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Michael Nothnagel

University of Cologne
University of Kiel

173

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7126

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Analysis of single nucleotide polymorphisms in chronic beryllium disease.

2021 Respiratory Research
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Ultra-rare constrained missense variants in the epilepsies: Shared and specific enrichment patterns in neuronal gene-sets 2021.04.18.440264

2021
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Development and Evaluation of the Ancestry Informative Marker Panel of the VISAGE Basic Tool.

2021 Genes
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Evaluation of supervised machine-learning methods for predicting appearance traits from DNA.

2021 Forensic Science International-genetics
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Author response for "Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran"

2021
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What Makes a Hot-Spring Habitat “Hot” for the Hot-Spring Snake: Distributional Data and Niche Modelling for the Genus Thermophis (Serpentes, Colubridae)

2021 Diversity
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Correction to: Towards a fine-scale picture of European genetic diversity.

2021 European Journal of Human Genetics
- Michael Nothnagel
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Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.

2021 Clinical Genetics
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Towards a fine-scale picture of European genetic diversity.

2020 European Journal of Human Genetics
- Michael Nothnagel
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The exhaustive genomic scan approach, with an application to rare-variant association analysis.

2020 European Journal of Human Genetics
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