Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve

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Publication Details

Journal
Heart
Published
2024-12-10
DOI
https://doi.org/10.1136/heartjnl-2024-324669
Citations
4
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
0.94

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article

Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve

Dawn S. Hui, Margot De Marco, Anthony Caffarelli, Anna Sabaté-Rotés et al.
4 citations
Heart
Congenital heart defects research
0.94
article

Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve

Dawn S. Hui, Margot De Marco, Anthony Caffarelli, Anna Sabaté-Rotés, Courtney McNeely, Siddharth K. Prakash, Ilenia Foffa, Yuli Y. Kim, Anji T. Yetman, Justin T. Tretter, Steven Grant Carlisle, Kim L. McBride, Malenka M. Bissell, Rodolfo Citro, Dianna M. Milewicz, Julie De Backer, Héctor I. Michelena, Maria Grazia Andreassi, Chiara Pensa, Laura Muiño Mosquera, Simon C. Body, Abi Watts, Helene DiGregorio, Sara Mansoorshahi
article en
4 citations

Abstract

No abstract available for this paper.
HeartVol. 111(5)
Boston University (US), Hoag Memorial Hospital Presbyterian (US), Cleveland Clinic (US), University of Salerno (IT), Mayo Clinic (US), Children's Hospital of Philadelphia (US), The University of Texas at San Antonio Health Science Center (US), University of Calgary (CA), Ghent University Hospital (BE), Ghent University (BE), University of Oxford (GB), Istituto di Fisiologia Clinica (IT), Vall d'Hebron Hospital Universitari (ES), Ospedali Riuniti San Giovanni di Dio e Ruggi d'Aragona (IT), The University of Texas Health Science Center (US), University of Nebraska Medical Center (US), University of Pennsylvania (US), The University of Texas Health Science Center at Houston (US)
University of Texas at Austin, National Institutes of Health, Department of Mechanical Engineering, University of Texas at Austin
Good health and well-being
Openalex Percentile: Top 24%
Congenital heart defects research
0.94
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