Evidence map›Paper›PMID 33390902›Full record

ArticleFrontiers in molecular neuroscience2020

GABA Measurement in a Neonatal Fragile X Syndrome Mouse Model Using

Samantha T Reyes, Sanaz Mohajeri, Karolina Krasinska, Scarlett G Guo, Meng Gu, Laura Pisani, Jarrett Rosenberg, Daniel M Spielman, Frederick T Chin

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in molecular neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Sub-MicroliterJournal of neurochemistry · 2025
    Article
  3. Review
  4. Targeted Treatments for Fragile X Syndrome.Advances in neurobiology · 2023
    Article
  5. Review
  6. 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

9 authors at 1 institution in 1 country.

Samantha T ReyesDepartment of Radiology, Stanford University, Stanford, CA, United States.
Sanaz MohajeriDepartment of Radiology, Stanford University, Stanford, CA, United States.
Karolina KrasinskaStanford University Mass Spectrometry Laboratory, Stanford University, Stanford, CA, United States.
Scarlett G GuoDepartment of Radiology, Stanford University, Stanford, CA, United States.
Meng GuDepartment of Radiology, Stanford University, Stanford, CA, United States.
Laura PisaniDepartment of Radiology, Stanford University, Stanford, CA, United States.
Jarrett RosenbergDepartment of Radiology, Stanford University, Stanford, CA, United States.
Daniel M SpielmanDepartment of Radiology, Stanford University, Stanford, CA, United States.
Frederick T ChinDepartment of Radiology, Stanford University, Stanford, CA, United States.
Stanford University · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
Training and DisseminationP41EB015891 · NIBIB · STANFORD UNIVERSITY · PI GLOVER, GARY H · 2012 to 2019
$10.7M
Cross-Species Multi-Modal Neuroimaging to Investigate GABA Physiology in Fragile X SyndromeR01HD084214 · NICHD · STANFORD UNIVERSITY · PI CHIN, FREDERICK T · 2014 to 2018
$2.7M
Robust 1H MRSI of GABA, Glutamate, Glutamine, and Glutathione R01MH110683 · NIMH · STANFORD UNIVERSITY · PI SPIELMAN, DANIEL M · 2017 to 2020
$1.5M
Upgrade of the Stanford GE-Varian Experimental MRI Scanner to the Current Model MS10RR026917 · NCRR · STANFORD UNIVERSITY · PI MOSELEY, MICHAEL E · 2010 to 2010
$497k
NCRR NIH HHS S10 RR026917NIBIB NIH HHS P41 EB015891NICHD NIH HHS R01 HD084214NIMH NIH HHS R01 MH110683
6 · The paper itself

Abstract

Fragile X syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder and inherited cause of intellectual disability that affects approximately one in 7,000 males and one in 11,000 females. In FXS, the

Indexed as

1H-MRSFmr1 knockoutfragile X syndromeGABALC-MS/MSmouseneonatal

Identifiers

PMID33390902
PMCPMC7775297
OpenAlexW3111700687

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.