Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 48

1.

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.

2.

Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami.

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

Eur J Hum Genet. 2010 May;18(5):569-74. doi: 10.1038/ejhg.2009.210. Epub 2009 Nov 25.

3.

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.

4.

The European GWAS-identified risk SNP rs457717 within IQGAP2 is not associated with age-related hearing impairment in Han male Chinese population.

Luo H, Wu H, Shen H, Chen H, Yang T, Huang Z, Jin X, Pang X, Li L, Hu X, Jiang X, Fan Z, Li J.

Eur Arch Otorhinolaryngol. 2016 Jul;273(7):1677-87. doi: 10.1007/s00405-015-3711-9. Epub 2015 Jul 18.

PMID:
26187738
5.

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.

6.

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.

7.

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.

8.

Hearing ability with age in northern European women: a new web-based approach to genetic studies.

Wolber LE, Steves CJ, Spector TD, Williams FM.

PLoS One. 2012;7(4):e35500. doi: 10.1371/journal.pone.0035500. Epub 2012 Apr 30.

9.

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
10.

Test for association of common variants in GRM7 with alcohol consumption.

Melroy-Greif WE, Vadasz C, Kamens HM, McQueen MB, Corley RP, Stallings MC, Hopfer CJ, Krauter KS, Brown SA, Hewitt JK, Ehringer MA.

Alcohol. 2016 Sep;55:43-50. doi: 10.1016/j.alcohol.2015.10.005. Epub 2016 Aug 31.

11.

A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.

Hoffmann TJ, Keats BJ, Yoshikawa N, Schaefer C, Risch N, Lustig LR.

PLoS Genet. 2016 Oct 20;12(10):e1006371. doi: 10.1371/journal.pgen.1006371. eCollection 2016 Oct.

12.

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
13.

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.

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

Am J Hum Genet. 2008 Sep;83(3):401-7. doi: 10.1016/j.ajhg.2008.08.002. Epub 2008 Aug 28.

14.

Molecular genetic epidemiology of age-related hearing impairment.

Uchida Y, Sugiura S, Ando F, Nakashima T, Shimokata H.

Auris Nasus Larynx. 2011 Dec;38(6):657-65. doi: 10.1016/j.anl.2011.02.005. Epub 2011 May 20. Review.

PMID:
21601397
15.

Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.

Fransen E, Bonneux S, Corneveaux JJ, Schrauwen I, Di Berardino F, White CH, Ohmen JD, Van de Heyning P, Ambrosetti U, Huentelman MJ, Van Camp G, Friedman RA.

Eur J Hum Genet. 2015 Jan;23(1):110-5. doi: 10.1038/ejhg.2014.56. Epub 2014 Jun 18.

16.

Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways.

Girotto G, Pirastu N, Sorice R, Biino G, Campbell H, d'Adamo AP, Hastie ND, Nutile T, Polasek O, Portas L, Rudan I, Ulivi S, Zemunik T, Wright AF, Ciullo M, Hayward C, Pirastu M, Gasparini P.

J Med Genet. 2011 Jun;48(6):369-74. doi: 10.1136/jmg.2010.088310. Epub 2011 Apr 14.

PMID:
21493956
17.

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies.

Hao K, Chudin E, McElwee J, Schadt EE.

BMC Genet. 2009 Jun 16;10:27. doi: 10.1186/1471-2156-10-27.

18.
19.

A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies.

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

Eur J Hum Genet. 2011 Mar;19(3):347-52. doi: 10.1038/ejhg.2010.179. Epub 2010 Dec 8.

20.

Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.

Muglia P, Tozzi F, Galwey NW, Francks C, Upmanyu R, Kong XQ, Antoniades A, Domenici E, Perry J, Rothen S, Vandeleur CL, Mooser V, Waeber G, Vollenweider P, Preisig M, Lucae S, Müller-Myhsok B, Holsboer F, Middleton LT, Roses AD.

Mol Psychiatry. 2010 Jun;15(6):589-601. doi: 10.1038/mp.2008.131. Epub 2008 Dec 23.

PMID:
19107115

Supplemental Content

Support Center