Hunt SC - Search Results

1

Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations.

North KE, Franceschini N, Avery CL, Baird L, Graff M, Leppert M, Chung JH, Zhang J, Hanis C, Boerwinkle E, Volcik KA, Grove ML, Mosley TH, Gu C, Heiss G, Pankow JS, Couper DJ, Ballantyne CM, Linda Kao WH, Weder AB, Cooper RS, Ehret GB, O'Connor AA, Chakravarti A, Hunt SC. North KE, et al. Among authors: hunt sc. Acta Diabetol. 2010 Dec;47 Suppl 1(Suppl 1):199-207. doi: 10.1007/s00592-009-0162-z. Epub 2009 Oct 24. Acta Diabetol. 2010. PMID: 19855918 Free PMC article.

2

Familial history of stroke and stroke risk. The Family Heart Study.

Liao D, Myers R, Hunt S, Shahar E, Paton C, Burke G, Province M, Heiss G. Liao D, et al. Stroke. 1997 Oct;28(10):1908-12. doi: 10.1161/01.str.28.10.1908. Stroke. 1997. PMID: 9341694

3

Genome scans for blood pressure and hypertension: the National Heart, Lung, and Blood Institute Family Heart Study.

Hunt SC, Ellison RC, Atwood LD, Pankow JS, Province MA, Leppert MF. Hunt SC, et al. Hypertension. 2002 Jul;40(1):1-6. doi: 10.1161/01.hyp.0000022660.28915.b1. Hypertension. 2002. PMID: 12105129

4

A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study.

Coon H, Eckfeldt JH, Leppert MF, Myers RH, Arnett DK, Heiss G, Province MA, Hunt SC. Coon H, et al. Among authors: hunt sc. Hum Genet. 2002 Sep;111(3):263-9. doi: 10.1007/s00439-002-0773-8. Epub 2002 Jul 31. Hum Genet. 2002. PMID: 12215839

5

Regarding "Testing for population subdivision and association in four case-control studies".

Pankow JS, Province MA, Hunt SC, Arnett DK. Pankow JS, et al. Among authors: hunt sc. Am J Hum Genet. 2002 Dec;71(6):1478-80. doi: 10.1086/344582. Am J Hum Genet. 2002. PMID: 12515254 Free PMC article. No abstract available.

6

Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript.

Dunn DM, Ishigami T, Pankow J, von Niederhausern A, Alder J, Hunt SC, Leppert MF, Lalouel JM, Weiss RB. Dunn DM, et al. Among authors: hunt sc. J Hum Genet. 2002;47(12):665-76. doi: 10.1007/s100380200102. J Hum Genet. 2002. PMID: 12522688

7

A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program.

Province MA, Kardia SL, Ranade K, Rao DC, Thiel BA, Cooper RS, Risch N, Turner ST, Cox DR, Hunt SC, Weder AB, Boerwinkle E; National Heart, Lung and Blood Institute Family Blood Pressure Program. Province MA, et al. Among authors: hunt sc. Am J Hypertens. 2003 Feb;16(2):144-7. doi: 10.1016/s0895-7061(02)03248-x. Am J Hypertens. 2003. PMID: 12559682

8

Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study.

Hopkins PN, Heiss G, Ellison RC, Province MA, Pankow JS, Eckfeldt JH, Hunt SC. Hopkins PN, et al. Among authors: hunt sc. Circulation. 2003 Aug 5;108(5):519-23. doi: 10.1161/01.CIR.0000081777.17879.85. Epub 2003 Jul 7. Circulation. 2003. PMID: 12847072

9

Positional identification of hypertension susceptibility genes on chromosome 2.

Barkley RA, Chakravarti A, Cooper RS, Ellison RC, Hunt SC, Province MA, Turner ST, Weder AB, Boerwinkle E; Family Blood Pressure Program. Barkley RA, et al. Among authors: hunt sc. Hypertension. 2004 Feb;43(2):477-82. doi: 10.1161/01.HYP.0000111585.76299.f7. Epub 2004 Jan 19. Hypertension. 2004. PMID: 14732741

10

Evidence for a gene on chromosome 13 influencing postural systolic blood pressure change and body mass index.

North KE, Rose KM, Borecki IB, Oberman A, Hunt SC, Miller MB, Blangero J, Almasy L, Pankow JS. North KE, et al. Among authors: hunt sc. Hypertension. 2004 Apr;43(4):780-4. doi: 10.1161/01.HYP.0000118921.66329.da. Epub 2004 Feb 16. Hypertension. 2004. PMID: 14967843

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