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