Sawona Biswas
- Genetics top 5%
- Genomics and Rare Diseases 8
- BRCA gene mutations in cancer 4
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
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- Hearing, Cochlea, Tinnitus, Genetics 1
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- Ethics in Clinical Research 3
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- Platelet Disorders and Treatments 2
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- Congenital heart defects research 2
- Co-authors
- Timothy W. YuLauren MassinghamDanny E. MillerJennifer MalinowskiKandamurugu ManickamHutton M. KearneyLaurie DemmerFuki M. Hisama
- Partner nations
- United StatesUnited KingdomSweden
In The Last Decade
Sawona Biswas
13 papers receiving 507 citations
Hit Papers
Peers
Comparison fields: 5 of 63
- Genetics 374
- Pediatrics, Perinatology and Child Health 88
- Sensory Systems 18
- Cancer Research 40
- Otorhinolaryngology 11
Countries citing papers authored by Sawona Biswas
This map shows the geographic impact of Sawona Biswas'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 Sawona Biswas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sawona Biswas more than expected).
Fields of papers citing papers by Sawona Biswas
This network shows the impact of papers produced by Sawona Biswas. 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 Sawona Biswas. The network helps show where Sawona Biswas may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Sawona Biswas, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)breakdown → | 2021 | 288 |
| 2 | 2020 | 16 | |
| 3 | 2018 | 5 | |
| 4 | 2018 | 27 | |
| 5 | 2018 | 59 | |
| 6 | 2018 | 30 | |
| 7 | 2017 | 22 | |
| 8 | 2017 | 13 | |
| 9 | 2016 | 11 | |
| 10 | 2016 | 1 | |
| 11 | 2015 | 14 | |
| 12 | 2015 | 26 | |
| 13 | 2013 | 1 |
About Sawona Biswas
Sawona Biswas is a scholar working on Genetics, Otorhinolaryngology and Sensory Systems, having authored 13 papers that have together received 513 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), BRCA gene mutations in cancer (4 papers), Ethics in Clinical Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Platelet Disorders and Treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). The work is most often cited by research in Genetics (374 citations), Pediatrics, Perinatology and Child Health (88 citations) and Sensory Systems (18 citations). Sawona Biswas has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include Timothy W. Yu, Lauren Massingham, Danny E. Miller, Jennifer Malinowski, Kandamurugu Manickam, Hutton M. Kearney, Laurie Demmer, Fuki M. Hisama, Monica R. McClain and Barbara A. Bernhardt. Their work appears in journals such as Blood, Human Mutation and Genetics in Medicine.
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.