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15 results for “SOD1 MUTATION”

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ClinicalTrials.gov32/100

Safety, Tolerability, and Activity Study of ISIS SOD1Rx to Treat Familial Amyotrophic Lateral Sclerosis (ALS) Caused by SOD1 Gene Mutations

ClinicalTrials.gov study NCT01041222. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Safety and Tolerance of RAG-17 in Amyotrophic Lateral Sclerosis Patients With SOD1 Gene Mutation

ClinicalTrials.gov study NCT05903690. IPD Sharing: NO. Countries: 1. Publications: 9.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov28/100

First in Human (FIH) Study of ALN-SOD in Adult Participants With Amyotrophic Lateral Sclerosis Associated With Mutation in the SOD1 Gene (SOD1-ALS)

ClinicalTrials.gov study NCT06351592. IPD Sharing: YES. Countries: 5. Publications: 0.

controlledIPD-YESFeb 2026View details →
geo24/100

Transcriptomic alteration of SOD1-G93A mutation and leptin deficiency in the adipose tissue

GEO Series GSE248515. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenDec 2023View details →
geo24/100

PWC dataset for genome-wide association study of modifiers of risk of canine degenerative myelopathy in dogs homozygous for SOD1 mutation

GEO Series GSE80735. Canis lupus familiaris. 46 samples. Type: SNP genotyping by SNP array.

openGEO-OpenJun 2016View details →
geo24/100

Integrated profiling of iPSC-derived motor neurons carrying C9orf72, FUS, TARDBP, or SOD1 mutations

GEO Series GSE299997. Homo sapiens. 156 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2025View details →
geo24/100

RNA-seq analysis revealed aberrant gene expression in motor neurons derived from ALS patient iPSCs bearing SOD1+/A272C mutation

GEO Series GSE95089. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2017View details →
ClinicalTrials.gov24/100

Frequency of SOD1 and C9orf72 Gene Mutations in French ALS

ClinicalTrials.gov study NCT04819555. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo24/100

A knockout mutation associated with juvenile paroxysmal dyskinesia in Markiesje dogs indicates SOD1 pleiotropy

GEO Series GSE166712. Canis lupus familiaris. 5 samples. Type: Genome variation profiling by high throughput sequencing.

openGEO-OpenMar 2021View details →
geo24/100

Expression of a miRNA targeting mutated SOD1 in astrocytes induces motoneuron plasticity and improves neuromuscular function in ALS mice

GEO Series GSE148901. Mus musculus. 13 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJan 2022View details →
ClinicalTrials.gov20/100

Extended Study of RAG-17 in the Treatment of Amyotrophic Lateral Sclerosis Patients With SOD1 Gene Mutation

ClinicalTrials.gov study NCT07077668. IPD Sharing: NO. Countries: 0. Publications: 0.

closedIPD-NOFeb 2026View details →
geo20/100

Downstream Effects of Mutations in SOD1 and TARDBP Converge on Gene Expression Impairment in Patient-Derived Motor Neurons

GEO Series GSE210969. Homo sapiens. 16 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.

openGEO-OpenAug 2022View details →
geo16/100

Transcriptomic profiling of electrophysiologically characterized human iPSC-derived motor neurons having SOD1 A4V mutation

GEO Series GSE138120. Homo sapiens. 192 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenOct 2023View details →
geo16/100

Boxer dataset for genome-wide association study of modifiers of risk of canine degenerative myelopathy in dogs homozygous for SOD1 mutation

GEO Series GSE80315. Canis lupus familiaris. 25 samples. Type: SNP genotyping by SNP array.

openGEO-OpenJun 2016View details →
zenodo12/100

Dataset related to article " Behavioural and cognitive phenotypes of patients with amyotrophic lateral sclerosis carrying SOD1 mutations" (manuscript submitted)

<p>Clinical and neuropsychological anonymized data of patients involved in the study presented in the submitted article mentioned at title&nbsp;</p>

restrictedFeb 2022View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record