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The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders

Molecular psychiatry, 2018-01, Vol.23 (1), p.6-14

2018

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CACNA1C (rs1006737) is associated with schizophrenia

Molecular psychiatry, 2010-02, Vol.15 (2), p.119-121

2010

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The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark

Psychological medicine, 2018-01, Vol.48 (2), p.305-314

2018

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Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder

Molecular psychiatry, 2006-12, Vol.11 (12), p.1126-1138

2006

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Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF

Translational psychiatry, 2015-11, Vol.5 (11), p.e677-e677

2015

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CACNA1C hypermethylation is associated with bipolar disorder

Translational psychiatry, 2016-06, Vol.6 (6), p.e831-e831

2016

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Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls

Psychological medicine, 2019-05, Vol.49 (7), p.1166-1173

2019

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Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders

Thorax, 2008-12, Vol.63 (12), p.1064-1069

2008

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Polymorphisms in the ALOX12 gene and osteoporosis

Osteoporosis international, 2011-08, Vol.22 (8), p.2249-2259

2011

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Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

Molecular psychiatry, 2014-03, Vol.19 (3), p.325-333

2014

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Polymorphisms of Muscle Genes Are Associated with Bone Mass and Incident Osteoporotic Fractures in Caucasians

Calcified tissue international, 2013-05, Vol.92 (5), p.467-476

2013

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ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

Molecular psychiatry, 2018-02, Vol.23 (2), p.263-270

2018

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Epigenome-wide association study of depression symptomatology in elderly monozygotic twins

Translational psychiatry, 2019-09, Vol.9 (1), p.214-14, Article 214

2019

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High loading of polygenic risk in cases with chronic schizophrenia

Molecular psychiatry, 2016-07, Vol.21 (7), p.969-974

2016

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Significant linkage to chromosome 12q24.32–q24.33 and identification of SFRS8 as a possible asthma susceptibility gene

Thorax, 2006-10, Vol.61 (10), p.874-879

2006

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Investigating the causal relationship between neuroticism and depression via Mendelian randomization

Acta psychiatrica Scandinavica, 2019-04, Vol.139 (4), p.395-397

2019

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Blood DNA methylation age is not associated with cognitive functioning in middle-aged monozygotic twins

Neurobiology of aging, 2017-02, Vol.50, p.60-63

2017

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Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM

Psychological medicine, 2019, Vol.49 (2), p.351-351

2019

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Fine‐scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp

Allergy (Copenhagen), 2004-01, Vol.59 (1), p.88-94

2004

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Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder

Molecular psychiatry, 2002-08, Vol.7 (7), p.745-754

2002

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COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity

Acta psychiatrica Scandinavica, 2017-07, Vol.136 (1), p.85-95

2017

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Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

Journal of medical genetics, 2001-12, Vol.38 (12), p.e43-43

2001

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Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

Translational psychiatry, 2017-02, Vol.7 (2), p.e1034-e1034

2017

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Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases

Journal of medical genetics, 2006-03, Vol.43 (3), p.e10-e10

2006

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Risk of schizophrenia in relation to parental origin and genome-wide divergence

Psychological medicine, 2012-07, Vol.42 (7), p.1515-1521

2012

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The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders

CACNA1C (rs1006737) is associated with schizophrenia

The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark

Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder

Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF

CACNA1C hypermethylation is associated with bipolar disorder

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls

Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders

Polymorphisms in the ALOX12 gene and osteoporosis

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

Polymorphisms of Muscle Genes Are Associated with Bone Mass and Incident Osteoporotic Fractures in Caucasians

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

Epigenome-wide association study of depression symptomatology in elderly monozygotic twins

High loading of polygenic risk in cases with chronic schizophrenia

Significant linkage to chromosome 12q24.32–q24.33 and identification of SFRS8 as a possible asthma susceptibility gene

Investigating the causal relationship between neuroticism and depression via Mendelian randomization

Blood DNA methylation age is not associated with cognitive functioning in middle-aged monozygotic twins

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM

Fine‐scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp

Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder

COMT Val158Met and MTHFR C677T moderate risk of schizophrenia in response to childhood adversity

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases

Risk of schizophrenia in relation to parental origin and genome-wide divergence

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