|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
|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
|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), 1-15, 2013
|Mechanisms leading to uniparental disomy and their clinical consequences|
Bioessays 22 (5), 452-459, 2000
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome|
G Gillessen-Kaesbach, W Robinson, D Lohmann, S Kaya-Westerloh, ...
Human genetics 96 (6), 638-643, 1995
|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
|Modification of 15q11—q13 DNA methylation imprints in unique Angelman and Prader—Willi patients|
CC Glenn, RD Nicholls, WP Robinson, S Saitoh, N Nllkawa, A Schlnzel, ...
Human molecular genetics 2 (9), 1377-1382, 1993
JP Robinson, M Cohn
IEEE Transactions on Computers 100 (1), 17-23, 1981