FAC MEDICINA
Centro
McGill University
Montreal, CanadáPublicaciones en colaboración con investigadores/as de McGill University (21)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Erratum to: Mapping the human genetic architecture of COVID-19 (Nature, (2021), 600, 7889, (472-477), 10.1038/s41586-021-03767-x)
Nature
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Quantitative aortography for assessment of aortic regurgitation in the era of percutaneous aortic valve replacement
Frontiers in Cardiovascular Medicine, Vol. 10
2022
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A first update on mapping the human genetic architecture of COVID-19
Nature
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Improved cancer-related fatigue in a randomised clinical trial: methylphenidate no better than placebo
BMJ Supportive and Palliative Care, Vol. 12, Núm. 2, pp. 226-234
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
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Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (Nature, (2022), 611, 7934, (115-123), 10.1038/s41586-022-05165-3)
Nature
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Stroke genetics informs drug discovery and risk prediction across ancestries
Nature, Vol. 611, Núm. 7934, pp. 115-123
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Tranexamic Acid in Patients Undergoing Noncardiac Surgery
New England Journal of Medicine, Vol. 386, Núm. 21, pp. 1996-1997
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Whole-genome sequencing reveals host factors underlying critical COVID-19
Nature, Vol. 607, Núm. 7917, pp. 97-103
2021
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Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Journal of Clinical Investigation, Vol. 131, Núm. 23
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Mapping the human genetic architecture of COVID-19
Nature, Vol. 600, Núm. 7889, pp. 472-477
2020
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Nature Genetics, Vol. 52, Núm. 1, pp. 56-73
2017
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Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Nature Genetics, Vol. 49, Núm. 5, pp. 680-691
2016
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Developmental programming: State-of-the-science and future directions-Summary from a Pennington Biomedical symposium
Obesity, Vol. 24, Núm. 5, pp. 1018-1026
2015
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Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
JAMA - Journal of the American Medical Association, Vol. 313, Núm. 13, pp. 1347-1361
2014
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Genetic implication of a novel thiamine transporter in human hypertension
Journal of the American College of Cardiology, Vol. 63, Núm. 15, pp. 1542-1555
2013
2012
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Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
Cancer Epidemiology Biomarkers and Prevention, Vol. 21, Núm. 4, pp. 645-657
2011
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International distribution and age estimation of the Portuguese BRCA2 c.156-157insAlu founder mutation
Breast Cancer Research and Treatment, Vol. 127, Núm. 3, pp. 671-679