Alsmadi O - Search Results

1

MC4R Variant rs17782313 Associates With Increased Levels of DNAJC27, Ghrelin, and Visfatin and Correlates With Obesity and Hypertension in a Kuwaiti Cohort.

Hammad MM, Abu-Farha M, Hebbar P, Cherian P, Al Khairi I, Melhem M, Alkayal F, Alsmadi O, Thanaraj TA, Al-Mulla F, Abubaker J. Hammad MM, et al. Among authors: alsmadi o. Front Endocrinol (Lausanne). 2020 Jul 7;11:437. doi: 10.3389/fendo.2020.00437. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32733386 Free PMC article.

2

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.

3

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.

4

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.

5

Major histocompatibility complex class II deficiency in Kuwait: clinical manifestations, immunological findings and molecular profile.

Al-Herz W, Alsmadi O, Melhem M, Recher M, Frugoni F, Notarangelo LD. Al-Herz W, et al. Among authors: alsmadi o. J Clin Immunol. 2013 Apr;33(3):513-9. doi: 10.1007/s10875-012-9831-8. Epub 2012 Nov 10. J Clin Immunol. 2013. PMID: 23143406

6

Genetic substructure of Kuwaiti population reveals migration history.

Alsmadi O, Thareja G, Alkayal F, Rajagopalan R, John SE, Hebbar P, Behbehani K, Thanaraj TA. Alsmadi O, et al. PLoS One. 2013 Sep 16;8(9):e74913. doi: 10.1371/journal.pone.0074913. eCollection 2013. PLoS One. 2013. PMID: 24066156 Free PMC article.

7

Leptin in association with common variants of MC3R mediates hypertension.

Alsmadi O, Melhem M, Hebbar P, Thareja G, John SE, Alkayal F, Behbehani K, Thanaraj TA. Alsmadi O, et al. Am J Hypertens. 2014 Jul;27(7):973-81. doi: 10.1093/ajh/hpt285. Epub 2014 Feb 2. Am J Hypertens. 2014. PMID: 24487982

8

ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.

Behbehani R, Melhem M, Alghanim G, Behbehani K, Alsmadi O. Behbehani R, et al. Among authors: alsmadi o. Br J Ophthalmol. 2014 Jun;98(6):826-31. doi: 10.1136/bjophthalmol-2013-304140. Epub 2014 Feb 25. Br J Ophthalmol. 2014. PMID: 24568867 Free PMC article.

9

Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry.

Alsmadi O, John SE, Thareja G, Hebbar P, Antony D, Behbehani K, Thanaraj TA. Alsmadi O, et al. PLoS One. 2014 Jun 4;9(6):e99069. doi: 10.1371/journal.pone.0099069. eCollection 2014. PLoS One. 2014. PMID: 24896259 Free PMC article.

10

Response to leptin and nitric oxide in blood pressure regulation in humans.

Alsmadi O, Melhem M, Hebbar P, Channanath A, Thareja G, John SE, Alkayal F, Behbehani K, Thanaraj TA. Alsmadi O, et al. Am J Hypertens. 2014 Nov;27(11):1429-30. doi: 10.1093/ajh/hpu178. Epub 2014 Oct 1. Am J Hypertens. 2014. PMID: 25273037 Free PMC article. No abstract available.

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