Evidence map›Paper›PMID 31673015›Full record

ArticleScientific reports2019

Molecular signatures of retinal ganglion cells revealed through single cell profiling.

Lauren A Laboissonniere, Jillian J Goetz, Gregory M Martin, Ran Bi, Terry J S Lund, Laura Ellson, Madison R Lynch, Bailey Mooney, Hannah Wickham, Peng Liu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Review
  3. A complete spatial map of mouse retinal ganglion cells reveals density and gene expression specializations.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Single-Cell Transcriptomics onBiomedicines · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Role of PKN1 in Retinal Cell Type Formation.International journal of molecular sciences · 2024
    Article
  13. Multi-omics in exploring the pathophysiology of diabetic retinopathy.Frontiers in cell and developmental biology · 2024
    Review
  14. Patch-seq: Advances and Biological Applications.Cellular and molecular neurobiology · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Viral Vector-Induced Ocular Hypertension in Mice.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  19. Article
  20. Tools and Biomarkers for the Study of Retinal Ganglion Cell Degeneration.International journal of molecular sciences · 2022
    Review
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

12 authors at 4 institutions in 2 countries.

Lauren A LaboissonniereDepartment of Molecular Genetics and Microbiology 2033 Mowry Road, University of Florida, Gainesville, FL, 32610, USA.
Jillian J GoetzDepartments of Ophthalmology and Physiology, Feinberg School of Medicine Northwestern University, Chicago, IL, 60611, USA.
Gregory M MartinOregon Health and Science University, Portland, OR, 97239, USA.
Ran BiDepartment of Statistics, 2117 Snedecor Hall, Iowa State University, Ames, IA, 50011, USA.ORCID http://orcid.org/0000-0002-7977-1427
Terry J S LundDepartment of Genetics, Development and Cell Biology 2437 Pammel Drive, 2114 Molecular Biology, Iowa State University, Ames, IA, 50011, USA.
Laura EllsonDepartment of Genetics, Development and Cell Biology 2437 Pammel Drive, 2114 Molecular Biology, Iowa State University, Ames, IA, 50011, USA.
Madison R LynchDepartment of Genetics, Development and Cell Biology 2437 Pammel Drive, 2114 Molecular Biology, Iowa State University, Ames, IA, 50011, USA.
Bailey MooneyDepartment of Genetics, Development and Cell Biology 2437 Pammel Drive, 2114 Molecular Biology, Iowa State University, Ames, IA, 50011, USA.
Hannah WickhamDepartment of Genetics, Development and Cell Biology 2437 Pammel Drive, 2114 Molecular Biology, Iowa State University, Ames, IA, 50011, USA.
Peng LiuDepartment of Statistics, 2117 Snedecor Hall, Iowa State University, Ames, IA, 50011, USA.
Gregory W SchwartzDepartments of Ophthalmology and Physiology, Feinberg School of Medicine Northwestern University, Chicago, IL, 60611, USA.
Jeffrey M TrimarchiEmmune, Inc, 14155 U.S Highway 1, Juno Beach, FL, 33408, USA. jtrimarc@iastate.edu.
Iowa State University · USNorthwestern University · USEmmune (United States) · USOregon Health & Science University · US

Funding

Novel circuit mapping strategies to reverse engineer the retinaDP2EY026770 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHWARTZ, GREGORY WILLIAM · 2015 to 2015
$2.3M
NEI NIH HHS DP2 EY026770
6 · The paper itself

Abstract

Retinal ganglion cells can be classified into more than 40 distinct subtypes, whether by functional classification or transcriptomics. The examination of these subtypes in relation to their physiology, projection patterns, and circuitry would be greatly facilitated through the identification of specific molecular identifiers for the generation of transgenic mice. Advances in single cell transcriptomic profiling have enabled the identification of molecular signatures for cellular subtypes that are only rarely found. Therefore, we used single cell profiling combined with hierarchical clustering and correlate analyses to identify genes expressed in distinct populations of Parvalbumin-expressing cells and functionally classified RGCs. RGCs were manually isolated based either upon fluorescence or physiological distinction through cell-attached recordings. Microarray hybridization and RNA-Sequencing were employed for the characterization of transcriptomes and in situ hybridization was utilized to further characterize gene candidate expression. Gene candidates were identified based upon cluster correlation, as well as expression specificity within physiologically distinct classes of RGCs. Further, we identified Prph, Ctxn3, and Prkcq as potential candidates for ipRGC classification in the murine retina. The use of these genes, or one of the other newly identified subset markers, for the generation of a transgenic mouse would enable future studies of RGC-subtype specific function, wiring, and projection.

Indexed as

Gene Expression ProfilingGene Expression RegulationOligonucleotide Array Sequence AnalysisSingle-Cell AnalysisAnimalsEye ProteinsMiceMice, TransgenicRetinal Ganglion CellsEye Proteins

Identifiers

PMID31673015
PMCPMC6823391
OpenAlexW2982599496

What OpenQuestion 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 OpenQuestion graph.