| 1 |
copy number variations
(2614 times)
|
Genetics, Medical
(612 times)
|
SNPs (187 times)
CMA (135 times)
aCGH (130 times)
|
2006 Bias of selection on human copy-number variants.
|
| 2 |
Copy Number Variants
(58 times)
|
Genetics, Medical
(13 times)
|
ASD (4 times)
SNP (4 times)
ASDs (3 times)
|
2007 Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome.
|
| 3 |
choroidal neovascularizations
(14 times)
|
Ophthalmology
(11 times)
|
OCT (6 times)
AMD (5 times)
OCTA (3 times)
|
2001 Optical coherence tomography (OCT) findings in normal retina and laser-induced choroidal neovascularization in rats.
|
| 4 |
choroidal neovascular membranes
(7 times)
|
Ophthalmology
(7 times)
|
AMD (2 times)
ICG (1 time)
OCT (1 time)
|
1995 Indocyanine green angiography and choroidal neovascularization obscured by hemorrhage.
|
| 5 |
contingent negative variations
(7 times)
|
Neurology
(6 times)
|
AEP (1 time)
BPs (1 time)
ECDs (1 time)
|
1975 Reliability of the contingent negative variation and the auditory evoked potential.
|
| 6 |
choroidal new vessels
(3 times)
|
Ophthalmology
(3 times)
|
AMD (2 times)
RPE (2 times)
BCVA (1 time)
|
1999 Drusen in age-related macular degeneration: pathogenesis, natural course, and laser photocoagulation-induced regression.
|
| 7 |
canine noroviruses
(1 time)
|
Allergy and Immunology
(1 time)
|
---
|
2014 Seroprevalence of canine norovirus in 14 European countries.
|
| 8 |
cell-engineered nanovesicles
(1 time)
|
Biocompatible Materials
(1 time)
|
ESC (1 time)
|
2017 Cell-Engineered Nanovesicle as a Surrogate Inducer of Contact-Dependent Stimuli.
|
| 9 |
chromosome number variations
(1 time)
|
Medicine
(1 time)
|
SILAC (1 time)
SNP (1 time)
|
2013 Proteomic and genomic analyses of antimony resistant Leishmania infantum mutant.
|
| 10 |
Classic neovessels
(1 time)
|
Ophthalmology
(1 time)
|
---
|
2003 [Alternative therapies for choroidal neovessels resulting from age-related macular degeneration].
|
| 11 |
copy number structural variations
(1 time)
|
Neoplasms
(1 time)
|
BL (1 time)
EBV (1 time)
NGS (1 time)
|
2016 Genome-wide Analysis of Epstein-Barr Virus (EBV) Integration and Strain in C666-1 and Raji Cells.
|
| 12 |
copy number variations detected
(1 time)
|
Pediatrics
(1 time)
|
---
|
2015 Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances.
|
| 13 |
duplications-copy number variations
(1 time)
|
Reproductive Medicine
(1 time)
|
PGD-A (1 time)
|
2017 Diagnosis and clinical management of duplications and deletions.
|
| 14 |
PurposeCopy-number variants
(1 time)
|
Genetics, Medical
(1 time)
|
CRISPR (1 time)
|
2018 Noncoding copy-number variations are associated with congenital limb malformation.
|
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