Michael D. Kessler

8.3k citations
55 papers · 4.3k · 5 hit papers · h-index 25

Impact in

  • Genetics top 1%
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Genetic Mapping and Diversity in Plants and Animals
  • Hematology top 5%
    • Acute Myeloid Leukemia Research

Papers in

    • Genetic Associations and Epidemiology 19
    • Genomics and Rare Diseases 10
    • Genomic variations and chromosomal abnormalities 5
    • Genetic diversity and population structure 4
    • BRCA gene mutations in cancer 4
    • Myeloproliferative Neoplasms: Diagnosis and Treatment 3
    • RNA modifications and cancer 5

Michael D. Kessler

50 papers receiving 4.2k citations

Michael D. Kessler's Hit Papers

Clonal haematopoiesis and risk of chronic liver disease 2023 · 149 citations
1490+1+3Years since publication4008001.2k

Peers

Michael D. Kessler
Comparison fields: 5 of 139
  • Genetics 1.8k
  • Hematology 309
  • Cancer Research 361
  • Genetics 231
  • Molecular Biology 1.5k
Replace Lauren Margolin with:
Lauren Margolin United States
Angel C. Y. Mak United States
Mollie A. Minear United States
Peter VandeHaar United States
Kevin Sandow United States
Ren‐Hua Chung Taiwan
Leslie S. Emery United States
Pramod Anugu United States
Lynette Ekunwe United States
Tomasz Żemojtel Germany
Michael D. Kessler relative to Lauren Margolin United States Lauren Margolin's profile →
Citations per field
00.5×1.7×
Lauren Margolin · 1×
Citations per year

Countries citing papers authored by Michael D. Kessler

Since Specialization
Citations

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

Fields of papers citing papers by Michael D. Kessler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael D. Kessler. 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 Michael D. Kessler. The network helps show where Michael D. Kessler may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 55 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
Exome sequencing and analysis of 454,787 UK Biobank participants
Hit paper breakdown →
2021591
3 2013298
4
Common and rare variant associations with clonal haematopoiesis phenotypes
Hit paper breakdown →
2022211
5
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
Hit paper breakdown →
2022205
6 2020161
7
Clonal haematopoiesis and risk of chronic liver disease
Hit paper breakdown →
2023149
8 2022123
9 2021122
10 2018119
11 201886
12 202371
13 202070
14 202267
15 202361
16 201659
17 202448
18 202246
19 201743
20 201841

About Michael D. Kessler

Michael D. Kessler is a scholar working on Genetics, Molecular Biology, Cancer Research, Genetics and Hematology, having authored 55 papers that have together received 4.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (19 papers), Genomics and Rare Diseases (10 papers), Cancer Genomics and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (5 papers), Genetic diversity and population structure (4 papers), BRCA gene mutations in cancer (4 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers). The work is most often cited by research in Genetics (1.8k citations), Hematology (309 citations), Cancer Research (361 citations), Genetics (231 citations) and Molecular Biology (1.5k citations). Michael D. Kessler has collaborated with scholars based in United States, Russia and Estonia. Frequent co-authors include Jianghan Qu, Meng Zhou, Andrew D. Smith, Jun Zhou, Qiang Song, Tyler H. Garvin, Fang Fang, Benjamin E. Decato, Timothy D. O’Connor and Matthew D. Dean. Their work appears in journals such as Nature, Nature Communications, Nature Genetics, Proceedings of the National Academy of Sciences and iScience.

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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