Summary of GenTAC Research

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Collapse  <img src='/DesktopModules/BHSoftDocumentManager/images/folder.gif' /> Summary of Research Summary of Research
GEN01 - Sequencing of Known Genes for Thoracic Aortic Aneurysms and Dissection in the GENTAC Cohort
GEN02 - Circulating TGF-ß in Marfan Syndrome
GEN03 - CNV in the GENTAC cohort
GEN04 - Association of Aortic Annular Dilatation with Aortic Regurgitation in Patients with Thoracic Aortic Aneurysms
GEN05 - Role of Mast Cells, Local ANG II Formation, and TGF-ß Expression in Aortic Aneurysms in Marfan and Marfan Related Syndromes
GEN06 - Long-term implications of acute dissection as primary indication for aortic root replacement in Marfan syndrome patients
GEN08 - Exome sequencing in cardiovascular phenotypes resulting from rare variants
GEN09 - Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissection
GEN15 - Impact of Image Analysis Method on Diagnostic and Therapeutic Classification of Patients with Thoracic Aortic Aneurysms
GEN16 - Replication of Genome Wide Association Study for Thoracic Aortic Disease using GENTAC cohort of Bicuspid Aortic Valve and Thoracic Aortic Disease (2 Phases)
GEN17 - Genetic Polymorphisms Predisposing to Sporadic Thoracic Aortic Aneurysms and Dissections: Role in Cardiovascular Disease in Turner Syndrome Patients
GEN18 - Descending Thoracic Aortic Diameter in Acute Type B Dissection: Impact of Connective Tissue Disorders. Insights of GenTAC registry
GEN19 - Predictors of Aortic Dissection in Patients with Bicuspid Aortic Valve Disease
GEN20 – Analysis of left ventricular size and systolic function in patients with Marfan syndrome and other genetically triggered thoracic aortic aneurysms
GEN22 - Gender-related differences in genetically triggered aortic disease
GEN24 - The effect of calcium channel blocker therapy on patients with Marfan syndrome
GEN27 - Aortic Aneurysm Associated with Bicuspid Aortic Valve: Relation to Hemodynamics, Valve Morphology and Gender
GEN29 - Pilot Data on Medication Use in Bicuspid Valve Patients
GEN30 - Genetic Risks for Bicuspid Aortic Valve Disease
GEN32 - Genetic Associations with Bicuspid Aortic Valve
GEN33 - Burden of rare exomic variants in patients with thoracic aortic dissections
GEN34 - The Turner Syndrome aortopathy in the context of other genetically triggered aortic diseases
GEN36 - GenTAC Dissection: Prevalence, Pattern, and Prognostic Implications of Aortic Dissection among Patients with Genetically Medicated Thoracic Aortic Aneurysm
GEN37 - The relationship between aortic and PA diameter among individuals with genetic conditions of the thoracic aorta: A report from the GenTAC registry
GEN39 - Outcomes of valve sparing aortic root replacement procedures in patients with genetically-transmitted thoracic aortic aneurysms
GEN40 - Parental Analysis of Rare Copy Number Variants in GENTAC Patients with Early Onset Aortic Disease
GEN42 - Identification of Functional Variants for Sporadic TAAD
GEN43 - Association of bicuspid aortic valve with Marfan syndrome or Loeys Dietz: two strikes?
GEN48 - Pregnancy and Aortic Outcomes in Women with Bicuspid Aortic Valve Disease
GEN49 - Are unicuspid and bicuspid aortic valve different phenotypes of the same disease? An insight from the GenTAC registry
GEN50 - A unified protocol for analysis of the aorta results in high reproducibility of measurements across imaging modalities. The GenTAC iCORE experience.
GEN51 - The Impact of Medical Therapy in Early- Versus Late-Stage Thoracic Aortic Aneurysm
GEN52 - Management of the vascular abnormalities associated with vascular Ehlers–Danlos syndrome
GEN53 - Investigation the Role of Notch Signaling in Marfan Syndrome
GEN54 - Validation of the vertebral tortuosity index as a new imaging biomarker to predict adverse cardiovascular events in connective tissue disorders
GEN55 - Cardiomyopathy in MFS
GEN56 - Clinical, Radiologic, and Genetic Factors Influencing Rapid Enlargement of the Descending Thoracic Aorta after Aortic Dissection
GEN57 - Factors Associated with Quality of Life in Marfan syndrome patients
GEN58 - Allergic and Gastrointestinal Disease in Connective Tissue Disorders
GEN59 - Ocular Phenotype in Marfan syndrome
GEN60 - Pneumothoraces and other lung complications in Aneurysm syndromes
GEN61 - Exploring the Link of BAV and HoFH in Primary Care Cohorts with Cardiovascular Disease
GEN63 - Determinants of Pregnancy Outcomes in Marfan Syndrome
GEN64 - Cardiac Phenotype in Loeys Dietz Patients Enrolled in GenTAC
GEN65 - Impact of the implementation of an imaging core lab for measuring the aorta in GenTAC, a national registry of genetically-related diseases of the aorta.