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Medicine

D-Index
79
Citations
25320
World Ranking
17474
National Ranking
658

Overview

Juul T. Wijnen is affiliated with Leiden University Medical Center in the Netherlands. Their scholarly work primarily intersects the fields of pathology and forensic medicine, cancer research, and molecular biology.

Their research focuses on key topics such as genetic factors in colorectal cancer, cancer genomics and diagnostics, and DNA repair mechanisms.

Recent publications by Juul T. Wijnen include:

  • A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants, 2021, Scientific Reports
  • Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers, 2020, UNC Libraries
  • Issue Information, 2021, NMR in Biomedicine
  • Issue Information, 2020, NMR in Biomedicine
  • Issue Information, 2020, NMR in Biomedicine

Juul T. Wijnen frequently collaborates with several co-authors, including Joseph A. Helpern, EX Wu, T Bathen, Zaver M. Bhujwalla, and Lavinia Spain. Each of these collaborators has contributed to multiple publications alongside Wijnen.

The majority of Wijnen's publications appear in the journal NMR in Biomedicine, with 26 publications, followed by Scientific Reports and UNC Libraries, with one publication each.

Best Publications

  • Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

    John Burn;Anne Marie Gerdes;Finlay MacRae;Jukka Pekka Mecklin

  • Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

    HF Vasen;JT Wijnen;FH Menko;JH Kleibeuker

  • Peutz–Jeghers syndrome: a systematic review and recommendations for management

    A. D. Beggs;A. R. Latchford;H. F. A. Vasen;G. Moslein

  • Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

    Hans F A Vasen;Ignacio Blanco;Katja Aktan-Collan;Jessica P Gopie

  • Guidelines for the clinical management of familial adenomatous polyposis (FAP)

    H. F. A Vasen;G. Moslein;A. Alonso;S. Aretz

  • Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)

    Hans F.A. Vasen;Gabriele Möslein;Angel Alonso;Inge Bernstein

  • The risk of extra‐colonic, extra‐endometrial cancer in the Lynch syndrome

    Patrice Watson;Hans F.A. Vasen;Jukka Pekka Mecklin;Inge Bernstein

  • A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

    Ian P.M. Tomlinson;Emily Webb;Luis Carvajal-Carmona;Peter Broderick

  • Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

    Pål Møller;Toni T Seppälä;Inge Bernstein;Inge Bernstein;Elke Holinski-Feder

  • Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

    Pal Moller;Toni Seppala;Inge Bernstein;Inge Bernstein;Elke Holinski-Feder

  • Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.

    Yvonne M C Hendriks;Anja Wagner;Hans Morreau;Fred Menko

  • Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

    Timothy R. Rebbeck;Nandita Mitra;Fei Wan;Olga M. Sinilnikova

  • Familial endometrial cancer in female carriers of MSH6 germline mutations

    J Wijnen;W de Leeuw;H Vasen;H van der Klift

  • Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

    JT Wijnen;Hfa Vasen;PM Khan;AH Zwinderman

  • Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

    Bryony A Thompson;Bryony A Thompson;Amanda B Spurdle;John-Paul Plazzer;Marc S Greenblatt

  • MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers : A study of hereditary nonpolyposis colorectal cancer families

    H. F.A. Vasen;A. Stormorken;F. H. Menko;F. M. Nagengast

  • Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

    Catherine M Phelan;Karoline B Kuchenbaecker;Karoline B Kuchenbaecker;Jonathan P Tyrer;Siddhartha P Kar

  • 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

  • Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

    Fergus J. Couch;Xianshu Wang;Lesley McGuffog;Andrew Lee

  • Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer

    John Burn;Anne-Marie Gerdes;Finlay Macrae;Jukka-Pekka Mecklin

Frequent Co-Authors

Hans F. A. Vasen
Hans F. A. Vasen Leiden University
Riccardo Fodde
Riccardo Fodde Erasmus MC
Frederik J. Hes
Frederik J. Hes Vrije Universiteit Brussel
Peter Devilee
Peter Devilee Leiden University Medical Center
Tom van Wezel
Tom van Wezel Leiden University Medical Center
Rodney J. Scott
Rodney J. Scott University of Newcastle Australia
P. Meera Khan
P. Meera Khan Leiden University
Hans Morreau
Hans Morreau Leiden University Medical Center
Fred H. Menko
Fred H. Menko Netherlands Cancer Institute
Pål Møller
Pål Møller Oslo University Hospital

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