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Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population.

Park H, Lee S, Kim HJ, Ju YS, Shin JY, Hong D, von Grotthuss M, Lee DS, Park C, Kim JH, Kim B, Yoo YJ, Cho SI, Sung J, Lee C, Kim JI, Seo JS.

J Med Genet. 2012 Dec;49(12):747-52. doi: 10.1136/jmedgenet-2012-101209. Epub 2012 Nov 1.


A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.

Oikkonen J, Huang Y, Onkamo P, Ukkola-Vuoti L, Raijas P, Karma K, Vieland VJ, Järvelä I.

Mol Psychiatry. 2015 Feb;20(2):275-82. doi: 10.1038/mp.2014.8. Epub 2014 Mar 11.


Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music.

Ukkola-Vuoti L, Kanduri C, Oikkonen J, Buck G, Blancher C, Raijas P, Karma K, Lähdesmäki H, Järvelä I.

PLoS One. 2013;8(2):e56356. doi: 10.1371/journal.pone.0056356. Epub 2013 Feb 27.


Assessing musical abilities objectively: construction and validation of the profile of music perception skills.

Law LN, Zentner M.

PLoS One. 2012;7(12):e52508. doi: 10.1371/journal.pone.0052508. Epub 2012 Dec 28.


A family-based association study after genome-wide linkage analysis identified two genetic loci for renal function in a Mongolian population.

Park H, Kim HJ, Lee S, Yoo YJ, Ju YS, Lee JE, Cho SI, Sung J, Kim JI, Seo JS.

Kidney Int. 2013 Feb;83(2):285-92. doi: 10.1038/ki.2012.389. Epub 2012 Dec 19.


Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

Auer PL, Johnsen JM, Johnson AD, Logsdon BA, Lange LA, Nalls MA, Zhang G, Franceschini N, Fox K, Lange EM, Rich SS, O'Donnell CJ, Jackson RD, Wallace RB, Chen Z, Graubert TA, Wilson JG, Tang H, Lettre G, Reiner AP, Ganesh SK, Li Y.

Am J Hum Genet. 2012 Nov 2;91(5):794-808. doi: 10.1016/j.ajhg.2012.08.031. Epub 2012 Oct 25.


Linkage disequilibrium pattern and age-at-diagnosis are critical for replicating genetic associations across ethnic groups in leprosy.

Alter A, Fava VM, Huong NT, Singh M, Orlova M, Van Thuc N, Katoch K, Thai VH, Ba NN, Abel L, Mehra N, Alcaïs A, Schurr E.

Hum Genet. 2013 Jan;132(1):107-16. doi: 10.1007/s00439-012-1227-6. Epub 2012 Sep 29.


Association of single nucleotide polymorphisms of IL23R and IL17 with ulcerative colitis risk in a Chinese Han population.

Yu P, Shen F, Zhang X, Cao R, Zhao X, Liu P, Tu H, Yang X, Shi R, Zhang H.

PLoS One. 2012;7(9):e44380. doi: 10.1371/journal.pone.0044380. Epub 2012 Sep 11.


Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population.

Tang XF, Zhang Z, Hu DY, Xu AE, Zhou HS, Sun LD, Gao M, Gao TW, Gao XH, Chen HD, Xie HF, Tu CX, Hao F, Wu RN, Zhang FR, Liang L, Pu XM, Zhang JZ, Han JW, Pan GP, Wu JQ, Li K, Su MW, Du WD, Zhang WJ, Liu JJ, Xiang LH, Yang S, Zhou YW, Zhang XJ.

J Invest Dermatol. 2013 Feb;133(2):403-10. doi: 10.1038/jid.2012.320. Epub 2012 Sep 6.


Further evidence for the association of genetic variants of ZNF804A with schizophrenia and a meta-analysis for genome-wide significance variant rs1344706.

Zhang R, Yan JD, Valenzuela RK, Lu SM, Du XY, Zhong B, Ren J, Zhao SH, Gao CG, Wang L, Guo TW, Ma J.

Schizophr Res. 2012 Oct;141(1):40-7. doi: 10.1016/j.schres.2012.07.013. Epub 2012 Aug 5.


Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility.

Hou S, Xiao X, Li F, Jiang Z, Kijlstra A, Yang P.

Hum Genet. 2012 Dec;131(12):1841-50. doi: 10.1007/s00439-012-1200-4. Epub 2012 Jul 25.


Polymorphisms in the CTNND2 gene and 11q24.1 genomic region are associated with pathological myopia in a Chinese population.

Yu Z, Zhou J, Chen X, Zhou X, Sun X, Chu R.

Ophthalmologica. 2012;228(2):123-9. doi: 10.1159/000338188. Epub 2012 Jun 29.


Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.

Dyment DA, Cader MZ, Chao MJ, Lincoln MR, Morrison KM, Disanto G, Morahan JM, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC, Ramagopalan SV.

Neurology. 2012 Jul 31;79(5):406-11. doi: 10.1212/WNL.0b013e3182616fc4. Epub 2012 Jun 27.


Association of CLCNKB haplotypes and hypertension in Mongolian and Han populations.

Su X, Chang P, Liu Z, Yan M, Liu G, Cui H.

Clin Exp Hypertens. 2012;34(7):482-7. doi: 10.3109/10641963.2012.666602. Epub 2012 May 11.


Genetic variation and human longevity.

Soerensen M.

Dan Med J. 2012 May;59(5):B4454.


An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error.

Abbott D, Li YJ, Guggenheim JA, Metlapally R, Malecaze F, Calvas P, Rosenberg T, Paget S, Zayats T, Mackey DA, Feng S, Young TL.

Mol Vis. 2012;18:720-9. Epub 2012 Mar 26.


Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.

Radhakrishna U, Nath SK, McElreavey K, Ratnamala U, Sun C, Maiti AK, Gagnebin M, Béna F, Newkirk HL, Sharp AJ, Everman DB, Murray JC, Schwartz CE, Antonarakis SE, Butler MG.

J Med Genet. 2012 Apr;49(4):270-6. doi: 10.1136/jmedgenet-2012-100826.


Association between genetic variants of the ADD1 and GNB3 genes and blood pressure response to the cold pressor test in a Chinese Han population: the GenSalt Study.

Wang L, Chen S, Zhao Q, Hixson JE, Rao DC, Jaquish CE, Huang J, Lu X, Chen J, Cao J, Li J, Li H, He J, Liu DP, Gu D; GenSalt Collaborative Research Group.

Hypertens Res. 2012 Aug;35(8):805-10. doi: 10.1038/hr.2012.38. Epub 2012 Apr 5.


Fine mapping study reveals novel candidate genes for carotid intima-media thickness in Dominican Republican families.

Wang L, Beecham A, Zhuo D, Dong C, Blanton SH, Rundek T, Sacco RL.

Circ Cardiovasc Genet. 2012 Apr 1;5(2):234-41. doi: 10.1161/CIRCGENETICS.111.961763. Epub 2012 Mar 14.


The sound of music: differentiating musicians using a fast, musical multi-feature mismatch negativity paradigm.

Vuust P, Brattico E, Seppänen M, Näätänen R, Tervaniemi M.

Neuropsychologia. 2012 Jun;50(7):1432-43. doi: 10.1016/j.neuropsychologia.2012.02.028. Epub 2012 Mar 6.

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