M. Sagi
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Reproductive Medicine top 10%
Papers in
-
- DNA Repair Mechanisms 1
- Genetics 5
- BRCA gene mutations in cancer 2
- Connective tissue disorders research 2
- Co-authors
- Joël Zlotogora (5 shared papers)Tara Cohen (2 shared papers)Dvorah Abeliovich (4 shared papers)N. Weinberg (3 shared papers)Tamar Peretz (3 shared papers)Israela Lerer (2 shared papers)G Amir (1 shared paper)Norman Heching (1 shared paper)
- Journals
- Clinical Genetics (1 paper)Neurology (1 paper)Prenatal Diagnosis (1 paper)Clinical and Experimental Dermatology (1 paper)Cancer Research (1 paper)
- Partner nations
- IsraelKazakhstanUnited States
In The Last Decade
M. Sagi
17 papers receiving 688 citations
Peers
Comparison fields: 5 of 55
- Genetics 434
- Reproductive Medicine 64
- Pediatrics, Perinatology and Child Health 108
- Cancer Research 59
- Pathology and Forensic Medicine 68
Countries citing papers authored by M. Sagi
This map shows the geographic impact of M. Sagi'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. Sagi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Sagi more than expected).
Fields of papers citing papers by M. Sagi
This network shows the impact of papers produced by M. Sagi. 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. Sagi. The network helps show where M. Sagi may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Sagi, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women. | 1997 | 295 |
| 2 | The blepharophimosis, ptosis, and epicanthus inversus syndrome: delineation of two types. | 1983 | 186 |
| 3 | 2009 | 46 | |
| 4 | Further localization of X-linked hydrocephalus in the chromosomal region Xq28. | 1992 | 41 |
| 5 | 1992 | 39 | |
| 6 | 1989 | 24 | |
| 7 | 1995 | 22 | |
| 8 | 1989 | 15 | |
| 9 | 1992 | 12 | |
| 10 | 2008 | 9 | |
| 11 | 2013 | 9 | |
| 12 | 2024 | 3 | |
| 13 | 2022 | 2 | |
| 14 | 2006 | 2 | |
| 15 | 2021 | 2 | |
| 16 | 2013 | 1 | |
| 17 | 2021 | 1 | |
| 18 | 2023 | 1 | |
| 19 | 2008 | 0 | |
| 20 | 2008 | 0 |
About M. Sagi
M. Sagi is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Organic Chemistry, having authored 21 papers that have together received 710 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (2 papers), Connective tissue disorders research (2 papers), Lysosomal Storage Disorders Research (2 papers), Prenatal Screening and Diagnostics (2 papers), DNA Repair Mechanisms (1 paper), Trypanosoma species research and implications (1 paper), Biomedical Research and Pathophysiology (1 paper) and Child Abuse and Related Trauma (1 paper). The work is most often cited by research in Genetics (434 citations), Reproductive Medicine (64 citations), Pediatrics, Perinatology and Child Health (108 citations), Cancer Research (59 citations) and Pathology and Forensic Medicine (68 citations). M. Sagi has collaborated with scholars based in Israel, Kazakhstan and United States. Frequent co-authors include Joël Zlotogora, Tara Cohen, Dvorah Abeliovich, N. Weinberg, Tamar Peretz, Israela Lerer, G Amir, Norman Heching, Luna Kaduri and S. Merin. Their work appears in journals such as Clinical Genetics, Neurology, Prenatal Diagnosis, Clinical and Experimental Dermatology and Cancer Research.
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.