Please enable Javascript

Labmeeting uses lots of Javascript - basically you can't use the site without it. So please enable Javascript in your browser. If your browser does not support Javascript, we recommend Firefox.

Papers authored by Sijmons RH

Collect these papers and discover other ones on Labmeeting. Learn more.

Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patients.

+ cite this

+ View Abstract

Ferreira AM, Westers H, Sousa S, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, Reuvekamp PT, Seruca R, Kleibeuker JH, Hollema H, Sijmons RH, and Hofstra RM

The Journal of pathology 219(1):96-102, 2009 Sep - Who cited this? | PubMed ID: 19521971 | Fulltext

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

+ cite this

+ View Abstract

Niessen RC, Hofstra RM, Westers H, Ligtenberg MJ, Kooi K, Jager PO, de Groote ML, Dijkhuizen T, Olderode-Berends MJ, Hollema H, Kleibeuker JH, and Sijmons RH

Genes, chromosomes & cancer 48(8):737-44, 2009 Aug - Who cited this? | PubMed ID: 19455606 | Fulltext

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

+ cite this

+ View Abstract

Ferreira AM, Westers H, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, van der Zee AG, Hollema H, Kleibeuker JH, Sijmons RH, and Hofstra RM

Genes, chromosomes & cancer 48(7):552-7, 2009 Jul - Who cited this? | PubMed ID: 19373783 | Fulltext

PMS2 involvement in patients suspected of Lynch syndrome.

+ cite this

+ View Abstract

Niessen RC, Kleibeuker JH, Westers H, Jager PO, Rozeveld D, Bos KK, Boersma-van Ek W, Hollema H, Sijmons RH, and Hofstra RM

Genes, chromosomes & cancer 48(4):322-9, 2009 Apr - Who cited this? | PubMed ID: 19132747 | Fulltext

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

+ cite this

+ View Abstract

Ou J, Rasmussen M, Westers H, Andersen SD, Jager PO, Kooi KA, Niessen RC, Eggen BJ, Nielsen FC, Kleibeuker JH, Sijmons RH, Rasmussen LJ, and Hofstra RM

Genes, chromosomes & cancer 48(4):340-50, 2009 Apr - Who cited this? | PubMed ID: 19156873 | Fulltext

Sharing data between LSDBs and central repositories.

+ cite this

+ View Abstract

den Dunnen JT, Sijmons RH, Andersen PS, Vihinen M, Beckmann JS, Rossetti S, Talbot CC, Hardison RC, Povey S, and Cotton RG

Human mutation 30(4):493-5, 2009 Apr - Who cited this? | PubMed ID: 19306393 | Fulltext

Planning the human variome project: the Spain report.

+ cite this

+ View Abstract

Kaput J, Cotton RG, Hardman L, Watson M, Al Aqeel AI, Al-Aama JY, Al-Mulla F, Alonso S, Aretz S, Auerbach AD, Bapat B, Bernstein IT, Bhak J, Bleoo SL, Blöcker H, Brenner SE,

(show remaining authors)

Human mutation 30(4):496-510, 2009 Apr - Who cited this? | PubMed ID: 19306394 | Fulltext

Management of extracolonic tumours in patients with Lynch syndrome.

+ cite this

+ View Abstract

Koornstra JJ, Mourits MJ, Sijmons RH, Leliveld AM, Hollema H, and Kleibeuker JH

The lancet oncology 10(4):400-8, 2009 Apr - Who cited this? | PubMed ID: 19341971 | Fulltext

Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in lynch syndrome.

+ cite this

+ View Abstract

Wijnen JT, Brohet RM, van Eijk R, Jagmohan-Changur S, Middeldorp A, Tops CM, van Puijenbroek M, Ausems MG, Gómez García E, Hes FJ, Hoogerbrugge N, Menko FH, van Os TA, Sijmons RH, Verhoef S, Wagner A,

(show remaining authors)

Gastroenterology 136(1):131-7, 2009 Jan - Who cited this? | PubMed ID: 19010329 | Fulltext

Hereditary Cancer in Clinical Practice transfers to BioMed Central.

+ cite this

Lubiński J, Sijmons RH, and Scott RJ

Hereditary cancer in clinical practice 7(1):1, 2009 - Who cited this? | PubMed ID: 19338678 | Fulltext

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

+ cite this

+ View Abstract

Ou J, Niessen RC, Vonk J, Westers H, Hofstra RM, and Sijmons RH

Human mutation 29(11):1337-41, 2008 Nov - Who cited this? | PubMed ID: 18951442 | Fulltext

Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes.

+ cite this

+ View Abstract

Greenblatt MS, Brody LC, Foulkes WD, Genuardi M, Hofstra RM, Olivier M, Plon SE, Sijmons RH, Sinilnikova O, Spurdle AB, and IARC Unclassified Genetic Variants Working Group

Human mutation 29(11):1273-81, 2008 Nov - Who cited this? | PubMed ID: 18951438 | Fulltext

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

+ cite this

+ View Abstract

Stulp RP, Herkert JC, Karrenbeld A, Mol B, Vos YJ, and Sijmons RH

Hereditary cancer in clinical practice 6(1):15-21, 2008 - Who cited this? | PubMed ID: 19706203 | Fulltext

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

+ cite this

+ View Abstract

Sijmons RH

Hereditary cancer in clinical practice 6(1):22-57, 2008 - Who cited this? | PubMed ID: 19706204 | Fulltext

Clinical and genetic aspects of testicular germ cell tumours.

+ cite this

+ View Abstract

Holzik MF, Sijmons RH, Hoekstra-Weebers JE, Sleijfer DT, and Hoekstra HJ

Hereditary cancer in clinical practice 6(1):3-14, 2008 - Who cited this? | PubMed ID: 19715611 | Fulltext

The common sense model of self-regulation and psychological adjustment to predictive genetic testing: a prospective study.

+ cite this

+ View Abstract

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, Van Gool AR, Klijn JG, and Tibben A

Psycho-oncology 16(12):1121-9, 2007 Dec - Who cited this? | PubMed ID: 17328098 | Fulltext

Functional analysis helps to clarify the clinical importance of unclassified variants in DNA mismatch repair genes.

+ cite this

+ View Abstract

Ou J, Niessen RC, Lützen A, Sijmons RH, Kleibeuker JH, de Wind N, Rasmussen LJ, and Hofstra RM

Human mutation 28(11):1047-54, 2007 Nov - Who cited this? | PubMed ID: 17594722 | Fulltext

Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.

+ cite this

+ View Abstract

Hes FJ, van der Luijt RB, Janssen AL, Zewald RA, de Jong GJ, Lenders JW, Links TP, Luyten GP, Sijmons RH, Eussen HJ, Halley DJ, Lips CJ, Pearson PL, van den Ouweland AM, and Majoor-Krakauer DF

Clinical genetics 72(2):122-9, 2007 Aug - Who cited this? | PubMed ID: 17661816 | Fulltext

A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships.

+ cite this

+ View Abstract

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, Van Gool AR, Klijn JG, Riedijk SR, van Dooren S, and Tibben A

Psycho-oncology 16(4):320-8, 2007 Apr - Who cited this? | PubMed ID: 16909428 | Fulltext

Getting rid of the PMS2 pseudogenes: mission impossible?.

+ cite this

Niessen RC, Kleibeuker JH, Jager PO, Sijmons RH, and Hofstra RM

Human mutation 28(4):414; author reply 415, 2007 Apr - Who cited this? | PubMed ID: 17139668 | Fulltext

Comparison of individuals opting for BRCA1/2 or HNPCC genetic susceptibility testing with regard to coping, illness perceptions, illness experiences, family system characteristics and hereditary cancer distress.

+ cite this

+ View Abstract

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, Van Gool AR, Klijn JG, and Tibben A

Patient education and counseling 65(1):58-68, 2007 Jan - Who cited this? | PubMed ID: 16872788 | Fulltext

Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study.

+ cite this

+ View Abstract

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, van Gool AR, Klijn JG, and Tibben A

Clinical genetics 71(1):35-42, 2007 Jan - Who cited this? | PubMed ID: 17204044 | Fulltext

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

+ cite this

+ View Abstract

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, Van Gool AR, Klijn JG, and Tibben A

European journal of cancer (Oxford, England : 1990) 43(1):71-7, 2007 Jan - Who cited this? | PubMed ID: 17045473 | Fulltext

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

+ cite this

+ View Abstract

Gerkes EH, de Jong MM, Sijmons RH, and Vellenga E

Hereditary cancer in clinical practice 5(2):72-8, 2007 - Who cited this? | PubMed ID: 19725987 | Fulltext

Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer.

+ cite this

+ View Abstract

Niessen RC, Berends MJ, Wu Y, Sijmons RH, Hollema H, Ligtenberg MJ, de Walle HE, de Vries EG, Karrenbeld A, Buys CH, van der Zee AG, Hofstra RM, and Kleibeuker JH

Gut 55(12):1781-8, 2006 Dec - Who cited this? | PubMed ID: 16636019 | Fulltext

Re-analysis of the Xq27-Xq28 region suggests a weak association of an X-linked gene with sporadic testicular germ cell tumour without cryptorchidism.

+ cite this

+ View Abstract

Lutke Holzik MF, Hoekstra HJ, Sijmons RH, Sonneveld DJ, van der Steege G, Sleijfer DT, and Nolte IM

European journal of cancer (Oxford, England : 1990) 42(12):1869-74, 2006 Aug - Who cited this? | PubMed ID: 16797968 | Fulltext

Experience of parental cancer in childhood is a risk factor for psychological distress during genetic cancer susceptibility testing.

+ cite this

+ View Abstract

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, Van Gool AR, Klijn JG, and Tibben A

Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 17(7):1090, 2006 Jul - Who cited this? | PubMed ID: 16600981 | Fulltext

MUTYH and the mismatch repair system: partners in crime?.

+ cite this

+ View Abstract

Niessen RC, Sijmons RH, Ou J, Olthof SG, Osinga J, Ligtenberg MJ, Hogervorst FB, Weiss MM, Tops CM, Hes FJ, de Bock GH, Buys CH, Kleibeuker JH, and Hofstra RM

Human genetics 119(1-2):206-11, 2006 Mar - Who cited this? | PubMed ID: 16408224 | Fulltext

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

+ cite this

+ View Abstract

Stulp RP, Vos YJ, Mol B, Karrenbeld A, de Raad M, van der Mijle HJ, and Sijmons RH

World journal of gastroenterology : WJG 12(5):809, 2006 Feb 7 - Who cited this? | PubMed ID: 16521201 | Fulltext

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP).

+ cite this

+ View Abstract

Nielsen M, Franken PF, Reinards TH, Weiss MM, Wagner A, van der Klift H, Kloosterman S, Houwing-Duistermaat JJ, Aalfs CM, Ausems MG, Bröcker-Vriends AH, Gomez Garcia EB, Hoogerbrugge N, Menko FH, Sijmons RH, Verhoef S,

(show remaining authors)

Journal of medical genetics 42(9), 2005 Sep - Who cited this? | PubMed ID: 16140997 | Fulltext

[More hereditary intestinal cancer can be detected if patients with colorectal carcinoma that are selected by the pathologist are examined for microsatellite instability].

+ cite this

+ View Abstract

de Bruin JH, Kievit W, Ligtenberg MJ, Nagengast FM, Adang EM, Ruers TJ, Kleibeuker JH, Sijmons RH, van Krieken JH, and Hoogerbrugge N

Nederlands tijdschrift voor geneeskunde 149(32):1792-8, 2005 Aug 6 - Who cited this? | PubMed ID: 16121665 | Fulltext

Colorectal cancer and the CHEK2 1100delC mutation.

+ cite this

+ View Abstract

de Jong MM, Nolte IM, Te Meerman GJ, van der Graaf WT, Mulder MJ, van der Steege G, Bruinenberg M, Schaapveld M, Niessen RC, Berends MJ, Sijmons RH, Hofstra RM, de Vries EG, and Kleibeuker JH

Genes, chromosomes & cancer 43(4):377-82, 2005 Aug - Who cited this? | PubMed ID: 15852425 | Fulltext

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

+ cite this

+ View Abstract

Domingo E, Niessen RC, Oliveira C, Alhopuro P, Moutinho C, Espín E, Armengol M, Sijmons RH, Kleibeuker JH, Seruca R, Aaltonen LA, Imai K, Yamamoto H, Schwartz S, and Hofstra RM

Oncogene 24(24):3995-8, 2005 Jun 2 - Who cited this? | PubMed ID: 15782118 | Fulltext

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

+ cite this

de Groot JW, Sijmons RH, Links TP, Plukker JT, and Hofstra RM

Journal of pediatric gastroenterology and nutrition 40(2):226-9, 2005 Feb - Who cited this? | PubMed ID: 15699703 | Fulltext

The human leukocyte antigen region and colorectal cancer risk.

+ cite this

+ View Abstract

de Jong MM, Niens M, Nolte IM, te Meerman GJ, van der Graaf WT, Mulder MJ, van der Steege G, Bruinenberg M, Schaapveld M, Sijmons RH, Hofstra RM, de Vries EG, and Kleibeuker JH

Diseases of the colon and rectum 48(2):303-6, 2005 Feb - Who cited this? | PubMed ID: 15714243 | Fulltext

Cost effectiveness of a new strategy to identify HNPCC patients.

+ cite this

+ View Abstract

Kievit W, de Bruin JH, Adang EM, Severens JL, Kleibeuker JH, Sijmons RH, Ruers TJ, Nagengast FM, Vasen HF, van Krieken JH, Ligtenberg MJ, and Hoogerbrugge N

Gut 54(1):97-102, 2005 Jan - Who cited this? | PubMed ID: 15591512 | Fulltext

Absence of constitutional Y chromosome AZF deletions in patients with testicular germ cell tumors.

+ cite this

+ View Abstract

Lutke Holzik MF, Storm K, Sijmons RH, D'hollander M, Arts EG, Verstraaten ML, Sleijfer DT, and Hoekstra HJ

Urology 65(1):196-201, 2005 Jan - Who cited this? | PubMed ID: 15667903 | Fulltext

No association between the Arg201Gly polymorphism of the DCC gene and colorectal cancer.

+ cite this

+ View Abstract

de Jong MM, te Meerman GJ, van der Graaf WT, de Vries EG, Nolte IM, Mulder MJ, Bruinenberg M, van der Steege G, Schaapveld M, Sijmons RH, Hofstra RM, and Kleibeuker JH

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 36(12):821-3, 2004 Dec - Who cited this? | PubMed ID: 15646429 | Fulltext

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status.

+ cite this

+ View Abstract

Oliveira C, Westra JL, Arango D, Ollikainen M, Domingo E, Ferreira A, Velho S, Niessen R, Lagerstedt K, Alhopuro P, Laiho P, Veiga I, Teixeira MR, Ligtenberg M, Kleibeuker JH, Sijmons RH,

(show remaining authors)

Human molecular genetics 13(19):2303-11, 2004 Oct 1 - Who cited this? | PubMed ID: 15294875 | Fulltext

No association between two MLH3 variants (S845G and P844L)and colorectal cancer risk.

+ cite this

+ View Abstract

de Jong MM, Hofstra RM, Kooi KA, Westra JL, Berends MJ, Wu Y, Hollema H, van der Sluis T, van der Graaf WT, de Vries EG, Schaapveld M, Sijmons RH, te Meerman GJ, and Kleibeuker JH

Cancer genetics and cytogenetics 152(1):70-1, 2004 Jul 1 - Who cited this? | PubMed ID: 15193445 | Fulltext

Genetic predisposition to testicular germ-cell tumours.

+ cite this

+ View Abstract

Lutke Holzik MF, Rapley EA, Hoekstra HJ, Sleijfer DT, Nolte IM, and Sijmons RH

The lancet oncology 5(6):363-71, 2004 Jun - Who cited this? | PubMed ID: 15172357 | Fulltext

Hereditary non-polyposis colorectal cancer: identification of mutation carriers and assessing pathogenicity of mutations.

+ cite this

+ View Abstract

Niessen RC, Sijmons RH, Berends MJ, Ou J, Hofstra RM, and Kleibeuker JH

Scandinavian journal of gastroenterology. Supplement(241):70-7, 2004 - Who cited this? | PubMed ID: 15696853 | Fulltext

Toward new strategies to select young endometrial cancer patients for mismatch repair gene mutation analysis.

+ cite this

+ View Abstract

Berends MJ, Wu Y, Sijmons RH, van der Sluis T, Ek WB, Ligtenberg MJ, Arts NJ, ten Hoor KA, Kleibeuker JH, de Vries EG, Mourits MJ, Hollema H, Buys CH, Hofstra RM, and van der Zee AG

Journal of clinical oncology : official journal of the American Society of Clinical Oncology 21(23):4364-70, 2003 Dec 1 - Who cited this? | PubMed ID: 14645426 | Fulltext

Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds.

+ cite this

+ View Abstract

Scheenstra R, Rijcken FE, Koornstra JJ, Hollema H, Fodde R, Menko FH, Sijmons RH, Bijleveld CM, and Kleibeuker JH

Gut 52(6):898-9, 2003 Jun - Who cited this? | PubMed ID: 12740349 | Fulltext

Acceptable age for prophylactic surgery in children with multiple endocrine neoplasia type 2a.

+ cite this

+ View Abstract

Kahraman T, de Groot JW, Rouwe C, Hofstra RM, Links TP, Sijmons RH, and Plukker JT

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology 29(4):331-5, 2003 May - Who cited this? | PubMed ID: 12711285 | Fulltext

Syndromic aspects of testicular carcinoma.

+ cite this

+ View Abstract

Lutke Holzik MF, Sijmons RH, Sleijfer DT, Sonneveld DJ, Hoekstra-Weebers JE, van Echten-Arends J, and Hoekstra HJ

Cancer 97(4):984-92, 2003 Feb 15 - Who cited this? | PubMed ID: 12569597 | Fulltext

Testicular carcinoma and HLA Class II genes.

+ cite this

+ View Abstract

Sonneveld DJ, Lutke Holzik MF, Nolte IM, Sleijfer DT, van der Graaf WT, Bruinenberg M, Sijmons RH, Hoekstra HJ, and Te Meerman GJ

Cancer 95(9):1857-63, 2002 Nov 1 - Who cited this? | PubMed ID: 12404278 | Fulltext

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

+ cite this

+ View Abstract

de Jong MM, Nolte IM, te Meerman GJ, van der Graaf WT, de Vries EG, Sijmons RH, Hofstra RM, and Kleibeuker JH

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 11(11):1332-52, 2002 Nov - Who cited this? | PubMed ID: 12433710 | Fulltext

BRCA1 and BRCA2 heterozygosity and repair of X-ray-induced DNA damage.

+ cite this

+ View Abstract

Nieuwenhuis B, Van Assen-Bolt AJ, Van Waarde-Verhagen MA, Sijmons RH, Van der Hout AH, Bauch T, Streffer C, and Kampinga HH

International journal of radiation biology 78(4):285-95, 2002 Apr - Who cited this? | PubMed ID: 12020440 | Fulltext

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant.

+ cite this

+ View Abstract

Berends MJ, Wu Y, Sijmons RH, Mensink RG, van der Sluis T, Hordijk-Hos JM, de Vries EG, Hollema H, Karrenbeld A, Buys CH, van der Zee AG, Hofstra RM, and Kleibeuker JH

American journal of human genetics 70(1):26-37, 2002 Jan - Who cited this? | PubMed ID: 11709755 | Fulltext

Search Google Scholar for Sijmons RH

Join Labmeeting

Organize and search your PDF collection
Collect papers
Search millions of papers
Keep up to date with paper alerts
Read your papers from anywhere
Recommend papers to colleagues
Manage your lab

Labmeeting is a web service for researchers. Sign up with your academic email address.

Individuals or corporations not affiliated with an academic institution can request a trial subscription.

Papers authored by Sijmons RH

Join Labmeeting

Sponsored Product