Publications
variant mitigates Alzheimer disease pathophysiology in vivo and postmortem.. Neurol Genet. 4(1):e216.
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2018. Transcriptome sequencing of the anterior cingulate in bipolar disorder: dysregulation of G protein-coupled receptors.. Am J Psychiatry. 172(11):1131-40.
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2015. A polymorphism in the glutamate metabotropic receptor 7 is associated with cognitive deficits in the early phases of psychosis.. Schizophr Res.
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2020. Polygenic scores differentially predict developmental trajectories of subtypes of social withdrawal in childhood.. J Child Psychol Psychiatry. 62(11):1320-1329.
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2021. No evidence for GADL1 variation as a bipolar disorder susceptibility factor in a Caucasian lithium-responsive cohort.. Am J Psychiatry. 172(1):94-5.
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2015. Mutation burden of rare variants in schizophrenia candidate genes.. PLoS One. 10(6):e0128988.
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2019. Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study.. Bipolar Disord.
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2018. Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.. PLoS One. 12(2):e0171595.
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2017. .
2021.
Genome-wide association study reveals two new risk loci for bipolar disorder.. Nat Commun. 5:3339.
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2014. Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.. Hum Mol Genet. 25(15):3383-3394.
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2016. Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.. Lancet. 387(10023):1085-93.
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2018. Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males.. Am J Med Genet B Neuropsychiatr Genet.
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2018. DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression.. BMC Psychiatry. 16(1):286.
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2016. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors.. Biol Psychiatry. 91(3):313-327.
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2022. A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1.. Sci Rep. 8(1):12173.
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2018. The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder.. Neurobiol Aging. 49:218.e13-218.e15.
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2017. Decreased global methylation in patients with bipolar disorder who respond to lithium.. Int J Neuropsychopharmacol. 17(4):561-9.
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2014. De novo variants in sporadic cases of childhood onset schizophrenia.. Eur J Hum Genet. 24(6):944-8.
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2016. A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.. Am J Med Genet A. 170A(5):1225-35.
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