Evidence map›Paper›PMID 32922348›Full record

ArticleFrontiers in neurology2020

Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome.

Luca Pagliaroli, Andrea Vereczkei, Shanmukha Sampath Padmanabhuni, Zsanett Tarnok, Luca Farkas, Peter Nagy, Renata Rizzo, Tomasz Wolanczyk, Urszula Szymanska, Mira Kapisyzi and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 16 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

17 authors at 8 institutions in 5 countries.

Luca PagliaroliInstitute of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary.
Andrea VereczkeiInstitute of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary.
Shanmukha Sampath PadmanabhuniDepartment of Molecular Biology and Genetics, Democritus University of Thrace, Alexandroupoli, Greece.
Zsanett TarnokVadaskert Clinic for Child and Adolescent Psychiatry, Budapest, Hungary.
Luca FarkasVadaskert Clinic for Child and Adolescent Psychiatry, Budapest, Hungary.
Peter NagyVadaskert Clinic for Child and Adolescent Psychiatry, Budapest, Hungary.
Renata RizzoMaterno Infantile and Radiological Science Department, University of Catania, Catania, Italy.
Tomasz WolanczykDepartment of Child Psychiatry, Medical University of Warsaw, Warsaw, Poland.
Urszula SzymanskaDepartment of Child Psychiatry, Medical University of Warsaw, Warsaw, Poland.
Mira KapisyziUniversity Hospital Center "Mother Theresa," Tirana, Albania.
Entela BashaUniversity Hospital Center "Mother Theresa," Tirana, Albania.
Anastasia KoumoulaDepartment of Child and Adolescent Psychiatry, Sismanoglio General Hospital of Attica, Athens, Greece.
Christos AndroutsosDepartment of Child and Adolescent Psychiatry, Sismanoglio General Hospital of Attica, Athens, Greece.
Vaia TsironiDepartment of Child and Adolescent Psychiatry, Sismanoglio General Hospital of Attica, Athens, Greece.
Iordanis KaragiannidisDepartment of Molecular Biology and Genetics, Democritus University of Thrace, Alexandroupoli, Greece.
Peristera PaschouDepartment of Molecular Biology and Genetics, Democritus University of Thrace, Alexandroupoli, Greece.
Csaba BartaInstitute of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary.
Democritus University of Thrace · GRSemmelweis University · HUVadaskert Alapítvány a Gyermekek Lelki Egészségéért · HUGeneral Hospital of Attica · GRMedical University of Warsaw · PLMother Teresa Hospital · ALSismanoglio General Hospital · GRUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

3'UTRgenetic variationmicroRNASNPTourette Syndrome

Identifiers

PMID32922348
PMCPMC7457023
OpenAlexW3049329302

What OpenQuestion holds

Textmetadata
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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.