Sameer Chavan

9.2k citations
57 papers · 5.4k · 7 hit papers · h-index 28

Impact in

  • Genetics top 1%
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Hematology top 2%
    • Acute Myeloid Leukemia Research

Papers in

    • Genetic Associations and Epidemiology 27
    • Genomics and Rare Diseases 8
    • Myeloproliferative Neoplasms: Diagnosis and Treatment 3
    • Asthma and respiratory diseases 7

Sameer Chavan

56 papers receiving 5.3k citations

Sameer Chavan's Hit Papers

Clonal haematopoiesis and risk of chronic liver disease 2023 · 149 citations
1490+2+4Years since publication4008001.2k

Peers

Sameer Chavan
Comparison fields: 5 of 143
  • Genetics 1.9k
  • Hematology 517
  • Genetics 358
  • Cancer Research 427
  • Immunology 528
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Citations per field
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Citations per year

Countries citing papers authored by Sameer Chavan

Since Specialization
Citations

This map shows the geographic impact of Sameer Chavan'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 Sameer Chavan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sameer Chavan more than expected).

Fields of papers citing papers by Sameer Chavan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sameer Chavan. 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 Sameer Chavan. The network helps show where Sameer Chavan may publish in the future.

Co-authors

The 25 scholars most cited alongside Sameer Chavan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sameer Chavan Line = papers co-authored together Sameer Chavan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 57 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Hit paper breakdown →
20211281
2
Mapping the human genetic architecture of COVID-19
Hit paper breakdown →
2021641
3
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Hit paper breakdown →
2020544
4
Genetic diversity fuels gene discovery for tobacco and alcohol use
Hit paper breakdown →
2022264
5
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Hit paper breakdown →
2022249
6 2018249
7
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
Hit paper breakdown →
2022205
8 2020161
9
Clonal haematopoiesis and risk of chronic liver disease
Hit paper breakdown →
2023149
10 2018129
11 2016123
12 2021122
13 201498
14 201886
15 201975
16 202371
17 202369
18 202267
19 202263
20 201659

About Sameer Chavan

Sameer Chavan is a scholar working on Genetics, Physiology, Dermatology, Molecular Biology and Hematology, having authored 57 papers that have together received 5.4k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (27 papers), Genomics and Rare Diseases (8 papers), Asthma and respiratory diseases (7 papers), Bioinformatics and Genomic Networks (6 papers), Dermatology and Skin Diseases (5 papers), RNA modifications and cancer (5 papers), Cancer Genomics and Diagnostics (4 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers). The work is most often cited by research in Genetics (1.9k citations), Hematology (517 citations), Genetics (358 citations), Cancer Research (427 citations) and Immunology (528 citations). Sameer Chavan has collaborated with scholars based in United States, United Kingdom and Barbados. Frequent co-authors include Hilary S. Parker, Jeffrey T. Leek, Alexander V. Favorov, Elana Judith Fertig, Christine H. Chung, Michael Considine, Sarah Cherian, Pratip Shil, Claire E Malley and Gerald T. Nepom. Their work appears in journals such as Nature Communications, Journal of Allergy and Clinical Immunology, Nature, Nature Genetics and Cell Genomics.

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.

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