Michael Nothnagel

18PUBLICATIONS
59CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Spatial statisticsNeurogeneticsGenome structure and regulationEpigenetics (incl. genome methylation and epigenomics)
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Publications (18)

|Nov 30, 2025
Genetic risk factor identification for common epilepsies guided by integrative omics data analysis.

Ashwini Mushunuri, Oluyomi Adesoji, Roland Krause

|Jan 03, 2024
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease.

Sophie A Riesmeijer, Zoha Kamali, Michael Ng

|Dec 11, 2023
SMapper: visualizing spatial prevalence data of all types, including sparse and incomplete datasets.

Lynn Khellaf, Arwin Ralf, Khanh Toan Nguyen

|Dec 05, 2022
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.

Nina Ishorst, Leonie Henschel, Frederic Thieme

|May 27, 2022
Benchmarking of univariate pleiotropy detection methods applied to epilepsy.

Oluyomi M Adesoji, Herbert Schulz, Patrick May

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