An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP).

Gu C, Hunt SC, Kardia S, Turner ST, Chakravarti A, Schork N, Olshen R, Curb D, Jaquish C, Boerwinkle E, Rao DC: An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP). Hum Genet 121:577-590, 2007. PMID 17372766.

Multiple Essential Hypertension Susceptibility Genes On Chromosome 1q.

Chang YP, Liu X, Ikeda MA, Kim JDO, Layton M, Weder A, Cooper R, Kardia S, Rao DC, Hunt S, Luke A, Boerwinkle E, Chakravarti A: Multiple Essential Hypertension Susceptibility Genes On Chromosome 1q. Amer J Hum Genet 80:253-264, 2007. PMID 17236131. PMC1785356.

The fate of 12 recessive mutations in a single village.

Zlotogora J, et al: The fate of 12 recessive mutations in a single village. Ann Hum Genet 71:202-208, 2007. PMID 17331080.

Cutting GR and the CF Twin and Sibling Study: Relative contribution of genetic and non-genetic modifiers to intestinal obstruction in cystic fibrosis.

Blackman SM, Deering-Brose R, McWilliams R, Naughton K, Coleman B, Lai T, Algire M, Beck S, Hoover-Fong J, Hamosh A, Fallin MD, West K, Arking DE, Chakravarti A, Cutler D, Cutting GR and the CF Twin and Sibling Study: Relative contribution of genetic and non-genetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology 131:1030-1039, 2006. PMID 17030173. PMC1764617.

Human embryonic stem cells have a unique epigenetic signature.

Bibikova M, Chudin E, Wu B, Zhou L, Garcia EW, Liu Y, Shin S, Plaia TW, Auerbach JM, Arking DE, Gonzalez R, Crook J, Davidson B, Schulz TC, Robins A, Khanna A, Sartipy P, Hyllner J, Vanguri P, Savant-Bhonsale S, Smith AK, Chakravarti A, Maitra A, Rao M, Barker DL, Loring JF, Fan JB: Human embryonic stem cells have a unique epigenetic signature. Genome Res 16:1075-1083, 2006. PMID 16899657. PMC1557765.

Identifying Allelic Loss and Homozygous Deletions in Pancreatic Cancer Without Matched Normals Using High-density SNP Arrays.

Calhoun ES, Hucl T, Gallmeier E, West KM, Arking DE, Maitra A, Iacobuzio-Donahue CA, Chakravarti A, Hruban RH, Kern SE: Identifying Allelic Loss and Homozygous Deletions in Pancreatic Cancer Without Matched Normals Using High-density SNP Arrays. Cancer Res 66:7920-7928, 2006. PMID 16912165.

A common genetic variant in the nNOS regulator CAPON modulates cardiac repolarization (QT interval).

Arking DE, Pfeufer A, Post W, Kao WHL, Ikeda M, West K, Kashuk C, Akyol M, Perz S, Jalilzadeh S, Illig T, Wichmann HE, Marban E, Kaab S, Spooner PM, Meitinger T, Chakravarti A: A common genetic variant in the nNOS regulator CAPON modulates cardiac repolarization (QT interval). Nat Genet 38:644-651, 2006. PMID 16648850.

Variation in the ciliary neurotrophic factor gene and muscle strength in older Caucasian women.

Arking DE, Walston J, Fallin D, Li T, Beamer B, Xue QL, Fried LP, Chakravarti A: Variation in the ciliary neurotrophic factor gene and muscle strength in older Caucasian women. J Amer Geriat Soc 54:823-826, 2006. PMID 16696750.

Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program.

Laramie JM, Wilk JB, Hunt SC, Ellison RC, Chakravarti A, Boerwinkle E, Myers RH: Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program. BMC Med Genet 7:17, 2006. PMID 16509988. PMC1413518.

The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.

Chang YP, Kim JD, Schwander K, Rao DC, Miller MB, Weder AB, Cooper RS, Schork NJ, Province MA, Morrison AC, Kardia SL, Quertermous T, Chakravarti A: The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program. Eur J Hum Genet 14:469-477, 2006. PMID 16493446.