Evgeny Vasilyev
4PUBLICATIONS
15CO-AUTHORS
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Publications (4)
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|Jul 01, 2022
A Founder Mutation in the POMC 5'-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA.Iuliia Viakhireva, Natalia Kalinchenko, Evgeny Vasilyev
|Mar 24, 2020
[Somatic mutations in the androgen receptor gene as the cause of androgen insensitivity syndrome].N Y Kalinchenko, A A Kolodkina, V M Petrov
|Jul 05, 2019
[Hereditary Cushing's syndrome caused by primary bilateral macronodular adrenal hyperplasia due to ARMC5 mutation with concomitant primary hyperparathyroidism: the first known case in Russia].E O Mamedova, E V Vasilyev, V M Petrov
|Sep 22, 2018
High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism.Nina Makretskaya, Olga Bezlepkina, Anna Kolodkina
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Frequent Collaborators
3 joint publications
Anatoly Tiulpakov
2 joint publications
Natalia Kalinchenko
2 joint publications
V M Petrov
1 joint publications
A A Kolodkina
1 joint publications
E O Mamedova
1 joint publications
N S Izmailova
1 joint publications
S A Buryakina
1 joint publications
L Y Rozhinskaya
1 joint publications
Z E Belaya
1 joint publications
Nina Makretskaya
