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Genome-wide association study of therapeutic opioid dosing identifies a novel locus upstream of OPRM1

Molecular psychiatry, 2017-03, Vol.22 (3), p.346-352

2017

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APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study

Molecular psychiatry, 2014-03, Vol.19 (3), p.351-357

2014

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A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

Molecular psychiatry, 2011-09, Vol.16 (9), p.949-959

2011

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Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

Nature (London), 2014-07, Vol.511 (7508), p.236-240

2014

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Rare structural variation of synapse and neurotransmission genes in autism

Molecular psychiatry, 2012-04, Vol.17 (4), p.402-411

2012

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Src kinase as a mediator of convergent molecular abnormalities leading to NMDAR hypoactivity in schizophrenia

Molecular psychiatry, 2015-09, Vol.20 (9), p.1091-1100

2015

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Connectome-wide network analysis of youth with Psychosis-Spectrum symptoms

Molecular psychiatry, 2015-12, Vol.20 (12), p.1508-1515

2015

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

Molecular psychiatry, 2010-06, Vol.15 (6), p.637-646

2010

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RNA-seq analysis of amygdala tissue reveals characteristic expression profiles in schizophrenia

Translational psychiatry, 2017-08, Vol.7 (8), p.e1203-e1203

2017

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Association between polygenic risk for schizophrenia, neurocognition and social cognition across development

Translational psychiatry, 2016-10, Vol.6 (10), p.e924-e924

2016

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High rate of disease-related copy number variations in childhood onset schizophrenia

Molecular psychiatry, 2014-05, Vol.19 (5), p.568-572

2014

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The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

Molecular psychiatry, 2015-04, Vol.20 (4), p.454-458

2015

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Psychiatric gene discoveries shape evidence on ADHD’s biology

Molecular psychiatry, 2016-09, Vol.21 (9), p.1202-1207

2016

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A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD

Molecular psychiatry, 2012-07, Vol.17 (7), p.741-747

2012

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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Molecular psychiatry, 2017-02, Vol.22 (2), p.321-322

2017

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Analysing biological pathways in genome-wide association studies

Nature reviews. Genetics, 2010-12, Vol.11 (12), p.843-854

2010

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Extended haplotype association study in Crohn’s disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3

Genes and immunity, 2013-07, Vol.14 (5), p.310-316

2013

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The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females

Genes and immunity, 2015-10, Vol.16 (7), p.495-498

2015

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Remapping the type I diabetes association of the CTLA4 locus

Genes and immunity, 2009-12, Vol.10 (Suppl 1), p.S27-S32

2009

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Targeted resequencing identifies defective variants of decoy receptor 3 in pediatric-onset inflammatory bowel disease

Genes and immunity, 2013-10, Vol.14 (7), p.447-452

2013

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Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity

International Journal of Obesity, 2012-01, Vol.36 (1), p.80-83

2012

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The ubiquitin ligase adaptor Ndfip1 regulates T cell-mediated gastrointestinal inflammation and inflammatory bowel disease susceptibility

Mucosal immunology, 2011-05, Vol.4 (3), p.314-324

2011

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The type I diabetes association of the IL2RA locus

Genes and immunity, 2009-12, Vol.10 (Suppl 1), p.S42-S48

2009

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Genome-wide association study of therapeutic opioid dosing identifies a novel locus upstream of OPRM1

APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

Rare structural variation of synapse and neurotransmission genes in autism

Src kinase as a mediator of convergent molecular abnormalities leading to NMDAR hypoactivity in schizophrenia

Connectome-wide network analysis of youth with Psychosis-Spectrum symptoms

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

RNA-seq analysis of amygdala tissue reveals characteristic expression profiles in schizophrenia

Association between polygenic risk for schizophrenia, neurocognition and social cognition across development

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

High rate of disease-related copy number variations in childhood onset schizophrenia

The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

Psychiatric gene discoveries shape evidence on ADHD’s biology

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD

Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Analysing biological pathways in genome-wide association studies

Extended haplotype association study in Crohn’s disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3

The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females

Remapping the type I diabetes association of the CTLA4 locus

Targeted resequencing identifies defective variants of decoy receptor 3 in pediatric-onset inflammatory bowel disease

Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity

The ubiquitin ligase adaptor Ndfip1 regulates T cell-mediated gastrointestinal inflammation and inflammatory bowel disease susceptibility

The type I diabetes association of the IL2RA locus

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains

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