Elon Pras
Impact in
- Biochemistry top 2%
- Amino Acid Enzymes and Metabolism
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Papers in
-
- Connexins and lens biology 6
- Genetics 21
- Genetics and Neurodevelopmental Disorders 6
- BRCA gene mutations in cancer 4
- Co-authors
- Eran Pras (12 shared papers)Moshe Frydman (15 shared papers)Hadas Lahat (9 shared papers)Etgar Levy‐Nissenbaum (5 shared papers)Haike Reznik‐Wolf (21 shared papers)Boleslaw Goldman (5 shared papers)Nadir Arber (6 shared papers)Ehud I. Assia (3 shared papers)
- Journals
- The American Journal of Human Genetics (5 papers)Journal of Medical Genetics (3 papers)European Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)Human Genetics (2 papers)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Elon Pras
93 papers receiving 2.8k citations
Peers
Comparison fields: 5 of 123
- Biochemistry 271
- Clinical Biochemistry 202
- Urology 172
- Ophthalmology 216
- Cardiology and Cardiovascular Medicine 427
Countries citing papers authored by Elon Pras
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
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-authors
The 25 scholars most cited alongside Elon Pras, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 97 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 189 | |
| 2 | 1994 | 169 | |
| 3 | A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family. | 2000 | 146 |
| 4 | 2011 | 129 | |
| 5 | 2007 | 114 | |
| 6 | 2012 | 111 | |
| 7 | 2003 | 108 | |
| 8 | 2008 | 95 | |
| 9 | 2002 | 92 | |
| 10 | 2013 | 82 | |
| 11 | 1994 | 78 | |
| 12 | 1992 | 73 | |
| 13 | 2004 | 69 | |
| 14 | Mutations in the SLC3A1 transporter gene in cystinuria. | 1995 | 67 |
| 15 | 2001 | 62 | |
| 16 | Cone-rod dystrophy and a frameshift mutation in the PROM1 gene. | 2009 | 59 |
| 17 | 1991 | 59 | |
| 18 | 2006 | 57 | |
| 19 | Molecular analysis of cystinuria in Libyan Jews: exclusion of the SLC3A1 gene and mapping of a new locus on 19q. | 1997 | 54 |
| 20 | 2010 | 47 |
About Elon Pras
Elon Pras is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cardiology and Cardiovascular Medicine and Rheumatology, having authored 97 papers that have together received 2.9k indexed citations. Recurring topics across this work include Amino Acid Enzymes and Metabolism (9 papers), Folate and B Vitamins Research (8 papers), Connexins and lens biology (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Cardiac electrophysiology and arrhythmias (5 papers), Kidney Stones and Urolithiasis Treatments (5 papers) and BRCA gene mutations in cancer (4 papers). The work is most often cited by research in Biochemistry (271 citations), Clinical Biochemistry (202 citations), Urology (172 citations), Ophthalmology (216 citations) and Cardiology and Cardiovascular Medicine (427 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 The American Journal of Human Genetics, Journal of Medical Genetics, European Journal of Medical Genetics, Prenatal Diagnosis and Human 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.