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Functional impact of global rare copy number variation in autism spectrum disorders.Nature, 2010, 466 (7304), pp.368-72. ⟨10.1038/nature09146⟩
Journal articles
inserm-00521387v1
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A genome-wide scan for common alleles affecting risk for autism.Human Molecular Genetics, 2010, 19 (20), pp.4072-82. ⟨10.1093/hmg/ddq307⟩
Journal articles
inserm-00521391v1
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Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipidsNature Genetics, 2019, 51 (4), pp.636-648. ⟨10.1038/s41588-019-0378-y⟩
Journal articles
pasteur-03278554v1
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