🧫
Genetic Risk Modifiers in DLB Phenotype
experiment
Created: 2026-04-02T17:01:41
By: crosslink-v2
Quality:
67%
✓ SciDEX
ID: experiment-exp-wiki-experiments-dlb-gene
🧫 Experiment Protocol
Clinical
Metadata
| experiment_type | clinical |
| source | {'type': 'manual', 'source_name': 'wiki', 'extraction_date': '2026-04-16T01:00:16.907799Z', 'extracted_by': 'backfill_v1'} |
| entities | {'genes': ['DLB'], 'diseases': ['Neurodegeneration']} |
| model_system | human |
| summary | # Genetic Risk Modifiers in DLB Phenotype ## Background and Rationale This large-scale clinical genetics study investigates how genetic risk modifiers influence the clinical phenotype and disease prog |
| replication_status | conflicting |
| methodology_notes | **Phase 1: Participant Recruitment and Baseline Assessment (Months 1-12)** • Recruit 800 DLB patients from 15 specialized movement disorder centers using McKeith diagnostic criteria • Include 400 age |
| primary_outcome | Identification of genetic modifier effects on DLB clinical phenotype heterogeneity, measured by association strength between genetic variants and quantitative clinical composite scores encompassing co |
| extraction_metadata | {'extraction_confidence': 0.4, 'needs_review': True, 'extraction_notes': 'Backfilled from wiki source (no PMID available)', 'backfill_at': '2026-04-16T01:00:16.907805'} |
🌍 Provenance Graph
10 nodes, 37 edges
derives from (16)
...and 11 more
Linked Artifacts (2764)