Evidence map›Paper›PMID 40671338›Full record

ArticleBrain : a journal of neurology2025

Genetic testing for SCA27B in Korean multiple system atrophy.

Joshua Laß, Michele Berselli, Doug Rioux, Susen Schaake, Jordan Follett, Jonathan E Bravo, Alexander D Veit, William Ronchetti, Sarah B Reiff, Matthew J Huentelman and 7 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain : a journal of neurology, 2025. 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

17 authors.

Joshua LaßInstitute of Neurogenetics, University of Lübeck, Lübeck 23538, Germany.
Michele BerselliDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0001-8577-9137
Doug RiouxDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
Susen SchaakeInstitute of Neurogenetics, University of Lübeck, Lübeck 23538, Germany.
Jordan FollettMcKnight Brain Institute, Department of Neurology, College of Medicine, University of Florida, Gainesville, FL 32611, USA.
Jonathan E BravoMcKnight Brain Institute, Department of Neurology, College of Medicine, University of Florida, Gainesville, FL 32611, USA.
Alexander D VeitDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
William RonchettiDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
Sarah B ReiffDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
Matthew J HuentelmanNeurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ 85004, USA.
Dana VuzmanDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.
Pamela BowerMission MSA (Formerly MSA Coalition), McLean, VA 22102, USA.
Vikram KhuranaDivision of Movement Disorders, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Joanne TrinhInstitute of Neurogenetics, University of Lübeck, Lübeck 23538, Germany.
Beomseok JeonDepartment of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul 03080, Korea.
Han-Joon KimDepartment of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul 03080, Korea.
Matthew J FarrerMcKnight Brain Institute, Department of Neurology, College of Medicine, University of Florida, Gainesville, FL 32611, USA.

Funding

Blavatnik Clinical Pilot AwardClinical & Translational Genomics InstituteMission Multiple System AtrophyParkinson's disease researchThe Chan Zuckerberg Initiative EOSS5 2022-309591The Department of Biomedical InformaticsThe Park Lab at Harvard Medical School
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID40671338
PMCPMC12677904

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.