webinar register page

Webinar banner
Heart University Contemporary Questions in Congenital Heart Disease Webinar #6- Cardiovascular Genetics: Everything you wanted to know but were afraid to ask.
Heart University Contemporary Questions in Congenital Heart Disease

Webinar #6- Cardiovascular Genetics: Everything you wanted to know but were afraid to ask.

Panelists and Topics:
David Winlaw, Surgeon, Cincinnati Children's Hospital Medical Center, OH, USA.
Should we sequence everyone if money were no object?

Martina Brueckner, Pediatric Cardiologist, Yale School of Medicine, CT, USA.
Have variants of unknown significance become significant?

Bruce Gelb, Pediatric Cardiologist, Mount Sinai, NY, USA.
Has the bench finally reached the bedside in Noonan Syndrome?

Tom Parks, Academic Clinical Fellow/Registrar in Infectious Disease, London School of Hygiene and Tropical Medicine and Wellcome Trust Centre for Human Genetics, Cambridge, UK.
Will an understanding of genetic predisposition to rheumatic heart disease change treatment in low-resource settings?

Julie De Backer, ACHD Cardiologist, Ghent University, Belgium.
Marfan and ARBs - does the bedside need to re-inform the bench?

Moderators:
K. Nicole Weaver, Clinical Geneticist, Cincinnati Children's Hospital Medical Center, OH, USA.
Seema Mital, Pediatric Cardiologist, Sick Kids, Toronto, CA.

**You can receive a certificate of attendance, after viewing the recording. Instructions for downloading this certificate are available with the webinar recording. We are currently working on CME and CEU’s for this webinar. We will notify you once this is available.

Dec 9, 2020 10:00 AM in Eastern Time (US and Canada)

* Required information
Loading

By registering, I agree to the Privacy Statement and Terms of Service.

Register

Speakers

K. Nicole Weaver, MD
Clinical Geneticist @Cincinnati Children's Hospital Medical Center, OH, USA.
Clinical expertise lies in the areas of cardiovascular, craniofacial and biochemical genetics. Co-director of the Cincinnati Children’s Cardiovascular Genetics Clinic, which provides care to children and adults with diagnoses, such as Marfan, Loeys Dietz, Williams and vascular Ehlers Danlos syndromes. A member of the Costello Syndrome Family Network (CSFN) Professional Advisory Board since 2015, and an activate participant in CSFN meetings for the last five years. Understanding the natural history of rare genetic diagnoses is a particular concern for parents, and therefore understanding the medical concerns of adults with Costello syndrome became a focus of my clinical research.
Seema Mital, MD, FACC, FAHA, FRCP(C)
Head of Cardiovascular Research Cardiology Staff Cardiologist - Heart Function and Transplant Program Cardiology @The Hospital for Sick Children
Mital has a strong translational research program. She has extensive experience in the genetics/genomics of congenital heart disease and heart failure, personalized medicine and clinical trials. She established the SickKids Heart Centre Biobank, a multi-centre biorepository of children and adults with childhood onset heart disease for genomics research, one of the largest international repositories of its kind. She is the Scientific Co-lead of the Ted Rogers Centre for Heart Research Cardiac Precision Medicine Program established in November 2014. Her research interests include genomics, pharmacogenomics and stem cell applications to model childhood heart disease and discover new therapies.