🧪 Experiments

16 proposed experiments from the Forge — designed to validate, falsify, and explore hypotheses

16
Total Experiments
0.71
Avg Score
0.52
Avg Feasibility
171
Clinical
202
Validation
27
Falsification
All Types animal_model (7)cell_biology (8)clinical (171)computational (12)exploratory (242)falsification (27)gene_expression (6)genetic_association (16)in-vitro (4)in_vitro (2)in-vivo (5)in_vivo (8)neuropathology (14)validation (202)
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genetic_association 0.50
Bulk RNA sequencing of 866 brain samples revealed significantly higher (~two-fold) overall burden of somatic single-nucl
🧬 cancer driver genes; clonal hematopoiesis genes (CSF1R) 🏥 Alzheimer's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Molecular-barcoded deep (>1000X) gene panel sequencing showed enrichment of sSNVs and sIndels in cancer driver genes in
🧬 cancer driver genes; CSF1R; clonal hematopoiesis genes 🏥 Alzheimer's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
GWANN identified 18 genes associated with family history of AD in UK Biobank, including 6 previously known AD genes (APO
🧬 APOE, BIN1, SORL1, ADAM10, APH1B, SPI1, PCDH9, NRG3, ROR1, LINGO2, SMYD3, LRRC7 🏥 Alzheimer's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Individuals with SNCA pathogenic variants reported painful dystonia, lower extremity pain, dorsal pain, and upper back p
🧬 SNCA 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Painful lower limb dystonia and lower back pain are prominent symptoms in PRKN carriers.
🧬 PRKN 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Continual correlation noted between LRRK2 mutations and pain emergence, though conflicting research outcomes pose challe
🧬 LRRK2 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
PINK1 mutation carriers frequently report experiencing pain.
🧬 PINK1 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Pain has been frequently reported as an initial symptom and the most troublesome one in GBA1-PD patients compared to tho
🧬 GBA1 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Evidence regarding pain in ATP13A2 pathogenic variants is limited and insufficient.
🧬 ATP13A2 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Evidence regarding pain in VPS35 pathogenic variants is limited and insufficient.
🧬 VPS35 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Evidence regarding pain in DNAJC6 pathogenic variants is limited and insufficient.
🧬 DNAJC6 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Evidence regarding pain in FBXO7 pathogenic variants is limited and insufficient.
🧬 FBXO7 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Evidence regarding pain in SYNJ1 pathogenic variants is limited and insufficient.
🧬 SYNJ1 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Participants carrying the APOE epsilon 4 allele showed more rapid biomarker changes (decreasing Aβ42:Aβ40 and increasing
🧬 APOE 🏥 Alzheimer's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Identification of a vulnerable subtype of dopaminergic neurons co-expressing Sox6 and Anxa1 that shows selective vulnera
🧬 Sox6, Anxa1 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
genetic_association 0.50
Generated a knock-in Cre mouse line for Anxa1+ dopaminergic neurons to enable targeted manipulation of this population.
🧬 ANXA1 🏥 Parkinson's disease 🔗 1 hyp
💰 N/A ⏱ N/A ✅ 0.00 ✨ 0.00
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