Evidence map›Paper›PMID 31608113›Full record

ReviewFrontiers in genetics2019

Development and Clinical Translation of Approved Gene Therapy Products for Genetic Disorders.

Alireza Shahryari, Marie Saghaeian Jazi, Saeed Mohammadi, Hadi Razavi Nikoo, Zahra Nazari, Elaheh Sadat Hosseini, Ingo Burtscher, Seyed Javad Mowla, Heiko Lickert

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed, 3 pooled it
11.4field-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

119 citing papers in PubMed, 3 syntheses or guidelines pooled it, 254 citations in OpenAlex.

  1. Pooled it
  2. Lentivirus- or AAV-mediated gene therapy interventions in ischemic stroke: A systematic review of preclinicalJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Pooled it
  3. Recombinant Human Adenovirus-Medicina (Kaunas, Lithuania) · 2021
    Pooled it
  4. Article
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  9. RAB40C regulates SNX9 stabilityCentral-European journal of immunology · 2026
    Article
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  11. Review
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59 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

9 authors at 4 institutions in 2 countries.

Alireza ShahryariInstitute of Diabetes and Regeneration Research, Helmholtz Zentrum München, Neuherberg, Germany.
Marie Saghaeian JaziStem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Saeed MohammadiStem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Hadi Razavi NikooInfectious Disease Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Zahra NazariDepartment of Biology, School of Basic Sciences, Golestan University, Gorgan, Iran.
Elaheh Sadat HosseiniDepartment of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Ingo BurtscherInstitute of Diabetes and Regeneration Research, Helmholtz Zentrum München, Neuherberg, Germany.
Seyed Javad MowlaDepartment of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Heiko LickertInstitute of Diabetes and Regeneration Research, Helmholtz Zentrum München, Neuherberg, Germany.
Helmholtz Zentrum München · DEGolestan University · IRGolestan University of Medical Sciences · IRTarbiat Modares University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The field of gene therapy is striving more than ever to define a path to the clinic and the market. Twenty gene therapy products have already been approved and over two thousand human gene therapy clinical trials have been reported worldwide. These advances raise great hope to treat devastating rare and inherited diseases as well as incurable illnesses. Understanding of the precise pathomechanisms of diseases as well as the development of efficient and specific gene targeting and delivery tools are revolutionizing the global market. Currently, human cancers and monogenic disorders are indications number one. The elevated prevalence of genetic disorders and cancers, clear gene manipulation guidelines and increasing financial support for gene therapy in clinical trials are major trends. Gene therapy is presently starting to become commercially profitable as a number of gene and cell-based gene therapy products have

Indexed as

cell-based gene therapyclinicdruggene therapygenetic disease

Identifiers

PMID31608113
PMCPMC6773888
OpenAlexW2969783143

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.