Sat Dev Batish
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
Papers in
- Genetics 19
- BRCA gene mutations in cancer 9
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 4
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- Genetic Neurodegenerative Diseases 9
- Hereditary Neurological Disorders 8
- 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)David Ivan Kutler (2 shared papers)Bhuvanesh Singh (2 shared papers)Orna Levran (11 shared papers)James R. Lupski (5 shared papers)
- Journals
- Human Mutation (6 papers)Nature Genetics (5 papers)The American Journal of Human Genetics (3 papers)Blood (3 papers)Neuromuscular Disorders (2 papers)
- Partner nations
- United StatesGermanyAustralia
In The Last Decade
Sat Dev Batish
58 papers receiving 5.3k citations
Peers
Comparison fields: 5 of 107
- Genetics 1.7k
- Cancer Research 760
- Molecular Biology 3.2k
- Psychiatry and Mental health 530
- Hematology 360
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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 609 | |
| 2 | 2006 | 521 | |
| 3 | 2007 | 426 | |
| 4 | 2009 | 391 | |
| 5 | 2011 | 363 | |
| 6 | 2005 | 303 | |
| 7 | 2003 | 301 | |
| 8 | 1996 | 262 | |
| 9 | 2001 | 178 | |
| 10 | 2003 | 153 | |
| 11 | 2014 | 152 | |
| 12 | 2010 | 121 | |
| 13 | 2011 | 110 | |
| 14 | 2007 | 109 | |
| 15 | 2007 | 109 | |
| 16 | 1997 | 103 | |
| 17 | 1997 | 103 | |
| 18 | 2001 | 93 | |
| 19 | 2010 | 89 | |
| 20 | 2002 | 85 |
About Sat Dev Batish
Sat Dev Batish is a scholar working on Genetics, Cellular and Molecular Neuroscience, Molecular Biology, Neurology and Cancer Research, having authored 59 papers that have together received 5.5k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (22 papers), Genetic Neurodegenerative Diseases (9 papers), BRCA gene mutations in cancer (9 papers), Hereditary Neurological Disorders (8 papers), Mitochondrial Function and Pathology (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Carcinogens and Genotoxicity Assessment (5 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (1.7k citations), Cancer Research (760 citations), Molecular Biology (3.2k citations), Psychiatry and Mental health (530 citations) and Hematology (360 citations). Sat Dev Batish has collaborated with scholars based in United States, Germany and Australia. Frequent co-authors include Arleen D. Auerbach, Helmut Hanenberg, Philip F. Giampietro, Jaya M. Satagopan, David Ivan Kutler, Bhuvanesh Singh, Orna Levran, James R. Lupski, Charles F. Towne and Feng Zhang. Their work appears in journals such as Human Mutation, Nature Genetics, The American Journal of Human Genetics, Blood and Neuromuscular Disorders.
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.