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Cited by in F6Publishing
For: Nakouzi G, Kreidieh K, Yazbek S. A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services. J Community Genet 2015;6:83-105. [PMID: 25261319 DOI: 10.1007/s12687-014-0203-3] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.1] [Reference Citation Analysis]
Number Citing Articles
1 Hamad L, Kreidieh K, Hamdan MB, Nakouzi G, Yazbek S. Mapping the Diverse Genetic Disorders and Rare Diseases Among the Syrian Population: Implications on Refugee Health and Health Services in Host Countries. J Immigr Minor Health 2020;22:1347-67. [PMID: 32172498 DOI: 10.1007/s10903-020-00987-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Haber M, Doumet-Serhal C, Scheib C, Xue Y, Danecek P, Mezzavilla M, Youhanna S, Martiniano R, Prado-Martinez J, Szpak M, Matisoo-Smith E, Schutkowski H, Mikulski R, Zalloua P, Kivisild T, Tyler-Smith C. Continuity and Admixture in the Last Five Millennia of Levantine History from Ancient Canaanite and Present-Day Lebanese Genome Sequences. Am J Hum Genet 2017;101:274-82. [PMID: 28757201 DOI: 10.1016/j.ajhg.2017.06.013] [Cited by in Crossref: 58] [Cited by in F6Publishing: 43] [Article Influence: 11.6] [Reference Citation Analysis]
3 Jaffal L, Joumaa WH, Assi A, Helou C, Condroyer C, El Dor M, Cherfan G, Zeitz C, Audo I, Zibara K, El Shamieh S. Novel Missense Mutations in BEST1 Are Associated with Bestrophinopathies in Lebanese Patients. Genes (Basel) 2019;10:E151. [PMID: 30781664 DOI: 10.3390/genes10020151] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
4 Hamad L, Kreidieh K, Nakouzi G, Lyon E, Yazbek S. Recommended measures for the efficient care of patients with genetic disorders during the COVID-19 pandemic in low and middle income countries. Am J Med Genet A 2020;182:2841-6. [PMID: 33067931 DOI: 10.1002/ajmg.a.61879] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Vatsyayan A, Sharma P, Gupta S, Sandhu S, Venu SL, Sharma V, Badaoui B, Azedine K, Youssef S, Rajab A, Fayez A, Madinur S, Ranawat A, Pandhare K, Ramachandran S, Sivasubbu S, Scaria V. DALIA- a comprehensive resource of Disease Alleles in Arab population. PLoS One 2021;16:e0244567. [PMID: 33439861 DOI: 10.1371/journal.pone.0244567] [Reference Citation Analysis]
6 Nair P, Sabbagh S, Mansour H, Fawaz A, Hmaimess G, Noun P, Dagher R, Megarbane H, Hana S, Alame S, Lamaa M, Hasbini D, Farah R, Rajab M, Stora S, El-Tourjuman O, Abou Jaoude P, Chalouhi G, Sayad R, Gillart AC, Al-Ali M, Delague V, El-Hayek S, Mégarbané A. Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases. Mol Genet Genomic Med 2018;6:1041-52. [PMID: 30293248 DOI: 10.1002/mgg3.480] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 1.8] [Reference Citation Analysis]
7 Bizzari S, Nair P, Deepthi A, Hana S, Al-Ali MT, Megarbané A, El-Hayek S. Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders. Genes (Basel) 2021;12:1518. [PMID: 34680914 DOI: 10.3390/genes12101518] [Reference Citation Analysis]