Pauline Chaste
Pauline Chaste
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Alıntı yapanlar
Alıntı yapanlar
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
Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders
B Hofvander, R Delorme, P Chaste, A Nydén, E Wentz, O Ståhlberg, ...
BMC psychiatry 9 (1), 1-9, 2009
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
Autism risk factors: genes, environment, and gene-environment interactions
P Chaste, M Leboyer
Dialogues in clinical neuroscience 14 (3), 281, 2012
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
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 Genet 8 (2), e1002521, 2012
Common genetic variants, acting additively, are a major source of risk for autism
L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ...
Molecular autism 3 (1), 1-13, 2012
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
R Toro, M Konyukh, R Delorme, C Leblond, P Chaste, F Fauchereau, ...
Trends in genetics 26 (8), 363-372, 2010
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly
JD Buxbaum, G Cai, P Chaste, G Nygren, J Goldsmith, J Reichert, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007
Association between the TPH gene A218C polymorphism and suicidal behavior: a meta‐analysis
F Bellivier, P Chaste, A Malafosse
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 124 …, 2004
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders
C Depienne, D Moreno-De-Luca, D Heron, D Bouteiller, A Gennetier, ...
Biological psychiatry 66 (4), 349-359, 2009
Predictors of treatment response in pediatric obsessive-compulsive disorder
GS Ginsburg, JN Kingery, KL Drake, MA Grados
Journal of the American Academy of Child & Adolescent Psychiatry 47 (8), 868-878, 2008
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
P Chaste, L Klei, SJ Sanders, V Hus, MT Murtha, JK Lowe, AJ Willsey, ...
Biological psychiatry 77 (9), 775-784, 2015
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait
P Chaste, L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ...
Biological psychiatry 74 (8), 576-584, 2013
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
P Chaste, N Clement, O Mercati, JL Guillaume, R Delorme, HG Botros, ...
PloS one 5 (7), e11495, 2010
The role of causal and intentional judgments in moral reasoning in individuals with high functioning autism
M Buon, E Dupoux, P Jacob, P Chaste, M Leboyer, T Zalla
Journal of autism and developmental disorders 43 (2), 458-470, 2013
Genetic variations of the melatonin pathway in patients with attention‐deficit and hyperactivity disorders
P Chaste, N Clement, HG Botros, JL Guillaume, M Konyukh, C Pagan, ...
Journal of pineal research 51 (4), 394-399, 2011
Individuals with autism spectrum disorders do not use social stereotypes in irony comprehension
T Zalla, F Amsellem, P Chaste, F Ervas, M Leboyer, M Champagne-Lavau
PloS one 9 (4), e95568, 2014
Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders
C Pagan, H Goubran-Botros, R Delorme, M Benabou, N Lemière, ...
Scientific reports 7 (1), 1-11, 2017
Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q 11.2, Specifically Breakpoints 1 to 2
P Chaste, SJ Sanders, KN Mohan, L Klei, Y Song, MT Murtha, V Hus, ...
Autism Research 7 (3), 355-362, 2014
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