Coon H - Search Results

1

Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p.

Drayna D, Coon H, Kim UK, Elsner T, Cromer K, Otterud B, Baird L, Peiffer AP, Leppert M; Utah Genetic Reference Project. Drayna D, et al. Among authors: coon h. Hum Genet. 2003 May;112(5-6):567-72. doi: 10.1007/s00439-003-0911-y. Epub 2003 Mar 6. Hum Genet. 2003. PMID: 12624758

2

Genomic scan for genes predisposing to schizophrenia.

Coon H, Jensen S, Holik J, Hoff M, Myles-Worsley M, Reimherr F, Wender P, Waldo M, Freedman R, Leppert M, et al. Coon H, et al. Am J Med Genet. 1994 Mar 15;54(1):59-71. doi: 10.1002/ajmg.1320540111. Am J Med Genet. 1994. PMID: 7909992

3

A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance.

Coon H, Jensen S, Hoff M, Holik J, Plaetke R, Reimherr F, Wender P, Leppert M, Byerley W. Coon H, et al. Am J Hum Genet. 1993 Jun;52(6):1234-49. Am J Hum Genet. 1993. PMID: 8503452 Free PMC article.

4

Linkage analysis of schizophrenia: the D1 dopamine receptor gene and several flanking DNA markers.

Jensen S, Plaetke R, Holik J, Hoff M, Myles-Worsley M, Leppert M, Coon H, Vest K, Freedman R, Waldo M, et al. Jensen S, et al. Among authors: coon h. Hum Hered. 1993 Jan-Feb;43(1):58-62. doi: 10.1159/000154115. Hum Hered. 1993. PMID: 8514328

5

Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q.

Hobbs MR, Pole AR, Pidwirny GN, Rosen IB, Zarbo RJ, Coon H, Heath H 3rd, Leppert M, Jackson CE. Hobbs MR, et al. Among authors: coon h. Am J Hum Genet. 1999 Feb;64(2):518-25. doi: 10.1086/302259. Am J Hum Genet. 1999. PMID: 9973288 Free PMC article.

6

Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families.

Myles-Worsley M, Coon H, McDowell J, Brenner C, Hoff M, Lind B, Bennett P, Freedman R, Clementz B, Byerley W. Myles-Worsley M, et al. Among authors: coon h. Am J Med Genet. 1999 Oct 15;88(5):544-50. Am J Med Genet. 1999. PMID: 10490714

7

Evidence for a major gene accounting for mild elevation in LDL cholesterol: the NHLBI Family Heart Study.

Coon H, Leppert MF, Kronenberg F, Province MA, Myers RH, Arnett DK, Eckfeldt JH, Heiss G, Williams RR, Hunt SC. Coon H, et al. Ann Hum Genet. 1999 Sep;63(Pt 5):401-12. doi: 10.1046/j.1469-1809.1999.6350401.x. Ann Hum Genet. 1999. PMID: 10735582

8

Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study.

Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF. Coon H, et al. Arterioscler Thromb Vasc Biol. 2000 Oct;20(10):2275-80. doi: 10.1161/01.atv.20.10.2275. Arterioscler Thromb Vasc Biol. 2000. PMID: 11031215

9

Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study.

Coon H, Leppert MF, Eckfeldt JH, Oberman A, Myers RH, Peacock JM, Province MA, Hopkins PN, Heiss G. Coon H, et al. Arterioscler Thromb Vasc Biol. 2001 Dec;21(12):1969-76. doi: 10.1161/hq1201.100228. Arterioscler Thromb Vasc Biol. 2001. PMID: 11742872

10

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. Hum Genet. 2002 Sep;111(3):263-9. doi: 10.1007/s00439-002-0773-8. Epub 2002 Jul 31. Hum Genet. 2002. PMID: 12215839

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