Susanne Motameny
8PUBLICATIONS
134CO-AUTHORS
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Publications (8)
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|Sep 30, 2024
NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling.Friederike Hanssen, Gisela Gabernet, Famke Bäuerle
|Nov 03, 2022
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.Guillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki
|Jun 16, 2021
Long-lived macrophage reprogramming drives spike protein-mediated inflammasome activation in COVID-19.Sebastian J Theobald, Alexander Simonis, Theodoros Georgomanolis
|Jun 20, 2020
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.Eszter Balogh, Jennifer C Chandler, Máté Varga
|May 14, 2020
Author Correction: Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy.Inês do Carmo G Gonçalves, Johanna Brecht, Maximilian P Thelen
|Sep 18, 2018
Depletion of Nesprin-2 is associated with an embryonic lethal phenotype in mice.Carmen Mroß, Marija Marko, Martina Munck
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Frequent Collaborators
3 joint publications
Maximilian P Thelen
3 joint publications
Darius Ebrahimi-Fakhari
3 joint publications
David Vilchez
3 joint publications
Mustafa Sahin
3 joint publications
Min Jeong Kye
1 joint publications
Eszter Balogh
1 joint publications
Jennifer C Chandler
1 joint publications
Máté Varga
1 joint publications
Gusztáv Schay
1 joint publications
Regina Légrádi
