Follow
Bernadette Rogé
Bernadette Rogé
Professor, CERPPS (UT2), TMBI (Univ. Toulouse)
Verified email at univ-tlse2.fr - Homepage
Title
Cited by
Cited by
Year
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
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
CM Durand, C Betancur, TM Boeckers, J Bockmann, P Chaste, ...
Nature genetics 39 (1), 25-27, 2007
18552007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
16452007
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13472018
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
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
7762009
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
Visual social attention in autism spectrum disorder: Insights from eye tracking studies
Q Guillon, N Hadjikhani, S Baduel, B Rogé
Neuroscience & Biobehavioral Reviews 42, 279-297, 2014
5452014
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
International Molecular Genetic Study of Autism Consortium
Human Molecular Genetics 7 (3), 571-578, 1998
5011998
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
Microcephaly and macrocephaly in autism
E Fombonne, B Rogé, J Claverie, S Courty, J Fremolle
Journal of autism and developmental disorders 29, 113-119, 1999
4471999
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
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
Increased perception of loudness in autism
S Khalfa, N Bruneau, B Rogé, N Georgieff, E Veuillet, JL Adrien, ...
Hearing research 198 (1-2), 87-92, 2004
2962004
Prevention and treatment of post-partum depression: a controlled randomized study on women at risk
H Chabrol, F Teissedre, M Saint-Jean, N Teisseyre, B Roge, E Mullet
Psychological medicine 32 (6), 1039-1047, 2002
2722002
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
Autisme, comprendre et agir-3e éd.: Santé, éducation, insertion
B Rogé
Dunod, 2022
2012022
Early processing of emotional faces in children with autism: An event-related potential study
M Batty, E Meaux, K Wittemeyer, B Rogé, MJ Taylor
Journal of experimental child psychology 109 (4), 430-444, 2011
1572011
Use of early intervention for young children with autism spectrum disorder across Europe
E Salomone, Š Beranová, F Bonnet-Brilhault, M Briciet Lauritsen, ...
Autism 20 (2), 233-249, 2016
1542016
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q
International Molecular Genetic Study of Autism Consortium
Human Molecular Genetics 10 (9), 973-982, 2001
1512001
The system can't perform the operation now. Try again later.
Articles 1–20