Cormand
Cormand
Unknown affiliation
Verified email at ub.edu
TitleCited byYear
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, 2013
14902013
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome
DBV de Bernabé, S Currier, A Steinbrecher, J Celli, E van Beusekom, ...
The American Journal of Human Genetics 71 (5), 1033-1043, 2002
7072002
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
3842019
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), eaap8757, 2018
3602018
The genetics of attention deficit/hyperactivity disorder in adults, a review
B Franke, SV Faraone, P Asherson, J Buitelaar, CHD Bau, ...
Molecular psychiatry 17 (10), 960-987, 2012
3132012
Genome-wide association analysis identifies susceptibility loci for migraine without aura
T Freilinger, V Anttila, B De Vries, R Malik, M Kallela, GM Terwindt, ...
Nature genetics 44 (7), 777, 2012
2822012
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ...
Nature genetics 48 (8), 856-866, 2016
2592016
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
M Arcos-Burgos, M Jain, MT Acosta, S Shively, H Stanescu, D Wallis, ...
Molecular psychiatry 15 (11), 1053-1066, 2010
2182010
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
T Network, C O'Dushlaine, L Rossin, PH Lee, L Duncan, NN Parikshak, ...
Nature neuroscience 18 (2), 199, 2015
1872015
Genetic evidence of heterogeneity in intrahepatic cholestasis of pregnancy
M Savander, A Ropponen, K Avela, N Weerasekera, B Cormand, ...
Journal of medical genetics 40 (8), 640-640, 2003
1792003
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD
B Franke, AA Vasquez, S Johansson, M Hoogman, J Romanos, ...
Neuropsychopharmacology 35 (3), 656-664, 2010
1742010
Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease
B Cormand, H Pihko, M Bayes, L Valanne, P Santavuori, B Talim, ...
Neurology 56 (8), 1059-1069, 2001
1712001
A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotype
DBV de Bernabé, H Van Bokhoven, E Van Beusekom, W Van den Akker, ...
Journal of medical genetics 40 (11), 845-848, 2003
1692003
Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2 A, DDC and MAOB
M Ribases, JA Ramos-Quiroga, A Hervas, R Bosch, A Bielsa, ...
Molecular psychiatry 14 (1), 71-85, 2009
1582009
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping
B Cormand, K Avela, H Pihko, P Santavuori, B Talim, H Topaloglu, ...
The American Journal of Human Genetics 64 (1), 126-135, 1999
1511999
Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder
M Ribasés, A Hervás, JA Ramos-Quiroga, R Bosch, A Bielsa, ...
Biological psychiatry 63 (10), 935-945, 2008
1202008
Unusual expression of Gaucher's disease: cardiovascular calcifications in three sibs homozygous for the D409H mutation.
A Chabas, B Cormand, D Grinberg, JM Burguera, S Balcells, JL Merino, ...
Journal of medical genetics 32 (9), 740-742, 1995
1181995
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
1152015
Fusion of the human gene for the polyubiquitination coeffector UEV1 with Kua, a newly identified gene
TM Thomson, JJ Lozano, N Loukili, R Carrió, F Serras, B Cormand, ...
Genome research 10 (11), 1743-1756, 2000
1002000
Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study
M Ribases, JA Ramos‐Quiroga, C Sanchez‐Mora, R Bosch, V Richarte, ...
Genes, Brain and Behavior 10 (2), 149-157, 2011
902011
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