Evidence map›Paper›PMID 35028775›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2022

A novel homozygous mutation in TBK1 gene causing ALS-FTD.

Laura Libonati, Marco Ceccanti, Chiara Cambieri, Davide Colavito, Federica Moret, Ilenia Fiorini, Maurizio Inghilleri

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 1 institution in 1 country.

Laura LibonatiRare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy. laura.libonati@uniroma1.it.ORCID http://orcid.org/0000-0002-4323-3598
Marco CeccantiRare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
Chiara CambieriRare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
Davide ColavitoResearch & Innovation S.R.L. (R&I Genetics), 35127, Padova, Italy.
Federica MoretRare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
Ilenia FioriniRare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
Maurizio InghilleriRare Neuromuscular Diseases Centre, Department of Human Neurosciences, Sapienza University, Viale dell'università 30, 00185, Rome, Italy.
Sapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Amyotrophic Lateral SclerosisFrontotemporal DementiaProtein Serine-Threonine KinasesGenetic Association StudiesHomozygoteHumansMutationProtein Serine-Threonine KinasesTBK1 protein, human

Identifiers

PMID35028775
OpenAlexW4205852741

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.