Medicine & Life Sciences
United Arab Emirates
100%
Genes
67%
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
47%
Phenotype
46%
Gaucher-like disease
42%
Genome-Wide Association Study
39%
Mutation
38%
Type I Schindler Disease
38%
Ethylmalonic encephalopathy
37%
Matrix Metalloproteinase 15
34%
Transaldolase
33%
Enzymes
33%
Primary Hypertrophic Osteoarthropathy
32%
Inborn Errors Metabolism
32%
Saposins
31%
Mucopolysaccharidosis VI
30%
Etoricoxib
30%
GM1 Gangliosidosis
30%
Mitochondrial Diseases
29%
Failure to Thrive
29%
Microcephaly
29%
Galactosidases
28%
Leigh Disease
28%
SARS Virus
28%
Glycogen Storage Disease Type II
27%
Pharmaceutical Databases
27%
electron-transferring-flavoprotein dehydrogenase
26%
Exome
26%
Drug Repositioning
26%
Hearing Loss
25%
Gaucher Disease
25%
Chromosomes, Human, Pair 2
25%
Genetic Databases
25%
Liver Transplantation
24%
Propionates
24%
Cholestasis
24%
Citrulline
24%
Serine
24%
Mitochondrial Genome
24%
Quadriplegia
23%
Tandem Mass Spectrometry
23%
Lupus Nephritis
23%
Jaundice
22%
Genetic Heterogeneity
22%
Amino Acid Substitution
22%
Electron Transport Complex IV
22%
Liquid Chromatography
22%
Lysosomes
21%
Siblings
21%
Machine Learning
21%
Corpus Callosum
21%
Metabolomics
21%
Genetic Variation
20%
Citric Acid
20%
Child
20%
Scoliosis
20%
sulfur dioxygenase
20%
Glucosylceramidase
20%
Inborn Genetic Diseases
19%
Seizures
19%
Population
19%
Virulence
19%
Computer Simulation
19%
Cardiomyopathies
18%
Liver Diseases
18%
Molecular Biology
18%
Intellectual Disability
18%
Fibroblasts
17%
Haplotypes
17%
Arginine
17%
Obstetrics
17%
Opioid Analgesics
16%
Fatty Acids
16%
Microcephaly with spastic quadriplegia
15%
Whole Exome Sequencing
15%
Nitric Oxide
15%
Early Diagnosis
15%
China
15%
Hepatocellular Carcinoma
15%
Comorbidity
14%
Biomarkers
14%
Electron Transport
14%
Cardiovascular Diseases
13%
Propionic Acidemia
13%
Nonsense Codon
12%
Pharmacology
12%
Enzyme Replacement Therapy
12%
Databases
12%
Hydrogen Sulfide
12%
Missense Mutation
12%
Therapeutics
12%
Mothers
11%
propionyl-coenzyme A
10%
2-methylbutyrylglycine
10%
Neutral Amino Acid Transport Systems
10%
Electron-Transferring Flavoproteins
10%
Glycerol
10%
4-(2-(N,N-dimethylamino)ethylaminosulfonyl)-7-(2-aminoethylamino)-2,1,3-benzoxadiazole
9%
Neurologic Manifestations
9%
Nonsense Mediated mRNA Decay
9%