Keren Boris

17PUBLICATIONS
410CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Cellular nervous systemNeurogeneticsImmunogenetics (incl. genetic immunology)
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Publications (17)

|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

Perrine Charles

3 joint publications

Laurence Faivre

3 joint publications

Matias Wagner

3 joint publications

Cas Simons