List of bibliographic references
Number of relevant bibliographic references: 7.
List of associated KwdEn.i
Nombre de documents | Descripteur |
5 | Humans |
3 | Alzheimer Disease (genetics) |
3 | Genome-Wide Association Study |
3 | Male |
2 | Adult |
2 | Aged |
2 | Case-Control Studies |
2 | Female |
2 | Genetic Predisposition to Disease |
2 | Middle Aged |
2 | Pedigree |
1 | ATP Binding Cassette Transporter, Sub-Family G, Member 1 |
1 | ATP-Binding Cassette Transporters (genetics) |
1 | Age of Onset |
1 | Aged, 80 and over |
1 | Alcoholism |
1 | Alzheimer Disease (diagnosis) |
1 | Alzheimer Disease (epidemiology) |
1 | Amino Acid Sequence |
1 | Brain (pathology) |
1 | Bruch Membrane (metabolism) |
1 | CHD2 |
1 | Carrier Proteins (genetics) |
1 | Child |
1 | Child Development Disorders, Pervasive (genetics) |
1 | Chromosome Mapping |
1 | Chromosomes, Human, Pair 18 |
1 | Chromosomes, Human, Pair 9 |
1 | Copy Number Variation |
1 | DNA Copy Number Variations |
1 | DNA Mutational Analysis |
1 | Dementia (diagnosis) |
1 | Dementia (etiology) |
1 | Exome |
1 | Extracellular Matrix (metabolism) |
1 | Fibrillin-2 |
1 | Fibrillins |
1 | GDI1 |
1 | Gene Regulatory Networks |
1 | Genetic Association Studies |
1 | Genetic Loci (genetics) |
1 | Genetic Variation |
1 | Genetic variant |
1 | Genotype |
1 | HDAC4 |
1 | Heat-Shock Proteins (genetics) |
1 | High-Throughput Nucleotide Sequencing |
1 | Hippocampus (metabolism) |
1 | Hippocampus (pathology) |
1 | Locus |
1 | Macular Degeneration (diagnosis) |
1 | Macular Degeneration (genetics) |
1 | Meta-Analysis as Topic |
1 | Metabolic Networks and Pathways (genetics) |
1 | Microfilament Proteins (genetics) |
1 | Microfilament Proteins (metabolism) |
1 | Models, Molecular |
1 | Molecular Sequence Data |
1 | Multigene Family |
1 | Mutation |
1 | N-Acetylgalactosaminyltransferases (genetics) |
1 | Odds Ratio |
1 | Pancreatitis |
1 | Phenotype |
1 | Plaque, Amyloid |
1 | Polymorphism, Single Nucleotide |
1 | Polymorphism, Single Nucleotide (genetics) |
1 | Prospective Studies |
1 | Protein Conformation |
1 | Protein Stability |
1 | Quantitative Trait Loci |
1 | Receptors, Antigen, B-Cell (genetics) |
1 | Retina (metabolism) |
1 | Retina (pathology) |
1 | Risk |
1 | Risk Factors |
1 | SETD5 |
1 | Sequence Alignment |
1 | Sequence Deletion |
1 | Sporadic |
1 | autism |
1 | de novo |
1 | gene networks |
1 | inherited |
1 | pathways |
1 | rare CNV |
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