about
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorderHost-microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseA genome-wide association study of anorexia nervosa.Involvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosateVariant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopeciaLocalization of a gene for syndactyly type 1 to chromosome 2q34-q36.Evidence for linkage of spelling disability to chromosome 15Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.Common variants conferring risk of schizophreniaThe neuronal transporter gene SLC6A15 confers risk to major depressionMicroduplications of 16p11.2 are associated with schizophreniaGenome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderDisruption of the neurexin 1 gene is associated with schizophreniaLarge recurrent microdeletions associated with schizophreniaA genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorderTwo variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorderIncreased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type IIIMonoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteersNovel genetic loci underlying human intracranial volume identified through genome-wide associationIdentification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor geneAssociation between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorderHypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosinThe hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approachGenome-wide association study reveals two new risk loci for bipolar disorderCloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopeciaMultiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.Identification of mutations in the human hairless gene in two new families with congenital atrichiaGenetic relationship between five psychiatric disorders estimated from genome-wide SNPs4th Pediatric Allergy and Asthma Meeting (PAAM)Genome-wide association study of alcohol dependenceGenome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociGene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohortA genome-wide association study in 574 schizophrenia trios using DNA poolingStudying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINSGenome-wide association of mood-incongruent psychotic bipolar disorder.Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia lociA mega-analysis of genome-wide association studies for major depressive disorderGenome-wide association study in German patients with attention deficit/hyperactivity disorder.A genome-wide association study of attempted suicide.
P50
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P50
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Sven Cichon
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P1053
B-9618-2014
H-8803-2013
P106
P21
P31
P3829
P496
0000-0002-9475-086X
P569
2000-01-01T00:00:00Z