M Shohat
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 5%
- BRCA gene mutations in cancer
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 11
- Connective tissue disorders research 5
- BRCA gene mutations in cancer 2
- Genomic variations and chromosomal abnormalities 2
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- Inflammasome and immune disorders 2
- Co-authors
- David L. Rimoin (4 shared papers)Helen E. Gruber (3 shared papers)Lutfi Jaber (4 shared papers)Uziel Beller (1 shared paper)BL Weber (1 shared paper)Bella Kaufman (1 shared paper)Shlomit Eisenberg (1 shared paper)Raphael Catane (1 shared paper)
- Journals
- Clinical Genetics (3 papers)Archives of Disease in Childhood (3 papers)Journal of Medical Genetics (2 papers)European Journal of Pediatrics (1 paper)The Journal of Pediatrics (1 paper)
- Partner nations
- IsraelUnited StatesNetherlands
In The Last Decade
M Shohat
27 papers receiving 869 citations
Peers
Comparison fields: 5 of 85
- Sensory Systems 61
- Genetics 343
- Rheumatology 97
- Pediatrics, Perinatology and Child Health 118
- Reproductive Medicine 50
Countries citing papers authored by M Shohat
This map shows the geographic impact of M Shohat'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 M Shohat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Shohat more than expected).
Fields of papers citing papers by M Shohat
This network shows the impact of papers produced by M Shohat. 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 M Shohat. The network helps show where M Shohat may publish in the future.
Co-authors
The 25 scholars most cited alongside M Shohat, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families. | 1997 | 246 |
| 2 | 1992 | 85 | |
| 3 | 1998 | 51 | |
| 4 | 1991 | 51 | |
| 5 | 1985 | 48 | |
| 6 | 1989 | 47 | |
| 7 | 1987 | 47 | |
| 8 | 2017 | 46 | |
| 9 | 1996 | 41 | |
| 10 | 2008 | 40 | |
| 11 | 1997 | 36 | |
| 12 | 1988 | 27 | |
| 13 | 2006 | 25 | |
| 14 | 1990 | 22 | |
| 15 | Autosomal dominant transmission of isolated congenital vertical talus. | 1989 | 22 |
| 16 | 1994 | 13 | |
| 17 | 1993 | 10 | |
| 18 | 2004 | 9 | |
| 19 | 2017 | 8 | |
| 20 | 1996 | 8 |
About M Shohat
M Shohat is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 29 papers that have together received 913 indexed citations. Recurring topics across this work include Connective tissue disorders research (5 papers), Prenatal Screening and Diagnostics (4 papers), Metabolism and Genetic Disorders (2 papers), Child Nutrition and Water Access (2 papers), BRCA gene mutations in cancer (2 papers), Cholesterol and Lipid Metabolism (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Inflammasome and immune disorders (2 papers). The work is most often cited by research in Sensory Systems (61 citations), Genetics (343 citations), Rheumatology (97 citations), Pediatrics, Perinatology and Child Health (118 citations) and Reproductive Medicine (50 citations). M Shohat has collaborated with scholars based in Israel, United States and Netherlands. Frequent co-authors include David L. Rimoin, Helen E. Gruber, Lutfi Jaber, Uziel Beller, BL Weber, Bella Kaufman, Shlomit Eisenberg, Raphael Catane, Gila Hornreich and D. Halle. Their work appears in journals such as Clinical Genetics, Archives of Disease in Childhood, Journal of Medical Genetics, European Journal of Pediatrics and The Journal of Pediatrics.
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.