Michael Nothnagel

Joseph Stelzmann Str. 26
Koeln, NW 50931, Germany

Last Updated: 09/26/2026

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Found 83 publications

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Journal: medRxiv : the preprint server for health sciences

Published: March 13, 2026

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Journal: medRxiv : the preprint server for health sciences

Published: March 13, 2026

MatchY: A software implementation of pedigree-based calculation of Y-STR match probabilities.

MatchY: A software implementation of pedigree-based calculation of Y-STR match probabilities.

Journal: Forensic science international. Genetics

Published: January 09, 2026

Exploring Paleogene Tibet's warm temperate environments through target enrichment and phylogenetic niche modelling of Himalayan spiny frogs (Paini, Dicroglossidae).

Exploring Paleogene Tibet's warm temperate environments through target enrichment and phylogenetic niche modelling of Himalayan spiny frogs (Paini, Dicroglossidae).

Journal: Molecular ecology

Published: March 06, 2024

Systematic assessment of COVID-19 host genetics using whole genome sequencing data.

Systematic assessment of COVID-19 host genetics using whole genome sequencing data.

Journal: PLoS pathogens

Published: February 17, 2024

Polygenic risk scores for nicotine use and family history of smoking are associated with smoking behaviour.

Polygenic risk scores for nicotine use and family history of smoking are associated with smoking behaviour.

Journal: Drug and alcohol dependence

Published: December 28, 2023

Conserved missense variant pathogenicity and correlated phenotypes across paralogous genes.

Conserved missense variant pathogenicity and correlated phenotypes across paralogous genes.

Journal: Genome biology

Published: December 14, 2023

SMapper: visualizing spatial prevalence data of all types, including sparse and incomplete datasets.

SMapper: visualizing spatial prevalence data of all types, including sparse and incomplete datasets.

Journal: Bioinformatics advances

Published: July 06, 2023

Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.

Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.

Journal: Molecular genetics & genomic medicine

Published: August 08, 2022

CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online.

CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online.

Journal: Bioinformatics (Oxford, England)

Published: June 14, 2022

A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease.

A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease.

Journal: Nature communications

Published: June 07, 2022

Development and evaluations of the ancestry informative markers of the VISAGE Enhanced Tool for Appearance and Ancestry.

Development and evaluations of the ancestry informative markers of the VISAGE Enhanced Tool for Appearance and Ancestry.

Journal: Forensic science international. Genetics

Published: June 03, 2022

Showing 1-12 of 83

Last Updated: 09/26/2026