Ayupova, Guzel,
Litvinov, Sergey,
Akhmetova, Vita,
Minniakhmetov, Ildar,
Mokrysheva, Natalia,
Khusainova, Rita (2024) regulator gene (CFTR) mutations in the
population, which is determined by
genetic diversity and ethnicity
Dzhaubermezov, M.,
Ekomasova, N.,
Mustafin, R.,
Gabidullina, L.,
Galimova, Y.,
Nurgalieva, A.,
Valova, Y.,
Prokofyeva, D.,
Khusnutdinova, E. (2022) individuals of 5 Finno-Permic
populations from the territories
of the European part of the Russian Federation
TIMASHEVA, Y.R.,
NASIBULLIN, T.R.,
MUSTAFINA, O.E.,
BALKHIYAROVA, Z.R.,
PROKOPENKO, I.,
AVZALETDINOVA, D.S.,
MORUGOVA, T.V. (2019) Background
Genome-wide association studies have captured a large proportion of
genetic variation
Ivanova, E.,
Gilyazova, I.,
Pavlov, V.,
Izmailov, A.,
Gimalova, G.,
Karunas, A.,
Prokopenko, I.,
Khusnutdinova, E. (2022) risk of developing disease outcomes from the general
population. Clear cell renal cell carcinoma (cc
Bikbova, M.M.,
Usubova, E.L.,
Oganisyana, K.Kh.,
Lobov, S.L.,
Khasanovad, R.R.,
Dzhemilevab, L.U.,
Khusnutdinova, E.K. (2017)
topography and its thinning, stretching, and protrusion. The hereditary or
genetic theory of keratoconus
in the development of blood pressure elevation. The
population of Tatars residing in the Volga-Ural region of Russia
Timasheva, Y,
Nasibullin, TR,
Tuktarova, IA,
Erdman, VV,
Galiullin, TR,
Zaplakhova, OV,
Bakhtiiarova, KZ (2022) sclerosis in
populations of European ancestry, but the associations are not always reproducible in other
Shnayder, N.A.,
Novitsky, M.A.,
Neznanov, N.G.,
Limankin, O.V.,
Asadullin, A.R.,
Petrov, A.V.,
Dmitrenko, D.V.,
Narodova, E.A.,
Popenko, N.V.,
Nasyrova, R.F. (2022) to the general
population. The comorbidity between schizophrenia and depression suggests a potential coincidence