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Amélie C Pinard (Amélie Pinard)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 5

Top Venues

Circulation. Genomic and precision medicine

Molecular genetics & genomic medicine

Neurology

Genetics in medicine : official journal of the American College of Medical Genetics

University of Texas Health Science Center at Houston

Aix-Marseille University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Texas Health Science Center at Houston Feb 1o 2017

United States

Postdoctoral Research Fellow :: Internal medicine

Education History

Aix-Marseille University Oct 1o 2012 - Jul 6o 2016

France

PHD :: Medical Genetics and Functional Genomics

Publications

Alana C Cecchi, Maura L Boerio, Isabella Marin, Amélie C Pinard, Dianna M Milewicz
Preventing Acute Aortic Dissections: The Power of Familial Screening and Risk Assessment. Journal of the American Heart Association 11 (8) (2022)
Maura L Boerio, Nicole Engelhardt, Sanmati Cuddapah, Jessica I Gold, Isabella C Marin, Amélie C Pinard, Dong-Chuan Guo, Siddharth K Prakash, Dianna M Milewicz
Further Evidence That ARIH1 Rare Variants Predispose to Thoracic Aortic Disease. Circulation. Genomic and precision medicine (2022)
Amélie C Pinard, Maximillian D J Fiander, Alana C Cecchi, Andrea L Rideout, Mohamed Azouz, Stuart M Fraser, P Daniel McNeely, Simon Walling, Sarah C Novara, Anna C E Hurst, Dongchuan Guo, Sandhya Parkash, Michael J Bamshad, Deborah A Nickerson, Anthony M Vandersteen, Dianna M Milewicz
Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy. Neurology 96 (13) (2021)
Fadi I Musfee, Dongchuan Guo, Amélie C Pinard, Ellen M Hostetler, Elizabeth E Blue, Deborah A Nickerson, null null, Michael J Bamshad, Dianna M Milewicz, Siddharth K Prakash
Rare deleterious variants of NOTCH1, GATA4, SMAD6, and ROBO4 are enriched in BAV with early onset complications but not in BAV with heritable thoracic aortic disease. Molecular genetics & genomic medicine 8 (10) (2020)
Amélie C Pinard, Stéphanie Guey, Dongchuan Guo, Alana C Cecchi, Natasha Kharas, Stephanie Wallace, Ellen S Regalado, Ellen M Hostetler, Anjail Z Sharrief, Françoise Bergametti, Manoëlle Kossorotoff, Nathanaelle Ibos-Augé, Markus Kraemer, Michael J Bamshad, Deborah A Nickerson, Edward R Smith, Elisabeth Tournier-Lasserve, Dianna M Milewicz
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)

Amélie C Pinard.css-eqlu8i{font-size:small;padding-left:4px;} (Amélie Pinard)

Publication Activity (10 Years)

Top Topics

Top Venues

Amélie C Pinard (Amélie Pinard)