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Page 1
Predisposition locus for major depression at chromosome 12q22-12q23.2.
Abkevich V, Camp NJ, Hensel CH, Neff CD, Russell DL, Hughes DC, Plenk AM, Lowry MR, Richards RL, Carter C, Frech GC, Stone S, Rowe K, Chau CA, Cortado K, Hunt A, Luce K, O'Neil G, Poarch J, Potter J, Poulsen GH, Saxton H, Bernat-Sestak M, Thompson V, Gutin A, Skolnick MH, Shattuck D, Cannon-Albright L. Abkevich V, et al. Among authors: hensel ch. Am J Hum Genet. 2003 Dec;73(6):1271-81. doi: 10.1086/379978. Epub 2003 Nov 5. Am J Hum Genet. 2003. PMID: 14606042 Free PMC article.
A major predisposition locus for severe obesity, at 4p15-p14.
Stone S, Abkevich V, Hunt SC, Gutin A, Russell DL, Neff CD, Riley R, Frech GC, Hensel CH, Jammulapati S, Potter J, Sexton D, Tran T, Gibbs D, Iliev D, Gress R, Bloomquist B, Amatruda J, Rae PM, Adams TD, Skolnick MH, Shattuck D. Stone S, et al. Among authors: hensel ch. Am J Hum Genet. 2002 Jun;70(6):1459-68. doi: 10.1086/340670. Epub 2002 Apr 15. Am J Hum Genet. 2002. PMID: 11957135 Free PMC article.
Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders.
Camp NJ, Lowry MR, Richards RL, Plenk AM, Carter C, Hensel CH, Abkevich V, Skolnick MH, Shattuck D, Rowe KG, Hughes DC, Cannon-Albright LA. Camp NJ, et al. Among authors: hensel ch. Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):85-93. doi: 10.1002/ajmg.b.30177. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15806581
Linkage of body mass index to chromosome 20 in Utah pedigrees.
Hunt SC, Abkevich V, Hensel CH, Gutin A, Neff CD, Russell DL, Tran T, Hong X, Jammulapati S, Riley R, Weaver-Feldhaus J, Macalma T, Richards MM, Gress R, Francis M, Thomas A, Frech GC, Adams TD, Shattuck D, Stone S. Hunt SC, et al. Among authors: hensel ch. Hum Genet. 2001 Sep;109(3):279-85. doi: 10.1007/s004390100581. Hum Genet. 2001. PMID: 11702208
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
Matsunami N, Hadley D, Hensel CH, Christensen GB, Kim C, Frackelton E, Thomas K, da Silva RP, Stevens J, Baird L, Otterud B, Ho K, Varvil T, Leppert T, Lambert CG, Leppert M, Hakonarson H. Matsunami N, et al. Among authors: hensel ch. PLoS One. 2013;8(1):e52239. doi: 10.1371/journal.pone.0052239. Epub 2013 Jan 14. PLoS One. 2013. PMID: 23341896 Free PMC article.
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.
Matsunami N, Hensel CH, Baird L, Stevens J, Otterud B, Leppert T, Varvil T, Hadley D, Glessner JT, Pellegrino R, Kim C, Thomas K, Wang F, Otieno FG, Ho K, Christensen GB, Li D, Prekeris R, Lambert CG, Hakonarson H, Leppert MF. Matsunami N, et al. Among authors: hensel ch. Mol Autism. 2014 Jan 27;5(1):5. doi: 10.1186/2040-2392-5-5. Mol Autism. 2014. PMID: 24467814 Free PMC article.
29 results