Coon H - Search Results

1

Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma.

Darlington TM, Pimentel R, Smith K, Bakian AV, Jerominski L, Cardon J, Camp NJ, Callor WB, Grey T, Singleton M, Yandell M, Renshaw PF, Yurgelun-Todd DA, Gray D, Coon H. Darlington TM, et al. Among authors: coon h. Transl Psychiatry. 2014 Oct 21;4(10):e471. doi: 10.1038/tp.2014.111. Transl Psychiatry. 2014. PMID: 25335167 Free PMC article.

2

Tryptophan hydroxylase polymorphisms in suicide victims.

Bennett PJ, McMahon WM, Watabe J, Achilles J, Bacon M, Coon H, Grey T, Keller T, Tate D, Tcaciuc I, Workman J, Gray D. Bennett PJ, et al. Among authors: coon h. Psychiatr Genet. 2000 Mar;10(1):13-7. doi: 10.1097/00041444-200010010-00003. Psychiatr Genet. 2000. PMID: 10909123

3

Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method.

Camp NJ, Neuhausen SL, Tiobech J, Polloi A, Coon H, Myles-Worsley M. Camp NJ, et al. Among authors: coon h. Am J Hum Genet. 2001 Dec;69(6):1278-89. doi: 10.1086/324590. Epub 2001 Oct 19. Am J Hum Genet. 2001. PMID: 11668428 Free PMC article.

4

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat.

Hunt SC, Hasstedt SJ, Coon H, Camp NJ, Cawthon RM, Wu LL, Hopkins PN. Hunt SC, et al. Among authors: coon h. Kidney Int. 2002 Oct;62(4):1143-8. doi: 10.1111/j.1523-1755.2002.kid557.x. Kidney Int. 2002. PMID: 12234284 Free article.

5

Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees.

Camp NJ, Hopkins PN, Hasstedt SJ, Coon H, Malhotra A, Cawthon RM, Hunt SC. Camp NJ, et al. Among authors: coon h. Hypertension. 2003 Sep;42(3):322-8. doi: 10.1161/01.HYP.0000084874.85653.46. Epub 2003 Jul 21. Hypertension. 2003. PMID: 12874090

6

Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees.

Hunt SC, Coon H, Hasstedt SJ, Cawthon RM, Camp NJ, Wu LL, Hopkins PN. Hunt SC, et al. Among authors: coon h. Am J Hypertens. 2004 Jun;17(6):511-5. doi: 10.1016/j.amjhyper.2004.02.019. Am J Hypertens. 2004. PMID: 15177524

7

Model-fitting and linkage analysis of sodium-lithium countertransport.

Hasstedt SJ, Camp NJ, Hopkins PN, Coon H, McKinney JT, Cawthon RM, Hunt SC. Hasstedt SJ, et al. Among authors: coon h. Eur J Hum Genet. 2004 Dec;12(12):1055-61. doi: 10.1038/sj.ejhg.5201262. Eur J Hum Genet. 2004. PMID: 15383825

8

Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree.

Coon H, Matsunami N, Stevens J, Miller J, Pingree C, Camp NJ, Thomas A, Krasny L, Lainhart J, Leppert MF, McMahon W. Coon H, et al. Hum Hered. 2005;60(4):220-6. doi: 10.1159/000090546. Epub 2006 Jan 2. Hum Hered. 2005. PMID: 16391490

9

Linkage analysis of Tourette syndrome in a large Utah pedigree.

Knight S, Coon H, Johnson M, Leppert MF, Camp NJ, McMahon WM; Tourette Syndrome Association International Consortium for Genetics. Knight S, et al. Among authors: coon h. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):656-662. doi: 10.1002/ajmg.b.31035. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19777563 Free PMC article.

10

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees.

Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon WM. Coon H, et al. Mol Autism. 2010 Apr 8;1(1):8. doi: 10.1186/2040-2392-1-8. Mol Autism. 2010. PMID: 20678250 Free PMC article.

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