Meyer BF - Search Results

1

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population.

Imtiaz F, Taibah K, Ramzan K, Bin-Khamis G, Kennedy S, Al-Mubarak B, Trabzuni D, Allam R, Al-Mostafa A, Sogaty S, Al-Shaikh AH, Bamukhayyar SS, Meyer BF, Al-Owain M. Imtiaz F, et al. Among authors: meyer bf. BMC Med Genet. 2011 Jul 4;12:91. doi: 10.1186/1471-2350-12-91. BMC Med Genet. 2011. PMID: 21726435 Free PMC article.

2

Novel PRG4 mutations underlie CACP in Saudi families.

Alazami AM, Al-Mayouf SM, Wyngaard CA, Meyer B. Alazami AM, et al. Hum Mutat. 2006 Feb;27(2):213. doi: 10.1002/humu.9399. Hum Mutat. 2006. PMID: 16429407

3

Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria.

Al-Sayed M, Alahmed S, Alsmadi O, Khalil H, Rashed MS, Imtiaz F, Meyer BF. Al-Sayed M, et al. Among authors: meyer bf. J Inherit Metab Dis. 2005;28(6):877-83. doi: 10.1007/s10545-005-0081-2. J Inherit Metab Dis. 2005. PMID: 16435180

4

Frequency of common HFE variants in the Saudi population: a high throughput molecular beacon-based study.

Alsmadi OA, Al-Kayal F, Al-Hamed M, Meyer BF. Alsmadi OA, et al. Among authors: meyer bf. BMC Med Genet. 2006 May 3;7:43. doi: 10.1186/1471-2350-7-43. BMC Med Genet. 2006. PMID: 16672055 Free PMC article.

5

Novel mutations underlying nephrogenic diabetes insipidus in Arab families.

Carroll P, Al-Mojalli H, Al-Abbad A, Al-Hassoun I, Al-Hamed M, Al-Amr R, Butt AI, Meyer BF. Carroll P, et al. Among authors: meyer bf. Genet Med. 2006 Jul;8(7):443-7. doi: 10.1097/01.gim.0000223554.46981.7a. Genet Med. 2006. PMID: 16845277 Free article.

6

Recessive cornea plana in the Kingdom of Saudi Arabia.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Ophthalmology. 2006 Oct;113(10):1773-8. doi: 10.1016/j.ophtha.2006.04.026. Ophthalmology. 2006. PMID: 17011957

7

Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.

Al-Sayed M, Imtiaz F, Alsmadi OA, Rashed MS, Meyer BF. Al-Sayed M, et al. Among authors: meyer bf. BMC Med Genet. 2006 Dec 16;7:86. doi: 10.1186/1471-2350-7-86. BMC Med Genet. 2006. PMID: 17173698 Free PMC article.

8

The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.

Imtiaz F, Savilahti E, Sarnesto A, Trabzuni D, Al-Kahtani K, Kagevi I, Rashed MS, Meyer BF, Järvelä I. Imtiaz F, et al. Among authors: meyer bf. J Med Genet. 2007 Oct;44(10):e89. doi: 10.1136/jmg.2007.051631. J Med Genet. 2007. PMID: 17911653 Free PMC article.

9

Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes.

Alsmadi O, Al-Rubeaan K, Wakil SM, Imtiaz F, Mohamed G, Al-Saud H, Al-Saud NA, Aldaghri N, Mohammad S, Meyer BF. Alsmadi O, et al. Among authors: meyer bf. Diabetes Metab Res Rev. 2008 Feb;24(2):137-40. doi: 10.1002/dmrr.777. Diabetes Metab Res Rev. 2008. PMID: 17922473

10

Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population.

Alsmadi O, Al-Rubeaan K, Mohamed G, Alkayal F, Al-Saud H, Al-Saud NA, Al-Daghri N, Mohammad S, Meyer BF. Alsmadi O, et al. Among authors: meyer bf. BMC Med Genet. 2008 Jul 26;9:72. doi: 10.1186/1471-2350-9-72. BMC Med Genet. 2008. PMID: 18655717 Free PMC article.

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