Yoel Hirsch

459 total citations
18 papers, 131 citations indexed

About

Yoel Hirsch is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Yoel Hirsch has authored 18 papers receiving a total of 131 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Cell Biology and 5 papers in Genetics. Recurrent topics in Yoel Hirsch's work include RNA regulation and disease (6 papers), Mitochondrial Function and Pathology (3 papers) and Cellular transport and secretion (3 papers). Yoel Hirsch is often cited by papers focused on RNA regulation and disease (6 papers), Mitochondrial Function and Pathology (3 papers) and Cellular transport and secretion (3 papers). Yoel Hirsch collaborates with scholars based in United States, Israel and Australia. Yoel Hirsch's co-authors include John Pappas, Wendy K. Chung, Rachel Rabin, Elaine H. Zackai, David A. Zeevi, Josef Ekstein, Kanji Okumoto, Beth Keena, Akemi Tanaka and Yuichi Abe and has published in prestigious journals such as The American Journal of Human Genetics, Human Genetics and Frontiers in Genetics.

In The Last Decade

Yoel Hirsch

14 papers receiving 129 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoel Hirsch United States 7 93 39 36 17 9 18 131
Wenbao Hu China 7 80 0.9× 40 1.0× 21 0.6× 46 2.7× 9 1.0× 11 155
Vafa Keser Canada 6 154 1.7× 67 1.7× 28 0.8× 8 0.5× 9 1.0× 8 178
Mélanie Quilès France 4 152 1.6× 33 0.8× 65 1.8× 14 0.8× 5 0.6× 6 192
Kimberly W. Keefe United States 5 114 1.2× 131 3.4× 25 0.7× 10 0.6× 6 0.7× 12 260
Damien Haye France 9 83 0.9× 41 1.1× 16 0.4× 10 0.6× 5 0.6× 10 131
Rebecca Willaert United States 6 84 0.9× 76 1.9× 54 1.5× 6 0.4× 12 1.3× 8 185
Kristin D. Kernohan Canada 4 69 0.7× 38 1.0× 9 0.3× 11 0.6× 4 0.4× 4 112
Mariet W. Elting Netherlands 3 44 0.5× 26 0.7× 11 0.3× 8 0.5× 12 1.3× 3 94
Mona Mohammad Almramhi United Kingdom 8 117 1.3× 58 1.5× 56 1.6× 7 0.4× 2 0.2× 13 189
Olga Zurita Spain 9 251 2.7× 63 1.6× 30 0.8× 5 0.3× 6 0.7× 14 285

Countries citing papers authored by Yoel Hirsch

Since Specialization
Citations

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

Fields of papers citing papers by Yoel Hirsch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoel Hirsch

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

All Works

18 of 18 papers shown
1.
Brownstein, Zippora, Yoel Hirsch, Hagar Mor‐Shaked, et al.. (2025). A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF. Human Genomics. 19(1). 112–112.
2.
Rabin, Rachel, Yoel Hirsch, Kevin T. Booth, et al.. (2024). ARSA Variant Associated With Late Infantile Metachromatic Leukodystrophy and Carrier Rate in Individuals of Ashkenazi Jewish Ancestry. American Journal of Medical Genetics Part A. 197(3). e63919–e63919.
3.
Hirsch, Yoel, Hanna Mandel, Tova Hershkovitz, et al.. (2022). Vici syndrome in Israel: Clinical and molecular insights. Frontiers in Genetics. 13. 991721–991721.
4.
Maxwell, Kristina G., Wenjuan Ye, Punn Augsornworawat, et al.. (2022). Multidimensional analysis and therapeutic development using patient iPSC–derived disease models of Wolfram syndrome. JCI Insight. 7(18). 18 indexed citations
5.
Rabin, Rachel, Yoel Hirsch, Wendy K. Chung, et al.. (2022). Expanding the phenotypic spectrum of COLEC10‐Related 3MC syndrome: A glimpse into COLEC10‐Related 3MC syndrome in the Ashkenazi Jewish population. American Journal of Medical Genetics Part A. 188(10). 3110–3117. 1 indexed citations
6.
Azaiez, Héla, Qiuju Wang, Lei Xu, et al.. (2021). The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study. Human Genetics. 141(3-4). 853–863. 8 indexed citations
7.
Helman, Guy, Ayelet Zerem, Sarah Woidill, et al.. (2021). Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121. 11–19. 4 indexed citations
8.
9.
Zeevi, David A., et al.. (2021). Recommendation of premarital genetic screening in the Syrian Jewish community based on mutation carrier frequencies within Syrian Jewish cohorts. Molecular Genetics & Genomic Medicine. 9(8). e1756–e1756. 6 indexed citations
10.
Daum, Hagit, Mythily Ganapathi, Yoel Hirsch, et al.. (2021). Bi‐allelic PAGR1 variants are associated with microcephaly and a severe neurodevelopmental disorder: Genetic evidence from two families. American Journal of Medical Genetics Part A. 188(1). 336–342. 6 indexed citations
11.
Rabin, Rachel, et al.. (2021). Severe epileptic encephalopathy associated with compound heterozygosity of THG1L variants in the Ashkenazi Jewish population. American Journal of Medical Genetics Part A. 185(5). 1589–1597. 5 indexed citations
12.
Muir, Alison M., Jennifer L. Cohen, Sarah E. Sheppard, et al.. (2020). Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities. The American Journal of Human Genetics. 106(5). 623–631. 19 indexed citations
13.
Boyden, Lynn M., Lihi Atzmony, Claire Hamilton, et al.. (2019). Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia. The American Journal of Human Genetics. 105(5). 1023–1029. 18 indexed citations
14.
15.
Lyon, Gholson J., Elaine Marchi, Vardiella Meiner, et al.. (2019). VAC14 syndrome in two siblings with retinitis pigmentosa and neurodegeneration with brain iron accumulation. Molecular Case Studies. 5(6). a003715–a003715. 12 indexed citations
16.
Rabin, Rachel, Yoel Hirsch, David A. Zeevi, et al.. (2019). Study of carrier frequency of Warsaw breakage syndrome in the Ashkenazi Jewish population and presentation of two cases. American Journal of Medical Genetics Part A. 179(10). 2144–2151. 13 indexed citations
17.
Tanaka, Akemi, Kanji Okumoto, Shigehiko Tamura, et al.. (2018). A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder. Molecular Case Studies. 5(1). a003483–a003483. 15 indexed citations
18.
Chiang, John, et al.. (2017). Founder Ashkenazi Jewish mutations of large deletion in the inherited retinal dystrophy genes. Ophthalmic Genetics. 39(1). 135–136. 2 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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