Meyer BF - Search Results

1

A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.

Wakil SM, Ram R, Muiya NP, Andres E, Mazhar N, Hagos S, Alshahid M, Meyer BF, Morahan G, Dzimiri N. Wakil SM, et al. Among authors: meyer bf. Clin Genet. 2016 Dec;90(6):518-525. doi: 10.1111/cge.12761. Epub 2016 Mar 8. Clin Genet. 2016. PMID: 26879886

2

Relevance of apolipoprotein E polymorphism for coronary artery disease in the Saudi population.

Dzimiri N, Meyer BF, Hussain SS, Basco C, Afrane B, Halees Z. Dzimiri N, et al. Among authors: meyer bf. Arch Pathol Lab Med. 1999 Dec;123(12):1241-5. doi: 10.5858/1999-123-1241-ROAEPF. Arch Pathol Lab Med. 1999. PMID: 10583930 Free article.

3

Angiotensin-converting enzyme polymorphism and the risk of coronary heart disease in the Saudi male population.

Dzimiri N, Basco C, Moorji A, Meyer BF. Dzimiri N, et al. Among authors: meyer bf. Arch Pathol Lab Med. 2000 Apr;124(4):531-4. doi: 10.5858/2000-124-0531-ACEPAT. Arch Pathol Lab Med. 2000. PMID: 10747309 Free article.

4

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.

Bohlega S, Abu-Amero SN, Wakil SM, Carroll P, Al-Amr R, Lach B, Al-Sayed Y, Cupler EJ, Meyer BF. Bohlega S, et al. Among authors: meyer bf. Neurology. 2004 May 11;62(9):1518-21. doi: 10.1212/01.wnl.0000123255.92062.37. Neurology. 2004. PMID: 15136674

5

Phenotypic variation and allelic heterogeneity in young patients with Papillon-Lefèvre syndrome.

Ullbro C, El-Samadi S, Boumah C, Al-Yousef N, Wakil S, Twetman S, Alfadley A, Thestrup-Pedersen K, Meyer B. Ullbro C, et al. Acta Derm Venereol. 2006;86(1):3-7. doi: 10.1080/00015550510011619. Acta Derm Venereol. 2006. PMID: 16585980 Free article.

6

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

7

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.

8

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. Among authors: meyer bf. 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.

9

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. Among authors: meyer bf. 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

10

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. Elhawari S, et al. Among authors: meyer bf. Atherosclerosis. 2010 Mar;209(1):152-4. doi: 10.1016/j.atherosclerosis.2009.09.005. Epub 2009 Sep 9. Atherosclerosis. 2010. PMID: 19782985

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