Judith Conroy
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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
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, 2012
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, 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
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
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
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
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
Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population
J Conroy, E Meally, G Kearney, M Fitzgerald, M Gill, L Gallagher
Molecular psychiatry 9 (6), 587-593, 2004
TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function
F Gómez-Herreros, JHM Schuurs-Hoeijmakers, M McCormack, ...
Nature genetics 46 (5), 516, 2014
Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31
R Segurado, J Conroy, E Meally, M Fitzgerald, M Gill, L Gallagher
American Journal of Psychiatry 162 (11), 2182-2184, 2005
Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder
Z Hawi, R Segurado, J Conroy, K Sheehan, N Lowe, A Kirley, D Shields, ...
The American Journal of Human Genetics 77 (6), 958-965, 2005
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
Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: Preferential transmission of the MAO‐A 941G …
K Domschke, K Sheehan, N Lowe, A Kirley, C Mullins, R O'sullivan, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 134 …, 2005
Inflammatory bowel disease: the role of inflammatory cytokine gene polymorphisms
J Balding, WJ Livingstone, J Conroy, L Mynett-Johnson, DG Weir, ...
Mediators of inflammation 13, 1970
Identification of a mutation in LARS as a novel cause of infantile hepatopathy
JP Casey, P McGettigan, N Lynam-Lennon, M McDermott, R Regan, ...
Molecular genetics and metabolism 106 (3), 351-358, 2012
The variable phenotypes of KCNQ‐related epilepsy
NM Allen, M Mannion, J Conroy, SA Lynch, A Shahwan, B Lynch, ...
Epilepsia 55 (9), e99-e105, 2014
First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotype
J Casey, R Kawaguchi, M Morrissey, H Sun, P McGettigan, JE Nielsen, ...
Human mutation 32 (12), 1417-1426, 2011
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
D Hadley, Z Wu, C Kao, A Kini, A Mohamed-Hadley, K Thomas, ...
Nature communications 5, 4074, 2014
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