McGill University

University / College


Location: Montreal, Canada (CA) CA

ISNI: 0000000419368649

ROR: https://ror.org/01pxwe438

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk (2018) Lu Y, Beeghly-Fadiel A, Wu L, Guo X, Li B, Schildkraut JM, Im HK, et al. Journal article DNA methylation-based classification of central nervous system tumours (2018) Capper D, Jones DTW, Sill M, Hovestadt V, Schrimpf D, Sturm D, Koelsche C, et al. Journal article Neoadjuvant trastuzumab, pertuzumab, and chemotherapy versus trastuzumab emtansine plus pertuzumab in patients with HER2-positive breast cancer (KRISTINE): a randomised, open-label, multicentre, phase 3 trial (2018) Hurvitz SA, Martin M, Symmans WF, Jung KH, Huang CS, Thompson AM, Harbeck N, et al. Journal article A point mutation in the Ncr1 signal peptide impairs the development of innate lymphoid cell subsets (2018) Almeida FF, Tognarelli S, Marcais A, Kueh AJ, Friede ME, Liao Y, Willis SN, et al. Journal article Chloroquine exposure triggers distinct cellular responses in sensitive versus resistant Plasmodium falciparum parasites (2018) Reiling SJ, Krohne G, Friedrich O, Geary TG, Rohrbach P Journal article, Original article Hereditary SWI/SNF complex deficiency syndromes (2018) Agaimy A, Foulkes WD Journal article Biphasic papillary renal cell carcinoma is a rare morphological variant with frequent multifocality: a study of 28 cases (2018) Trpkov K, Athanazio D, Magi-Galluzzi C, Yilmaz H, Clouston D, Agaimy A, Williamson SR, et al. Journal article Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study (2018) Whelan CD, Altmann A, Botia JA, Jahanshad N, Hibar DP, Absil J, Alhusaini S, et al. Journal article Patterns and predictors of skin score change in early diffuse systemic sclerosis from the European Scleroderma Observational Study (2018) Herrick AL, Peytrignet S, Lunt M, Pan X, Hesselstrand R, Mouthon L, Silman AJ, 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