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Items: 1 to 20 of 80

1.

GRM7 variants confer susceptibility to age-related hearing impairment.

Friedman RA, Van Laer L, Huentelman MJ, Sheth SS, Van Eyken E, Corneveaux JJ, Tembe WD, Halperin RF, Thorburn AQ, Thys S, Bonneux S, Fransen E, Huyghe J, Pyykkö I, Cremers CW, Kremer H, Dhooge I, Stephens D, Orzan E, Pfister M, Bille M, Parving A, Sorri M, Van de Heyning PH, Makmura L, Ohmen JD, Linthicum FH Jr, Fayad JN, Pearson JV, Craig DW, Stephan DA, Van Camp G.

Hum Mol Genet. 2009 Feb 15;18(4):785-96. doi: 10.1093/hmg/ddn402. Epub 2008 Dec 1.

2.

Association of GRM7 variants with different phenotype patterns of age-related hearing impairment in an elderly male Han Chinese population.

Luo H, Yang T, Jin X, Pang X, Li J, Chai Y, Li L, Zhang Y, Zhang L, Zhang Z, Wu W, Zhang Q, Hu X, Sun J, Jiang X, Fan Z, Huang Z, Wu H.

PLoS One. 2013 Oct 11;8(10):e77153. doi: 10.1371/journal.pone.0077153. eCollection 2013.

3.

GRM7 variants associated with age-related hearing loss based on auditory perception.

Newman DL, Fisher LM, Ohmen J, Parody R, Fong CT, Frisina ST, Mapes F, Eddins DA, Robert Frisina D, Frisina RD, Friedman RA.

Hear Res. 2012 Dec;294(1-2):125-32. doi: 10.1016/j.heares.2012.08.016. Epub 2012 Oct 25.

4.

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment.

Van Laer L, Van Eyken E, Fransen E, Huyghe JR, Topsakal V, Hendrickx JJ, Hannula S, Mäki-Torkko E, Jensen M, Demeester K, Baur M, Bonaconsa A, Mazzoli M, Espeso A, Verbruggen K, Huyghe J, Huygen P, Kunst S, Manninen M, Konings A, Diaz-Lacava AN, Steffens M, Wienker TF, Pyykkö I, Cremers CW, Kremer H, Dhooge I, Stephens D, Orzan E, Pfister M, Bille M, Parving A, Sorri M, Van de Heyning PH, Van Camp G.

Hum Mol Genet. 2008 Jan 15;17(2):159-69. Epub 2007 Oct 6.

5.

A genome-wide association study for age-related hearing impairment in the Saami.

Van Laer L, Huyghe JR, Hannula S, Van Eyken E, Stephan DA, Mäki-Torkko E, Aikio P, Fransen E, Lysholm-Bernacchi A, Sorri M, Huentelman MJ, Van Camp G.

Eur J Hum Genet. 2010 Jun;18(6):685-93. doi: 10.1038/ejhg.2009.234. Epub 2010 Jan 13.

6.

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.

Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N, O'Donovan MC, Owen MJ.

Mol Psychiatry. 2010 Nov;15(11):1101-11. doi: 10.1038/mp.2009.96. Epub 2009 Sep 29.

PMID:
19786960
7.

Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population.

Gaj P, Maryan N, Hennig EE, Ledwon JK, Paziewska A, Majewska A, Karczmarski J, Nesteruk M, Wolski J, Antoniewicz AA, Przytulski K, Rutkowski A, Teumer A, Homuth G, Starzyńska T, Regula J, Ostrowski J.

PLoS One. 2012;7(4):e35307. doi: 10.1371/journal.pone.0035307. Epub 2012 Apr 19.

8.

Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder.

Kandaswamy R, McQuillin A, Curtis D, Gurling H.

Am J Med Genet B Neuropsychiatr Genet. 2014 Jun;165B(4):365-72. doi: 10.1002/ajmg.b.32239. Epub 2014 May 8.

9.

Association of cadherin23 single nucleotide polymorphism with age-related hearing impairment in Han Chinese.

Hwang JH, Liu KS, Wu CC, Liu TC.

Otolaryngol Head Neck Surg. 2012 Sep;147(3):531-4. doi: 10.1177/0194599812446904. Epub 2012 May 11.

PMID:
22581638
10.

Association study of polymorphisms in the group III metabotropic glutamate receptor genes, GRM4 and GRM7, with schizophrenia.

Shibata H, Tani A, Chikuhara T, Kikuta R, Sakai M, Ninomiya H, Tashiro N, Iwata N, Ozaki N, Fukumaki Y.

Psychiatry Res. 2009 May 15;167(1-2):88-96. doi: 10.1016/j.psychres.2007.12.002. Epub 2009 Apr 7.

PMID:
19351574
11.

Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population.

Bonneux S, Fransen E, Van Eyken E, Van Laer L, Huyghe J, Van de Heyning P, Voets A, Gerards M, Stassen AP, Hendrickx AT, Smeets HJ, Van Camp G.

Mitochondrion. 2011 Sep;11(5):729-34. doi: 10.1016/j.mito.2011.05.008. Epub 2011 May 30.

PMID:
21645648
12.

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment.

Van Eyken E, Van Camp G, Fransen E, Topsakal V, Hendrickx JJ, Demeester K, Van de Heyning P, Mäki-Torkko E, Hannula S, Sorri M, Jensen M, Parving A, Bille M, Baur M, Pfister M, Bonaconsa A, Mazzoli M, Orzan E, Espeso A, Stephens D, Verbruggen K, Huyghe J, Dhooge I, Huygen P, Kremer H, Cremers CW, Kunst S, Manninen M, Pyykkö I, Lacava A, Steffens M, Wienker TF, Van Laer L.

J Med Genet. 2007 Sep;44(9):570-8. Epub 2007 May 18.

13.

Assessment of heterogeneity between European Populations: a Baltic and Danish replication case-control study of SNPs from a recent European ulcerative colitis genome wide association study.

Andersen V, Ernst A, Sventoraityte J, Kupcinskas L, Jacobsen BA, Krarup HB, Vogel U, Jonaitis L, Denapiene G, Kiudelis G, Balschun T, Franke A.

BMC Med Genet. 2011 Oct 13;12:139. doi: 10.1186/1471-2350-12-139.

14.

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.

15.

Caucasian and Asian specific rheumatoid arthritis risk loci reveal limited replication and apparent allelic heterogeneity in north Indians.

Prasad P, Kumar A, Gupta R, Juyal RC, Thelma BK.

PLoS One. 2012;7(2):e31584. doi: 10.1371/journal.pone.0031584. Epub 2012 Feb 15.

16.

Environmental and genetic factors in age-related hearing impairment.

Bovo R, Ciorba A, Martini A.

Aging Clin Exp Res. 2011 Feb;23(1):3-10. Review.

PMID:
21499014
17.

Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome.

Krumbiegel M, Pasutto F, Schlötzer-Schrehardt U, Uebe S, Zenkel M, Mardin CY, Weisschuh N, Paoli D, Gramer E, Becker C, Ekici AB, Weber BH, Nürnberg P, Kruse FE, Reis A.

Eur J Hum Genet. 2011 Feb;19(2):186-93. doi: 10.1038/ejhg.2010.144. Epub 2010 Sep 1.

18.

A genome-wide association study of a coronary artery disease risk variant.

Lee JY, Lee BS, Shin DJ, Woo Park K, Shin YA, Joong Kim K, Heo L, Young Lee J, Kyoung Kim Y, Jin Kim Y, Bum Hong C, Lee SH, Yoon D, Jung Ku H, Oh IY, Kim BJ, Lee J, Park SJ, Kim J, Kawk HK, Lee JE, Park HK, Lee JE, Nam HY, Park HY, Shin C, Yokota M, Asano H, Nakatochi M, Matsubara T, Kitajima H, Yamamoto K, Kim HL, Han BG, Cho MC, Jang Y, Kim HS, Euy Park J, Lee JY.

J Hum Genet. 2013 Mar;58(3):120-6. doi: 10.1038/jhg.2012.124. Epub 2013 Jan 31.

PMID:
23364394
19.

Genome-wide association study of coronary artery disease in the Japanese.

Takeuchi F, Yokota M, Yamamoto K, Nakashima E, Katsuya T, Asano H, Isono M, Nabika T, Sugiyama T, Fujioka A, Awata N, Ohnaka K, Nakatochi M, Kitajima H, Rakugi H, Nakamura J, Ohkubo T, Imai Y, Shimamoto K, Yamori Y, Yamaguchi S, Kobayashi S, Takayanagi R, Ogihara T, Kato N.

Eur J Hum Genet. 2012 Mar;20(3):333-40. doi: 10.1038/ejhg.2011.184. Epub 2011 Oct 5.

20.

Shared genetic factors for age at natural menopause in Iranian and European women.

Rahmani M, Earp MA, Ramezani Tehrani F, Ataee M, Wu J, Treml M, Nudischer R, P-Behnami S; ReproGen Consortium, Perry JR, Murabito JM, Azizi F, Brooks-Wilson A.

Hum Reprod. 2013 Jul;28(7):1987-94. doi: 10.1093/humrep/det106. Epub 2013 Apr 16.

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