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Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group.
Ghosh S, Karanjawala ZE, Hauser ER, Ally D, Knapp JI, Rayman JB, Musick A, Tannenbaum J, Te C, Shapiro S, Eldridge W, Musick T, Martin C, Smith JR, Carpten JD, Brownstein MJ, Powell JI, Whiten R, Chines P, Nylund SJ, Magnuson VL, Boehnke M, Collins FS. Ghosh S, et al. Among authors: collins fs. Genome Res. 1997 Feb;7(2):165-78. doi: 10.1101/gr.7.2.165. Genome Res. 1997. PMID: 9049634 Free article.
The geneticist's approach to complex disease.
Ghosh S, Collins FS. Ghosh S, et al. Among authors: collins fs. Annu Rev Med. 1996;47:333-53. doi: 10.1146/annurev.med.47.1.333. Annu Rev Med. 1996. PMID: 8712786 Review.
Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search.
Smith JR, Freije D, Carpten JD, Grönberg H, Xu J, Isaacs SD, Brownstein MJ, Bova GS, Guo H, Bujnovszky P, Nusskern DR, Damber JE, Bergh A, Emanuelsson M, Kallioniemi OP, Walker-Daniels J, Bailey-Wilson JE, Beaty TH, Meyers DA, Walsh PC, Collins FS, Trent JM, Isaacs WB. Smith JR, et al. Among authors: collins fs. Science. 1996 Nov 22;274(5291):1371-4. doi: 10.1126/science.274.5291.1371. Science. 1996. PMID: 8910276
A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.
Kittles RA, Baffoe-Bonnie AB, Moses TY, Robbins CM, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent JM, Collins FS, Mousses S, Bailey-Wilson J, Furbert-Harris P, Dunston G, Powell IJ, Carpten JD. Kittles RA, et al. Among authors: collins fs. J Med Genet. 2006 Jun;43(6):507-11. doi: 10.1136/jmg.2005.035790. Epub 2005 Sep 9. J Med Genet. 2006. PMID: 16155194 Free PMC article.
715 results