Elena V. Semina

6.5k total citations · 1 hit paper
98 papers, 4.9k citations indexed

About

Elena V. Semina is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Elena V. Semina has authored 98 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 52 papers in Genetics and 15 papers in Genetics. Recurrent topics in Elena V. Semina's work include Ocular Disorders and Treatments (27 papers), Developmental Biology and Gene Regulation (24 papers) and Connexins and lens biology (14 papers). Elena V. Semina is often cited by papers focused on Ocular Disorders and Treatments (27 papers), Developmental Biology and Gene Regulation (24 papers) and Connexins and lens biology (14 papers). Elena V. Semina collaborates with scholars based in United States, Canada and France. Elena V. Semina's co-authors include Linda M. Reis, Jeffrey C. Murray, Wallace L.M. Alward, Brad A. Amendt, Pierre Bitoun, Rebecca S. Reiter, Nancy J. Leysens, Tord Hjalt, Rebecca C. Tyler and Nicole A. Datson and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Elena V. Semina

95 papers receiving 4.8k 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.

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

1996 720 citations Elena V. Semina, Pierre Bitoun et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Elena V. Semina United States	36	3.6k	2.0k	836	682	416	98	4.9k
Hélène Dollfus France	42	4.8k 1.3×	3.0k 1.5×	1.2k 1.5×	344 0.5×	674 1.6×	178	6.7k
Douglas B. Gould United States	30	2.0k 0.6×	836 0.4×	883 1.1×	420 0.6×	531 1.3×	72	3.9k
Philip J. Gage United States	31	2.4k 0.7×	1.0k 0.5×	290 0.3×	529 0.8×	227 0.5×	52	3.7k
Ruth Ashery‐Padan Israel	44	4.7k 1.3×	1.1k 0.5×	566 0.7×	819 1.2×	781 1.9×	80	6.0k
Jean‐Michel Rozet France	34	3.8k 1.0×	1.2k 0.6×	1.8k 2.1×	471 0.7×	500 1.2×	120	4.5k
Tsutomu Kume United States	39	3.8k 1.1×	715 0.4×	339 0.4×	351 0.5×	781 1.9×	93	5.2k
Noriyuki Azuma Japan	28	1.5k 0.4×	644 0.3×	783 0.9×	784 1.1×	215 0.5×	139	2.6k
Tim Jordan United Kingdom	14	2.8k 0.8×	1.1k 0.6×	499 0.6×	656 1.0×	295 0.7×	14	3.5k
Nicola Ragge United Kingdom	29	1.1k 0.3×	1.2k 0.6×	333 0.4×	288 0.4×	164 0.4×	74	2.6k
Y Ninomiya Japan	38	2.1k 0.6×	1.1k 0.6×	182 0.2×	379 0.6×	755 1.8×	81	4.4k

Countries citing papers authored by Elena V. Semina

Since Specialization

Citations

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

Fields of papers citing papers by Elena V. Semina

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena V. Semina

This figure shows the co-authorship network connecting the top 25 collaborators of Elena V. Semina. A scholar is included among the top collaborators of Elena V. Semina 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 Elena V. Semina. Elena V. Semina 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

Ceroni, Fabiola, Richard Holt, Елена А. Сорокина, et al.. (2024). Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development. Nature Communications. 15(1). 9245–9245. 2 indexed citations

Khanna, Cheryl L., James B. Smadbeck, Sarah H. Johnson, et al.. (2024). Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld‐Rieger Syndrome. American Journal of Medical Genetics Part A. 194(5). e63542–e63542. 2 indexed citations

Reis, Linda M., et al.. (2024). In Vivo Assessment of Retinal Phenotypes in Axenfeld–Rieger Syndrome. Investigative Ophthalmology & Visual Science. 65(4). 20–20.

Reis, Linda M., David J. Amor, Raad A. Haddad, et al.. (2023). Alternative Genetic Diagnoses in Axenfeld–Rieger Syndrome Spectrum. Genes. 14(10). 1948–1948. 5 indexed citations

Daruich, Alejandra, Melinda K. Duncan, Matthieu P. Robert, et al.. (2022). Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches. Progress in Retinal and Eye Research. 95. 101133–101133. 33 indexed citations

Muheisen, Sanaa, et al.. (2022). CRISPR-Cas9-mediated functional dissection of the foxc1 genomic region in zebrafish identifies critical conserved cis-regulatory elements. Human Genomics. 16(1). 49–49. 4 indexed citations

Reis, Linda M., Mohit Maheshwari, Donald Basel, et al.. (2022). Novel Genetic Diagnoses in Septo-Optic Dysplasia. Genes. 13(7). 1165–1165. 8 indexed citations

Reis, Linda M., Donald Basel, Julie McCarrier, David V. Weinberg, & Elena V. Semina. (2020). Compound heterozygous splicing CDON variants result in isolated ocular coloboma. Clinical Genetics. 98(5). 486–492. 4 indexed citations

Reis, Linda M., Carlos Zamora, Omar Abdul‐Rahman, et al.. (2019). Novel variants in CDH2 are associated with a new syndrome including Peters anomaly. Clinical Genetics. 97(3). 502–508. 14 indexed citations

10.

Reis, Linda M., Елена А. Сорокина, Sanaa Muheisen, et al.. (2019). De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome. The American Journal of Human Genetics. 105(2). 425–433. 25 indexed citations

11.

Happ, Hannah C., Kala F. Schilter, Eric Weh, Linda M. Reis, & Elena V. Semina. (2016). 8q21.11 microdeletion in two patients with syndromic peters anomaly. American Journal of Medical Genetics Part A. 170(9). 2471–2475. 16 indexed citations

12.

Happ, Hannah C., Eric Weh, Deborah M. Costakos, Linda M. Reis, & Elena V. Semina. (2016). Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract. BMC Medical Genetics. 17(1). 64–64. 6 indexed citations

13.

Reis, Linda M., et al.. (2015). Novel mutations in PAX6, OTX2 and NDP in anophthalmia, microphthalmia and coloboma. European Journal of Human Genetics. 24(4). 535–541. 60 indexed citations

14.

Brémond‐Gignac, Dominique, Pierre Bitoun, Linda M. Reis, et al.. (2010). Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia.. PubMed. 16. 1705–11. 43 indexed citations

15.

Сорокина, Елена А., et al.. (2008). Mip Represents a Potential Direct Downstream Target of Pitx3 Transcription Factor. Investigative Ophthalmology & Visual Science. 49(13). 2791–2791. 1 indexed citations

16.

Sakazume, Satoru, et al.. (2007). Functional analysis of human mutations in homeodomain transcription factor PITX3. BMC Molecular Biology. 8(1). 84–84. 28 indexed citations

17.

Zinkevich, Natalya S., D.V. Bosenko, Rebecca C. Tyler, & Elena V. Semina. (2006). Studies of Zebrafish pitx2 Demonstrate Conservation of Expression and Function With the Human Gene. Investigative Ophthalmology & Visual Science. 47(13). 5631–5631.

18.

Hjalt, Tord & Elena V. Semina. (2005). Current molecular understanding of Axenfeld–Rieger syndrome. Expert Reviews in Molecular Medicine. 7(25). 1–17. 72 indexed citations

19.

Bosenko, D.V., Natalya S. Zinkevich, Rebecca C. Tyler, Brian A. Link, & Elena V. Semina. (2004). Sequence and expression of zebrafish optineurin gene suggests conserved function in vertebrate eye. Investigative Ophthalmology & Visual Science. 45(13). 4408–4408. 1 indexed citations

20.

Brooks, Brian P., Sayoko E. Moroi, Catherine A. Downs, et al.. (2004). A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome. Ophthalmic Genetics. 25(1). 57–62. 24 indexed citations

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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