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Ellen M Wijsman
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Year
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
E Levy-Lahad, W Wasco, P Poorkaj, DM Romano, J Oshima, ...
Science 269 (5226), 973-977, 1995
35771995
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
23142010
Positional cloning of the Werner's syndrome gene
CE Yu, J Oshima, YH Fu, EM Wijsman, F Hisama, R Alisch, S Matthews, ...
Science 272 (5259), 258-262, 1996
20621996
Tau is a candidate gene for chromosome 17 frontotemporal dementia
P Poorkaj, TD Bird, E Wijsman, E Nemens, RM Garruto, L Anderson, ...
Annals of neurology 43 (6), 815-825, 1998
17241998
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
16512007
Replicating genotype–phenotype associations
Nature 447 (7145), 655-660, 2007
16092007
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13672018
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14
GD Schellenberg, TD Bird, EM Wijsman, HT Orr, L Anderson, E Nemens, ...
Science 258 (5082), 668-671, 1992
13581992
A familial Alzheimer's disease locus on chromosome 1
E Levy-Lahad, EM Wijsman, E Nemens, L Anderson, KAB Goddard, ...
Science 269 (5226), 970-973, 1995
11121995
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
10642014
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
7532013
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
7182010
Writing problems in developmental dyslexia: Under-recognized and under-treated
VW Berninger, KH Nielsen, RD Abbott, E Wijsman, W Raskind
Journal of school psychology 46 (1), 1-21, 2008
5612008
Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case‐control study
GP Jarvik, EM Wijsman, WA Kukull, GD Schellenberg, C Yu, EB Larson
Neurology 45 (6), 1092-1096, 1995
4921995
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
4452012
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia
H Liu, SC Heath, C Sobin, JL Roos, BL Galke, ML Blundell, M Lenane, ...
Proceedings of the National Academy of Sciences 99 (6), 3717-3722, 2002
4172002
A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis
C Helms, L Cao, JG Krueger, EM Wijsman, F Chamian, D Gordon, ...
Nature genetics 35 (4), 349-356, 2003
3912003
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region
K Kamino, HT Orr, H Payami, EM Wijsman, ME Alonso, SM Pulst, ...
American journal of human genetics 51 (5), 998, 1992
3771992
Meta-analysis of 32 genome-wide linkage studies of schizophrenia
MYM Ng, DF Levinson, SV Faraone, BK Suárez, LE DeLisi, T Arinami, ...
Molecular psychiatry 14 (8), 774-785, 2009
3632009
Neurocognitive and electrophysiological evidence of altered face processing in parents of children with autism: Implications for a model of abnormal development of social brain …
G Dawson, SJ Webb, E Wijsman, G Schellenberg, A Estes, J Munson, ...
Development and psychopathology 17 (3), 679-697, 2005
3572005
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