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Top Articles

#TitleJournalYearCitations
1Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutationsNature Genetics2000798
2American Society of Anaesthesiologists physical status classificationIndian Journal of Anaesthesia2011571
3Sequence variability in the 5' non-coding region of hepatitis C virus: identification of a new virus type and restrictions on sequence diversityJournal of General Virology1993444
4Ribavirin and interferon alfa-2a for severe Middle East respiratory syndrome coronavirus infection: a retrospective cohort studyLancet Infectious Diseases, The2014434
5Clinical aspects and outcomes of 70 patients with Middle East respiratory syndrome coronavirus infection: a single-center experience in Saudi ArabiaInternational Journal of Infectious Diseases2014427
6Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosusNature Genetics2011366
7Severe Bile Salt Export Pump Deficiency: 82 Different ABCB11 Mutations in 109 FamiliesGastroenterology2008331
8Isolated C-terminal tail of FGF23 alleviates hypophosphatemia by inhibiting FGF23-FGFR-Klotho complex formationProceedings of the National Academy of Sciences of the United States of America2010327
9Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis–renal dysfunction–cholestasis (ARC) syndromeNature Genetics2004313
10Meta-Analysis of Navigation vs Conventional Total Knee ArthroplastyJournal of Arthroplasty2012297
11Clinical exome sequencing: results from 2819 samples reflecting 1000 familiesEuropean Journal of Human Genetics2017291
12PERCUTANEOUS DOUBLE-BALLOON MITRAL VALVOTOMY FOR RHEUMATIC MITRAL-VALVE STENOSISLancet, The1986284
13Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndromeNature Genetics2001277
14N-acetyltransferase1989268
15ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani SyndromeAmerican Journal of Human Genetics2004255
16A 0-1 goal programming model for nurse schedulingComputers and Operations Research2005209
17The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomesHuman Genetics2017209
18Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growthHuman Molecular Genetics2007202
19Brucellar and tuberculous spondylitis: comparative imaging features.Radiology1989187
20Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yieldMolecular Psychiatry2017187
21Moringa oleifera as an Anti-Cancer Agent against Breast and Colorectal Cancer Cell LinesPLoS ONE2015186
22Differences in presentation and progression between severe FIC1 and BSEP deficienciesJournal of Hepatology2010182
23Predicting outcome among intensive care unit patients using computerised trend analysis of daily Apache II scores corrected for organ system failureIntensive Care Medicine1988169
24Role of MR imaging in the management of spinal infections.American Journal of Roentgenology1992169
25Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C OxidaseAmerican Journal of Human Genetics2008165
26Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain SizeAmerican Journal of Human Genetics2003163
27Granulomatous spinal infections: MR imaging.Radiology1990159
28Vitamin D Deficiency and Chronic Low Back Pain in Saudi ArabiaSpine2003159
29Cancer-Associated Thrombosis: An OverviewClinical Medicine Insights: Oncology2014151
30Chemotherapy Compared with Bone Marrow Transplantation for Adults with Acute Lymphoblastic Leukemia in First RemissionAnnals of Internal Medicine1991145
31A family cluster of Middle East Respiratory Syndrome Coronavirus infections related to a likely unrecognized asymptomatic or mild caseInternational Journal of Infectious Diseases2013145
32Continuous Enteral Feeding: A Major Cause of Pneumonia among Ventilated Intensive Care Unit PatientsJournal of Parenteral and Enteral Nutrition1990143
33Causes and effects of road traffic accidents in Saudi ArabiaPublic Health2000140
34Smoking habits in the Middle East and North Africa: Results of the BREATHE studyRespiratory Medicine2012134
35NeurobrucellosisNeurology1989131
36Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome2003130
37Predicting deaths among intensive care unit patientsCritical Care Medicine1988125
38Expanding the genetic heterogeneity of intellectual disabilityHuman Genetics2017122
39Characterizing the morbid genome of ciliopathiesGenome Biology2016118
40Childhood Absence Epilepsy with Tonic-Clonic Seizures and Electroencephalogram 3–4-Hz Spike and Multispike–Slow Wave Complexes: Linkage to Chromosome 8q24American Journal of Human Genetics1998117
41AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeJournal of Medical Genetics2005116
42Causes and effects of road traffic accidents in Saudi ArabiaPublic Health2000116
43Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseasesJournal of Allergy and Clinical Immunology2016115
44In search of triallelism in Bardet–Biedl syndromeEuropean Journal of Human Genetics2012111
45A system for assessing the severity and progression of occlusal tooth wearJournal of Oral Rehabilitation1993108
46Treatment of Middle East respiratory syndrome with a combination of lopinavir/ritonavir and interferon-β1b (MIRACLE trial): statistical analysis plan for a recursive two-stage group sequential randomized controlled trialTrials2020108
47Fluconazole improves survival in septic shock: A randomized double-blind prospective studyCritical Care Medicine2003104
48Middle East respiratory syndrome coronavirus in childrenJournal of King Abdulaziz University, Islamic Economics2015100
49Seroepidemiology of Hepatitis B virus infection in Saudi children 8 years after a mass hepatitis B vaccination programmeJournal of Infection199999
50Microalbuminuria in Patients With NIDDM: An OverviewDiabetes Care199698