Soma Das
Impact in
- Genetics top 0.05%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Molecular Biology top 0.2%
Papers in
-
- Cancer therapeutics and mechanisms 10
- DNA Repair Mechanisms 9
- Genetics 45
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 14
- Genomics and Rare Diseases 14
- Genetic Syndromes and Imprinting 9
- Co-authors
- Sherri J. Bale (6 shared papers)Wayne W. Grody (3 shared papers)Madhuri Hegde (2 shared papers)Elaine Lyon (2 shared papers)Heidi L. Rehm (3 shared papers)Sue Richards (2 shared papers)David Bick (2 shared papers)Julie M. Gastier‐Foster (1 shared paper)
- Journals
- Blood (11 papers)Genetics in Medicine (9 papers)Journal of Clinical Oncology (7 papers)Human Mutation (5 papers)Clinical Genetics (5 papers)
- Partner nations
- United StatesIndiaCanada
In The Last Decade
Soma Das
149 papers receiving 27.0k citations
Soma Das's Hit Papers
Peers
Comparison fields: 5 of 175
- Genetics 8.7k
- Molecular Biology 10.0k
- Clinical Biochemistry 888
- Genetics 1.3k
- Cancer Research 1.7k
Countries citing papers authored by Soma Das
This map shows the geographic impact of Soma Das'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 Soma Das with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Soma Das more than expected).
Fields of papers citing papers by Soma Das
This network shows the impact of papers produced by Soma Das. 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 Soma Das. The network helps show where Soma Das may publish in the future.
Co-authors
The 25 scholars most cited alongside Soma Das, 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 154 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Hit paper breakdown → | 2015 | 19638 |
| 2 | Genetic Variants in the UDP-glucuronosyltransferase 1A1 Gene Predict the Risk of Severe Neutropenia of Irinotecan Hit paper breakdown → | 2004 | 697 |
| 3 | ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 Hit paper breakdown → | 2008 | 574 |
| 4 | UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity Hit paper breakdown → | 2002 | 524 |
| 5 | 2019 | 227 | |
| 6 | 2005 | 224 | |
| 7 | 2008 | 186 | |
| 8 | 2011 | 181 | |
| 9 | 1999 | 165 | |
| 10 | 2007 | 156 | |
| 11 | 2005 | 150 | |
| 12 | 2017 | 145 | |
| 13 | 2005 | 143 | |
| 14 | Interethnic difference in the allelic distribution of human epidermal growth factor receptor intron 1 polymorphism. | 2003 | 137 |
| 15 | 2002 | 136 | |
| 16 | 2012 | 133 | |
| 17 | 2004 | 126 | |
| 18 | 2002 | 124 | |
| 19 | 2001 | 114 | |
| 20 | 2008 | 105 |
About Soma Das
Soma Das is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Oncology and Public Health, Environmental and Occupational Health, having authored 154 papers that have together received 27.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (14 papers), Acute Lymphoblastic Leukemia research (12 papers), Cancer therapeutics and mechanisms (10 papers), DNA Repair Mechanisms (9 papers), Genetic Syndromes and Imprinting (9 papers) and Neonatal Health and Biochemistry (9 papers). The work is most often cited by research in Genetics (8.7k citations), Molecular Biology (10.0k citations), Clinical Biochemistry (888 citations), Genetics (1.3k citations) and Cancer Research (1.7k citations). Soma Das has collaborated with scholars based in United States, India and Canada. Frequent co-authors include Sherri J. Bale, Wayne W. Grody, Madhuri Hegde, Elaine Lyon, Heidi L. Rehm, Sue Richards, David Bick, Julie M. Gastier‐Foster, Nazneen Aziz and Karl V. Voelkerding. Their work appears in journals such as Blood, Genetics in Medicine, Journal of Clinical Oncology, Human Mutation and Clinical 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.