| h-gap-5c6cec3e-m2 | plasma GFAP separates causal from compensatory states in: Blood-brain barrier pe | 0.35 | 0.69 | plasma GFAP | active | 2026-04-26 | SDA-2026-04-26-gap-20260426-001501 |
| h-gap-2f2e5b80-m2 | plasma LPS-binding protein separates causal from compensatory states in: How doe | 0.35 | 0.69 | plasma LPS-binding protein | active | 2026-04-26 | SDA-2026-04-26-gap-20260425-224724 |
| h-gap-456a357b-m3 | protective chromatin remodeling defines the therapeutic window for: Are DNA meth | 0.35 | 0.66 | protective chromatin remodeling | active | 2026-04-26 | SDA-2026-04-26-gap-debate-20260410-111542-7f40fe3e |
| h-gap-92152803-m1 | ubiquitylation-dependent turnover is the actionable driver in: How do ALS-linked | 0.34 | 0.74 | ubiquitylation-dependent turnover | active | 2026-04-26 | SDA-2026-04-26-gap-pubmed-20260410-181402-259766ab |
| h-gap-e7852b55-m1 | age-linked CpG drift is the actionable driver in: Are age-related DNA methylatio | 0.34 | 0.74 | age-linked CpG drift | active | 2026-04-26 | SDA-2026-04-26-gap-debate-20260410-112902-5b3fc173 |
| h-gap-456a357b-m1 | age-linked CpG drift is the actionable driver in: Are DNA methylation changes in | 0.34 | 0.74 | age-linked CpG drift | active | 2026-04-26 | SDA-2026-04-26-gap-debate-20260410-111542-7f40fe3e |
| h-ccefee49 | SIRT3 Mitochondrial Activation to Counter Hub-Specific Energetic Vulnerability | 0.34 | 0.30 | SIRT3 Mitochondrial | proposed | 2026-04-26 | SDA-2026-04-16-frontier-connectomics-84acb35a |
| h-59d95760 | Epigenetic Age Acceleration Moderates the Amyloid-to-Tau Conversion Cascade — A | 0.34 | 0.17 | MAPT | active | 2026-04-26 | SDA-2026-04-25-gap-epi-clock-biomarker-20260425-222549 |
| h-gap-2f2e5b80-m1 | TLR4 priming is the actionable driver in: How does gut microbiome dysbiosis cont | 0.34 | 0.74 | TLR4 priming | active | 2026-04-26 | SDA-2026-04-26-gap-20260425-224724 |
| h-gap-456a357b-m2 | ATAC-seq accessibility separates causal from compensatory states in: Are DNA met | 0.34 | 0.69 | ATAC-seq accessibility | active | 2026-04-26 | SDA-2026-04-26-gap-debate-20260410-111542-7f40fe3e |
| h-74cfd51e | Phosphatidylserine Decarboxylase (PISD) Restoration to Correct Mitochondrial Mem | 0.34 | 0.40 | PISD | proposed | 2026-04-26 | SDA-2026-04-16-frontier-lipidomics-dcdbc360 |
| h-gap-2f2e5b80-m3 | microglial inflammasome tone defines the therapeutic window for: How does gut mi | 0.34 | 0.66 | microglial inflammasome tone | active | 2026-04-26 | SDA-2026-04-26-gap-20260425-224724 |
| h-var-1aef6fec24 | Magnetofection-Enhanced IGFBPL1 Delivery via Superparamagnetic Iron Oxide Nanopa | 0.34 | 0.26 | IGFBPL1 | proposed | 2026-04-27 | SDA-2026-04-06-gap-debate-20260406-062045-6addd0cf |
| h-f4c6f2d080 | Poorly lipidated APOE4 particles are preferentially routed through LDLR/LRP1 int | 0.34 | 0.19 | LRP1 | proposed | 2026-04-25 | SDA-2026-04-25-gapdebate-f4c8357045 |
| h-b67ff2c9 | Ferroptosis as Primary Driver of Motor Neuron Death | 0.34 | 0.35 | | proposed | 2026-04-18 | SDA-2026-04-18-gap-debate-20260417-032952-48bdcbea |
| h-var-f632822c7c | FUS-Enhanced AAV-PHP.eB Delivery of IGFBPL1 to Microglia | 0.34 | 0.26 | IGFBPL1 | proposed | 2026-04-27 | SDA-2026-04-06-gap-debate-20260406-062045-6addd0cf |
| h-SDA-2026-04-26-gap | Pre-Symptomatic Dawn-Administration for Phase-Advance Targeting | 0.34 | 0.27 | MT2 receptor (Gq/11 coupling); PER1/2; SCN pacemaking neuron | proposed | 2026-04-26 | SDA-2026-04-26-gap-pubmed-20260411-090734-1be1b913 |
| h-SDA-2026-04-26-gap | Individual Baseline Variability in p-tau217 Half-Life Dictates Cessation Thresho | 0.34 | 0.33 | CST3, AQP4 | proposed | 2026-04-26 | SDA-2026-04-26-gap-debate-20260417-033134-20519caa |
| h-gap-92152803-m2 | K48/K63 ubiquitin chain balance separates causal from compensatory states in: Ho | 0.33 | 0.69 | K48/K63 ubiquitin chain balance | active | 2026-04-26 | SDA-2026-04-26-gap-pubmed-20260410-181402-259766ab |
| h-25276acb00 | CHMP2B vs. CHMP2A Subunit Targeting Creates a Therapeutic Window in ESCRT-Depend | 0.33 | 0.32 | CHMP2B, CHMP2A, CHMP4B | proposed | 2026-04-22 | SDA-2026-04-06-gap-debate-20260406-062052-7bcf4b6c |
| h-var-73d2ff30c1 | Novel Hypothesis on Metabolic Dysregulation in Neurodegeneration | 0.33 | 0.30 | SLC16A1 (MCT1) | archived | 2026-04-17 | |
| h-gap-92152803-m3 | proteasome shuttle failure defines the therapeutic window for: How do ALS-linked | 0.33 | 0.66 | proteasome shuttle failure | active | 2026-04-26 | SDA-2026-04-26-gap-pubmed-20260410-181402-259766ab |
| h-gap-e7852b55-m2 | ATAC-seq accessibility separates causal from compensatory states in: Are age-rel | 0.33 | 0.69 | ATAC-seq accessibility | active | 2026-04-26 | SDA-2026-04-26-gap-debate-20260410-112902-5b3fc173 |
| h-gap-e7852b55-m3 | protective chromatin remodeling defines the therapeutic window for: Are age-rela | 0.33 | 0.66 | protective chromatin remodeling | active | 2026-04-26 | SDA-2026-04-26-gap-debate-20260410-112902-5b3fc173 |
| h-8530ac03f6 | TFUS Restores CCK Interneuron Dysfunction via Mitochondrial Dynamics Restoration | 0.33 | 0.28 | Piezo1 (PIEZO1), Drp1 (DNM1L), OPA1, MFN2, Calcineurin (PPP3 | proposed | 2026-04-28 | SRB-2026-04-28-h-var-a4975bdd96 |
| h-cef0dd34 | Plasma p-tau217-Triggered Exosome Dosing Maximizes lncRNA-0021 Therapeutic Windo | 0.32 | 0.15 | CSF p-tau217 (biomarker), lncRNA-0021, hUC-MSC exosomes | promoted | 2026-04-17 | SDA-2026-04-16-gap-pubmed-20260410-150509-76c40dac |
| h-29335102 | Multi-Clock Ensemble Discordance as a Parkinson's Disease Prodrome Detector — Ep | 0.32 | 0.12 | DNA, IDS, PD | active | 2026-04-26 | SDA-2026-04-25-gap-epi-clock-biomarker-20260425-222549 |
| h-af33e758af | Prostacyclin (PGI2) Signaling via IP Receptor | 0.32 | 0.25 | PTGIR (IP receptor); PTGS2 (COX-2) | proposed | 2026-04-26 | SDA-2026-04-26-gap-pubmed-20260410-170057-a2f72fd8-debate |
| h-66b49ac5 | Combination Gene Therapy Targeting RGS6 and Parkin or PINK1 to Address Mitochond | 0.32 | 0.15 | PINK1 | proposed | 2026-04-18 | SDA-2026-04-17-gap-pubmed-20260410-145520-5692b02e |
| h-965864b650 | Partial Agonist/SPP1 Splice Variant Strategy: Splice-Switching Therapeutics | 0.31 | 0.30 | SPP1 splicing factors | proposed | 2026-04-21 | SDA-2026-04-07-gap-pubmed-20260406-062118-2cdbb0dd |
| h-d799fa0468 | Combination RGS6 restoration plus D2-pathway modulation | 0.31 | 0.18 | RGS6 | proposed | 2026-04-26 | SDA-2026-04-26-gap-pubmed-20260410-145520-5692b02e-debate |
| h-4e806018 | Astrocyte-Neuron Lactate Shuttle Enhancement via Pharmacological Activation of M | 0.31 | 0.35 | SLC16A3 (MCT4) | proposed | 2026-04-26 | SDA-2026-04-16-frontier-metabolomics-f03b09d9 |
| f9810557-7cc1-410f-b | Test hypothesis 2 | 0.30 | 0.02 | | proposed | 2026-04-27 | |
| ffaac8bd-77eb-41be-b | Test hypothesis 2 | 0.30 | 0.02 | | proposed | 2026-04-27 | |
| 453a9291-591a-492d-8 | Test hypothesis 2 | 0.30 | 0.02 | | proposed | 2026-04-27 | |
| 6a908861-12e7-4518-9 | Test hypothesis 2 | 0.30 | 0.02 | | proposed | 2026-04-27 | |
| mlsm-axis-parkinsons | [Archived Hypothesis] | 0.30 | 0.30 | | archived | 2026-04-17 | legacy-pre-pipeline-import-v1 |
| mitochondrial-dynami | [Archived Hypothesis] | 0.30 | 0.45 | | archived | 2026-04-17 | legacy-pre-pipeline-import-v1 |
| h-test-123 | [Archived Hypothesis] | 0.30 | 0.00 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| non-dopaminergic-neu | [Archived Hypothesis] | 0.30 | 0.45 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| sirtuin-dysfunction- | [Archived Hypothesis] | 0.30 | 0.45 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| mitochondria-lysosom | [Archived Hypothesis] | 0.30 | 0.45 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| metal-ion-synuclein- | [Archived Hypothesis] | 0.30 | 0.30 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| pathologic-synergy-o | [Archived Hypothesis] | 0.30 | 0.45 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| h-nonexistent | [Archived Hypothesis] | 0.30 | 0.00 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| cellular-senescence- | [Archived Hypothesis] | 0.30 | 0.45 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| h-nonexistent-123 | [Archived Hypothesis] | 0.30 | 0.00 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| purinergic-signaling | [Archived Hypothesis] | 0.30 | 0.30 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| retromer-endosomal-s | [Archived Hypothesis] | 0.30 | 0.55 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |
| h_001 | [Archived Hypothesis] | 0.30 | 0.00 | | archived | 2026-04-16 | legacy-pre-pipeline-import-v1 |