PubMed

Characterization of CTNS mutations in Arab patients with cystinosis.

Aldahmesh MA, Humeidan A, Almojalli HA, Khan AO, Rajab M, AL-Abbad AA, Meyer BF, Alkuraya FS.

Ophthalmic Genet. 2009 Dec;30(4):185-9.PMID: 19852576 [PubMed - in process]Related articles

Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.

Morales J, Al-Sharif L, Khalil DS, Shinwari JM, Bavi P, Al-Mahrouqi RA, Al-Rajhi A, Alkuraya FS, Meyer BF, Al Tassan N.

Am J Hum Genet. 2009 Nov;85(5):558-68.PMID: 19836009 [PubMed - in process]Related articles

A study of the role of the myocyte-specific enhancer factor-2A gene in coronary artery disease.

Elhawari S, Al-Boudari O, Muiya P, Khalak H, Andres E, Al-Shahid M, Al-Dosari M, Meyer BF, Al-Mohanna F, Dzimiri N.

Atherosclerosis. 2009 Sep 9. [Epub ahead of print]PMID: 19782985 [PubMed - as supplied by publisher]Related articles

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.

Ann Hum Genet. 2009 Sep;73(Pt 5):475-83. Epub 2009 Jun 16.PMID: 19624571 [PubMed - in process]Related articles

Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations.

Al-Dirbashi OY, Shaheen R, Al-Sayed M, Al-Dosari M, Makhseed N, Abu Safieh L, Santa T, Meyer BF, Shimozawa N, Alkuraya FS.

Am J Med Genet A. 2009 Jun;149A(6):1219-23.PMID: 19449432 [PubMed - indexed for MEDLINE]Related articles

Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia.

Aldahmesh MA, Khan AO, Meyer BF, Alkuraya FS.

Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4142-5. Epub 2009 Apr 15.PMID: 19369245 [PubMed - indexed for MEDLINE]Related articles

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.

BMC Res Notes. 2009 Mar 24;2:48.PMID: 19309528 [PubMed - in process]Related articlesFree article

Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example.

Aldahmesh MA, Abu-Safieh L, Khan AO, Al-Hassnan ZN, Shaheen R, Rajab M, Monies D, Meyer BF, Alkuraya FS.

Am J Med Genet A. 2009 Feb 15;149A(4):662-5.PMID: 19283855 [PubMed - indexed for MEDLINE]Related articles

Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.

Kaya N, Imtiaz F, Colak D, Al-Sayed M, Al-Odaib A, Al-Zahrani F, Al-Mubarak BR, Al-Owain M, Al-Dhalaan H, Chedrawi A, Al-Hassnan Z, Coskun S, Sakati N, Ozand P, Meyer BF.

Genet Med. 2008 Sep;10(9):675-84.PMID: 18978679 [PubMed - indexed for MEDLINE]Related articles

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.

Eur J Hum Genet. 2009 Jan;17(1):14-21. Epub 2008 Aug 13.PMID: 18701883 [PubMed - indexed for MEDLINE]Related articles

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.

BMC Med Genet. 2008 Jul 26;9:72.PMID: 18655717 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Diabetes Metab Res Rev. 2008 Feb;24(2):137-40.PMID: 17922473 [PubMed - indexed for MEDLINE]Related articles

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.

J Med Genet. 2007 Oct;44(10):e89.PMID: 17911653 [PubMed - indexed for MEDLINE]Related articles

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

Al-Sayed M, Imtiaz F, Alsmadi OA, Rashed MS, Meyer BF.

BMC Med Genet. 2006 Dec 16;7:86.PMID: 17173698 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Genet Med. 2006 Jul;8(7):443-7.PMID: 16845277 [PubMed - indexed for MEDLINE]Related articles

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.

Clin Chem. 2006 Jul;52(7):1439-40. No abstract available. PMID: 16798975 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

BMC Med Genet. 2006 May 3;7:43.PMID: 16672055 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

J Inherit Metab Dis. 2005;28(6):877-83.PMID: 16435180 [PubMed - indexed for MEDLINE]Related articles

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.

Diabetes Care. 2006 Jan;29(1):171-2. No abstract available. PMID: 16373923 [PubMed - indexed for MEDLINE]Related articlesFree article

Strategies for the prevention of hereditary diseases in a highly consanguineous population.

Meyer BF.

Ann Hum Biol. 2005 Mar-Apr;32(2):174-9. Review.PMID: 16096214 [PubMed - indexed for MEDLINE]Related articles