Smitha Kumble
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
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- Metabolism and Genetic Disorders
Papers in
- Genetics 10
- Genomics and Rare Diseases 7
- Connective tissue disorders research 2
- Genomic variations and chromosomal abnormalities 2
- Genetic Syndromes and Imprinting 1
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- Celiac Disease Research and Management 1
- Co-authors
- Ravi Savarirayan (2 shared papers)Michael S. Hildebrand (1 shared paper)Brigid M. Regan (1 shared paper)Matthew Frank Hunter (1 shared paper)Andrew Paul Fennell (1 shared paper)Zornitza Stark (2 shared papers)Samuel Frank Berkovic (1 shared paper)Ella Jane Wilkins (1 shared paper)
- Journals
- Genetics in Medicine (3 papers)Journal of Clinical Immunology (1 paper)JAMA (1 paper)Expert Opinion on Emerging Drugs (1 paper)Obstetrical & Gynecological Survey (1 paper)
- Partner nations
- AustraliaUnited StatesDenmark
In The Last Decade
Smitha Kumble
12 papers receiving 475 citations
Peers
Comparison fields: 5 of 57
- Genetics 325
- Clinical Biochemistry 30
- Pediatrics, Perinatology and Child Health 53
- Cancer Research 40
- Genetics 25
Countries citing papers authored by Smitha Kumble
This map shows the geographic impact of Smitha Kumble'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 Smitha Kumble with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Smitha Kumble more than expected).
Fields of papers citing papers by Smitha Kumble
This network shows the impact of papers produced by Smitha Kumble. 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 Smitha Kumble. The network helps show where Smitha Kumble may publish in the future.
Co-authors
The 25 scholars most cited alongside Smitha Kumble, 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 | 2020 | 191 | |
| 2 | 2018 | 140 | |
| 3 | 2021 | 66 | |
| 4 | 2020 | 29 | |
| 5 | 2022 | 14 | |
| 6 | 2021 | 14 | |
| 7 | 2017 | 8 | |
| 8 | Chondrodysplasia Punctata 2, X-Linked | 2020 | 5 |
| 9 | 2020 | 4 | |
| 10 | 2021 | 3 | |
| 11 | 2023 | 2 | |
| 12 | 2022 | 2 |
About Smitha Kumble
Smitha Kumble is a scholar working on Genetics, Gastroenterology, Cancer Research, Pediatrics, Perinatology and Child Health and Infectious Diseases, having authored 12 papers that have together received 478 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Connective tissue disorders research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Viral gastroenteritis research and epidemiology (1 paper), RNA regulation and disease (1 paper), Genetic Syndromes and Imprinting (1 paper), Prenatal Screening and Diagnostics (1 paper) and Celiac Disease Research and Management (1 paper). The work is most often cited by research in Genetics (325 citations), Clinical Biochemistry (30 citations), Pediatrics, Perinatology and Child Health (53 citations), Cancer Research (40 citations) and Genetics (25 citations). Smitha Kumble has collaborated with scholars based in Australia, United States and Denmark. Frequent co-authors include Ravi Savarirayan, Michael S. Hildebrand, Brigid M. Regan, Matthew Frank Hunter, Andrew Paul Fennell, Zornitza Stark, Samuel Frank Berkovic, Ella Jane Wilkins, Carolyn Ellaway and Sulekha Rajagopalan. Their work appears in journals such as Genetics in Medicine, Journal of Clinical Immunology, JAMA, Expert Opinion on Emerging Drugs and Obstetrical & Gynecological Survey.
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.