| Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations (“glomangiomas”) P Brouillard, LM Boon, JB Mulliken, O Enjolras, M Ghassibé, ML Warman, ... The American Journal of Human Genetics 70 (4), 866-874, 2002 | 360 | 2002 |
| Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium … RLL de Lima, SA Hoper, M Ghassibe, ME Cooper, NK Rorick, S Kondo, ... Genetics in medicine 11 (4), 241-247, 2009 | 165 | 2009 |
| Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect P Brouillard, M Ghassibé, A Penington, LM Boon, A Dompmartin, ... Journal of Medical Genetics 42 (2), e13-e13, 2005 | 151 | 2005 |
| Orofacial clefts embryology, classification, epidemiology, and genetics G Nasreddine, J El Hajj, M Ghassibe-Sabbagh Mutation Research/Reviews in Mutation Research 787, 108373, 2021 | 144 | 2021 |
| Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population M Ghassibé, B Bayet, N Revencu, C Verellen-Dumoulin, Y Gillerot, ... European journal of human genetics 13 (11), 1239-1242, 2005 | 126 | 2005 |
| Large scale association analysis identifies three susceptibility loci for coronary artery disease S Saade, JB Cazier, M Ghassibe-Sabbagh, S Youhanna, DA Badro, ... PloS one 6 (12), e29427, 2011 | 103 | 2011 |
| Genetic and environmental influences on total plasma homocysteine and its role in coronary artery disease risk M Ghassibe-Sabbagh, DE Platt, S Youhanna, AB Abchee, K Stewart, ... Atherosclerosis 222 (1), 180-186, 2012 | 99 | 2012 |
| Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene M Mustapha, N Salem, V Delague, E Chouery, M Ghassibeh, M Rai, ... Journal of medical genetics 38 (10), e36-e36, 2001 | 95 | 2001 |
| Y-chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populations DA Badro, B Douaihy, M Haber, SC Youhanna, A Salloum, ... PloS one 8 (1), e54616, 2013 | 90 | 2013 |
| Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene M Ghassibé, N Revencu, B Bayet, Y Gillerot, R Vanwijck, ... Journal of medical genetics 41 (2), e15-e15, 2004 | 84 | 2004 |
| Afghanistan's ethnic groups share a Y-chromosomal heritage structured by historical events M Haber, DE Platt, MA Bonab, SC Youhanna, DF Soria-Hernanz, ... PloS one 7 (3), e34288, 2012 | 76 | 2012 |
| FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish M Ghassibe-Sabbagh, L Desmyter, T Langenberg, F Claes, O Boute, ... The American Journal of Human Genetics 88 (2), 150-161, 2011 | 72 | 2011 |
| Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis J Hager, Y Kamatani, JB Cazier, S Youhanna, M Ghassibe-Sabbagh, ... PloS one 7 (6), e38663, 2012 | 68 | 2012 |
| Differences in osteogenic and odontogenic differentiation potential of DPSCs and SHED J Sabbagh, M Ghassibe-Sabbagh, M Fayyad-Kazan, F Al-Nemer, ... Journal of Dentistry 101, 103413, 2020 | 57 | 2020 |
| T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility M Ghassibe-Sabbagh, M Haber, AK Salloum, Y Al-Sarraj, Y Akle, K Hirbli, ... Scientific reports 4 (1), 7351, 2014 | 41 | 2014 |
| Multivariate epidemiologic analysis of type 2 diabetes mellitus risks in the Lebanese population M Ghassibe-Sabbagh, M Deeb, AK Salloum, F Mouzaya, M Haber, ... Diabetology & Metabolic Syndrome 6, 1-12, 2014 | 33 | 2014 |
| IRF6 screening of syndromic and a priori non-syndromic cleft lip and palate patients: identification of a new type of minor VWS sign L Desmyter, M Ghassibé, N Revencu, O Boute, M Lees, G François, ... Molecular Syndromology 1 (2), 67-74, 2010 | 31 | 2010 |
| Association of hypertension with coronary artery disease onset in the Lebanese population A Milane, J Abdallah, R Kanbar, G Khazen, M Ghassibe-Sabbagh, ... Springerplus 3, 1-7, 2014 | 27 | 2014 |
| Orofacial clefting: update on the role of genetics M Ghassibé, B Bayet, N Revencu, L Desmyter, C Verellen-Dumoulin, ... B ENT, 20, 2006 | 27 | 2006 |
| Impact of inflammation, gene variants, and cigarette smoking on coronary artery disease risk M Merhi, S Demirdjian, E Hariri, N Sabbah, S Youhanna, ... Inflammation Research 64, 415-422, 2015 | 26 | 2015 |
