Keren Boris
16PUBLICATIONS
401CO-AUTHORS
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Publications (16)
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|Sep 19, 2024
Germline mutations in a G protein identify signaling cross-talk in T cells.Hyoungjun Ham, Huie Jing, Ian T Lamborn
|Sep 10, 2024
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina
|Apr 02, 2024
Mono and biallelic variants in HCN2 cause severe neurodevelopmental disorders.Clara Houdayer, A Marie Phillips, Marie Chabbert
|Aug 11, 2023
A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report.Yeboah Kofi Gyening, Keren Boris, Mignot Cyril
|Jul 14, 2023
Deep Characterization of a Greek Patient with Desmin-Related Myofibrillar Myopathy and Cardiomyopathy.Constantinos Papadopoulos, Edoardo Malfatti, Corinne Métay
|May 31, 2023
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production.Frédéric Ebstein, Sébastien Küry, Victoria Most
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Frequent Collaborators
3 joint publications
Matias Wagner
3 joint publications
Laurence Faivre
3 joint publications
Perrine Charles
3 joint publications
Cas Simons
2 joint publications
Paulino Gomez-Puertas
2 joint publications
Steffen Syrbe
2 joint publications
Reza Maroofian
2 joint publications
Bert Callewaert
2 joint publications
Rikke S Møller
2 joint publications
Mignot Cyril
