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Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
Circulation. 2009 Nov 3;120(18):1752-60. doi: 10.1161/CIRCULATIONAHA.109.863076. Epub 2009 Oct 19.
Circulation. 2009.
PMID: 19841300
Free PMC article.
The structure of common genetic variation in United States populations.
Guthery SL, Salisbury BA, Pungliya MS, Stephens JC, Bamshad M.
Guthery SL, et al. Among authors: pungliya ms.
Am J Hum Genet. 2007 Dec;81(6):1221-31. doi: 10.1086/522239. Epub 2007 Oct 16.
Am J Hum Genet. 2007.
PMID: 17999361
Free PMC article.
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Genetic variability and evolution of two pharmacologically important classes of genes.
Pungliya MS, Salisbury BA, Nandabalan K, Stephens JC.
Pungliya MS, et al.
Pharmacogenomics. 2004 Jan;5(1):115-27. doi: 10.1517/phgs.5.1.115.25684.
Pharmacogenomics. 2004.
PMID: 14683423
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SNP and haplotype variation in the human genome.
Salisbury BA, Pungliya M, Choi JY, Jiang R, Sun XJ, Stephens JC.
Salisbury BA, et al.
Mutat Res. 2003 May 15;526(1-2):53-61. doi: 10.1016/s0027-5107(03)00014-9.
Mutat Res. 2003.
PMID: 12714183
Review.
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DNA variability of human genes.
Schneider JA, Pungliya MS, Choi JY, Jiang R, Sun XJ, Salisbury BA, Stephens JC.
Schneider JA, et al. Among authors: pungliya ms.
Mech Ageing Dev. 2003 Jan;124(1):17-25. doi: 10.1016/s0047-6374(02)00165-3.
Mech Ageing Dev. 2003.
PMID: 12618002
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Genome-wide association of haplotype markers to gene expression levels.
Windemuth A, Kumar M, Nandabalan K, Koshy B, Xu C, Pungliya M, Judson R.
Windemuth A, et al.
Cold Spring Harb Symp Quant Biol. 2003;68:89-107. doi: 10.1101/sqb.2003.68.89.
Cold Spring Harb Symp Quant Biol. 2003.
PMID: 15338607
No abstract available.
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Computational methods for single-point and multipoint analysis of genetic variants associated with a simulated complex disorder in a general population.
Shoemaker CA, Pungliya M, Sao Pedro MA, Ruiz C, Alvarez SA, Ward M, Ryder EF, Krushkal J.
Shoemaker CA, et al.
Genet Epidemiol. 2001;21 Suppl 1:S738-45. doi: 10.1002/gepi.2001.21.s1.s738.
Genet Epidemiol. 2001.
PMID: 11793771
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