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Medicine

D-Index
72
Citations
21561
World Ranking
19801
National Ranking
9862

Overview

Paul J. Goodfellow is affiliated with The Ohio State University in the United States. Their research primarily focuses on cancer, particularly genetic factors and molecular mechanisms related to colorectal, endometrial, cervical, and ovarian cancers.

The scientist's recent publications include:

  • Germline and Somatic Tumor Testing in Epithelial Ovarian Cancer: ASCO Guideline, 2020, Journal of Clinical Oncology
  • Evaluation of treatment effects in patients with endometrial cancer and POLE mutations: An individual patient data meta-analysis, 2021, Cancer
  • Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative, 2021, JCO Precision Oncology
  • Characterization of mismatch-repair/microsatellite instability-discordant endometrial cancers, 2023, Cancer
  • Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patients, 2020, Gynecologic Oncology

Frequent co-authors collaborating with Paul J. Goodfellow include:

  • David E. Cohn
  • Casey Cosgrove
  • Adrian A. Suarez
  • Heather Hampel
  • Rachel Pearlman

Paul J. Goodfellow has frequently published in the following venues:

  • Gynecologic Oncology
  • Cancer
  • Journal of Clinical Oncology
  • JCO Precision Oncology
  • The Oncologist

Their main fields of study are Medicine and Biochemistry, Genetics and Molecular Biology. Within these fields, significant subfields of study include:

  • Pathology and Forensic Medicine
  • Cancer Research
  • Obstetrics and Gynecology
  • Genetics
  • Reproductive Medicine

Their research covers key topics such as:

  • Genetic factors in colorectal cancer
  • Cancer Genomics and Diagnostics
  • Endometrial and Cervical Cancer Treatments
  • Ovarian cancer diagnosis and treatment
  • BRCA gene mutations in cancer
  • Cancer-related molecular mechanisms research
  • DNA Repair Mechanisms

Best Publications

  • Integrated genomic characterization of endometrial carcinoma

    Gad Getz;Stacey B. Gabriel;Kristian Cibulskis;Eric Lander

  • Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC

    Helen Donis-Keller;Shenshen Dou;David Chi;Katrin M. Carlson

  • Genome remodelling in a basal-like breast cancer metastasis and xenograft

    Li Ding;Matthew J C Ellis;Shunqiang Li;David E. Larson

  • Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.

    Katrin M. Carlson;Shenshen Dou;David Chi;Nancy Scavarda

  • DICER1 Mutations in Familial Pleuropulmonary Blastoma

    D. Ashley Hill;D. Ashley Hill;Jennifer Ivanovich;John R. Priest;Christina A. Gurnett

  • Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.

    Rachel Pearlman;Wendy L Frankel;Benjamin Swanson;Weiqiang Zhao

  • Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

    N. E. Simpson;K. K. Kidd;P. J. Goodfellow;H. McDermid

  • Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene.

    Alison J. Whelan;Detlef Bartsch;Paul J. Goodfellow

  • Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.

    Pamela Pollock;Michael Gartside;L. Dejeza;Matthew Powell

  • Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

    Roger L Milne;Roger L Milne;Karoline B Kuchenbaecker;Karoline B Kuchenbaecker;Kyriaki Michailidou;Kyriaki Michailidou;Jonathan Beesley

  • MLH1 Promoter Methylation and Gene Silencing is the Primary Cause of Microsatellite Instability in Sporadic Endometrial Cancers

    Sally B. Simpkins;Tina Bocker;Elizabeth M. Swisher;David G. Mutch

  • Patterns and functional implications of rare germline variants across 12 cancer types

    Charles Lu;Mingchao Xie;Michael C. Wendl;Jiayin Wang;Jiayin Wang

  • A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

    Christopher A. Haiman;Gary K. Chen;Celine M. Vachon;Federico Canzian

  • The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

    Claire Braybrook;Kit Doudney;Ana Carolina B. Marçano;Alfred Arnason

  • Epigenetic Repression of microRNA-129-2 Leads to Overexpression of SOX4 Oncogene in Endometrial Cancer

    Yi Wen Huang;Joseph C. Liu;Daniel E. Deatherage;Jingqin Luo

  • Use of mutation profiles to refine the classification of endometrial carcinomas.

    Melissa K McConechy;Jiarui Ding;Jiarui Ding;Maggie Cu Cheang;Kimberly C Wiegand

  • Integrated analysis of germline and somatic variants in ovarian cancer

    Krishna L. Kanchi;Kimberly J. Johnson;Kimberly J. Johnson;Charles Lu;Michael D. McLellan

  • Ovarian and endometrial endometrioid carcinomas have distinct CTNNB1 and PTEN mutation profiles

    Melissa K McConechy;Jiarui Ding;Janine Senz;Winnie Yang

  • Parent-of-origin effects in multiple endocrine neoplasia type 2B.

    Katrin M. Carlson;John Bracamontes;Charles E. Jackson;Robin Clark

  • Germline and Somatic Tumor Testing in Epithelial Ovarian Cancer: ASCO Guideline.

    Panagiotis A. Konstantinopoulos;Barbara Norquist;Christina Lacchetti;Deborah Armstrong

Frequent Co-Authors

David G. Mutch
David G. Mutch Washington University in St. Louis
David E. Cohn
David E. Cohn The Ohio State University
Samuel A. Wells
Samuel A. Wells National Cancer Institute
Heather Hampel
Heather Hampel The Ohio State University
Feng Gao
Feng Gao Linköping University
feng gao
feng gao Duke University
Li Ding
Li Ding Washington University in St. Louis
Elaine R. Mardis
Elaine R. Mardis The Ohio State University
Tim H M Huang
Tim H M Huang The University of Texas Health Science Center at San Antonio
Richard K. Wilson
Richard K. Wilson Nationwide Children's Hospital

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