List of works - Christiane Wolf

A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

scientific article

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder

scientific article published on 17 April 2015

Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol

scientific article published on 10 June 2015

CEACAM6 gene variants in inflammatory bowel disease

scientific article (publication date: 29 April 2011)

Common genetic variants influence human subcortical brain structures

scientific article

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.

scientific article

Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

scientific article

EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units

scientific article

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

scientific article

Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis

scientific journal article

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

scientific article

Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

scientific article

Imaging genetics of FOXP2 in dyslexia

scientific article published on 7 September 2011

Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population

scientific article

Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI

scientific article published on 7 February 2015

Novel genetic loci underlying human intracranial volume identified through genome-wide association

scientific article (publication date: 3 October 2016)

PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites

scientific article

Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach

scientific article

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

scientific article

The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations

scientific article published on 6 July 2015

The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

scientific article

The genetic architecture of the human cerebral cortex

scientific article

The neuronal transporter gene SLC6A15 confers risk to major depression

scientific article

Variations in the WDR36 gene in German patients with normal tension glaucoma

scientific article

White Matter Lesion Progression: Genome-Wide Search for Genetic Influences

scientific article

List of works by Christiane Wolf

A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder

Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol

CEACAM6 gene variants in inflammatory bowel disease

Common genetic variants influence human subcortical brain structures

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.

Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

Imaging genetics of FOXP2 in dyslexia

Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population

Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI

Novel genetic loci underlying human intracranial volume identified through genome-wide association

PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites

Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations

The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

The genetic architecture of the human cerebral cortex

The neuronal transporter gene SLC6A15 confers risk to major depression

Variations in the WDR36 gene in German patients with normal tension glaucoma

White Matter Lesion Progression: Genome-Wide Search for Genetic Influences