222 related articles for article (PubMed ID: 15520224)
1. Localization of cancer susceptibility genes by genome-wide single-nucleotide polymorphism linkage-disequilibrium mapping.
Mitra N; Ye TZ; Smith A; Chuai S; Kirchhoff T; Peterlongo P; Nafa K; Phillips MS; Offit K; Ellis NA
Cancer Res; 2004 Nov; 64(21):8116-25. PubMed ID: 15520224
[TBL] [Abstract][Full Text] [Related]
2. The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.
Foulkes WD; Thiffault I; Gruber SB; Horwitz M; Hamel N; Lee C; Shia J; Markowitz A; Figer A; Friedman E; Farber D; Greenwood CM; Bonner JD; Nafa K; Walsh T; Marcus V; Tomsho L; Gebert J; Macrae FA; Gaff CL; Paillerets BB; Gregersen PK; Weitzel JN; Gordon PH; MacNamara E; King MC; Hampel H; De La Chapelle A; Boyd J; Offit K; Rennert G; Chong G; Ellis NA
Am J Hum Genet; 2002 Dec; 71(6):1395-412. PubMed ID: 12454801
[TBL] [Abstract][Full Text] [Related]
3. Ashkenazi Jewish population frequency of the Bloom syndrome gene 2281 delta 6ins7 mutation.
Roa BB; Savino CV; Richards CS
Genet Test; 1999; 3(2):219-21. PubMed ID: 10464671
[TBL] [Abstract][Full Text] [Related]
4. Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping.
Ellis NA; Kirchhoff T; Mitra N; Ye TZ; Chuai S; Huang H; Nafa K; Norton L; Neuhausen S; Gordon D; Struewing JP; Narod S; Offit K
Genet Epidemiol; 2006 Jan; 30(1):48-61. PubMed ID: 16206141
[TBL] [Abstract][Full Text] [Related]
5. Clinical and genetic findings in an Ashkenazi Jewish population with colorectal neoplasms.
Zauber NP; Sabbath-Solitare M; Marotta S; Zauber AG; Foulkes W; Chan M; Turner F; Bishop DT
Cancer; 2005 Aug; 104(4):719-29. PubMed ID: 15959913
[TBL] [Abstract][Full Text] [Related]
6. Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population.
Li L; Eng C; Desnick RJ; German J; Ellis NA
Mol Genet Metab; 1998 Aug; 64(4):286-90. PubMed ID: 9758720
[TBL] [Abstract][Full Text] [Related]
7. High frequency of a common Bloom syndrome Ashkenazi mutation among Jews of Polish origin.
Shahrabani-Gargir L; Shomrat R; Yaron Y; Orr-Urtreger A; Groden J; Legum C
Genet Test; 1998; 2(4):293-6. PubMed ID: 10464606
[TBL] [Abstract][Full Text] [Related]
8. The coding region of the Bloom syndrome BLM gene and of the CBL proto-oncogene is mutated in genetically unstable sporadic gastrointestinal tumors.
Calin G; Herlea V; Barbanti-Brodano G; Negrini M
Cancer Res; 1998 Sep; 58(17):3777-81. PubMed ID: 9731483
[TBL] [Abstract][Full Text] [Related]
9. A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene.
Straughen JE; Johnson J; McLaren D; Proytcheva M; Ellis N; German J; Groden J
Hum Mutat; 1998; 11(2):175-8. PubMed ID: 9482582
[TBL] [Abstract][Full Text] [Related]
10. The HNPCC associated MSH2*1906G-->C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population.
Sun S; Greenwood CM; Thiffault I; Hamel N; Chong G; Foulkes WD
J Med Genet; 2005 Oct; 42(10):766-8. PubMed ID: 16199548
[TBL] [Abstract][Full Text] [Related]
11. The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry.
Ellis NA; Ciocci S; Proytcheva M; Lennon D; Groden J; German J
Am J Hum Genet; 1998 Dec; 63(6):1685-93. PubMed ID: 9837821
[TBL] [Abstract][Full Text] [Related]
12. A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer.
Froggatt NJ; Green J; Brassett C; Evans DG; Bishop DT; Kolodner R; Maher ER
J Med Genet; 1999 Feb; 36(2):97-102. PubMed ID: 10051005
[TBL] [Abstract][Full Text] [Related]
13. A636P is associated with early-onset colon cancer in Ashkenazi Jews.
Guillem JG; Rapaport BS; Kirchhoff T; Kolachana P; Nafa K; Glogowski E; Finch R; Huang H; Foulkes WD; Markowitz A; Ellis NA; Offit K
J Am Coll Surg; 2003 Feb; 196(2):222-5. PubMed ID: 12595050
[TBL] [Abstract][Full Text] [Related]
14. A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region.
Baffoe-Bonnie AB; Smith JR; Stephan DA; Schleutker J; Carpten JD; Kainu T; Gillanders EM; Matikainen M; Teslovich TM; Tammela T; Sood R; Balshem AM; Scarborough SD; Xu J; Isaacs WB; Trent JM; Kallioniemi OP; Bailey-Wilson JE
Hum Genet; 2005 Aug; 117(4):307-16. PubMed ID: 15906096
[TBL] [Abstract][Full Text] [Related]
15. Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome.
Ellis NA; Roe AM; Kozloski J; Proytcheva M; Falk C; German J
Am J Hum Genet; 1994 Sep; 55(3):453-60. PubMed ID: 8079989
[TBL] [Abstract][Full Text] [Related]
16. Physical mapping of the bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1.
Straughen J; Ciocci S; Ye TZ; Lennon DN; Proytcheva M; Alhadeff B; Goodfellow P; German J; Ellis NA; Groden J
Genomics; 1996 Jul; 35(1):118-28. PubMed ID: 8661112
[TBL] [Abstract][Full Text] [Related]
17. Haplotype and linkage disequilibrium architecture for human cancer-associated genes.
Bonnen PE; Wang PJ; Kimmel M; Chakraborty R; Nelson DL
Genome Res; 2002 Dec; 12(12):1846-53. PubMed ID: 12466288
[TBL] [Abstract][Full Text] [Related]
18. Clinical features of Bloom syndrome and function of the causative gene, BLM helicase.
Kaneko H; Kondo N
Expert Rev Mol Diagn; 2004 May; 4(3):393-401. PubMed ID: 15137905
[TBL] [Abstract][Full Text] [Related]
19. BLM heterozygosity and the risk of colorectal cancer.
Gruber SB; Ellis NA; Scott KK; Almog R; Kolachana P; Bonner JD; Kirchhoff T; Tomsho LP; Nafa K; Pierce H; Low M; Satagopan J; Rennert H; Huang H; Greenson JK; Groden J; Rapaport B; Shia J; Johnson S; Gregersen PK; Harris CC; Boyd J; Rennert G; Offit K
Science; 2002 Sep; 297(5589):2013. PubMed ID: 12242432
[No Abstract] [Full Text] [Related]
20. Colorectal cancer and polymorphisms in DNA repair genes WRN, RMI1 and BLM.
Frank B; Hoffmeister M; Klopp N; Illig T; Chang-Claude J; Brenner H
Carcinogenesis; 2010 Mar; 31(3):442-5. PubMed ID: 19945966
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
