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Richard Anney
Richard Anney
在 cardiff.ac.uk 的电子邮件经过验证
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11th Meeting of the Irish Society of Human Genetics, Friday 12th September 2008
F Sharkey, N Wilkie, E Maher, D FitzPatrick, R O'Shea, E Treacy, ...
The Ulster Medical Journal 78 (1), 65-74, 2009
2009
16th Meeting of the Irish Society of Human Genetics, Friday 6th September 2013.: Postgraduate Centre, Belfast Health and Social Care Trust.
J Casey, H Murphy, S Ennis, S Lynch, L Bradley, R Mabrouk, A Paterson, ...
The Ulster Medical Journal 82 (3), 197-204, 2013
2013
17th Meeting of the Irish Society of Human Genetics, Friday 5th September 2014.: Trinity Centre for Health Sciences, St James's Hospital, Dublin.
P Morrison, E Campbell, F Kennedy, A Russell, W Smithson, L Parsons, ...
The Ulster Medical Journal 83 (3), 186-199, 2014
2014
2001.‘‘
DP Hopkins, PA Briss, CJ Ricard, CG Husten, VG Carande-Kulis, ...
Reviews of Evidence Regarding Interventions to Reduce Tobacco Use and …, 0
607
27. USING A TRIO-BASED GENETIC DESIGN FOR INVESTIGATING THE AETIOLOGY OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)
J Martin, M Wray, SS Agha, K Lewis, R Anney, M O'Donovan, A Thapar, ...
European Neuropsychopharmacology 51, e54-e55, 2021
2021
34NOVEL INSIGHT INTO THE AETIOLOGY OF AUTISM SPECTRUM DISORDER GAINED BY INTEGRATING FUNCTIONAL DATA WITH GENOME-WIDE ASSOCIATION SUMMARY STATISTICS
O Pain, A Pocklington, R Anney
European Neuropsychopharmacology 29, S1085-S1086, 2019
2019
39 Allelic expression imbalance at interleukin 18 and chemokine cxcl 16 in patients with acute coronary syndromes
JM Gahan, MM Byrne, E Connolly, SG Gray, RJL Anney, RT Murphy, ...
Heart 101 (Suppl 5), A22-A22, 2015
2015
5-HTT and DRD4 genotypes are associated with emotional liability in children with ADHD
T Banaschewski, B Franke, EA Taylor, EJS Sonuga-Barke, W Schlotz, ...
第十九届世界儿童及青少年精神卫生与相关学科学术会议摘要集, 2010
2010
A CLOSER LOOK AT MISSINGNESS: THE IMPLICATIONS OF NON-RANDOM MISSINGNESS ON FALSE POSITIVE ASSOCIATION IN GENOTYPE CALLING APPROACHES FOR GENOME WIDE ASSOCIATION DATA.
R Anney, E Kenny, C O'Dushlaine, J Su, B Franke, B Neale, S Faraone, ...
Ulster Medical Journal 78 (1), 2009
2009
A cross-sectional study investigating sleep difficulties on internalising and externalising problems in autistic patients
JZ Ang, T Dinneen, R Anney, L Gallagher
A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings
EJS Sonuga-Barke, R Kumsta, W Schlotz, J Lasky-Su, R Marco, ...
Biological psychiatry 70 (3), 230-236, 2011
682011
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder
J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ...
Biological psychiatry 83 (12), 1044-1053, 2018
1802018
A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants
SJRA Chawner, JL Doherty, RJL Anney, KM Antshel, CE Bearden, ...
American Journal of Psychiatry 178 (1), 77-86, 2021
702021
A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3
S Connolly, R Anney, L Gallagher, EA Heron
European Journal of Human Genetics 25 (2), 234-239, 2017
482017
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
7832009
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
7202010
A genomewide scan for common alleles affecting risk for autism.
R SEGURADO, RJL ANNEY, J MC GRATH, N BOLSHAKOVA, M GILL, ...
Oxford University Press, 2010
2010
A high density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies replicated linkage regions on chromosomes 9 and 16
P Asherson, K Zhou, RJL Anney, B Franke, JK Buitelaar, R Ebstein, M Gill, ...
A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16
P Asherson, K Zhou, RJL Anney, B Franke, J Buitelaar, R Ebstein, M Gill, ...
Molecular psychiatry 13 (5), 514-521, 2008
952008
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
2292012
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