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Medicine

D-Index
85
Citations
22281
World Ranking
14754
National Ranking
565

Overview

Jan H. Kleibeuker is affiliated with the University Medical Center Groningen in the Netherlands. Their professional focus centers around research in a clinical and medical academic environment.

Details regarding recent papers, co-authors, publication venues, book publications, fields and subfields of study, main research topics, and awards are not provided in the available data. As such, a comprehensive overview based on these aspects cannot be constructed.

Their association with a prominent medical center suggests involvement in medical research, likely contributing to advancements aligned with the institution's focus on healthcare and clinical studies.

Further specific information about Jan H. Kleibeuker's scientific contributions, research areas, or publication record is not available at this time.

Best Publications

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

    HF Vasen;JT Wijnen;FH Menko;JH Kleibeuker

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

    JT Wijnen;Hfa Vasen;PM Khan;AH Zwinderman

  • 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

  • Anastomotic biliary strictures after liver transplantation: Causes and consequences

    Robert C. Verdonk;Carlijn I. Buis;Robert J. Porte;Eric J. van der Jagt

  • Red meat and colon cancer: the cytotoxic and hyperproliferative effects of dietary heme.

    A. L. A. Sesink;D. S. M. L. Termont;J. H. Kleibeuker;R. Van Der Meer

  • Decrease in mortality in Lynch syndrome families because of surveillance.

    Andrea E. de Jong;Yvonne M.C. Hendriks;Jan H. Kleibeuker;Sybrand Y. de Boer

  • Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

    Ying Wu;Maran J.W. Berends;Rob G.J. Mensink;Claudia Kempinga

  • Endoscopic regression of Barrett’s oesophagus during omeprazole treatment; a randomised double blind study

    F T M Peters;S Ganesh;E J Kuipers;W J Sluiter

  • Diagnostic tests for Helicobacter pylori: a prospective evaluation of their accuracy, without selecting a single test as the gold standard.

    J C Thijs;A A van Zwet;W J Thijs;H B Oey

  • Increased risk of fundic gland polyps during long-term proton pump inhibitor therapy.

    Mathilde Jalving;Jan Koornstra;J. Wesseling;Hendrika Boezen

  • Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility.

    M M de Jong;I M Nolte;G J te Meerman;W T A van der Graaf

  • Molecular and Clinical Characteristics of MSH6 Variants: An Analysis of 25 Index Carriers of a Germline Variant

    Maran J.W. Berends;Ying Wu;Rolf H. Sijmons;Rob G.J. Mensink

  • Extra-intestinal manifestations of familial adenomatous polyposis.

    Emma J. Groen;Annemieke Roos;Friso L. Muntinghe;Roelien H. Enting

  • One to 2-Year Surveillance Intervals Reduce Risk of Colorectal Cancer in Families With Lynch Syndrome

    Hans F.A. Vasen;Mohamed Abdirahman;Richard Brohet;Alexandra M.J. Langers

  • Expression of nitric oxide synthases and formation of nitrotyrosine and reactive oxygen species in inflammatory bowel disease

    G. Dijkstra;H. Moshage;H. M. Van Dullemen;A. De Jager-Krikken

  • Surveillance for hereditary nonpolyposis colorectal cancer: a long-term study on 114 families.

    Wouter H de Vos tot Nederveen Cappel;Fokko M Nagengast;Gerrit Griffioen;Fred H Menko

  • PREVALENCE AND CHARACTERIZATION OF NEUTROPHIL CYTOPLASMIC ANTIBODIES IN AUTOIMMUNE LIVER-DISEASES

    A. H. L. Mulder;G. Horst;E. B. Haagsma;P. C. Limburg

  • Management of extracolonic tumours in patients with Lynch syndrome

    Jan J Koornstra;Marian J E Mourits;Rolf H Sijmons;Annemarie M Leliveld

  • The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC.

    Andrea E. De Jong;Hans Morreau;Marjo Van Puijenbroek;Paul H.C. Eilers

  • Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.

    Renee C. Niessen;Robert M. W. Hofstra;Helga Westers;Marjolijn J. L. Ligtenberg

Frequent Co-Authors

Hans F. A. Vasen
Hans F. A. Vasen Leiden University
Rolf H. Sijmons
Rolf H. Sijmons University of Groningen
Harry Hollema
Harry Hollema University Medical Center Groningen
Elisabeth G.E. de Vries
Elisabeth G.E. de Vries University Medical Center Groningen
Robert M.W. Hofstra
Robert M.W. Hofstra Erasmus University Rotterdam
Ilja M. Nolte
Ilja M. Nolte University Medical Center Groningen
Juul T. Wijnen
Juul T. Wijnen Leiden University Medical Center
Fred H. Menko
Fred H. Menko Netherlands Cancer Institute
Rinse K. Weersma
Rinse K. Weersma University Medical Center Groningen
Charles H.C.M. Buys
Charles H.C.M. Buys University of Groningen

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