R01HL111459

NIH – National Heart, Lung, and Blood Institute

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Cardiac imaging and biomarkers for assessing myocardial fibrosis in children with hypertrophic cardiomyopathy

Kirmani, S., Woodard, P. K., Shi, L., Hamza, T. H., Canter, C. E., Colan, S. D., Pahl, E., Towbin, J. A., Webber, S. A., Rossano, J. W., Everitt, M. D., Molina, K. M., Kantor, P. F., Jefferies, J. L., Feingold, B., Addonizio, L. J., Ware, S. M., Chung, W. K., Ballweg, J. A., … Lipshultz, S. E. (2023). Cardiac imaging and biomarkers for assessing myocardial fibrosis in children with hypertrophic cardiomyopathy. American Heart Journal, 264, 153–162. https://doi.org/10.1016/j.ahj.2023.06.005
Authors:
Sonya Kirmani
Pamela K Woodard
Ling Shi
Taye H Hamza
Charles E Canter
Steven D Colan
Elfriede Pahl
Jeffrey A Towbin
Steven A Webber
Joseph W Rossano
Melanie D Everitt
Kimberly M Molina
Paul F Kantor
John L Jefferies
Brian Feingold
Linda J Addonizio
Stephanie M Ware
Wendy K Chung
Jean A Ballweg
Teresa M Lee
Neha Bansal
Hiedy Razoky
Jason Czachor
Fatima I Lunze
Edward Marcus
Paul Commean
James D Wilkinson
Steven E Lipshultz
Affiliated Authors:
Linda J Addonizio
Wendy K Chung
Teresa M Lee
Columbia Affiliation:
Subjects:
Contrast Media (MeSH)
Cardiomyopathy, Hypertrophic (MeSH)
Grants:
R01CA211996 (NIH – National Cancer Institute)
R01HL137558 (NIH – National Heart, Lung, and Blood Institute)
R01HL139968 (NIH – National Heart, Lung, and Blood Institute)
R01HL109090 (NIH – National Heart, Lung, and Blood Institute)
R01HL111459 (NIH – National Heart, Lung, and Blood Institute)
R01HL053392 (NIH – National Heart, Lung, and Blood Institute)
Publication Type:
Article
Unique ID:
10.1016/j.ahj.2023.06.005
PMID:
37315879
DOI:
10.1016/j.ahj.2023.06.005
Journal:
American Heart Journal
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record
View Scopus Record

Record Created:

The genetic architecture of pediatric cardiomyopathy

Ware, S. M., Bhatnagar, S., Dexheimer, P. J., Wilkinson, J. D., Sridhar, A., Fan, X., Shen, Y., Tariq, M., Schubert, J. A., Colan, S. D., Shi, L., Canter, C. E., Hsu, D. T., Bansal, N., Webber, S. A., Everitt, M. D., Kantor, P. F., Rossano, J. W., Pahl, E., … Lipshultz, S. E. (2022). The genetic architecture of pediatric cardiomyopathy. The American Journal of Human Genetics, 109(2), 282–298. https://doi.org/10.1016/j.ajhg.2021.12.006
Authors:
Stephanie M. Ware
Surbhi Bhatnagar
Phillip J. Dexheimer
James D. Wilkinson
Arthi Sridhar
Xiao Fan
Yufeng Shen
Muhammad Tariq
Jeffrey A. Schubert
Steven D. Colan
Ling Shi
Charles E. Canter
Daphne T. Hsu
Neha Bansal
Steven A. Webber
Melanie D. Everitt
Paul F. Kantor
Joseph W. Rossano
Elfriede Pahl
Paolo Rusconi
Teresa M. Lee
Jeffrey A. Towbin
Ashwin K. Lal
Wendy K. Chung
Erin M. Miller
Bruce Aronow
Lisa J. Martin
Steven E. Lipshultz
Affiliated Authors:
Xiao Fan
Yufeng Shen
Teresa M. Lee
Wendy K. Chung
Columbia Affiliation:
Subjects:
Diagnosis and Management of Hypertrophic Cardiomyopathy (OpenAlex Topic)
Molecular Mechanisms of Cardiac Development and Regeneration (OpenAlex Topic)
Diagnosis and Management of Arrhythmogenic Right Ventricular Cardiomyopathy (OpenAlex Topic)
Cardiomyopathy, Dilated (MeSH)
Exome (MeSH)
Gene Expression Regulation (MeSH)
Genotype (MeSH)
Inheritance Patterns (MeSH)
Author Keywords:
ancestry
bioinformatics
clinical interpretation
exome
heart
infant
molecular diagnosis
variant
Grants:
R01CA211996 (NIH – National Cancer Institute)
R01HL109090 (NIH – National Heart, Lung, and Blood Institute)
R01HL111459 (NIH – National Heart, Lung, and Blood Institute)
R01HL139968 (NIH – National Heart, Lung, and Blood Institute)
K23HL138231 (NIH – National Heart, Lung, and Blood Institute)
R01HL137558 (NIH – National Heart, Lung, and Blood Institute)
R01HL053392 (NIH – National Heart, Lung, and Blood Institute)
Publication Type:
Article
Unique ID:
10.1016/j.ajhg.2021.12.006
PMID:
35026164
DOI:
10.1016/j.ajhg.2021.12.006
Journal:
American Journal of Human Genetics
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record
View Web of Science Record
View PubMed Record
View OpenAlex Record

Record Created:

Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents

Ahimaz, P., Sabatello, M., Qian, M., Wang, A., Miller, E. M., Parrott, A., Lal, A. K., Chatfield, K. C., Rossano, J. W., Ware, S. M., Parent, J. J., Kantor, P., Yue, L., Wynn, J., Lee, T. M., Addonizio, L. J., Appelbaum, P. S., & Chung, W. K. (2021). Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents. Circulation: Genomic and Precision Medicine, 14(4). https://doi.org/10.1161/circgen.120.003189
Authors:
Priyanka Ahimaz
Maya Sabatello
Min Qian
Aijin Wang
Erin M. Miller
Ashley Parrott
Ashwin K. Lal
Kathryn C. Chatfield
Joseph W. Rossano
Stephanie M. Ware
John J. Parent
Paul Kantor
Lisa Yue
Julia Wynn
Teresa M. Lee
Linda J. Addonizio
Paul S. Appelbaum
Wendy K. Chung
Affiliated Authors:
Priyanka Ahimaz
Maya Sabatello
Min Qian
Aijin Wang
Lisa Yue
Julia Wynn
Teresa M. Lee
Linda J. Addonizio
Paul S. Appelbaum
Wendy K. Chung
Columbia Affiliation:
Subjects:
Cardiomyopathies (MeSH)
Emotions (MeSH)
Genetic Testing (MeSH)
Parents (MeSH)
Surveys and Questionnaires (MeSH)
Cardiac Resynchronization Therapy in Heart Failure (OpenAlex Topic)
Diagnosis and Management of Hypertrophic Cardiomyopathy (OpenAlex Topic)
Genetic Research on BRCA Mutations and Cancer Risk (OpenAlex Topic)
Author Keywords:
behavior
cardiomyopathies
family
genetic testing
psychology
Grants:
R01HL111459 (NIH – National Heart, Lung, and Blood Institute)
RM1HG007257 (NIH – National Human Genome Research Institute)
K01HG008653 (NIH – National Human Genome Research Institute)
R01HG010365 (NIH – National Human Genome Research Institute)
Publication Type:
Article
Unique ID:
10.1161/CIRCGEN.120.003189
PMID:
34255550
DOI:
10.1161/CIRCGEN.120.003189
Journal:
Circulation: Genomic and Precision Medicine
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record
View Web of Science Record
View OpenAlex Record
View PubMed Record

Record Created:

Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study

Ware, S. M., Wilkinson, J. D., Tariq, M., Schubert, J. A., Sridhar, A., Colan, S. D., Shi, L., Canter, C. E., Hsu, D. T., Webber, S. A., Dodd, D. A., Everitt, M. D., Kantor, P. F., Addonizio, L. J., Jefferies, J. L., Rossano, J. W., Pahl, E., Rusconi, P., … Chung, W. K. (2021). Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study. Journal of the American Heart Association, 10(9). https://doi.org/10.1161/jaha.120.017731
Authors:
Stephanie M Ware
James D Wilkinson
Muhammad Tariq
Jeffrey A Schubert
Arthi Sridhar
Steven D Colan
Ling Shi
Charles E Canter
Daphne T Hsu
Steven A Webber
Debra A Dodd
Melanie D Everitt
Paul F Kantor
Linda J Addonizio
John L Jefferies
Joseph W Rossano
Elfriede Pahl
Paolo Rusconi
Wendy K Chung
Teresa Lee
Jeffrey A Towbin
Ashwin K Lal
Surbhi Bhatnagar
Bruce Aronow
Phillip J Dexheimer
Lisa J Martin
Erin M Miller
Lynn A Sleeper
Hiedy Razoky
Jason Czachor
Steven E Lipshultz
Affiliated Authors:
Linda J Addonizio
Wendy K Chung
Teresa Lee
Subjects:
Diagnosis and Management of Hypertrophic Cardiomyopathy (OpenAlex Topic)
Diagnosis and Management of Arrhythmogenic Right Ventricular Cardiomyopathy (OpenAlex Topic)
Gene Therapy for Spinal Muscular Atrophy (OpenAlex Topic)
Cardiomyopathies (MeSH)
Genetic Predisposition to Disease (MeSH)
Genetic Testing (MeSH)
Registries (MeSH)
Author Keywords:
exome
heart failure
infant
molecular
mutation
Grants:
R01HL111459 (NIH – National Heart, Lung, and Blood Institute)
Publication Type:
Article
Unique ID:
10.1161/jaha.120.017731
PMID:
33906374
DOI:
10.1161/jaha.120.017731
Journal:
Journal of the American Heart Association
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record
View OpenAlex Record
View Web of Science Record
View Scopus Record

Record Created:

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