Elon Pras

4.2k total citations
37 papers, 2.4k citations indexed

About

Elon Pras is a scholar working on Molecular Biology, Immunology and Surgery. According to data from OpenAlex, Elon Pras has authored 37 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 18 papers in Immunology and 12 papers in Surgery. Recurrent topics in Elon Pras's work include Inflammasome and immune disorders (27 papers), interferon and immune responses (13 papers) and Cholesterol and Lipid Metabolism (8 papers). Elon Pras is often cited by papers focused on Inflammasome and immune disorders (27 papers), interferon and immune responses (13 papers) and Cholesterol and Lipid Metabolism (8 papers). Elon Pras collaborates with scholars based in Israel, United States and Poland. Elon Pras's co-authors include Mordechai Pras, Avi Livneh, Daniel L. Kastner, Pnina Langevitz, Shai Padeh, Yael Shinar, Hadas Lahat, Etgar Levy‐Nissenbaum, Michael Eldar and Doron Lancet and has published in prestigious journals such as New England Journal of Medicine, Circulation and The American Journal of Human Genetics.

In The Last Decade

Elon Pras

36 papers receiving 2.3k citations

Peers

Elon Pras

IMMUN

CCM

NEPHR

SURGE

Joan Urmson Canada

Olivia Boyer France

Yoshiyuki Ohtomo Japan

Vanita Shah United Kingdom

Betina Macho France

Konstantinos Savvatis Germany

Cécile Braudeau France

Jean Michel Goujon France

Anke Strey Germany

Heike Göbel Germany

Joan Urmson Canada

Elon Pras

277 ×0.1

886 ×1.0

IMMUN

60 ×0.1

CCM

189 ×0.5

NEPHR

565 ×1.5

SURGE

Citations per year, relative to Elon Pras Elon Pras (= 1×) peers Joan Urmson

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

Vardi, Moshe Y., Biana Dubinsky‐Pertzov, Asaf Shemer, et al.. (2024). Behavior of biometric parameters during clinical hours. Journal Français d Ophtalmologie. 47(9). 104296–104296. 1 indexed citations

Lidar, Merav, Yael Shinar, Haike Reznik‐Wolf, et al.. (2018). A high and equal prevalence of the Q703K variant in NLRP3 patients with autoinflammatory symptoms and ethnically matched controls.. PubMed. 35 Suppl 108(6). 82–85. 5 indexed citations

Soriano, Alessandra & Elon Pras. (2014). Familial Mediterranean fever: genetic update.. PubMed. 16(5). 274–6. 6 indexed citations

Berkun, Yackov, Amir Karban, Shai Padeh, et al.. (2012). NOD2/CARD15 Gene Mutations in Patients with Familial Mediterranean Fever. Seminars in Arthritis and Rheumatism. 42(1). 84–88. 18 indexed citations

Marek‐Yagel, Dina, Yackov Berkun, Shai Padeh, et al.. (2010). Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean Fever. Arthritis Care & Research. 62(9). 1294–1298. 13 indexed citations

Padeh, Shai, Avi Livneh, Elon Pras, et al.. (2010). Familial Mediterranean Fever in the First Two Years of Life: A Unique Phenotype of Disease in Evolution. The Journal of Pediatrics. 156(6). 985–989. 44 indexed citations

Marek‐Yagel, Dina, Yackov Berkun, Shai Padeh, et al.. (2009). Clinical disease among patients heterozygous for familial mediterranean fever. Arthritis & Rheumatism. 60(6). 1862–1866. 152 indexed citations

Ben‐Zeev, Bruria, Etgar Levy‐Nissenbaum, Hadas Lahat, et al.. (2002). Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews. Human Genetics. 111(2). 214–218. 27 indexed citations

Levy‐Nissenbaum, Etgar, Michael Eldar, Qing Wang, et al.. (2001). Genetic Analysis of Brugada Syndrome in Israel: Two Novel Mutations and Possible Genetic Heterogeneity. Genetic Testing. 5(4). 331–334. 13 indexed citations

10.

Pras, Elon, I Aksentijevich, Yael Shinar, Daniel L. Kastner, & Anat Achiron. (2001). Lack of Evidence for an Association between Two Genetic Polymorphisms in the Tumor Necrosis Factor Receptor 1 Gene and Multiple Sclerosis in Ashkenazi Jews. European Neurology. 46(3). 153–155. 1 indexed citations

11.

Lahat, Hadas, Elon Pras, Nili Avidan, et al.. (2001). A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel. The American Journal of Human Genetics. 69(6). 1378–1384. 461 indexed citations

12.

Pras, Elon, et al.. (1999). Refined Mapping of the CSNU3 Gene to a 1.8-Mb Region on Chromosome 19q13.1 Using Historical Recombinants in Libyan Jewish Cystinuria Patients. Genomics. 60(2). 248–250. 9 indexed citations

13.

Torosyan, Yelizaveta, Jonathan Samuels, Michael Centola, et al.. (1999). Mutation and Haplotype Studies of Familial Mediterranean Fever Reveal New Ancestral Relationships and Evidence for a High Carrier Frequency with Reduced Penetrance in the Ashkenazi Jewish Population. The American Journal of Human Genetics. 64(4). 949–962. 219 indexed citations

14.

Livneh, Avi, Pnina Langevitz, Yael Shinar, et al.. (1999). MEFV mutation analysis in patients suffering from amyloidosis of familial Mediterranean fever. Amyloid. 6(1). 1–6. 158 indexed citations

15.

Padeh, Shai, Naphtali Brezniak, Debora Zemer, et al.. (1999). Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome: Clinical characteristics and outcome. The Journal of Pediatrics. 135(1). 98–101. 199 indexed citations

16.

Shinar, Yael, Elon Pras, Itzhak Siev‐Ner, et al.. (1998). Analysis of Allelic Association Between D6S461 Marker and Multiple Sclerosis in Ashkenazi and Iraqi Jewish Patients. Journal of Molecular Neuroscience. 11(3). 265–270. 7 indexed citations

17.

Pras, Eran, et al.. (1998). Clinical differences between North African and Iraqi Jews with familial Mediterranean fever. American Journal of Medical Genetics. 75(2). 216–219. 213 indexed citations

18.

Aksentijevich, Ivona, Luis Gruberg, Elon Pras, et al.. (1993). Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?. Human Genetics. 91(6). 527–534. 6 indexed citations

19.

Pras, Elon, Ivona Aksentijevich, Luis Gruberg, et al.. (1992). Mapping of a Gene Causing Familial Mediterranean Fever to the Short Arm of Chromosome 16. New England Journal of Medicine. 326(23). 1509–1513. 193 indexed citations

20.

Gruberg, Luis, Ivona Aksentijevich, Elon Pras, Daniel L. Kastner, & Mordechai Pras. (1992). Mapping of the Familial Mediterranean Fever Gene to Chromosome 16. American Journal of Reproductive Immunology. 28(3-4). 241–242. 7 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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