Yvonne J Vos

Yvonne J Vos

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Yvonne J Vos

Yvonne J Vos

Publications by authors named "Yvonne J Vos"

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Cancer Risks for PMS2-Associated Lynch Syndrome.

J Clin Oncol 2018 10 30;36(29):2961-2968. Epub 2018 Aug 30.

Sanne W. ten Broeke, Heleen M. van der Klift, Carli M.J. Tops, Manon Suerink, Frederik J. Hes, Hans F.A. Vasen, Juul T. Wijnen, and Maartje Nielsen, Leiden University Medical Center, Leiden; Encarna Gomez Garcia, Maastricht University Medical Center, Maastricht; Nicoline Hoogerbrugge, Arjen R. Mensenkamp, and Liesbeth Spruijt, Radboud University Medical Center, Nijmegen; Tom G.W. Letteboer, University Medical Center, Utrecht; Theo A.M. van Os and Egbert J.W. Redeker, Academic Medical Center, Amsterdam; Maran J.W. Olderode-Berends and Yvonne J. Vos, University of Groningen; University Medical Center Groningen, Groningen; Anja Wagner, Erasmus Medical Center, Rotterdam, the Netherlands; Stefan Aretz, University of Bonn; University Hospital Bonn, Bonn; Christoph Engel, Leipzig University; Medizinisch Genetisches Zentrum Bayerstr, Leipzig; Magnus von Knebel Doeberitz, University of Heidelberg; German Cancer Research Center, Heidelberg; Pål Møller, University of Witten-Herdecke, Wuppertal; Nils Rahner, Heinrich-Heine-University, Düsseldorf; Hans K. Schackert, Technische Universität Dresden, Dresden; Verena Steinke-Lange, Medizinische Klinik und Poliklinik IV Campus Innenstadt, Klinikum der Universität München, Munich, Germany; Pål Møller, The Norwegian Radium Hospital; Oslo University Hospital, Oslo, Norway; Inge Bernstein, Hvidovre Hospital, Hvidovre, and Aalborg University Hospital, Aalborg, Denmark; Daniel D. Buchanan, Mark Clendenning, John L. Hopper, Mark A. Jenkins, Christophe Rosty, Ingrid Winship, and Aung Ko Win, The University of Melbourne; Daniel D. Buchanan, Ingrid Winship, and Aung Ko Win, Royal Melbourne Hospital, Parkville, Melbourne, Victoria; Rodney Scott, University of Newcastle, Newcastle, New South Wales, Australia; Albert de la Chapelle, Heather L. Hampel, Rachel Pearlman, and Leigha Senter, The Ohio State University Comprehensive Cancer Center, Columbus, OH; Gabriel Capella and Marta Pineda, Institut d'Investigació Biomédica de Bellvitge, Barcelona, Spain; Steven Gallinger, Mount Sinai Hospital, Toronto, Ontario, Canada; Jane C. Figueiredo and Robert Haile, Cedars-Sinai Medical Center, Los Angeles, CA; Loic Le Marchand, University of Hawaii Cancer Center, Honolulu, HI; Annika Lindblom, Karolinska Institutet; Karolinska University Hospital, Stockholm, Sweden; Noralane M. Lindor, Mayo Clinic Arizona, Scottsdale, AZ; Polly A. Newcomb, Fred Hutchinson Cancer Research Center; University of Washington, Seattle, WA; and Stephen Thibodeau, Mayo Clinic, Rochester, MN.

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http://ascopubs.org/doi/10.1200/JCO.2018.78.4777
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http://dx.doi.org/10.1200/JCO.2018.78.4777DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349460PMC
October 2018

Unusual Course of Lafora Disease.

Epilepsia Open 2016 12 25;1(3-4):136-139. Epub 2016 Aug 25.

Department of Neurology University Medical Centre Groningen University of Groningen Groningen the Netherlands.

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http://dx.doi.org/10.1002/epi4.12009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719837PMC
December 2016

Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsy.

Eur J Paediatr Neurol 2016 May 8;20(3):489-92. Epub 2016 Jan 8.

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

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http://dx.doi.org/10.1016/j.ejpn.2015.12.014DOI Listing
May 2016

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

Mutation Analysis in Glycogen Storage Disease Type III Patients in the Netherlands: Novel Genotype-Phenotype Relationships and Five Novel Mutations in the AGL Gene.

JIMD Rep 2013 16;7:19-26. Epub 2012 Mar 16.

Department of Metabolic Diseases, Beatrix Children's Hospital, University Medical Centre Groningen, University of Groningen, 30.001, 9700 RB, Groningen, The Netherlands,

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http://dx.doi.org/10.1007/8904_2012_134DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575051PMC
February 2013

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

An updated and upgraded L1CAM mutation database.

Hum Mutat 2010 Jan;31(1):E1102-9

Department of Genetics, University Medical Centre Groningen, University of Groningen, P.O. Box 30001, 9700 RB Groningen, The Netherlands.

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http://dx.doi.org/10.1002/humu.21172DOI Listing
January 2010

Nephrogenic diabetes insipidus in a patient with L1 syndrome: a new report of a contiguous gene deletion syndrome including L1CAM and AVPR2.

Am J Med Genet A 2008 Jul;146A(14):1853-8

Department of Pediatric Nephrology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://doi.wiley.com/10.1002/ajmg.a.32386
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http://dx.doi.org/10.1002/ajmg.a.32386DOI Listing
July 2008

Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia.

Eur J Hum Genet 2008 Jun 30;16(6):673-9. Epub 2008 Jan 30.

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

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http://www.nature.com/articles/5202012
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http://dx.doi.org/10.1038/sj.ejhg.5202012DOI Listing
June 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

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

Shah-Waardenburg syndrome and PCWH associated with SOX10 mutations: a case report and review of the literature.

Eur J Paediatr Neurol 2006 Jan 28;10(1):11-7. Epub 2006 Feb 28.

Department of Medical Genetics, University Medical Centre Groningen, Groningen University, Box 30.001, 9700 RB Groningen, The Netherlands.

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http://dx.doi.org/10.1016/j.ejpn.2005.10.004DOI Listing
January 2006

Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?

Hum Genet 2003 Feb 21;112(2):105-9. Epub 2002 Nov 21.

Department of Biosciences, Division of Genetics, University of Helsinki, Viikinkaari 5, 00014 Helsinki, Finland.

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http://dx.doi.org/10.1007/s00439-002-0866-4DOI Listing
February 2003

X-linked hydrocephalus: a novel missense mutation in the L1CAM gene.

Pediatr Neurol 2002 Oct;27(4):293-6

Department of Pediatrics, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al Ain.

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http://dx.doi.org/10.1016/s0887-8994(02)00440-xDOI Listing
October 2002