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AVPR1A MAIN EFFECT AND OXTR-BY-ENVIRONMENT INTERPLAY IN INDIVIDUAL DIFFERENCES IN DEPRESSION LEVEL
KAZANTSEVA, A.V., DAVYDOVA, YU.D., ENIKEEVA, R.F., LOBASKOVA, M.M., MUSTAFIN, R.N., MALYKH, S.B., TAKHIROVA, Z.R., KHUSNUTDINOVA, E.K. (2020)
MENTAL DISORDER
ГЕНЕТИЧЕСКИЕ ОСНОВЫ ПРЕДРАСПОЛОЖЕННОСТИ К ДЕПРЕССИВНЫМ РАССТРОЙСТВАМ
GENETIC BASIS OF DEPRESSIVE DISORDERS
ДАВЫДОВА, Ю.Д., ЕНИКЕЕВА, Р.Ф., КАЗАНЦЕВА, А.В., МУСТАФИН, Р.Н., РОМАНОВА, А.Р., МАЛЫХ, С.Б., ХУСНУТДИНОВА, Э.К., Davydova Yu.D., Enikeeva R.F., Kazantseva A.V., Mustafin R.N., Romanova A.R., Malykh S.B., Khusnutdinova E.K.2 (2019)
GENETIC BASIS OF DEPRESSIVE DISORDERS
A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia
Romanov, G.P., Pshennikova, V.G., Lashin, S.A., Solovyev, A.V., Teryutin, F.M., Cherdonova, A.M., Borisova, T.V., Sazonov, N.N., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A., Barashkov, N.A. (2020)
genetic disorder
Epigenetic Mechanisms of the Influence of Physical Activity on the Development of Atherosclerosis
Mustafin, R.N., Khusnutdinova, E.K. (2024)
but also inhibits the progression of an already developed disease with a decrease in vascular stenosis
ЛЕЧЕНИЕ И ОСОБЕННОСТИ ТЕЧЕНИЯ НАСЛЕДСТВЕННОГО РАКА ЯИЧНИКОВ
TREATMENT AND FEATURES OF HEREDITARY OVARIAN CANCER
Фаисханова, Р.Р., Сакаева, Д.Д., Хуснутдинова, Э.К., Faiskhanova, R.R., Sakaeva, D.D., Khusnutdinova, E.K. (2021)
THE INFLUENCE OF GENES, miRNAs AND RETROELEMENTS ON PSYCHOLOGICAL WELL-BEING
Mustafin, R.N., Khusnutdinova, E.K. (2024)
transposons, are associated with major depressive disorder. The data obtained indicate the influence
ANALYSIS OF CLINICAL MANIFESTATIONS OF NEUROFIBROMATOSIS TYPE 1 IN PATIENTS WITH NONSENSE PATHOGENIC VARIANTS IN THE NF1 GENE FROM THE REPUBLIC OF BASHKORTOSTAN
Mustafin, R.N., Bermisheva, M.A., Karunas, A.S., Akhmetshin, A.A., Monakhova, A.S., Khusnutdinova, E.K. (2025)
and subcutaneous tumors, plexiform neurofibromas, skeletal abnormalities and cognitive disorders. The study
МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЕ ОСНОВЫ РАЗВИТИЯ ОСТРОГО ПАНКРЕАТИТА
MOLECULAR-GENETIC BASES OF DEVELOPMENT OF ACUTE PANCREATITIS
ИМАЕВА, А.К., НУРГАЛИЕВА, А. Х., ГАЛЛЯМОВА, Л.Ф., МУСТАФИН, Т.И., САФИНОВА, Л.Ш., ХУСНУТДИНОВА, Э.К., IMAEVA, A.K., NURGALIEVA, A.KH., GALLYAMOVA, L.F., MUSTAFIN, T.I., SAFMOVA, L.SH., KHUSNUTDINOVA, E.K. (2020)
МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН
MAJOR MUTATION IN THE SPAST GENE IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA FROM THE REPUBLIC OF BASHKORTOSTAN
KHIDIYATOVA, I.M., AKHMETGALEYEVA, A.F., YANKINA, M.A., KHUSNUTDINOVA, E.K., SHAVALIEVA, V.V., SAIFULLINA, E.V., MAGZHANOV, R.V., IDRISOVA, R.F., ХИДИЯТОВА И.М., АХМЕТГАЛЕЕВА А.Ф., САЙФУЛЛИНА Е.В., ИДРИСОВА Р.Ф., ЯНКИНА М.А., ШАВАЛИЕВА В.В., МАГЖАНОВ Р.В., ХУСНУТДИНОВА Э.К. (2019)
Hereditary spastic paraplegia (HSP) is a group of neurodegenerative disorders with a predominant
A NOVEL PATHOGENIC VARIANT C.975G>A (P.TRP325*) IN THE POU3F4 GENE IN YAKUT FAMILY (EASTERN SIBERIA, RUSSIA) WITH THE X-LINKED DEAFNESS-2 (DFNX2)
BARASHKOV, N.A., KLAROV, L.A., TERYUTIN, F.M., SOLOVYEV, A.V., PSHENNIKOVA, V.G., ROMANOV, G.P., TOMSKY, M.I., FEDOROVA, S.A., KONNIKOVA, E.E., TOBOKHOV, A.V., MOROZOV, I.V., BONDAR, A.A., POSUKH, O.L., DZHEMILEVA, L.U., KHUSNUTDINOVA, E.K. (2018)
(enlargement of semicircular canals and postural disorders) clinical DFNX2 features in affected males with c.975

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