Medicine and Dentistry
Diagnosis
78%
Patient
72%
Disease
67%
Family
43%
Therapeutic Procedure
28%
Limb
26%
Genetic Disorder
26%
Gene
26%
Pathogenesis
25%
Syndrome
21%
Vocal Folds
21%
Dentinogenesis Imperfecta
21%
Calcification
21%
Sudden Death
21%
Rheumatoid Arthritis
21%
Dysplasia
21%
Epileptic Seizure
21%
DeJerine-Sottas Disease
21%
Neurodegeneration
21%
Developmental Delay
20%
Sibling
18%
Growth
18%
Spasticity
18%
Female
15%
Analysis
15%
Constipation
14%
Scoliosis
14%
Gastroesophageal Reflux
14%
Genetic Counseling
14%
Corpus Callosum Agenesis
13%
Pregnancy
11%
Autosomal Recessive Inheritance
11%
White Matter
10%
Failure to Thrive
10%
Magnetic Resonance Imaging
10%
Atrophy
10%
Exome Sequencing
9%
Cerebellum Atrophy
9%
Microcephaly
9%
Hypotonia
9%
Symptom
9%
Programmed Cell Death
8%
Elastin
8%
Aortic Root
8%
Emphysema
8%
Embryonic Hemoglobin
7%
Drug Therapy
7%
Spastic Paraplegia
7%
Child
7%
Iron
7%
Biochemistry, Genetics and Molecular Biology
Gene
100%
Spectrum
51%
Regulatory Element
43%
Genetics
39%
Exon
34%
Germline
32%
Genomics
28%
SMARCA2
21%
Transcription
21%
Helicase
21%
NIPBL
21%
Induced Pluripotent Stem Cell
21%
SMARCA4
21%
FA2H
21%
Genetic Divergence
21%
Iron
16%
SLC3A1
16%
SLC7A9
16%
Protocadherin
14%
Haplotype
14%
SWI/SNF
13%
Genetic Counseling
12%
Proband
11%
Exome Sequencing
10%
Chromosome 2 (Human)
10%
Reductase
10%
Candidate Gene
10%
Fat
10%
Nervous System Development
10%
Transmembrane Domain
10%
Autosomal Recessive Disorder
10%
Protein
7%
Karyotype
7%
Membrane
7%
Transposable Element
7%
Next Generation Sequencing
6%
Knockout Model
5%
Conformation
5%
Isoform
5%
Missense
5%
Neuroscience
Genotype
73%
Muscle Disorder
43%
Electroencephalography
30%
Paraplegia
28%
Appetite
21%
Brain Imaging
21%
Morphogen
21%
Brain Development
21%
Forebrain
21%
De Lange Syndrome
21%
Angelman Syndrome
21%
Pediatric Neurology
21%
Southern Blot
16%
Hereditary Spastic Paraplegia
14%
Central Nervous System
10%
Charcot-Marie-Tooth Disease
10%
Hypotonia
9%
Brain
8%
Linkage Disequilibrium
7%
Ethnicity
7%
Cerebellar Cortex
7%
Magnetic Resonance Imaging
7%
Microcephaly
7%
Codon
7%
Dystonia
7%
Neurodegenerative Disorder
7%
Behavior (Neuroscience)
5%
Transcription Factors
5%
Seizure
5%
Dysarthria
5%
White Matter
5%
Epilepsy
5%
Social Behavior
5%
Disease Modeling
5%
Hippocampus
5%
Cognition
5%