Biochemistry, Genetics and Molecular Biology
Platelet
100%
Genetics
76%
Whole Genome Sequencing
64%
Thrombocytopenia
55%
Megakaryocyte
39%
Gene Expression
34%
Allele
32%
High Throughput Sequencing
29%
Phenotype
28%
Mitochondrial DNA
26%
Mouse
25%
Isoform
24%
Thrombocyte Function
24%
Transcription Factors
22%
RNA Sequencing
22%
Pedigree
21%
Coagulopathy
19%
Stem Cell
19%
Messenger RNA
18%
Genome Sequencing
18%
Germ Cell
17%
Thrombopoiesis
16%
Missense
16%
Germline
16%
B Cell
16%
Autosomal Dominant Inheritance
16%
Exon
15%
Exome Sequencing
15%
Genetic Disorder
14%
Intellectual Disability
14%
Genome Wide Association Study
13%
Telomere Length
13%
Helicase
13%
Penetrance
13%
Ploidy
13%
Epigenetics
13%
Fibrinolysis
13%
Thrombomodulin
13%
Genotyping
13%
RNA Sequence
12%
Next Generation Sequencing
12%
Autosomal Recessive Inheritance
12%
Genetic Screening
12%
Haplotype
11%
Microarrays
11%
Actin
10%
Genome-Wide Association Study
10%
Proband
10%
Receptor Tyrosine Kinase
9%
Indel
9%
Keyphrases
Platelet Dysfunction
49%
Whole Genome Sequencing
47%
Platelets
47%
Megakaryocytes
40%
Rare Diseases
32%
Human Phenotype Ontology
29%
High-throughput Sequencing
28%
Gene Expression
27%
Macrothrombocytopenia
26%
Bleeding Disorders
25%
Mitochondrial DNA
23%
Thrombocytopenia
23%
Rare Variants
22%
Primary Immunodeficiency
22%
Pathogenic Variants
22%
Whole-genome Sequence Data
21%
Platelet Function
21%
Thrombotic
21%
Autosomal Dominant
20%
Gain-of-function mutation
20%
Bleeding
20%
Biallelic
19%
Transcription Factor
18%
Expression Level
16%
Disease Risk
16%
Agnostic
16%
Pedigree
16%
Proplatelet Formation
14%
Molecular Diagnostics
14%
Loss Function
14%
Myelofibrosis
14%
Monogenic
14%
Inherited Platelet Disorders
13%
Etiology
13%
Telomere Length
13%
NFKB1
13%
Ploidy
13%
Coagulopathy
13%
Nuclear Mitochondrial DNA
13%
Fibrinolysis
13%
Breast Cancer
13%
RNA-seq Data
13%
Thrombomodulin
13%
Platelet Isolation
13%
Multi-mapping
13%
Epilepsy
13%
DNA Segment
13%
Next-generation Sequencing
13%
RNA Sequencing (RNA-seq)
12%
Intellectual Disability
12%
Medicine and Dentistry
Platelet
54%
Thrombocytopenia
50%
Platelet Disorder
41%
Disease
33%
Bleeding
30%
Bleeding Disorder
30%
Diagnosis
22%
Human Phenotype Ontology
22%
Megakaryocyte
21%
Autosomal Dominant Inheritance
19%
Thrombocyte Dysfunction
19%
Thrombocytopoiesis
16%
Myelofibrosis
16%
Genome Wide Association Study
15%
Breast Cancer
13%
Allele
13%
Coagulopathy
13%
Transcriptomics
13%
Whole Genome Sequencing
13%
Rare Disease
13%
Autosomal Recessive Inheritance
12%
Genetic Disorder
11%
Protein Tyrosine Kinase
10%
Next Generation Sequencing
10%
Molecular Diagnosis
10%
In Vitro
10%
Prematurity
9%
Neonatal Intensive Care Unit
9%
Thrombosis
9%
Hearing Impairment
9%
Thrombocyte Function
9%
Actin
9%
Neonate
8%
Epileptic Absence
8%
Pedigree
8%
Platelet Reactivity
7%
Homeostasis
7%
Phenotype
7%
Exon
7%
Thromboplastin
7%
Blood Stasis
7%
Isotopes of Calcium
6%
MYH9
6%
Bone Pathology
6%
Cluster Analysis
6%
Methenamine
6%
Guanine
6%
STAT6 Protein
6%
Diacylglycerol
6%
Atopy
6%
