Evidence map›Paper›PMID 30160596›Full record

ArticleAutophagy2019

Mitochondrial dysfunction and mitophagy defect triggered by heterozygous GBA mutations.

Hongyu Li, Ahrom Ham, Thong Chi Ma, Sheng-Han Kuo, Ellen Kanter, Donghoon Kim, Han Seok Ko, Yi Quan, Sergio Pablo Sardi, Aiqun Li and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Autophagy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 1 pooled it
11.5field-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

140 citing papers in PubMed, 1 synthesis or guideline pooled it, 236 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Species-dependent activities of the PINK1-parkin axis.Translational neurodegeneration · 2026
    Review
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  5. Article
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  18. Article
  19. Autophagy-lysosomal pathway in neurodegeneration.Molecular neurodegeneration advances · 2026
    Review
  20. Article

80 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

14 authors at 4 institutions in 1 country.

Hongyu Lia Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Ahrom Hama Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Thong Chi Maa Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Sheng-Han Kuoa Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Ellen Kantera Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Donghoon Kimb Department of Neurology and Institute for Cell Engineering , Johns Hopkins University , Baltimore , MD , USA.
Han Seok Kob Department of Neurology and Institute for Cell Engineering , Johns Hopkins University , Baltimore , MD , USA.
Yi Quana Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Sergio Pablo Sardic Neuroscience Therapeutic Area , Sanofi , Framingham , MA , USA.
Aiqun Lid The New York Stem Cell Foundation , Columbia University Medical Center , New York , NY , USA.
Ottavio Arancioe Departments of Pathology and Cell Biology , Columbia University Medical Center , New York , NY , USA.
Un Jung Kanga Department of Neurology , Columbia University Medical Center , New York , NY , USA.
David Sulzera Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Guomei Tanga Department of Neurology , Columbia University Medical Center , New York , NY , USA.
Columbia University Irving Medical Center · USJohns Hopkins University · USNew York Stem Cell Foundation · USSanofi (United States) · US

Funding

Understanding Mechanisms of a-synuclein pathologyP50NS038377 · NINDS · JOHNS HOPKINS UNIVERSITY · PI ROSENTHAL, LIANA ISA SHAPIRO · 1998 to 2019
$38.8M
Cellular and Molecular Basis for Cognitive Impairment Associated with Glucocerebrosidase (GBA1) MutationR01NS104390 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TANG, GUOMEI · 2018 to 2022
$1.8M
Glucocerebrosidase Biology and It's Role in Parkinson's DiseaseR01NS082205 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KO, HANSEOK · 2013 to 2017
$1.8M
Extracellular tau oligomers and Alzheimer diseaseR01AG049402 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ARANCIO, OTTAVIO · 2015 to 2019
$1.6M
The role of glucocerebrosidase and chaperone_mediated autophagy in Parkinsons disK08NS083738 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KUO, SHENG-HAN · 2013 to 2017
$940k
Mitochondrial dysfunction due to aberrant mTOR-regulated mitophagy in autismK01MH096956 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TANG, GUOMEI · 2013 to 2016
$734k
NIA NIH HHS R01 AG049402NIMH NIH HHS K01 MH096956NINDS NIH HHS K08 NS083738NINDS NIH HHS P50 NS038377NINDS NIH HHS R01 NS082205NINDS NIH HHS R01 NS104390
6 · The paper itself

Abstract

Heterozygous mutations in GBA, the gene encoding the lysosomal enzyme glucosylceramidase beta/β-glucocerebrosidase, comprise the most common genetic risk factor for Parkinson disease (PD), but the mechanisms underlying this association remain unclear. Here, we show that in Gba

Indexed as

AnimalsCell Line, TumorGene ExpressionGlucosylceramidaseGyrus CinguliHumansLysosomesMiceMice, KnockoutMitochondriaMitochondrial MembranesMitophagyMutationParkinson DiseaseProto-Oncogene MasReactive Oxygen SpeciesGlucosylceramidaseMAS1 protein, humanProto-Oncogene MasReactive Oxygen SpeciesAutophagyglucocerebrosidasemitochondrial dysfunctionmitophagyParkinson disease

Identifiers

PMID30160596
PMCPMC6287702
OpenAlexW2888867513

What OpenQuestion 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 OpenQuestion graph.