Medicine & Life Sciences
Mutation
100%
Frontotemporal Lobar Degeneration
79%
Frontotemporal Dementia
73%
Genes
44%
Phenotype
43%
Exome
40%
Dementia
36%
Whole Exome Sequencing
32%
MELAS Syndrome
31%
Microtubule-Associated Proteins
30%
Intellectual Disability
29%
Neurodevelopmental Disorders
29%
Brain Diseases
28%
Brain
27%
Atrophy
25%
Epilepsy
24%
Seizures
23%
Chromosomes, Human, Pair 9
21%
Angelman Syndrome
20%
Age of Onset
20%
Alexander Disease
20%
Magnetic Resonance Imaging
17%
White Matter
17%
Loss of Function Mutation
16%
Mitochondrial Diseases
16%
Friedreich Ataxia
16%
Genetic Association Studies
16%
Muscle Hypotonia
16%
Late Onset Disorders
16%
Multiple Sclerosis
15%
Progranulins
14%
Genetic Testing
14%
Kennerknecht Sorgo Oberhoffer syndrome
13%
Neuroimaging
13%
Translational Medical Research
13%
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations
13%
Failure to Thrive
13%
Nervous System Diseases
13%
Stroke
12%
Woodhouse Sakati syndrome
12%
Mitochondrial Complex III Deficiency
12%
Cerebroretinal Microangiopathy with Calcifications and Cysts
12%
Open Reading Frames
12%
Population Biological Variation
12%
Missense Mutation
11%
Kleefstra Syndrome
11%
Biomarkers
11%
Gene Components
11%
Uridine Diphosphate Glucose Dehydrogenase
10%