Nouran Adly

Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin et al. · Cell Reports · 2014 · 465 citations · Full text

LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency

Abdullah Alangari, Abdulrahman Alsultan, Nouran Adly et al. · Journal of Allergy and Clinical Immunology · 2012 · 244 citations · Full text

Primary Immunodeficiency, Immunogenetics, Autoimmune Disease +12

Recessive Mutations in DOCK6, Encoding the Guanidine Nucleotide Exchange Factor DOCK6, Lead to Abnormal Actin Cytoskeleton Organization and Adams-Oliver Syndrome

Ranad Shaheen, Eissa Faqeih, Asma Sunker et al. · The American Journal of Human Genetics · 2011 · 139 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +6

Printed microelectrode arrays on soft materials: from PDMS to hydrogels

Nouran Adly, Sabrina Weidlich, Silke Seyock et al. · npj Flexible Electronics · 2018 · 130 citations · Full text

Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

Mohammed A. Aldahmesh, Arif O. Khan, Hisham Alkuraya et al. · The American Journal of Human Genetics · 2013 · 128 citations · Full text

Ophthalmology, Severe Myopia, Genetic Disorder +3