S. Deryabina

In Silico Analysis Revealed Five Novel High-Risk Single-Nucleotide Polymorphisms (rs200384291, rs201163886, rs193141883, rs201139487, and rs201723157) in ELANE Gene Causing Autosomal Dominant Severe Congenital Neutropenia 1 and Cyclic Hematopoiesis

I. Tuzankina, K. Shinwari, Guojun Liu, 2022, TheScientificWorldJournal.

Analysis of the TREC and KREC Levels in the Dried Blood Spots of Healthy Newborns with Different Gestational Ages and Weights

M. A. Bolkov, I. Tuzankina, K. Shinwari, 2022, Acta naturae.

RETROSPECTIVE DIAGNOSIS OF PRIMARY IMMUNODEFICIENCIES FOR CHILDREN IN SVERDLOVSK REGION

I. Tuzankina, S. Deryabina, E. Vlasova, 2016 .

A Novel Bruton’s Tyrosine Kinase Mutation in Russian Patient with X-Linked Agammaglobulinemia

I. Tuzankina, M. Bolkov, A. Pavlova, 2017 .

Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis

Liu Guojun, I. Tuzankina, K. Shinwari, 2021, TheScientificWorldJournal.

Family Members with Congenital Heart Disease and Hypogammaglobulinemia

I. Tuzankina, M. Bolkov, S. Deryabina, 2019, Pediatric Immunology.