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Nature Cardiovascular Research
|
April 20, 2026
PCBP1 regulates alternative splicing of AARS2 in congenital cardiomyopathy
Yao Wei Lu, Zhuomin Liang, Kerry Dorr, et al.
Genome Medicine
|
May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease
Alexander Hsieh, Sarah U Morton, Jon A L Willcox, et al.
JAMA Cardiology
|
October 21, 2020
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease
Sarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Circulation
|
April 25, 2024
SPTLC3 Is Essential for Complex I Activity and Contributes to Ischemic Cardiomyopathy
Anna Kovilakath, Adolfo G Mauro, Yolander A Valentine, et al.
Circulation. Genomic and Precision Medicine
|
May 11, 2023
Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease
Min Young Jang, Parth N Patel, Alexandre C Pereira, et al.
Circulation. Genomic and Precision Medicine
|
February 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study
Emily L Griffin, Shannon N Nees, Sarah U Morton, et al.
Circulation Research
|
February 9, 2021
Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency
Tarsha Ward, Warren Tai, Sarah Morton, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2020
De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease
Marko T Boskovski, Jason Homsy, Meena Nathan, et al.
Neuroimage
|
July 5, 2024
Identifying novel data-driven subgroups in congenital heart disease using multi-modal measures of brain structure
Marlee M Vandewouw, Ami Norris-Brilliant, Anum Rahman, et al.
JAMA Network Open
|
January 26, 2023
Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease
Sarah U Morton, Ami Norris-Brilliant, Sean Cunningham, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 76) with videos related to
Sort By:
Page
of 8
Nature Cardiovascular Research
|
April 20, 2026
PCBP1 regulates alternative splicing of AARS2 in congenital cardiomyopathy
Yao Wei Lu, Zhuomin Liang, Kerry Dorr, et al.
Genome Medicine
|
May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease
Alexander Hsieh, Sarah U Morton, Jon A L Willcox, et al.
JAMA Cardiology
|
October 21, 2020
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease
Sarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Circulation
|
April 25, 2024
SPTLC3 Is Essential for Complex I Activity and Contributes to Ischemic Cardiomyopathy
Anna Kovilakath, Adolfo G Mauro, Yolander A Valentine, et al.
Circulation. Genomic and Precision Medicine
|
May 11, 2023
Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease
Min Young Jang, Parth N Patel, Alexandre C Pereira, et al.
Circulation. Genomic and Precision Medicine
|
February 21, 2023
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study
Emily L Griffin, Shannon N Nees, Sarah U Morton, et al.
Circulation Research
|
February 9, 2021
Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency
Tarsha Ward, Warren Tai, Sarah Morton, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2020
De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease
Marko T Boskovski, Jason Homsy, Meena Nathan, et al.
Neuroimage
|
July 5, 2024
Identifying novel data-driven subgroups in congenital heart disease using multi-modal measures of brain structure
Marlee M Vandewouw, Ami Norris-Brilliant, Anum Rahman, et al.
JAMA Network Open
|
January 26, 2023
Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease
Sarah U Morton, Ami Norris-Brilliant, Sean Cunningham, et al.
Page
of 8