Mohammed S. Al-Dosari

Mutation in <i>MPDZ</i> causes severe congenital hydrocephalus

Mohammed S. Al-Dosari, Mohammed Al‐Owain, Maha Tulbah et al. · Journal of Medical Genetics · 2012 · 108 citations

Life Sciences, Genetics, Molecular Genetics +12

POC1A Truncation Mutation Causes a Ciliopathy in Humans Characterized by Primordial Dwarfism

Ranad Shaheen, Eissa Faqeih, Hanan E. Shamseldin et al. · The American Journal of Human Genetics · 2012 · 83 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

A Ni(<scp>ii</scp>)MOF-based hypersensitive dual-function luminescent sensor towards the 3-nitrotyrosine biomarker and 6-propyl-2-thiouracil antithyroid drug in urine

Wen‐Cui Li, Liying Liu, Xiaoting Li et al. · Journal of Materials Chemistry B · 2024 · 60 citations

Natural Sciences, Biomedical Engineering, Pharmacology +17

Distribution of selected gene polymorphisms of UGT1A1 in a Saudi population

Khalid M. Alkharfy, Amal M. Alghamdi, Khawla M. Bagulb et al. · Archives of Medical Science · 2013 · 12 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Two novel cobalt-based coordination polymers for electrochemical sensing of trace ciprofloxacin

Ruifang Xiang, Tianrui Qin, Yichen Liu et al. · Microchemical Journal · 2024 · 10 citations

Natural Sciences, Chemistry, Materials Science +16