Publications of Christiane Wolf
All genres
Journal Article (32)
2020
Journal Article
15 (7), e0236421 (2020)
Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgery. PLOS ONE 2017
Journal Article
211 (2), pp. 70 - 76 (2017)
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. BRITISH JOURNAL OF PSYCHIATRY
Journal Article
8, 1511 (2017)
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. NATURE COMMUNICATIONS 2016
Journal Article
21 (2), pp. 189 - 197 (2016)
GWAS for executive function and processing speed suggests involvement of the CADM2 gene. MOLECULAR PSYCHIATRY 2015
Journal Article
46 (11), pp. 3048 - 3057 (2015)
White Matter Lesion Progression Genome-Wide Search for Genetic Influences. STROKE
Journal Article
10 (8), e0135807 (2015)
Solid Organ Transplantation in Patients with Inflammatory Bowel Diseases (IBD): Analysis of Transplantation Outcome and IBD Activity in a Large Single Center Cohort. PLOS ONE
Journal Article
10 (7), e0116044 (2015)
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. PLOS ONE
Journal Article
15, 126 (2015)
Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol. BMC PSYCHIATRY
Journal Article
13, 86 (2015)
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder. BMC MEDICINE
Journal Article
77 (8), pp. 749 - 763 (2015)
Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. BIOLOGICAL PSYCHIATRY
Journal Article
520 (7546), pp. 224 - 229 (2015)
Common genetic variants influence human subcortical brain structures. NATURE
Journal Article
279, pp. 46 - 49 (2015)
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. JOURNAL OF NEUROIMMUNOLOGY
Journal Article
47 (1), pp. 78 - + (2015)
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection. NATURE GENETICS 2014
Journal Article
9 (11), e108503 (2014)
The NOD2 p.Leu1007fsX1008 Mutation (rs2066847) Is a Stronger Predictor of the Clinical Course of Crohn's Disease than the FOXO3A Intron Variant rs12212067. PLOS ONE
Journal Article
8 (2), pp. 153 - 182 (2014)
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. SI: Genetic Neuroimaging in Aging and Age-Related Diseases
Journal Article
35 (2), pp. 378 - 386 (2014)
Abdominal obesity and lower gray matter volume: a Mendelian randomization study. NEUROBIOLOGY OF AGING 2013
Journal Article
8 (6), e64872 (2013)
A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. PLOS ONE
Journal Article
8 (6), e64947 (2013)
Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach. PLOS ONE 2012
Journal Article
159B (3), pp. 263 - 273 (2012)
Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics
Journal Article
20 (2), pp. 224 - 229 (2012)
Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics