Hunt SC - Search Results

1

The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study.

Franceschini N, North KE, Arnett D, Pankow JS, Chung JH, Baird L, Leppert MF, Eckfeldt JH, Boerwinkle E, Gu CC, Lewis CE, Myers RH, Turner ST, Weder A, Kao WH, Mosley TH, Chakravarti A, Kramer H, Zhang J, Hunt SC. Franceschini N, et al. Among authors: hunt sc. Am J Hypertens. 2009 May;22(5):552-8. doi: 10.1038/ajh.2009.41. Epub 2009 Mar 5. Am J Hypertens. 2009. PMID: 19265784 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

Gender difference in diastolic function in hypertension (the HyperGEN study).

Bella JN, Palmieri V, Kitzman DW, Liu JE, Oberman A, Hunt SC, Hopkins PN, Rao DC, Arnett DK, Devereux RB. Bella JN, et al. Among authors: hunt sc. Am J Cardiol. 2002 May 1;89(9):1052-6. doi: 10.1016/s0002-9149(02)02274-9. Am J Cardiol. 2002. PMID: 11988194

4

Influence of apolipoprotein E, smoking, and alcohol intake on carotid atherosclerosis: National Heart, Lung, and Blood Institute Family Heart Study.

Djoussé L, Myers RH, Province MA, Hunt SC, Eckfeldt JH, Evans G, Peacock JM, Ellison RC. Djoussé L, et al. Among authors: hunt sc. Stroke. 2002 May;33(5):1357-61. doi: 10.1161/01.str.0000014325.54063.1a. Stroke. 2002. PMID: 11988615

5

Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study.

DeWan AT, Arnett DK, Miller MB, Peacock JM, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt JH. DeWan AT, et al. Among authors: hunt sc. Am J Hum Genet. 2002 Jul;71(1):204-5. doi: 10.1086/340730. Am J Hum Genet. 2002. PMID: 12068377 Free PMC article. No abstract available.

6

Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees.

Kronenberg F, Coon H, Ellison RC, Borecki I, Arnett DK, Province MA, Eckfeldt JH, Hopkins PN, Hunt SC. Kronenberg F, et al. Among authors: hunt sc. Eur J Hum Genet. 2002 Jun;10(6):367-74. doi: 10.1038/sj.ejhg.5200818. Eur J Hum Genet. 2002. PMID: 12080388

7

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

8

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

9

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.

10

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

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