13 results for author:"Berends M." in Literature citations
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| Is colorectal surveillance indicated in patients with PTEN mutations? Nieuwenhuis M.H., Kets C.M., Murphy-Ryan M., Colas C., Moller P., Hes F.J., Hodgson S.V., Olderode-Berends M.J., Aretz S., Heinimann K. et al. Colorectal Dis 14:e562-6(2012) · Mapped (3) |
| Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines. Herkert J.C., Niessen R.C., Olderode-Berends M.J., Veenstra-Knol H.E., Vos Y.J., van der Klift H.M., Scheenstra R., Tops C.M., Karrenbeld A., Peters F.T. et al. Eur. J. Cancer 47:965-982(2011) · Mapped (4) |
| A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum. Van Reeuwijk J., Olderode-Berends M.J., Van den Elzen C., Brouwer O.F., Roscioli T., Van Pampus M.G., Scheffer H., Brunner H.G., Van Bokhoven H., Hol F.A. Clin. Genet. 78:275-281(2010) · Mapped (1) |
| Acquired mutations in TET2 are common in myelodysplastic syndromes. Langemeijer S.M.C., Kuiper R.P., Berends M., Knops R., Aslanyan M.G., Massop M., Stevens-Linders E., van Hoogen P., van Kessel A.G., Raymakers R.A.P. et al. |
| Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome. Niessen R.C., Hofstra R.M., Westers H., Ligtenberg M.J., Kooi K., Jager P.O., de Groote M.L., Dijkhuizen T., Olderode-Berends M.J., Hollema H. et al. Genes Chromosomes Cancer 48:737-744(2009) · Mapped (31) |
| 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. Niessen R.C., Berends M.J., Wu Y., Sijmons R.H., Hollema H., Ligtenberg M.J., de Walle H.E., de Vries E.G., Karrenbeld A., Buys C.H. et al. Gut 55:1781-1788(2006) · Mapped (48) |
| Colorectal cancer and the CHEK2 1100delC mutation. de Jong M.M., Nolte I.M., Te Meerman G.J., van der Graaf W.T., Mulder M.J., van der Steege G., Bruinenberg M., Schaapveld M., Niessen R.C., Berends M.J. et al. Genes Chromosomes Cancer 43:377-382(2005) · Mapped (3) |
| No association between two MLH3 variants (S845G and P844L)and colorectal cancer risk. de Jong M.M., Hofstra R.M., Kooi K.A., Westra J.L., Berends M.J., Wu Y., Hollema H., van der Sluis T., van der Graaf W.T., de Vries E.G. et al. Cancer Genet. Cytogenet. 152:70-71(2004) · Mapped (6) |
| Toward new strategies to select young endometrial cancer patients for mismatch repair gene mutation analysis. Berends M.J., Wu Y., Sijmons R.H., van der Sluis T., Ek W.B., Ligtenberg M.J., Arts N.J., ten Hoor K.A., Kleibeuker J.H., de Vries E.G. et al. J. Clin. Oncol. 21:4364-4370(2003) · Mapped (48) |
| Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant. Berends M.J.W., Wu Y., Sijmons R.H., Mensink R.G.J., van der Sluis T., Hordijk-Hos J.M., de Vries E.G.E., Hollema H., Karrenbeld A., Buys C.H.C.M. et al. Am. J. Hum. Genet. 70:26-37(2002) · UniProtKB (1) · Mapped (5) |
| A role for MLH3 in hereditary nonpolyposis colorectal cancer. Wu Y., Berends M.J.W., Sijmons R.H., Mensink R.G.J., Verlind E., Kooi K.A., van der Sluis T., Kempinga C., van der Zee A.G.J., Hollema H. et al. |
| Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms. Wu Y., Berends M.J.W., Post J.G., Mensink R.G.J., Verlind E., van der Sluis T., Kempinga C., Sijmons R.H., van der Zee A.G.J., Hollema H. et al. Gastroenterology 120:1580-1587(2001) · UniProtKB (1) |
| Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. Wu Y., Berends M.J.W., Mensink R.G.J., Kempinga C., Sijmons R.H., van Der Zee A.G.J., Hollema H., Kleibeuker J.H., Buys C.H.C.M., Hofstra R.M.W. Am. J. Hum. Genet. 65:1291-1298(1999) · UniProtKB (1) |