaicism for trisomy 2

Prenatal diagnosis

Shaffer, LG and Langlois, S and McCaskill, C and Main, DM and Robinson, WP and Barrett, IJ and Kalousek, DK

The origin of maternal uniparental disomy 15.

AMERICAN JOURNAL OF MEDICAL GENETICS

Robinson, WP and Langlois, S and Bernasconi, F and Clark, S and Christian, S and Ledbetter, DH and GillessenKaesbach, G and Horsthemke, B and Lerer, I and Abeliovich, D and others

Delineation of 7q11. 2 deletions associated with Williams--Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion

Genomics

Robinson, WP and Waslynka, J and Bernasconi, F and Wang, M and Clark, S and Kotzot, D and Schinzel, A

Phenotype of maternal UPD(14)

Am. J. Med. Genet.

Wendy P. Robinson and Sylvie Langlois

A comparison of phenotype in patients with Prader-Willi syndrome (PWS) resulting from interstitial deletion and uniparental disomy.

AMERICAN JOURNAL OF MEDICAL GENETICS

Mitchell, J and Langlois, S and GillessenKaesbach, G and Horsthemke, B and Michaelis, R and Schinzel, AA and Abelovich, S and Lerer, I and Schuffenhauer, S and Guitart, M and others

Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases

American journal of medical genetics

Kalousek, DK and Langlois, S and Robinson, WP and Telenius, A and Bernard, L and Barrett, IJ and Howard-Peebles, PN and Wilson, RD

Phenotype of maternal UPD (14)

American journal of medical genetics

Robinson, Wendy P and Langlois, Sylvie

Molecular studies of translocations and trisomy involving chromosome 13

American journal of medical genetics

Robinson, WP and Bernasconi, F and Dutly, F and Lefort, G and Romain, DR and Binkert, F and Schinzel, AA

Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.

American journal of human genetics

Benlian, Pascale and Foubert, Luc and Gagne, Eric and Bernard, Lynn and De Gennes, JL and Langlois, Sylvie and Robinson, Wendy and Hayden, Michael

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: Sex specific differences

American journal of medical genetics

Mitchell, John and Schinzel, Albert and Langlois, Sylvie and Gillessen-Kaesbach, Gabriele and Schuffenhauer, Simone and Michaelis, Ron and Abeliovich, Dvorah and Lerer, Isabel and Christian, Susan and Guitart, Miriam and others

Kallmann syndrome in a boy with at (1; 10) translocation detected by reverse chromosome painting.

Journal of medical genetics

Schinzel, Albert and Lorda-Sanchez, Isabel and Binkert, Franz and Carter, NP and Bebb, CE and Ferguson-Smith, Malcolm A and Eiholzer, Urs and Zachmann, Milo and Robinson, Wendy P

Sex-specific meiotic recombination in the Prader"Willi/Angelman syndrome imprinted region

Human molecular genetics

Robinson, Wendy P and Lalande, Marc

Uniparental disomy 7 in Silver"Russell syndrome and primordial growth retardation

Human molecular genetics

Kotzot, Dieter and Schmitt, Silke and Bernasconi, Fabiana and Robinson, Wendy P and Lurie, Iosif W and Ilyina, Helena and Mhes, Kroly and Hamel, Ben CJ and Otten, Barto J and Hergersberg, Martin and others

Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.

American journal of human genetics

Robinson, WP and Binkert, F and Bernasconi, F and Lorda-Sanchez, I and Werder, EA and Schinzel, AA

Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus

European journal of pediatrics

Kotzot, D and Bernasconi, F and Brecevic, L and Robinson, WP and Kiss, P and Kosztolanyi, G and Lurie, IW and Superti-Furga, A and Schinzel, A

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.

American journal of human genetics

Christian, SL and Robinson, WP and Huang, B and Mutirangura, A and Line, MR and Nakao, Mitsuyoshi and Surti, U and Chakravarti, A and Ledbetter, DH

THE ORIGIN OF TRISOMY CONFINED TO THE PLACENTA

AMERICAN JOURNAL OF HUMAN GENETICS

ROBINSON, WP and LANGLOIS, S and BARRETT, I and CLARK, S and BERNARD, L and KALOUSEK, DK

Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome

Human genetics

Gillessen-Kaesbach, Gabriele and Robinson, Wendy and Lohmann, Dietmar and Kaya-Westerloh, Sabine and Passarge, Eberhard and Horsthemke, Bernhard

An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like features.

Clinical dysmorphology

Schinzel, AA and Robinson, WP and Binkert, F and Fanconi, A

Fine Mapping of 8 Additional Short Tandem Repeats (Strs) and Expansion of the Yac Contig within the Prader-Willi-Angelman-Syndrome Critical Region on Chromosome-15q11. 2-] Q12

Cytogenetics and Cell Genetics

Christian, SL and Robinson, WP and Mutirangura, A and Nakao, M and Beaudet, AL and Ledbetter, DH

Detection of aberrant DNA methylation in unique Prader"Willi syndrome patients and its diagnostic implications

Human molecular genetics

Buiting, Karin and Dittrich, Brbel and Robinson, Wendy P and Guitart, Mirlam and Abeliovich, Dvorah and Lerer, Israela and Horsthemke, Bernhard

Maternal uniparental disomy 22 has no impact on the phenotype.

American journal of human genetics

Schinzel, Albert A and Basaran, S and Bernasconi, Fabiana and Karaman, B and Yksel-Apak, M and Robinson, WP

DETECTION OF ABERRANT DNA METHYLATION IN UNIQUE PRADER-WILLI-SYNDROME PATIENTS AND ITS DIAGNOSTIC IMPLICATIONS (VOL 3, PG 893, 1994)

HUMAN MOLECULAR GENETICS

BUITING, K and DITTRICH, B and ROBINSON, WP and GUITART, M and ABELIOVICH, D and LERER, I and HORSTHEMKE, B

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?

American journal of medical genetics

Bottani, Armand and Robinson, WP and Delozier-Blanchet, CD and Engel, E and Morris, MA and Schmitt, B and Thun-Hohenstein, L and Schinzel, A

Fine Mapping of 5 Additional Short Tandem Repeats (Strs) within the Prader Willi/Angelman Syndrome Critical Region on Chromosome 15q11. 2-12

Journal of Cellular Biochemistry

Christian, SL and Mutirangura, A and Robinson, WP and Nakao, M and Beaudet, AL and Ledbetter, DH

RECOMBINATION IN THE PERICENTROMERIC REGION OF CHROMOSOME 15Q

CYTOGENETICS AND CELL GENETICS

ROBINSON, WP and CHRISTIAN, SL and LEDBETTER, DH and SCHINZEL, AA

A somatic origin of homologous Robertsonian translocations and isochromosomes

American journal of human genetics

Robinson, WP and Bernasconi, F and Basaran, S and Yksel-Apak, M and Neri, G and Serville, F and Balicek, P and Haluza, R and Farah, LMS and Lleci, G and others

Multiple origins of X chromosome tetrasomy.

Journal of medical genetics

Robinson, WP and Binkert, F and Schinzel, AA and Basaran, S and Mikelsaar, R

Molecular studies of free and translocation trisomy

American Journal of Human Genetics

Robinson, WP and Bernasconi, F and Lefort, G

Angelman Syndrome due to paternal uniparental disomy of chromosome 15

Bottani, A

Intrachromosomal triplication of 15q11-q13.

Journal of medical genetics

Schinzel, AA and Brecevic, L and Bernasconi, F and Binkert, F and Berthet, F and Wuilloud, A and Robinson, WP

DUPLICATION OF CHROMOSOME-15Q IN PRADER-WILLI AND ANGELMAN SYNDROMES-A GENE DOSAGE PARADOX

AMERICAN JOURNAL OF HUMAN GENETICS

Mutirangura, A and Kuwano, A and Robinson, WP and Greenberg, F and Malcolm, S and Ledbetter, DH

Parental origin of the supernumerary chromosome in trisomy 18

Clinical genetics

Ya-gang, Xie and Robinson, Wendy P and Spiegel, Roland and Binkert, Franz and Ruefenacht, Urszula and Schinzel, Albert A

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup (15) chromosome.

Journal of medical genetics

Robinson, Wendy P and Wagstaff, Joseph and Bernasconi, Fabiana and Baccichetti, Carlo and Artifoni, Lina and Franzoni, Emilio and Suslak, Lorraine and Shih, Ling-Yu and Aviv, Hannah and Schinzel, Albert A

Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombination

Human genetics

Robinson, Wendy P and Spiegel, Roland and Schinzel, Albert A

Robertsonian translocations between homologous chromosomes are somatic events

AMERICAN JOURNAL OF HUMAN GENETICS

Robinson, WP and Bernasconi, F and Blouin, JL and BASARAN, S and NERI, G and ZIZKA, J and ANTONARAKIS, SE and SCHINZEL, AA

Molecular definition of the Prader"Willi syndrome chromosome region and orientation of the SNRPN gene

Human molecular genetics

Bulting, Karin and Dlttrich, Brbel and Gro, Stephanle and Greger, Valerle and Lalande, Marc and Robinson, Wendy and Mutirangura, Apiwat and Ledbetter, David and Horsthemke, Bernhard

Modification of 15q11"q13 DNA methylation imprints in unique Angelman and Prader"Willi patients

Human molecular genetics

Glenn, Christopher C and Nicholls, Robert D and Robinson, Wendy P and Saitoh, Shinjl and Nllkawa, Norlo and Schlnzel, Albert and Horsthemke, Bernhard and Driscoll, Daniel J

Nondisjunction of chromosome 15: origin and recombination.

American journal of human genetics

Robinson, WP and Bernasconi, F and Mutirangura, A and Ledbetter, DH and Langlois, S and Malcolm, S and Morris, MA and Schinzel, AA

Homozygous parent affected sib pair method for detecting disease predisposing variants: application to insulin dependent diabetes mellitus

Genetic epidemiology

Robinson, Wendy P and Barbosa, Jose and Rich, Steven S and Thomson, Glenys

Exclusively paternal X chromosomes in a girl with short stature

Human genetics

Schinzel, Albert A and Robinson, Wendy P and Binkert, Franz and Torresani, Toni and Werder, Edmond A

C2. B. 8 Reading disequilibrium patterns

HLA 1991: Proceedings of the Eleventh International Histocompatibility Workshop and Conference, Held in Yokohama, Japan, 6-13 November, 1991

THOMSON, GLENYS and KLITZ, WILLIAM and ROBINSON, WENDY

Prader-Willi or Angelman syndrome in familial 15q11 q13 deletion of maternal origin?

Human genetics

Schinzel, Albert and Robinson, Wendy P and Bottani, Armand and Yagang, Xie and Prader, Andrea

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

Human genetics

Dittrich, Brbel and Robinson, Wendy P and Knoblauch, Hans and Buiting, Karin and Schmidt, Kerstin and Gillessen-Kaesbach, Gabriele and Horsthemke, Bernhard

Clinical and molecular analysis of five inv dup (15) patients.

European journal of human genetics: EJHG

Robinson, WP and Binkert, F and Gine, R and Vazquez, C and Mller, W and Rosenkranz, W and Schinzel, A

Reduced recombination and paternal age effect in Klinefelter syndrome

Human genetics

Lorda-Sanchez, Isabel and Binkert, Franz and Maechler, Marco and Robinson, Wendy P and Schinzel, Albert A

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader--Willi syndrome critical region

Nature genetics

z{\c{c}}elik, Tayfun and Leff, Stuart and Robinson, Wendy and Donlon, Tim and Lalande, Marc and Sanjines, Elvira and Schinzel, Albert and Francke, Uta

Clinical, molecular, and cytogenetic survey of potential Prader-Willi syndrome patients

Prader-Willi Syndrome

Robinson, WP and Bottani, A and Yagang, X and Balakrishnan, J and Binkert, F and Mchler, M and Prader, A and Schinzel, A

Increased parental ages and uniparental disomy 15: a paternal age effect?

European journal of human genetics: EJHG

Robinson, WP and Lorda-Sanchez, I and Malcolm, S and Langlois, S and Schuffenhauer, S and Knoblauch, H and Horsthemke, B and Schinzel, AA

Three-locus systems impose additional constraints on pairwise disequilibria.

Genetics

Robinson, Wendy P and Asmussen, MA and Thomson, G

Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA data.

Genetics

Robinson, Wendy P and Cambon-Thomsen, Anne and Borot, Nicolas and Klitz, W and Thomson, G

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.

American journal of human genetics

Robinson, Wendy P and Bottani, Armand and Xie, YG and Balakrishman, Jaya and Binkert, Franz and Mchler, M and Prader, A and Schinzel, A

Population genetics of HLA

Evolution at the molecular level

Hedrick, Philip W and Klitz, William and Robinson, Wendy P and Kuhner, Mary K and Thomson, Glenys

Familial congenital laryngeal abductor paralysis: different expression in a family with one male and three females affected.

Journal of medical genetics

Schinzel, A and Hof, Erika and Dangel, P and Robinson, Wendy

HLA and insulin gene associations with IDDM

Genetic epidemiology

Thomson, G and Robinson, WP and Kuhner, MK and Joe, S and Klitz, W

HLA--Bw60 increases susceptibility to ankylosing spondylitis in HLA--B27+ patients

Arthritis & Rheumatism

Robinson, Wendy P and Van Der Linden, Sjef M and Khan, Muhammad A and Rentsch, Hans-Ueli and Cats, Arnold and Russell, Anthony and Thomson, Glenys

Clues to IDDM pathogenesis from genetic and serological traits in multiply affected families

Genetic epidemiology

Klitz, William and Kuhner, Mary K and Robinson, Wendy and Esposito, Michael and Thomson, Glenys

Population genetic analysis of selection and disease associations at the HLA gene family

Robinson, Wendy Paige

Affected sib pair IBS methods: detection of linkage and genetic models.

Progress in clinical and biological research

Motro, Uzi and Thomson, Glenys and Kuhner, Mary K and Robinson, Wendy P

Disease associations and disequilibrium mapping.

Progress in clinical and biological research

Robinson, Wendy P and Kramer, Patricia and Payami, Haydeh and Motro, Uzi and Esposito, Michael S and Thomson, Glenys

Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus

American journal of human genetics

Thomson, Glenys and Robinson, Wendy P and Kuhner, Mary K and Joe, Sharon and MacDonald, Michael J and Gottschall, Jerome L and Barbosa, Jose and Rich, Stephen S and Bertrams, Jrg and Baur, Max P and others

Letters to JMG

Green, A and McIntosh, I and Cenarro, A and Artieda, M and Castillo, S and Mozas, P and Reyes, G and Tejedor, D and Alonso, R and Mata, P and others

Mosaicism

Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics

Robinson, Wendy P

Chromosomal Genetic Disease: Numerical Aberrations

eLS

Robinson, Wendy P and McFadden, Deborah E