Yuri V. Sergeev

5.5k total citations · 1 hit paper
86 papers, 3.8k citations indexed

About

Yuri V. Sergeev is a scholar working on Molecular Biology, Cell Biology and Ophthalmology. According to data from OpenAlex, Yuri V. Sergeev has authored 86 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 31 papers in Cell Biology and 20 papers in Ophthalmology. Recurrent topics in Yuri V. Sergeev's work include Retinal Development and Disorders (25 papers), melanin and skin pigmentation (23 papers) and Connexins and lens biology (20 papers). Yuri V. Sergeev is often cited by papers focused on Retinal Development and Disorders (25 papers), melanin and skin pigmentation (23 papers) and Connexins and lens biology (20 papers). Yuri V. Sergeev collaborates with scholars based in United States, China and Japan. Yuri V. Sergeev's co-authors include Paul T. Wingfield, Monika B. Dolinska, J. Fielding Hejtmancik, Oleg V. Tsodikov, M. Thomas Record, Charles E. Egwuagu, Renxi Wang, Cheng‐Rong Yu, Sung-Hye Kim and Ivy M. Dambuza and has published in prestigious journals such as Journal of Clinical Investigation, Nature Medicine and PLoS ONE.

In The Last Decade

Yuri V. Sergeev

85 papers receiving 3.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Interleukin-35 induces regulatory B cells that suppress autoimmune disease

2014 583 citations Monika B. Dolinska, Yuri V. Sergeev et al. profile →

Peers

Countries citing papers authored by Yuri V. Sergeev

Since Specialization

Citations

This map shows the geographic impact of Yuri V. Sergeev'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 Yuri V. Sergeev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yuri V. Sergeev more than expected).

Fields of papers citing papers by Yuri V. Sergeev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yuri V. Sergeev. 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 Yuri V. Sergeev. The network helps show where Yuri V. Sergeev may publish in the future.

Co-authorship network of co-authors of Yuri V. Sergeev

This figure shows the co-authorship network connecting the top 25 collaborators of Yuri V. Sergeev. A scholar is included among the top collaborators of Yuri V. Sergeev 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 Yuri V. Sergeev. Yuri V. Sergeev 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	Genetic mutations disrupt the coordinated mode of tyrosinase's intra‐melanosomal domain 2025 ·Protein Science ·(unknown), Yuri V. Sergeev	2
2	Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B 2023 ·The American Journal of Human Genetics ·Stacie K. Loftus, M. Gillis, (unknown), Laura L. Baxter, (unknown), Dawn E. Watkins‐Chow, Frank X. Donovan, Yuri V. Sergeev, William S. Oetting, William J. Pavan, David R. Adams	8
3	Evaluating the Cysteine-Rich and Catalytic Subdomains of Human Tyrosinase and OCA1-Related Mutants Using 1 μs Molecular Dynamics Simulation 2023 ·International Journal of Molecular Sciences ·(unknown), Yuri V. Sergeev	3
4	Protein Biochemistry and Molecular Modeling of the Intra-Melanosomal Domain of Human Recombinant Tyrp2 Protein and OCA8-Related Mutant Variants 2022 ·International Journal of Molecular Sciences ·Monika B. Dolinska, (unknown), (unknown), Yuri V. Sergeev	6
5	The Role of Flagship Universities in a Region: Transformation Models 2019 ·Voprosy Obrazovaniya/ Educational Studies Moscow ·(unknown), (unknown), (unknown), (unknown), Yuri V. Sergeev	19
6	Dynamic analysis of human tyrosinase intra-melanosomal domain and mutant variants to further understand oculocutaneous albinism type 1 2018 ·Journal of Analytical & Pharmaceutical Research ·S. Katie Farney, Monika B. Dolinska, Yuri V. Sergeev	5
7	The consequences of deglycosylation of recombinant intra-melanosomal domain of human tyrosinase 2017 ·Biological Chemistry ·Monika B. Dolinska, Yuri V. Sergeev	10
8	Unfolding mutation screen for inherited eye disease 2016 ·Investigative Ophthalmology & Visual Science ·Caitlyn L McCafferty, Yuri V. Sergeev	1
9	Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness 2016 ·The American Journal of Human Genetics ·Aman George, Dina J. Zand, Robert B. Hufnagel, Ruchi Sharma, Yuri V. Sergeev, Janet M. Legare, Gregory M. Rice, (unknown), (unknown), Laura H. Tetri, David M. Gamm, Kapil Bharti, Brian P. Brooks	70
10	CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability 2016 ·Scientific Reports ·Yuriko Minegishi, Xunlun Sheng, Kazutoshi Yoshitake, Yuri V. Sergeev, Daisuke Iejima, Yoshio Shibagaki, Norikazu Monma, Kazuho Ikeo, Masaaki Furuno, (unknown), Yani Liu, Weining Rong, Seisuke Hattori, Takeshi Iwata	30
11	Modulation of V-ATPase by βA3/A1-Crystallin in Retinal Pigment Epithelial Cells 2015 ·Advances in experimental medicine and biology ·Mallika Valapala, Yuri V. Sergeev, Eric F. Wawrousek, Stacey Hose, J. Samuel Zigler, Debasish Sinha	7
12	Novel mutation in FBN1 causes ectopia lentis and varicose great saphenous vein in one Chinese autosomal dominant family. 2014 ·PubMed ·Qing Fu, Peng Liu, Qingsheng Lu, Feng Wang, Hui Wang, Wei Shen, Fei Xu, Lin Liu, Yuri V. Sergeev, Ruifang Sui	4
13	Molecular modeling of functional domain of ABCA4: towards understanding the genotype-to-phenotype relationships in Stargardt’s disease 2013 ·Investigative Ophthalmology & Visual Science ·Yuri V. Sergeev, Katherine Pogrebniak, (unknown), Wadih M. Zein, Kerry Goetz, (unknown), Crandall E. Peeler, Thiran Jayasundera, Brian P. Brooks, Paul A. Sieving	1
14	DNA Variations in Oculocutaneous Albinism: An Updated Mutation List and Current Outstanding Issues in Molecular Diagnostics 2013 ·Human Mutation ·Dimitre R. Simeonov, Xinjing Wang, Chen Wang, Yuri V. Sergeev, Monika B. Dolinska, Matthew Bower, Roxanne Fischer, (unknown), Genia Dubrovsky, Joan Z. Balog, Marjan Huizing, (unknown), Wadih M. Zein, William A. Gahl, Brian P. Brooks, David R. Adams	102
15	Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypes 2013 ·Human Molecular Genetics ·Yuri V. Sergeev, Susan Vitale, Paul A. Sieving, Ajoy Vincent, Anthony G. Robson, Anthony T. Moore, Andrew R. Webster, Graham E. Holder	33
16	X-Linked Retinoschisis: RS1 Mutation Severity and Age Affect the ERG Phenotype in a Cohort of 68 Affected Male Subjects 2011 ·Investigative Ophthalmology & Visual Science ·(unknown), Catherine A. Cukras, Amy Turriff, Yuri V. Sergeev, Susan Vitale, Ronald A. Bush, Paul A. Sieving	50
17	Loss-of-Function Mutations in Rab Escort Protein 1 (REP-1) Affect Intracellular Transport in Fibroblasts and Monocytes of Choroideremia Patients 2009 ·PLoS ONE ·(unknown), Jennifer J. Barb, Yuri V. Sergeev, (unknown), Christopher Silvin, Peter J. Munson, Ian M. MacDonald	41
18	Mutations in KCNJ13 Cause Autosomal-Dominant Snowflake Vitreoretinal Degeneration 2008 ·The American Journal of Human Genetics ·J. Fielding Hejtmancik, Xiaodong Jiao, Anren Li, Yuri V. Sergeev, Xiaoyan Ding, Anil K. Sharma, Chi‐Chao Chan, Igor Medina, Albert O. Edwards	77
19	β-Crystallin association 2004 ·Experimental Eye Research ·J. Fielding Hejtmancik, Paul T. Wingfield, Yuri V. Sergeev	51
20	Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2 2004 ·The American Journal of Human Genetics ·Anren Li, Xiaodong Jiao, Francis L. Munier, Daniel F. Schorderet, Wenliang Yao, Fumino Iwata, Mutsuko Hayakawa, Atsushi Kanai, (unknown), Richard A. Lewis, John R. Heckenlively, Richard G. Weleber, Elias I. Traboulsi, Qingjiong Zhang, Xueshan Xiao, Muriel I. Kaiser‐Kupfer, Yuri V. Sergeev, J. Fielding Hejtmancik	207

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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