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14 results for “FTLD”

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ClinicalTrials.gov32/100

Identification of New FTLD Genes

ClinicalTrials.gov study NCT02363062. IPD Sharing: Not stated. Countries: 1. Publications: 2.

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

Neuroinflammation in FTLD

ClinicalTrials.gov study NCT06870838. IPD Sharing: NO. Countries: 1. Publications: 1.

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

tDCS and Speech Therapy for Motor Speech Disorders Caused by FTLD Syndromes: a Feasibility Study

ClinicalTrials.gov study NCT04883229. IPD Sharing: NO. Countries: 0. Publications: 5.

closedIPD-NOFeb 2026View details →
geo24/100

A TDP-43 acetylation-mimic mutation that disrupts RNA-binding drives FTLD-like neurodegeneration in a mouse model of sporadic TDP-43 proteinopathy

GEO Series GSE216294. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJan 2023View details →
geo24/100

Neuronal VCP loss of function recapitulates FTLD-TDP pathology

GEO Series GSE178257. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2021View details →
ClinicalTrials.gov24/100

A Multi-Modal Remote Monitoring Platform for Frontotemporal Lobar Degeneration (FTLD) Syndromes

ClinicalTrials.gov study NCT05956834. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

PET Imaging Tau Accumulation in FTLD and Atypical Alzheimer's Using [18F]-PI-2620

ClinicalTrials.gov study NCT05456503. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
geo20/100

Loss of TMEM106B potentiates lysosomal and FTLD-like pathology in progranulin deficient mice [neuroinflammation panel]

GEO Series GSE155066. Mus musculus. 18 samples. Type: Other.

openGEO-OpenJul 2020View details →
geo20/100

Expression data from postmortem human brain samples with and without FTLD-U

GEO Series GSE13162. Homo sapiens. 56 samples. Type: Expression profiling by array.

openGEO-OpenOct 2008View details →
geo20/100

Loss of TMEM106B potentiates lysosomal and FTLD-like pathology in progranulin deficient mice [neuropathology panel]

GEO Series GSE155065. Mus musculus. 12 samples. Type: Other.

openGEO-OpenJul 2020View details →
dryad20/100

Frontotemporal Lobar Degeneration (FTLD)

Open the record for dataset details and reuse information.

publicJun 2013View details →
geo12/100

Single-cell dissection of the primary motor cortex in ALS and FTLD patients.

GEO Series GSE174332. Homo sapiens. 66 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJul 2021View details →
zenodo12/100

RawData_CathepsinD_NTA_FTLD

<p>RawData table (excel file) shows sample code, category as diagnostic group, age and age at onset (&le;55, 56-65- 66-75, &gt;75), the raw NTA file name, raw values of cathepsin D in sEVs and in plasma. Raw NTA data of each sample analyzed consists of .csv file generated by Nano-Sight NS300 Instrument. NTA .csv file contains information about EV concentration (particles/ml, particles/frame), size (mean, mode, SD) and size distribution (D10, D50 and D90).</p>

restrictedAug 2022View details →
zenodo8/100

RawData_NGS_FTLD

<p>A targeted deep sequencing of 98 genes belonging to the lysosomal pathway, selected based on their high expression in multiple brain regions, was performed in 127 subjects (n=74 GRN mutation carriers and n=53 C9orf72 pathological expansion carriers). Sequencing reads were aligned versus the hg19 reference genome using bwa software (mem algorithm, 0.7.17-r1188). Subsequently, duplicated read marking has been performed using Picard and the single-nucleotide variant (SNV) and insertion/deletion (INDEL) calling have been carried out using the Haplotype Caller module of Genome Analysis Toolkit (GATK, version 4.1.8) software over the target region. The Single-Nucleotide Polymorphism Database (dbSNP; v151) was used as the variant reference database. A genomic variant call format (gVCF; version 4.1.8) has been created for each sample.</p> <p>This research was funded by the Italian Ministry of Health, Italy, Ricerca Finalizzata, (grant RF-2016-02361492).</p>

restrictedAug 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