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Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
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In: American journal of human genetics, vol 99, iss 3 (2016)
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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
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In: ISSN: 1931-7557 ; EISSN: 1931-7565 ; Brain imaging and behavior (Brain Imaging Behav) ; https://hal-pasteur.archives-ouvertes.fr/pasteur-01967166 ; Brain imaging and behavior (Brain Imaging Behav), Secaucus, NJ : Springer, 2014, 8 (2), pp.152-182. ⟨10.1007/s11682-013-9269-5⟩ (2014)
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Individual common variants exert weak effects on the risk for autism spectrum disorders.
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In: ISSN: 0964-6906 ; EISSN: 1460-2083 ; Human Molecular Genetics ; https://www.hal.inserm.fr/inserm-00723650 ; Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (21), pp.4781-92. ⟨10.1093/hmg/dds301⟩ (2012)
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4 |
Individual common variants exert weak effects on the risk for autism spectrum disorders
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5 |
Individual common variants exert weak effects on risk for Autism Spectrum Disorders
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6 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
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7 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
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8 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
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Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
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Evidence for a Language Quantitative Trait Locus on Chromosome 7q in Multiplex Autism Families
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