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Fabian Brand

Showing results (11-20 of 17) with videos related to

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Human Mutation|September 15, 2022
Next-generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen-de Vries syndromeFabian Brand, Aswinkumar Vijayananth, Tzung-Chien Hsieh, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|June 6, 2023
[Optimisation of risk and crisis communication of governments, authorities and public health institutions-challenges in long-lasting crises illustrated by the COVID-19 pandemic]Annett Schulze, Fabian Brand, Dinah Kristin Leschzyk, et al.
F1000Research|September 30, 2024
NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant callingFriederike Hanssen, Gisela Gabernet, Famke Bäuerle, et al.
Human Genomics|January 24, 2026
Genetic contribution to severe COVID-19 in adults under 60 years without major comorbidities in the German National Pandemic Cohort Network (NAPKON)Ayda Abolhassani, T Madhusankha Alawathurage, Axel Schmidt, et al.
Plos Pathogens|December 23, 2024
Systematic assessment of COVID-19 host genetics using whole genome sequencing dataAxel Schmidt, Nicolas Casadei, Fabian Brand, et al.
Plos Genetics|November 3, 2022
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics InitiativeGuillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Human Mutation|September 15, 2022
Next-generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen-de Vries syndromeFabian Brand, Aswinkumar Vijayananth, Tzung-Chien Hsieh, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|June 6, 2023
[Optimisation of risk and crisis communication of governments, authorities and public health institutions-challenges in long-lasting crises illustrated by the COVID-19 pandemic]Annett Schulze, Fabian Brand, Dinah Kristin Leschzyk, et al.
F1000Research|September 30, 2024
NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant callingFriederike Hanssen, Gisela Gabernet, Famke Bäuerle, et al.
Human Genomics|January 24, 2026
Genetic contribution to severe COVID-19 in adults under 60 years without major comorbidities in the German National Pandemic Cohort Network (NAPKON)Ayda Abolhassani, T Madhusankha Alawathurage, Axel Schmidt, et al.
Plos Pathogens|December 23, 2024
Systematic assessment of COVID-19 host genetics using whole genome sequencing dataAxel Schmidt, Nicolas Casadei, Fabian Brand, et al.
Plos Genetics|November 3, 2022
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics InitiativeGuillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
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