Elon Pras

6.2k total citations
96 papers, 2.9k citations indexed

About

Elon Pras is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elon Pras has authored 96 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 30 papers in Genetics and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elon Pras's work include Prenatal Screening and Diagnostics (10 papers), Amino Acid Enzymes and Metabolism (10 papers) and Folate and B Vitamins Research (8 papers). Elon Pras is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Amino Acid Enzymes and Metabolism (10 papers) and Folate and B Vitamins Research (8 papers). Elon Pras collaborates with scholars based in Israel, United States and Germany. Elon Pras's 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 and has published in prestigious journals such as New England Journal of Medicine, Circulation and Nature Genetics.

In The Last Decade

Elon Pras

93 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elon Pras Israel 29 1.2k 557 451 331 324 96 2.9k
Bruce Bennetts Australia 31 1.3k 1.1× 1.4k 2.5× 140 0.3× 139 0.4× 98 0.3× 101 3.2k
Allan M. Lund Denmark 32 1.1k 0.9× 876 1.6× 77 0.2× 68 0.2× 674 2.1× 171 3.3k
Reijo Norio Finland 36 1.1k 0.9× 1.8k 3.2× 154 0.3× 53 0.2× 137 0.4× 69 3.6k
Boleslaw Goldman Israel 22 746 0.6× 575 1.0× 179 0.4× 73 0.2× 122 0.4× 74 1.7k
Swapan K. Nath United States 32 838 0.7× 960 1.7× 100 0.2× 96 0.3× 278 0.9× 103 3.9k
Masafumi Ito Japan 31 1.2k 1.0× 594 1.1× 145 0.3× 36 0.1× 247 0.8× 175 3.9k
Paige Kaplan United States 42 1.6k 1.3× 841 1.5× 194 0.4× 28 0.1× 1.5k 4.6× 135 5.7k
Yoshinori Okada Japan 33 889 0.7× 229 0.4× 242 0.5× 78 0.2× 509 1.6× 315 4.0k
Tommy Martinsson Sweden 49 3.3k 2.7× 1.0k 1.9× 287 0.6× 54 0.2× 629 1.9× 202 6.3k
James H. Garvin United States 32 722 0.6× 95 0.2× 121 0.3× 85 0.3× 364 1.1× 127 3.2k

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

20 of 20 papers shown
1.
Yaron, Yuval, Michal Berkenstadt, Doron M. Behar, et al.. (2025). Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening. npj Digital Medicine. 8(1). 183–183.
2.
Lesman‐Segev, Orit H., Nofar Mor, Ortal Barel, et al.. (2023). Adult-onset Alexander disease among patients of Jewish Syrian descent. Neurogenetics. 24(4). 303–310. 3 indexed citations
3.
Dori, Amir, Michael Arad, Yishay Wasserstrum, et al.. (2023). Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features. Annals of Clinical and Translational Neurology. 10(4). 553–567. 3 indexed citations
4.
Eliyahu, Aviva, Ortal Barel, Lior Greenbaum, et al.. (2022). Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay. Frontiers in Pediatrics. 10. 844845–844845. 10 indexed citations
5.
Achiron, R., et al.. (2016). Very Early In-Utero Diagnosis of Walker-Warburg Phenotype: The Cutting Edge of Technology. SHILAP Revista de lepidopterología. 2(2). E54–E57. 7 indexed citations
6.
Pras, Eran, et al.. (2015). Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration. Journal of Medical Genetics. 52(7). 484–492. 20 indexed citations
7.
Laitman, Yael, Michal Berkenstadt, Daphna Weissglas‐Volkov, et al.. (2015). The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers. Cancer Genetics. 209(3). 70–74. 24 indexed citations
8.
Grinshpun‐Cohen, Julia, et al.. (2014). Factors that affect the decision to undergo amniocentesis in women with normal Down syndrome screening results: it is all about the age. Health Expectations. 18(6). 2306–2317. 17 indexed citations
9.
Peled, Yael, Michael Gramlich, Guy Yoskovitz, et al.. (2013). Titin Mutation in Familial Restrictive Cardiomyopathy. International Journal of Cardiology. 171(1). 24–30. 80 indexed citations
10.
Chen, Jianjun, Zhiwei Ma, Xiaodong Jiao, et al.. (2011). Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts. The American Journal of Human Genetics. 88(6). 827–838. 127 indexed citations
11.
Fischetti, Lucia, George Dedoussis, Helen Michelakakis, et al.. (2008). Twenty-Four Novel Mutations Identified in a Cohort of 85 Patients by Direct Sequencing of the SLC3A1 and SLC7A9 Cystinuria Genes. Genetic Testing. 12(3). 351–355. 11 indexed citations
12.
Frydman, Moshe, et al.. (2008). Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome. The American Journal of Human Genetics. 82(5). 1217–1222. 95 indexed citations
13.
Shalev, Stavit, Eliezer Shalev, Elon Pras, et al.. (2006). Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome. Prenatal Diagnosis. 26(9). 782–784. 26 indexed citations
14.
Lahat, Hadas, Elon Pras, & Michael Eldar. (2004). A missense mutation in CASQ2 is associated with autosomal recessive catecholamine‐induced polymorphic ventricular tachycardia in Bedouin families from Israel. Annals of Medicine. 36(sup1). 87–91. 27 indexed citations
15.
Levy‐Nissenbaum, Etgar, Regina C. Betz, Moshe Frydman, et al.. (2003). Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin. Nature Genetics. 34(2). 151–153. 108 indexed citations
16.
Kreiss, Yitshak, et al.. (2000). The Founder Mutations in the BRCA1 , BRCA2 , and ATM Genes in Moroccan Jewish Women with Breast Cancer. Genetic Testing. 4(4). 403–407. 10 indexed citations
17.
Toren, Amos, Ninette Amariglio, Galit Rozenfeld-Granot, et al.. (1999). Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13. The American Journal of Human Genetics. 65(6). 1711–1717. 23 indexed citations
18.
Pras, Elon, et al.. (1998). A splicing mutation (891+4A→G) in SLC3A1 leads to exon 4 skipping and causes cystinuria in a Moslem Arab family. Human Mutation. 11(S1). S28–S30. 10 indexed citations
19.
Pras, Elon, H. Ralph Schumacher, Daniel L. Kastner, & Ronald L. Wilder. (1996). Lack of evidence of mycobacteria in synovial tissue from patients with rheumatoid arthritis. Arthritis & Rheumatism. 39(12). 2080–2081. 7 indexed citations
20.
Pras, Elon, Nadir Arber, Ivona Aksentijevich, et al.. (1994). Localization of a gene causing cystinuria to chromosome 2p. Nature Genetics. 6(4). 415–419. 77 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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