Evidence map›Paper›PMID 37578141›Full record

ArticleHuman gene therapy2023

Developing a Gene Therapy for the Treatment of Autosomal Dominant Alzheimer's Disease.

Benjamin Moore, Apurwa Sharma, Martin Goulet, Tracey Suter, Carolyn Pelletier, Ruoxi Hu, Eric Schaeffer, Raymond J Kelleher

Open access · greenAbstract read
In one paragraph

Article in Human gene therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Benjamin MooreParos Bio, Boston, Massachusetts, USA.
Apurwa SharmaParos Bio, Boston, Massachusetts, USA.
Martin GouletParos Bio, Boston, Massachusetts, USA.
Tracey SuterParos Bio, Boston, Massachusetts, USA.ORCID 0000-0002-7091-2297
Carolyn PelletierParos Bio, Boston, Massachusetts, USA.
Ruoxi HuParos Bio, Boston, Massachusetts, USA.
Eric SchaefferParos Bio, Boston, Massachusetts, USA.ORCID 0009-0008-3892-6163
Raymond J KelleherDepartment of Neurology, and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Parsons (United States) · USHarvard University · US

Funding

Presenilin dysfunction in the brainR01NS075346 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI KELLEHER, RAYMOND J · 2011 to 2020
$4.7M
Research Mentoring in Neurology and Translational Research on Alzheimers DiseaseK24NS093185 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI KELLEHER, RAYMOND J · 2016 to 2020
$940k
NINDS NIH HHS K24 NS093185NINDS NIH HHS R01 NS075346
6 · The paper itself

Abstract

Autosomal dominant Alzheimer's disease (ADAD) is a rare early-onset form of Alzheimer's disease, caused by dominant mutations in one of three genes: presenilin 1, presenilin 2, and amyloid β precursor protein (APP). Mutations in the presenilin 1 gene (

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAmyloid Precursor Protein SecretasesAnimalsGenetic TherapyHumansMiceMutationPresenilin-1Tissue DistributionAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAmyloid Precursor Protein SecretasesPresenilin-1AAV gene therapyAlzheimer's diseaseCNS deliverypresenilin

Identifiers

PMID37578141
PMCPMC10623074
OpenAlexW4385798920

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.