Wendy Robinson - Publications

Affiliations: 
Medical Genetics University of British Columbia, Vancouver, Vancouver, BC, Canada 

151 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Martinez VD, Cohn DE, Telkar N, Minatel BC, Pewarchuk ME, Marshall EA, Price EM, Robinson WP, Lam WL. Profiling the small non-coding RNA transcriptome of the human placenta. Scientific Data. 8: 166. PMID 34215751 DOI: 10.1038/s41597-021-00948-1  1
2021 Cohn DE, Barros-Filho MC, Minatel BC, Pewarchuk ME, Marshall EA, Vucic EA, Sage AP, Telkar N, Stewart GL, Jurisica I, Reis PP, Robinson WP, Lam WL. Reactivation of Multiple Fetal miRNAs in Lung Adenocarcinoma. Cancers. 13. PMID 34072436 DOI: 10.3390/cancers13112686  1
2021 Inkster AM, Yuan V, Konwar C, Matthews AM, Brown CJ, Robinson WP. A cross-cohort analysis of autosomal DNA methylation sex differences in the term placenta. Biology of Sex Differences. 12: 38. PMID 34044884 DOI: 10.1186/s13293-021-00381-4  1
2021 Robinson WP, Del Gobbo GF. Mistakes Are Common; Should We Worry about Them? Trends in Molecular Medicine. PMID 33994120 DOI: 10.1016/j.molmed.2021.04.008  1
2021 Del Gobbo GF, Yuan V, Robinson WP. 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. PMID 33750025 DOI: 10.1002/ajmg.a.62183  1
2021 Del Gobbo GF, Yin Y, Choufani S, Butcher EA, Wei J, Rajcan-Separovic E, Bos H, von Dadelszen P, Weksberg R, Robinson WP, Yuen RKC. Genomic imbalances in the placenta are associated with poor fetal growth. Molecular Medicine (Cambridge, Mass.). 27: 3. PMID 33413077 DOI: 10.1186/s10020-020-00253-4  1
2021 Yuan V, Hui D, Yin Y, Peñaherrera MS, Beristain AG, Robinson WP. Cell-specific characterization of the placental methylome. Bmc Genomics. 22: 6. PMID 33407091 DOI: 10.1186/s12864-020-07186-6  1
2019 Treissman J, Yuan V, Baltayeva J, Le HT, Castellana B, Robinson WP, Beristain AG. Low oxygen enhances trophoblast column growth by potentiating differentiation of the extravillous lineage and promoting LOX activity. Development (Cambridge, England). PMID 31871275 DOI: 10.1242/dev.181263  1
2019 Cho RY, Peñaherrera MS, Du Souich C, Huang L, Mwenifumbo J, Nelson TN, Elliott AM, Adam S, Eydoux P, Yang GX, Chijiwa C, Van Allen MI, Friedman JM, Robinson WP, et al. Renpenning syndrome in a female. American Journal of Medical Genetics. Part A. PMID 31840929 DOI: 10.1002/ajmg.a.61451  1
2019 Del Gobbo GF, Konwar C, Robinson WP. The significance of the placental genome and methylome in fetal and maternal health. Human Genetics. PMID 31555906 DOI: 10.1007/S00439-019-02058-W  1
2019 Yuan V, Price EM, Del Gobbo G, Mostafavi S, Cox B, Binder AM, Michels KB, Marsit C, Robinson WP. Accurate ethnicity prediction from placental DNA methylation data. Epigenetics & Chromatin. 12: 51. PMID 31399127 DOI: 10.1186/S13072-019-0296-3  1
2019 Lee Y, Choufani S, Weksberg R, Wilson SL, Yuan V, Burt A, Marsit C, Lu AT, Ritz B, Bohlin J, Gjessing HK, Harris JR, Magnus P, Binder AM, Robinson WP, et al. Placental epigenetic clocks: estimating gestational age using placental DNA methylation levels. Aging. PMID 31235674 DOI: 10.18632/aging.102049  1
2019 Konwar C, Manokhina I, Terry J, Inkster AM, Robinson WP. Altered levels of placental miR-338-3p and miR-518b are associated with acute chorioamnionitis and IL6 genotype. Placenta. 82: 42-45. PMID 31174625 DOI: 10.1016/J.Placenta.2019.05.009  1
2019 Konwar C, Del Gobbo GF, Terry J, Robinson WP. Association of a placental Interleukin-6 genetic variant (rs1800796) with DNA methylation, gene expression and risk of acute chorioamnionitis. Bmc Medical Genetics. 20: 36. PMID 30795743 DOI: 10.1186/S12881-019-0768-0  1
2019 Konwar C, Del Gobbo G, Yuan V, Robinson WP. Considerations when processing and interpreting genomics data of the placenta. Placenta. PMID 30642669 DOI: 10.1016/J.Placenta.2019.01.006  1
2018 Magee LA, Synnes AR, von Dadelszen P, Hutfield AM, Chanoine JP, Côté AM, Devlin AM, Dorling J, Gafni A, Ganzevoort W, Helewa ME, Hutton EK, Koren G, Lee SK, Mcarthur D, ... ... Robinson WP, et al. CHIPS-Child: Testing the developmental programming hypothesis in the offspring of the CHIPS trial. Pregnancy Hypertension. 14: 15-22. PMID 30527103 DOI: 10.1016/J.Preghy.2018.04.021  1
2018 Konwar C, Price EM, Wang LQ, Wilson SL, Terry J, Robinson WP. DNA methylation profiling of acute chorioamnionitis-associated placentas and fetal membranes: insights into epigenetic variation in spontaneous preterm births. Epigenetics & Chromatin. 11: 63. PMID 30373633 DOI: 10.1186/S13072-018-0234-9  1
2018 Qiao Y, Bagheri H, Tang F, Badduke C, Martell S, Lewis SME, Robinson W, Connolly MB, Arbour L, Rajcan-Separovic E. Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication. European Journal of Medical Genetics. PMID 29908350 DOI: 10.1016/J.Ejmg.2018.06.010  1
2018 Price EM, Robinson WP. Adjusting for Batch Effects in DNA Methylation Microarray Data, a Lesson Learned. Frontiers in Genetics. 9: 83. PMID 29616078 DOI: 10.3389/fgene.2018.00083  1
2018 Del Gobbo GF, Price EM, Hanna CW, Robinson WP. No evidence for association of677C>T and 1298A>C variants with placental DNA methylation. Clinical Epigenetics. 10: 34. PMID 29564022 DOI: 10.1186/S13148-018-0468-1  1
2018 Leavey K, Wilson SL, Bainbridge SA, Robinson WP, Cox BJ. Epigenetic regulation of placental gene expression in transcriptional subtypes of preeclampsia. Clinical Epigenetics. 10: 28. PMID 29507646 DOI: 10.1186/S13148-018-0463-6  1
2017 Wilson SL, Robinson WP. Utility of DNA methylation to assess placental health. Placenta. PMID 29273273 DOI: 10.1016/J.Placenta.2017.12.013  1
2017 Wilson SL, Leavey K, Cox B, Robinson WP. Mining DNA methylation alterations towards a classification of placental pathologies. Human Molecular Genetics. PMID 29092053 DOI: 10.1093/Hmg/Ddx391  1
2017 Matthews AM, Tarailo-Graovac M, Price EM, Blydt-Hansen I, Ghani A, Drögemöller BI, Robinson WP, Ross CJ, Wasserman WW, Siden H, van Karnebeek CD. 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. PMID 28778789 DOI: 10.1016/j.ejmg.2017.07.015  1
2017 Manokhina I, Del Gobbo GF, Konwar C, Wilson SL, Robinson WP. Placental biomarkers for assessing fetal health. Human Molecular Genetics. PMID 28595268 DOI: 10.1093/Hmg/Ddx210  1
2017 Barha CK, Salvante KG, Hanna CW, Wilson SL, Robinson WP, Altman RM, Nepomnaschy PA. Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers. Plos One. 12: e0177869. PMID 28542264 DOI: 10.1371/Journal.Pone.0177869  1
2017 Qiao Y, Badduke C, Tang F, Cowieson D, Martell S, Lewis SME, Peñaherrera MS, Robinson WP, Volchuk A, Rajcan-Separovic E. Whole exome sequencing of families with 1q21.1 microdeletion or microduplication. American Journal of Medical Genetics. Part A. PMID 28475290 DOI: 10.1002/ajmg.a.38247  1
2017 de Goede OM, Lavoie PM, Robinson WP. Cord blood hematopoietic cells from preterm infants display altered DNA methylation patterns. Clinical Epigenetics. 9: 39. PMID 28428831 DOI: 10.1186/s13148-017-0339-1  1
2017 Edgar RD, Jones MJ, Robinson WP, Kobor MS. An empirically driven data reduction method on the human 450K methylation array to remove tissue specific non-variable CpGs. Clinical Epigenetics. 9: 11. PMID 28184257 DOI: 10.1186/S13148-017-0320-Z  1
2016 Wilson SL, Liu Y, Robinson WP. Placental telomere length decline with gestational age differs by sex and TERT, DNMT1, and DNMT3A DNA methylation. Placenta. 48: 26-33. PMID 27871469 DOI: 10.1016/J.Placenta.2016.10.001  1
2016 de Goede OM, Lavoie PM, Robinson WP. Characterizing the hypomethylated DNA methylation profile of nucleated red blood cells from cord blood. Epigenomics. PMID 27687885 DOI: 10.2217/epi-2016-0069  1
2016 Manokhina I, Singh TK, Robinson WP. Cell-Free Placental DNA in Maternal Plasma in Relation to Placental Health and Function. Fetal Diagnosis and Therapy. PMID 27562338 DOI: 10.1159/000448707  1
2016 Becker-Santos DD, Thu KL, English JC, Pikor LA, Martinez VD, Zhang M, Vucic EA, Luk MT, Carraro A, Korbelik J, Piga D, Lhomme NM, Tsay MJ, Yee J, MacAulay CE, ... ... Robinson WP, et al. Developmental transcription factor NFIB is a putative target of oncofetal miRNAs and is associated with tumour aggressiveness in lung adenocarcinoma. The Journal of Pathology. PMID 27357447 DOI: 10.1002/Path.4765  1
2016 Price EM, Peñaherrera MS, Portales-Casamar E, Pavlidis P, Van Allen MI, McFadden DE, Robinson WP. Profiling placental and fetal DNA methylation in human neural tube defects. Epigenetics & Chromatin. 9: 6. PMID 26889207 DOI: 10.1186/S13072-016-0054-8  1
2016 Hanna CW, Peñaherrera MS, Saadeh H, Andrews S, McFadden DE, Kelsey G, Robinson WP. Pervasive polymorphic imprinted methylation in the human placenta. Genome Research. PMID 26769960 DOI: 10.1101/Gr.196139.115  1
2016 Barha CK, Hanna CW, Salvante KG, Wilson SL, Robinson WP, Altman RM, Nepomnaschy PA. Number of Children and Telomere Length in Women: A Prospective, Longitudinal Evaluation. Plos One. 11: e0146424. PMID 26731744 DOI: 10.1371/Journal.Pone.0146424  1
2015 Wilson SL, Blair JD, Hogg K, Langlois S, von Dadelszen P, Robinson WP. Placental DNA methylation at term reflects maternal serum levels of INHA and FN1, but not PAPPA, early in pregnancy. Bmc Medical Genetics. 16: 111. PMID 26654447 DOI: 10.1186/S12881-015-0257-Z  1
2015 Manokhina I, Wilson SL, Robinson WP. Noninvasive nucleic acid-based approaches to monitor placental health and predict pregnancy-related complications. American Journal of Obstetrics and Gynecology. 213: S197-206. PMID 26428499 DOI: 10.1016/J.Ajog.2015.07.010  1
2015 de Goede OM, Razzaghian HR, Price EM, Jones MJ, Kobor MS, Robinson WP, Lavoie PM. Nucleated red blood cells impact DNA methylation and expression analyses of cord blood hematopoietic cells. Clinical Epigenetics. 7: 95. PMID 26366232 DOI: 10.1186/S13148-015-0129-6  1
2015 Aghababaei M, Hogg K, Perdu S, Robinson WP, Beristain AG. ADAM12-directed ectodomain shedding of E-cadherin potentiates trophoblast fusion. Cell Death and Differentiation. PMID 25909890 DOI: 10.1038/cdd.2015.44  1
2015 Sirrs S, van Karnebeek CD, Peng X, Shyr C, Tarailo-Graovac M, Mandal R, Testa D, Dubin D, Carbonetti G, Glynn SE, Sayson B, Robinson WP, Han B, Wishart D, Ross CJ, et al. Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms. Orphanet Journal of Rare Diseases. 10: 38. PMID 25885783 DOI: 10.1186/S13023-015-0248-3  1
2015 Tarailo-Graovac M, Sinclair G, Stockler-Ipsiroglu S, Van Allen M, Rozmus J, Shyr C, Biancheri R, Oh T, Sayson B, Lafek M, Ross CJ, Robinson WP, Wasserman WW, Rossi A, van Karnebeek CD. The genotypic and phenotypic spectrum of PIGA deficiency. Orphanet Journal of Rare Diseases. 10: 23. PMID 25885527 DOI: 10.1186/s13023-015-0243-8  1
2015 Uhlmann WR, Peñaherrera MS, Robinson WP, Milunsky JM, Nicholson JM, Albin RL. 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. 167: 1152-60. PMID 25736541 DOI: 10.1002/ajmg.a.37009  1
2015 Robinson WP, Price EM. The human placental methylome. Cold Spring Harbor Perspectives in Medicine. 5: a023044. PMID 25722473 DOI: 10.1101/Cshperspect.A023044  1
2015 Barbaux S, Erwich JJ, Favaron PO, Gil S, Gallot D, Golos TG, Gonzalez-Bulnes A, Guibourdenche J, Heazell AE, Jansson T, Laprévote O, Lewis RM, Miller RK, Monk D, Novakovic B, ... ... Robinson W, et al. 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. 36: S5-10. PMID 25703592 DOI: 10.1016/J.Placenta.2015.01.196  1
2015 Hu Y, Blair JD, Yuen RK, Robinson WP, von Dadelszen P. Genome-wide DNA methylation identifies trophoblast invasion-related genes: Claudin-4 and Fucosyltransferase IV control mobility via altering matrix metalloproteinase activity. Molecular Human Reproduction. 21: 452-65. PMID 25697377 DOI: 10.1093/molehr/gav007  1
2015 Wen J, Hanna CW, Martell S, Leung PC, Lewis SM, Robinson WP, Stephenson MD, Rajcan-Separovic E. Functional consequences of copy number variants in miscarriage. Molecular Cytogenetics. 8: 6. PMID 25674159 DOI: 10.1186/s13039-015-0109-8  1
2015 Filges I, Manokhina I, Peñaherrera MS, McFadden DE, Louie K, Nosova E, Friedman JM, Robinson WP. Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants. Molecular Human Reproduction. 21: 339-46. PMID 25504873 DOI: 10.1093/molehr/gau112  1
2014 Manokhina I, Singh TK, Peñaherrera MS, Robinson WP. Quantification of cell-free DNA in normal and complicated pregnancies: overcoming biological and technical issues. Plos One. 9: e101500. PMID 24987984 DOI: 10.1371/journal.pone.0101500  1
2014 Brown LA, Rupps R, Peñaherrera MS, Robinson WP, Patel MS, Eydoux P, Boerkoel CF. 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. 164: 1587-94. PMID 24668696 DOI: 10.1002/ajmg.a.36490  1
2014 Hogg K, Robinson WP, Beristain AG. Activation of endocrine-related gene expression in placental choriocarcinoma cell lines following DNA methylation knock-down. Molecular Human Reproduction. 20: 677-89. PMID 24623739 DOI: 10.1093/molehr/gau020  1
2014 Blair JD, Langlois S, McFadden DE, Robinson WP. Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsia. Placenta. 35: 216-22. PMID 24462402 DOI: 10.1016/j.placenta.2014.01.001  1
2014 Hogg K, Price EM, Robinson WP. Improved reporting of DNA methylation data derived from studies of the human placenta. Epigenetics : Official Journal of the Dna Methylation Society. 9: 333-7. PMID 24394602 DOI: 10.4161/Epi.27648  1
2014 Ackerman WE, Adamson L, Carter AM, Collins S, Cox B, Elliot MG, Ermini L, Gruslin A, Hoodless PA, Huang J, Kniss DA, McGowen MR, Post M, Rice G, Robinson W, et al. 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. 35: S10-4. PMID 24315655 DOI: 10.1016/J.Placenta.2013.11.011  1
2014 Qiao Y, Mondal K, Trapani V, Wen J, Carpenter G, Wildin R, Price EM, Gibbons RJ, Eichmeyer J, Jiang R, DuPont B, Martell S, Lewis SM, Robinson WP, O'Driscoll M, et al. Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes. Human Mutation. 35: 58-62. PMID 24130152 DOI: 10.1002/Humu.22465  1
2013 Towle R, Truong D, Hogg K, Robinson WP, Poh CF, Garnis C. Global analysis of DNA methylation changes during progression of oral cancer. Oral Oncology. 49: 1033-42. PMID 24035722 DOI: 10.1016/J.Oraloncology.2013.08.005  1
2013 Blair JD, Yuen RK, Lim BK, McFadden DE, von Dadelszen P, Robinson WP. Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset pre-eclampsia. Molecular Human Reproduction. 19: 697-708. PMID 23770704 DOI: 10.1093/molehr/gat044  1
2013 Hogg K, Blair JD, McFadden DE, von Dadelszen P, Robinson WP. Early onset pre-eclampsia is associated with altered DNA methylation of cortisol-signalling and steroidogenic genes in the placenta. Plos One. 8: e62969. PMID 23667551 DOI: 10.1371/journal.pone.0062969  1
2013 Hanna CW, McFadden DE, Robinson WP. DNA methylation profiling of placental villi from karyotypically normal miscarriage and recurrent miscarriage. The American Journal of Pathology. 182: 2276-84. PMID 23583422 DOI: 10.1016/j.ajpath.2013.02.021  1
2013 Schroeder DI, Blair JD, Lott P, Yu HO, Hong D, Crary F, Ashwood P, Walker C, Korf I, Robinson WP, LaSalle JM. The human placenta methylome. Proceedings of the National Academy of Sciences of the United States of America. 110: 6037-42. PMID 23530188 DOI: 10.1073/Pnas.1215145110  1
2013 Manokhina I, Hanna CW, Stephenson MD, McFadden DE, Robinson WP. Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage. Molecular Human Reproduction. 19: 539-44. PMID 23515668 DOI: 10.1093/molehr/gat019  1
2013 Jacob KJ, Robinson WP, Lefebvre L. Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth. Clinical Genetics. 84: 326-34. PMID 23495910 DOI: 10.1111/Cge.12143  1
2013 Price ME, Cotton AM, Lam LL, Farré P, Emberly E, Brown CJ, Robinson WP, Kobor MS. Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array. Epigenetics & Chromatin. 6: 4. PMID 23452981 DOI: 10.1186/1756-8935-6-4  1
2013 Yuen RK, Chen B, Blair JD, Robinson WP, Nelson DM. Hypoxia alters the epigenetic profile in cultured human placental trophoblasts. Epigenetics : Official Journal of the Dna Methylation Society. 8: 192-202. PMID 23314690 DOI: 10.4161/epi.23400  1
2013 Hogg K, Blair JD, von Dadelszen P, Robinson WP. Hypomethylation of the LEP gene in placenta and elevated maternal leptin concentration in early onset pre-eclampsia. Molecular and Cellular Endocrinology. 367: 64-73. PMID 23274423 DOI: 10.1016/j.mce.2012.12.018  1
2013 Novakovic B, Gordon L, Robinson WP, Desoye G, Saffery R. 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. 24: 282-8. PMID 22901689 DOI: 10.1016/j.jnutbio.2012.06.006  1
2012 Hu Y, Yuen R, Eastabrook G, Dutz J, Tan R, von Dadelszen P, Robinson W. PP065. dNK and dNK-CM mediated alterations of DNA methylation in extravillous cytotrophoblasts (EVTS). Pregnancy Hypertension. 2: 277. PMID 26105388 DOI: 10.1016/J.Preghy.2012.04.176  1
2012 Yong PJ, McFadden DE, Robinson WP. Protein kinase profiling in miscarriage: implications for the pathogenesis of trisomic pregnancy. Journal of Obstetrics and Gynaecology Canada : Jogc = Journal D'Obstã©Trique Et Gynã©Cologie Du Canada : Jogc. 34: 1141-8. PMID 23231796  1
2012 Hogg K, Price EM, Hanna CW, Robinson WP. Prenatal and perinatal environmental influences on the human fetal and placental epigenome. Clinical Pharmacology and Therapeutics. 92: 716-26. PMID 23047650 DOI: 10.1038/clpt.2012.141  1
2012 Price EM, Robinson WP. Response to: "Response to Different measures of 'genome-wide' DNA methylation exhibit unique properties in placental and somatic tissues. Epigenetics. 7: 965. PMID 22864533 DOI: 10.4161/Epi.21623  1
2012 Niederhoffer KY, Peñaherrera M, Pugash D, Rupps R, Arbour L, Tessier F, Choufani S, Zhao C, Manokhina I, Shuman C, Robinson WP, Weksberg R, Boerkoel CF. Beckwith-Wiedemann syndrome in sibs discordant for IC2 methylation. American Journal of Medical Genetics. Part A. 158: 1662-9. PMID 22615066 DOI: 10.1002/Ajmg.A.35377  1
2012 Price EM, Cotton AM, Peñaherrera MS, McFadden DE, Kobor MS, Robinson W. Different measures of "genome-wide" DNA methylation exhibit unique properties in placental and somatic tissues. Epigenetics : Official Journal of the Dna Methylation Society. 7: 652-63. PMID 22531475 DOI: 10.4161/Epi.20221  1
2012 Hanna CW, Bloom MS, Robinson WP, Kim D, Parsons PJ, vom Saal FS, Taylor JA, Steuerwald AJ, Fujimoto VY. 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 (Oxford, England). 27: 1401-10. PMID 22381621 DOI: 10.1093/Humrep/Des038  1
2012 Hanna CW, Blair JD, Stephenson MD, Robinson WP. Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage. Reproductive Biomedicine Online. 24: 251-3. PMID 22197129 DOI: 10.1016/j.rbmo.2011.10.013  1
2012 Ackerman WE, Bulmer JN, Carter AM, Chaillet JR, Chamley L, Chen CP, Chuong EB, Coleman SJ, Collet GP, Croy BA, de Mestre AM, Dickinson H, Ducray J, Enders AC, Fogarty NM, ... ... Robinson WP, et al. IFPA Meeting 2011 workshop report III: Placental immunology; epigenetic and microRNA-dependent gene regulation; comparative placentation; trophoblast differentiation; stem cells. Placenta. 33: S15-22. PMID 22154501 DOI: 10.1016/J.Placenta.2011.11.022  1
2011 Yuen RK, Manokhina I, Robinson WP. Are we ready for DNA methylation-based prenatal testing? Epigenomics. 3: 387-90. PMID 22126197 DOI: 10.2217/epi.11.62  1
2011 Novakovic B, Yuen RK, Gordon L, Penaherrera MS, Sharkey A, Moffett A, Craig JM, Robinson WP, Saffery R. Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors. Bmc Genomics. 12: 529. PMID 22032438 DOI: 10.1186/1471-2164-12-529  1
2011 Cohen CJ, Rebollo R, Babovic S, Dai EL, Robinson WP, Mager DL. Placenta-specific expression of the Interleukin-2 (IL-2) receptor β subunit from an endogenous retroviral promoter Journal of Biological Chemistry. 286: 35543-35552. PMID 21865161 DOI: 10.1074/jbc.M111.227637  1
2011 Yuen RK, Jiang R, Peñaherrera MS, McFadden DE, Robinson WP. Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies. Epigenetics & Chromatin. 4: 10. PMID 21749726 DOI: 10.1186/1756-8935-4-10  1
2011 Yong PJ, McFadden DE, Robinson WP. Developmental origin of chorionic villus cultures from spontaneous abortion and chorionic villus sampling. Journal of Obstetrics and Gynaecology Canada : Jogc = Journal D'Obstã©Trique Et Gynã©Cologie Du Canada : Jogc. 33: 449-52. PMID 21639964  1
2011 Cotton AM, Lam L, Affleck JG, Wilson IM, Peñaherrera MS, McFadden DE, Kobor MS, Lam WL, Robinson WP, Brown CJ. Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation. Human Genetics. 130: 187-201. PMID 21597963 DOI: 10.1007/s00439-011-1007-8  1
2011 Yuen RK, Neumann SM, Fok AK, Peñaherrera MS, McFadden DE, Robinson WP, Kobor MS. Extensive epigenetic reprogramming in human somatic tissues between fetus and adult. Epigenetics & Chromatin. 4: 7. PMID 21545704 DOI: 10.1186/1756-8935-4-7  1
2011 Yuen RK, Robinson WP. Review: A high capacity of the human placenta for genetic and epigenetic variation: implications for assessing pregnancy outcome. Placenta. 32: S136-41. PMID 21281965 DOI: 10.1016/j.placenta.2011.01.003  1
2011 Bourque DK, Peñaherrera MS, Yuen RK, Van Allen MI, McFadden DE, Robinson WP. The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders. Clinical Genetics. 79: 169-75. PMID 20507345 DOI: 10.1111/J.1399-0004.2010.01443.X  1
2010 Ngai YF, Chijiwa C, Mercimek-Mahmutoglu S, Stewart L, Yong SL, Robinson WP, Gibson WT. 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. 152: 2784-90. PMID 20979189 DOI: 10.1002/ajmg.a.33172  1
2010 Avila L, Yuen RK, Diego-Alvarez D, Peñaherrera MS, Jiang R, Robinson WP. Evaluating DNA methylation and gene expression variability in the human term placenta. Placenta. 31: 1070-7. PMID 20947161 DOI: 10.1016/j.placenta.2010.09.011  1
2010 Rajcan-Separovic E, Diego-Alvarez D, Robinson WP, Tyson C, Qiao Y, Harvard C, Fawcett C, Kalousek D, Philipp T, Somerville MJ, Stephenson MD. Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss. Human Reproduction (Oxford, England). 25: 2913-22. PMID 20847186 DOI: 10.1093/humrep/deq202  1
2010 Hanna CW, Bretherick KL, Liu CC, Stephenson MD, Robinson WP. Genetic variation within the hypothalamus-pituitary-ovarian axis in women with recurrent miscarriage. Human Reproduction (Oxford, England). 25: 2664-71. PMID 20716560 DOI: 10.1093/humrep/deq211  1
2010 Yuen RK, Peñaherrera MS, von Dadelszen P, McFadden DE, Robinson WP. DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia. European Journal of Human Genetics : Ejhg. 18: 1006-12. PMID 20442742 DOI: 10.1038/ejhg.2010.63  1
2010 Peñaherrera MS, Weindler S, Van Allen MI, Yong SL, Metzger DL, McGillivray B, Boerkoel C, Langlois S, Robinson WP. Methylation profiling in individuals with Russell-Silver syndrome. American Journal of Medical Genetics. Part A. 152: 347-55. PMID 20082469 DOI: 10.1002/Ajmg.A.33204  1
2010 Bourque DK, Avila L, Peñaherrera M, von Dadelszen P, Robinson WP. Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia. Placenta. 31: 197-202. PMID 20060582 DOI: 10.1016/J.Placenta.2009.12.003  1
2010 Robinson WP, Peñaherrera MS, Jiang R, Avila L, Sloan J, McFadden DE, Langlois S, von Dadelszen P. Assessing the role of placental trisomy in preeclampsia and intrauterine growth restriction. Prenatal Diagnosis. 30: 1-8. PMID 19918961 DOI: 10.1002/pd.2409  1
2010 Bretherick KL, Fairbrother N, Avila L, Harbord SH, Robinson WP. Fertility and aging: do reproductive-aged Canadian women know what they need to know? Fertility and Sterility. 93: 2162-8. PMID 19296943 DOI: 10.1016/J.Fertnstert.2009.01.064  1
2009 Yuen RK, Avila L, Peñaherrera MS, von Dadelszen P, Lefebvre L, Kobor MS, Robinson WP. Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes. Plos One. 4: e7389. PMID 19838307 DOI: 10.1371/Journal.Pone.0007389  1
2009 Yong PJ, von Dadelszen P, McFadden DE, Barrett IJ, Kalousek DK, Robinson WP. Placental weight in pregnancies with trisomy confined to the placenta. Journal of Obstetrics and Gynaecology Canada : Jogc = Journal D'Obstã©Trique Et Gynã©Cologie Du Canada : Jogc. 31: 605-10. PMID 19761633  1
2009 Cotton AM, Avila L, Penaherrera MS, Affleck JG, Robinson WP, Brown CJ. Inactive X chromosome-specific reduction in placental DNA methylation. Human Molecular Genetics. 18: 3544-52. PMID 19586922 DOI: 10.1093/hmg/ddp299  1
2009 Hanna CW, Bretherick KL, Gair JL, Fluker MR, Stephenson MD, Robinson WP. Telomere length and reproductive aging. Human Reproduction (Oxford, England). 24: 1206-11. PMID 19202142 DOI: 10.1093/humrep/dep007  1
2008 Nagarajan RP, Patzel KA, Martin M, Yasui DH, Swanberg SE, Hertz-Picciotto I, Hansen RL, Van de Water J, Pessah IN, Jiang R, Robinson WP, LaSalle JM. MECP2 promoter methylation and X chromosome inactivation in autism. Autism Research : Official Journal of the International Society For Autism Research. 1: 169-78. PMID 19132145 DOI: 10.1002/Aur.24  1
2008 Minks J, Robinson WP, Brown CJ. A skewed view of X chromosome inactivation. The Journal of Clinical Investigation. 118: 20-3. PMID 18097476 DOI: 10.1172/JCI34470  1
2008 Bretherick KL, Hanna CW, Currie LM, Fluker MR, Hammond GL, Robinson WP. Estrogen receptor alpha gene polymorphisms are associated with idiopathic premature ovarian failure. Fertility and Sterility. 89: 318-24. PMID 17706202 DOI: 10.1016/j.fertnstert.2007.03.008  1
2008 Bretherick KL, Hanna CW, Currie LM, Fluker MR, Hammond GL, Robinson WP. Estrogen receptor α gene polymorphisms are associated with idiopathic premature ovarian failure Obstetrical and Gynecological Survey. 63: 435-436. DOI: 10.1097/01.ogx.0000318078.78865.25  1
2007 Robinson WP, Slee J, Smith N, Murch A, Watson SK, Lam WL, McFadden DE. Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5. American Journal of Medical Genetics. Part A. 143: 1752-9. PMID 17593542 DOI: 10.1002/ajmg.a.31800  1
2007 Bretherick KL, Metzger DL, Chanoine JP, Panagiotopoulos C, Watson SK, Lam WL, Fluker MR, Brown CJ, Robinson WP. Skewed X-chromosome inactivation is associated with primary but not secondary ovarian failure. American Journal of Medical Genetics. Part A. 143: 945-51. PMID 17431892 DOI: 10.1002/ajmg.a.31679  1
2007 Robinson WP, McGillivray B, Friedman JM. Pregnancy and postnatal outcome of mosaic isochromosome 20q. Prenatal Diagnosis. 27: 143-5. PMID 17191261 DOI: 10.1002/pd.1636  1
2007 Robinson WP, Lauzon JL, Innes AM, Lim K, Arsovska S, McFadden DE. Origin and outcome of pregnancies affected by androgenetic/biparental chimerism. Human Reproduction (Oxford, England). 22: 1114-22. PMID 17185351 DOI: 10.1093/humrep/del462  1
2007 Hirschfeld AF, Jiang R, Robinson WP, McFadden DE, Turvey SE. Toll-like receptor 4 polymorphisms and idiopathic chromosomally normal miscarriage. Human Reproduction (Oxford, England). 22: 440-3. PMID 16982657 DOI: 10.1093/humrep/del377  1
2006 Yong PJ, Langlois S, von Dadelszen P, Robinson W. The association between preeclampsia and placental trisomy 16 mosaicism. Prenatal Diagnosis. 26: 956-61. PMID 16874839 DOI: 10.1002/Pd.1534  1
2006 Langlois S, Yong PJ, Yong SL, Barrett I, Kalousek DK, Miny P, Exeler R, Morris K, Robinson WP. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism. Prenatal Diagnosis. 26: 548-58. PMID 16683298 DOI: 10.1002/pd.1457  1
2006 McFadden DE, Robinson WP. Phenotype of triploid embryos. Journal of Medical Genetics. 43: 609-12. PMID 16236813 DOI: 10.1136/jmg.2005.037747  1
2006 Bretherick K, Gair J, Robinson WP. The association of skewed X chromosome inactivation with aneuploidy in humans. Cytogenetic and Genome Research. 111: 260-5. PMID 16192703 DOI: 10.1159/000086898  0.32
2006 Kaiser-Rogers KA, McFadden DE, Livasy CA, Dansereau J, Jiang R, Knops JF, Lefebvre L, Rao KW, Robinson WP. Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia. Journal of Medical Genetics. 43: 187-92. PMID 15908568 DOI: 10.1136/Jmg.2005.033571  1
2005 Bretherick KL, Fluker MR, Robinson WP. FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure. Human Genetics. 117: 376-82. PMID 16078053 DOI: 10.1007/s00439-005-1326-8  1
2005 Robinson WP, McGillivray B, Lewis ME, Arbour L, Barrett I, Kalousek DK. Prenatally detected trisomy 20 mosaicism. Prenatal Diagnosis. 25: 239-44. PMID 15791659 DOI: 10.1002/pd.1121  1
2003 Beever CL, Peñaherrera MS, Langlois S, Robinson WR. X chromosome inactivation patterns in Russell-Silver syndrome patients and their mothers. American Journal of Medical Genetics. Part A. 123: 231-5. PMID 14608642 DOI: 10.1002/ajmg.a.20317  1
2003 Beever C, Lai BP, Baldry SE, Peñaherrera MS, Jiang R, Robinson WP, Brown CJ. Methylation of ZNF261 as an assay for determining X chromosome inactivation patterns. American Journal of Medical Genetics. Part A. 120: 439-41. PMID 12838571 DOI: 10.1002/ajmg.a.20045  1
2003 Ma S, Yuen BH, Penaherrera M, Koehn D, Ness L, Robinson W. ICSI and the transmission of X-autosomal translocation: a three-generation evaluation of X;20 translocation: case report. Human Reproduction (Oxford, England). 18: 1377-82. PMID 12832360 DOI: 10.1093/Humrep/Deg247  0.4
2002 McFadden DE, Jiang R, Langlois S, Robinson WP. Dispermy--origin of diandric triploidy: brief communication. Human Reproduction (Oxford, England). 17: 3037-8. PMID 12456599  1
2002 Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK. Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism. Prenatal Diagnosis. 22: 1076-85. PMID 12454962 DOI: 10.1002/pd.483  1
2001 Robinson WP, McFadden DE, Stephenson MD. The origin of abnormalities in recurrent aneuploidy/polyploidy. American Journal of Human Genetics. 69: 1245-54. PMID 11675616 DOI: 10.1086/324468  1
2001 Rajcan-Separovic E, Robinson WP, Stephenson M, Pantzar T, Arbour L, McFadden D, Guscott J. Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13). American Journal of Medical Genetics. 99: 320-4. PMID 11252000 DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1173>3.0.CO;2-1  1
2000 Robinson WP, Christian SL, Kuchinka BD, Peñaherrera MS, Das S, Schuffenhauer S, Malcolm S, Schinzel AA, Hassold TJ, Ledbetter DH. Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15 Clinical Genetics. 57: 349-358. PMID 10852369 DOI: 10.1034/J.1399-0004.2000.570505.X  1
1999 Bernard LE, Peñaherrera MS, Van Allen MI, Wang MS, Yong SL, Gareis F, Langlois S, Robinson WP. Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases. American Journal of Medical Genetics. 87: 230-6. PMID 10564876 DOI: 10.1002/(SICI)1096-8628(19991126)87:3<230::AID-AJMG7>3.0.CO;2-S  1
1999 Wang MS, Schinzel A, Kotzot D, Balmer D, Casey R, Chodirker BN, Gyftodimou J, Petersen MB, Lopez-Rangel E, Robinson WP. 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. 86: 34-43. PMID 10440826 DOI: 10.1002/(SICI)1096-8628(19990903)86:1<34::AID-AJMG7>3.0.CO;2-4  1
1999 Morton CC, Christian SL, Donlon TA, Driscoll DJ, Fink JK, Gabriel JM, Gotway G, Greally JM, Hitchins MP, Howard HC, Ji Y, Leonard S, Lerner T, Magenis E, Malcolm S, ... ... Robinson WP, et al. Report of the fourth international workshop on human chromosome 15 mapping 1997. Cytogenetics and Cell Genetics. 84: 12-21. PMID 10343092 DOI: 10.1159/000015203  1
1999 Robinson WP, Bernasconi F, Lau A, McFadden DE. Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment. American Journal of Medical Genetics. 84: 34-42. PMID 10213044 DOI: 10.1002/(SICI)1096-8628(19990507)84:1<34::AID-AJMG8>3.0.CO;2-7  1
1998 Field LL, Tobias R, Robinson WP, Paisey R, Bain S. Maternal uniparental disomy of chromosome 1 with no apparent phenotypic effects [1] American Journal of Human Genetics. 63: 1216-1220. PMID 9758608 DOI: 10.1086/302050  1
1998 Harrison KJ, Teshima IE, Silver MM, Jay V, Unger S, Robinson WP, James A, Levin A, Chitayat D. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies. American Journal of Medical Genetics. 79: 103-7. PMID 9741467 DOI: 10.1002/(Sici)1096-8628(19980901)79:2<103::Aid-Ajmg5>3.0.Co;2-R  1
1998 Robinson WP, Kuchinka BD, Bernasconi F, Petersen MB, Schulze A, Brondum-Nielsen K, Christian SL, Ledbetter DH, Schinzel AA, Horsthemke B, Schuffenhauer S, Michaelis RC, Langlois S, Hassold TJ. Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination. Human Molecular Genetics. 7: 1011-9. PMID 9580665 DOI: 10.1093/Hmg/7.6.1011  1
1998 Robinson WP, Dutly F, Nicholls RD, Bernasconi F, Peñaherrera M, Michaelis RC, Abeliovich D, Schinzel AA. The mechanisms involved in formation of deletions and duplications of 15q11-q13. Journal of Medical Genetics. 35: 130-6. PMID 9580159 DOI: 10.1136/Jmg.35.2.130  1
1997 Lau AW, Brown CJ, Peñaherrera M, Langlois S, Kalousek DK, Robinson WP. Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism. American Journal of Human Genetics. 61: 1353-61. PMID 9399909 DOI: 10.1086/301651  1
1997 Brown CJ, Robinson WP. XIST expression and X-chromosome inactivation in human preimplantation embryos American Journal of Human Genetics. 61: 5-8. PMID 9245976 DOI: 10.1086/513914  1
1997 Robinson WP, Horsthemke B, Leonard S, Malcolm S, Morton C, Nicholls RD, Ritchie RJ, Rogan P, Schultz R, Schwartz S, Sharp J, Trent R, Wevrick R, Williamson M, Knoll JH. Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., Canada Cytogenetics and Cell Genetics. 76: 1-13. PMID 9154113 DOI: 10.1159/000134500  1
1996 Shaffer LG, Langlois S, McCaskill C, Main DM, Robinson WP, Barrett IJ, Kalousek DK. Analysis of nine pregnancies with confined placental mosaicism for trisomy 2. Prenatal Diagnosis. 16: 899-905. PMID 8938058 DOI: 10.1002/(SICI)1097-0223(199610)16:10<899::AID-PD960>3.0.CO;2-M  1
1996 Mitchell J, Schinzel A, Langlois S, Gillessen-Kaesbach G, Schuffenhauer S, Michaelis R, Abeliovich D, Lerer I, Christian S, Guitart M, McFadden DE, Robinson WP. Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences. American Journal of Medical Genetics. 65: 133-6. PMID 8911605 DOI: 10.1002/(Sici)1096-8628(19961016)65:2<133::Aid-Ajmg10>3.0.Co;2-R  1
1996 Schinzel A, Lorda-Sanchez I, Binkert F, Carter NP, Bebb CE, Ferguson-Smith MA, Eiholzer U, Zachmann M, Robinson WP. Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting. Journal of Medical Genetics. 32: 957-61. PMID 8825924 DOI: 10.1136/Jmg.32.12.957  0.44
1996 Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA. Molecular studies of translocations and trisomy involving chromosome 13. American Journal of Medical Genetics. 61: 158-63. PMID 8669444 DOI: 10.1002/(SICI)1096-8628(19960111)61:2<158::AID-AJMG11>3.0.CO;2-T  1
1996 Robinson WP, Waslynka J, Bernasconi F, Wang M, Clark S, Kotzot D, Schinzel A. 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. 34: 17-23. PMID 8661020 DOI: 10.1006/geno.1996.0237  1
1995 Robinson WP, Lalande M. Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region. Human Molecular Genetics. 4: 801-6. PMID 7633438 DOI: 10.1093/Hmg/4.5.801  1
1995 Kotzot D, Schmitt S, Bernasconi F, Robinson WP, Lurie IW, Ilyina H, Méhes K, Hamel BC, Otten BJ, Hergersberg M. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Human Molecular Genetics. 4: 583-7. PMID 7633407 DOI: 10.1093/Hmg/4.4.583  1
1994 Robinson WP, Binkert F, Schinzel AA, Basaran S, Mikelsaar R. Multiple origins of X chromosome tetrasomy [4] Journal of Medical Genetics. 31: 424-425. PMID 8064828 DOI: 10.1136/jmg.31.5.424  1
1994 Bottani A, Robinson WP, DeLozier-Blanchet CD, Engel E, Morris MA, Schmitt B, Thun-Hohenstein L, Schinzel A. Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype? American Journal of Medical Genetics. 51: 35-40. PMID 8030667 DOI: 10.1002/Ajmg.1320510109  0.32
1994 Schinzel AA, Brecevic L, Bernasconi F, Binkert F, Berthet F, Wuilloud A, Robinson WP. Intrachromosomal triplication of 15q11-q13. Journal of Medical Genetics. 31: 798-803. PMID 7837257 DOI: 10.1136/jmg.31.10.798  1
1993 Robinson WP, Wagstaff J, Bernasconi F, Baccichetti C, Artifoni L, Franzoni E, Suslak L, Shih LY, Aviv H, Schinzel AA. 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. 30: 756-60. PMID 8411071 DOI: 10.1136/jmg.30.9.756  1
1993 Schinzel AA, Robinson WP, Binkert F, Torresani T, Werder EA. Exclusively paternal X chromosomes in a girl with short stature. Human Genetics. 92: 175-8. PMID 8370585 DOI: 10.1007/BF00219687  0.68
1993 Glenn CC, Nicholls RD, Robinson WP, Saitoh S, Niikawa N, Schinzel A, Horsthemke B, Driscoll DJ. Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients. Human Molecular Genetics. 2: 1377-82. PMID 8242060 DOI: 10.1093/HMG/2.9.1377  0.48
1993 Buiting K, Dittrich B, Gross S, Greger V, Lalande M, Robinson W, Mutirangura A, Ledbetter D, Horsthemke B. Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene. Human Molecular Genetics. 2: 1991-4. PMID 8111365 DOI: 10.1093/Hmg/2.12.1991  1
1992 Schinzel A, Robinson WP, Bottani A, Yagang X, Prader A. Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin? Human Genetics. 88: 361-2. PMID 1733842 DOI: 10.1007/Bf00197279  0.48
1992 Lorda-Sanchez I, Binkert F, Maechler M, Robinson WP, Schinzel AA. Reduced recombination and paternal age effect in Klinefelter syndrome. Human Genetics. 89: 524-30. PMID 1353053 DOI: 10.1007/BF00219178  0.6
1992 Ozçelik T, Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, Francke U. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nature Genetics. 2: 265-9. PMID 1303277 DOI: 10.1038/Ng1292-265  1
1990 Schinzel A, Hof E, Dangel P, Robinson W. Familial congenital laryngeal abductor paralysis: different expression in a family with one male and three females affected. Journal of Medical Genetics. 27: 715-716. PMID 2277390 DOI: 10.1136/Jmg.27.11.715  0.48
1989 Klitz W, Kuhner MK, Robinson W, Esposito M, Thomson G. Clues to IDDM pathogenesis from genetic and serological traits in multiply affected families. Genetic Epidemiology. 6: 117-22. PMID 2567254 DOI: 10.1002/Gepi.1370060122  0.52
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