Shinu Ansari

Genomic analysis of primordial dwarfism reveals novel disease genes

Ranad Shaheen, Eissa Faqeih, Shinu Ansari et al. · Genome Research · 2014 · 167 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by <i>TMEM38B</i> mutation

Ranad Shaheen, Anas M. Alazami, Muneera Alshammari et al. · Journal of Medical Genetics · 2012 · 142 citations

Medicine, Genetics, Molecular Genetics +17

Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome

Ranad Shaheen, Mona Aglan, Kim M. Keppler‐Noreuil et al. · The American Journal of Human Genetics · 2013 · 132 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

Mutations in CSPP1, Encoding a Core Centrosomal Protein, Cause a Range of Ciliopathy Phenotypes in Humans

Ranad Shaheen, Hanan E. Shamseldin, Catrina M. Loucks et al. · The American Journal of Human Genetics · 2013 · 89 citations · Full text

Veterinary Medicine, Pathobiology, Pathology +4

Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes

Ranad Shaheen, Eissa Faqeih, Muneera Alshammari et al. · European Journal of Human Genetics · 2012 · 72 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17