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2020Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia., Nat Commun 2020 Oct; 11(1): 5272.
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2020Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia., Mol Psychiatry 2020 Oct; (): .
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2020Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome., Am J Psychiatry 2020 Sep; (): appiajp202019080834.
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2019Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia, Transl Psychiatry. 2019 Feb 11;9(1):77.
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2019Both rare and common genetic variants contribute to autism in the Faroe Islands., NPJ Genom Med 2019 ; 4(): 1.
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2018Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples., JAMA Psychiatry 2018 05; 75(5): 447-457.
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2016CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders, Mol. Psychiatry 2017 04;22(4):625-633.
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201511q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures., Am J Med Genet A 2015 Dec; 167A(12): 3019-30.
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2015A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability, Eur. J. Hum. Genet. 2016 Jun;24(6):838-43.
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2014Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments., PLoS Genet 2014 Sep; 10(9): e1004580.
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2014Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders, PLoS ONE 2014;9(3):e88600.
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2014Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders, Hum. Genet. 2014 Jun;133(6):781-92.
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2013Heterozygous FA2H mutations in autism spectrum disorders, BMC Med. Genet. 2013;14:124.
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2013The emerging role of SHANK genes in neuropsychiatric disorders, Dev Neurobiol 2014 Feb;74(2):113-22.
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2012Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway, J. Pineal Res. 2013 Jan;54(1):46-57.
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2012Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders., PLoS Genet 2012 Feb; 8(2): e1002521.
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2011Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders., J Pineal Res 2011 Nov; 51(4): 394-9.