Evidence map›Paper›PMID 38136995›Full record

ArticleGenes2023

Research on the Pathogenesis of Cognitive and Neurofunctional Impairments in Patients with Noonan Syndrome: The Role of Rat Sarcoma-Mitogen Activated Protein Kinase Signaling Pathway Gene Disturbances.

Natalia Braun-Walicka, Agnieszka Pluta, Tomasz Wolak, Edyta Maj, Agnieszka Maryniak, Monika Gos, Anna Abramowicz, Aleksandra Landowska, Ewa Obersztyn, Jerzy Bal

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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

10 authors at 3 institutions in 1 country.

Natalia Braun-WalickaThe Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0001-9212-7989
Agnieszka PlutaThe Bioimaging Research Center, World Hearing Center, Institute of Physiology and Pathology of Hearing, Kajetany, 05-830 Nadarzyn, Poland.
Tomasz WolakThe Bioimaging Research Center, World Hearing Center, Institute of Physiology and Pathology of Hearing, Kajetany, 05-830 Nadarzyn, Poland.ORCID 0000-0002-6473-8392
Edyta MajThe Bioimaging Research Center, World Hearing Center, Institute of Physiology and Pathology of Hearing, Kajetany, 05-830 Nadarzyn, Poland.
Agnieszka MaryniakThe Faculty of Psychology, University of Warsaw, 00-183 Warsaw, Poland.ORCID 0000-0001-7213-6554
Monika GosThe Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Anna AbramowiczThe Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0001-6574-4826
Aleksandra LandowskaThe Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.ORCID 0000-0002-5920-1312
Ewa ObersztynThe Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Jerzy BalThe Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
Institute of Physiology and Pathology of Hearing · PLMedical University of Warsaw · PLUniversity of Warsaw · PL

Funding

National Science Center 2016/21/N/HS6/02891
6 · The paper itself

Abstract

Noonan syndrome (NS) is one of the most common genetic conditions inherited mostly in an autosomal dominant manner with vast heterogeneity in clinical and genetic features. Patients with NS might have speech disturbances, memory and attention deficits, limitations in daily functioning, and decreased overall intelligence. Here, 34 patients with Noonan syndrome and 23 healthy controls were enrolled in a study involving gray and white matter volume evaluation using voxel-based morphometry (VBM), white matter connectivity measurements using diffusion tensor imaging (DTI), and resting-state functional magnetic resonance imaging (rs-fMRI). Fractional anisotropy (FA) and mean diffusivity (MD) probability distributions were calculated. Cognitive abilities were assessed using the Stanford Binet Intelligence Scales. Reductions in white matter connectivity were detected using DTI in NS patients. The rs-fMRI revealed hyper-connectivity in NS patients between the sensorimotor network and language network and between the sensorimotor network and salience network in comparison to healthy controls. NS patients exhibited decreased verbal and nonverbal IQ compared to healthy controls. The assessment of the microstructural alterations of white matter as well as the resting-state functional connectivity (rsFC) analysis in patients with NS may shed light on the mechanisms responsible for cognitive and neurofunctional impairments.

Indexed as

Diffusion Tensor ImagingNoonan SyndromeCognitionHumansMagnetic Resonance ImagingMitogen-Activated Protein KinasesProto-Oncogene Proteins p21(ras)Signal TransductionMitogen-Activated Protein KinasesProto-Oncogene Proteins p21(ras)cognitive impairmentsfunctional magnetic resonance imagingintelligence testsNoonan syndrome

Identifiers

PMID38136995
PMCPMC10742480
OpenAlexW4389286410

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.