В. Л. Сурин

580 total citations
72 papers, 381 citations indexed

About

В. Л. Сурин is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, В. Л. Сурин has authored 72 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Hematology, 28 papers in Molecular Biology and 17 papers in Genetics. Recurrent topics in В. Л. Сурин's work include Hemophilia Treatment and Research (17 papers), Cancer-related gene regulation (10 papers) and Platelet Disorders and Treatments (10 papers). В. Л. Сурин is often cited by papers focused on Hemophilia Treatment and Research (17 papers), Cancer-related gene regulation (10 papers) and Platelet Disorders and Treatments (10 papers). В. Л. Сурин collaborates with scholars based in Russia, Mongolia and Germany. В. Л. Сурин's co-authors include Oleg A. Ermakov, Anna Sergeeva, Л. П. Менделеева, Maria Suntsova, Maxim Sorokin, Нуршат Гайфуллин, Andrew Garazha, Anton Buzdin, Evgeniy Simonov and Vladimir Prassolov and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

В. Л. Сурин

54 papers receiving 364 citations

Peers

Countries citing papers authored by В. Л. Сурин

Since Specialization

Citations

This map shows the geographic impact of В. Л. Сурин's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by В. Л. Сурин with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites В. Л. Сурин more than expected).

Fields of papers citing papers by В. Л. Сурин

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by В. Л. Сурин. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by В. Л. Сурин. The network helps show where В. Л. Сурин may publish in the future.

Co-authorship network of co-authors of В. Л. Сурин

This figure shows the co-authorship network connecting the top 25 collaborators of В. Л. Сурин. A scholar is included among the top collaborators of В. Л. Сурин based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with В. Л. Сурин. В. Л. Сурин is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Hereditary combined deficiency of factors V and VIII: observations in the Russian population 2024 ·(unknown), (unknown), (unknown), В. Л. Сурин, (unknown), (unknown), (unknown), (unknown)	0
2	Analysis of microsatellite instability in primary mediastinal large B-cell lymphoma: Focus on PD-L1/PD-L2 and CIITA 2024 ·(unknown), (unknown), (unknown), В. Л. Сурин, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), С. М. Куликов, (unknown), А. М. Ковригина, Andrey Sudarikov	0
3	KRAS/NRAS Gene Mutations and the Efficacy of Bortezomib-Based Triplet Induction Therapy in Patients with Newly Diagnosed Multiple Myeloma 2024 ·SHILAP Revista de lepidopterología ·Anna Sergeeva, В. Л. Сурин, (unknown), (unknown), (unknown), С. М. Куликов, Л. П. Менделеева	0
4	Traditional multilocus phylogeny fails to fully resolve Palearctic ground squirrels (Spermophilus) relationships but reveals a new species endemic to West Siberia 2024 ·Molecular Phylogenetics and Evolution ·Evgeniy Simonov, (unknown), (unknown), (unknown), (unknown), В. Л. Сурин, Vera A. Matrosova, (unknown), (unknown), (unknown), Ф.Н. Голенищев, Oleg A. Ermakov	1
5	Active spread of β‐thalassemia beyond the thalassemia belt: A study on a Russian population 2024 ·Clinical Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), Liliya Doronina, В. Л. Сурин	0
6	Total knee arthroplasty in a female with a severe form of hemophilia A 2023 ·(unknown), (unknown), (unknown), (unknown), (unknown), В. Л. Сурин	0
7	Molecular Genetic Analysis of Russian Patients with Coagulation Factor FVII Deficiency 2023 ·Genes ·(unknown), (unknown), (unknown), Tatiana Abramova, (unknown), В. Л. Сурин	1
8	Spectrum of Causative Mutations in Patients with Hemophilia A in Russia 2023 ·Genes ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), В. Л. Сурин	0
9	Thrombotic thrombocytopenic purpura in pregnancy. Giving birth or not giving birth, that is the question 2022 ·G. М. Galstyan, R.G. Shmakov, (unknown), (unknown), (unknown), В. Л. Сурин, (unknown), (unknown), Evgeniya Polushkina, (unknown), (unknown), Pyregov A.V. Pyregov, (unknown), (unknown), (unknown)	3
10	New missense mutation p.Trp387Ser affecting the functionally important TrpXXTrp motif in the TSR1 repeat of ADAMTS13 metalloproteinase: Case report 2022 ·Clinical and Experimental Pharmacology and Physiology ·(unknown), (unknown), В. Л. Сурин, (unknown), (unknown)	0
11	Thrombosis in patients with hereditary fibrinogen deficiency 2022 ·(unknown), (unknown), В. Л. Сурин, (unknown), (unknown), (unknown), (unknown), (unknown)	0
12	Diagnosis and choice of haemostatic therapy during surgery in patients with combined coagulation factor V and VIII defi ciency 2021 ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), В. Л. Сурин, (unknown), (unknown), (unknown)	2
13	Cytogenetic and Molecular Genetic Abnormalities of CIITA Gene in Patients with Primary Mediastinal (Thymic) Large B-Cell Lymphoma 2021 ·SHILAP Revista de lepidopterología ·(unknown), В. Л. Сурин, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Anna Sergeeva, (unknown)	2
14	Detection of activating mutations in RAS/RAF/MEK/ERK and JAK/STAT signaling pathways 2020 ·SHILAP Revista de lepidopterología ·(unknown), Е. Н. Паровичникова, В. Л. Сурин, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Andrey Sudarikov, Savchenko Vg	0
15	CONGENITAL FACTOR V DEFICIENCY: CASE REPORTS 2019 ·(unknown), (unknown), (unknown), В. Л. Сурин, (unknown), (unknown), (unknown), G. М. Galstyan, (unknown)	4
16	Molecular genetic study of acute intermittent porphyria in Russia: HMBS gene mutation spectrum and problem of penetrance 2019 ·Clinical Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), В. Л. Сурин	6
17	PILOT RESEARCH OF A GENETIC PREDISPOSITION FOR CLINICAL MANIFESTATIONS OF ACUTE INTERMITTENT PORPHYRIA 2019 ·(unknown), (unknown), (unknown), (unknown), В. Л. Сурин	0
18	MOLECULAR GENETIC STRUCTURE OF MULTIPLE MYELOMA TUMOUR CELLS PRIOR TO TREATMENT AND AT THE TIME OF RELAPSE: SHORT REVIEW AND CASE REPORT 2019 ·Anna Sergeeva, Tatiana Abramova, В. Л. Сурин, (unknown), (unknown), (unknown), Anton Buzdin, Л. П. Менделеева	2
19	Hereditary afibrinogenemia: A literature review and clinical observations 2016 ·Terapevticheskii arkhiv ·(unknown), В. Л. Сурин, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2
20	[Three new mutations in the porphobilinogen deaminase gene, detected in acute intermittent porphyria patients from Russia]. 2001 ·PubMed ·В. Л. Сурин, (unknown), (unknown), (unknown), (unknown), (unknown)	4

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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