Evidence map›Paper›PMID 36100231›Full record

ReviewAnnual review of pathology2023

Genetics and Pathogenesis of Parkinson's Syndrome.

Hui Ye, Laurie A Robak, Meigen Yu, Matthew Cykowski, Joshua M Shulman

Open access · hybridAbstract readReview
In one paragraph

Review in Annual review of pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 241 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
241citing papers in PubMed, 6 pooled it
43.2field-weighted citation impact, top 1% 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

241 citing papers in PubMed, 6 syntheses or guidelines pooled it, 368 citations in OpenAlex.

  1. Pooled it
  2. Altered regional spontaneous brain activity in Parkinson's disease: a meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Pooled it
  3. Pooled it
  4. The Role of miRNAs in Parkinson's Disease: A Systematic Review.International journal of molecular sciences · 2025
    Pooled it
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181 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Hui YeDepartment of Neurology, Baylor College of Medicine, Houston, Texas, USA; email: Hui.Ye@bcm.edu, Joshua.Shulman@bcm.edu.
Laurie A RobakJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA.
Meigen YuJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA.
Matthew CykowskiDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA; email: mdcykowski@houstonmethodist.org.
Joshua M ShulmanDepartment of Neurology, Baylor College of Medicine, Houston, Texas, USA; email: Hui.Ye@bcm.edu, Joshua.Shulman@bcm.edu.
Baylor College of Medicine · USNeurological Research Institute · USMethodist Hospital · US

Funding

Functional Genomic Dissection of Alzheimer's Disease in Humans and Drosophila ModelsU01AG072439 · NIA · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J, BOTAS, JUAN · 2021 to 2025
$8.4M
Age-related TDP-43 neuropathology: using disease-driving mechanisms to guide classificationRF1NS118584 · NINDS · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CYKOWSKI, MATTHEW DANIEL, NELSON, PETER T. · 2020 to 2020
$3.2M
Parkinson's disease susceptibility in carriers of lysosomal storage disorder genesK08NS112467 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI ROBAK, LAURIE A · 2019 to 2023
$939k
Metabolo-Genetic Dissection of GBA and Lysosomal Genes in Parkinson's Disease and Lewy Body DementiaR21AG068961 · NIA · BAYLOR COLLEGE OF MEDICINE · PI SHULMAN, JOSHUA M · 2020 to 2021
$440k
INTERACTIONS BETWEEN LYSOSOMAL STORAGE DISORDER GENES, SPHINGOLIPID HOMEOSTASIS, AND ALPHA-SYNUCLEIN MECHANISMS IN PARKINSON'S DISEASEF31NS115364 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI YU, MEIGEN · 2020 to 2021
$79k
NIA NIH HHS R21 AG068961NIA NIH HHS U01 AG072439NINDS NIH HHS F31 NS115364NINDS NIH HHS K08 NS112467NINDS NIH HHS RF1 NS118584
6 · The paper itself

Abstract

Parkinson's disease (PD) is clinically, pathologically, and genetically heterogeneous, resisting distillation to a single, cohesive disorder. Instead, each affected individual develops a virtually unique form of Parkinson's syndrome. Clinical manifestations consist of variable motor and nonmotor features, and myriad overlaps are recognized with other neurodegenerative conditions. Although most commonly characterized by alpha-synuclein protein pathology throughout the central and peripheral nervous systems, the distribution varies and other pathologies commonly modify PD or trigger similar manifestations. Nearly all PD is genetically influenced. More than 100 genes or genetic loci have been identified, and most cases likely arise from interactions among many common and rare genetic variants. Despite its complex architecture, insights from experimental genetic dissection coalesce to reveal unifying biological themes, including synaptic, lysosomal, mitochondrial, andimmune-mediated mechanisms of pathogenesis. This emerging understanding of Parkinson's syndrome, coupled with advances in biomarkers and targeted therapies, presages successful precision medicine strategies.

Indexed as

Parkinson DiseaseHumansMitochondriaMutationalpha-synucleinfunctional genomicsGBAheterogeneityLRRK2lysosomemitochondriaoligogenicparkinsonismParkinson's diseasesynapse

Identifiers

PMID36100231
PMCPMC10290758
OpenAlexW4295753421

What Socratic holds

Textmetadata
LicenceCC BY
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.