Sat Dev Batish
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
Papers in
-
- DNA Repair Mechanisms 20
- Mitochondrial Function and Pathology 5
- Genetics 16
- BRCA gene mutations in cancer 8
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Arleen D. Auerbach (21 shared papers)Helmut Hanenberg (13 shared papers)Philip F. Giampietro (6 shared papers)Jaya M. Satagopan (3 shared papers)Bhuvanesh Singh (2 shared papers)David I. Kutler (2 shared papers)Orna Levran (11 shared papers)James R. Lupski (5 shared papers)
- Journals
- Human Mutation (5 papers)Nature Genetics (4 papers)Blood (3 papers)Proceedings of the National Academy of Sciences (2 papers)Neurogenetics (2 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Sat Dev Batish
49 papers receiving 3.5k citations
Sat Dev Batish's Hit Papers
Peers
Comparison fields: 5 of 94
- Genetics 1.2k
- Cancer Research 563
- Molecular Biology 2.3k
- Hematology 269
- Otorhinolaryngology 75
Countries citing papers authored by Sat Dev Batish
This map shows the geographic impact of Sat Dev Batish'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 Sat Dev Batish with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sat Dev Batish more than expected).
Fields of papers citing papers by Sat Dev Batish
This network shows the impact of papers produced by Sat Dev Batish. 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 Sat Dev Batish. The network helps show where Sat Dev Batish may publish in the future.
Co-authors
The 25 scholars most cited alongside Sat Dev Batish, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A 20-year perspective on the International Fanconi Anemia Registry (IFAR) Hit paper breakdown → | 2003 | 533 |
| 2 | 2006 | 456 | |
| 3 | 2009 | 337 | |
| 4 | 2005 | 283 | |
| 5 | 2003 | 269 | |
| 6 | 2001 | 159 | |
| 7 | 2014 | 135 | |
| 8 | 2003 | 123 | |
| 9 | 2010 | 98 | |
| 10 | 1997 | 97 | |
| 11 | 2011 | 97 | |
| 12 | 1997 | 95 | |
| 13 | 2001 | 81 | |
| 14 | 2007 | 78 | |
| 15 | 2002 | 71 | |
| 16 | 2005 | 67 | |
| 17 | 2005 | 63 | |
| 18 | 2007 | 61 | |
| 19 | 2015 | 48 | |
| 20 | A neglected lesbian health concern: cervical neoplasia. | 1996 | 46 |
About Sat Dev Batish
Sat Dev Batish is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Cancer Research, having authored 50 papers that have together received 3.6k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (20 papers), Genetic Neurodegenerative Diseases (9 papers), BRCA gene mutations in cancer (8 papers), Hereditary Neurological Disorders (7 papers), Genomic variations and chromosomal abnormalities (5 papers), Carcinogens and Genotoxicity Assessment (5 papers), Mitochondrial Function and Pathology (5 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Genetics (1.2k citations), Cancer Research (563 citations), Molecular Biology (2.3k citations), Hematology (269 citations) and Otorhinolaryngology (75 citations). Sat Dev Batish has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Arleen D. Auerbach, Helmut Hanenberg, Philip F. Giampietro, Jaya M. Satagopan, Bhuvanesh Singh, David I. Kutler, Orna Levran, James R. Lupski, Charles F. Towne and Feng Zhang. Their work appears in journals such as Human Mutation, Nature Genetics, Blood, Proceedings of the National Academy of Sciences and Neurogenetics.
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.