Evidence map›Paper›PMID 31692906›Full record

ArticleScience advances2019

CRISPR-Cas9-mediated therapeutic editing of

Dong Hyun Jo, Dong Woo Song, Chang Sik Cho, Un Gi Kim, Kyu Jun Lee, Kihwang Lee, Sung Wook Park, Daesik Kim, Jin Hyoung Kim, Jin-Soo Kim and 3 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 100 citations in OpenAlex.

  1. Review
  2. Article
  3. A Translational Roadmap for Neurological Nonsense Mutation Disorders.International journal of molecular sciences · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Genetic engineering and the eye.Eye (London, England) · 2025
    Review
  10. Review
  11. Review
  12. Suppressor tRNA in gene therapy.Science China. Life sciences · 2024
    Review
  13. Review
  14. Review
  15. A New Generation of Gene Therapies as the Future of Wet AMD Treatment.International journal of molecular sciences · 2024
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article

7 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

13 authors at 5 institutions in 1 country.

Dong Hyun JoFight Against Angiogenesis-Related Blindness (FARB) Laboratory, Clinical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0002-6320-6829
Dong Woo SongToolGen Inc., Seoul, Republic of Korea.ORCID 0000-0001-9700-7759
Chang Sik ChoFight Against Angiogenesis-Related Blindness (FARB) Laboratory, Clinical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
Un Gi KimToolGen Inc., Seoul, Republic of Korea.
Kyu Jun LeeToolGen Inc., Seoul, Republic of Korea.
Kihwang LeeDepartment of Ophthalmology, Ajou University School of Medicine, Suwon, Republic of Korea.ORCID 0000-0003-0478-8758
Sung Wook ParkFight Against Angiogenesis-Related Blindness (FARB) Laboratory, Clinical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0001-8151-6663
Daesik KimCenter for Genome Engineering, Institute for Basic Science (IBS), Seoul, Republic of Korea.
Jin Hyoung KimFight Against Angiogenesis-Related Blindness (FARB) Laboratory, Clinical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
Jin-Soo KimCenter for Genome Engineering, Institute for Basic Science (IBS), Seoul, Republic of Korea.
Seokjoong KimToolGen Inc., Seoul, Republic of Korea.
Jeong Hun KimFight Against Angiogenesis-Related Blindness (FARB) Laboratory, Clinical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-2957-1766
Jung Min LeeToolGen Inc., Seoul, Republic of Korea.ORCID 0000-0002-8249-2920
Seoul National University · KRToolGen (South Korea) · KRSeoul National University Hospital · KRHandong Global University · KRInstitute for Basic Science · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leber congenital amaurosis (LCA), one of the leading causes of childhood-onset blindness, is caused by autosomal recessive mutations in several genes including

Indexed as

Gene EditingAnimalscis-trans-IsomerasesCRISPR-Cas SystemsDependovirusDisease Models, AnimalGenomeLeber Congenital AmaurosisMaleMiceMice, Inbred C57BLMutationPhenotypeRecombinational DNA RepairRetinaRetinoid Isomerohydrolasecis-trans-IsomerasesRetinoid Isomerohydrolase

Identifiers

PMID31692906
PMCPMC6821465
OpenAlexW2982498219

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.