Biochemistry, Genetics and Molecular Biology
BCL11A
100%
Genetics
83%
Genotype Phenotype Correlation
83%
Autosomal Dominant Inheritance
61%
Regulatory Element
50%
Genomics
50%
ASCL1
50%
Exon
40%
Germline
37%
Gene Expression
37%
Missense Mutation
37%
Germ Cell
37%
Haploinsufficiency
33%
Pioneer Factor
31%
SMARCA2
25%
Transcription
25%
Helicase
25%
NIPBL
25%
Induced Pluripotent Stem Cell
25%
SMARCA4
25%
FA2H
25%
Genetic Divergence
25%
SLC3A1
25%
SLC7A9
25%
Exome Sequencing
25%
Candidate Gene
25%
Cholesterol Synthesis
25%
Dysferlin
25%
Phospholipase A2
25%
Body Weight
25%
Enhancer Region
25%
Chromatin Remodeling
25%
Exon Skipping
25%
Founder Effect
25%
Alternative Splicing
25%
Transcription Factor
22%
Protocadherin
16%
Cystine
16%
Haplotype
16%
Allele
16%
Genetic Counseling
16%
SWI/SNF
15%
Proband
13%
Isoform
13%
Chromosome 2 (Human)
12%
Reductase
12%
Nervous System Development
12%
Transmembrane Domain
12%
Autosomal Recessive Disorder
12%
Genetic Variation
12%
Neuroscience
BCL11A
75%
Neurodegeneration
75%
Exome Sequencing
56%
Muscle Disorder
50%
Exon
50%
Paraplegia
33%
Brain Development
27%
Brain Imaging
25%
Morphogen
25%
De Lange Syndrome
25%
Angelman Syndrome
25%
Pediatric Neurology
25%
Central Nervous System
25%
Charcot-Marie-Tooth Disease
25%
Nuclear Pore Complex
25%
Intergenic Region
25%
Phospholipase A2 Group VI
25%
Dysferlin
25%
Haploinsufficiency
25%
Stem Cell
25%
Energy Expenditure
25%
Uniparental Disomy
25%
Chromosome 2
25%
Germ Cell
25%
Human Chromosome
25%
Genetic Variation
25%
Face
25%
Pantothenate Kinase-Associated Neurodegeneration
25%
Alternative Splicing
25%
Exon Skipping
25%
Phospholipase A2
25%
Ataxia
25%
Southern Blot
18%
Hereditary Spastic Paraplegia
16%
Haplotype
16%
Hypotonia
14%
Muscular Dystrophy
13%
Microcephaly
12%
Point Mutation
12%
Magnetic Resonance Imaging
11%
Hemoglobin F
8%
Transcription Factors
8%
Cerebellar Cortex
8%
Magnetic Resonance Imaging
8%
Codon
8%
Dystonia
8%
Neurodegenerative Disorder
8%
Leukodystrophy
8%
Linkage Disequilibrium
8%
Sarcolemma
8%
Medicine and Dentistry
Neurodegeneration
50%
Infantile Neuroaxonal Dystrophy
50%
Disease
45%
Genetic Disorder
41%
Autosomal Dominant Inheritance
41%
Diseases
35%
Limb
30%
Developmental Delay
29%
Sudden Death
25%
Rheumatoid Arthritis
25%
Dysplasia
25%
Clubfoot
25%
Cutis Laxa
25%
Cholesterol Synthesis
25%
Inflammatory Arthritis
25%
DeJerine-Sottas Disease
25%
Vocal Folds
25%
Epileptic Seizure
25%
Dentinogenesis Imperfecta
25%
Phospholipase A2
25%
Focal Dermal Hypoplasia
25%
Spasticity
20%
Phospholipase A2 Group VI
20%
Corpus Callosum Agenesis
20%
Pantothenate Kinase-Associated Neurodegeneration
20%
Brain Imaging
18%
Polyarthritis
16%
Constipation
16%
Scoliosis
16%
Gastroesophageal Reflux
16%
Genetic Counseling
16%
Microcephaly
16%
Exome Sequencing
16%
Exon
15%
Cerebellum Atrophy
14%
Hypotonia
14%
Autosomal Recessive Inheritance
13%
Bone Dysplasia
13%
Prematurity
13%
Failure to Thrive
12%
Oxidoreductase
12%
Autosomal Recessive Disorder
12%
Magnetic Resonance Imaging
12%
Rhythm
12%
Skin Biopsy
12%
Tumor Spheroid
10%
Neurologic Disease
10%
Transforming Growth Factor Beta
10%
Programmed Cell Death
10%
Elastin
10%
