Evidence map›Paper›PMID 35705095›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2022

Worldwide use of factor IX Padua for hemophilia B gene therapy.

Benjamin J Samelson-Jones

Abstract readComment
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Gene therapy for hemophilia - From basic science to first approvals of "one-and-done" therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. First hemophilia B gene therapy approved: More than two decades in the making.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Benjamin J Samelson-JonesPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; The Raymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia, 5028 Colket Translational Research Center 3501 Civic Center Blvd., Philadelphia, PA 19104, USA; Department of Pediatrics, Division of Hematology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: samelsonjonesb@chop.edu.

Funding

Rational Development of Bioengineered Factor IX Variants for Hemophilia B TherapyK08HL140078 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI SAMELSON-JONES, BEN J · 2018 to 2021
$638k
NHLBI NIH HHS K08 HL140078
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Hemophilia BDependovirusFactor IXGenetic TherapyHumansFactor IXfactor IX-Padua

Identifiers

PMID35705095
PMCPMC9263299

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.