M. Thibeault

发表

Growth and development of islet autoimmunity and type 1 diabetes in children genetically at risk

C. de Beaufort, H. Siljander, A. Hämäläinen, 2021, Diabetologia.

Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease

S. Scherer, A. C. Lionel, C. Marshall, 2012, PLoS genetics.

Correction: Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease

S. Scherer, A. C. Lionel, C. Marshall, 2013, PLoS Genetics.

Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.

P. Awadalla, Christoph Preuss, G. Andelfinger, 2016, The Canadian journal of cardiology.

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm

Steven J. M. Jones, D. Labuda, H. Dietz, 2014, Nature Genetics.

Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in Quebec

R. Rozen, M. Dubé, G. Andelfinger, 2011, Cardiology in the Young.

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

M. Hurles, A. McCallion, A. Franco‐Cereceda, 2019, Nature Genetics.

Regional differences in milk and complementary feeding patterns in infants participating in an international nutritional type 1 diabetes prevention trial

C. de Beaufort, H. Siljander, V. Tillmann, 2017, Maternal & child nutrition.

Use of vitamin D supplements during infancy in an international feeding trial

C. de Beaufort, H. Siljander, V. Tillmann, 2013, Public Health Nutrition.

Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease

P. Awadalla, B. Godard, Christoph Preuss, 2016, PLoS genetics.

Evaluation of the Intermittent Exotropia Questionnaire using Rasch analysis.

David B. Petersen, Andrew J. Toole, Jayne M. Silver, 2015, JAMA ophthalmology.