Evidence map›Paper›PMID 30793977›Full record

ArticleHuman gene therapy2019

New Human Chromosomal Sites with "Safe Harbor" Potential for Targeted Transgene Insertion.

Stefan Pellenz, Michael Phelps, Weiliang Tang, Blake T Hovde, Ryan B Sinit, Wenqing Fu, Hui Li, Eleanor Chen, Raymond J Monnat

Open access · greenAbstract read
In one paragraph

Article in Human gene therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Challenges and opportunities of human iPSC-derived NK as "Off-the-shelf" cellular therapies.Journal of experimental & clinical cancer research : CR · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Science advances · 2024
    Article
  14. TALEN-mediated intron editing of HSPCs enables transgene expression restricted to the myeloid lineage.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. bioRxiv : the preprint server for biology · 2023
    Article
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

9 authors at 1 institution in 1 country.

Stefan Pellenz1Department of Pathology, University of Washington, Seattle, Washington.
Michael Phelps1Department of Pathology, University of Washington, Seattle, Washington.
Weiliang Tang1Department of Pathology, University of Washington, Seattle, Washington.
Blake T Hovde2Department of Genome Sciences, University of Washington, Seattle, Washington.
Ryan B Sinit1Department of Pathology, University of Washington, Seattle, Washington.
Wenqing Fu2Department of Genome Sciences, University of Washington, Seattle, Washington.
Hui Li1Department of Pathology, University of Washington, Seattle, Washington.
Eleanor Chen1Department of Pathology, University of Washington, Seattle, Washington.
Raymond J Monnat1Department of Pathology, University of Washington, Seattle, Washington.
University of Washington · US

Funding

Tumor mutation signaturesP01CA077852 · NCI · UNIVERSITY OF WASHINGTON · PI MONNAT, RAYMOND J · 1999 to 2019
$26.0M
INTERDISCIPLINARY TRAINING IN GENOMIC SCIENCEST32HG000035 · NHGRI · UNIVERSITY OF WASHINGTON · PI Bruce Colston Trapnell · 1995 to 2026
$24.2M
NEW LAGLIDADG HOMING ENDONUCLEASES FOR GENOME ENGINEERING (Component 2 of 11)RL1CA133831 · NCI · UNIVERSITY OF WASHINGTON · PI MONNAT, RAYMOND J · 2007 to 2011
$1.9M
NCI NIH HHS P01 CA077852NCI NIH HHS RL1 CA133831NHGRI NIH HHS T32 HG000035
6 · The paper itself

Abstract

This study identified 35 new sites for targeted transgene insertion that have the potential to serve as new human genomic "safe harbor" sites (SHS). SHS potential for these 35 sites, located on 16 chromosomes, including both arms of the human X chromosome, and for the existing human SHS

Indexed as

Chromosomes, HumanMutagenesis, InsertionalTransgenesBase SequenceCell LineChromosome BreakpointsCRISPR-Cas SystemsGene EditingGene ExpressionGene Knock-In TechniquesGene TargetingGenetic LociGenome, HumanGeographic MappingHumansCas9 nucleasesgene therapygenome editinghuman genome“safe harbor” sitetransgene insertion site

Identifiers

PMID30793977
PMCPMC6648220
OpenAlexW2916758974

What OpenQuestion holds

Textmetadata
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.