Evidence map›Paper›PMID 41439479›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2026

Pathogenic or Likely Pathogenic GRN Variants Are Found in 0.1% of Parkinson's Disease Patients.

Christian A Ganoza, Ana Westenberger, Jefri J Paul, Filipa Curado, Jörg Rennecke, Sumanth Mannepalli, Emir Zonic, Deepa Saravanakumar, Omid Paknia, Ruslan Al-Ali and 22 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2026. 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
–field-weighted citation impact
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.

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

32 authors.

Christian A GanozaCENTOGENE GmbH, Rostock, Germany.ORCID https://orcid.org/0000-0002-5891-5372
Ana WestenbergerInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.ORCID https://orcid.org/0000-0001-8062-6959
Jefri J PaulCENTOGENE GmbH, Rostock, Germany.
Filipa CuradoCENTOGENE GmbH, Rostock, Germany.
Jörg RenneckeCENTOGENE GmbH, Rostock, Germany.
Sumanth MannepalliCENTOGENE GmbH, Rostock, Germany.
Emir ZonicCENTOGENE GmbH, Rostock, Germany.
Deepa SaravanakumarCENTOGENE GmbH, Rostock, Germany.
Omid PakniaCENTOGENE GmbH, Rostock, Germany.
Ruslan Al-AliCENTOGENE GmbH, Rostock, Germany.
Björn-Hergen LaabsInstitute of Medical Biometry and Statistics, University of Lübeck, University Medical Center Schleswig-Holstein, Lübeck, Germany.ORCID https://orcid.org/0000-0002-9265-5738
Ilona CsotiGertrudis Klinik Biskirchen, Leun-Biskirchen, Germany.
Franco ValzaniaNeurology Unit, Neuromotor and Rehabilitation Department, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Wim VandenbergheDepartment of Neurology, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0002-9758-5062
Katrin ReetzSection of Neurodegeneration, Department of Neurology, RWTH Aachen University, Aachen, Germany.ORCID https://orcid.org/0000-0002-9730-9228
Mitra AfshariDepartment of Neurology and Rehabilitation, University of Illinois, Chicago, USA.ORCID https://orcid.org/0000-0003-4803-953X
Sharon Hassin-BaerFaculty of Medical and Health Sciences Medicine, Tel Aviv University, Tel Aviv, Israel.
Erich Talamoni FonoffLaboratory of Neuroscience, Hospital Sírio-Libanês, São Paulo, Brazil.
Doreen GruberMovement Disorders Clinic, Beelitz-Heilstätten, Germany.
Anna de RosaDepartment of Neurosciences and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
Thomas MusacchioDepartment of Neurology, Würzburg University Hospital, Würzburg, Germany.
Patricia de Carvalho AguiarHospital Israelita Albert Einstein, São Paulo, Brazil.
Anna NegrottiDepartment of General and Specialized Medicine, Neurology Unit, University Hospital of Parma, Parma, Italy.
Vitor TumasDepartment of Neurosciences and Behavioral Sciences, Ribeirao Preto Medical School of University of São Paulo, São Paulo, Brazil.
Juan Carlos Gomez-EstebanNeurodegenerative Diseases Group, BioBizkaia Research Institute, Barakaldo, Spain.
Tanya GurevichMovement Disorders Unit, Neurological Institute, Tel Aviv Sourasky Medical Center, Tel Aviv University, Tel Aviv, Israel.
Nicola PaveseClinical Ageing Research Unit, Newcastle University, Newcastle, UK.ORCID https://orcid.org/0000-0002-6801-6194
Jaime KulisevskyMovement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.ORCID https://orcid.org/0000-0003-4870-1431
Esther SammlerMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, University of Dundee, Dundee, UK.ORCID https://orcid.org/0000-0003-3218-7116
Christine KleinInstitute of Neurogenetics, University of Lübeck, Lübeck, Germany.ORCID https://orcid.org/0000-0003-2102-3431
Peter BauerCENTOGENE GmbH, Rostock, Germany.
Christian BeetzCENTOGENE GmbH, Rostock, Germany.ORCID https://orcid.org/0000-0001-7061-2895

Funding

Denali Therapeutics
6 · The paper itself

Abstract

backgroundParkinsonism may be observed in multiple neurodegenerative diseases, including GRN-associated frontotemporal dementia (FTD-GRN), complicating the differential diagnosis of Parkinson's disease (PD).

objectivesTo investigate the presence of GRN variants in a large group of PD patients.

methodsWe analyzed GRN variants in >18,500 PD patients and compared sociodemographic, genetic, and clinical data between individuals with and without GRN variants.

resultsTwenty-four (0.13%) PD patients harbored 16 unique pathogenic or likely pathogenic GRN variants. Our GRN variant-positive PD patients had a higher male-to-female ratio and a younger age at onset compared with FTD-GRN patients reported in the literature. Patients with GRN variants showed higher rates of impaired olfactory function and more severe motor symptoms than GRN variant-negative patients.

conclusionsFTD-GRN may be indistinguishable from PD. Therefore, comprehensive genetic testing, including GRN analysis, is recommended for patients with clinically diagnosed parkinsonism/PD to guide disease management and prognosis. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Frontotemporal DementiaParkinson DiseaseProgranulinsAgedFemaleHumansMaleMiddle AgedGRN protein, humanProgranulinsage at onsetfrontotemporal dementiaFTDgenetic variantsGRNGRN‐associated frontotemporal dementiamale‐to‐female ratioparkinsonismParkinson's disease

Identifiers

PMID41439479
PMCPMC13067306

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.