Evidence map›Paper›PMID 36609826›Full record

ArticleMolecular neurobiology2023

Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients.

Nicole Piera Palomba, Giorgio Fortunato, Giuseppe Pepe, Nicola Modugno, Sara Pietracupa, Immacolata Damiano, Giada Mascio, Federica Carrillo, Luca Giovanni Di Giovannantonio, Laura Ianiro and 11 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. What We Know About TMEM175 in Parkinson's Disease.CNS neuroscience & therapeutics · 2025
    Review
  8. Review
  9. Lysosome quality control in health and neurodegenerative diseases.Cellular & molecular biology letters · 2024
    Review
  10. Review
  11. Review
  12. 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

21 authors at 5 institutions in 2 countries.

Nicole Piera Palomba *IRCCS INM Neuromed, Pozzilli, IS, Italy.
Giorgio Fortunato *Institute of Genetics and Biophysics, Adriano Buzzati-Traverso", National Research Council, Naples, Italy.
Giuseppe PepeIRCCS INM Neuromed, Pozzilli, IS, Italy.
Nicola ModugnoIRCCS INM Neuromed, Pozzilli, IS, Italy.
Sara PietracupaIRCCS INM Neuromed, Pozzilli, IS, Italy.
Immacolata DamianoInstitute of Genetics and Biophysics, Adriano Buzzati-Traverso", National Research Council, Naples, Italy.
Giada MascioIRCCS INM Neuromed, Pozzilli, IS, Italy.
Federica CarrilloInstitute of Genetics and Biophysics, Adriano Buzzati-Traverso", National Research Council, Naples, Italy.
Luca Giovanni Di GiovannantonioInstitute of Genetics and Biophysics, Adriano Buzzati-Traverso", National Research Council, Naples, Italy.
Laura IaniroIRCCS INM Neuromed, Pozzilli, IS, Italy.
Katiuscia MartinelloIRCCS INM Neuromed, Pozzilli, IS, Italy.
Viola VolpatoDementia Research Institute, Cardiff University, Cardiff, UK.
Vincenzo DesiatoIRCCS INM Neuromed, Pozzilli, IS, Italy.
Riccardo AcriIRCCS INM Neuromed, Pozzilli, IS, Italy.
Marianna StortoIRCCS INM Neuromed, Pozzilli, IS, Italy.
Ferdinando NicolettiIRCCS INM Neuromed, Pozzilli, IS, Italy.
Caleb WebberDementia Research Institute, Cardiff University, Cardiff, UK.
Antonio SimeoneInstitute of Genetics and Biophysics, Adriano Buzzati-Traverso", National Research Council, Naples, Italy.
Sergio FucileIRCCS INM Neuromed, Pozzilli, IS, Italy.
Vittorio MaglioneIRCCS INM Neuromed, Pozzilli, IS, Italy.
Teresa EspositoIRCCS INM Neuromed, Pozzilli, IS, Italy. teresa.esposito@igb.cnr.it.ORCID http://orcid.org/0000-0002-7879-8441
Istituto Neurologico Mediterraneo · ITInstitute of Genetics and Biophysics · ITUK Dementia Research Institute · GBUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Oxford · GB

Funding

Ministero della Salute RF 2019-12370224Ministero della Salute Ricerca corrente
6 · The paper itself

Abstract

Parkinson's disease (PD) represents the most common neurodegenerative movement disorder. We recently identified 16 novel genes associated with PD. In this study, we focused the attention on the common and rare variants identified in the lysosomal K

Indexed as

Neurodegenerative DiseasesParkinson DiseaseDopaminergic NeuronsHumansIon ChannelsLysosomesPotassium ChannelsIon ChannelsPotassium ChannelsTMEM175 protein, humanAssociation studyAutophagy-lysosomal pathwayElectrophysiology analysisMutation analysisParkinson’s diseaseTMEM175

Identifiers

PMID36609826
PMCPMC9984355
OpenAlexW4313639148

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.