| 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 | 723 | 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), 4, 2013 | 577 | 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 | 467 | 1988 |
| Mechanisms leading to uniparental disomy and their clinical consequences WP Robinson Bioessays 22 (5), 452-459, 2000 | 429 | 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 | 383 | 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 | 351 | 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 | 332 | 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 | 327 | 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 | 313 | 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 | 270 | 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 | 269 | 1997 |
| 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 | 253 | 2013 |
| 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 (4), 376-382, 2005 | 252 | 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 (3), 313-315, 1992 | 247 | 1992 |
| 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), 529, 2011 | 225 | 2011 |
| 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 | 225 | 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 | 221 | 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 | 217 | 1995 |
| 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 | 207 | 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 | 191 | 2012 |
Carolyn J. BrownProfessor, Medical Genetics, Life Sciences Institute, University of British ColumbiaVerified email at ubc.ca
