Evidence map›Paper›PMID 34158098›Full record

ArticleGenome medicine2021

Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.

Na Zhu, Emilia M Swietlik, Carrie L Welch, Michael W Pauciulo, Jacob J Hagen, Xueya Zhou, Yicheng Guo, Johannes Karten, Divya Pandya, Tobias Tilly and 19 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Genome medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Molecular Function and Contribution ofAmerican journal of respiratory and critical care medicine · 2023
    Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors.

Na Zhu *Department of Pediatrics, Columbia University Irving Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA.
Emilia M Swietlik *Department of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Carrie L Welch *Department of Pediatrics, Columbia University Irving Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA.
Michael W Pauciulo *Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Jacob J HagenDepartment of Pediatrics, Columbia University Irving Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA.
Xueya ZhouDepartment of Pediatrics, Columbia University Irving Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA.
Yicheng GuoDepartment of Systems Biology, Columbia University, New York, NY, USA.
Johannes Karten42Genetics, Belfast, Ireland.
Divya PandyaDepartment of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Tobias TillyDepartment of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Katie A LutzDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Jennifer M MartinDepartment of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Carmen M TreacyDepartment of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Erika B RosenzweigDepartment of Pediatrics, Columbia University Irving Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA.
Usha KrishnanDepartment of Pediatrics, Columbia University Irving Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA.
Anna W ColemanDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Claudia Gonzaga-JaureguiRegeneron Pharmaceuticals, New York, NY, USA.
Allan LawrieDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Richard C TrembathDepartment of Medical and Molecular Genetics, King's College London, London, UK.
Martin R WilkinsNational Heart & Lung Institute, Imperial College London, London, UK.
Regeneron Genetics Center
PAH Biobank Enrolling Centers’ Investigators
NIHR BioResource for Translational Research - Rare Diseases
National Cohort Study of Idiopathic and Heritable PAH
Nicholas W Morrell *Department of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Yufeng Shen *Department of Systems Biology, Columbia University, New York, NY, USA.
Stefan Gräf *Department of Medicine, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
William C Nichols *Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Wendy K Chung *Department of Pediatrics, Columbia University Irving Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA. wkc15@columbia.edu.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
National Biological Sample and Data Repository for PAHR24HL105333 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI NICHOLS, WILLIAM C · 2012 to 2016
$10.1M
Medical Research Council MR/K020919/1NCATS NIH HHS UL1 TR001863NHLBI NIH HHS R24 HL105333
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34158098
PMCPMC8220777

What OpenQuestion holds

Textmetadata
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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.