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American Journal of Human Genetics|May 22, 2021
Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorderHolger Hengel, Shabab B Hannan, Sarah Dyack, et al.Nature|May 27, 2021
Swarm Learning for decentralized and confidential clinical machine learningStefanie Warnat-Herresthal, Hartmut Schultze, Krishnaprasad Lingadahalli Shastry, 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.Nature Communications|February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxiaBenita Menden, Rana D Incebacak Eltemur, German Demidov, 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.Npj Biodiversity|September 17, 2024
The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomicsAnn M Mc Cartney, Giulio Formenti, Alice Mouton, et al.Pageof 10