Hofman A - Search Results

1

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, Baird PN, Vitart V, Paterson AD, Mitchell P, Saw SM, Fossarello M, Kazmierkiewicz K, Murgia F, Portas L, Schache M, Richardson A, Xie J, Wang JJ, Rochtchina E; DCCT/EDIC Research Group; Viswanathan AC, Hayward C, Wright AF, Polasek O, Campbell H, Rudan I, Oostra BA, Uitterlinden AG, Hofman A, Rivadeneira F, Amin N, Karssen LC, Vingerling JR, Hosseini SM, Döring A, Bettecken T, Vatavuk Z, Gieger C, Wichmann HE, Wilson JF, Fleck B, Foster PJ, Topouzis F, McGuffin P, Sim X, Inouye M, Holliday EG, Attia J, Scott RJ, Rotter JI, Meitinger T, Bailey-Wilson JE. Stambolian D, et al. Among authors: hofman a. Hum Mol Genet. 2013 Jul 1;22(13):2754-64. doi: 10.1093/hmg/ddt116. Epub 2013 Mar 7. Hum Mol Genet. 2013. PMID: 23474815 Free PMC article.

2

Association between genetic variation in the gene for insulin-like growth factor-I and low birthweight.

Vaessen N, Janssen JA, Heutink P, Hofman A, Lamberts SW, Oostra BA, Pols HA, van Duijn CM. Vaessen N, et al. Among authors: hofman a. Lancet. 2002 Mar 23;359(9311):1036-7. doi: 10.1016/s0140-6736(02)08067-4. Lancet. 2002. PMID: 11937187

3

The risk and natural course of age-related maculopathy: follow-up at 6 1/2 years in the Rotterdam study.

van Leeuwen R, Klaver CC, Vingerling JR, Hofman A, de Jong PT. van Leeuwen R, et al. Among authors: hofman a. Arch Ophthalmol. 2003 Apr;121(4):519-26. doi: 10.1001/archopht.121.4.519. Arch Ophthalmol. 2003. PMID: 12695249

4

Association of 5' estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk.

van Meurs JB, Schuit SC, Weel AE, van der Klift M, Bergink AP, Arp PP, Colin EM, Fang Y, Hofman A, van Duijn CM, van Leeuwen JP, Pols HA, Uitterlinden AG. van Meurs JB, et al. Among authors: hofman a. Hum Mol Genet. 2003 Jul 15;12(14):1745-54. doi: 10.1093/hmg/ddg176. Hum Mol Genet. 2003. PMID: 12837697 Free article.

5

Association between an insulin-like growth factor I gene promoter polymorphism and bone mineral density in the elderly: the Rotterdam Study.

Rivadeneira F, Houwing-Duistermaat JJ, Vaessen N, Vergeer-Drop JM, Hofman A, Pols HA, Van Duijn CM, Uitterlinden AG. Rivadeneira F, et al. Among authors: hofman a. J Clin Endocrinol Metab. 2003 Aug;88(8):3878-84. doi: 10.1210/jc.2002-021813. J Clin Endocrinol Metab. 2003. PMID: 12915683 Free article.

6

Relationship between refraction and prevalent as well as incident age-related maculopathy: the Rotterdam Study.

Ikram MK, van Leeuwen R, Vingerling JR, Hofman A, de Jong PT. Ikram MK, et al. Among authors: hofman a. Invest Ophthalmol Vis Sci. 2003 Sep;44(9):3778-82. doi: 10.1167/iovs.03-0120. Invest Ophthalmol Vis Sci. 2003. PMID: 12939291 Free article.

7

Cdx-2 polymorphism in the promoter region of the human vitamin D receptor gene determines susceptibility to fracture in the elderly.

Fang Y, van Meurs JB, Bergink AP, Hofman A, van Duijn CM, van Leeuwen JP, Pols HA, Uitterlinden AG. Fang Y, et al. Among authors: hofman a. J Bone Miner Res. 2003 Sep;18(9):1632-41. doi: 10.1359/jbmr.2003.18.9.1632. J Bone Miner Res. 2003. PMID: 12968672 Free article.

8

Epidemiology of age-related maculopathy: a review.

van Leeuwen R, Klaver CC, Vingerling JR, Hofman A, de Jong PT. van Leeuwen R, et al. Among authors: hofman a. Eur J Epidemiol. 2003;18(9):845-54. doi: 10.1023/a:1025643303914. Eur J Epidemiol. 2003. PMID: 14561043 Review.

9

A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands.

Aulchenko YS, Vaessen N, Heutink P, Pullen J, Snijders PJ, Hofman A, Sandkuijl LA, Houwing-Duistermaat JJ, Edwards M, Bennett S, Oostra BA, van Duijn CM. Aulchenko YS, et al. Among authors: hofman a. Diabetes. 2003 Dec;52(12):3001-4. doi: 10.2337/diabetes.52.12.3001. Diabetes. 2003. PMID: 14633863

10

Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.

Croes EA, Alizadeh BZ, Bertoli-Avella AM, Rademaker T, Vergeer-Drop J, Dermaut B, Houwing-Duistermaat JJ, Wientjens DP, Hofman A, Van Broeckhoven C, van Duijn CM. Croes EA, et al. Among authors: hofman a. Eur J Hum Genet. 2004 May;12(5):389-94. doi: 10.1038/sj.ejhg.5201161. Eur J Hum Genet. 2004. PMID: 14970845

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