Veronica J Vieland
Veronica J Vieland
The Research Institute at Nationwide Children's Hospital & The Ohio State University
Geverifieerd e-mailadres voor - Homepage
Geciteerd door
Geciteerd door
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
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, A Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984-995, 2013
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
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking
Nature 461 (7265), 802-808, 2009
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
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
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
A major susceptibility locus for specific language impairment is located on 13q21
CW Bartlett, JF Flax, MW Logue, VJ Vieland, AS Bassett, P Tallal, ...
The American Journal of Human Genetics 71 (1), 45-55, 2002
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
T Network, ...
Nature neuroscience 18 (2), 199, 2015
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
Adolescent suicide attempters: response to suicide-prevention programs
D Shaffer, V Vieland, A Garland, M Rojas, M Underwood, C Busner
Jama 264 (24), 3151-3155, 1990
Evidence supporting WNT2 as an autism susceptibility gene
TH Wassink, J Piven, VJ Vieland, J Huang, RE Swiderski, J Pietila, ...
American journal of medical genetics 105 (5), 406-413, 2001
Examination of AVPR1a as an autism susceptibility gene
TH Wassink, J Piven, VJ Vieland, J Pietila, RJ Goedken, SE Folstein, ...
Molecular psychiatry 9 (10), 968-972, 2004
The impact of curriculum-based suicide prevention programs for teenagers
D Shaffer, ANN Garland, V Vieland, M Underwood, C Busner
Journal of the American Academy of Child & Adolescent Psychiatry 30 (4), 588-596, 1991
Incorporating language phenotypes strengthens evidence of linkage to autism
Y Bradford, J Haines, H Hutcheson, M Gardiner, T Braun, V Sheffield, ...
American journal of medical genetics 105 (6), 539-547, 2001
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131 (4), 565-579, 2012
Results of a genome‐wide genetic screen for panic disorder
JA Knowles, AJ Fyer, VJ Vieland, MM Weissman, SE Hodge, GA Heiman, ...
American journal of medical genetics 81 (2), 139-147, 1998
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Molecular autism 8, 1-17, 2017
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder
R Maier, G Moser, GB Chen, S Ripke, D Absher, I Agartz, H Akil, F Amin, ...
The American Journal of Human Genetics 96 (2), 283-294, 2015
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–20