Biochemistry, Genetics and Molecular Biology
Genetic Screening
100%
Genetics
81%
Missense
56%
Germ Cell
51%
Germline
46%
Preimplantation
43%
Mole (Insectivora)
43%
BRCA1
43%
Exome Sequencing
37%
DNA Mismatch Repair
37%
Cohort Study
33%
Aneuploidy
32%
Population
32%
BMPR1A
32%
BRCA2
32%
Penetrance
27%
Mosaicism
27%
Microsatellite DNA
26%
Genotyping
25%
Next Generation Sequencing
24%
Whole Genome Sequencing
24%
MLH1
21%
MSH2
21%
Genetic Disorder
21%
Cancer Staging
21%
Mitochondrial Disease
21%
MSH6
20%
STK11
19%
Autosomal Dominant Inheritance
19%
Point Mutation
18%
Triploidy
18%
Prevalence
17%
DNA Extraction
16%
Genetic Counseling
15%
Allele
14%
Pedigree
13%
Trophoblast
13%
Gene Sequence
13%
Genetic Predisposition
12%
Cancer Incidence
12%
Awareness
12%
Gene Repair
12%
Exon
12%
Genome Sequencing
10%
Cross Sectional Study
10%
Mental Retardation
10%
Candidate Gene
10%
Quantitative Technique
10%
Homeobox
10%
Dermatan Sulfate
10%
Type I Collagen
10%
Microphthalmia-Associated Transcription Factor
10%
BAP1
10%
Comorbidity
10%
Mortality Rate
10%
Leigh's Disease
10%
Retinitis pigmentosa
10%
ATP Synthase
10%
Apolipoprotein E
10%
Methylenetetrahydrofolate Reductase
10%
Gene Linkage
10%
Bone Development
10%
OPN1LW
10%
Buccal Mucosa
10%
Chromosome 13
10%
Factor H
10%
Chromosome 11
10%
Body Height
10%
Transfection
10%
Consanguinity
10%
SCO1
10%
Phosphorylase Kinase
10%
X-Linked Hypophosphatemia
10%
Rickets
10%
Autosomal Recessive Inheritance
10%
Loss of Heterozygosity
10%
TLR4
10%
Age-Related Maculopathy Susceptibility 2
10%
Attitude
10%
Myeloid
10%
Aggrecan
10%
Trisomy 21
10%
Gene Deletion
10%
SCN8A
10%
Angioedema
10%
ALPL
10%
Autosomal Dominant Polycystic Kidney
10%
Phosphorylase
10%
Genetic Trait
10%
PMS2
9%
Alkaline Phosphatase
9%
PKD1
9%
CDKN2B
8%
MUTYH
8%
Blastocyst
8%
Porosity
7%
Immunostaining
7%
Morphology
6%
Vascular Endothelial Growth Factor
5%
Ovary Function
5%
Medicine and Dentistry
Hereditary Nonpolyposis Colorectal Cancer
77%
Malignant Neoplasm
71%
Genetic Screening
59%
Diseases
55%
Rokitansky Syndrome
54%
Colorectal Cancer
50%
DNA Mismatch Repair
46%
Molar Pregnancy
36%
Hereditary Colorectal Cancer
32%
Peutz Jeghers Syndrome
32%
Diagnosis
28%
Cancer Risk
26%
Symptom
24%
Cross Sectional Study
23%
Polyposis
23%
Autosomal Dominant Inheritance
23%
Exome Sequencing
22%
Hypophosphatasia
21%
Cancer Staging
21%
Salpingooophorectomy
21%
Hysterectomy
21%
Gestational Trophoblastic Disease
21%
Hypodontia
21%
Maternal Blood
21%
Neoplasm
20%
Epileptic Seizure
18%
Disease Predisposition
18%
Cohort Analysis
18%
Colonoscopy
18%
Clinical Genetics
16%
Sensorineural Hearing Loss
16%
Prevalence
15%
Prostate Cancer
15%
Counseling
15%
Cancer Diagnosis
14%
Awareness
14%
Childbirth
14%
Congenital Malformation
13%
Renal Cyst
13%
Point Mutation
13%
Gene Repair
13%
Stomach Polyposis
13%
Drug Therapy
13%
Clinical Finding
12%
Cancer Susceptibility
12%
Personalized Medicine
12%
Penetrance
12%
Pervasive Developmental Disorder
12%
Pedigree
12%
Vagina Aplasia
12%
Clinical Management
11%
Trophoblast
11%
Genetic Counseling
11%
Retrospective Cohort Study
11%
Bone Strength
11%
Hazard Ratio
11%
Polycystic Kidney Disease
10%
Disorders of Mitochondrial Functions
10%
Lactic Acidosis
10%
Familial Disease
10%
Cancer Therapy
10%
Left Coronary Artery
10%
Genetic Disorder
10%
Arthrogryposis
10%
Marfan Syndrome
10%
Apoplexy
10%
Limb Defect
10%
Nosology
10%
Megalin
10%
Elastin
10%
Hypoparathyroidism
10%
Maternal Welfare
10%
Dizziness
10%
Chondrodysplasia
10%
Overdiagnosis
10%
Patient Characteristics
10%
Drusen
10%
Homeobox
10%
Achondroplasia
10%
Attitude
10%
Phosphorylase Kinase
10%
Gastric Finding
10%
X Linked Hypophosphatemic Rickets
10%
Early Cancer Diagnosis
10%
Tracheoesophageal Fistula
10%
Imperforate Anus
10%
Esophageal Atresia
10%
Mitochondrial Encephalopathy
10%
Bone Malformation
10%
Proteinase
10%
Epimerase
10%
Parathyroid Hormone
10%
Diet Therapy
10%
Vagus Nerve Stimulation
10%
Cone Dystrophy
10%
Buccal Mucosa
10%
Hybrid Gene
10%
Ketogenic Diet
10%
Nemaline Myopathy
10%
Acute Lymphoblastic Leukemia
10%
Keyphrases
Lynch Syndrome
43%
Pathogenic Variants
23%
Peutz-Jeghers Syndrome
21%
Conceptus
21%
Aneuploidy
21%
Mismatch Repair
21%
Hydatidiform Mole
21%
Androgenetic
18%
Whole Genome Sequencing
16%
Denmark
14%
Mismatch Repair Genes
13%
Triploid
12%
Cancer Predisposition Syndrome
12%
Mosaicism
12%
Phenotypic Spectrum
12%
Colorectal Cancer
11%
Familial Cancer
11%
Short-rib Polydactyly Syndromes
10%
Ataxia
10%
Retinitis pigmentosa
10%
NARP Syndrome
10%
Mitochondrial mutations
10%
Genetic Aspects
10%
Palmoplantar Keratoderma
10%
Type I Collagen
10%
Osteogenesis Imperfecta
10%
Overlap Syndrome
10%
Ehlers-Danlos Syndrome
10%
Myopia
10%
SLITRK6
10%
Greek Population
10%
Glaucoma
10%
Lysyl Oxidase
10%
Methylenetetrahydrofolate Reductase Polymorphism
10%
Apolipoprotein E
10%
Rokitansky Syndrome
10%
Pseudoexfoliation Syndrome
10%
Familial Occurrence
10%
Genotyping Techniques
10%
Craniosynostosis
10%
Partial Trisomy 6p
10%
ECEL1
10%
Arthrogryposis multiplex Congenita
10%
HDAC8
10%
Large Fontanelles
10%
Hypertelorism
10%
Cornelia De Lange Syndrome (CdLS)
10%
Blue Cone Monochromacy
10%
X Chromosome Inactivation
10%
Complement Factor H Gene
10%
Interstitial Deletion
10%
Body Dysmorphic Disorder
10%
Protein-truncating Variants
10%
Homeobox
10%
CABP2
10%
Gastric Phenotype
10%
Information Letters
10%
Genetic Network
10%
GABRD
10%
Mitochondrial Encephalopathy
10%
Von Hippel-Lindau Disease
10%
Clinical Genetics
10%
Say-Barber-Biesecker-Young-Simpson Syndrome
10%
KAT6B
10%
Informal Learning Opportunities
10%
Juvenile Polyposis Syndrome
10%
Breast Cancer Risk
10%
Case-comparison Study
10%
Dermatan Sulfate Epimerase
10%
Protein Kinase B
10%
Achondroplasia
10%
Mitochondrial Disease
10%
SCO1
10%
Ocular Albinism
10%
Sudden Sensorineural Hearing Loss (SSNHL)
10%
Late-stage Cancer
10%
Disease Pattern
10%
Aneuploidy Screening
10%
Morning Report
10%
Screening Cancer
10%
Sensorineural Hearing Impairment
10%
HARS2
10%
Perrault Syndrome
10%
Gene Variants
10%
Elastin Gene
10%
Cutis Laxa
10%
Myeloid Neoplasms
10%
Germline Predisposition
10%
Late-onset Colorectal Cancer
10%
Autosomal Dominant Cutis Laxa
10%
Salpingo-oophorectomy
10%
Spinocerebellar Ataxia Type 14
10%
Aberrant Splicing
10%
ARMS2 Gene
10%
Preimplantation Genetic Testing for Aneuploidy (PGT-A)
10%
TARS2
10%
TLR4 Gene Polymorphism
10%
Result Comparison
10%
Cancer Treatment
10%
Female Prevalence
10%