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Medicine

D-Index
82
Citations
34609
World Ranking
15892
National Ranking
7996

Overview

Tom Walsh is affiliated with the University of Washington in the United States and conducts research primarily within the fields of Biochemistry, Genetics, and Molecular Biology, with a significant focus also on Medicine.

Their scholarly output includes a substantial number of publications across multiple subfields, notably Genetics, Molecular Biology, Surgery, Cancer Research, and Immunology.

Key research topics addressed by Tom Walsh cover the following areas:

  • BRCA gene mutations in cancer
  • Cancer Genomics and Diagnostics
  • RNA and protein synthesis mechanisms
  • Genetic factors in colorectal cancer
  • Genomics and Rare Diseases
  • Genomic variations and chromosomal abnormalities
  • Hearing, Cochlea, Tinnitus, Genetics

The scientist's recent published papers include:

  • Targeted long-read sequencing identifies missing disease-causing variation, 2021, The American Journal of Human Genetics
  • Genetics of schizophrenia in the South African Xhosa, 2020, Science
  • Germline variants drive myelodysplastic syndrome in young adults, 2021, Leukemia
  • Genomic analysis of inherited hearing loss in the Palestinian population, 2020, Proceedings of the National Academy of Sciences
  • Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots", 2020, Genetics in Medicine

Tom Walsh frequently collaborates with several coauthors, notably:

  • Mary-Claire King
  • Süleyman Gülsüner
  • Jon McClellan
  • Ming K. Lee
  • Karen Mulligan

Their work is published in a range of scientific journals, with multiple contributions to:

  • Biological Psychiatry
  • Journal of Medical Genetics
  • International Journal of Gynecological Cancer
  • Proceedings of the National Academy of Sciences
  • Genome Research

Tom Walsh has also contributed to the publication of a book titled Implementing Information Security in Healthcare released by HIMSS Publishing eBooks in 2020.

Best Publications

  • Strong Association of De Novo Copy Number Mutations with Autism

    Jonathan Sebat;B. Lakshmi;Dheeraj Malhotra;Jennifer Troge

  • Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

    Tom Walsh;Jon M. McClellan;Shane E. McCarthy;Anjené M. Addington

  • Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer

    Colin C. Pritchard;Joaquin Mateo;Michael F. Walsh;Navonil De Sarkar

  • Kirsten ras mutations in patients with colorectal cancer: the ‘RASCAL II’ study

    H. J. N. Andreyev;A. R. Norman;D. Cunningham;J. Oates

  • Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

    Tom Walsh;Silvia Casadei;Ming K. Lee;Christopher C. Pennil

  • Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas

    Kathryn P. Pennington;Tom Walsh;Maria I. Harrell;Ming K. Lee

  • Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

    Tom Walsh;Silvia Casadei;Kathryn Hale Coats;Elizabeth Swisher

  • Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

    Heather C Mefford;Andrew J Sharp;Carl Baker;Andy Itsara

  • Microduplications of 16p11.2 are Associated with Schizophrenia

    Shane E. McCarthy;Vladimir Makarov;George Kirov;Anjene M. Addington

  • Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial.

    Mary Claire King;Sam Wieand;Kathryn Hale;Ming Lee

  • Inherited Mutations in Women With Ovarian Carcinoma

    Barbara M. Norquist;Maria I. Harrell;Mark F. Brady;Tom Walsh

  • Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy

    Paulina Navon Elkan;Sarah B. Pierce;Reeval Segel;Reeval Segel;Tom Walsh

  • A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

    Santhosh Girirajan;Jill A. Rosenfeld;Gregory M. Cooper;Francesca Antonacci

  • Ten Genes for Inherited Breast Cancer

    Tom Walsh;Mary Claire King

  • Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network

    Suleyman Gulsuner;Tom Walsh;Amanda C. Watts;Ming K. Lee

  • Widespread RNA Editing of Embedded Alu Elements in the Human Transcriptome

    Dennis D.Y. Kim;Thomas T.Y. Kim;Thomas Walsh;Yoshifumi Kobayashi

  • Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

    Tom Walsh;Ming K. Lee;Silvia Casadei;Anne M. Thornton

  • Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

    Michael O. Dorschner;Laura M. Amendola;Emily H. Turner;Peggy D. Robertson

  • Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy

    Michael Y. Zhang;Jane E. Churpek;Siobán B. Keel;Tom Walsh

  • Actionable exomic incidental findings in 6503 participants: challenges of variant classification

    Laura M. Amendola;Michael O. Dorschner;Peggy D. Robertson;Joseph S. Salama

Frequent Co-Authors

Mary Claire King
Mary Claire King University of Washington
Ming K. Lee
Ming K. Lee University of Washington
Colin C. Pritchard
Colin C. Pritchard University of Washington
Michael L. Littman
Michael L. Littman Brown University
Elizabeth M. Swisher
Elizabeth M. Swisher University of Washington
Robert W. Stackman
Robert W. Stackman Florida Atlantic University
Karen B. Avraham
Karen B. Avraham Tel Aviv University
Akiko Shimamura
Akiko Shimamura Harvard University
Jonathan Sebat
Jonathan Sebat University of California, San Diego

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