Yuval Yogev

497 total citations
28 papers, 243 citations indexed

About

Yuval Yogev is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Yuval Yogev has authored 28 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Genetics. Recurrent topics in Yuval Yogev's work include Genomics and Rare Diseases (5 papers), RNA modifications and cancer (4 papers) and CRISPR and Genetic Engineering (3 papers). Yuval Yogev is often cited by papers focused on Genomics and Rare Diseases (5 papers), RNA modifications and cancer (4 papers) and CRISPR and Genetic Engineering (3 papers). Yuval Yogev collaborates with scholars based in Israel, United States and Czechia. Yuval Yogev's co-authors include Ohad S. Birk, Ohad Wormser, Daniel Halpérin, Yonatan Perez, Rotem Kadir, Zamir Shorer, Ilan Shelef, Libe Gradstein, Raz Zarivach and Hagit Flusser and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Yuval Yogev

25 papers receiving 239 citations

Peers

Yuval Yogev

GENET

PHYSI

CCM

Emma M. Lessieur United States

Priscilla R. Prestes Australia

Hideaki Ohtsubo Japan

Alessandra M. Norris United States

Arthur Sorlin France

Fılız Hazan Türkiye

Martin Krenn Austria

Andrea Yuste United States

Chiara Panicucci Italy

Aude Angelini United States

Emma M. Lessieur United States

Yuval Yogev

150 ×1.1

37 ×0.7

GENET

45 ×1.4

26 ×0.9

PHYSI

17 ×0.7

CCM

Citations per year, relative to Yuval Yogev Yuval Yogev (= 1×) peers Emma M. Lessieur

Countries citing papers authored by Yuval Yogev

Since Specialization

Citations

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

Fields of papers citing papers by Yuval Yogev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuval Yogev

This figure shows the co-authorship network connecting the top 25 collaborators of Yuval Yogev. A scholar is included among the top collaborators of Yuval Yogev 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 Yuval Yogev. Yuval Yogev 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

Michelson, Marina, et al.. (2024). Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene. Clinical Genetics. 105(6). 671–675.

Cohen, Idan, H W Levi, Yuval Yogev, et al.. (2024). Heterozygous THBS2 pathogenic variant causes Ehlers–Danlos syndrome with prominent vascular features in humans and mice. European Journal of Human Genetics. 32(5). 550–557. 7 indexed citations

Yogev, Yuval, Moshe Schaffer, Ohad Wormser, et al.. (2024). A role of BPTF in viral oncogenicity delineated through studies of heritable Kaposi sarcoma. Journal of Medical Virology. 96(2). e29436–e29436. 1 indexed citations

Yogev, Yuval, Ohad Wormser, Daniel Halpérin, et al.. (2024). VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19. Human Genetics. 143(5). 695–701. 5 indexed citations

Yogev, Yuval, et al.. (2023). De‐novo “germline second hit” loss‐of‐heterozygosity RBP3 deletion mutation causing recessive high myopia. Clinical Genetics. 104(5). 571–576. 2 indexed citations

Wormser, Ohad, Yonatan Perez, Libe Gradstein, et al.. (2023). IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma. npj Genomic Medicine. 8(1). 22–22. 1 indexed citations

Halpérin, Daniel, Yuval Yogev, Ohad Wormser, et al.. (2023). SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice. Journal of Medical Genetics. 61(2). 117–124.

Simonovsky, Eyal, Idan Hekselman, Omer Basha, et al.. (2023). Predicting molecular mechanisms of hereditary diseases by using their tissue‐selective manifestation. Molecular Systems Biology. 19(8). e11407–e11407. 5 indexed citations

Halpérin, Daniel, Yuval Yogev, Ohad Wormser, et al.. (2022). A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13‐q21.3. Clinical Genetics. 102(2). 123–129. 2 indexed citations

10.

Lior, Yotam, Yuval Yogev, Reut Riff, et al.. (2022). Fractional exhaled Nitric Oxide (FeNO) level as a predictor of COVID-19 disease severity. Nitric Oxide. 124. 68–73. 16 indexed citations

11.

Yogev, Yuval, Yair Sadaka, Yael Feinstein, et al.. (2022). Transcript-Based Diagnosis and Expanded Phenotype of an Intronic Mutation in TPM3 Myopathy. Molecular Diagnosis & Therapy. 26(5). 561–568. 2 indexed citations

12.

Halpérin, Daniel, Rotem Kadir, Ohad Wormser, et al.. (2021). CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice. Nature Communications. 12(1). 6187–6187. 23 indexed citations

13.

Halpérin, Daniel, Ohad Wormser, Yuval Yogev, et al.. (2020). Phenotypic variability and mutation hotspot in COX15‐related Leigh syndrome. American Journal of Medical Genetics Part A. 182(6). 1506–1512. 9 indexed citations

14.

Halpérin, Daniel, et al.. (2020). Novel MTMR2 mutation causing severe Charcot-Marie-Tooth type 4B1 disease: a case report. Neurogenetics. 21(4). 301–304. 2 indexed citations

15.

Yogev, Yuval. (2020). A humoral solution: Autologous blood products and tissue repair. Cellular Immunology. 356. 104178–104178. 3 indexed citations

16.

Yogev, Yuval, Lior Zeller, Raz Zarivach, et al.. (2019). Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenase. Journal of Clinical Investigation. 129(12). 5163–5168. 29 indexed citations

17.

Halpérin, Daniel, Yuval Yogev, Ohad Wormser, et al.. (2019). A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I. Annals of Human Genetics. 83(5). 361–366. 5 indexed citations

18.

Straussberg, Rachel, Ruijuan Xu, Izolda Mileva, et al.. (2019). DEGS1 variant causes neurological disorder. European Journal of Human Genetics. 27(11). 1668–1676. 31 indexed citations

19.

Halpérin, Daniel, Rotem Kadir, Yonatan Perez, et al.. (2018). SEC31A mutation affects ER homeostasis, causing a neurological syndrome. Journal of Medical Genetics. 56(3). 139–148. 27 indexed citations

20.

Yogev, Yuval, Yonatan Perez, Iris Noyman, et al.. (2017). Progressive hereditary spastic paraplegia caused by a homozygous KY mutation. European Journal of Human Genetics. 25(8). 966–972. 13 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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