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1,395 results
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Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer.
Grady WM, Willis J, Guilford PJ, Dunbier AK, Toro TT, Lynch H, Wiesner G, Ferguson K, Eng C, Park JG, Kim SJ, Markowitz S. Grady WM, et al. Nat Genet. 2000 Sep;26(1):16-7. doi: 10.1038/79120. Nat Genet. 2000. PMID: 10973239
E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer.
Guilford PJ, Hopkins JB, Grady WM, Markowitz SD, Willis J, Lynch H, Rajput A, Wiesner GL, Lindor NM, Burgart LJ, Toro TT, Lee D, Limacher JM, Shaw DW, Findlay MP, Reeve AE. Guilford PJ, et al. Hum Mutat. 1999;14(3):249-55. doi: 10.1002/(SICI)1098-1004(1999)14:3<249::AID-HUMU8>3.0.CO;2-9. Hum Mutat. 1999. PMID: 10477433
Hereditary diffuse gastric cancer: association with lobular breast cancer.
Schrader KA, Masciari S, Boyd N, Wiyrick S, Kaurah P, Senz J, Burke W, Lynch HT, Garber JE, Huntsman DG. Schrader KA, et al. Fam Cancer. 2008;7(1):73-82. doi: 10.1007/s10689-007-9172-6. Fam Cancer. 2008. PMID: 18046629 Free PMC article. Review.
An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer.
Lynch HT, Watson P, Tinley S, Snyder C, Durham C, Lynch J, Kirnarsky Y, Serova O, Lenoir G, Lerman C, Narod SA. Lynch HT, et al. Cancer Genet Cytogenet. 1999 Mar;109(2):91-8. doi: 10.1016/s0165-4608(98)00165-4. Cancer Genet Cytogenet. 1999. PMID: 10087939
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.
Phelan CM, Rebbeck TR, Weber BL, Devilee P, Ruttledge MH, Lynch HT, Lenoir GM, Stratton MR, Easton DF, Ponder BA, Cannon-Albright L, Larsson C, Goldgar DE, Narod SA. Phelan CM, et al. Nat Genet. 1996 Mar;12(3):309-11. doi: 10.1038/ng0396-309. Nat Genet. 1996. PMID: 8589723
Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond.
Hansford S, Kaurah P, Li-Chang H, Woo M, Senz J, Pinheiro H, Schrader KA, Schaeffer DF, Shumansky K, Zogopoulos G, Santos TA, Claro I, Carvalho J, Nielsen C, Padilla S, Lum A, Talhouk A, Baker-Lange K, Richardson S, Lewis I, Lindor NM, Pennell E, MacMillan A, Fernandez B, Keller G, Lynch H, Shah SP, Guilford P, Gallinger S, Corso G, Roviello F, Caldas C, Oliveira C, Pharoah PD, Huntsman DG. Hansford S, et al. JAMA Oncol. 2015 Apr;1(1):23-32. doi: 10.1001/jamaoncol.2014.168. JAMA Oncol. 2015. PMID: 26182300 Clinical Trial.
[Hereditary diffuse gastric cancer (HDGC): presentation of a family with a new mutation of the CDH1 gene].
Van Domselaar F, Correa D, Vaccaro C, Redal M, Van Domselaar R, Huntsman D, Kaurah P, Senz J, Lynch H. Van Domselaar F, et al. Acta Gastroenterol Latinoam. 2007 Sep;37(3):158-63. Acta Gastroenterol Latinoam. 2007. PMID: 17955726 Spanish.
A polymorphic stop codon in BRCA2.
Mazoyer S, Dunning AM, Serova O, Dearden J, Puget N, Healey CS, Gayther SA, Mangion J, Stratton MR, Lynch HT, Goldgar DE, Ponder BA, Lenoir GM. Mazoyer S, et al. Nat Genet. 1996 Nov;14(3):253-4. doi: 10.1038/ng1196-253. Nat Genet. 1996. PMID: 8896551 No abstract available.
The risk of breast cancer in BRCA1 and BRCA2 mutation carriers without a first-degree relative with breast cancer.
Metcalfe KA, Lubinski J, Gronwald J, Huzarski T, McCuaig J, Lynch HT, Karlan B, Foulkes WD, Singer CF, Neuhausen SL, Senter L, Eisen A, Sun P, Narod SA; Hereditary Breast Cancer Clinical Study Group. Metcalfe KA, et al. Clin Genet. 2018 May;93(5):1063-1068. doi: 10.1111/cge.13191. Epub 2018 Mar 25. Clin Genet. 2018. PMID: 29206279
Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat.
Rebbeck TR, Kantoff PW, Krithivas K, Neuhausen S, Blackwood MA, Godwin AK, Daly MB, Narod SA, Garber JE, Lynch HT, Weber BL, Brown M. Rebbeck TR, et al. Am J Hum Genet. 1999 May;64(5):1371-7. doi: 10.1086/302366. Am J Hum Genet. 1999. PMID: 10205268 Free PMC article.
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