Global and National Burden of Diseases and Injuries Among Children and Adolescents Between 1990 and 2013: Findings From the Global Burden of Disease 2013 Study | JAMA Pediatrics | 2016 | 347 |
Oncogenic PI3K mutations are as common as AKT1 and SMO mutations in meningioma | Neuro-Oncology | 2016 | 144 |
Plasma Lipidomic Profiles Improve on Traditional Risk Factors for the Prediction of Cardiovascular Events in Type 2 Diabetes Mellitus | Circulation | 2016 | 133 |
Health in times of uncertainty in the eastern Mediterranean region, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013 | The Lancet Global Health | 2016 | 117 |
Antimicrobials: a global alliance for optimizing their rational use in intra-abdominal infections (AGORA) | World Journal of Emergency Surgery | 2016 | 95 |
Characterizing the morbid genome of ciliopathies | Genome Biology | 2016 | 89 |
Middle East Respiratory Syndrome Coronavirus: What Does a Radiologist Need to Know? | American Journal of Roentgenology | 2016 | 87 |
Secondary analysis of outcomes after 11,085 hip fracture operations from the prospective UK Anaesthesia Sprint Audit of Practice (ASAP-2) | Anaesthesia | 2016 | 86 |
Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases | Journal of Allergy and Clinical Immunology | 2016 | 80 |
Multiple introductions of MERS-CoV in a 2014 hospital outbreak in Riyadh, Saudi Arabia | International Journal of Infectious Diseases | 2016 | 78 |
A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognition | Human Genetics | 2016 | 78 |
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases | Journal of Allergy and Clinical Immunology | 2016 | 76 |
A Comparative Study of Clinical Presentation and Risk Factors for Adverse Outcome in Patients Hospitalised with Acute Respiratory Disease Due to MERS Coronavirus or Other Causes | PLoS ONE | 2016 | 76 |
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies | Genetics in Medicine | 2016 | 73 |
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue | Human Genetics | 2016 | 61 |
Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate | BMC Medical Genomics | 2016 | 58 |
Age-based analysis of pediatric upper airway dimensions using computed tomography imaging | Pediatric Pulmonology | 2016 | 50 |
Description of a Hospital Outbreak of Middle East Respiratory Syndrome in a Large Tertiary Care Hospital in Saudi Arabia | Infection Control and Hospital Epidemiology | 2016 | 48 |
The Current Use of Social Media in Neurosurgery | World Neurosurgery | 2016 | 46 |
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy | American Journal of Human Genetics | 2016 | 45 |
Incidence, Predictors, and Postoperative Complications of Blood Transfusion in Thoracic and Lumbar Fusion Surgery: An Analysis of 13,695 Patients from the American College of Surgeons National Surgical Quality Improvement Program Database | Global Spine Journal | 2016 | 38 |
The Most Cited Works in Aneurysmal Subarachnoid Hemorrhage: A Bibliometric Analysis of the 100 Most Cited Articles | World Neurosurgery | 2016 | 37 |
Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort | Genetics in Medicine | 2016 | 35 |
Perceived stress and associated factors among medical students | Journal of Family and Community Medicine | 2016 | 35 |
Bimanual Psychomotor Performance in Neurosurgical Resident Applicants Assessed Using NeuroTouch, a Virtual Reality Simulator | Journal of Surgical Education | 2016 | 35 |