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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
23062010
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
10582014
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
LC Tsoi, SL Spain, J Knight, E Ellinghaus, PE Stuart, F Capon, J Ding, ...
Nature genetics 44 (12), 1341-1348, 2012
10452012
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
MJ Greenway, PM Andersen, C Russ, S Ennis, S Cashman, C Donaghy, ...
Nature genetics 38 (4), 411-413, 2006
8342006
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
7512013
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
7152010
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature neuroscience 18 (2), 199-209, 2015
5172015
A medium-density genetic linkage map of the bovine genome
W Barendse, D Vaiman, SJ Kemp, Y Sugimoto, SM Armitage, JL Williams, ...
Mammalian Genome 8, 21-28, 1997
4861997
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
4552017
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
4422012
Geospatial resolution of human and bacterial diversity with city-scale metagenomics
E Afshinnekoo, C Meydan, S Chowdhury, D Jaroudi, C Boyer, N Bernstein, ...
Cell systems 1 (1), 72-87, 2015
3312015
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
3272017
A PCR‐based sex‐determination assay in cattle based on the bovine amelogenin locus
S Ennis, TF Gallagher
Animal Genetics 25 (6), 425-427, 1994
3081994
A novel candidate region for ALS on chromosome 14q11. 2
MJ Greenway, MD Alexander, S Ennis, BJ Traynor, B Corr, E Frost, ...
Neurology 63 (10), 1936-1938, 2004
2632004
Marketing theory and practice
MJ Baker, O Badot, K Bernard, S Brown, D Brownlie, S Carter, KC Chan, ...
Springer, 1995
2511995
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, 565-579, 2012
2282012
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
2202015
Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders
EM Kenny, P Cormican, S Furlong, E Heron, G Kenny, C Fahey, ...
Molecular psychiatry 19 (8), 872-879, 2014
2092014
Unexplained early onset epileptic encephalopathy: exome screening and phenotype expansion
NM Allen, J Conroy, A Shahwan, B Lynch, RG Correa, SDJ Pena, ...
Epilepsia 57 (1), e12-e17, 2016
1932016
Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism
CT Correia, AM Coutinho, AF Sequeira, IG Sousa, L Lourenco Venda, ...
Genes, Brain and behavior 9 (7), 841-848, 2010
1662010
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