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 Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.
Academic Article Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With?Coronary Artery?Disease.
Academic Article Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Academic Article Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans.
Academic Article HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders.
Academic Article Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.
Academic Article Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia.
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 Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts.
Academic Article Evidence of Inbreeding in Hodgkin Lymphoma.
Academic Article Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin.
Academic Article Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.
Academic Article Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression.
Academic Article Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification.
Academic Article IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.
Academic Article Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients.
Academic Article Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder.
Academic Article Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
Academic Article Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.
Concept Gene Frequency
Academic Article Genetic and functional analyses implicate microRNA 499A in bipolar disorder development.

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  • Gene Frequency
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