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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Nucleic acids research, 2010-09, Vol.38 (16), p.e164-e164

2010

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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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Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

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

2014

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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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NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases

Human genetics, 2021-12, Vol.140 (12), p.1665-1678

2021

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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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Risk of pre‐eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case–control study

BJOG : an international journal of obstetrics and gynaecology, 2021-01, Vol.128 (1), p.55-65

2021

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Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche

Human reproduction (Oxford), 2021-06, Vol.36 (7), p.1999-2010

2021

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Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population

American journal of human genetics, 2005-03, Vol.76 (3), p.505-509

2005

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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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Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients

Journal of medical genetics, 2011-01, Vol.48 (1), p.1-9

2011

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Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders

Clinical genetics, 2016-02, Vol.89 (2), p.163-172

2016

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Attention-Deficit Hyperactivity Disorder and Pharmacotherapy—Past, Present, and Future: A Review of the Changing Landscape of Drug Therapy

Therapeutic innovation & regulatory science, 2015-09, Vol.49 (5), p.632-642

2015

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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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Crohn's Disease and Genetic Hitchhiking at IBD5

Molecular biology and evolution, 2012-01, Vol.29 (1), p.101-111

2012

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Case–control association analysis of polymorphisms in the delta-opioid receptor, OPRD1 , with cocaine and opioid addicted populations

Drug and alcohol dependence, 2013-01, Vol.127 (1), p.122-128

2013

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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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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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Contribution of ADAM33 polymorphisms to the population risk of asthma

Thorax, 2005-04, Vol.60 (4), p.274-276

2005

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OP0282 The Association of PTPN22 RS2476601 with Juvenile Idiopathic Arthritis is Specific to Females

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.179-179

2015

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IL-13-dependent autocrine signaling mediates altered responsiveness of IgE-sensitized airway smooth muscle

American journal of physiology. Lung cellular and molecular physiology, 2002-03, Vol.282 (3), p.520-L528

2002

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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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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

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

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

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

NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases

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

Risk of pre‐eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case–control study

Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche

Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population

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

Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients

Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders

Attention-Deficit Hyperactivity Disorder and Pharmacotherapy—Past, Present, and Future: A Review of the Changing Landscape of Drug Therapy

Analysing biological pathways in genome-wide association studies

Crohn's Disease and Genetic Hitchhiking at IBD5

Case–control association analysis of polymorphisms in the delta-opioid receptor, OPRD1 , with cocaine and opioid addicted populations

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

Remapping the type I diabetes association of the CTLA4 locus

Contribution of ADAM33 polymorphisms to the population risk of asthma

OP0282 The Association of PTPN22 RS2476601 with Juvenile Idiopathic Arthritis is Specific to Females

IL-13-dependent autocrine signaling mediates altered responsiveness of IgE-sensitized airway smooth muscle

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

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