Anatoly Tiulpakov

9PUBLICATIONS
35CO-AUTHORS
Gene mappingNeurogeneticsMedical infection agents (incl. prions)Infant and child healthSolid tumours
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Publications (9)

|Jun 26, 2026
Clinical and Genetic Characterization of a Russian Family with Bardet-Biedl Syndrome Carrying a Previously Undescribed Missense Variant and a Recurrent Pathogenic Frameshift Variant in BBS7 Gene.

|Aug 11, 2022
Spectrum of neuro-developmental disorders in children with congenital hyperinsulinism due to activating mutations in GLUD1.

Sommayya Aftab, Diliara Gubaeva, Jayne A L Houghton

|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

|Jun 01, 2022
Early transition to sulfonylurea therapy in infant with DEND syndrome due to F132L ABCC8 mutation.

Yulia Tikhonovich, Elena Petryaykina, Natalya Zubkova

|Mar 24, 2020
[Virilizing ovarian tumor: the challenges of differential diagnosis].

M F Kalashnikova, N V Likhodey, A N Tiulpakov

|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

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Frequent Collaborators

3 joint publications

Evgeny Vasilyev

2 joint publications

V M Petrov

2 joint publications

Natalia Kalinchenko

1 joint publications

E O Mamedova