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Items: 1 to 20 of 98

1.

Common variants in the GDF5-UQCC region are associated with variation in human height.

Sanna S, Jackson AU, Nagaraja R, Willer CJ, Chen WM, Bonnycastle LL, Shen H, Timpson N, Lettre G, Usala G, Chines PS, Stringham HM, Scott LJ, Dei M, Lai S, Albai G, Crisponi L, Naitza S, Doheny KF, Pugh EW, Ben-Shlomo Y, Ebrahim S, Lawlor DA, Bergman RN, Watanabe RM, Uda M, Tuomilehto J, Coresh J, Hirschhorn JN, Shuldiner AR, Schlessinger D, Collins FS, Davey Smith G, Boerwinkle E, Cao A, Boehnke M, Abecasis GR, Mohlke KL.

Nat Genet. 2008 Feb;40(2):198-203. doi: 10.1038/ng.74. Epub 2008 Jan 13.

2.

Positive selection on the osteoarthritis-risk and decreased-height associated variants at the GDF5 gene in East Asians.

Wu DD, Li GM, Jin W, Li Y, Zhang YP.

PLoS One. 2012;7(8):e42553. doi: 10.1371/journal.pone.0042553. Epub 2012 Aug 14.

3.

A common variant of HMGA2 is associated with adult and childhood height in the general population.

Weedon MN, Lettre G, Freathy RM, Lindgren CM, Voight BF, Perry JR, Elliott KS, Hackett R, Guiducci C, Shields B, Zeggini E, Lango H, Lyssenko V, Timpson NJ, Burtt NP, Rayner NW, Saxena R, Ardlie K, Tobias JH, Ness AR, Ring SM, Palmer CN, Morris AD, Peltonen L, Salomaa V; Diabetes Genetics Initiative; Wellcome Trust Case Control Consortium, Davey Smith G, Groop LC, Hattersley AT, McCarthy MI, Hirschhorn JN, Frayling TM.

Nat Genet. 2007 Oct;39(10):1245-50. Epub 2007 Sep 2.

4.

A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis.

Miyamoto Y, Mabuchi A, Shi D, Kubo T, Takatori Y, Saito S, Fujioka M, Sudo A, Uchida A, Yamamoto S, Ozaki K, Takigawa M, Tanaka T, Nakamura Y, Jiang Q, Ikegawa S.

Nat Genet. 2007 Apr;39(4):529-33. Epub 2007 Mar 25.

PMID:
17384641
5.

Genetic variation in the GDF5 region is associated with osteoarthritis, height, hip axis length and fracture risk: the Rotterdam study.

Vaes RB, Rivadeneira F, Kerkhof JM, Hofman A, Pols HA, Uitterlinden AG, van Meurs JB.

Ann Rheum Dis. 2009 Nov;68(11):1754-60. doi: 10.1136/ard.2008.099655. Epub 2008 Nov 24.

PMID:
19029166
6.

Deep sequencing of GDF5 reveals the absence of rare variants at this important osteoarthritis susceptibility locus.

Dodd AW, Rodriguez-Fontenla C, Calaza M, Carr A, Gomez-Reino JJ, Tsezou A, Reynard LN, Gonzalez A, Loughlin J.

Osteoarthritis Cartilage. 2011 Apr;19(4):430-4. doi: 10.1016/j.joca.2011.01.014. Epub 2011 Jan 31.

7.

Genetic regulation of adult stature.

Lettre G.

Curr Opin Pediatr. 2009 Aug;21(4):515-22. doi: 10.1097/MOP.0b013e32832c6dce. Review.

PMID:
19455035
8.

An SNP in the 5'-UTR of GDF5 is associated with osteoarthritis susceptibility in Europeans and with in vivo differences in allelic expression in articular cartilage.

Southam L, Rodriguez-Lopez J, Wilkins JM, Pombo-Suarez M, Snelling S, Gomez-Reino JJ, Chapman K, Gonzalez A, Loughlin J.

Hum Mol Genet. 2007 Sep 15;16(18):2226-32. Epub 2007 Jul 6.

9.

Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2.

Takeshita H, Fujihara J, Soejima M, Koda Y, Kimura-Kataoka K, Ono R, Yuasa I, Iida R, Ueki M, Nagao M, Yasuda T.

Electrophoresis. 2011 Jul;32(14):1844-51. doi: 10.1002/elps.201100128.

PMID:
21769890
10.

A meta-analysis of European and Asian cohorts reveals a global role of a functional SNP in the 5' UTR of GDF5 with osteoarthritis susceptibility.

Chapman K, Takahashi A, Meulenbelt I, Watson C, Rodriguez-Lopez J, Egli R, Tsezou A, Malizos KN, Kloppenburg M, Shi D, Southam L, van der Breggen R, Donn R, Qin J, Doherty M, Slagboom PE, Wallis G, Kamatani N, Jiang Q, Gonzalez A, Loughlin J, Ikegawa S.

Hum Mol Genet. 2008 May 15;17(10):1497-504. doi: 10.1093/hmg/ddn038. Epub 2008 Feb 24.

11.

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele.

Hodge JC, T Cuenco K, Huyck KL, Somasundaram P, Panhuysen CI, Stewart EA, Morton CC.

Hum Genet. 2009 Apr;125(3):257-63. doi: 10.1007/s00439-008-0621-6. Epub 2009 Jan 9.

12.

Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height.

Bouatia-Naji N, Marchand M, Cavalcanti-Proença C, Daghmoun S, Durand E, Tichet J, Marre M, Balkau B, Froguel P, Lévy-Marchal C.

Eur J Endocrinol. 2009 Apr;160(4):557-60. doi: 10.1530/EJE-08-0794. Epub 2009 Jan 12.

13.

Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.

Shriner D, Adeyemo A, Gerry NP, Herbert A, Chen G, Doumatey A, Huang H, Zhou J, Christman MF, Rotimi CN.

PLoS One. 2009 Dec 22;4(12):e8398. doi: 10.1371/journal.pone.0008398.

14.

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.

Scuteri A, Sanna S, Chen WM, Uda M, Albai G, Strait J, Najjar S, Nagaraja R, Orrú M, Usala G, Dei M, Lai S, Maschio A, Busonero F, Mulas A, Ehret GB, Fink AA, Weder AB, Cooper RS, Galan P, Chakravarti A, Schlessinger D, Cao A, Lakatta E, Abecasis GR.

PLoS Genet. 2007 Jul;3(7):e115.

15.

Vitamin D receptor gene haplotype is associated with body height and bone size.

Fang Y, van Meurs JB, Rivadeneira F, van Schoor NM, van Leeuwen JP, Lips P, Pols HA, Uitterlinden AG.

J Clin Endocrinol Metab. 2007 Apr;92(4):1491-501. Epub 2007 Jan 9.

PMID:
17213281
16.

Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.

Chan Y, Holmen OL, Dauber A, Vatten L, Havulinna AS, Skorpen F, Kvaløy K, Silander K, Nguyen TT, Willer C, Boehnke M, Perola M, Palotie A, Salomaa V, Hveem K, Frayling TM, Hirschhorn JN, Weedon MN.

PLoS Genet. 2011 Dec;7(12):e1002439. doi: 10.1371/journal.pgen.1002439. Epub 2011 Dec 29.

17.

Genome-wide association analysis identifies 20 loci that influence adult height.

Weedon MN, Lango H, Lindgren CM, Wallace C, Evans DM, Mangino M, Freathy RM, Perry JR, Stevens S, Hall AS, Samani NJ, Shields B, Prokopenko I, Farrall M, Dominiczak A; Diabetes Genetics Initiative; Wellcome Trust Case Control Consortium, Johnson T, Bergmann S, Beckmann JS, Vollenweider P, Waterworth DM, Mooser V, Palmer CN, Morris AD, Ouwehand WH; Cambridge GEM Consortium, Zhao JH, Li S, Loos RJ, Barroso I, Deloukas P, Sandhu MS, Wheeler E, Soranzo N, Inouye M, Wareham NJ, Caulfield M, Munroe PB, Hattersley AT, McCarthy MI, Frayling TM.

Nat Genet. 2008 May;40(5):575-83. doi: 10.1038/ng.121. Epub 2008 Apr 6.

18.

Characterization of common genetic variants in cathepsin K and testing for association with bone mineral density in a large cohort of perimenopausal women from Scotland.

Giraudeau FS, McGinnis RE, Gray IC, O'Brien EJ, Doncaster KE, Spurr NK, Ralston SH, Reid DM, Wood J.

J Bone Miner Res. 2004 Jan;19(1):31-41.

19.

Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data.

Elliott KS, Chapman K, Day-Williams A, Panoutsopoulou K, Southam L, Lindgren CM, Arden N, Aslam N, Birrell F, Carluke I, Carr A, Deloukas P, Doherty M, Loughlin J, McCaskie A, Ollier WE, Rai A, Ralston S, Reed MR, Spector TD, Valdes AM, Wallis GA, Wilkinson M, Zeggini E; GIANT consortium; arcOGEN consortium.

Ann Rheum Dis. 2013 Jun;72(6):935-41. doi: 10.1136/annrheumdis-2012-202081. Epub 2012 Sep 6.

20.

Genetic variation in candidate genes like the HMGA2 gene in the extremely tall.

Hendriks AE, Brown MR, Boot AM, Oostra BA, Drop SL, Parks JS.

Horm Res Paediatr. 2011;76(5):307-13. doi: 10.1159/000330764. Epub 2011 Sep 14.

PMID:
21921580
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