V. O

Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein.

H. Ostrer, Robert Huether, A. Chamberlin, 2019, Human molecular genetics.

Rapid Next-Generation Sequencing Method for Prediction of Prostate Cancer Risks.

H. Ostrer, V. Fofanov, S. Freedland, 2019, The Journal of molecular diagnostics : JMD.

POLYMORPHISM OF APOLIPOPROTEIN A1 GENE AND LIPID PROFILE OF BLOOD SERUM IN THE EVENKI AND BURYAT POPULATIONS

T. Bairova, M. Darenskaya, V. O, 2015 .

Biallelic mutations in FLNB cause a skeletal dysplasia with 46,XY gonadal dysgenesis by activating β‐catenin

H. Ostrer, K. Upadhyay, B. Taragin, 2018, Clinical genetics.