Leslie G. Biesecker

39.3k citations
305 papers · 15.4k indexed · 6 hit papers · h-index 65

Impact in

  • Genetics top 0.05%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • BRCA gene mutations in cancer
    • Genetic Syndromes and Imprinting

Papers in

    • Genomics and Rare Diseases 79
    • Genomic variations and chromosomal abnormalities 47
    • BRCA gene mutations in cancer 42
    • Genetic and Kidney Cyst Diseases 21

Leslie G. Biesecker

294 papers receiving 15.1k citations

Hit Papers

Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework 2019 · 310 citations
310201320262017202150010001.5k

Peers

Leslie G. Biesecker
Comparison fields: 5 of 177
  • Genetics 8.1k
  • Developmental Biology 333
  • Cancer Research 1.5k
  • Molecular Biology 6.6k
  • Pathology and Forensic Medicine 1.3k
Replace Michael J. Bamshad with:
Michael J. Bamshad United States
Han G. Brunner Netherlands
Michael Krawczak Germany
Ethylin Wang Jabs United States
Elaine H. Zackai United States
Valérie Cormier‐Daire France
David Bick United States
Nazneen Aziz United States
Fowzan S. Alkuraya Saudi Arabia
Julie M. Gastier‐Foster United States
Leslie G. Biesecker relative to Michael J. Bamshad United States Michael J. Bamshad's profile →
Citations per field
00.5×1.5×1.9×
Michael J. Bamshad · 1×
Citations per year

Countries citing papers authored by Leslie G. Biesecker

Since Specialization
Citations

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

Fields of papers citing papers by Leslie G. Biesecker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leslie G. Biesecker. 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 Leslie G. Biesecker. The network helps show where Leslie G. Biesecker may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown
#Work
1 20246
2 20248
3 20230
4 20231
5 202215
6 202115
7 20212
8 202042
9 201924
10 201924
11 201814
12 20183
13 201718
14 201619
15 2015156
16 20148
17 201330
18 201136
19
Identificación de una nueva mutación en el gen CDMP-1 causante de la braquidactilia tipo C en una familia colombiana
20011
20 19982

About Leslie G. Biesecker

Leslie G. Biesecker is a scholar working on Genetics, Developmental Biology, Genetics, Cancer Research and Rheumatology, having authored 305 papers that have together received 15.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (79 papers), Genomic variations and chromosomal abnormalities (47 papers), Vascular Malformations and Hemangiomas (43 papers), BRCA gene mutations in cancer (42 papers), Hedgehog Signaling Pathway Studies (37 papers), Cancer Genomics and Diagnostics (25 papers), Genetic and Kidney Cyst Diseases (21 papers) and Soft tissue tumor case studies (20 papers). The work is most often cited by research in Genetics (8.1k citations), Developmental Biology (333 citations), Cancer Research (1.5k citations), Molecular Biology (6.6k citations) and Pathology and Forensic Medicine (1.3k citations). Leslie G. Biesecker has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Heidi L. Rehm, Nancy B. Spinner, Barbara B. Biesecker, Jennifer J. Johnston, Julie C. Sapp, Steven M. Harrison, Robert L. Nussbaum, John M. Graham, Robert C. Green and Jonathan S. Berg. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Human Mutation, Journal of Medical Genetics and Clinical 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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