Viktoria Zakharova
5PUBLICATIONS
89CO-AUTHORS
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Publications (5)
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|Dec 11, 2024
Mild Congenital Hyperinsulinism Caused by Mutation in Human Glucokinase Gene.Leila Salikhovna Sozaeva, Sabina Kalandarovna Ismailova, Irina Yurievna Chernyak
|Dec 06, 2024
A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations.Natalia Borbaran Bravo, Ekaterina Deordieva, Larissa Doll
|Jan 08, 2024
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation.Andrea Accogli, Saurabh Shakya, Taewoo Yang
|Sep 02, 2022
Cancer-causing MAP2K1 mutation in a mosaic patient with cardio-facio-cutaneous syndrome and immunodeficiency.Victorya Zakharova, Elena Raykina, Irina Mersiyanova
|May 05, 2021
Constrained chromatin accessibility in PU.1-mutated agammaglobulinemia patients.Carole Le Coz, David N Nguyen, Chun Su
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Frequent Collaborators
1 joint publications
Leila Salikhovna Sozaeva
1 joint publications
Sabina Kalandarovna Ismailova
1 joint publications
Irina Yurievna Chernyak
1 joint publications
Sergey Vladimirovich Popov
1 joint publications
Igor Sergeevich Chugunov
1 joint publications
Carole Le Coz
1 joint publications
David N Nguyen
1 joint publications
Chun Su
1 joint publications
Brian E Nolan
1 joint publications
Amanda V Albrecht
