Badii R - Search Results

1

The Molecular Basis of α-Thalassemia in the Qatari Pediatric Population.

Kamal M, Abu-Sirriya S, Abu-Dayya A, Al-Khatib H, Abu-Ramadan H, Petrou M, Amer A, Badii R, Kleanthous M. Kamal M, et al. Among authors: badii r. Hemoglobin. 2015;39(5):350-4. doi: 10.3109/03630269.2015.1060606. Epub 2015 Jul 10. Hemoglobin. 2015. PMID: 26161810

2

A common mutation in the CBS gene explains a high incidence of homocystinuria in the Qatari population.

El-Said MF, Badii R, Bessisso MS, Shahbek N, El-Ali MG, El-Marikhie M, El-Zyoid M, Salem MS, Bener A, Hoffmann GF, Zschocke J. El-Said MF, et al. Among authors: badii r. Hum Mutat. 2006 Jul;27(7):719. doi: 10.1002/humu.9436. Hum Mutat. 2006. PMID: 16786517

3

GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.

Khalifa Alkowari M, Girotto G, Abdulhadi K, Dipresa S, Siam R, Najjar N, Badii R, Gasparini P. Khalifa Alkowari M, et al. Among authors: badii r. Int J Audiol. 2012 Mar;51(3):181-5. doi: 10.3109/14992027.2011.625983. Epub 2011 Nov 21. Int J Audiol. 2012. PMID: 22103400

4

Type 2 Diabetes Risk Allele Loci in the Qatari Population.

O'Beirne SL, Salit J, Rodriguez-Flores JL, Staudt MR, Abi Khalil C, Fakhro KA, Robay A, Ramstetter MD, Al-Azwani IK, Malek JA, Zirie M, Jayyousi A, Badii R, Al-Nabet Al-Marri A, Chiuchiolo MJ, Al-Shakaki A, Chidiac O, Gharbiah M, Bener A, Stadler D, Hackett NR, Mezey JG, Crystal RG. O'Beirne SL, et al. Among authors: badii r. PLoS One. 2016 Jul 6;11(7):e0156834. doi: 10.1371/journal.pone.0156834. eCollection 2016. PLoS One. 2016. PMID: 27383215 Free PMC article.

5

Ancestry-related distribution of Runs of homozygosity and functional variants in Qatari population.

Mezzavilla M, Cocca M, Maisano Delser P, Badii R, Abbaszadeh F, Hadi KA, Giorgia G, Gasparini P. Mezzavilla M, et al. Among authors: badii r. BMC Genom Data. 2022 Sep 21;23(1):73. doi: 10.1186/s12863-022-01087-1. BMC Genom Data. 2022. PMID: 36131251 Free PMC article.

6

Lack of association between the Pro12Ala polymorphism of the PPAR-gamma 2 gene and type 2 diabetes mellitus in the Qatari consanguineous population.

Badii R, Bener A, Zirie M, Al-Rikabi A, Simsek M, Al-Hamaq AO, Ghoussaini M, Froguel P, Wareham NJ. Badii R, et al. Acta Diabetol. 2008 Mar;45(1):15-21. doi: 10.1007/s00592-007-0013-8. Epub 2007 Sep 6. Acta Diabetol. 2008. PMID: 17805473

7

Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients.

Vozzi D, Morgan A, Vuckovic D, D'Eustacchio A, Abdulhadi K, Rubinato E, Badii R, Gasparini P, Girotto G. Vozzi D, et al. Among authors: badii r. Gene. 2014 Jun 1;542(2):209-16. doi: 10.1016/j.gene.2014.03.033. Epub 2014 Mar 20. Gene. 2014. PMID: 24657061

8

Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families.

Alkowari MK, Vozzi D, Bhagat S, Krishnamoorthy N, Morgan A, Hayder Y, Logendra B, Najjar N, Gandin I, Gasparini P, Badii R, Girotto G, Abdulhadi K. Alkowari MK, et al. Among authors: badii r. Mutat Res. 2017 Aug;800-802:29-36. doi: 10.1016/j.mrfmmm.2017.05.001. Epub 2017 May 4. Mutat Res. 2017. PMID: 28501645

9

Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population.

O'Beirne SL, Salit J, Rodriguez-Flores JL, Staudt MR, Abi Khalil C, Fakhro KA, Robay A, Ramstetter MD, Malek JA, Zirie M, Jayyousi A, Badii R, Al-Nabet Al-Marri A, Bener A, Mahmoud M, Chiuchiolo MJ, Al-Shakaki A, Chidiac O, Stadler D, Mezey JG, Crystal RG. O'Beirne SL, et al. Among authors: badii r. PLoS One. 2018 Sep 13;13(9):e0199837. doi: 10.1371/journal.pone.0199837. eCollection 2018. PLoS One. 2018. PMID: 30212457 Free PMC article. Clinical Trial.

10

Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits.

Thareja G, Al-Sarraj Y, Belkadi A, Almotawa M; Qatar Genome Program Research (QGPR) Consortium; Suhre K, Albagha OME. Thareja G, et al. Nat Commun. 2021 Feb 23;12(1):1250. doi: 10.1038/s41467-021-21381-3. Nat Commun. 2021. PMID: 33623009 Free PMC article.

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