Keyphrases
Cytopenia
72%
Thalassemia
55%
Pediatric Patients
53%
Myelodysplastic Syndrome
51%
Clinical Presentation
47%
Immune Thrombocytopenia
46%
Israel
46%
Neutropenia
43%
Fanconi Anemia
39%
Congenital Neutropenia
38%
Clinical Characteristics
37%
Pediatric Immune Thrombocytopenia
36%
Congenital Anemia
34%
Haploinsufficiency
34%
Head-and-neck Squamous Cell Carcinoma (HNSCC)
34%
Metagenomic Next-generation Sequencing (mNGS)
30%
Anemia
27%
Leukemia
27%
Molecular Diagnostics
26%
Globin
26%
Hematopoietic Stem Cells
26%
Transcription Factor
25%
Pediatric Hematology
25%
Whole Exome Sequencing
25%
Next-generation Sequencing
25%
Germ Cells
25%
Novel mutation
24%
Macrocytic Anemia
24%
GATA2
24%
Bleeding
23%
Erythroblasts
21%
Pediatric
21%
Splenectomy
20%
Response to Treatment
20%
Biallelic
20%
Laboratory Features
20%
Intravenous Immunoglobulin (IVIg)
20%
Oncology Patients
20%
MPL mutation
19%
Genetic Diagnosis
19%
Stem Cell Transplantation
19%
Leukemia Predisposition
19%
Hemoglobin A2
19%
Hematological Malignancies
19%
Thrombocytopenia
19%
Platelet Count
18%
Bone Marrow
18%
Hematopoietic Stem Cell Transplantation
18%
Pediatric Intensive Care Unit
17%
Prediction Accuracy
17%
Medicine and Dentistry
Pediatrics
100%
Idiopathic Thrombocytopenic Purpura
72%
Cytopenia
69%
Neutropenia
58%
Anemia
52%
Myelodysplastic Syndrome
47%
Thalassemia
43%
Next Generation Sequencing
42%
Disease Predisposition
40%
Fanconi Anemia
37%
Leukemia
37%
Bleeding
36%
Pediatrics Patient
35%
Head and Neck Squamous Cell Carcinoma
34%
Diseases
34%
Platelet
29%
Thrombocytopenia
25%
Pediatric Hematology
25%
Immunoglobulin
23%
Bone Marrow Failure
21%
Somatics
21%
Stem Cell
21%
Exome Sequencing
21%
Infection
21%
Erythrocyte
20%
Splenectomy
20%
Hematologic Malignancy
20%
Adverse Event
20%
Intensive Care
19%
Disease
19%
Germ Cell
19%
Adverse Effect
19%
Oncology
17%
Scoring System
17%
Sepsis
17%
Essential Thrombocythaemia
17%
Corpus Luteum
17%
Thrombocyte Function
17%
Neonatal Thrombocytopenia
17%
Rhesus D Antibody
17%
Alpha-Thalassemia
17%
Blood Disorder
17%
Gray Platelet Syndrome
17%
Microcytosis
17%
Diamond-Blackfan Anemia
17%
Systemic Lupus Erythematosus
17%
Immune Dysregulation
17%
Genetic Variation
17%
Kidney Graft
17%
Hydroxychloroquine
17%
Biochemistry, Genetics and Molecular Biology
Myeloid
61%
Genetics
55%
Globin
37%
Germ Cell
35%
Haploinsufficiency
34%
Thrombocytopenia
30%
Transcription Factors
30%
Exome Sequencing
29%
Cell Function
24%
Bone Marrow Failure
23%
Hemoglobin A2
23%
Nonsense Mutation
21%
Stem Cell
21%
Genomics
21%
Missense
19%
T Cell
19%
Germline
18%
G6PC3
17%
Hemocyte
17%
Microcytosis
17%
Diamond-Blackfan Anemia
17%
Erythropoiesis
17%
Genetic Background
17%
Patient Compliance
17%
Megakaryocytopoiesis
17%
Iron Chelation
17%
Tumor Suppressor Gene
17%
BRCA1
17%
GATA2
17%
Congenital Amegakaryocytic Thrombocytopenia
17%
Serum Iron
17%
Genetic Variation
17%
Point Mutation
17%
Telomere
17%
Proteomics
17%
Genetic Divergence
17%
Galectin-3
17%
Cancer Cell
17%
Uridine
17%
Hematopoietic Cell
16%
Chelation
15%
Maturation
15%
Protein Function
14%
Mean Corpuscular Volume
11%
Blood Cell Count
11%
Heterozygosity
11%
Allele
10%
SH2B3
10%
Next Generation Sequencing
10%
Genetic Disorder
10%
