| Year |
Citation |
Score |
| 2024 |
Shannon MJ, McNeill GL, Koksal B, Baltayeva J, Wächter J, Castellana B, Peñaherrera MS, Robinson WP, Leung PCK, Beristain AG. Single-cell assessment of primary and stem cell-derived human trophoblast organoids as placenta-modeling platforms. Developmental Cell. PMID 38359834 DOI: 10.1016/j.devcel.2024.01.023 |
0.693 |
|
| 2023 |
Khan A, Inkster AM, Peñaherrera MS, King S, Kildea S, Oberlander TF, Olson DM, Vaillancourt C, Brain U, Beraldo EO, Beristain AG, Clifton VL, Gobbo GFD, Lam WL, Metz GA, ... ... Robinson WP, et al. The application of epiphenotyping approaches to DNA methylation array studies of the human placenta. Research Square. PMID 37461679 DOI: 10.21203/rs.3.rs-3069705/v1 |
0.771 |
|
| 2022 |
Inkster AM, Konwar C, Peñaherrera MS, Brain U, Khan A, Price EM, Schuetz JM, Portales-Casamar É, Burt A, Marsit CJ, Vaillancourt C, Oberlander TF, Robinson WP. Profiling placental DNA methylation associated with maternal SSRI treatment during pregnancy. Scientific Reports. 12: 22576. PMID 36585414 DOI: 10.1038/s41598-022-26071-8 |
0.788 |
|
| 2021 |
Martinez VD, Sage AP, Minatel BC, Marshall EA, Price EM, Becker-Santos DD, Robinson WP, Lam WL. Human placental piwi-interacting RNA transcriptome is characterized by expression from the DLK1-DIO3 imprinted region. Scientific Reports. 11: 14981. PMID 34294738 DOI: 10.1038/s41598-021-93885-3 |
0.461 |
|
| 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 |
0.419 |
|
| 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 |
0.767 |
|
| 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 |
0.301 |
|
| 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 |
0.65 |
|
| 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 |
0.728 |
|
| 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 |
0.721 |
|
| 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 |
0.757 |
|
| 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 |
0.476 |
|
| 2019 |
Savage P, Monk D, Hernandez Mora JR, van der Westhuizen N, Rauw J, Tinker A, Robinson W, Song Q, Seckl MJ, Fisher RA. A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutations. Bmc Cancer. 19: 744. PMID 31357948 DOI: 10.1186/S12885-019-5906-8 |
0.36 |
|
| 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 |
0.663 |
|
| 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 |
0.683 |
|
| 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 |
0.753 |
|
| 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 |
0.713 |
|
| 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 |
0.639 |
|
| 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 |
0.803 |
|
| 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 |
0.344 |
|
| 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 |
0.442 |
|
| 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 |
0.744 |
|
| 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 |
0.644 |
|
| 2017 |
Wilson SL, Robinson WP. Utility of DNA methylation to assess placental health. Placenta. PMID 29273273 DOI: 10.1016/J.Placenta.2017.12.013 |
0.684 |
|
| 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 |
0.689 |
|
| 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 |
0.446 |
|
| 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 |
0.801 |
|
| 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 |
0.764 |
|
| 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 |
0.721 |
|
| 2017 |
Konwar C, Price M, Del Gobbo G, Wilson S, Terry J, Robinson W. Genetic and epigenetic profiling of acute chorioamnionitis associated placentas Placenta. 57: 304. DOI: 10.1016/J.Placenta.2017.07.253 |
0.781 |
|
| 2017 |
Robinson W. Genetic and epigenetic changes in the placenta in intrauterine growth restriction (IUGR) Placenta. 57: 242. DOI: 10.1016/J.Placenta.2017.07.072 |
0.314 |
|
| 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 |
0.688 |
|
| 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 |
0.765 |
|
| 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 |
0.823 |
|
| 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 |
0.764 |
|
| 2016 |
Leavey K, Wilson S, Bainbridge S, Robinson W, Cox B. Epigenetic regulation of placental gene expression in transcriptional subclasses of preeclampsia Placenta. 45: 122-123. DOI: 10.1016/J.Placenta.2016.06.213 |
0.661 |
|
| 2016 |
Wilson SL, Leavey K, von Dadelszen P, Cox B, Robinson WP. Unravelling the relationship between early and late-onset preeclampsia. What does the placental DNA methylation profile reveal? Placenta. 45: 114. DOI: 10.1016/J.Placenta.2016.06.184 |
0.671 |
|
| 2016 |
Konwar C, Price EM, Robinson WP. Using DNA methylation signatures in placental tissue and cells to gain insight into chorioamnionitis Placenta. 45: 113. DOI: 10.1016/J.Placenta.2016.06.180 |
0.775 |
|
| 2016 |
Del Gobbo G, Price EM, Hanna C, Robinson W. Placental MTHFR 677C>T genotypes in pregnancy pathologies Placenta. 45: 112. DOI: 10.1016/J.Placenta.2016.06.177 |
0.723 |
|
| 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 |
0.684 |
|
| 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 |
0.633 |
|
| 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 |
0.43 |
|
| 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 |
0.692 |
|
| 2015 |
Robinson WP, Price EM. The human placental methylome. Cold Spring Harbor Perspectives in Medicine. 5: a023044. PMID 25722473 DOI: 10.1101/Cshperspect.A023044 |
0.535 |
|
| 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 |
0.647 |
|
| 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 |
0.694 |
|
| 2015 |
Bagheri H, Wen J, Hanna CW, Tang F, Martell S, Qiao Y, Leung P, Robinson W, Stephenson M, Rajcan-Separovic E. MG-123 Genomics of early pregnancy loss Journal of Medical Genetics. 52: A6.1-A6. DOI: 10.1136/Jmedgenet-2015-103577.15 |
0.715 |
|
| 2015 |
Hanna C, Penaherrera M, Saadeh H, McFadden D, Kelsey G, Robinson W. Transient and placenta-specific imprinting in human development Placenta. 36: A39. DOI: 10.1016/J.Placenta.2015.07.303 |
0.78 |
|
| 2015 |
Leavey K, Wilson S, Bainbridge S, Robinson W, Cox B. An integrated transcriptional, epigenetic, and clinical analysis of preeclamptic placentas Placenta. 36: A7. DOI: 10.1016/J.Placenta.2015.07.206 |
0.64 |
|
| 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 |
0.733 |
|
| 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 |
0.729 |
|
| 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 |
0.309 |
|
| 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 |
0.362 |
|
| 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 |
0.506 |
|
| 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 |
0.428 |
|
| 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 |
0.684 |
|
| 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 |
0.319 |
|
| 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 |
0.722 |
|
| 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 |
0.688 |
|
| 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 |
0.358 |
|
| 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 |
0.639 |
|
| 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 |
0.304 |
|
| 2013 |
Blair J, Yuen R, Lim B, McFadden D, von Dadelszen P, Robinson W. Widespread DNA hypomethylation at gene enhancer and low CpG density regions in placentas associated with early-onset preeclampsia Placenta. 34: A86. DOI: 10.1016/J.Placenta.2013.06.254 |
0.714 |
|
| 2013 |
Hu Y, Blair J, Yuen R, Robinson W, von Dadelszen P. Decidual natural killer cells regulate FUT4 expression in EVT through DNA enhancer methylation Placenta. 34: A68-A69. DOI: 10.1016/J.Placenta.2013.06.206 |
0.665 |
|
| 2013 |
Peñaherrera M, Price M, Blair J, Van Allen M, McFadden D, Robinson W. Quantification of DNA methylation at imprinted domains in the placenta Placenta. 34: A66. DOI: 10.1016/J.Placenta.2013.06.198 |
0.746 |
|
| 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 |
0.686 |
|
| 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 |
0.568 |
|
| 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 |
0.731 |
|
| 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 |
0.451 |
|
| 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 |
0.753 |
|
| 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 |
0.557 |
|
| 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 |
0.695 |
|
| 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 |
0.643 |
|
| 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 |
0.632 |
|
| 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 |
0.813 |
|
| 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 |
0.815 |
|
| 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 |
0.499 |
|
| 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 |
0.324 |
|
| 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 |
0.816 |
|
| 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 |
0.659 |
|
| 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 |
0.704 |
|
| 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 |
0.653 |
|
| 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 |
0.78 |
|
| 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 |
0.695 |
|
| 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 |
0.747 |
|
| 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 |
0.738 |
|
| 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 |
0.735 |
|
| 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 |
0.687 |
|
| 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 |
0.562 |
|
| 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 |
0.744 |
|
| 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 |
0.75 |
|
| 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 |
0.767 |
|
| 2008 |
Ghahremani M, Hannah CW, Peneherrera M, Bretherick KL, Fluker MR, Robinson WP. EPIGENETIC ALTERATIONS ASSOCIATED WITH PREMATURE OVARIAN FAILURE Clinical & Investigative Medicine. 31: 11. DOI: 10.25011/cim.v31i4.4804 |
0.794 |
|
| 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 |
0.765 |
|
| 2008 |
Ghahremani M, Hanna C, Bretherick K, Penaherrera M, Fluker M, Robinson W. Epigenetic alterations associated with premature ovarian failure Fertility and Sterility. 90: S122-S123. DOI: 10.1016/j.fertnstert.2008.07.125 |
0.779 |
|
| 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 |
0.305 |
|
| 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 |
0.768 |
|
| 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 |
0.62 |
|
| 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 |
0.531 |
|
| 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 |
0.806 |
|
| 2005 |
Gair JL, Arbour L, Rupps R, Jiang R, Bruyère H, Robinson WP. Recurrent trisomy 21: four cases in three generations. Clinical Genetics. 68: 430-5. PMID 16207210 DOI: 10.1111/J.1399-0004.2005.00512.X |
0.326 |
|
| 2005 |
Robinson WP, Peñaherrera MS, Gair J, Hatakeyama C, Ma S. X-chromosome inactivation and telomere size in newborns resulting from intracytoplasmic sperm injection. American Journal of Medical Genetics. Part A. 343-5. PMID 16097000 DOI: 10.1002/ajmg.a.30886 |
0.775 |
|
| 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 |
0.753 |
|
| 2005 |
Hatakeyama C, Anderson CL, Beever CL, Peñaherrera MS, Brown CJ, Robinson WP. The dynamics of X-inactivation skewing as women age. Clinical Genetics. 66: 327-32. PMID 15355435 DOI: 10.1111/J.1399-0004.2004.00310.X |
0.414 |
|
| 2005 |
Hatakeyama C, Penaherrera M, Robinson W, Ma S. X-Chromosome Inactivation (XCI) in Newborns Conceived Through Intracytoplasmic Sperm Injection (ICSI) Fertility and Sterility. 84: S241. DOI: 10.1016/J.Fertnstert.2005.07.622 |
0.726 |
|
| 2004 |
Ma S, Tang SS, Yuen BH, Bruyere H, Peñaherrera M, Robinson WP. Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case report. Human Reproduction (Oxford, England). 18: 2298-301. PMID 14585877 DOI: 10.1093/Humrep/Deg462 |
0.725 |
|
| 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 |
0.732 |
|
| 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 |
0.735 |
|
| 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 |
0.734 |
|
| 2002 |
Penaherrea M, Ma S, Yuen BH, Brown C, Robinson W. X-Chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t(X;20) case Fertility and Sterility. 78: S255-S256. DOI: 10.1016/S0015-0282(02)04085-2 |
0.314 |
|
| 2001 |
Ma S, Robinson W, Lam R, Yuen BH. Maternal origin of monosomy 21 derived from ICSI. Human Reproduction (Oxford, England). 16: 1100-3. PMID 11387276 DOI: 10.1093/Humrep/16.6.1100 |
0.367 |
|
| 2001 |
Peñaherrera MS, Barrett IJ, Brown CJ, Langlois S, Yong SL, Lewis S, Bruyère H, Howard-Peebles PN, Kalousek DK, Robinson WP. An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta. Clinical Genetics. 58: 436-46. PMID 11149612 DOI: 10.1034/J.1399-0004.2000.580603.X |
0.36 |
|
| 2001 |
Brown CJ, Robinson WP. The causes and consequences of random and non-random X chromosome inactivation in humans. Clinical Genetics. 58: 353-63. PMID 11140834 DOI: 10.1034/J.1399-0004.2000.580504.X |
0.326 |
|
| 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 |
0.525 |
|
| 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 |
0.486 |
|
| 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 |
0.509 |
|
| 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 |
0.462 |
|
| 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 |
0.737 |
|
| 1997 |
Robinson WP, Langlois S, Schuffenhauer S, Horsthemke B, Michaelis RC, Christian S, Ledbetter DH, Schinzel A. Cytogenetic and age-dependent risk factors associated with uniparental disomy 15. Prenatal Diagnosis. 16: 837-44. PMID 8905898 DOI: 10.1002/(Sici)1097-0223(199609)16:9<837::Aid-Pd956>3.0.Co;2-7 |
0.509 |
|
| 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 |
0.464 |
|
| 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 |
0.461 |
|
| 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 |
0.484 |
|
| 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 |
0.461 |
|
| 1996 |
Gillessen-Kaesbach G, Robinson W, Lohmann D, Kaya-Westerloh S, Passarge E, Horsthemke B. Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome. Human Genetics. 96: 638-43. PMID 8522319 DOI: 10.1007/Bf00210291 |
0.31 |
|
| 1994 |
Ya-gang X, Robinson WP, Spiegel R, Binkert F, Ruefenacht U, Schinzel AA. Parental origin of the supernumerary chromosome in trisomy 18. Clinical Genetics. 44: 57-61. PMID 8275560 DOI: 10.1111/j.1399-0004.1993.tb03847.x |
0.51 |
|
| 1994 |
Robinson WP, Lorda-Sanchez I, Malcolm S, Langlois S, Schuffenhauer S, Knoblauch H, Horsthemke B, Schinzel AA. Increased parental ages and uniparental disomy 15: a paternal age effect? European Journal of Human Genetics : Ejhg. 1: 280-6. PMID 8081941 DOI: 10.1159/000472425 |
0.487 |
|
| 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 |
0.45 |
|
| 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 |
0.487 |
|
| 1994 |
Buiting K, Dittrich B, Robinson WP, Guitart M, Abeliovich D, Lerer I, Horsthemke B. Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implications. Human Molecular Genetics. 3: 893-5. PMID 7951232 DOI: 10.1093/HMG/3.6.893 |
0.314 |
|
| 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 |
0.45 |
|
| 1994 |
SCHINZEL AA, ROBINSON WP, BINKERT F, FANCONI A. An interstitial deletion of proximal 8q (q11???q13) in a girl with Silver-russell syndrome-like features Clinical Dysmorphology. 3: 63???69. DOI: 10.1097/00019605-199401000-00009 |
0.414 |
|
| 1993 |
Robinson WP, Spiegel R, Schinzel AA. Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombination. Human Genetics. 91: 181-4. PMID 8462978 DOI: 10.1007/BF00222722 |
0.473 |
|
| 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 |
0.468 |
|
| 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 |
0.48 |
|
| 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 |
0.532 |
|
| 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 |
0.341 |
|
| 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 |
0.451 |
|
| 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 |
0.493 |
|
| 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 |
0.574 |
|
| 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 |
0.511 |
|
| 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 |
0.731 |
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