Wendy P Robinson
Wendy P Robinson
University of British Columbia
Verified email at bcchr.ca - Homepage
Cited by
Cited by
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
WP Robinson
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
Counting sequences
JP Robinson, M Cohn
IEEE Transactions on Computers 100 (1), 17-23, 1981
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