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Catalina Betancur
Catalina Betancur
INSERM U1130, CNRS UMR 8246, Sorbonne Université
Verified email at inserm.fr
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
22062010
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), 984-994, 2013
22022013
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
S Jamain, H Quach, C Betancur, M Rĺstam, C Colineaux, IC Gillberg, ...
Nature Genetics 34 (1), 27-29, 2003
21052003
Patterns and rates of exonic de novo mutations in autism spectrum disorders
BM Neale, Y Kou, L Liu, A Ma’Ayan, KE Samocha, A Sabo, CF Lin, ...
Nature 485 (7397), 242-245, 2012
19202012
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
17632007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
16112007
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
13112020
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
11992018
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting
C Betancur
Brain Research 1380, 42-77, 2011
11202011
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
10092014
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
7372009
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
6912010
Abnormal melatonin synthesis in autism spectrum disorders
J Melke, HG Botros, P Chaste, C Betancur, G Nygren, H Anckarsäter, ...
Molecular Psychiatry 13 (1), 90-98, 2008
5672008
Meta-analysis of SHANK mutations in autism spectrum disorders: a gradient of severity in cognitive Impairments
CS Leblond, C Nava, A Polge, J Gauthier, G Huguet, S Lumbroso, ...
PLoS Genetics 10 (9), e1004580, 2014
5452014
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
The Network and Pathway Analysis Subgroup of the Psychiatric Genomics Consortium
Nature Neuroscience 18 (2), 199-209, 2015
4932015
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
CS Leblond, J Heinrich, R Delorme, C Proepper, C Betancur, G Huguet, ...
PLoS Genetics 8 (2), e1002521, 2012
4492012
Individual common variants exert weak effects on 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
4292012
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, 2017
4172017
Linkage and association of the glutamate receptor 6 gene with autism
S Jamain, C Betancur, H Quach, A Philippe, M Fellous, B Giros, C Gillberg, ...
Molecular Psychiatry 7 (3), 302-310, 2002
4002002
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
C Betancur, T Sakurai, JD Buxbaum
Trends in Neurosciences 32 (7), 402-412, 2009
3292009
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