R. Aljelaify

发表

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

Mohamed Abouelhoda, Yong Xiong, Fowzan S Alkuraya, 2015, Cell reports.

Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human

C. Mellersh, S. Katayama, K. Krjutškov, 2023, Genome Medicine.

Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family

Musa Alharbi, M. Abedalthagafi, A. Zhou, 2018, npj Genomic Medicine.

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

M. Temsah, F. Alkuraya, Y. Xiong, 2015, Cell reports.

Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family

Musa Alharbi, M. Abedalthagafi, A. Zhou, 2018, npj Genomic Medicine.

Behavioural Effects of Adult Vitamin D Deficiency in BALB/c Mice Are not Associated with Proliferation or Survival of Neurons in the Adult Hippocampus

R. Sullivan, T. Burne, Kyna-Anne Conn, 2016, PloS one.

New insights into the genomic landscape of meningiomas identified FGFR3 in a subset of patients with favorable prognoses

M. Abedalthagafi, M. Abouelhoda, Abdullah Alobaid, 2019, Oncotarget.

Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency.

S. Ramkissoon, Musa Alharbi, M. Abedalthagafi, 2018, The oncologist.

Methylation Profiling of Medulloblastoma in a Clinical Setting Permits Sub-classification and Reveals New Outcome Predictions

M. Snuderl, Musa Alharbi, J. Serrano, 2020, Frontiers in Neurology.