Biochemistry, Genetics and Molecular Biology
Allele
40%
Amino Acids
8%
Axon
12%
Basal Body
8%
Binding Protein
6%
Binding Site
32%
Blood Lipids
6%
Blood Pressure
17%
Body Mass
19%
Caenorhabditis Elegans
39%
Candidate Gene
16%
Cell Fate
16%
Cell Proliferation
6%
Chlamydomonas
13%
Chlamydomonas reinhardtii
19%
CHRNA5
9%
Cilium
11%
DNA Binding
6%
DNA Methylation
17%
DNA Sequence
14%
DNA-binding Protein
7%
Dynamics
9%
Dynein
14%
Early Growth Response Factor 1
6%
Enhancer Region
19%
Enzyme
11%
Epigenetics
16%
Epigenome
10%
Exome
12%
Exome Sequencing
14%
Exon
9%
Family Life
11%
Fibroblast
6%
Flagellum
9%
Gene Control
8%
Gene Expression
41%
Gene Expression Profiling
7%
Gene Linkage
25%
Gene Locus
9%
Genetic Architecture
6%
Genetic Determinism
10%
Genetic Divergence
34%
Genetic Epidemiology
6%
Genetic Risk
8%
Genetic Variation
11%
Genetics
100%
Genome Wide Association Study
11%
Genome-Wide Association Study
33%
Genomics
55%
Genotyping
26%
Germ Cell
26%
Germline
15%
Haplotype
11%
HDL-Cholesterol
8%
Homeostasis
6%
Human Genetics
6%
Human Genome
6%
Intellectual Disability
9%
Kinase
7%
Lifespan
9%
Linkage Analysis
14%
Lipid
21%
Locus Control Region
6%
Messenger RNA
16%
Metabolic Pathway
11%
Methylation
15%
MicroRNA
6%
Missense
14%
Nerve Fiber Degeneration
10%
Neuroblast
6%
Next Generation Sequencing
7%
Nicotinamide Adenine Dinucleotide
7%
Offspring
8%
Phosphotransferase
7%
Precursor
9%
Prevalence
6%
Proband
14%
Programmed Cell Death
7%
Promoter Region
30%
Protein-DNA Interaction
7%
Quantitative Trait
7%
Quantitative Trait Locus
9%
Rare Variant
12%
Receptor Gene
7%
Regulatory Element
9%
Regulatory Sequence
10%
RNA
16%
RNA Sequence
8%
Single Nucleotide Polymorphism
25%
Single-Nucleotide Polymorphism
36%
Stem Cell
14%
Transcription
17%
Transcription Factors
54%
Transcriptome
7%
Transcriptomics
7%
Transposable Element
15%
Triglyceride
12%
Whole Genome Sequencing
10%
Wild Type
14%
Zebra Fish
7%
Keyphrases
African American
18%
African Ancestry
6%
Aging
8%
Alzheimer's Disease
9%
Autism
14%
Autism Spectrum Disorder
10%
Axon
12%
Axonal Degeneration
15%
Basal Body
9%
Binding Site
22%
Blood Pressure
16%
Body Mass Index
14%
Caenorhabditis Elegans
39%
Cell Fate
8%
Central Nervous System
13%
Chlamydomonas
13%
Chlamydomonas Reinhardtii
22%
CHRNA5
9%
Cilia
9%
Ciliary
7%
Cis-regulatory Elements
8%
Confidence Interval
7%
Coronary Artery Disease
11%
De-novo mutations
6%
Diabetes
8%
DNA Methylation (DNAm)
12%
DNA Sequencing
13%
DNA-binding Proteins
7%
Drosophilidae
27%
Dynein
9%
Early Growth Response Protein 1 (EGR1)
10%
Epigenome
8%
Epigenomics
7%
European American
9%
European Ancestry
13%
Exome Sequencing
8%
Family Study
15%
Fasting Plasma Glucose
9%
Flagella
10%
Gene Expression
32%
Gene Regulation
9%
Gene Regulatory Network
9%
Genetic Analysis
10%
Genetic Epidemiology
9%
Genetic Factors
7%
Genetic Studies
8%
Genetic Variants
15%
Genetic Variation
8%
Genome Scan
10%
Genome Sequencing
9%
Genome-wide Association Study
29%
Genotype
14%
Germ Cells
17%
Glial Cell Line-derived Neurotrophic Factor
11%
Heart Blood
16%
Heart-lung
16%
Heritability
9%
High-density Lipoprotein Cholesterol (HDL-C)
9%
Hypertension
13%
Intellectual Disability
7%
Linkage Analysis
11%
Lipids
8%
LOD Score
8%
Long Life Family Study
14%
Meta-analysis
30%
Metabolic Syndrome
10%
Methylation
7%
Microglia
7%
MicroRNA
7%
Missense Variants
7%
Mouse Model
8%
National Heart
16%
Nerve Growth Factor
6%
Neurodevelopmental Disorders
18%
Neurturin
11%
NGFI-A
7%
NHLBI
15%
Nicotinamide Adenine Dinucleotide (NAD+)
15%
Nicotine Dependence
15%
Obesity
14%
Odds Ratio
8%
Polymorphism
11%
Proband
10%
Protein-DNA Interaction
7%
Quantitative Trait Loci
9%
Quantitative Traits
7%
Rare Variants
10%
Regulatory Elements
6%
SARM1
12%
Schwann Cells
11%
Single nucleotide Polymorphism
27%
SNP
18%
Transcription Factor
41%
Transcription Factor Binding Sites
9%
Transposable Elements
10%
Triglycerides
9%
Tumor
7%
Type 2 Diabetes Mellitus (T2DM)
9%
Virus
7%
Whole Genome Sequencing
10%