Evidence map›Paper›PMID 40640177›Full record

Observational studyNature communications2025

Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery.

W Scott Watkins, Edgar J Hernandez, Thomas A Miller, Nathan R Blue, Raquel Mae Zimmerman, Eric R Griffiths, Erwin Frise, Daniel Bernstein, Marko T Boskovski, Martina Brueckner and 16 more

Abstract readObservational Study
In one paragraph

Observational study in Nature communications, 2025. 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. Article
  2. Genetics of Congenital Heart Disease.Clinics in perinatology · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors.

W Scott WatkinsDepartment of Human Genetics, University of Utah, Salt Lake City, UT, 84112, USA.
Edgar J HernandezDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, 84108, USA.
Thomas A MillerDepartment of Pediatrics, Maine Medical Center, Portland, ME, USA.
Nathan R BlueDepartment of Obstetrics and Gynecology, University of Utah, Salt Lake City, UT, 84112, USA.ORCID http://orcid.org/0000-0003-2187-3428
Raquel Mae ZimmermanDepartment of Biomedical Informatics, University of Utah, Salt Lake City, UT, 84108, USA.
Eric R GriffithsPediatric Cardiothoracic Surgery, University of Utah, Salt Lake City, UT, USA.ORCID http://orcid.org/0000-0001-7679-5151
Erwin FriseFabric Genomics Inc, Oakland, CA, 94612, USA.ORCID http://orcid.org/0000-0002-9281-4567
Daniel BernsteinDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID http://orcid.org/0000-0001-7761-5853
Marko T BoskovskiDepartment of Surgery, University of California, San Francisco, CA, 94143, USA.
Martina BruecknerDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, 06510, USA.ORCID http://orcid.org/0000-0003-0347-5389
Wendy K ChungDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0003-3438-5685
J William GaynorDivision of Cardiothoracic Surgery, Department of Surgery, Children's Hospital of Philadelphia, and the Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0001-7955-5604
Bruce D GelbMindich Child Health and Development Institute and Departments of Pediatrics and Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID http://orcid.org/0000-0001-8527-5027
Elizabeth GoldmuntzDivision of Cardiology, Children's Hospital of Philadelphia, Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-2936-4396
Peter J GruberDepartment of Surgery, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-7356-905X
Jane W NewburgerDepartment of Cardiology, Boston Children's Hospital, and Department of Pediatrics, Harvard Medical School, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0002-7794-9017
Amy E RobertsDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Sarah U MortonDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-7816-2646
John E MayerDepartment of Cardiovascular Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0002-5849-2971
Christine E SeidmanDepartments of Genetics and Medicine, Harvard Medical School, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0001-6380-1209
Jonathan G SeidmanDepartments of Genetics and Medicine, Harvard Medical School, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0002-9082-3566
Yufeng ShenDepartments of Systems Biology and Biomedical Informatics, Columbia University, New York, NY, 10032, USA.
Michael WagnerDivision of Biomedical Informatics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
H Joseph YostMolecular Medicine Program, University of Utah, Salt Lake City, UT, 84112, USA.ORCID http://orcid.org/0000-0003-2961-5669
Mark YandellDepartment of Human Genetics, University of Utah, Salt Lake City, UT, 84112, USA. myandell@genetics.utah.edu.ORCID http://orcid.org/0000-0002-9497-4505
Martin Tristani-FirouziNora Eccles Harrison Cardiovascular Research and Training Institute, and Division of Pediatric Cardiology, Salt Lake City, UT, 84108, USA. Martin.Tristani@utah.edu.ORCID http://orcid.org/0000-0001-5916-442X

Funding

Administrative Coordinating Center: Cardiovascular Development and Pediatric Cardiac Genomics ConsortiaU01HL131003 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI CNOTA, JAMES, OLLBERDING, NICHOLAS J · 2016 to 2024
$54.8M
CTSA UM1 Program at University of UtahUM1TR004409 · NCATS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI RACHEL HESS, Jennifer Juhl Majersik · 2023 to 2026
$21.9M
The Genetic Basis of Conotruncal DefectsU01HL098153 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI GOLDMUNTZ, ELIZABETH · 2009 to 2014
$4.3M
Molecular approaches to gene identification in congenital heart diseaseU01HL098163 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHUNG, WENDY K, WARBURTON, DOROTHY P. · 2009 to 2014
$3.9M
Genetics of Hypoplastic Left Heart SyndromeUM1HL128761 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI BERNSTEIN, DANIEL, SRIVASTAVA, DEEPAK · 2015 to 2019
$2.5M
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
Identifying unrecognized genetic causes of congenital heart diseaseR01HL162356 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI William Tswenching Pu, CHRISTINE E SEIDMAN · 2024 to 2026
$2.3M
Genetics of conotruncal defects and associated neurodevelopmental outcomesUM1HL098123 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GELB, BRUCE D · 2015 to 2019
$2.3M
Genetics and genomics of congenital heart disease and associated neurodevelopmental abnormalitiesUM1HL098162 · NHLBI · YALE UNIVERSITY · PI BRUECKNER, MARTINA, GUPTA, ABHA RANI · 2015 to 2019
$2.2M
Bridging the Gap between Genomics and Clinical Outcomes in CHDU01HL128711 · NHLBI · UNIVERSITY OF UTAH · PI TRISTANI-FIROUZI, MARTIN, YANDELL, MARK DOUGLAS · 2020 to 2024
$2.1M
Bridging the Gap between Genomics and Clinical Outcomes in CHDUM1HL128711 · NHLBI · UNIVERSITY OF UTAH · PI TRISTANI-FIROUZI, MARTIN, YANDELL, MARK DOUGLAS · 2015 to 2019
$2.0M
Integration of RNA and Genome Sequences to Identify Genetic Risk in Hypoplastic Left Heart SyndromeK08HL157653 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI Sarah Uhler Morton · 2022 to 2026
$840k
NCATS NIH HHS UM1 TR004409NHLBI NIH HHS K08 HL157653NHLBI NIH HHS R01 HL162356NHLBI NIH HHS U01 HL098153NHLBI NIH HHS U01 HL098163NHLBI NIH HHS U01 HL128711NHLBI NIH HHS U01 HL131003NHLBI NIH HHS UM1 HL098123NHLBI NIH HHS UM1 HL098147NHLBI NIH HHS UM1 HL098162NHLBI NIH HHS UM1 HL128711NHLBI NIH HHS UM1 HL128761
6 · The paper itself

Abstract

While exome and whole genome sequencing have transformed medicine by elucidating the genetic underpinnings of both rare and common complex disorders, its utility to predict clinical outcomes remains understudied. Here, we use artificial intelligence (AI) technologies to explore the predictive value of whole exome sequencing in forecasting clinical outcomes following surgery for congenital heart defects (CHD). We report results for a prospective observational cohort study of 2,253 CHD patients from the Pediatric Cardiac Genomics Consortium with a broad range of complex heart defects, pre- and post-operative clinical variables and exome sequencing. Damaging genotypes in chromatin-modifying and cilia-related genes are associated with an elevated risk of adverse post-operative outcomes, including mortality, cardiac arrest and prolonged mechanical ventilation. The impact of damaging genotypes is further amplified in the context of specific CHD phenotypes, surgical complexity and extra-cardiac anomalies. The absence of a damaging genotype in chromatin-modifying and cilia-related genes is also informative, reducing the risk for some adverse postoperative outcomes. Thus, genome sequencing enriches the ability to forecast outcomes following congenital cardiac surgery.

Indexed as

Cardiac Surgical ProceduresHeart Defects, CongenitalWhole Genome SequencingChildChild, PreschoolExome SequencingFemaleForecastingGenotypeHumansInfantInfant, NewbornMaleProspective StudiesTreatment Outcome

Identifiers

PMID40640177
PMCPMC12246213

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.