Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
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Hoffmann, Per
One or more keywords matched the following items that are connected to Hoffmann, Per
Item TypeName
Academic Article Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.
Academic Article Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.
Academic Article Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.
Academic Article Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Academic Article Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders.
Academic Article Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Academic Article Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Academic Article Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
Academic Article Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature.
Academic Article Genetics of dyslexia: the evolving landscape.
Academic Article A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Academic Article Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
Academic Article Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin.
Academic Article A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis.
Academic Article Analysis of shared heritability in common disorders of the brain.
Academic Article Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study.
Academic Article Genotype-phenotype feasibility studies on khat abuse, traumatic experiences and psychosis in Ethiopia.
Academic Article De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformation.
Academic Article Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
Academic Article The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Academic Article Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype.
Academic Article Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
Concept Phenotype
Academic Article Immunogenetics of lithium response and psychiatric phenotypes in patients with bipolar disorder.

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