| Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis C Toomes, J James, AJ Wood, CL Wu, D McCormick, N Lench, C Hewitt, ... Nature genetics 23 (4), 421-424, 1999 | 651 | 1999 |
| Molecular characterization of β‐thalassemia in Egyptians IR Hussein, SA Temtamy, A El‐Beshlawy, C Fearon, Z Shalaby, ... Human mutation 2 (1), 48-52, 1993 | 74 | 1993 |
| Association of angiotensin converting enzyme gene (I/D) polymorphism with hypertension and type 2 diabetes HM Zarouk WA, Hussein IR, Esmaeil NN, Raslan HM, Reheim HA, Moguib O, Emara ... Bratisl Lek Listy 113 ((1)), 14-8, 2012 | 64 | 2012 |
| Thalassemia prevalence and status in Egypt A El-Beshlawy, N Kaddah, L Rageb, I Hussein, G Mouktar, A Moustafa, ... Pediatric research 45 (5), 760-760, 1999 | 49 | 1999 |
| MOLECULAR BASIS OF β-THALASSEMIA IN THE WESTERN PROVINCE OF SAUDI ARABIA: IDENTIFICATION OF RARE β-THALASSEMIA MUTATIONS AQ Abuzenadah, Hussein, Damanhouri, A-Sayes, Gari, Chaudhary, Zaher, Al-Attas Hemoglobin 35 ((4)), 346–357, 2011 | 42* | 2011 |
| Identification of Mediterranean β-thalassemia mutations by reverse dot-blot in Italians and Egyptians MS Rady, M Baffico, AS Khalifa, NM Heshmat, S El-Moselhy, ... Hemoglobin 21 (1), 59-69, 1997 | 29 | 1997 |
| Correction of aberrant pre-mRNA splicing by antisense oligonucleotides in β-thalassemia Egyptian patients with IVSI-110 mutation A El-Beshlawy, A Mostafa, I Youssry, H Gabr, IM Mansour, M El-Tablawy, ... Journal of pediatric hematology/oncology 30 (4), 281-284, 2008 | 23 | 2008 |
| Characterization of familial breast cancer in Saudi Arabia A Merdad, MA Gari, S Hussein, S Al-Khayat, H Tashkandi, J Al-Maghrabi, ... BMC genomics 16, 1-7, 2015 | 21 | 2015 |
| The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families IR Hussein, A El‐Beshlawy, A Salem, R Mosaad, N Zaghloul, L Ragab, ... Haemophilia 14 (5), 1082-1087, 2008 | 19 | 2008 |
| Identification of de novo and rare inherited copy number variants in children with syndromic congenital heart defects IR Hussein, RS Bader, AG Chaudhary, R Bassiouni, M Alquaiti, F Ashgan, ... Pediatric cardiology 39, 924-940, 2018 | 15 | 2018 |
| ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia C Shammas, T Papasavva, X Felekis, C Christophorou, H Roomere, ... Clinical chemistry and laboratory medicine 48 (12), 1713-1718, 2010 | 14 | 2010 |
| Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) Jeddah, Kingdom of Saudi Arabia. 30 November-3 December 2015 JW Shay, N Homma, R Zhou, MI Naseer, AG Chaudhary, M Al-Qahtani, ... BMC genomics 17, 1-78, 2016 | 13 | 2016 |
| An SP1-binding site polymorphism in the COLIAI gene and osteoporosis in Egyptian patients with thalassemia major HM Hamed, A Galal, MEL Ghamrawy, K Abd El Azeem, IR Hussein, ... Blood coagulation & fibrinolysis 22 (2), 81-85, 2011 | 13 | 2011 |
| Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability AG Chaudhary, IR Hussein, A Abuzenadah, M Gari, R Bassiouni, ... Pediatric neurology 50 (4), 368-376, 2014 | 11 | 2014 |
| Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia Hussein, Magbooli , Huwait , Chaudhary , Bader, Gari , Ashgan , Alquaiti ... Molecular Cytogenetics 9 (DOI 10.1186/s13039-016-0266-4), 1-13, 2016 | 9 | 2016 |
| Screening tor B-thalassemia mutations in Egypt by reverse dot blot hybridization IR Hussein, A ElBeshlawy, SA Temtamy, M Elawady, G ElKammah, ... BRITISH JOURNAL OF HAEMATOLOGY 93, 90-90, 1996 | 7 | 1996 |
| Genotypes, phenotypes in beta-thalassaemia and sickle cell anaemia in Egypt A El-Beshlawy, L Ragab, I Hussein, M El-Tagui JAC 6 (2), 147-151, 1995 | 7 | 1995 |
| Genetic studies of congenital heart defects in Egyptian patients IR Hussein, M El-Rubi, NA Helmy, HA Hussein, A El-Gerzawy, ... Res J Med Med Sci 4, 55-66, 2009 | 5 | 2009 |
| Phenotypic scoring in thalassemia intermedia and the impact of underlying molecular defects EB Ghada, EB Amal, S Howayda Aly, H Ibtessam R | 5 | 2003 |
| Prenatal Diagnosis of betathalassemia in Egypt IR Hussein, A El-Beshlawy, KR Gaber Egyptian J Hematol 25, 547-61, 2000 | 5 | 2000 |
