Mackay IJ - Search Results

1

Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.

Treloar SA, Wicks J, Nyholt DR, Montgomery GW, Bahlo M, Smith V, Dawson G, Mackay IJ, Weeks DE, Bennett ST, Carey A, Ewen-White KR, Duffy DL, O'connor DT, Barlow DH, Martin NG, Kennedy SH. Treloar SA, et al. Among authors: mackay ij. Am J Hum Genet. 2005 Sep;77(3):365-76. doi: 10.1086/432960. Epub 2005 Jul 21. Am J Hum Genet. 2005. PMID: 16080113 Free PMC article.

2

Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.

Zondervan KT, Treloar SA, Lin J, Weeks DE, Nyholt DR, Mangion J, MacKay IJ, Cardon LR, Martin NG, Kennedy SH, Montgomery GW. Zondervan KT, et al. Among authors: mackay ij. Hum Reprod. 2007 Mar;22(3):717-28. doi: 10.1093/humrep/del446. Epub 2006 Dec 11. Hum Reprod. 2007. PMID: 17158817

3

The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants.

van Heel DA, Dechairo BM, Dawson G, McGovern DP, Negoro K, Carey AH, Cardon LR, Mackay I, Jewell DP, Lench NJ. van Heel DA, et al. Hum Mol Genet. 2003 Oct 15;12(20):2569-75. doi: 10.1093/hmg/ddg281. Epub 2003 Aug 19. Hum Mol Genet. 2003. PMID: 12928481

4

Loci for regulation of bone mineral density in men and women identified by genome wide linkage scan: the FAMOS study.

Ralston SH, Galwey N, MacKay I, Albagha OM, Cardon L, Compston JE, Cooper C, Duncan E, Keen R, Langdahl B, McLellan A, O'Riordan J, Pols HA, Reid DM, Uitterlinden AG, Wass J, Bennett ST. Ralston SH, et al. Hum Mol Genet. 2005 Apr 1;14(7):943-51. doi: 10.1093/hmg/ddi088. Epub 2005 Mar 3. Hum Mol Genet. 2005. PMID: 15746152

5

Association of the TSHR gene with Graves' disease: the first disease specific locus.

Dechairo BM, Zabaneh D, Collins J, Brand O, Dawson GJ, Green AP, Mackay I, Franklyn JA, Connell JM, Wass JA, Wiersinga WM, Hegedus L, Brix T, Robinson BG, Hunt PJ, Weetman AP, Carey AH, Gough SC. Dechairo BM, et al. Eur J Hum Genet. 2005 Nov;13(11):1223-30. doi: 10.1038/sj.ejhg.5201485. Eur J Hum Genet. 2005. PMID: 16106256

6

Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.

Berry V, Francis P, Reddy MA, Collyer D, Vithana E, MacKay I, Dawson G, Carey AH, Moore A, Bhattacharya SS, Quinlan RA. Berry V, et al. Am J Hum Genet. 2001 Nov;69(5):1141-5. doi: 10.1086/324158. Epub 2001 Sep 27. Am J Hum Genet. 2001. PMID: 11577372 Free PMC article.

7

Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3).

Dechairo B, Dimon C, van Heel D, Mackay I, Edwards M, Scambler P, Jewell D, Cardon L, Lench N, Carey A. Dechairo B, et al. Eur J Hum Genet. 2001 Aug;9(8):627-33. doi: 10.1038/sj.ejhg.5200687. Eur J Hum Genet. 2001. PMID: 11528509

8

Evidence for a major gene for bone mineral density in idiopathic osteoporotic families.

Cardon LR, Garner C, Bennett ST, Mackay IJ, Edwards RM, Cornish J, Hegde M, Murray MA, Reid IR, Cundy T. Cardon LR, et al. Among authors: mackay ij. J Bone Miner Res. 2000 Jun;15(6):1132-7. doi: 10.1359/jbmr.2000.15.6.1132. J Bone Miner Res. 2000. PMID: 10841182 Free article.

9

Likelihood-based estimation of microsatellite mutation rates.

Whittaker JC, Harbord RM, Boxall N, Mackay I, Dawson G, Sibly RM. Whittaker JC, et al. Genetics. 2003 Jun;164(2):781-7. doi: 10.1093/genetics/164.2.781. Genetics. 2003. PMID: 12807796 Free PMC article.

10

LPIN2 is associated with type 2 diabetes, glucose metabolism, and body composition.

Aulchenko YS, Pullen J, Kloosterman WP, Yazdanpanah M, Hofman A, Vaessen N, Snijders PJ, Zubakov D, Mackay I, Olavesen M, Sidhu B, Smith VE, Carey A, Berezikov E, Uitterlinden AG, Plasterk RH, Oostra BA, van Duijn CM. Aulchenko YS, et al. Diabetes. 2007 Dec;56(12):3020-6. doi: 10.2337/db07-0338. Epub 2007 Sep 5. Diabetes. 2007. PMID: 17804763

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