Doron M. Behar

8.3k total citations
62 papers, 3.2k citations indexed

About

Doron M. Behar is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Doron M. Behar has authored 62 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 23 papers in Molecular Biology and 7 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Doron M. Behar's work include Forensic and Genetic Research (22 papers), Genetic diversity and population structure (8 papers) and Forensic Anthropology and Bioarchaeology Studies (6 papers). Doron M. Behar is often cited by papers focused on Forensic and Genetic Research (22 papers), Genetic diversity and population structure (8 papers) and Forensic Anthropology and Bioarchaeology Studies (6 papers). Doron M. Behar collaborates with scholars based in Israel, United States and United Kingdom. Doron M. Behar's co-authors include Richard Villems, Antonio Torroni, Saharon Rosset, Lluís Quintana‐Murci, Toomas Kivisild, Shay Tzur, Karl Skorecki, Mait Metspalu, Ene Metspalu and Chris Tyler‐Smith and has published in prestigious journals such as Science, The Lancet and Nature Communications.

In The Last Decade

Doron M. Behar

61 papers receiving 3.1k citations

Peers

Countries citing papers authored by Doron M. Behar

Since Specialization

Citations

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

Fields of papers citing papers by Doron M. Behar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Doron M. Behar. 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 Doron M. Behar. The network helps show where Doron M. Behar may publish in the future.

Co-authorship network of co-authors of Doron M. Behar

This figure shows the co-authorship network connecting the top 25 collaborators of Doron M. Behar. A scholar is included among the top collaborators of Doron M. Behar 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 Doron M. Behar. Doron M. Behar 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

#	Work	Indexed citations
1	Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening 2025 ·npj Digital Medicine ·Yuval Yaron, (unknown), Michal Berkenstadt, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Doron M. Behar, Elon Pras, Adi Reches, Alina Kurolap, Hagit Baris Feldman	0
2	Human Y chromosome haplogroup L1-M22 traces Neolithic expansion in West Asia and supports the Elamite and Dravidian connection 2024 ·iScience ·Ajai Kumar Pathak, (unknown), (unknown), (unknown), Doron M. Behar, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Hovhannes Sahakyan	2
3	Overcoming Challenges in Reproductive Health Applications by Deploying More Sensitive and Accurate Molecular Technologies 2019 ·Charlotte Brasch‐Andersen, Doron M. Behar, (unknown), Carmen Rubio	2
4	Preconception carrier screening yield: effect of variants of unknown significance in partners of carriers with clinically significant variants 2019 ·Genetics in Medicine ·Hila Fridman, Doron M. Behar, Shai Carmi, Ephrat Levy‐Lahad	23
5	The genetic legacy of continental scale admixture in Indian Austroasiatic speakers 2019 ·Scientific Reports ·(unknown), Luca Pagani, Ajai Kumar Pathak, Sulev Kõks, (unknown), Xuan Dung Ho, Gazi Nurun Nahar Sultana, (unknown), Md Asaduzzaman, Doron M. Behar, Yarin Hadid, Richard Villems, Gyaneshwer Chaubey, Toomas Kivisild, Mait Metspalu	28
6	Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing 2016 ·European Journal of Human Genetics ·Eyal Reinstein, Shay Tzur, Rony Cohen, Concetta Bormans, Doron M. Behar	21
7	Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C 2016 ·European Journal of Human Genetics ·Eyal Reinstein, Ana Gutiérrez‐Fernández, Shay Tzur, Concetta Bormans, Shai Marcu, Einav Tayeb-Fligelman, Chana Vinkler, Annick Raas‐Rothschild, (unknown), Meytal Landau, Mordechai Shohat, Xosé S. Puente, Doron M. Behar, Carlos López-Otı́n	33
8	Neolithic human mitochondrial haplogroup H genomes and the genetic origins of Europeans 2013 ·Wolfgang Haak, Paul Brotherton, Jennifer E.L. Templeton, Guido Brandt, Julien Soubrier, Christina Adler, Stephen M. Richards, (unknown), Robert Ganslmeier, Susanne Friederich, Veit Dresely, Mannis van Oven, Jonas Korlach, Simon Y. W. Ho, Lluís Quintana‐Murci, Doron M. Behar, Harald Meller, Kurt W. Alt, Alan Cooper	2
9	The Many Faces of Sensorineural Hearing Loss: One Founder and Two Novel Mutations Affecting One Family of Mixed Jewish Ancestry 2013 ·Genetic Testing and Molecular Biomarkers ·Doron M. Behar, Bella Davidov, Zippora Brownstein, Tamar Ben‐Yosef, Karen B. Avraham, Mordechai Shohat	7
10	Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency 2013 ·Journal of Lipid Research ·Doron M. Behar, Lina Basel‐Vanagaite, Fabian Glaser, Marielle Kaplan, Shay Tzur, Nurit Magal, Tal Eidlitz‐Markus, Y. Cohen, Galit Sarig, Concetta Bormans, Mordechai Shohat, Avraham Zeharia	24
11	Genetic Continuity in the Franco-Cantabrian Region: New Clues from Autochthonous Mitogenomes 2012 ·PLoS ONE ·Alberto Gómez‐Carballa, Anna Olivieri, Doron M. Behar, Alessandro Achilli, Antonio Torroni, Antonio Salas	21
12	The population genetics of chronic kidney disease: insights from the MYH9–APOL1 locus 2011 ·Nature Reviews Nephrology ·Saharon Rosset, Shay Tzur, Doron M. Behar, Walter G. Wasser, Karl Skorecki	56
13	Strong Maternal Khoisan Contribution to the South African Coloured Population: A Case of Gender-Biased Admixture 2010 ·The American Journal of Human Genetics ·Lluís Quintana‐Murci, Christine Harmant, Hélène Quach, Oleg Balanovsky, Valery Zaporozhchenko, (unknown), Paul D. van Helden, Eileen G. Hoal, Doron M. Behar	9
14	Four USH2A Founder Mutations Underlie the Majority of Usher Syndrome Type 2 Cases among Non-Ashkenazi Jews 2008 ·Genetic Testing ·(unknown), (unknown), (unknown), Doron M. Behar, Mordechai Shohat, Eyal Banin, Stavit A. Shalev, Reuven Sharony, Dror Sharon, Tamar Ben‐Yosef	21
15	Ashkenazi Jewish Centenarians Do Not Demonstrate Enrichment in Mitochondrial Haplogroup J 2008 ·PLoS ONE ·Liran I. Shlush, Gil Atzmon, Roni Weisshof, Doron M. Behar, (unknown), Nir Barzilai, Karl Skorecki	15
16	The Druze: A Population Genetic Refugium of the Near East 2008 ·PLoS ONE ·Liran I. Shlush, Doron M. Behar, Guennady Yudkovsky, Alan R. Templeton, Yarin Hadid, Fuad Basis, Michael F. Hammer, Shalev Itzkovitz, Karl Skorecki	41
17	Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora 2008 ·PLoS ONE ·Doron M. Behar, Ene Metspalu, Toomas Kivisild, Saharon Rosset, Shay Tzur, Yarin Hadid, Guennady Yudkovsky, Dror Rosengarten, Luı́sa Pereira, António Amorim, Ildus Kutuev, David Gurwitz, Batsheva Bonné‐Tamir, Richard Villems, Karl Skorecki	88
18	Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles 2006 ·Human Molecular Genetics ·Paul Verdu, Luis B. Barreiro, Étienne Patin, Antoine Gessain, Olivier Cassar, Judith R. Kidd, Kenneth K. Kídd, Doron M. Behar, Alain Froment, Évelyne Heyer, Lucas Sica, Jean‐Laurent Casanova, Laurent Abel, Lluís Quintana‐Murci	96
19	Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis 2004 ·Nature Genetics ·Orit Topaz, Daniel L. Shurman, Richard N. Bergman, Margarita Indelman, Paulina Ratajczak, (unknown), Ziad Khamaysi, Doron M. Behar, (unknown), (unknown), Israel Zelikovic, S. Raimer, (unknown), Gabriele Richard, Eli Sprecher	424
20	Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor 2004 ·The American Journal of Human Genetics ·Lluís Quintana‐Murci, Raphaëlle Chaix, R. Spencer Wells, Doron M. Behar, Hamid Sayar, Rosaria Scozzari, Chiara Rengo, Nadia Al-Zahery, Ornella Semino, A. Silvana Santachiara‐Benerecetti, Alfredo Coppa, Qasim Ayub, Aisha Mohyuddin, Chris Tyler‐Smith, S. Qasim Mehdi, Antonio Torroni, Ken McElreavey	317

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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