Fain PR - Search Results

1

A high resolution CEPH crossover mapping panel and integrated map of chromosome 11.

Fain PR, Kort EN, Yousry C, James MR, Litt M. Fain PR, et al. Hum Mol Genet. 1996 Oct;5(10):1631-6. doi: 10.1093/hmg/5.10.1631. Hum Mol Genet. 1996. PMID: 8894699

2

The CEPH consortium linkage map of human chromosome 11.

Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, Weissenbach J, Donis-Keller H, Gatti R, et al. Litt M, et al. Genomics. 1995 May 1;27(1):101-12. doi: 10.1006/geno.1995.1011. Genomics. 1995. PMID: 7665156 Free article.

3

A 2D crossover-based map of the human X chromosome as a model for map integration.

Fain PR, Kort EN, Chance PF, Nguyen K, Redd DF, Econs MJ, Barker DF. Fain PR, et al. Nat Genet. 1995 Mar;9(3):261-6. doi: 10.1038/ng0395-261. Nat Genet. 1995. PMID: 7773289

4

Localization of the highly polymorphic microsatellite DXS456 on the genetic linkage map of the human X chromosome.

Fain PR, Luty JA, Guo Z, Nguyen K, Barker DF, Litt M. Fain PR, et al. Genomics. 1991 Dec;11(4):1155-7. doi: 10.1016/0888-7543(91)90045-g. Genomics. 1991. PMID: 1686017

5

Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2.

Alkhateeb A, Stetler GL, Old W, Talbert J, Uhlhorn C, Taylor M, Fox A, Miller C, Dills DG, Ridgway EC, Bennett DC, Fain PR, Spritz RA. Alkhateeb A, et al. Among authors: fain pr. Hum Mol Genet. 2002 Mar 15;11(6):661-7. doi: 10.1093/hmg/11.6.661. Hum Mol Genet. 2002. PMID: 11912181

6

Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores.

Nechiporuk A, Fain P, Kort E, Nee LE, Frommelt E, Polinsky RJ, Korenberg JR, Pulst SM. Nechiporuk A, et al. Am J Med Genet. 1993 May 1;48(1):63-6. doi: 10.1002/ajmg.1320480113. Am J Med Genet. 1993. PMID: 8357039

7

A genomewide screen for generalized vitiligo: confirmation of AIS1 on chromosome 1p31 and evidence for additional susceptibility loci.

Fain PR, Gowan K, LaBerge GS, Alkhateeb A, Stetler GL, Talbert J, Bennett DC, Spritz RA. Fain PR, et al. Am J Hum Genet. 2003 Jun;72(6):1560-4. doi: 10.1086/375451. Epub 2003 Apr 18. Am J Hum Genet. 2003. PMID: 12707860 Free PMC article.

8

Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene.

You M, Wang D, Liu P, Vikis H, James M, Lu Y, Wang Y, Wang M, Chen Q, Jia D, Liu Y, Wen W, Yang P, Sun Z, Pinney SM, Zheng W, Shu XO, Long J, Gao YT, Xiang YB, Chow WH, Rothman N, Petersen GM, de Andrade M, Wu Y, Cunningham JM, Wiest JS, Fain PR, Schwartz AG, Girard L, Gazdar A, Gaba C, Rothschild H, Mandal D, Coons T, Lee J, Kupert E, Seminara D, Minna J, Bailey-Wilson JE, Amos CI, Anderson MW. You M, et al. Among authors: fain pr. Clin Cancer Res. 2009 Apr 15;15(8):2666-74. doi: 10.1158/1078-0432.CCR-08-2335. Epub 2009 Apr 7. Clin Cancer Res. 2009. PMID: 19351763 Free PMC article.

9

Refined physical and genetic mapping of the NF1 region on chromosome 17.

Fain PR, Goldgar DE, Wallace MR, Collins FS, Wright E, Nguyen K, Barker DF. Fain PR, et al. Am J Hum Genet. 1989 Nov;45(5):721-8. Am J Hum Genet. 1989. PMID: 2573276 Free PMC article.

10

Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab family.

Verge CF, Vardi P, Babu S, Bao F, Erlich HA, Bugawan T, Tiosano D, Yu L, Eisenbarth GS, Fain PR. Verge CF, et al. Among authors: fain pr. J Clin Invest. 1998 Oct 15;102(8):1569-75. doi: 10.1172/JCI3379. J Clin Invest. 1998. PMID: 9788970 Free PMC article.

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