Yarin Hadid

510 total citations
11 papers, 333 citations indexed

About

Yarin Hadid is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Yarin Hadid has authored 11 papers receiving a total of 333 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Yarin Hadid's work include Forensic and Genetic Research (4 papers), Mitochondrial Function and Pathology (2 papers) and Genetic diversity and population structure (2 papers). Yarin Hadid is often cited by papers focused on Forensic and Genetic Research (4 papers), Mitochondrial Function and Pathology (2 papers) and Genetic diversity and population structure (2 papers). Yarin Hadid collaborates with scholars based in Israel, United States and Estonia. Yarin Hadid's co-authors include Doron M. Behar, Karl Skorecki, Toomas Kivisild, Richard Villems, Shay Tzur, Batsheva Bonné‐Tamir, António Amorim, David Gurwitz, Ildus Kutuev and Luı́sa Pereira and has published in prestigious journals such as PLoS ONE, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Yarin Hadid

11 papers receiving 319 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yarin Hadid Israel	8	228	104	67	24	20	11	333
Carla Bini Italy	12	280 1.2×	205 2.0×	55 0.8×	11 0.5×	5 0.3×	57	442
Avinash Arvind Rasalkar India	6	216 0.9×	143 1.4×	89 1.3×	27 1.1×	6 0.3×	11	373
Patrycja Daca‐Roszak Poland	9	196 0.9×	192 1.8×	60 0.9×	6 0.3×	10 0.5×	21	342
Houssein Khodjet‐El‐Khil Tunisia	14	343 1.5×	140 1.3×	95 1.4×	5 0.2×	17 0.8×	32	491
Farha El‐Chennawi Egypt	13	118 0.5×	79 0.8×	40 0.6×	4 0.2×	15 0.8×	24	385
Pu Li China	5	258 1.1×	86 0.8×	59 0.9×	2 0.1×	8 0.4×	7	318
Óscar Acosta Peru	8	158 0.7×	61 0.6×	27 0.4×	2 0.1×	10 0.5×	30	247
Revathi Rajkumar India	9	130 0.6×	121 1.2×	38 0.6×	9 0.4×	26 1.3×	12	341
Jean-Michel Dugoujon France	12	409 1.8×	116 1.1×	171 2.6×	13 0.5×	3 0.1×	24	588

Countries citing papers authored by Yarin Hadid

Since Specialization

Citations

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

Fields of papers citing papers by Yarin Hadid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yarin Hadid

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

All Works

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11 of 11 papers shown

Shalata, Adel, Marina Bar‐Shai, Yarin Hadid, et al.. (2023). Danon Disease: Entire LAMP2 Gene Deletion with Unusual Clinical Presentation—Case Report and Review of the Literature. Genes. 14(8). 1539–1539. 5 indexed citations

Bejar, Jacob, et al.. (2023). Performance of CellDetect for detection of bladder cancer: Comparison with urine cytology and UroVysion. Urologic Oncology Seminars and Original Investigations. 41(6). 296.e1–296.e8. 10 indexed citations

Hadid, Yarin, et al.. (2022). Explainable machine learning for chronic lymphocytic leukemia treatment prediction using only inexpensive tests. Computers in Biology and Medicine. 145. 105490–105490. 13 indexed citations

Pagani, Luca, Ajai Kumar Pathak, Sulev Kõks, et al.. (2019). The genetic legacy of continental scale admixture in Indian Austroasiatic speakers. Scientific Reports. 9(1). 3818–3818. 28 indexed citations

Weiss, Karin, Nina Ekhilevitch, Lior Cohen, et al.. (2019). Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population. European Journal of Medical Genetics. 63(2). 103643–103643. 6 indexed citations

Sagi‐Dain, Lena, Amihood Singer, Yarin Hadid, et al.. (2018). Non-visualization of fetal gallbladder in microarray era – a retrospective cohort study and review of the literature. The Journal of Maternal-Fetal & Neonatal Medicine. 32(16). 2643–2648. 10 indexed citations

Shalata, Adel, Z. Leibovitz, Hongbing Li, et al.. (2018). Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and blood. Journal of Medical Genetics. 56(5). 340–346. 6 indexed citations

Shlush, Liran I., Doron M. Behar, Guennady Yudkovsky, et al.. (2008). The Druze: A Population Genetic Refugium of the Near East. PLoS ONE. 3(5). e2105–e2105. 41 indexed citations

Behar, Doron M., Ene Metspalu, Toomas Kivisild, et al.. (2008). Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora. PLoS ONE. 3(4). e2062–e2062. 88 indexed citations

10.

Behar, Doron M., Jason Blue-Smith, David F. Soria‐Hernanz, et al.. (2008). A novel 154-bp deletion in the human mitochondrial DNA control region in healthy individuals. Human Mutation. 29(12). 1387–1391. 8 indexed citations

11.

Behar, Doron M., Ene Metspalu, Toomas Kivisild, et al.. (2006). The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event. The American Journal of Human Genetics. 78(3). 487–497. 118 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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