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Genetics

D-Index
78
Citations
32490
World Ranking
1671
National Ranking
57

Overview

Graham J. Mann is affiliated with the Australian National University in Australia. Their research spans multiple domains within biochemistry, genetics, molecular biology, and medicine, with a significant focus on oncology and cancer research.

Their recent publications include:

  • FinnGen provides genetic insights from a well-phenotyped isolated population, 2023, Nature
  • Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection, 2021, Nature Medicine
  • Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes, 2022, JAMA Oncology
  • Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity, 2020, Nature Communications
  • Multiomic profiling of checkpoint inhibitor-treated melanoma: Identifying predictors of response and resistance, and markers of biological discordance, 2021, Cancer Cell

Their work is concentrated in the following main fields of study:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Subfields of study reflect their focused expertise and include:

  • Oncology
  • Molecular Biology
  • Genetics
  • Cancer Research
  • Immunology

Key topics explored in their research cover a range of cancer-related aspects and biomedical themes:

  • Cutaneous Melanoma Detection and Management
  • BRCA gene mutations in cancer
  • Cancer Genomics and Diagnostics
  • Genetic Associations and Epidemiology
  • Melanoma and MAPK Pathways
  • Health Systems, Economic Evaluations, Quality of Life
  • Immunotherapy and Immune Responses

Graham J. Mann frequently publishes in several specialized venues, indicating established engagement with the scientific community in their areas of study. These include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Communications
  • Nature
  • British Journal of Dermatology
  • Scientific Reports

Among their frequent co-authors are:

  • Richard A. Scolyer
  • Anne Ε. Cust
  • James S. Wilmott
  • Manjeet K. Bolla
  • Stig E. Bojesen

Best Publications

  • Pan-cancer analysis of whole genomes

    Peter J. Campbell;Gad Getz;Jan O. Korbel;Joshua M. Stuart

  • Genomic Classification of Cutaneous Melanoma

    Rehan Akbani;Kadir C. Akdemir;B. Arman Aksoy;Monique Albert

  • Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer.

    Katherine A. Hoadley;Christina Yau;Christina Yau;Toshinori Hinoue;Denise M. Wolf

  • Whole-genome landscapes of major melanoma subtypes

    Nicholas K. Hayward;Nicholas K. Hayward;James S. Wilmott;Nicola Waddell;Nicola Waddell;Peter A. Johansson

  • Prognostic and Clinicopathologic Associations of Oncogenic BRAF in Metastatic Melanoma

    Georgina V. Long;Alexander M. Menzies;Adnan M. Nagrial;Lauren E. Haydu

  • Genomic and Functional Approaches to Understanding Cancer Aneuploidy

    Alison M. Taylor;Alison M. Taylor;Juliann Shih;Gavin Ha;Gavin Ha;Galen F. Gao

  • Patterns of somatic structural variation in human cancer genomes

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

  • Geographical Variation in the Penetrance of CDKN2A Mutations for Melanoma

    D. Timothy Bishop;Florence Demenais;Alisa M. Goldstein;Wilma Bergman

  • Erratum: Comprehensive Characterization of Cancer Driver Genes and Mutations (ARTICLE (2018) 173(2) (371–385), (S009286741830237X), (10.1016/j.cell.2018.02.060))

    Matthew H. Bailey;Collin Tokheim;Eduard Porta-Pardo;Sohini Sengupta

  • A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

    Satoru Yokoyama;Susan L. Woods;Glen M. Boyle;Lauren G. Aoude

  • Genome-wide association study identifies three loci associated with melanoma risk.

    D Timothy Bishop;Florence Demenais;Mark M Iles;Mark Harland

  • Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma‐prone families from three continents

    Alisa M Goldstein;May Chan;Mark Harland;Nicholas K Hayward

  • High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL

    Alisa M. Goldstein;May Chan;Mark Harland;Elizabeth M. Gillanders

  • Dominant Negative ATM Mutations in Breast Cancer Families

    Georgia Chenevix-Trench;Amanda B. Spurdle;Magtouf Gatei;Helena Kelly

  • Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas

    Franz X. Schaub;Varsha Dhankani;Ashton C. Berger;Mihir Trivedi

  • Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

    Joshua D. Campbell;Joshua D. Campbell;Joshua D. Campbell;Christina Yau;Christina Yau;Reanne Bowlby;Yuexin Liu

  • UV-associated mutations underlie the etiology of MCV-negative Merkel cell carcinomas

    Stephen Q. Wong;Kelly Waldeck;Ismael A. Vergara;Jan Schröder;Jan Schröder;Jan Schröder

  • Circulating tumour DNA predicts response to anti-PD1 antibodies in metastatic melanoma.

    J.H. Lee;J.H. Lee;J.H. Lee;G.V. Long;S. Boyd;S. Lo

  • Genome-wide association study identifies three new melanoma susceptibility loci

    Jennifer H. Barrett;Mark M. Iles;Mark Harland;John C. Taylor

  • Common sequence variants on 20q11.22 confer melanoma susceptibility

    Kevin M. Brown;Stuart MacGregor;Grant W. Montgomery;David W. Craig

Frequent Co-Authors

Richard A. Scolyer
Richard A. Scolyer Royal Prince Alfred Hospital
Richard F. Kefford
Richard F. Kefford Macquarie University
Nicholas K. Hayward
Nicholas K. Hayward QIMR Berghofer Medical Research Institute
John F. Thompson
John F. Thompson University of Sydney
Georgina V. Long
Georgina V. Long University of Sydney
James S. Wilmott
James S. Wilmott University of Sydney
John L. Hopper
John L. Hopper University of Melbourne
Nadine A. Kasparian
Nadine A. Kasparian Cincinnati Children's Hospital Medical Center
Graham G. Giles
Graham G. Giles University of Melbourne
Susana Puig
Susana Puig University of Barcelona

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