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Journal of Cardiovascular Translational Research
|
May 28, 2017
Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity
Benjamin J Landis, Jeffrey A Schubert, Dongbing Lai, et al.
The Journal of Pediatrics
|
July 28, 2020
A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy
Amy R Shikany, Benjamin J Landis, Ashley Parrott, et al.
Molecular Genetics & Genomic Medicine
|
November 26, 2024
Performance of Dysmorphology-Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing
Benjamin M Helm, Lindsey R Helvaty, Erin Conboy, et al.
Cell & Bioscience
|
March 2, 2023
Activation of the Hedgehog signaling pathway leads to fibrosis in aortic valves
Dongsheng Gu, Arvin H Soepriatna, Wenjun Zhang, et al.
Genes
|
January 21, 2022
An Emergent Nexus between Striae and Thoracic Aortic Dissection
Benjamin J Landis, Courtney E Vujakovich, Lindsey R Elmore, et al.
Journal of Molecular and Cellular Cardiology Plus
|
July 18, 2025
Combined genome and transcriptome analysis identifies molecular signatures of aortic disease in patients with Marfan syndrome
Katherine B Stanley, Alexa V Mederos, Ethan H Barksdale, et al.
The Journal of Pediatrics
|
May 21, 2023
Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects
Matthew D Durbin, Korre Fairman, Lindsey R Helvaty, et al.
Journal of the American Heart Association
|
September 29, 2022
Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease
Benjamin J Landis, Benjamin M Helm, Jeremy L Herrmann, et al.
HGG Advances
|
December 17, 2021
Identification of a common polymorphism in <i>COQ8B</i> acting as a modifier of thoracic aortic aneurysm severity
Benjamin J Landis, Dongbing Lai, Dong-Chuan Guo, et al.
Research Square
|
April 2, 2024
Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart Defects
Matthew D Durbin, Lindsey R Helvaty, Alyx Posorske, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Journal of Cardiovascular Translational Research
|
May 28, 2017
Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity
Benjamin J Landis, Jeffrey A Schubert, Dongbing Lai, et al.
The Journal of Pediatrics
|
July 28, 2020
A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy
Amy R Shikany, Benjamin J Landis, Ashley Parrott, et al.
Molecular Genetics & Genomic Medicine
|
November 26, 2024
Performance of Dysmorphology-Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing
Benjamin M Helm, Lindsey R Helvaty, Erin Conboy, et al.
Cell & Bioscience
|
March 2, 2023
Activation of the Hedgehog signaling pathway leads to fibrosis in aortic valves
Dongsheng Gu, Arvin H Soepriatna, Wenjun Zhang, et al.
Genes
|
January 21, 2022
An Emergent Nexus between Striae and Thoracic Aortic Dissection
Benjamin J Landis, Courtney E Vujakovich, Lindsey R Elmore, et al.
Journal of Molecular and Cellular Cardiology Plus
|
July 18, 2025
Combined genome and transcriptome analysis identifies molecular signatures of aortic disease in patients with Marfan syndrome
Katherine B Stanley, Alexa V Mederos, Ethan H Barksdale, et al.
The Journal of Pediatrics
|
May 21, 2023
Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects
Matthew D Durbin, Korre Fairman, Lindsey R Helvaty, et al.
Journal of the American Heart Association
|
September 29, 2022
Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease
Benjamin J Landis, Benjamin M Helm, Jeremy L Herrmann, et al.
HGG Advances
|
December 17, 2021
Identification of a common polymorphism in <i>COQ8B</i> acting as a modifier of thoracic aortic aneurysm severity
Benjamin J Landis, Dongbing Lai, Dong-Chuan Guo, et al.
Research Square
|
April 2, 2024
Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart Defects
Matthew D Durbin, Lindsey R Helvaty, Alyx Posorske, et al.
Page
of 4