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Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

BMC genomics, 2015-07, Vol.16 (1), p.548-548, Article 548

2015

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Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

American journal of human genetics, 2012-10, Vol.91 (4), p.703-712

2012

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CtIP Mutations Cause Seckel and Jawad Syndromes

PLoS genetics, 2011-10, Vol.7 (10), p.e1002310-e1002310

2011

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Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction

Nature communications, 2021-09, Vol.12 (1), p.5276-5276, Article 5276

2021

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Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins

Frontiers in aging neuroscience, 2017-12, Vol.9, p.413-413

2017

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DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

PloS one, 2017-01, Vol.12 (1), p.e0170121-e0170121

2017

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Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers

PLoS genetics, 2014-07, Vol.10 (7), p.e1004488-e1004488

2014

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A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

Human genetics, 2020-05, Vol.139 (5), p.593-604

2020

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Polymorphism in serotonin receptor 3B is associated with pain catastrophizing

PloS one, 2013-11, Vol.8 (11), p.e78889-e78889

2013

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EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions

BMC genomics, 2015-11, Vol.16 (934), p.929-929, Article 929

2015

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Genome wide assessment of mRNA in astrocyte protrusions by direct RNA sequencing reveals mRNA localization for the intermediate filament protein nestin

Glia, 2013-11, Vol.61 (11), p.1922-1937

2013

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Depression, the Val66Met polymorphism, age, and gender influence the serum BDNF level

Journal of psychiatric research, 2012-09, Vol.46 (9), p.1118-1125

2012

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Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2016-12, Vol.171B (8), p.1013-1022

2016

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Hypomethylation of FAM63B in bipolar disorder patients

Clinical epigenetics, 2016-05, Vol.8 (53), p.52-52, Article 52

2016

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An association study of suicide and candidate genes in the serotonergic system

Journal of affective disorders, 2013-06, Vol.148 (2), p.291-298

2013

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Association of GRIN1 and GRIN2A-D With schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-12, Vol.156B (8), p.913-922

2011

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Nature genetics, 2016-05, Vol.48 (5), p.552-555

2016

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Endogenous and Antipsychotic-Related Risks for Diabetes Mellitus in Young People With Schizophrenia: A Danish Population-Based Cohort Study

The American journal of psychiatry, 2017-07, Vol.174 (7), p.686-694

2017

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Psychiatric Genomics: An Update and an Agenda

American Journal of Psychiatry, 2018-01, Vol.175 (1), p.15-27

2018

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Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Nature neuroscience, 2019-12, Vol.22 (12), p.1961

2019

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Support of association between BRD1 and both schizophrenia and bipolar affective disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-03, Vol.153B (2), p.582-591

2010

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Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

Molecular psychiatry, 2020-10, Vol.25 (10), p.2410-2421

2020

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A major role for common genetic variation in anxiety disorders

Molecular psychiatry, 2020-12, Vol.25 (12), p.3292-3303

2020

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Investigating the association between body fat and depression via Mendelian randomization

Translational psychiatry, 2019-08, Vol.9 (1), p.184-9, Article 184

2019

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Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

CtIP Mutations Cause Seckel and Jawad Syndromes

Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction

Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins

DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers

A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

Polymorphism in serotonin receptor 3B is associated with pain catastrophizing

EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions

Genome wide assessment of mRNA in astrocyte protrusions by direct RNA sequencing reveals mRNA localization for the intermediate filament protein nestin

Depression, the Val66Met polymorphism, age, and gender influence the serum BDNF level

Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population

Hypomethylation of FAM63B in bipolar disorder patients

An association study of suicide and candidate genes in the serotonergic system

Association of GRIN1 and GRIN2A-D With schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Endogenous and Antipsychotic-Related Risks for Diabetes Mellitus in Young People With Schizophrenia: A Danish Population-Based Cohort Study

Psychiatric Genomics: An Update and an Agenda

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Support of association between BRD1 and both schizophrenia and bipolar affective disorder

Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

A major role for common genetic variation in anxiety disorders

Investigating the association between body fat and depression via Mendelian randomization

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