Evidence map›Paper›PMID 32396742›Full record

ArticleCirculation. Genomic and precision medicine2020

Congenital Heart Defects Due to

Sarah U Morton, Radhika Agarwal, Jill A Madden, Casie A Genetti, Catherine A Brownstein, Francesc López-Giráldez, Jungmin Choi, Christine E Seidman, Jonathan G Seidman, Gholson J Lyon and 1 more

Open access · bronzeAbstract readCase ReportsLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Circulation. Genomic and precision medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. The roles of TAF1 in neuroscience and beyond.Royal Society open science · 2024
    Review
  2. Article
  3. Article
  4. Identification ofDiagnostics (Basel, Switzerland) · 2022
    Article
  5. Article
  6. 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

11 authors at 6 institutions in 2 countries.

Sarah U MortonDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital (S.U.M., P.B.A.).
Radhika AgarwalDepartment of Genetics (R.A., C.E.S., J.G.S.), Harvard Medical School.
Jill A MaddenDivision of Genetics and Genomics (J.A.M., C.A.G., C.A.B., P.B.A.), Boston Children's Hospital, MA.
Casie A GenettiDivision of Genetics and Genomics (J.A.M., C.A.G., C.A.B., P.B.A.), Boston Children's Hospital, MA.
Catherine A BrownsteinDivision of Genetics and Genomics (J.A.M., C.A.G., C.A.B., P.B.A.), Boston Children's Hospital, MA.
Francesc López-GiráldezYale Center for Genome Analysis, Department of Genetics, Yale University, CT (F.L.-G.).
Jungmin ChoiDepartment of Biomedical Sciences, Korea University College of Medicine, Seoul (J.C.).
Christine E SeidmanDepartment of Genetics (R.A., C.E.S., J.G.S.), Harvard Medical School.
Jonathan G SeidmanDepartment of Genetics (R.A., C.E.S., J.G.S.), Harvard Medical School.
Gholson J LyonInstitute for Basic Research in Developmental Disabilities, Staten Island (G.J.L.).
Pankaj B AgrawalDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital (S.U.M., P.B.A.).
Boston Children's Hospital · USHarvard University · USBrigham and Women's Hospital · USKorea University · JPThe Graduate Center, CUNY · USYale University · US

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
Yale Center for Mendelian GenomicsUM1HG006504 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, GUNEL, MURAT · 2016 to 2020
$14.8M
Genome Sequence-Based Screening for Childhood Risk and Newborn IllnessU19HD077671 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI BEGGS, ALAN H., GREEN, ROBERT C. · 2013 to 2018
$6.1M
NHGRI Genome Sequencing Program Coordinating CenterU24HG008956 · NHGRI · RUTGERS, THE STATE UNIV OF N.J. · PI BUYSKE, STEVEN G, MATISE, TARA C. · 2016 to 2020
$4.9M
Regulation of Cardiac Development in Health and DiseaseUM1HL098166 · NHLBI · HARVARD MEDICAL SCHOOL · PI PENNACCHIO, LEN ALEXANDER, PU, WILLIAM TSWENCHING · 2015 to 2019
$4.4M
The Genomic Basis of Congenital Heart Disease and Neurodevelopmental OutcomesUM1HL098147 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI NEWBURGER, JANE W., ROBERTS, AMY E · 2015 to 2019
$2.4M
SPEG is Critical in Skeletal Muscle Development and FunctionR01AR068429 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI AGRAWAL, PANKAJ B · 2015 to 2019
$1.9M
NCATS NIH HHS UL1 TR001863NHGRI NIH HHS U24 HG008956NHGRI NIH HHS UM1 HG006504NHLBI NIH HHS UM1 HL098147NHLBI NIH HHS UM1 HL098166NIAMS NIH HHS R01 AR068429NICHD NIH HHS U19 HD077671
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Mutation, MissenseChild, PreschoolHeart Defects, CongenitalHistone AcetyltransferasesHumansMaleTATA-Binding Protein Associated FactorsTranscription Factor TFIIDHistone AcetyltransferasesTATA-binding protein associated factor 250 kDaTATA-Binding Protein Associated FactorsTranscription Factor TFIIDdevelopmental delay disordersheart defects, congenitalmutations, missensewhole exome sequencing

Identifiers

PMID32396742
PMCPMC7329268
OpenAlexW3025072872

What OpenQuestion holds

Textmetadata
LicenceTDM
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.