| Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case–control study MD Stephenson, KA Awartani, WP Robinson Human reproduction 17 (2), 446-451, 2002 | 686 | 2002 |
| Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array EM Price, AM Cotton, LL Lam, P Farré, E Emberly, CJ Brown, ... Epigenetics & chromatin 6, 1-15, 2013 | 545 | 2013 |
| Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus G Thomson, WP Robinson, MK Kuhner, S Joe, MJ MacDonald, ... American journal of human genetics 43 (6), 799, 1988 | 464 | 1988 |
| Mechanisms leading to uniparental disomy and their clinical consequences WP Robinson Bioessays 22 (5), 452-459, 2000 | 418 | 2000 |
| The human placenta methylome DI Schroeder, JD Blair, P Lott, HOK Yu, D Hong, F Crary, P Ashwood, ... Proceedings of the national academy of sciences 110 (15), 6037-6042, 2013 | 346 | 2013 |
| Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation D Kotzot, S Schmitt, F Bernasconi, WP Robinson, IW Lurie, H Ilyina, ... Human molecular genetics 4 (4), 583-587, 1995 | 346 | 1995 |
| Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region T Özçelik, S Leff, W Robinson, T Donlon, M Lalande, E Sanjines, ... Nature genetics 2 (4), 265-269, 1992 | 328 | 1992 |
| Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients. WP Robinson, A Bottani, YG Xie, J Balakrishman, F Binkert, M Mächler, ... American journal of human genetics 49 (6), 1219, 1991 | 319 | 1991 |
| Fertility and aging: do reproductive-aged Canadian women know what they need to know? KL Bretherick, N Fairbrother, L Avila, SHA Harbord, WP Robinson Fertility and sterility 93 (7), 2162-2168, 2010 | 304 | 2010 |
| DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia RKC Yuen, MS Penaherrera, P Von Dadelszen, DE McFadden, ... European Journal of Human Genetics 18 (9), 1006-1012, 2010 | 259 | 2010 |
| 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 … WP Robinson, IJ Barrett, L Bernard, A Telenius, F Bernasconi, RD Wilson, ... American journal of human genetics 60 (4), 917, 1997 | 258 | 1997 |
| FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure KL Bretherick, MR Fluker, WP Robinson Human genetics 117, 376-382, 2005 | 250 | 2005 |
| Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13 B Dittrich, WP Robinson, H Knoblauch, K Buiting, K Schmidt, ... Human Genetics 90, 313-315, 1992 | 241 | 1992 |
| Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset pre-eclampsia JD Blair, RKC Yuen, BK Lim, DE McFadden, P von Dadelszen, ... Molecular human reproduction 19 (10), 697-708, 2013 | 234 | 2013 |
| Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia DK Bourque, L Avila, M Penaherrera, P Von Dadelszen, WP Robinson Placenta 31 (3), 197-202, 2010 | 230 | 2010 |
| HLA–Bw60 increases susceptibility to ankylosing spondylitis in HLA–B27+ patients WP Robinson, SM Van Der Linden, MA Khan, HU Rentsch, A Cats, ... Arthritis & Rheumatism: Official Journal of the American College of …, 1989 | 224 | 1989 |
| Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients. SL Christian, WP Robinson, B Huang, A Mutirangura, MR Line, M Nakao, ... American journal of human genetics 57 (1), 40, 1995 | 213 | 1995 |
| Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors B Novakovic, RK Yuen, L Gordon, MS Penaherrera, A Sharkey, A Moffett, ... BMC genomics 12, 1-14, 2011 | 210 | 2011 |
| Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia KA Kaiser-Rogers, DE Mcfadden, CA Livasy, J Dansereau, R Jiang, ... Journal of medical genetics 43 (2), 187-192, 2006 | 198 | 2006 |
| DNA methylation changes in whole blood is associated with exposure to the environmental contaminants, mercury, lead, cadmium and bisphenol A, in women undergoing ovarian … CW Hanna, MS Bloom, WP Robinson, D Kim, PJ Parsons, FS vom Saal, ... Human reproduction 27 (5), 1401-1410, 2012 | 181 | 2012 |
Carolyn J. BrownProfessor, Medical Genetics, Life Sciences Institute, University of British ColumbiaVerified email at ubc.ca
