Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
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Nothnagel, Michael
One or more keywords matched the following items that are connected to Nothnagel, Michael
Item TypeName
Academic Article Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing.
Academic Article Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.
Academic Article The impact of correlations between pigmentation phenotypes and underlying genotypes on genetic prediction of pigmentation traits.
Academic Article Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits.
Academic Article Female-specific association of C-C chemokine receptor 5 gene polymorphisms with L?fgren's syndrome.
Academic Article Genome-wide association analysis in primary sclerosing cholangitis.
Academic Article Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition.
Academic Article Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits.
Academic Article Evaluation of supervised machine-learning methods for predicting appearance traits from DNA.
Academic Article X chromosomal variation is associated with slow progression to AIDS in HIV-1-infected women.
Academic Article Association of inflammatory bowel disease risk loci with sarcoidosis, and its acute and chronic subphenotypes.
Academic Article Haplotypes of IL-12R?1 impact on the clinical phenotype of hidradenitis suppurativa.
Academic Article Diagnosing fatty liver disease: a comparative evaluation of metabolic markers, phenotypes, genotypes and established biomarkers.
Concept Phenotype
Academic Article Benchmarking of univariate pleiotropy detection methods applied to epilepsy.
Academic Article Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes.
Academic Article CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online.

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  • Phenotype
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