Theo dõi
Michella Ghassibe
Michella Ghassibe
Assistant Professor in Human Genetics, Lebanese American University
Email được xác minh tại lau.edu.lb
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
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
3652002
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
1652009
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
1492005
Orofacial clefts embryology, classification, epidemiology, and genetics
G Nasreddine, J El Hajj, M Ghassibe-Sabbagh
Mutation Research/Reviews in Mutation Research 787, 108373, 2021
1422021
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
1232005
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
1052011
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
972012
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
932001
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
882013
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
802004
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
742012
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
712012
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
712011
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
572020
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
392014
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
322014
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
292010
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
272015
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
272014
Orofacial clefting: update on the role of genetics
M Ghassibé, B Bayet, N Revencu, L Desmyter, C Verellen-Dumoulin, ...
B ENT, 20, 2006
272006
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