Medicine & Life Sciences
Mutation
100%
Frontotemporal Dementia
80%
Frontotemporal Lobar Degeneration
77%
Genes
46%
Dementia
40%
Phenotype
37%
Whole Exome Sequencing
36%
Microtubule-Associated Proteins
33%
Brain Diseases
30%
Neurodevelopmental Disorders
30%
Intellectual Disability
29%
Atrophy
27%
Epilepsy
26%
Exome
26%
Brain
26%
Seizures
25%
Chromosomes, Human, Pair 9
23%
MELAS Syndrome
22%
Angelman Syndrome
22%
Age of Onset
22%
Alexander Disease
22%
Magnetic Resonance Imaging
19%
Loss of Function Mutation
18%
Mitochondrial Diseases
18%
Friedreich Ataxia
18%
Genetic Association Studies
18%
Muscle Hypotonia
18%
Late Onset Disorders
17%
Multiple Sclerosis
17%
Progranulins
16%
White Matter
16%
Kennerknecht Sorgo Oberhoffer syndrome
15%
Genetic Testing
14%
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations
14%
Failure to Thrive
14%
Woodhouse Sakati syndrome
14%
Neuroimaging
13%
Mitochondrial Complex III Deficiency
13%
Cerebroretinal Microangiopathy with Calcifications and Cysts
13%
Open Reading Frames
13%
Population Biological Variation
13%
Missense Mutation
13%
Kleefstra Syndrome
12%
Gene Components
12%
Biomarkers
11%
Uridine Diphosphate Glucose Dehydrogenase
11%
Anesthetics
11%
Congenital Pain Insensitivity
11%
Granulins
11%