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Mohamed Abouelhoda
Mohamed Abouelhoda
King Faisal Specialist Hospital & Research Center, Cairo University,
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Title
Cited by
Cited by
Year
Replacing suffix trees with enhanced suffix arrays
MI Abouelhoda, S Kurtz, E Ohlebusch
Journal of discrete algorithms 2 (1), 53-86, 2004
9842004
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families
AM Alazami, N Patel, HE Shamseldin, S Anazi, MS Al-Dosari, F Alzahrani, ...
Cell reports 10 (2), 148-161, 2015
4492015
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
D Monies, M Abouelhoda, M AlSayed, Z Alhassnan, M Alotaibi, H Kayyali, ...
Human genetics 136, 921-939, 2017
2592017
Lessons learned from large-scale, first-tier clinical exome sequencing in a highly consanguineous population
D Monies, M Abouelhoda, M Assoum, N Moghrabi, R Rafiullah, ...
The American Journal of Human Genetics 104 (6), 1182-1201, 2019
2362019
Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield
S Anazi, S Maddirevula, E Faqeih, H Alsedairy, F Alzahrani, ...
Molecular psychiatry 22 (4), 615-624, 2017
2192017
The enhanced suffix array and its applications to genome analysis
MI Abouelhoda, S Kurtz, E Ohlebusch
Algorithms in Bioinformatics: Second International Workshop, WABI 2002 Rome …, 2002
1952002
A year of genomic surveillance reveals how the SARS-CoV-2 pandemic unfolded in Africa
TO Wilkinson E, Giovanetti M, Tegally H, .. Mohamed Abouelhoda..
Science, 2021
184*2021
Tavaxy: Integrating Taverna and Galaxy workflows with cloud computing support
M Abouelhoda, SA Issa, M Ghanem
BMC bioinformatics 13, 1-19, 2012
1662012
Characterizing the morbid genome of ciliopathies
R Shaheen, K Szymanska, B Basu, N Patel, N Ewida, E Faqeih, ...
Genome biology 17, 1-11, 2016
1502016
Expanding the genetic heterogeneity of intellectual disability
S Anazi, S Maddirevula, V Salpietro, YT Asi, S Alsahli, A Alhashem, ...
Human genetics 136, 1419-1429, 2017
1492017
Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases
SM Group
Genome Biology 16 (134), 2015
1382015
Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases
H Al-Mousa, M Abouelhoda, DM Monies, N Al-Tassan, A Al-Ghonaium, ...
Journal of Allergy and Clinical Immunology 137 (6), 1780-1787, 2016
1292016
Association of a Mutation in LACC1 With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis
SM Wakil, DM Monies, M Abouelhoda, N Al‐Tassan, H Al‐Dusery, ...
Arthritis & rheumatology 67 (1), 288-295, 2015
1292015
Optimal exact string matching based on suffix arrays
MI Abouelhoda, E Ohlebusch, S Kurtz
String Processing and Information Retrieval: 9th International Symposium …, 2002
1212002
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies
N Patel, MA Aldahmesh, H Alkuraya, S Anazi, H Alsharif, AO Khan, ...
Genetics in Medicine 18 (6), 554-562, 2016
1072016
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden
M Abouelhoda, T Sobahy, M El-Kalioby, N Patel, H Shamseldin, D Monies, ...
Genetics in Medicine 18 (12), 1244-1249, 2016
1012016
Genomic and phenotypic delineation of congenital microcephaly
R Shaheen, S Maddirevula, N Ewida, S Alsahli, GMH Abdel-Salam, ...
Genetics in Medicine 21 (3), 545-552, 2019
992019
Autozygome and high throughput confirmation of disease genes candidacy
S Maddirevula, F Alzahrani, M Al-Owain, MA Al Muhaizea, HR Kayyali, ...
Genetics in Medicine 21 (3), 736-742, 2019
962019
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families
B Al-Mubarak, M Abouelhoda, A Omar, H AlDhalaan, M Aldosari, ...
Scientific reports 7 (1), 5679, 2017
952017
Relative reduction of biological and phylogenetic diversity of the oral microbiota of diabetes and pre-diabetes patients
ATM Saeb, KA Al-Rubeaan, K Aldosary, GKU Raja, B Mani, ...
Microbial pathogenesis 128, 215-229, 2019
892019
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