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Items: 1 to 20 of 79

1.

A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.

Jongjaroenprasert W, Phusantisampan T, Mahasirimongkol S, Mushiroda T, Hirankarn N, Snabboon T, Chanprasertyotin S, Tantiwong P, Soonthornpun S, Rattanapichart P, Mamanasiri S, Himathongkam T, Ongphiphadhanakul B, Takahashi A, Kamatani N, Kubo M, Nakamura Y.

J Hum Genet. 2012 May;57(5):301-4. doi: 10.1038/jhg.2012.20. Epub 2012 Mar 8.

PMID:
22399142
2.

Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.

Cheung CL, Lau KS, Ho AY, Lee KK, Tiu SC, Lau EY, Leung J, Tsang MW, Chan KW, Yeung CY, Woo YC, Cheung EY, Hung VH, Pang HK, Hung CS, Sham PC, Kung AW.

Nat Genet. 2012 Sep;44(9):1026-9. doi: 10.1038/ng.2367. Epub 2012 Aug 5.

PMID:
22863731
3.

A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.

Ng CC, Yew PY, Puah SM, Krishnan G, Yap LF, Teo SH, Lim PV, Govindaraju S, Ratnavelu K, Sam CK, Takahashi A, Kubo M, Kamatani N, Nakamura Y, Mushiroda T.

J Hum Genet. 2009 Jul;54(7):392-7. doi: 10.1038/jhg.2009.49. Epub 2009 May 29.

PMID:
19478819
4.

Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis.

Chu PY, Cheng CJ, Tseng MH, Yang SS, Chen HC, Lin SH.

Clin Chim Acta. 2012 Dec 24;414:105-8. doi: 10.1016/j.cca.2012.08.004. Epub 2012 Aug 15.

PMID:
22910584
5.

Fine mapping analysis of a region of 20q13.33 identified five independent susceptibility loci for glioma in a Chinese Han population.

Song X, Zhou K, Zhao Y, Huai C, Zhao Y, Yu H, Chen Y, Chen G, Chen H, Fan W, Mao Y, Lu D.

Carcinogenesis. 2012 May;33(5):1065-71. doi: 10.1093/carcin/bgs117. Epub 2012 Mar 2.

PMID:
22387365
6.

Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population.

Jongjaroenprasert W, Chanprasertyotin S, Butadej S, Nakasatien S, Charatcharoenwitthaya N, Himathongkam T, Ongphiphadhanakul B.

Clin Endocrinol (Oxf). 2008 Apr;68(4):646-51. Epub 2007 Oct 29.

PMID:
17970773
7.

Genome-wide association study identifies PERLD1 as asthma candidate gene.

Anantharaman R, Andiappan AK, Nilkanth PP, Suri BK, Wang de Y, Chew FT.

BMC Med Genet. 2011 Dec 21;12:170. doi: 10.1186/1471-2350-12-170.

8.

The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis.

Li X, Yao S, Xiang Y, Zhang X, Wu X, Luo L, Huang H, Zhu M, Wan H, Hong D.

BMC Neurol. 2015 Mar 21;15:38. doi: 10.1186/s12883-015-0290-8.

9.

Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.

Nakabayashi K, Komaki G, Tajima A, Ando T, Ishikawa M, Nomoto J, Hata K, Oka A, Inoko H, Sasazuki T; Japanese Genetic Research Group for Eating Disorders (JGRED), Shirasawa S.

J Hum Genet. 2009 Sep;54(9):531-7. doi: 10.1038/jhg.2009.74. Epub 2009 Aug 14.

PMID:
19680270
10.

Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.

Low SK, Takahashi A, Cha PC, Zembutsu H, Kamatani N, Kubo M, Nakamura Y.

Hum Mol Genet. 2012 May 1;21(9):2102-10. doi: 10.1093/hmg/dds020. Epub 2012 Jan 27.

PMID:
22286173
11.

A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population.

Yoon KA, Park JH, Han J, Park S, Lee GK, Han JY, Zo JI, Kim J, Lee JE, Takahashi A, Kubo M, Nakamura Y, Lee JS.

Hum Mol Genet. 2010 Dec 15;19(24):4948-54. doi: 10.1093/hmg/ddq421. Epub 2010 Sep 28.

PMID:
20876614
12.

Genome-wide association study of pancreatic cancer in Japanese population.

Low SK, Kuchiba A, Zembutsu H, Saito A, Takahashi A, Kubo M, Daigo Y, Kamatani N, Chiku S, Totsuka H, Ohnami S, Hirose H, Shimada K, Okusaka T, Yoshida T, Nakamura Y, Sakamoto H.

PLoS One. 2010 Jul 29;5(7):e11824. doi: 10.1371/journal.pone.0011824.

13.

Genome-wide association study identifies TNFSF13 as a susceptibility gene for IgA in a South Chinese population in smokers.

Yang C, Jie W, Yanlong Y, Xuefeng G, Aihua T, Yong G, Zheng L, Youjie Z, Haiying Z, Xue Q, Min Q, Linjian M, Xiaobo Y, Yanling H, Zengnan M.

Immunogenetics. 2012 Oct;64(10):747-53. doi: 10.1007/s00251-012-0636-y. Epub 2012 Aug 3.

PMID:
22864923
14.

Genome-wide association study of serum albumin:globulin ratio in Korean populations.

Hong KW, Jin HS, Song D, Kwak HK, Kim SS, Kim Y.

J Hum Genet. 2013 Mar;58(3):174-7. doi: 10.1038/jhg.2012.130. Epub 2013 Jan 10.

PMID:
23303382
15.

A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease.

Kim JJ, Hong YM, Sohn S, Jang GY, Ha KS, Yun SW, Han MK, Lee KY, Song MS, Lee HD, Kim DS, Lee JE, Shin ES, Jang JH, Lee YS, Kim SY, Lee JY, Han BG, Wu JY, Kim KJ, Park YM, Seo EJ, Park IS, Lee JK; Korean Kawasaki Disease Genetics Consortium.

Hum Genet. 2011 May;129(5):487-95. doi: 10.1007/s00439-010-0937-x. Epub 2011 Jan 9.

PMID:
21221998
16.

A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease.

Mathias RA, Kim Y, Sung H, Yanek LR, Mantese VJ, Hererra-Galeano JE, Ruczinski I, Wilson AF, Faraday N, Becker LC, Becker DM.

BMC Med Genomics. 2010 Jun 7;3:22. doi: 10.1186/1755-8794-3-22.

17.

[Genome-wide association study of bronchial asthma in the Volga-Ural region of Russia].

Karunas AS, Iunusbaev BB, Fedorova IuIu, Gimalova GF, Ramazanova NN, Gur'eva LL, Mukhtarova LA, Zagidullin ShZ, Etkina EI, Khusnutdinova EK.

Mol Biol (Mosk). 2011 Nov-Dec;45(6):992-1003. Russian.

PMID:
22295569
18.

Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis.

Mahasirimongkol S, Yanai H, Mushiroda T, Promphittayarat W, Wattanapokayakit S, Phromjai J, Yuliwulandari R, Wichukchinda N, Yowang A, Yamada N, Kantipong P, Takahashi A, Kubo M, Sawanpanyalert P, Kamatani N, Nakamura Y, Tokunaga K.

J Hum Genet. 2012 Jun;57(6):363-7. doi: 10.1038/jhg.2012.35. Epub 2012 May 3.

PMID:
22551897
19.

Genome-wide association study on bipolar disorder in the Bulgarian population.

Yosifova A, Mushiroda T, Kubo M, Takahashi A, Kamatani Y, Kamatani N, Stoianov D, Vazharova R, Karachanak S, Zaharieva I, Dimova I, Hadjidekova S, Milanova V, Madjirova N, Gerdjikov I, Tolev T, Poryazova N, O'Donovan MC, Owen MJ, Kirov G, Toncheva D, Nakamura Y.

Genes Brain Behav. 2011 Oct;10(7):789-97. doi: 10.1111/j.1601-183X.2011.00721.x. Epub 2011 Aug 18.

20.

High-resolution whole-genome association study of Parkinson disease.

Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.

Am J Hum Genet. 2005 Nov;77(5):685-93. Epub 2005 Sep 9.

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