| A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot G Nemer, F Fadlalah, J Usta, M Nemer, G Dbaibo, M Obeid, F Bitar Human mutation 27 (3), 293-294, 2006 | 229 | 2006 |
| Parental consanguinity and congenital heart malformations in a developing country MM Nabulsi, H Tamim, M Sabbagh, MY Obeid, KA Yunis, FF Bitar American journal of medical genetics Part A 116 (4), 342-347, 2003 | 162 | 2003 |
| Consanguineous marriage and congenital heart defects: A case‐control study in the neonatal period Y Khalid, M Ghina, B Fadi, C Fadi, K May, R Joseph, G Makhoul, T Hala American journal of medical genetics Part A 140 (14), 1524-1530, 2006 | 146 | 2006 |
| Rheumatic fever in children: a 15-year experience in a developing country FF Bitar, P Hayek, M Obeid, W Gharzeddine, M Mikati, GS Dbaibo Pediatric cardiology 21, 119-122, 2000 | 111 | 2000 |
| Ocular pathology in congenital heart disease AM Mansour, FF Bitar, EI Traboulsi, KM Kassak, MY Obeid, A Megarbane, ... Eye 19 (1), 29-34, 2005 | 92 | 2005 |
| Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study TR Tromp, ML Hartgers, GK Hovingh, AJ Vallejo-Vaz, KK Ray, H Soran, ... The Lancet 399 (10326), 719-728, 2022 | 89 | 2022 |
| Long-term effects of acute and of chronic hypoxia on behavior and on hippocampal histology in the developing brain MA Mikati, MP Zeinieh, RM Kurdi, SA Harb, JA El Hokayem, RH Daderian, ... Developmental brain research 157 (1), 98-102, 2005 | 79 | 2005 |
| Doppler characterization of left ventricular diastolic function in β-thalassaemia major. Evidence for an early stage of impaired relaxation WS Gharzuddine, HK Kazma, IA Nuwayhid, FF Bitar, SF Koussa, ... European Journal of Echocardiography 3 (1), 47-51, 2002 | 77 | 2002 |
| Research in congenital heart disease: A comparative bibliometric analysis between developing and developed countries T Farhat, Z Abdul-Sater, M Obeid, M Arabi, K Diab, S Masri, Z Al Haless, ... Pediatric cardiology 34, 375-382, 2013 | 75 | 2013 |
| Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis Y Shigehara, S Okuda, G Nemer, A Chedraoui, R Hayashi, F Bitar, ... Human molecular genetics 25 (20), 4484-4493, 2016 | 71 | 2016 |
| Apoptosis and the activity of ceramide, Bax and Bcl-2 in the lungs of neonatal rats exposed to limited and prolonged hyperoxia AW Husari, GS Dbaibo, H Bitar, A Khayat, S Panjarian, M Nasser, FF Bitar, ... Respiratory research 7, 1-11, 2006 | 68 | 2006 |
| Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation AC Fahed, RM Safa, FF Haddad, FF Bitar, RR Andary, MT Arabi, ST Azar, ... Molecular genetics and metabolism 102 (2), 181-188, 2011 | 66 | 2011 |
| Transient hypertrophic cardiomyopathy in the newborn following multiple doses of antenatal corticosteroids KA Yunis, FF Bitar, P Hayek, SM Mroueh, M Mikati American journal of perinatology 16 (01), 17-21, 1999 | 64 | 1999 |
| Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype K Shibbani, AC Fahed, L Al‐Shaar, M Arabi, G Nemer, F Bitar, ... Clinical genetics 85 (2), 127-137, 2014 | 62 | 2014 |
| Paediatric infective endocarditis: 19-year experience at a tertiary care hospital in a developing country FF Bitar, RA Jawdi, GS Dbaibo, KA Yunis, W Gharzeddine, M Obeid Acta paediatrica (Oslo, Norway: 1992) 89 (4), 427-430, 2000 | 52 | 2000 |
| Patterns of congenital heart disease in unoperated adults: a 20‐year experience in a developing country H Hannoush, H Tamim, H Younes, S Arnaout, W Gharzeddine, H Dakik, ... Clinical cardiology 27 (4), 236-240, 2004 | 49 | 2004 |
| Effect of chronic hypoxia on leptin, insulin, adiponectin, and ghrelin JT Chaiban, FF Bitar, ST Azar Metabolism 57 (8), 1019-1022, 2008 | 48 | 2008 |
| Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysms L Abu-Safieh, EB Abboud, H Alkuraya, H Shamseldin, S Al-Enzi, L Al-Abdi, ... The American Journal of Human Genetics 89 (2), 313-319, 2011 | 47 | 2011 |
| Two heterozygous mutations in NFATC1 in a patient with Tricuspid Atresia Z Abdul-Sater, A Yehya, J Beresian, E Salem, A Kamar, S Baydoun, ... PloS one 7 (11), e49532, 2012 | 43 | 2012 |
| Aspergillus vertebral osteomyelitis in a child with a primary monocyte killing defect: response to GM-CSF therapy LA Jawdeh, R Haidar, F Bitar, S Mroueh, S Akel, N Nuwayri-Salti, ... Journal of Infection 41 (1), 97-100, 2000 | 43 | 2000 |
Sami SanjadProfessor of Pediatrics/Nephrology American University of Beirut Medical CenterVerified email at aub.edu.lb
