Ola H. Gebril

Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders

Miriam S. Reuter, Hasan Tawamie, Rebecca Buchert et al. · JAMA Psychiatry · 2017 · 246 citations

Life Sciences, Genetics, Molecular Genetics +17

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8

Kym M. Boycott, Chandree L. Beaulieu, Kristin D. Kernohan et al. · The American Journal of Human Genetics · 2015 · 231 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Brain haemosiderin in older people: pathological evidence for an ischaemic origin of magnetic resonance imaging (<scp>MRI</scp>) microbleeds

B. M. Janaway, Julie E. Simpson, Nigel Hoggard et al. · Neuropathology and Applied Neurobiology · 2013 · 85 citations · Full text

Medicine, Neurology, Neuroscience +17

The role of zinc supplementation on the metallothionein system in children with autism spectrum disorder

Nagwa A. Meguid, Geir Bjørklund, Ola H. Gebril et al. · Acta Neurologica Belgica · 2019 · 54 citations

Medicine, Nutrition, Nutritional Sciences +13

The health-related quality of life in normal and obese children

Sahar A. Khairy, Sally R. Eid, Lobna M. El Hadidy et al. · Egyptian Pediatric Association Gazette · 2016 · 34 citations · Full text

Medicine, Child Health, Pediatrics +17