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George A Porter

Showing results (61-70 of 76) with videos related to

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Nature Cardiovascular Research|April 20, 2026
PCBP1 regulates alternative splicing of AARS2 in congenital cardiomyopathyYao Wei Lu, Zhuomin Liang, Kerry Dorr, et al.
Genome Medicine|May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart diseaseAlexander 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 DiseaseSarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Circulation|April 25, 2024
SPTLC3 Is Essential for Complex I Activity and Contributes to Ischemic CardiomyopathyAnna 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 DiseaseMin 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 StudyEmily L Griffin, Shannon N Nees, Sarah U Morton, et al.
Circulation Research|February 9, 2021
Mechanisms of Congenital Heart Disease Caused by NAA15 HaploinsufficiencyTarsha 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 DiseaseMarko 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 structureMarlee 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 DiseaseSarah U Morton, Ami Norris-Brilliant, Sean Cunningham, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Nature Cardiovascular Research|April 20, 2026
PCBP1 regulates alternative splicing of AARS2 in congenital cardiomyopathyYao Wei Lu, Zhuomin Liang, Kerry Dorr, et al.
Genome Medicine|May 1, 2020
EM-mosaic detects mosaic point mutations that contribute to congenital heart diseaseAlexander 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 DiseaseSarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Circulation|April 25, 2024
SPTLC3 Is Essential for Complex I Activity and Contributes to Ischemic CardiomyopathyAnna 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 DiseaseMin 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 StudyEmily L Griffin, Shannon N Nees, Sarah U Morton, et al.
Circulation Research|February 9, 2021
Mechanisms of Congenital Heart Disease Caused by NAA15 HaploinsufficiencyTarsha 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 DiseaseMarko 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 structureMarlee 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 DiseaseSarah U Morton, Ami Norris-Brilliant, Sean Cunningham, et al.
Pageof 8