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Gene|January 31, 2012
Vanishing white matter disease caused by EIF2B2 mutation with the presentation of an adrenoleukodystrophy phenotypeAhmed Alsalem, Ranad Shaheen, Fowzan S AlkurayaJournal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|September 1, 2014
The ECEL1-related strabismus phenotype is consistent with congenital cranial dysinnervation disorderArif O Khan, Ranad Shaheen, Fowzan S AlkurayaAmerican Journal of Medical Genetics. Part A|June 21, 2017
Expanding the allelic disorders linked to TCTN1 to include Varadi syndrome (Orofaciodigital syndrome type VI)Mohammad M Al-Qattan, Ranad Shaheen, Fowzan S AlkurayaNeurogenetics|July 24, 2013
A truncating mutation in B3GNT1 causes severe Walker-Warburg syndromeRanad Shaheen, Eissa Faqeih, Shinu Ansari, et al.Journal of Medical Genetics|October 17, 2014
Mutation in PLK4, encoding a master regulator of centriole formation, defines a novel locus for primordial dwarfismRanad Shaheen, Saeed Al Tala, Agaadir Almoisheer, et al.Journal of Medical Genetics|June 5, 2010
Novel CENPJ mutation causes Seckel syndromeMohammed S Al-Dosari, Ranad Shaheen, Dilek Colak, et al.Human Genetics|August 29, 2016
Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizuresBrahim Tabarki, Nabil AlMajhad, Amal AlHashem, et al.Food Microbiology|March 16, 2010
Persistence strategies of Bacillus cereus spores isolated from dairy silo tanksRanad Shaheen, Birgitta Svensson, Maria A Andersson, et al.American Journal of Medical Genetics. Part A|August 3, 2016
The syndrome dysmorphic facies, renal agenesis, ambiguous genitalia, microcephaly, polydactyly and lissencephaly (DREAM-PL): Report of two additional patientsRanad Shaheen, Zakariya Al-Salam, Ayman W El-Hattab, et al.Human Genetics|July 5, 2015
Revisiting disease genes based on whole-exome sequencing in consanguineous populationsAhmed Shamia, Ranad Shaheen, Nouran Sabbagh, et al.Pageof 9