Satish Kumar Nandakumar

2.2k citations
17 papers · 1.4k · 1 hit paper · h-index 14

Impact in

  • Hematology top 2%
    • Acute Myeloid Leukemia Research
  • Genetics top 5%
    • Myeloproliferative Neoplasms: Diagnosis and Treatment
    • Hemoglobinopathies and Related Disorders

Papers in

    • Acute Myeloid Leukemia Research 7
    • Hematopoietic Stem Cell Transplantation 2
    • Hemoglobinopathies and Related Disorders 4
    • Myeloproliferative Neoplasms: Diagnosis and Treatment 3
    • Genetic Associations and Epidemiology 3

Satish Kumar Nandakumar

16 papers receiving 1.4k citations

Satish Kumar Nandakumar's Hit Papers

Inherited causes of clonal haematopoiesis in 97,691 whole genomes 2020 · 544 citations
5440+2+4Years since publication100200300400500

Peers

Satish Kumar Nandakumar
Comparison fields: 5 of 69
  • Hematology 514
  • Genetics 362
  • Cancer Research 193
  • Immunology 214
  • Molecular Biology 655
Replace Jason E. Farrar with:
Jason E. Farrar United States
Sherif Ibrahim United States
Keegan Q. Barry-Holson United States
Mark David Ewalt United States
Bala Bharathi Burugula United States
Suveg Pandey United States
Miriam Belmonte United Kingdom
Polynikis Kaimakis Netherlands
Kwok Peng Ng United States
Satish Kumar Nandakumar relative to Jason E. Farrar United States Jason E. Farrar's profile →
Citations per field
00.5×1.5×
Jason E. Farrar · 1×
Citations per year

Countries citing papers authored by Satish Kumar Nandakumar

Since Specialization
Citations

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

Fields of papers citing papers by Satish Kumar Nandakumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Satish Kumar Nandakumar. 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 Satish Kumar Nandakumar. The network helps show where Satish Kumar Nandakumar may publish in the future.

Co-authors

The 25 scholars most cited alongside Satish Kumar Nandakumar, 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 Satish Kumar Nandakumar Line = papers co-authored together Satish Kumar Nandakumar links everyone, so they are left out of the graph.

All Works

17 of 17 papers shown
#Work
1
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Hit paper breakdown →
2020544
2 2016231
3 2016121
4 2019112
5 2020108
6 201346
7 202243
8 201540
9 201637
10 202034
11 202027
12 202324
13 202121
14 201915
15 20209
16 20251
17 20250

About Satish Kumar Nandakumar

Satish Kumar Nandakumar is a scholar working on Hematology, Genetics, Cancer Research, Molecular Biology and Genetics, having authored 17 papers that have together received 1.4k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (7 papers), Epigenetics and DNA Methylation (5 papers), Hemoglobinopathies and Related Disorders (4 papers), Cancer Genomics and Diagnostics (3 papers), RNA modifications and cancer (3 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers), Genetic Associations and Epidemiology (3 papers) and Hematopoietic Stem Cell Transplantation (2 papers). The work is most often cited by research in Hematology (514 citations), Genetics (362 citations), Cancer Research (193 citations), Immunology (214 citations) and Molecular Biology (655 citations). Satish Kumar Nandakumar has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Vijay G. Sankaran, Jacob C. Ulirsch, Xiaolan Zhang, Peter Rogov, Ron Do, Tarjei S. Mikkelsen, Patrick E. McDonel, Alexandre Melnikov, Li Wang and Aviv Regev. Their work appears in journals such as Nature, Nature Communications, Journal of Clinical Immunology, Nature Genetics and Trends in 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.

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