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
19572010
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
18742003
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
17862013
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
16822012
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
15212007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature Genetics 39 (3), 319-328, 2007
14592007
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting
C Betancur
Brain Research 1380, 42-77, 2011
9442011
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
7692014
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), 2018
6682018
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking
Nature 461 (7265), 802-808, 2009
6612009
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
5982010
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
4762008
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
4072020
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
3812012
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
3672014
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
3612012
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
3542002
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
2952015
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
2902009
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
2632017
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