Université de Montréal

Co-producing active lifestyles as whole-system-approach: theory, intervention and knowledge-to-action implications (2019) Rütten A, Frahsa A, Abel T, Bergmann M, De Leeuw E, Hunter D, Jansen M, et al. Journal article Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk (2019) Yang Y, Wu L, Shu X, Lu Y, Shu XO, Cai Q, Beeghly-Fadiel A, et al. Journal article Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice (2019) Jønch AE, Douard E, Moreau C, Van Dijck A, Passeggeri M, Kooy F, Puechberty J, et al. Journal article 33-fold pulse compression down to 1.5 cycles in a 6-m-long hollow-core fiber (2018) Jeong YG, Piccoli R, Ferachou D, Cardin V, Chini M, Hadrich S, Limpert J, et al. Conference contribution High power hollow-core fiber compression of Yb lasers as ideal drivers for HHG (2018) Cardin V, Jeong YG, Fan G, Balciunas T, Piccoli R, Ferachou D, Limpert J, et al. Conference contribution Prognostic value of coronary computed tomographic angiography findings in asymptomatic individuals: a 6-year follow-up from the prospective multicentre international CONFIRM study (2018) Cho I, Al'Aref SJ, Berger A, Hartaigh BO, Gransar H, Valenti V, Lin FY, et al. Journal article Tuberculosis and impaired IL-23-dependent IFN-gamma immunity in humans homozygous for a common TYK2 missense variant (2018) Boisson-Dupuis S, Ramirez-Alejo N, Li Z, Patin E, Rao G, Kerner G, Lim CK, et al. Journal article CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, et al. Journal article The Coronary Artery Disease-Reporting and Data System (CAD-RADS): Prognostic and Clinical Implications Associated With Standardized Coronary Computed Tomography Angiography Reporting (2018) Xie JX, Cury RC, Leipsic J, Crim MT, Berman DS, Gransar H, Budoff MJ, et al. Journal article Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017) Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al. Journal article