Patil N - Search Results

1

Characterization of single-nucleotide polymorphisms in coding regions of human genes.

Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, Patil N, Shaw N, Lane CR, Lim EP, Kalyanaraman N, Nemesh J, Ziaugra L, Friedland L, Rolfe A, Warrington J, Lipshutz R, Daley GQ, Lander ES. Cargill M, et al. Among authors: patil n. Nat Genet. 1999 Jul;22(3):231-8. doi: 10.1038/10290. Nat Genet. 1999. PMID: 10391209

2

Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse.

Lindblad-Toh K, Winchester E, Daly MJ, Wang DG, Hirschhorn JN, Laviolette JP, Ardlie K, Reich DE, Robinson E, Sklar P, Shah N, Thomas D, Fan JB, Gingeras T, Warrington J, Patil N, Hudson TJ, Lander ES. Lindblad-Toh K, et al. Among authors: patil n. Nat Genet. 2000 Apr;24(4):381-6. doi: 10.1038/74215. Nat Genet. 2000. PMID: 10742102

3

Fine-scale recombination patterns differ between chimpanzees and humans.

Ptak SE, Hinds DA, Koehler K, Nickel B, Patil N, Ballinger DG, Przeworski M, Frazer KA, Pääbo S. Ptak SE, et al. Among authors: patil n. Nat Genet. 2005 Apr;37(4):429-34. doi: 10.1038/ng1529. Epub 2005 Feb 18. Nat Genet. 2005. PMID: 15723063 Free article.

4

Single-nucleotide polymorphism genotyping using microarrays.

Patil N, Nouri N, McAllister L, Matsukaki H, Ryder T. Patil N, et al. Curr Protoc Hum Genet. 2001 May;Chapter 2:Unit 2.9. doi: 10.1002/0471142905.hg0209s27. Curr Protoc Hum Genet. 2001. PMID: 18428273

5

A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation.

Patil N, Cox DR, Bhat D, Faham M, Myers RM, Peterson AS. Patil N, et al. Nat Genet. 1995 Oct;11(2):126-9. doi: 10.1038/ng1095-126. Nat Genet. 1995. PMID: 7550338

6

Sequence diversity in genes of lipid metabolism.

Garcia CK, Mues G, Liao Y, Hyatt T, Patil N, Cohen JC, Hobbs HH. Garcia CK, et al. Among authors: patil n. Genome Res. 2001 Jun;11(6):1043-52. doi: 10.1101/gr.172301. Genome Res. 2001. PMID: 11381031 Free PMC article.

7

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

Patil N, Berno AJ, Hinds DA, Barrett WA, Doshi JM, Hacker CR, Kautzer CR, Lee DH, Marjoribanks C, McDonough DP, Nguyen BT, Norris MC, Sheehan JB, Shen N, Stern D, Stokowski RP, Thomas DJ, Trulson MO, Vyas KR, Frazer KA, Fodor SP, Cox DR. Patil N, et al. Science. 2001 Nov 23;294(5547):1719-23. doi: 10.1126/science.1065573. Science. 2001. PMID: 11721056

8

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays.

Mei R, Galipeau PC, Prass C, Berno A, Ghandour G, Patil N, Wolff RK, Chee MS, Reid BJ, Lockhart DJ. Mei R, et al. Among authors: patil n. Genome Res. 2000 Aug;10(8):1126-37. doi: 10.1101/gr.10.8.1126. Genome Res. 2000. PMID: 10958631 Free PMC article.

9

Matching strategies for genetic association studies in structured populations.

Hinds DA, Stokowski RP, Patil N, Konvicka K, Kershenobich D, Cox DR, Ballinger DG. Hinds DA, et al. Among authors: patil n. Am J Hum Genet. 2004 Feb;74(2):317-25. doi: 10.1086/381716. Epub 2004 Jan 21. Am J Hum Genet. 2004. PMID: 14740319 Free PMC article.

10

A transcript map of the Down syndrome critical region on chromosome 21.

Peterson A, Patil N, Robbins C, Wang L, Cox DR, Myers RM. Peterson A, et al. Among authors: patil n. Hum Mol Genet. 1994 Oct;3(10):1735-42. doi: 10.1093/hmg/3.10.1735. Hum Mol Genet. 1994. PMID: 7849696

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