Biochemistry, Genetics and Molecular Biology
Neural Tube
100%
Candidate Gene
80%
Oxidative Stress
57%
Cilium
57%
Glucose Homeostasis
57%
Adrenoleukodystrophy
57%
Cell Migration
57%
Carbon Metabolism
57%
Folic Acid
57%
Cytoskeleton
57%
Cell Polarity
57%
Newborn Screening
57%
Exome Sequencing
40%
Genetics
37%
Signal Transduction
28%
Gene Ontology
28%
Cohort Study
28%
ABCD1
28%
Biological Functions
14%
Glucose Metabolism
14%
Lifespan
14%
Folate Metabolism
14%
Transcription Regulation
14%
Gene Frequency
11%
Missense
11%
Next Generation Sequencing
11%
Genotype Phenotype Correlation
9%
Very Long Chain Fatty Acid
9%
Alpha Oxidation
9%
Lysophosphatidylcholine
9%
Prevalence
9%
Dried Blood Spot
9%
Hematopoietic Stem Cell Transplantation
9%
Keyphrases
Myelomeningocele
57%
Signaling Genes
57%
Wnt Signaling
57%
Deleterious Variants
57%
Ultra-rare
57%
Mutational Burden
28%
Defect Risk
22%
Planar Cell Polarity
19%
Stress Network
11%
Canonical Wnt
9%
Sequence Data
9%
Wnt Signaling Pathway
9%
Mexican Population
9%
Publicly Available
9%
Signaling Network
9%
Gene Ontology Enrichment Analysis
9%
Mexican Americans
9%
GnomAD
9%
Fisher's Exact Test
9%
Combined Annotation-dependent Depletion
9%
Exome Sequencing
9%
Neural Tube Defects
9%
European Ancestry
9%
Canonical Wnt Signaling
9%
Mid-childhood
7%
C26:0-lysophosphatidylcholine
7%
Medicine and Dentistry
Adrenoleukodystrophy
57%
Newborn Screening
57%
Meningomyelocele
57%
ABCD1
21%
Cell Polarity
19%
Neonatal Infant
14%
Transcription Regulation
11%
Fisher Exact Test
9%
Signal Transduction
9%
Exome Sequencing
9%
Neural Tube Defect
9%
White Matter Disease
7%
Adrenal Insufficiency
7%
Adrenal Disease
7%
Clinically Isolated Syndrome
7%
Prevalence
7%
Very Long Chain Fatty Acid
7%
Neurologic Disease
7%
Epileptic Absence
7%
Hematopoietic Stem Cell Transplantation
7%
Family Counseling
7%
Quality of Life
7%
Genotype Phenotype Correlation
7%
Lysophosphatidylcholine
7%
Degenerative Disease
7%
Biological Marker
7%
Childbirth
7%
Spastic Paraplegia
7%
Dried Blood Spot
7%