Rolf Sijmons

Rolf Sijmons

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Rolf Sijmons

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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Genet Med 2019 Jul 24. Epub 2019 Jul 24.

Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.

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http://dx.doi.org/10.1038/s41436-019-0596-9DOI Listing
July 2019

Comprehensive Profiling of Primary and Metastatic ccRCC Reveals a High Homology of the Metastases to a Subregion of the Primary Tumour.

Cancers (Basel) 2019 Jun 12;11(6). Epub 2019 Jun 12.

Department of Genetics, University of Groningen, University Medical Center Groningen, HPC CB50, 9700 RB Groningen, The Netherlands.

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http://dx.doi.org/10.3390/cancers11060812DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628027PMC
June 2019

Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co-occurring FANCC and CHEK2 mutations.

Br J Haematol 2019 Mar 16;184(6):1071-1073. Epub 2018 May 16.

Department of Haematology, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands.

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http://dx.doi.org/10.1111/bjh.15265DOI Listing
March 2019

Systematic Review of the Prognostic Role of the Immune System After Surgery of Colorectal Liver Metastases.

Front Oncol 2019 19;9:148. Epub 2019 Mar 19.

Department of Hepato-Pancreato-Biliary Surgery and Liver Transplantation, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.

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http://dx.doi.org/10.3389/fonc.2019.00148DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433783PMC
March 2019

NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing.

BMC Bioinformatics 2018 Dec 17;19(1):531. Epub 2018 Dec 17.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/s12859-018-2557-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296037PMC
December 2018

How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial.

Patient Educ Couns 2018 09 8;101(9):1611-1619. Epub 2018 May 8.

Department of Medical Psychology, Academic Medical Centre, University of Amsterdam, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.pec.2018.05.009DOI Listing
September 2018

Reusability of coded data in the primary care electronic medical record: A dynamic cohort study concerning cancer diagnoses.

Int J Med Inform 2017 03 28;99:45-52. Epub 2016 Aug 28.

Julius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht, PO Box 85500, 3508 GA Utrecht, The Netherlands; Department of Public Health and Primary Care, Leiden University Medical Centre, PO Box 9600, 2300 RC Leiden, The Netherlands; Department of General Practice & Elderly Care Medicine and the EMGO Institute for Health and Care Research, VU University Medical Centre, PO Box 7507, 1007 MB Amsterdam, The Netherlands. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S13865056163019
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http://dx.doi.org/10.1016/j.ijmedinf.2016.08.004DOI Listing
March 2017

Prevalence and Progression of Pancreatic Cystic Precursor Lesions Differ Between Groups at High Risk of Developing Pancreatic Cancer.

Pancreas 2017 01;46(1):28-34

From the *Department of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam; †Department of Clinical Genetics, Academic Medical Center; and ‡Family Cancer Clinic Cancer Institute, Amsterdam; Departments of §Radiology and ∥Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam; ¶Department of Radiology, Academic Medical Center, Amsterdam; #Department of Genetics, University of Groningen, and **Department of Gastroenterology and Hepatology, University Medical Center, Groningen; Departments of ††Gastroenterology and Hepatology and ‡‡Clinical Genetics, University Medical Center, Utrecht; and §§Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam, the Netherlands.

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http://dx.doi.org/10.1097/MPA.0000000000000725DOI Listing
January 2017

GAVIN: Gene-Aware Variant INterpretation for medical sequencing.

Genome Biol 2017 01 16;18(1). Epub 2017 Jan 16.

University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/s13059-016-1141-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240400PMC
January 2017

Design and Feasibility of an Intervention to Support Cancer Genetic Counselees in Informing their At-Risk Relatives.

J Genet Couns 2016 12 22;25(6):1179-1187. Epub 2016 Apr 22.

Department of Medical Psychology, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1007/s10897-016-9948-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114329PMC
December 2016

Do GPs know their patients with cancer? Assessing the quality of cancer registration in Dutch primary care: a cross-sectional validation study.

BMJ Open 2016 09 15;6(9):e012669. Epub 2016 Sep 15.

Julius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht, Utrecht, The Netherlands.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030604PMC
http://dx.doi.org/10.1136/bmjopen-2016-012669DOI Listing
September 2016

SETD2: an epigenetic modifier with tumor suppressor functionality.

Oncotarget 2016 Aug;7(31):50719-50734

Department of Genetics, University of Groningen, University Medical Center Groningen, The Netherlands.

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http://dx.doi.org/10.18632/oncotarget.9368DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226616PMC
August 2016

Functional Studies on Primary Tubular Epithelial Cells Indicate a Tumor Suppressor Role of SETD2 in Clear Cell Renal Cell Carcinoma.

Neoplasia 2016 06 26;18(6):339-46. Epub 2016 May 26.

Department of Genetics, University of Groningen, University Medical Center Groningen, PO Box 30.001, 9700 RB Groningen, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.neo.2016.04.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916950PMC
June 2016

SORTA: a system for ontology-based re-coding and technical annotation of biomedical phenotype data.

Database (Oxford) 2015 18;2015. Epub 2015 Sep 18.

University of Groningen, University Medical Centre Groningen, Genomics Coordination Centre, Department of Genetics, Groningen, The Netherlands, University of Groningen, University Medical Center Groningen, Department of Epidemiology, Groningen, The Netherlands and LifeLines Cohort Study and Biobank, Groningen, The Netherlands

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http://dx.doi.org/10.1093/database/bav089DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574036PMC
May 2016

CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.

Hum Mutat 2016 May 24;37(5):457-64. Epub 2016 Feb 24.

University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/humu.22969DOI Listing
May 2016

Review: Clinical aspects of hereditary DNA Mismatch repair gene mutations.

DNA Repair (Amst) 2016 Feb 11;38:155-162. Epub 2015 Dec 11.

Department of Clinical Genetics, Erasmus Medical Center Rotterdam, P.O. Box 2040, 3000CA Rotterdam, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.dnarep.2015.11.018DOI Listing
February 2016

Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1.

Gastroenterology 2015 Oct 11;149(4):897-906.e19. Epub 2015 Jun 11.

Department of Pathology, Radboud university medical center, Nijmegen, The Netherlands; Department of Human Genetics, Radboud university medical center, Nijmegen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1053/j.gastro.2015.06.003DOI Listing
October 2015

ClinGen and Genetic Testing.

N Engl J Med 2015 10;373(14):1377

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http://dx.doi.org/10.1056/NEJMc1508700DOI Listing
October 2015

Development of the Informing Relatives Inventory (IRI): Assessing Index Patients' Knowledge, Motivation and Self-Efficacy Regarding the Disclosure of Hereditary Cancer Risk Information to Relatives.

Int J Behav Med 2015 Aug;22(4):551-60

Department of Medical Psychology, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands,

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http://dx.doi.org/10.1007/s12529-014-9455-xDOI Listing
August 2015

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.

J Clin Oncol 2015 Feb 15;33(4):319-25. Epub 2014 Dec 15.

Sanne W. ten Broeke, Carli M. Tops, Heleen M. van der Klift, Manon Suerink, Frederik J. Hes, Hans F. Vasen, Maartje Nielsen, and Juul T. Wijnen, Leiden University Medical Center; Hans F. Vasen, The Netherlands Foundation for the Detection of Hereditary Tumors, Leiden; Richard M. Brohet, Research Center Linnaeus Institute, Spaarne Hospital, Hoofddorp; Mary E. Velthuizen and Tom G.W. Letteboer, University Medical Center Utrecht, Utrecht; Encarna Gomez Garcia, Maastricht University Medical Center, Maastricht; Nicoline Hoogerbrugge, Arjen R. Mensenkamp, and Liesbeth Spruijt, Radboud University Medical Center, Nijmegen; Fred H. Menko, Vrije Universiteit, University Medical Center; Theo A. van Os and Bert J.W. Redeker, Academic Medical Center, Amsterdam; Rolf H. Sijmons and Yvonne J. Vos, University of Groningen, University Medical Center Groningen, Groningen; Anja Wagner, Erasmus University Medical Center, Rotterdam, the Netherlands; Inge Bernstein, Aalborg University Hospital, Aalborg; Inge Bernstein, Danish Hereditary Nonpolyposis Colorectal Cancer Registry, Hvidovre University Hospital Copenhagen, Denmark; Gabriel Capellá Munar, Hereditary Cancer Program, Catalan Institute of Oncology-Institut D'Investigació Biomèdica de Bellvitge, l'Hospitalet de Llobregat, Spain; Annika Lindblom, Karolinska Institutet, Karolinska University Hospital, Solna; Pal Moller, Research Group Inherited Cancer, Oslo University Hospital, Oslo, Norway; and Nils Rahner, Institute of Human Genetics, University of Dusseldorf, Dusseldorf, Germany.

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http://dx.doi.org/10.1200/JCO.2014.57.8088DOI Listing
February 2015

High frequency of RPL22 mutations in microsatellite-unstable colorectal and endometrial tumors.

Hum Mutat 2014 Dec;35(12):1442-5

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, 9700, RB, The Netherlands.

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http://dx.doi.org/10.1002/humu.22686DOI Listing
December 2014

New target genes in endometrial tumors show a role for the estrogen-receptor pathway in microsatellite-unstable cancers.

Hum Mutat 2014 Dec;35(12):1514-23

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands; Department of Pathomorphology, Medical College, Jagiellonian University, Krakow, Poland; Institute of Molecular Pathology and Immunology and Medical Faculty, University of Porto, Porto, Portugal.

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http://dx.doi.org/10.1002/humu.22700DOI Listing
December 2014

Charles Buys (1942-2014).

Eur J Hum Genet 2014 Dec;22(12):1343-4

Department of Clinical Genetics, University of Rotterdam, Erasmus MC, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1038/ejhg.2014.207DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231401PMC
December 2014

Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnostics.

Hum Mutat 2013 Jul 29;34(7):1035-42. Epub 2013 Apr 29.

Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/humu.22332DOI Listing
July 2013

Gene variants of unknown clinical significance in Lynch syndrome. An introduction for clinicians.

Fam Cancer 2013 Jun;12(2):181-7

Department of Genetics, University Medical Center Groningen, University of Groningen, Hanzeplein 1, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s10689-013-9629-8DOI Listing
June 2013

Prevalence of BRCA1 and BRCA2 Germline Mutations in Breast Cancer Women of Multiple Ethnic Region in Northwest China.

J Breast Cancer 2013 Mar 31;16(1):50-4. Epub 2013 Mar 31.

Department of Breast Surgery, Xinjiang Cancer Institute & Hospital, Xinjiang Medical University, Urumqi, China. ; Postdoctoral Research Station of Clinical Medicine, Xinjiang Medical University, Urumqi, China.

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https://synapse.koreamed.org/DOIx.php?id=10.4048/jbc.2013.16
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http://dx.doi.org/10.4048/jbc.2013.16.1.50DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625769PMC
March 2013

Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas.

J Med Genet 2012 Jun 25;49(6):362-5. Epub 2012 May 25.

Department of Gastroenterology & Hepatology, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1136/jmedgenet-2011-100563DOI Listing
June 2012

[Familial gastric cancer: diagnosis, treatment and periodic surveillance].

Ned Tijdschr Geneeskd 2011 ;155:A2731

Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis, Amsterdam, the Netherlands.

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September 2011

Malignant peritoneal mesothelioma in a patient with Li-Fraumeni syndrome.

J Clin Oncol 2011 Jun 4;29(17):e503-5. Epub 2011 Apr 4.

Ghent University Hospital, Ghent; the Research Foundation-Flanders, Brussels, Belgium.

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http://dx.doi.org/10.1200/JCO.2010.34.1933DOI Listing
June 2011

Screening for germline DND1 mutations in testicular cancer patients.

Fam Cancer 2010 Sep;9(3):439-42

Department of Genetics, University Medical Center Groningen, University of Groningen, PO Box 30001, 9700 RB, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s10689-010-9340-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921500PMC
September 2010

Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.

J Clin Oncol 2010 Jun 17;28(18):3008-14. Epub 2010 May 17.

Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Division of Psychosocial Research and Epidemiology, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1200/JCO.2009.27.2112DOI Listing
June 2010

Cell-free assay breakthrough for MLH1 variants.

Hum Mutat 2010 Mar;31(3)

University Medical Center Groningen, The Netherlands.

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http://dx.doi.org/10.1002/humu.21217DOI Listing
March 2010

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

Genes Chromosomes Cancer 2009 Aug;48(8):737-44

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/gcc.20678DOI Listing
August 2009

Do microsatellite instability profiles really differ between colorectal and endometrial tumors?

Genes Chromosomes Cancer 2009 Jul;48(7):552-7

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

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http://dx.doi.org/10.1002/gcc.20664DOI Listing
July 2009

PMS2 involvement in patients suspected of Lynch syndrome.

Genes Chromosomes Cancer 2009 Apr;48(4):322-9

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/gcc.20642DOI Listing
April 2009

Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome.

Genes Chromosomes Cancer 2009 Apr;48(4):340-50

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/gcc.20644DOI Listing
April 2009

Planning the human variome project: the Spain report.

Authors:
Jim Kaput Richard G H Cotton Lauren Hardman Michael Watson Aida I Al Aqeel Jumana Y Al-Aama Fahd Al-Mulla Santos Alonso Stefan Aretz Arleen D Auerbach Bharati Bapat Inge T Bernstein Jong Bhak Stacey L Bleoo Helmut Blöcker Steven E Brenner John Burn Mariona Bustamante Rita Calzone Anne Cambon-Thomsen Michele Cargill Paola Carrera Lawrence Cavedon Yoon Shin Cho Yeun-Jun Chung Mireille Claustres Garry Cutting Raymond Dalgleish Johan T den Dunnen Carlos Díaz Steven Dobrowolski M Rosário N dos Santos Rosemary Ekong Simon B Flanagan Paul Flicek Yoichi Furukawa Maurizio Genuardi Ho Ghang Maria V Golubenko Marc S Greenblatt Ada Hamosh John M Hancock Ross Hardison Terence M Harrison Robert Hoffmann Rania Horaitis Heather J Howard Carol Isaacson Barash Neskuts Izagirre Jongsun Jung Toshio Kojima Sandrine Laradi Yeon-Su Lee Jong-Young Lee Vera L Gil-da-Silva-Lopes Finlay A Macrae Donna Maglott Makia J Marafie Steven G E Marsh Yoichi Matsubara Ludwine M Messiaen Gabriela Möslein Mihai G Netea Melissa L Norton Peter J Oefner William S Oetting James C O'Leary Ana Maria Oller de Ramirez Mark H Paalman Jillian Parboosingh George P Patrinos Giuditta Perozzi Ian R Phillips Sue Povey Suyash Prasad Ming Qi David J Quin Rajkumar S Ramesar C Sue Richards Judith Savige Dagmar G Scheible Rodney J Scott Daniela Seminara Elizabeth A Shephard Rolf H Sijmons Timothy D Smith María-Jesús Sobrido Toshihiro Tanaka Sean V Tavtigian Graham R Taylor Jon Teague Thoralf Töpel Mollie Ullman-Cullere Joji Utsunomiya Henk J van Kranen Mauno Vihinen Elizabeth Webb Thomas K Weber Meredith Yeager Young I Yeom Seon-Hee Yim Hyang-Sook Yoo

Hum Mutat 2009 Apr;30(4):496-510

Division of Personalised Nutrition and Medicine, FDA/National Center for Toxicological Research, Jefferson, Arkansas 72079, USA.

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http://compbio.berkeley.edu/people/brenner/pubs/kaput-2009-h
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http://doi.wiley.com/10.1002/humu.20972
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http://dx.doi.org/10.1002/humu.20972DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879779PMC
April 2009

Management of extracolonic tumours in patients with Lynch syndrome.

Lancet Oncol 2009 Apr;10(4):400-8

Department of Gastroenterology and Hepatology, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands.

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https://linkinghub.elsevier.com/retrieve/pii/S14702045097004
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http://dx.doi.org/10.1016/S1470-2045(09)70041-5DOI Listing
April 2009

A database to support the interpretation of human mismatch repair gene variants.

Hum Mutat 2008 Nov;29(11):1337-41

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

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http://dx.doi.org/10.1002/humu.20907DOI Listing
November 2008

Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.

Hered Cancer Clin Pract 2008 Feb 15;6(1):15-21. Epub 2008 Feb 15.

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://hccpjournal.biomedcentral.com/articles/10.1186/1897-4
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http://dx.doi.org/10.1186/1897-4287-6-1-15DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735069PMC
February 2008

Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome.

Authors:
Rolf H Sijmons

Hered Cancer Clin Pract 2008 Feb 15;6(1):22-57. Epub 2008 Feb 15.

Department of Genetics, University Medical Center, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/1897-4287-6-1-22DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735164PMC
February 2008

Clinical and genetic aspects of testicular germ cell tumours.

Hered Cancer Clin Pract 2008 Feb 15;6(1):3-14. Epub 2008 Feb 15.

Department of Surgical Oncology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/1897-4287-6-1-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735737PMC
February 2008

Familial multiple myeloma: report on two families and discussion of screening options.

Hered Cancer Clin Pract 2007 Jun 15;5(2):72-8. Epub 2007 Jun 15.

Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands.

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http://hccpjournal.biomedcentral.com/articles/10.1186/1897-4
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http://dx.doi.org/10.1186/1897-4287-5-2-72DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2736995PMC
June 2007

Prognostic factors for hereditary cancer distress six months after BRCA1/2 or HNPCC genetic susceptibility testing.

Eur J Cancer 2007 Jan 11;43(1):71-7. Epub 2006 Oct 11.

Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, Westzeedijk 112-114, 3016 AH, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.ejca.2006.08.023DOI Listing
January 2007

MUTYH and the mismatch repair system: partners in crime?

Hum Genet 2006 Mar 12;119(1-2):206-11. Epub 2006 Jan 12.

Department of Medical Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s00439-005-0118-5DOI Listing
March 2006

First report of a de novo germline mutation in the MLH1 gene.

World J Gastroenterol 2006 Feb;12(5):809-11

Department of Clinical Genetics, University Medical Center Groningen, PO Box 30001, 9700 RB Groningen, The Netherlands.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066138PMC
http://dx.doi.org/10.3748/wjg.v12.i5.809DOI Listing
February 2006

BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes.

Oncogene 2005 Jun;24(24):3995-8

Molecular Oncology and Aging Research, Centre d'Investigacions en Bioquímica i Biologia Molecular (CIBBIM), Hospital Universitari Vall d'Hebron, Passeig Vall d'Hebron 119-129, Barcelona 08035, Spain.

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http://dx.doi.org/10.1038/sj.onc.1208569DOI Listing
June 2005

Medullary thyroid cancer in a patient with Hirschsprung disease with a C609Y germline RET-mutation.

J Pediatr Gastroenterol Nutr 2005 Feb;40(2):226-9

Department of Surgical Oncology, University Hospital Groningen, 9713 AW Groningen, The Netherlands.

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http://dx.doi.org/10.1097/00005176-200502000-00028DOI Listing
February 2005

The human leukocyte antigen region and colorectal cancer risk.

Dis Colon Rectum 2005 Feb;48(2):303-6

Department of Gastroenterology, University Hospital Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s10350-004-0801-yDOI Listing
February 2005

Clinical vignette: early-onset head and neck cancer: beware of fanconi anaemia!

Hered Cancer Clin Pract 2004 Jul 15;2(3):147-8. Epub 2004 Jul 15.

Department of Clinical Genetics, Groningen University Hospital, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/1897-4287-2-3-147DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392523PMC
July 2004

Familial cervical cancer: case reports, review and clinical implications.

Hered Cancer Clin Pract 2004 May 15;2(2):99-105. Epub 2004 May 15.

Department of Gynaecology, Groningen University Hospital, The Netherlands.

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http://dx.doi.org/10.1186/1897-4287-2-2-99DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840001PMC
May 2004

Syndromic aspects of testicular carcinoma.

Cancer 2003 Feb;97(4):984-92

Department of Surgical Oncology, University Medical Center Groningen, Groningen, The Netherlands.

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http://doi.wiley.com/10.1002/cncr.11155
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http://dx.doi.org/10.1002/cncr.11155DOI Listing
February 2003

Testicular carcinoma and HLA Class II genes.

Cancer 2002 Nov;95(9):1857-63

Department of Surgical Oncology, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/cncr.10903DOI Listing
November 2002

Low-penetrance genes and their involvement in colorectal cancer susceptibility.

Cancer Epidemiol Biomarkers Prev 2002 Nov;11(11):1332-52

Department of Gastroenterology, University Hospital Groningen, The Netherlands.

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November 2002