Elon Pras

6.2k citations

96 papers · 2.9k indexed · h-index 29

Molecular Biology top 10%
Genetics top 5%
Cardiology and Cardiovascular Medicine top 5%
Ophthalmology top 2%
Epidemiology top 10%

Co-authors: Eran Pras Moshe Frydman Hadas Lahat Etgar Levy‐Nissenbaum Haike Reznik‐Wolf Boleslaw Goldman Nadir Arber Ehud I. Assia
Topics: Prenatal Screening and Diagnostics (10 papers)Amino Acid Enzymes and Metabolism (10 papers)Folate and B Vitamins Research (8 papers)
Cited by: Biochemistry Ophthalmology Clinical Biochemistry
Journals: New England Journal of Medicine Circulation Nature Genetics
Partner nations: Israel United States Germany

In The Last Decade

Elon Pras

93 papers receiving 2.8k citations

Peers

Countries citing papers authored by Elon Pras

Since Specialization

Citations

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

Fields of papers citing papers by Elon Pras

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elon Pras

This figure shows the co-authorship network connecting the top 25 collaborators of Elon Pras. A scholar is included among the top collaborators of Elon Pras 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 Elon Pras. Elon Pras 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	Adult-onset Alexander disease among patients of Jewish Syrian descent 2023 ·Neurogenetics ·(unknown),(unknown),(unknown),(unknown),Orit H. Lesman‐Segev,Nofar Mor,Ortal Barel,Dan Dominissini,(unknown),Elon Pras,Lior Greenbaum,Sharon Hassin‐Baer	3
3	Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features 2023 ·Annals of Clinical and Translational Neurology ·Amir Dori,Michael Arad,Yishay Wasserstrum,Arthur Pollak,(unknown),Merav Ben‐David,(unknown),(unknown),Efrat Shavit‐Stein,Liran Domachevsky,Rafael Kuperstein,Dan Dominissini,(unknown),Menachem Sadeh,Elon Pras,Lior Greenbaum	3
4	Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay 2022 ·Frontiers in Pediatrics ·Aviva Eliyahu,Ortal Barel,Lior Greenbaum,(unknown),(unknown),Annick Raas‐Rothschild,Amihood Singer,Ifat Bar-Joseph,Vered Kunik,(unknown),Orna Staretz‐Chacham,Naomi Pode‐Shakked,Lily Bazak,Noa Ruhrman‐Shahar,Elon Pras,Moshe Frydman,Mordechai Shohat,Ben Pode‐Shakked	10
5	Very Early In-Utero Diagnosis of Walker-Warburg Phenotype: The Cutting Edge of Technology 2016 ·SHILAP Revista de lepidopterología ·R. Achiron,Eldad Katorza,Haike Reznik‐Wolf,Elon Pras,Debora Kidron,(unknown)	7
6	Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration 2015 ·Journal of Medical Genetics ·Eran Pras,(unknown),(unknown),(unknown),(unknown),Gershon Celniker,Ofer Isakov,Noam Shomron,Elon Pras	20
7	The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers 2015 ·Cancer Genetics ·Yael Laitman,(unknown),Michal Berkenstadt,(unknown),Daphna Weissglas‐Volkov,(unknown),Ifat Sarouk,Elon Pras,Eitan Friedman	24
8	Factors that affect the decision to undergo amniocentesis in women with normal Down syndrome screening results: it is all about the age 2014 ·Health Expectations ·Julia Grinshpun‐Cohen,Talya Miron‐Shatz,(unknown),Elon Pras	17
9	Titin Mutation in Familial Restrictive Cardiomyopathy 2013 ·International Journal of Cardiology ·Yael Peled,Michael Gramlich,Guy Yoskovitz,Micha S. Feinberg,Arnon Afek,Sylvie Polak‐Charcon,Elon Pras,Ben‐Ami Sela,Eli Konen,Omer Weissbrod,Dan Geiger,(unknown),Ludwig Thierfelder,Dov Freimark,Brenda Gerull,Michael Arad	80
10	Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts 2011 ·The American Journal of Human Genetics ·Jianjun Chen,Zhiwei Ma,Xiaodong Jiao,Robert N. Fariss,(unknown),Marc Kantorow,Eran Pras,Moshe Frydman,Elon Pras,Sheikh Riazuddin,J. Fielding Hejtmancik	127
11	Twenty-Four Novel Mutations Identified in a Cohort of 85 Patients by Direct Sequencing of the SLC3A1 and SLC7A9 Cystinuria Genes 2008 ·Genetic Testing ·(unknown),(unknown),Lucia Fischetti,George Dedoussis,(unknown),Helen Michelakakis,Leopoldo Zelante,Elon Pras,Luigi Bisceglia	11
12	Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome 2008 ·The American Journal of Human Genetics ·(unknown),Moshe Frydman,(unknown),Eran Pras,Uri Nir,Haike Reznik‐Wolf,Elon Pras	95
13	Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome 2006 ·Prenatal Diagnosis ·Stavit Shalev,Eliezer Shalev,Elon Pras,(unknown),Ephraim Gazit,Yuval Yaron,Ron Loewenthal	26
14	A missense mutation in CASQ2 is associated with autosomal recessive catecholamine‐induced polymorphic ventricular tachycardia in Bedouin families from Israel 2004 ·Annals of Medicine ·Hadas Lahat,Elon Pras,Michael Eldar	27
15	Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin 2003 ·Nature Genetics ·Etgar Levy‐Nissenbaum,Regina C. Betz,Moshe Frydman,Michel Simon,Hadas Lahat,(unknown),Boleslaw Goldman,Anette Bygum,(unknown),Axel M. Hillmer,Nathalie Jonca,Jaime Toribio,Roland Kruse,Georg Dewald,Sven Cichon,Christian Kubisch,Marina Guerrin,Guy Serre,Markus M. Nöthen,Elon Pras	108
16	The Founder Mutations in the BRCA1 , BRCA2 , and ATM Genes in Moroccan Jewish Women with Breast Cancer 2000 ·Genetic Testing ·Yitshak Kreiss,(unknown),Ruth Gershoni Baruch,Ephrat Levy‐Lahad,Elon Pras,Eitan Friedman	10
17	Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13 1999 ·The American Journal of Human Genetics ·Amos Toren,Ninette Amariglio,Galit Rozenfeld-Granot,Anthony Simon,F. Brok‐Simoni,Elon Pras,Gideon Rechavi	23
18	A splicing mutation (891+4A→G) in SLC3A1 leads to exon 4 skipping and causes cystinuria in a Moslem Arab family 1998 ·Human Mutation ·Elon Pras,(unknown),(unknown),Ivona Aksentijevich,Giora Katz,Daniel L. Kastner	10
19	Lack of evidence of mycobacteria in synovial tissue from patients with rheumatoid arthritis 1996 ·Arthritis & Rheumatism ·Elon Pras,H. Ralph Schumacher,Daniel L. Kastner,Ronald L. Wilder	7
20	Localization of a gene causing cystinuria to chromosome 2p 1994 ·Nature Genetics ·Elon Pras,Nadir Arber,Ivona Aksentijevich,Giora Katz,Jonathan Schapiro,(unknown),Luis Gruberg,(unknown),Uri Liberman,Jean Weissenbach,Mordechai Pras,Daniel L. Kastner	77

About Elon Pras

Elon Pras is a scholar working on Biochemistry, Genetics and Urology, having authored 96 papers that have together received 2.9k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Amino Acid Enzymes and Metabolism (10 papers) and Folate and B Vitamins Research (8 papers). The work is most often cited by research in Biochemistry (303 citations), Ophthalmology (331 citations) and Clinical Biochemistry (239 citations). Elon Pras has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Eran Pras, Moshe Frydman, Hadas Lahat, Etgar Levy‐Nissenbaum, Haike Reznik‐Wolf, Boleslaw Goldman, Nadir Arber, Ehud I. Assia, Yechezkel Sidi and Michael Eldar. Their work appears in journals such as New England Journal of Medicine, Circulation and Nature Genetics.

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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