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D-Index & Metrics

Biology and Biochemistry

D-Index
49
Citations
20104
World Ranking
17820
National Ranking
1406

Overview

Daniel Leongamornlert is a researcher affiliated with the Wellcome Sanger Institute in the United Kingdom. Their research spans Medicine and Biochemistry, Genetics and Molecular Biology, focusing extensively on hematology and cancer-related fields.

The primary areas of study for this scientist include:

  • Hematology
  • Molecular Biology
  • Cancer Research
  • Genetics
  • Public Health, Environmental and Occupational Health

They have contributed to numerous topics within biomedical research, including:

  • Cancer Genomics and Diagnostics
  • Acute Myeloid Leukemia Research
  • Acute Lymphoblastic Leukemia research
  • Chronic Myeloid Leukemia Treatments
  • Multiple Myeloma Research and Treatments
  • Chronic Lymphocytic Leukemia Research
  • Glycosylation and Glycoproteins Research

Their recent publications show active involvement in studies addressing somatic mutations, leukemia classifications, and cancer timing mechanisms. Notable recent papers include:

  • The mutational landscape of normal human endometrial epithelium, 2020, Nature
  • The mutational landscape of human somatic and germline cells, 2021, Nature
  • Convergent somatic mutations in metabolism genes in chronic liver disease, 2021, Nature
  • Unified classification and risk-stratification in Acute Myeloid Leukemia, 2022, Nature Communications
  • Timing the initiation of multiple myeloma, 2020, Nature Communications

Frequent co-authors with whom Daniel Leongamornlert has collaborated multiple times include:

  • Peter J. Campbell
  • Alex Cagan
  • Tim H. H. Coorens
  • Francesco Maura
  • Iñigo Martincorena

Their publications are regularly found in several key scientific venues, reflecting a consistent contribution to their fields of interest. These venues include:

  • Nature
  • Blood
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Communications
  • Blood Advances

Best Publications

  • The zebrafish reference genome sequence and its relationship to the human genome.

    Kerstin Howe;Matthew D. Clark;Carlos F. Torroja;Carlos F. Torroja;James Torrance

  • Multiple newly identified loci associated with prostate cancer susceptibility.

    Rosalind A Eeles;Rosalind A Eeles;Zsofia Kote-Jarai;Graham G Giles;Graham G Giles;Ali Amin Al Olama

  • Patterns of somatic structural variation in human cancer genomes

    Yilong Li;Nicola D Roberts;Jeremiah A Wala;Jeremiah A Wala;Ofer Shapira;Ofer Shapira

  • Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

    Fredrick R. Schumacher;Ali Amin Al Olama;Sonja I. Berndt;Sara Benlloch

  • Germline BRCA Mutations Are Associated With Higher Risk of Nodal Involvement, Distant Metastasis, and Poor Survival Outcomes in Prostate Cancer

    Elena Castro;Chee Goh;David Olmos;Ed Saunders

  • Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

    Rosalind A. Eeles;Ali Amin Al Olama;Sara Benlloch;Edward J. Saunders

  • DNA sequence and analysis of human chromosome 9

    A J Mungall;S A Palmer;S K Sims;C A Edwards

  • A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

    Ali Amin Al Olama;Zsofia Kote-Jarai;Sonja I. Berndt;David V. Conti

  • Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

    Rosalind A. Eeles;Zsofia Kote-Jarai;Ali Amin Al Olama;Graham G. Giles;Graham G. Giles

  • Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

    Colin S Cooper;Colin S Cooper;Rosalind Eeles;Rosalind Eeles;David C Wedge;Peter Van Loo;Peter Van Loo;Peter Van Loo

  • The DNA sequence and biological annotation of human chromosome 1

    S. G. Gregory;S. G. Gregory;K. F. Barlow;K. E. McLay;R. Kaul

  • BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients

    Z Kote-Jarai;D Leongamornlert;E Saunders;M Tymrakiewicz

  • The mutational landscape of normal human endometrial epithelium

    Luiza Moore;Luiza Moore;Daniel Leongamornlert;Tim H. H. Coorens;Mathijs A. Sanders;Mathijs A. Sanders

  • Effect of BRCA Mutations on Metastatic Relapse and Cause-specific Survival After Radical Treatment for Localised Prostate Cancer

    Elena Castro;Chee Goh;Daniel Leongamornlert;Ed Saunders

  • Germline BRCA1 mutations increase prostate cancer risk

    D Leongamornlert;N Mahmud;M Tymrakiewicz;E Saunders

  • Multiple Loci on 8q24 Associated With Prostate Cancer Susceptibility

    Ali Amin Al Olama;Zsofia Kote-Jarai;Graham G Giles;Graham G Giles;Michelle Guy

  • The DNA sequence and comparative analysis of human chromosome 20.

    P Deloukas;M E Earthrowl;D V Grafham;M Rubenfield

  • Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

    Z Kote-Jarai;Olama Aaa.;G G Giles;G G Giles;G Severi;G Severi

  • Mutational signatures of ionizing radiation in second malignancies.

    Sam Behjati;Gunes Gundem;David C. Wedge;David C. Wedge;Nicola D. Roberts

  • Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

    Zsofia Kote-Jarai;Ali Amin Al Olama;Graham G. Giles;Gianluca Severi

Frequent Co-Authors

Rosalind A. Eeles
Rosalind A. Eeles Institute of Cancer Research
Zsofia Kote-Jarai
Zsofia Kote-Jarai Institute of Cancer Research
David E. Neal
David E. Neal University of Cambridge
Graham G. Giles
Graham G. Giles University of Melbourne
Peter J. Campbell
Peter J. Campbell Wellcome Sanger Institute
Douglas F. Easton
Douglas F. Easton University of Cambridge
Kenneth W. Muir
Kenneth W. Muir University of Manchester
Freddie C. Hamdy
Freddie C. Hamdy University of Oxford
Lisa A. Cannon-Albright
Lisa A. Cannon-Albright University of Utah

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