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27 results

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Willingness to participate in genome testing: a survey of public attitudes from Qatar.
Abdul Rahim HF, Ismail SI, Hassan A, Fadl T, Khaled SM, Shockley B, Nasrallah C, Qutteina Y, Elmaghraby E, Yasin H, Darwish D, Fakhro KA, Badji R, Al-Muftah W, Afifi N, Althani A. Abdul Rahim HF, et al. J Hum Genet. 2020 Dec;65(12):1067-1073. doi: 10.1038/s10038-020-0806-y. Epub 2020 Jul 28. J Hum Genet. 2020. PMID: 32724056 Free PMC article.
Qatar genome: Insights on genomics from the Middle East.
Mbarek H, Devadoss Gandhi G, Selvaraj S, Al-Muftah W, Badji R, Al-Sarraj Y, Saad C, Darwish D, Alvi M, Fadl T, Yasin H, Alkuwari F, Razali R, Aamer W, Abbaszadeh F, Ahmed I, Mokrab Y, Suhre K, Albagha O, Fakhro K, Badii R, Ismail SI, Althani A; Qatar Genome Program Research Consortium. Mbarek H, et al. Among authors: al muftah w. Hum Mutat. 2022 Apr;43(4):499-510. doi: 10.1002/humu.24336. Epub 2022 Feb 20. Hum Mutat. 2022. PMID: 35112413
The QChip1 knowledgebase and microarray for precision medicine in Qatar.
Rodriguez-Flores JL, Messai-Badji R, Robay A, Temanni R, Syed N, Markovic M, Al-Khayat E, Qafoud F, Nawaz Z, Badii R, Al-Sarraj Y, Mbarek H, Al-Muftah W, Alvi M, Rostami MR, Cruzado JCM, Mezey JG, Shakaki AA, Malek JA, Greenblatt MB, Fakhro KA, Machaca K, Al-Nabet A, Afifi N, Brooks A, Ismail SI, Althani A, Crystal RG. Rodriguez-Flores JL, et al. Among authors: al muftah w. NPJ Genom Med. 2022 Jan 19;7(1):3. doi: 10.1038/s41525-021-00270-0. NPJ Genom Med. 2022. PMID: 35046417 Free PMC article.
A population study of clinically actionable genetic variation affecting drug response from the Middle East.
Jithesh PV, Abuhaliqa M, Syed N, Ahmed I, El Anbari M, Bastaki K, Sherif S, Umlai UK, Jan Z, Gandhi G, Manickam C, Selvaraj S, George C, Bangarusamy D, Abdel-Latif R, Al-Shafai M, Tatari-Calderone Z, Estivill X, Pirmohamed M; Qatar Genome Program Research Consortium. Jithesh PV, et al. NPJ Genom Med. 2022 Feb 15;7(1):10. doi: 10.1038/s41525-022-00281-5. NPJ Genom Med. 2022. PMID: 35169154 Free PMC article.
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.
Fallerini C, Picchiotti N, Baldassarri M, Zguro K, Daga S, Fava F, Benetti E, Amitrano S, Bruttini M, Palmieri M, Croci S, Lista M, Beligni G, Valentino F, Meloni I, Tanfoni M, Minnai F, Colombo F, Cabri E, Fratelli M, Gabbi C, Mantovani S, Frullanti E, Gori M, Crawley FP, Butler-Laporte G, Richards B, Zeberg H, Lipcsey M, Hultström M, Ludwig KU, Schulte EC, Pairo-Castineira E, Baillie JK, Schmidt A, Frithiof R; WES/WGS Working Group Within the HGI; GenOMICC Consortium; GEN-COVID Multicenter Study; Mari F, Renieri A, Furini S. Fallerini C, et al. Hum Genet. 2022 Jan;141(1):147-173. doi: 10.1007/s00439-021-02397-7. Epub 2021 Dec 10. Hum Genet. 2022. PMID: 34889978 Free PMC article.
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