Evidence map›Paper›PMID 29138314›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Imaging and quantifying ganglion cells and other transparent neurons in the living human retina.

Zhuolin Liu, Kazuhiro Kurokawa, Furu Zhang, John J Lee, Donald T Miller

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers.

0numbers the graph read from it
0cells of the map it votes in
144citing papers in PubMed
21.2field-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

144 citing papers in PubMed, 220 citations in OpenAlex.

  1. Cumulative Loss of Inner Retinal Neurons in Healthy and Glaucoma Subjects.Investigative ophthalmology & visual science · 2026
    Article
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  5. Observational
  6. Monitoring Gene Expression in Retina with synthetic serum markers.bioRxiv : the preprint server for biology · 2026
    Article
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  20. Review

84 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 2 institutions in 1 country.

Zhuolin LiuSchool of Optometry, Indiana University, Bloomington, IN 47405; liuzhuo@indiana.edu.
Kazuhiro KurokawaSchool of Optometry, Indiana University, Bloomington, IN 47405.
Furu ZhangSchool of Optometry, Indiana University, Bloomington, IN 47405.
John J LeePurdue School of Engineering and Technology, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202.
Donald T MillerSchool of Optometry, Indiana University, Bloomington, IN 47405.
Indiana University Bloomington · USUniversity of Indianapolis · US

Funding

Optical Imaging of the Photoreceptor-RPE ComplexR01EY018339 · NEI · TRUSTEES OF INDIANA UNIVERSITY · PI MILLER, DONALD T · 2007 to 2025
$7.7M
Core Support for Vision Research at Indiana UniversityP30EY019008 · NEI · TRUSTEES OF INDIANA UNIVERSITY · PI BURNS, STEPHEN A · 2009 to 2013
$2.1M
NEI NIH HHS P30 EY019008NEI NIH HHS R01 EY018339
6 · The paper itself

Abstract

Ganglion cells (GCs) are fundamental to retinal neural circuitry, processing photoreceptor signals for transmission to the brain via their axons. However, much remains unknown about their role in vision and their vulnerability to disease leading to blindness. A major bottleneck has been our inability to observe GCs and their degeneration in the living human eye. Despite two decades of development of optical technologies to image cells in the living human retina, GCs remain elusive due to their high optical translucency. Failure of conventional imaging-using predominately singly scattered light-to reveal GCs has led to a focus on multiply-scattered, fluorescence, two-photon, and phase imaging techniques to enhance GC contrast. Here, we show that singly scattered light actually carries substantial information that reveals GC somas, axons, and other retinal neurons and permits their quantitative analysis. We perform morphometry on GC layer somas, including projection of GCs onto photoreceptors and identification of the primary GC subtypes, even beneath nerve fibers. We obtained singly scattered images by: (

Indexed as

AdultAmacrine CellsCell CountHealthy VolunteersHumansMiddle AgedNerve FibersOptics and PhotonicsRetinal Bipolar CellsRetinal Cone Photoreceptor CellsRetinal Ganglion CellsRetinal Horizontal CellsTomography, Optical CoherenceVision, Ocularadaptive opticsoptical coherence tomographyorganelle motilityretinaretinal ganglion cells

Identifiers

PMID29138314
PMCPMC5715765
OpenAlexW2770144792

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.