| New data on the phylogeography and genetic diversity of the brown bear Ursus arctos Linnaeus, 1758 of Northeastern Eurasia (mtDNA control region … VV Salomashkina, MV Kholodova, OY Tuten’kov, NS Moskvitina, ... Biology Bulletin 41, 38-46, 2014 | 17 | 2014 |
| Systematics, evolution, and genetics of bears AC Kitchener, E Bellemain, X Ding, A Kopatz, V Kutschera, ... | 9 | 2020 |
| Mutational analysis of hemophilia B in Russia: molecular-genetic study VL Surin, EY Demidova, DS Selivanova, YA Luchinina, VV Salomashkina, ... Russian Journal of Genetics 52, 409-415, 2016 | 9 | 2016 |
| Factor XII deficiency: a clinical and molecular genetic study E Demidova, V Salomashkina, O Pshenichnikova, D Selivanova, ... International Journal of Hematology 117 (5), 678-683, 2023 | 6 | 2023 |
| Phylogeography of ancient and modern brown bears from eastern Eurasia AS Molodtseva, AI Makunin, VV Salomashkina, IG Kichigin, NV Vorobieva, ... Biological Journal of the Linnean Society 135 (4), 722-733, 2022 | 6 | 2022 |
| ABO* A and RHD variants in Russians LL Golovkina, A Stremoukhova, M Vasiljeva, T Pushkina, G Atroscchenko, ... Vox Sanguinis, Supplement 112 (S1), 218-218, 2017 | 6 | 2017 |
| Molecular serological characteristics of weak D antigen types of the Rhesus system LL Golovkina, AG Stremoukhova, TD Pushkina, RS Kalandarov, ... Terapevticheskii arkhiv 88 (7), 78-83, 2016 | 4 | 2016 |
| A founder effect in hemophilia A patients from Russian Ural region with a new p.(His634Arg) variant in F8 gene VV Salomashkina, OS Pshenichnikova, FG Perina, VL Surin Blood Coagulation & Fibrinolysis 33 (2), 124-129, 2022 | 3 | 2022 |
| First evidence of a brown bear on Wrangel Island, Russia UV Babiy, VV Salomashkina, PS Kulemeev, MV Kholodova, AR Gruzdev, ... Ursus 2022 (33e4), 1-8, 2022 | 3 | 2022 |
| Genetic variability of brown bear (Ursus arctos L., 1758) VV Salomashkina, MV Kholodova, UA Semenov, AS Muradov, ... Russian Journal of Genetics 53, 108-117, 2017 | 3 | 2017 |
| Spectrum of Causative Mutations in Patients with Hemophilia A in Russia O Pshenichnikova, V Salomashkina, J Poznyakova, D Selivanova, ... Genes 14 (2), 260, 2023 | 2 | 2023 |
| New missense mutation His2026Arg in the factor VIII gene was revealed in two female patients with clinical manifestation of hemophilia A VL Surin, VV Salomashkina, OS Pshenichnikova, FG Perina, ON Bobrova, ... Russian Journal of Genetics 54, 712-716, 2018 | 2 | 2018 |
| Molecular and genetic verification of von Willebrand disease type 2N DM Chernetskaya, VL Surin, VV Salomashkina, OS Pshenichnikova, ... Russ. J. Hematol. Transfusiology 67, 172-180, 2022 | 1 | 2022 |
| Literature review and clinical observation of acquired idiopathic hemophilia with a new missense mutation in the factor VIII gene (His2026Arg) VI Ershov, IY Gadaev, DA Budanova, FG Perina, VL Surin, ... Terapevticheskii arkhiv 90 (7), 118-122, 2018 | 1 | 2018 |
| Distribution of weak D types in Russians LL Golovkina, RS Kalandarov, AG Stremoukhova, TD Pushkina, ... HLA 87 (4), 287-287, 2016 | 1 | 2016 |
| Active spread of β‐thalassemia beyond the thalassemia belt: A study on a Russian population E Shchemeleva, VV Salomashkina, D Selivanova, N Tsvetaeva, ... Clinical Genetics 107 (1), 23-33, 2025 | | 2025 |
| P1622: GENE CONVERSION CASES FOUND DURING THE VON WILLEBRAND GENE STUDY D Chernetskaya, V Surin, V Salomashkina, O Pshenichnikova, ... HemaSphere 7 (S3), e944699b, 2023 | | 2023 |
| Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c. 396delG p. Val133Trpfs* 25 E Demidova, V Salomashkina, D Selivanova, E Litvin, N Karamyan, ... Hemoglobin 47 (2), 97-101, 2023 | | 2023 |
| Thrombosis in patients with hereditary fibrinogen deficiency EV Yakovleva, VV Salomashkina, VL Surin, DS Selivanova, PS Lavrova, ... Russian journal of hematology and transfusiology 67 (2), 193-201, 2022 | | 2022 |
| CLINICAL PHENOTYPE IN PATIENTS WITH HEREDITARY FACTOR XII DEFICIENCY E Yakovleva, E Demidova, V Surin, V Salomashkina, D Selivanova, ... HAEMOPHILIA 28, 113-114, 2022 | | 2022 |
