Hesham Aldhalaan

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 · 472 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed et al. · Human Genetics · 2017 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Expanding the genetic heterogeneity of intellectual disability

Shams Anazi, Sateesh Maddirevula, Vincenzo Salpietro et al. · Human Genetics · 2017 · 176 citations

Life Sciences, Genetics, Molecular Genetics +14

The clinical spectrum of homozygous <i>HOXA1</i> mutations

Thomas M. Bosley, Ibrahim A. Alorainy, Mustafa A. Salih et al. · American Journal of Medical Genetics Part A · 2008 · 122 citations

Life Sciences, Genetics, Molecular Genetics +17

Services for children with autism in the Kingdom of Saudi Arabia

Fahad Alnemary, Fahad Alnemary, Hesham Aldhalaan et al. · Autism · 2016 · 105 citations

Medicine, Health Policy, Pediatrics +10