Biochemistry, Genetics and Molecular Biology
Genetics
100%
Exome Sequencing
95%
Missense
73%
Wild Type
54%
Intellectual Disability
43%
Autosomal Recessive Inheritance
40%
Homozygosity
40%
Exon
38%
Body Height
35%
Endoglin
34%
Escherichia coli
34%
Succinic Acid
34%
Familial Hypercholesterolemia
34%
Endoplasmic Reticulum Stress
34%
Dysplasia
34%
Enzyme
31%
Microarrays
29%
Metabolic Network
29%
Messenger RNA
28%
Artificial Intelligence
26%
Inborn Error of Metabolism
26%
Pharmacogenomics
26%
Genetic Screening
26%
Gene Linkage
26%
Gene Mutation
25%
Genetic Disorder
23%
Gene Knockout
23%
Autosomal Dominant Inheritance
22%
Oxidoreductase
20%
Computer Model
20%
Genotyping
20%
LDL Receptor
19%
Single-Nucleotide Polymorphism
19%
Pharmacological Chaperone
17%
Galactose
17%
Phosphoenolpyruvate Carboxykinase
17%
PCK1
17%
Schindler Disease
17%
Metabolomics
17%
Leigh's Disease
17%
Zinc Ion
17%
Nonsense-Mediated Decay
17%
CDH23
17%
Maroteaux-Lamy Syndrome
17%
Citrulline
17%
Homocystinuria
17%
Liquid Chromatography-Mass Spectrometry
17%
RNA
17%
Wilms' Tumor
17%
Genetic Algorithm
17%
Haplotype
17%
Activin
17%
Mesangial Cell
17%
MAP1B
17%
Bromodomain Phd-Finger Transcription Factor
17%
Katanin
17%
PTBP2
17%
CDKL5
17%
WD40 Repeat
17%
Haploinsufficiency
17%
MicroRNA
17%
Copy-Number Variation
17%
Marker Gene
17%
Support Vector Machine
17%
CYP2D6
17%
Proteoglycan
17%
HLA-DQB1
17%
Prevalence
17%
Pharmacogenetic Variant
17%
ROR2
17%
PTPN22
17%
Internalization
17%
Oncogene
17%
Electronic Health Record
17%
Artificial Intelligence
17%
Mutant Protein
17%
Low-Density Lipoprotein
17%
Alpha-Mannosidosis
17%
NPR2
17%
Patient Participation
17%
Lung Function
17%
Respiratory Function
17%
Lysosomal Storage Disease
17%
Macromolecule
17%
Lysosome
17%
Breathing
17%
Genetic Test
17%
Attitude
17%
Sanger Sequencing
17%
Tendon Reflex
17%
CNTN1
17%
Stop Codon
17%
Chromosome 1
17%
Reductase
17%
Immune Checkpoints
17%
Carbonic Anhydrase
17%
Cell Junction
17%
Occludin
17%
Lymphoblast
17%
Blood Brain Barrier
17%
Ciprofloxacin
17%
Skeletal Muscle
17%
FUS
17%
Campylobacter Jejuni
17%
Dioxygenase
17%
Hydrogen Sulfide
17%
Zinc
17%
Sepiapterin Reductase
17%
Sodium-Glucose Cotransporter 2 Inhibitors
17%
Prenatal Growth
15%
SOD1
13%
Proteasome
13%
Nonsense Mutation
12%
Oxidative Stress
12%
Zebra Fish
12%
Phenocopy
11%
Creatine Kinase
11%
DNA Sequence
11%
Mitochondrial Membrane Potential
11%
Endoplasmic-Reticulum-Associated Protein Degradation
10%
Electron Transfer Flavoprotein B
10%
Nicotinamide Adenine Dinucleotide Phosphate
10%
TARDBP
10%
Mouse
9%
Reference Value
8%
Derivatization
8%
Fatty Acid Metabolism
8%
ETFDH
8%
Fatty Acid Blood Level
8%
Reconstruction
8%
DNA Modification
8%
Endoplasmic Reticulum Membrane
8%
Membrane
8%
Metabolic Engineering
8%
Protein Complexes
8%
Gene Expression Data
8%
Metabolite
8%
Protein Expression
8%
Reversed-Phase Chromatography
8%
Genome Sequencing
8%
Membrane Protein
8%
Technique in Genetics
8%
Gene Targeting
8%
POT1
8%
Gene Deletion
8%
Cyclic Guanosine Monophosphate
8%
Cross Sectional Study
8%
Morpholino
8%
Cas9
8%
Awareness
8%
Proline
8%
Genome Editing
8%
Anabolism
8%
Isozyme
8%
Orthology
8%
Retrospective Study
8%
Consanguinity
8%
CRISPR
8%
GJB2
8%
Newborn Period
8%
Large Intestine
8%
Standing
8%
Quality Control
8%
Genetic Divergence
8%
Protein Folding
8%
Cell Migration
7%
Hedgehog Signaling Pathway
7%
Unfolded Protein Response
7%
PITX2
6%
Cell Membrane
6%
Allele
6%
Gaucher's Disease
5%
Prosaposin
5%
Glucocerebroside
5%
Medline
5%
Medical Informatics
5%
Thrombopoietin
5%
Gene Discovery
5%
Gene Function
5%
POMGNT1
5%
Clinical Decision Making
5%
Oxygen Desaturation
5%
Intelligence
5%
Hypokalemia
5%
Protein Conformation
5%
Fibroblast Growth Factor
5%
Clinical Classification
5%
Scopus
5%
Patient Coding
5%
Solution and Solubility
5%
Next Generation Sequencing
5%
Propionyl-CoA
5%
PON1
5%
Mitochondrial DNA Depletion Syndrome
5%
Streptococcus Agalactiae
5%
Penetrance
5%
Conformation
5%
NPC1
5%
Cell Function
5%
Apelin
5%
Keyphrases
Bees Algorithm
34%
Metabolic Engineering
21%
Lactate Production
21%
Succinate Production
21%
Null Variants
17%
Pharmacological Chaperone
17%
Schindler Disease
17%
Gaucher
17%
Saposin C
17%
Phosphoenolpyruvate Carboxylase
17%
PCK1
17%
Leigh Syndrome
17%
Novel Phenotypes
17%
COX4I1
17%
Group Consensus
17%
Transaldolase
17%
Targeted Proteomics
17%
CDH23 Gene
17%
Neurogenetics
17%
MPS VI
17%
Variant Database
17%
Genomic Landscape
17%
Etoricoxib
17%
Serine Deficiency
17%
SLC4A1
17%
Spastic Tetraplegia
17%
Report Analysis
17%
Hypertrophic Osteoarthropathy
17%
Cobalamin C Deficiency
17%
Bioactivation
17%
Citrulline Supplementation
17%
Arginine Supplementation
17%
Overgrowth Syndrome
17%
Renal Dysplasia
17%
Fermentation Pathways
17%
Phishing Attack Detection
17%
Speech Detection
17%
Image-based Features
17%
Artificial Speech
17%
Long Short Time Memory
17%
Kinetic Parameters
17%
Junctional Adhesion Molecule
17%
Wnt Signaling
17%
Human Cognition
17%
Wnt Signaling Pathway
17%
Yeast Fermentation
17%
Unsupervised Machine Learning
17%
Dichotomizer
17%
Bent Bone Dysplasia
17%
Association Function
17%
Supervised Machine Learning
17%
Variant Impact
17%
Optimization Genetic Algorithm
17%
Genetic Flux
17%
Minimization of Metabolic Adjustment
17%
HHT2
17%
Gene Knockout
17%
SVM-RFE
17%
Cancer Prognostic Marker
17%
Synaptopodin
17%
Artificial Bee Colony Algorithm
17%
KIF7
17%
MiR-92a
17%
Epicardial Adipose
17%
Epicardial Adipose Tissue
17%
Cancer Classification
17%
Endoglin
17%
Endoplasmic Reticulum Quality Control
17%
Centriole
17%
Hereditary Hemorrhagic Telangiectasia
17%
Katanin P80
17%
KATNB1
17%
Human Cortical Development
17%
Methyltransferase
17%
GABPA
17%
Camptodactyly-arthropathy-coxa Vara-pericarditis
17%
Proteoglycan 4 (PRG4)
17%
Bat Algorithm
17%
Frameshift Variant
17%
Genetic Causation
17%
Copy number Analysis
17%
Human Accelerated Regions
17%
Autism Spectrum Disorder
17%
HLA-DQB1 Alleles
17%
WD Repeat Domain
17%
Cell Degradation
17%
Dynamic Flux Balance Analysis
17%
Desynchronization Transition
17%
In Silico
17%
Swahili Coast
17%
Innovative Potential
17%
Signal Shaping
17%
Meticillin-resistant Staphylococcus Aureus
17%
CYP2D6 Genotype
17%
Molecular Potential
17%
Southeast Asian Population
17%
Pharmacogenes
17%
Teratocarcinosarcoma
17%
CTNNB1 mutation
17%
Intraocular Mass
17%
PSMD12
17%
Secondary Associations
17%
PDLIM5
17%
Microorganisms
17%
Silver-Russell Syndrome
17%
Deep Generative Models
17%
INS Gene
17%
PTPN22
17%
Succinic
17%
Pathogenicity Prediction Tools
17%
Online Healthcare
17%
Expert Rules
17%
Mendelian Conditions
17%
Heterogeneous Cohorts
17%
Acromelic Dysplasia
17%
Urticarial Vasculitis
17%
DNASE1L3
17%
Mendelian Randomization
17%
PGx Testing
17%
CNTNAP1
17%
Neural Progenitor Cell Proliferation
17%
Cerebral Cortex Development
17%
EXOC7
17%
ELAC2
17%
PYCR2
17%
Hypomyelination
17%
Ellis-van Creveld Syndrome
17%
Subependymal
17%
JAM3
17%
Tight Junction Proteins
17%
Immune Checkpoint Inhibitors
17%
Cardio-obstetrics
17%
Orphanet
17%
KIAA1217
17%
Neonatal Presentation
17%
GyrA Gene
17%
Campylobacter Jejuni Infection
17%
Bilateral Sensorineural Hearing Loss
17%
Carbonic Anhydrase VA Deficiency
17%
Resistance Mechanisms
17%
Ethylmalonic Encephalopathy
17%
Ambroxol
17%
Novel Pathogenic mutation
17%
Sepiapterin Reductase
17%
Asfotase Alfa
17%
Hypophosphatasia
17%
Aging Biomarkers
17%
Kidney Transplant Recipients
17%
EVC2 Gene
13%
Statin-associated muscle Symptoms
13%
Higher Rank
11%
Founder Haplotype
11%
ASVspoof 2015
11%
Katanin
11%
Hyperammonemic Encephalopathy
11%
Tumor
11%
CUL7
10%
Intelligence Studies
10%
ASCT1
10%
Rational Modeling
10%
OptGene
10%
OptKnock
10%
Cytochrome P450 2D6 (CYP2D6)
9%
Central Bureau
8%
Microbial Strains
8%
Google Trends Data
8%
Cognition Deficits
8%
Segment Polarity Gene
8%
Human Homolog
8%
Iranian Families
8%
Splice Junction
8%
Exon Skipping
8%
Human Brain Development
8%
RNA Analysis
8%
Pathogenic Effects
8%
Fuzzy Database
8%
Pathway Marker
8%
Dendritic Growth
8%
Cortex Layers
8%
Metabolomics Methods
8%
Disease Biomarker
8%
Saturated-unsaturated
8%
Isotope Internal Standard
8%
Multiple Reaction Monitoring
8%
Branched-chain Fatty Acids
8%
Underivatized
8%
Production Rate
8%
Local Researcher
8%
OBSL1
8%
Techniques in Genetics
8%
Electronic Health Record Data
8%
Huntington's Chorea
8%
Rett Syndrome
8%
Neurological Drugs
8%
Cognitive Center
8%
Multisystem Atrophy
8%
Endocrine Pathways
8%
Humoral Pathway
8%
CYP2C9
8%
CASPR
8%
Medicine and Dentistry
Immune Checkpoint Inhibitor
34%
Rare Disease
34%
Neoplasm
24%
Genetic Screening
23%
Pharmacogenomics
23%
Cardiovascular Disease
19%
Personalized Medicine
18%
Metabolic Engineering
17%
Glycogen Storage Disease Type II
17%
Atorvastatin
17%
Rosuvastatin
17%
Early Diagnosis
17%
Statin
17%
Mendelian Randomization Analysis
17%
Methyltransferase
17%
Lysosomal Storage Disease
17%
Maroteaux-Lamy Syndrome
17%
Mannosidosis
17%
Adipose Tissue
17%
Medicine
17%
Genetic Marker
17%
Reelin
17%
Kidney Dysplasia
17%
Ciprofloxacin
17%
Systematic Review
17%
Quinolone Derivative
17%
Campylobacter Enteritis
17%
Pathogenicity
17%
Redox Signalling
17%
Canagliflozin
17%
Etoricoxib
17%
Osteoarthropathy
17%
Attitude
17%
Obstetrics
17%
Image Analysis
17%
Leigh's Disease
17%
Developmental Regression
17%
Next Generation Sequencing
17%
Dried Blood Spot
17%
Adverse Effect
17%
Observational Study
17%
Mutational Analysis
17%
Tetraplegia
17%
Cardiomyopathy
17%
Breast Cancer
17%
Citrulline
17%
Silver-Russell Syndrome
17%
Storage Disease
14%
Malignant Neoplasm
12%
Marker Gene
11%
Spirometry
11%
In Silico
10%
microRNA
9%
Bioethanol
8%
Gene Targeting
8%
Lung
8%
Genetic Disorder
8%
Cortex Layer II
8%
Medial Entorhinal Cortex
8%
Zinc Transporter
8%
Logistic Regression Analysis
7%
Dioxygenase
6%
Hydrogen Sulfide
6%
Awareness
6%
Diagnosis
6%
Cross Sectional Study
5%
Health Promotion
5%
Luminal A Breast Cancer
5%
Thrombopoietin
5%
Cytoreductive Surgery
5%
Debulking Surgery
5%
Blastema
5%
Neuroepithelium
5%
ICE (Chemotherapy)
5%
Bone Mass
5%
Point Mutation
5%
Quinolone
5%
Gene Mapping
5%
Bloody Diarrhea
5%
Campylobacter Jejuni
5%
Fanconi Anemia
5%
Immune System
5%
Propionyl-CoA
5%
Single Nucleotide Polymorphism
5%
Electronic Health Record
5%