Alsmadi O - Search Results

1

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).

Alsmadi O, Meyer BF, Alkuraya F, Wakil S, Alkayal F, Al-Saud H, Ramzan K, Al-Sayed M. Alsmadi O, et al. Eur J Hum Genet. 2009 Jan;17(1):14-21. doi: 10.1038/ejhg.2008.141. Epub 2008 Aug 13. Eur J Hum Genet. 2009. PMID: 18701883 Free PMC article.

2

The peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and type 2 diabetes in an Arab population.

Wakil SM, Al-Rubeaan K, Alsmadi O, Imtiaz F, Carroll P, Rajab M, Al-Katari S, Al-Katari M, Meyer BF. Wakil SM, et al. Among authors: alsmadi o. Diabetes Care. 2006 Jan;29(1):171-2. doi: 10.2337/diacare.29.1.171. Diabetes Care. 2006. PMID: 16373923 No abstract available.

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: alsmadi o. 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. 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

LCGreen I-based real-time PCR assays for detecting common ASL and HMGCL variants.

Alsmadi O, Alkayal F, Al-Sayed M, Rashed MS, Imtiaz F, Meyer BF. Alsmadi O, et al. Clin Chem. 2006 Jul;52(7):1439-40. doi: 10.1373/clinchem.2006.067538. Clin Chem. 2006. PMID: 16798975 No abstract available.

6

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. BMC Med Genet. 2006 Dec 16;7:86. doi: 10.1186/1471-2350-7-86. BMC Med Genet. 2006. PMID: 17173698 Free PMC article.

7

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. Diabetes Metab Res Rev. 2008 Feb;24(2):137-40. doi: 10.1002/dmrr.777. Diabetes Metab Res Rev. 2008. PMID: 17922473

8

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. BMC Med Genet. 2008 Jul 26;9:72. doi: 10.1186/1471-2350-9-72. BMC Med Genet. 2008. PMID: 18655717 Free PMC article.

9

Specific and complete human genome amplification with improved yield achieved by phi29 DNA polymerase and a novel primer at elevated temperature.

Alsmadi O, Alkayal F, Monies D, Meyer BF. Alsmadi O, et al. BMC Res Notes. 2009 Mar 24;2:48. doi: 10.1186/1756-0500-2-48. BMC Res Notes. 2009. PMID: 19309528 Free PMC article.

10

Haplotypes encompassing the KIAA0391 and PSMA6 gene cluster confer a genetic link for myocardial infarction and coronary artery disease.

Alsmadi O, Muiya P, Khalak H, Al-Saud H, Meyer BF, Al-Mohanna F, Alshahid M, Dzimiri N. Alsmadi O, et al. Ann Hum Genet. 2009 Sep;73(Pt 5):475-83. doi: 10.1111/j.1469-1809.2009.00534.x. Epub 2009 Jun 16. Ann Hum Genet. 2009. PMID: 19624571

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