Evidence map›Paper›PMID 32785033›Full record

ReviewInternational journal of molecular sciences2020

The Role of Alpha-Synuclein and Other Parkinson's Genes in Neurodevelopmental and Neurodegenerative Disorders.

C Alejandra Morato Torres, Zinah Wassouf, Faria Zafar, Danuta Sastre, Tiago Fleming Outeiro, Birgitt Schüle

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 61 citations in OpenAlex.

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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

6 authors at 2 institutions in 3 countries.

C Alejandra Morato TorresDepartment Pathology, Stanford University School of Medicine, Stanford, CA 94304, USA.
Zinah WassoufGerman Center for Neurodegenerative Diseases, 37075 Göttingen, Germany.
Faria ZafarDepartment Pathology, Stanford University School of Medicine, Stanford, CA 94304, USA.
Danuta SastreDepartment Pathology, Stanford University School of Medicine, Stanford, CA 94304, USA.
Tiago Fleming OuteiroGerman Center for Neurodegenerative Diseases, 37075 Göttingen, Germany.
Birgitt SchüleDepartment Pathology, Stanford University School of Medicine, Stanford, CA 94304, USA.ORCID 0000-0002-9952-5776
Stanford University · USGerman Center for Neurodegenerative Diseases · DE

Funding

Deutsche Forschungsgemeinschaft Germany's Excellence Strategy - EXC 2067/1- 390729940Deutsche Forschungsgemeinschaft SFB1286Michael J. Fox Foundation for Parkinson's Research Target Advancement Program
6 · The paper itself

Abstract

Neurodevelopmental and late-onset neurodegenerative disorders present as separate entities that are clinically and neuropathologically quite distinct. However, recent evidence has highlighted surprising commonalities and converging features at the clinical, genomic, and molecular level between these two disease spectra. This is particularly striking in the context of autism spectrum disorder (ASD) and Parkinson's disease (PD). Genetic causes and risk factors play a central role in disease pathophysiology and enable the identification of overlapping mechanisms and pathways. Here, we focus on clinico-genetic studies of causal variants and overlapping clinical and cellular features of ASD and PD. Several genes and genomic regions were selected for our review, including

Indexed as

AdolescentAdultAgedAged, 80 and overalpha-SynucleinAnimalsAutism Spectrum DisorderChildChild, PreschoolDiGeorge SyndromeDisease Models, AnimalFemaleFragile X Messenger Ribonucleoprotein 1Gene DosageHumansInfantalpha-SynucleinFragile X Messenger Ribonucleoprotein 1parkin proteinUbiquitin-Protein Ligases22q11.2 deletion syndromealpha-synucleinautism spectrum disordersneurodegenerationneuronal developmentPARK2Parkinson’s diseaseSNCAsynaptic dysfunction

Identifiers

PMID32785033
PMCPMC7460874
OpenAlexW3042852198

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.