Evidence map›Paper›PMID 41221603›Full record

ArticleCirculation. Genomic and precision medicine2025

Exploring

Clément Sauvestre, Amel Bouchatal, Claire Beneteau, Vincent Michaud, Pierre Blanc, Patrice Bouvagnet, Wendy K Chung, Julien Marcadier, Mary Ann Thomas, Helena Gásdal Karstensen and 7 more

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Circulation. Genomic and precision medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Clément SauvestreCHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).ORCID 0009-0001-5645-5560
Amel BouchatalCHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).
Claire BeneteauCHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).ORCID 0000-0002-1682-523X
Vincent MichaudCHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).ORCID 0000-0002-5788-392X
Pierre BlancLaboratoire SeqOIA-PFMG2025, Paris (P. Blanc).ORCID 0009-0003-8965-7171
Patrice BouvagnetCentre de Diagnostic Prénatal, Hôpital MFME, Fort de France, Martinique, France (P. Bouvagnet).ORCID 0000-0001-7583-0533
Wendy K ChungDepartment of Pediatrics, Boston Children's Hospital & Harvard Medical School, MA (W.K.C.).
Julien MarcadierDepartment of Pediatrics (J.M., M.A.T.).ORCID 0009-0003-2534-8273
Mary Ann ThomasDepartment of Pediatrics (J.M., M.A.T.).ORCID 0009-0006-8855-7445
Helena Gásdal KarstensenDepartment of Genetics, Center of Diagnostics, Copenhagen University Hospital-Rigshospitalet, Denmark (H.G.K., A.P.B.).ORCID 0000-0002-3871-969X
Alfred Peter BornDepartment of Genetics, Center of Diagnostics, Copenhagen University Hospital-Rigshospitalet, Denmark (H.G.K., A.P.B.).
Catherine BreenManchester Centre for Genomic Medicine, St Mary's Hospital (C. Breen).
Shiyi XiongShanghai 1st Maternity & Infant Hospital, Tongji University, China (S.X.).
Lesley C AdesDepartment of Clinical Genetics, Children's Hospital at Westmead, Sydney Children's Hospital Network, NSW, Australia (L.C.A.).
Abhijit DixitNottingham Univ Hospitals, United Kingdom (A.D.).ORCID 0000-0001-9240-0674
Mélanie FradinService de Génétique Médicale, CLAD Ouest, CHU de Rennes, France (M.F.).ORCID 0000-0002-2535-2198
Caroline RooryckCHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).ORCID 0000-0002-9789-3591

Funding

Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart diseaseU01HL153009 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHUNG, WENDY K, GELB, BRUCE D · 2020 to 2024
$2.3M
NHLBI NIH HHS U01 HL153009
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

coarctation of aortacongenital heart defectshaploinsuficiencyhypoplastic left heart syndromeRBFOX2

Identifiers

PMID41221603
PMCPMC12922010

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.