Valentina Labay

1.7k total citations
11 papers, 1.3k citations indexed

About

Valentina Labay is a scholar working on Molecular Biology, Urology and Sensory Systems. According to data from OpenAlex, Valentina Labay has authored 11 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Urology and 3 papers in Sensory Systems. Recurrent topics in Valentina Labay's work include Hearing, Cochlea, Tinnitus, Genetics (3 papers), Hair Growth and Disorders (3 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Valentina Labay is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (3 papers), Hair Growth and Disorders (3 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Valentina Labay collaborates with scholars based in Israel, United States and United Kingdom. Valentina Labay's co-authors include Raymonde Szargel, Nadine Cohen, Hanna Mandel, Andrew J. Griffith, Tomoko Makishima, Yefim Anbinder, Orly Elpeleg, Ann Saada, Corina Hartman and Drora Berkowitz and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Biochemistry.

In The Last Decade

Valentina Labay

11 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valentina Labay Israel 10 767 372 328 194 137 11 1.3k
Yuzo Tanabe Japan 19 912 1.2× 332 0.9× 27 0.1× 112 0.6× 141 1.0× 40 1.3k
Yelena Bykhovskaya United States 29 1.3k 1.7× 277 0.7× 485 1.5× 17 0.1× 59 0.4× 45 2.1k
Khushnooda Ramzan Saudi Arabia 18 644 0.8× 90 0.2× 230 0.7× 26 0.1× 55 0.4× 79 1.2k
Jerzy Bal Poland 19 486 0.6× 60 0.2× 85 0.3× 110 0.6× 62 0.5× 113 1.1k
Tarja Joensuu Finland 19 670 0.9× 24 0.1× 252 0.8× 141 0.7× 210 1.5× 31 1.3k
Christian Hamel France 20 1.2k 1.6× 141 0.4× 111 0.3× 26 0.1× 73 0.5× 39 1.5k
Soo Kyung Koo South Korea 15 503 0.7× 61 0.2× 153 0.5× 26 0.1× 63 0.5× 28 743
Teresa M. Gunn United States 22 717 0.9× 44 0.1× 65 0.2× 26 0.1× 200 1.5× 63 1.6k
Isabelle Russell‐Eggitt United Kingdom 26 1.1k 1.4× 36 0.1× 49 0.1× 47 0.2× 97 0.7× 58 2.4k
Bahareh Rabbani Iran 14 548 0.7× 32 0.1× 185 0.6× 21 0.1× 43 0.3× 48 1.1k

Countries citing papers authored by Valentina Labay

Since Specialization
Citations

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

Fields of papers citing papers by Valentina Labay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Valentina Labay. 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 Valentina Labay. The network helps show where Valentina Labay may publish in the future.

Co-authorship network of co-authors of Valentina Labay

This figure shows the co-authorship network connecting the top 25 collaborators of Valentina Labay. A scholar is included among the top collaborators of Valentina Labay 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 Valentina Labay. Valentina Labay is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Kawashima, Yoshiyuki, Gwenaëlle S. G. Géléoc, Kiyoto Kurima, et al.. (2011). Mechanotransduction in mouse inner ear hair cells requires transmembrane channel–like genes. Journal of Clinical Investigation. 121(12). 4796–4809. 315 indexed citations
2.
Labay, Valentina, et al.. (2010). Topology of Transmembrane Channel-like Gene 1 Protein. Biochemistry. 49(39). 8592–8598. 55 indexed citations
3.
Labay, Valentina, Gema Garrido, Anne C. Madeo, et al.. (2007). Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNASer(UCN) in sensorineural hearing loss. Clinical Genetics. 73(1). 50–54. 11 indexed citations
4.
Zelikovic, Israel, et al.. (2003). A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes. Kidney International. 63(1). 24–32. 122 indexed citations
5.
Belyantseva, Inna A., Valentina Labay, Erich T. Boger, Andrew J. Griffith, & Thomas B. Friedman. (2003). Stereocilia: the long and the short of it. Trends in Molecular Medicine. 9(11). 458–461. 18 indexed citations
6.
Mandel, Hanna, Raymonde Szargel, Valentina Labay, et al.. (2001). The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA. Nature Genetics. 29(3). 337–341. 430 indexed citations
7.
Sprecher, Eli, Gilles G. Lestringant, Raymonde Szargel, et al.. (2000). Reply. Journal of Investigative Dermatology. 115(4). 762–763. 2 indexed citations
8.
Raz, Tal, Valentina Labay, Raymonde Szargel, et al.. (2000). The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia geneSLC19A2 of eight families. Human Mutation. 16(1). 37–42. 48 indexed citations
9.
Sprecher, Eli, Gilles G. Lestringant, Raymonde Szargel, et al.. (1999). Atrichia with Papular Lesions Resulting from a Nonsense Mutation Within the Human Hairless Gene. Journal of Investigative Dermatology. 113(4). 687–690. 36 indexed citations
10.
Labay, Valentina, Tal Raz, Hanna Mandel, et al.. (1999). Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Nature Genetics. 22(3). 300–304. 207 indexed citations
11.
Sprecher, Eli, Richard N. Bergman, Raymonde Szargel, et al.. (1998). Atrichia with papular lesions maps to 8p in the region containing the human hairless gene. American Journal of Medical Genetics. 80(5). 546–550. 30 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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