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BMC Evolutionary Biology|June 8, 2010
WAMI: a web server for the analysis of minisatellite mapsMohamed Abouelhoda, Mohamed El-Kalioby, Robert GiegerichGenome Biology|November 26, 2016
Revisiting the morbid genome of Mendelian disordersMohamed Abouelhoda, Tariq Faquih, Mohamed El-Kalioby, et al.Transfusion Medicine Reviews|April 14, 2021
Knowledge Improvement of Blood Transfusion Safety Among Pediatricians: Post Educational InterventionShaimaa Sahmoud, Esraa M Ashry, Mohamed El Kalioby, et al.BMC Bioinformatics|January 4, 2013
Personalized cloud-based bioinformatics services for research and education: use cases and the elasticHPC packageMohamed El-Kalioby, Mohamed Abouelhoda, Jan Krüger, et al.Biomed Research International|May 28, 2013
Streaming support for data intensive cloud-based sequence analysisShadi A Issa, Romeo Kienzler, Mohamed El-Kalioby, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2016
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burdenMohamed Abouelhoda, Turki Sobahy, Mohamed El-Kalioby, et al.Human Genomics|September 28, 2016
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesDorota Monies, Hindi N Alhindi, Mohamed A Almuhaizea, et al.BMC Research Notes|June 9, 2016
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi familiesSaeed A Bohlega, Bashayer R Al-Mubarak, Eman A Alyemni, et al.Scientific Reports|July 20, 2017
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi familiesBashayer Al-Mubarak, Mohamed Abouelhoda, Aisha Omar, et al.Journal of Medical Genetics|February 11, 2016
Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panelMohamed H Al-Hamed, Wesam Kurdi, Nada Alsahan, et al.Pageof 2