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Items: 1 to 20 of 30

1.

Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.

Tin A, Woodward OM, Kao WH, Liu CT, Lu X, Nalls MA, Shriner D, Semmo M, Akylbekova EL, Wyatt SB, Hwang SJ, Yang Q, Zonderman AB, Adeyemo AA, Palmer C, Meng Y, Reilly M, Shlipak MG, Siscovick D, Evans MK, Rotimi CN, Flessner MF, Köttgen M, Cupples LA, Fox CS, Köttgen A; CARe and CHARGE Consortia.

Hum Mol Genet. 2011 Oct 15;20(20):4056-68. doi: 10.1093/hmg/ddr307. Epub 2011 Jul 18.

2.

Recent advances in renal urate transport: characterization of candidate transporters indicated by genome-wide association studies.

Anzai N, Jutabha P, Amonpatumrat-Takahashi S, Sakurai H.

Clin Exp Nephrol. 2012 Feb;16(1):89-95. doi: 10.1007/s10157-011-0532-z. Epub 2011 Nov 1. Review.

PMID:
22038265
3.

The genetics of hyperuricaemia and gout.

Reginato AM, Mount DB, Yang I, Choi HK.

Nat Rev Rheumatol. 2012 Oct;8(10):610-21. doi: 10.1038/nrrheum.2012.144. Epub 2012 Sep 4. Review.

4.

Genetics of gout.

Choi HK, Zhu Y, Mount DB.

Curr Opin Rheumatol. 2010 Mar;22(2):144-51. doi: 10.1097/BOR.0b013e32833645e8. Review.

PMID:
20110790
5.

The genetic basis of gout.

Merriman TR, Choi HK, Dalbeth N.

Rheum Dis Clin North Am. 2014 May;40(2):279-90. doi: 10.1016/j.rdc.2014.01.009. Epub 2014 Feb 19. Review.

PMID:
24703347
6.

Renal urate handling: clinical relevance of recent advances.

Anzai N, Enomoto A, Endou H.

Curr Rheumatol Rep. 2005 Jun;7(3):227-34. Review.

PMID:
15919000
7.

A 'complexity' of urate transporters.

Wright AF, Rudan I, Hastie ND, Campbell H.

Kidney Int. 2010 Sep;78(5):446-52. doi: 10.1038/ki.2010.206. Epub 2010 Jul 7. Review.

8.

An update on the genetic architecture of hyperuricemia and gout.

Merriman TR.

Arthritis Res Ther. 2015 Apr 10;17:98. doi: 10.1186/s13075-015-0609-2. Review.

9.

Urate transporters: an evolving field.

Anzai N, Endou H.

Semin Nephrol. 2011 Sep;31(5):400-9. doi: 10.1016/j.semnephrol.2011.08.003. Review.

PMID:
22000646
10.

Genetics of hyperuricemia and gout: implications for the present and future.

George RL, Keenan RT.

Curr Rheumatol Rep. 2013 Feb;15(2):309. doi: 10.1007/s11926-012-0309-8. Review.

PMID:
23307580
11.

Recent insights into the pathogenesis of hyperuricaemia and gout.

Riches PL, Wright AF, Ralston SH.

Hum Mol Genet. 2009 Oct 15;18(R2):R177-84. doi: 10.1093/hmg/ddp369. Review.

PMID:
19808794
12.

The genetic basis of hyperuricaemia and gout.

Merriman TR, Dalbeth N.

Joint Bone Spine. 2011 Jan;78(1):35-40. doi: 10.1016/j.jbspin.2010.02.027. Epub 2010 May 15. Review.

PMID:
20472486
13.

Associations between SLC2A9 polymorphisms and gout susceptibility : A meta-analysis.

Lee YH, Seo YH, Kim JH, Choi SJ, Ji JD, Song GG.

Z Rheumatol. 2017 Feb;76(1):64-70. doi: 10.1007/s00393-016-0070-x. Review.

PMID:
27052299
14.

[The epidemiology and genetic of gout].

Bardin T, Richette P.

Presse Med. 2011 Sep;40(9 Pt 1):830-5. doi: 10.1016/j.lpm.2011.04.012. Epub 2011 Jul 12. Review. French.

PMID:
21752574
15.

Genomic Influences on Hyperuricemia and Gout.

Merriman T.

Rheum Dis Clin North Am. 2017 Aug;43(3):389-399. doi: 10.1016/j.rdc.2017.04.004. Review.

PMID:
28711141
16.

Research progress in the genetics of hyperuricaemia and gout.

Zheng M, Ma JW.

Yi Chuan. 2016 Apr;38(4):300-13. doi: 10.16288/j.yczz.15-385. Review.

PMID:
27103454
17.

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.

Evangelou E, Kerkhof HJ, Styrkarsdottir U, Ntzani EE, Bos SD, Esko T, Evans DS, Metrustry S, Panoutsopoulou K, Ramos YF, Thorleifsson G, Tsilidis KK; arcOGEN Consortium, Arden N, Aslam N, Bellamy N, Birrell F, Blanco FJ, Carr A, Chapman K, Day-Williams AG, Deloukas P, Doherty M, Engström G, Helgadottir HT, Hofman A, Ingvarsson T, Jonsson H, Keis A, Keurentjes JC, Kloppenburg M, Lind PA, McCaskie A, Martin NG, Milani L, Montgomery GW, Nelissen RG, Nevitt MC, Nilsson PM, Ollier WE, Parimi N, Rai A, Ralston SH, Reed MR, Riancho JA, Rivadeneira F, Rodriguez-Fontenla C, Southam L, Thorsteinsdottir U, Tsezou A, Wallis GA, Wilkinson JM, Gonzalez A, Lane NE, Lohmander LS, Loughlin J, Metspalu A, Uitterlinden AG, Jonsdottir I, Stefansson K, Slagboom PE, Zeggini E, Meulenbelt I, Ioannidis JP, Spector TD, van Meurs JB, Valdes AM.

Ann Rheum Dis. 2014 Dec;73(12):2130-6. doi: 10.1136/annrheumdis-2012-203114. Epub 2013 Aug 29. Review.

18.

Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.

Peters U, Jiao S, Schumacher FR, Hutter CM, Aragaki AK, Baron JA, Berndt SI, Bézieau S, Brenner H, Butterbach K, Caan BJ, Campbell PT, Carlson CS, Casey G, Chan AT, Chang-Claude J, Chanock SJ, Chen LS, Coetzee GA, Coetzee SG, Conti DV, Curtis KR, Duggan D, Edwards T, Fuchs CS, Gallinger S, Giovannucci EL, Gogarten SM, Gruber SB, Haile RW, Harrison TA, Hayes RB, Henderson BE, Hoffmeister M, Hopper JL, Hudson TJ, Hunter DJ, Jackson RD, Jee SH, Jenkins MA, Jia WH, Kolonel LN, Kooperberg C, Küry S, Lacroix AZ, Laurie CC, Laurie CA, Le Marchand L, Lemire M, Levine D, Lindor NM, Liu Y, Ma J, Makar KW, Matsuo K, Newcomb PA, Potter JD, Prentice RL, Qu C, Rohan T, Rosse SA, Schoen RE, Seminara D, Shrubsole M, Shu XO, Slattery ML, Taverna D, Thibodeau SN, Ulrich CM, White E, Xiang Y, Zanke BW, Zeng YX, Zhang B, Zheng W, Hsu L; Colon Cancer Family Registry and the Genetics and Epidemiology of Colorectal Cancer Consortium.

Gastroenterology. 2013 Apr;144(4):799-807.e24. doi: 10.1053/j.gastro.2012.12.020. Epub 2012 Dec 22. Review.

19.

Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.

Schormair B, Zhao C, Bell S, Tilch E, Salminen AV, Pütz B, Dauvilliers Y, Stefani A, Högl B, Poewe W, Kemlink D, Sonka K, Bachmann CG, Paulus W, Trenkwalder C, Oertel WH, Hornyak M, Teder-Laving M, Metspalu A, Hadjigeorgiou GM, Polo O, Fietze I, Ross OA, Wszolek Z, Butterworth AS, Soranzo N, Ouwehand WH, Roberts DJ, Danesh J, Allen RP, Earley CJ, Ondo WG, Xiong L, Montplaisir J, Gan-Or Z, Perola M, Vodicka P, Dina C, Franke A, Tittmann L, Stewart AFR, Shah SH, Gieger C, Peters A, Rouleau GA, Berger K, Oexle K, Di Angelantonio E, Hinds DA, Müller-Myhsok B, Winkelmann J; 23andMe Research Team; DESIR study group.

Lancet Neurol. 2017 Nov;16(11):898-907. doi: 10.1016/S1474-4422(17)30327-7. Review.

20.

Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

Panagiotou OA, Evangelou E, Ioannidis JP.

Am J Epidemiol. 2010 Oct 15;172(8):869-89. doi: 10.1093/aje/kwq234. Epub 2010 Sep 28. Review.

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