Smitha Kumble
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 4
- Connective tissue disorders research 2
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
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- Ion channel regulation and function 1
- Co-authors
- Ravi Savarirayan (2 shared papers)Ingrid E. Scheffer (1 shared paper)David Mowat (1 shared paper)Alison Yeung (1 shared paper)Gemma Poke (1 shared paper)Ella Wilkins (1 shared paper)Michael S. Hildebrand (1 shared paper)Carolyn Ellaway (1 shared paper)
- Journals
- Human Molecular Genetics (1 paper)Expert Opinion on Emerging Drugs (1 paper)American Journal of Medical Genetics Part A (1 paper)Journal of Paediatrics and Child Health (1 paper)Europe PMC (PubMed Central) (1 paper)
- Partner nations
- AustraliaUnited StatesNew Zealand
In The Last Decade
Smitha Kumble
5 papers receiving 22 citations
Peers
Comparison fields: 5 of 15
- Genetics 11
- Physiology 1
- Genetics 2
- Speech and Hearing 1
- Health, Toxicology and Mutagenesis 2
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 | 2022 | 12 | |
| 2 | Chondrodysplasia Punctata 2, X-Linked | 2020 | 4 |
| 3 | 2021 | 3 | |
| 4 | 2022 | 2 | |
| 5 | 2023 | 1 |
About Smitha Kumble
Smitha Kumble is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Pediatrics, Perinatology and Child Health and Physiology, having authored 5 papers that have together received 22 indexed citations. Recurring topics across this work include Connective tissue disorders research (2 papers), Cardiac electrophysiology and arrhythmias (1 paper), Genomics and Rare Diseases (1 paper), NF-κB Signaling Pathways (1 paper), Genetic Syndromes and Imprinting (1 paper), Ion channel regulation and function (1 paper), Prenatal Screening and Diagnostics (1 paper) and Pain Mechanisms and Treatments (1 paper). The work is most often cited by research in Genetics (11 citations), Physiology (1 citation), Genetics (2 citations), Speech and Hearing (1 citation) and Health, Toxicology and Mutagenesis (2 citations). Smitha Kumble has collaborated with scholars based in Australia, United States and New Zealand. Frequent co-authors include Ravi Savarirayan, Ingrid E. Scheffer, David Mowat, Alison Yeung, Gemma Poke, Ella Wilkins, Michael S. Hildebrand, Carolyn Ellaway, Sulekha Rajagopalan and Samuel F. Berkovic. Their work appears in journals such as Human Molecular Genetics, Expert Opinion on Emerging Drugs, American Journal of Medical Genetics Part A, Journal of Paediatrics and Child Health and Europe PMC (PubMed Central).
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.