884 results on '"Dubé, Marie‐Pierre"'
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52. Supplementary Table 8 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
53. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals
54. Avoidance of Vitamin K−Rich Foods Is Common among Warfarin Users and Translates into Lower Usual Vitamin K Intakes
55. Opportunities for personalized approaches in heart failure
56. Supplementary Figure 1 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
57. Supplementary Figure 2 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
58. Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
59. Supplementary Table 6 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
60. Data from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
61. Supplementary Table 9 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
62. Supplementary Table 4 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
63. Supplementary Table 7 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
64. Supplementary Table 3 from Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors
65. Interplay Between Hereditary and Acquired Factors Determine Neutrophil Counts in Aging Individuals
66. Females present higher dose‐adjusted drug concentrations of metoprolol and allopurinol/oxypurinol than males
67. Cardiovascular pharmacogenomics; state of current knowledge and implementation in practice
68. Study of effect modifiers of genetically predicted CETP reduction
69. Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
70. Genetic Studies
71. ADCY9 (Adenylate Cyclase Type 9) Inactivation Protects From Atherosclerosis Only in the Absence of CETP (Cholesteryl Ester Transfer Protein)
72. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
73. Childhood maltreatment and leukocyte telomere length in men and women with chronic illness: an evaluation of moderating and mediating influences.
74. Whole-genome sequencing in French Canadians from Quebec
75. Childhood maltreatment and leukocyte telomere length in men and women with chronic illness: an evaluation of moderating and mediating influences
76. Low-dose colchicine and high-sensitivity C-reactive protein after myocardial infarction: A combined analysis using individual patient data from the COLCOT and LoDoCo-MI studies
77. ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol Levels
78. Impact of Selection Bias on Estimation of Subsequent Event Risk
79. CETP: Pharmacogenomics-Based Response to the CETP Inhibitor Dalcetrapib
80. Pharmacogenomics to Revive Drug Development in Cardiovascular Disease
81. Impact of regular physical activity on weekly warfarin dose requirement
82. Somatic Mosaic Chromosomal Alterations and Death of Cardiovascular Disease Causes among Cancer Survivors.
83. Somatic mosaic chromosomal alterations and death of cardiovascular disease causes among cancer survivors: an analysis of the UK Biobank
84. Do variants in the coding regions ofFOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?
85. Pharmacogenomic study of heart failure and candesartan response from the CHARM programme
86. An association study ofABCG2rs2231142 on the concentrations of allopurinol and its metabolites
87. Mutations in DCC Cause Congenital Mirror Movements
88. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia
89. Fetal Alcohol Spectrum Disorders: Gene-Environment Interactions, Predictive Biomarkers, and the Relationship Between Structural Alterations in the Brain and Functional Outcomes
90. Association between renal function and CYP3A5 genotype in heart transplant recipients treated with calcineurin inhibitors
91. Adenylate cyclase type 9 antagonizes cAMP accumulation and regulates endothelial signalling involved in atheroprotection
92. ExPheWas: a platform for cis-Mendelian randomization and gene-based association scans
93. Modifiers of (CAG)n instability in Machado–Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes
94. Pharmacogenomic approaches to lipid-regulating trials
95. Novel Mutations in the Amyloid Precursor Protein Gene within Moroccan Patients with Alzheimer's Disease
96. CE-482906-005 YIELD OF GENETIC TESTING IN EARLY-ONSET ATRIAL FIBRILLATION: A SUBSTUDY OF THE BRAIN-AF RANDOMIZED CLINICAL TRIAL
97. Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts
98. Leveraging large observational studies to discover genetic determinants of drug concentrations: A proof‐of‐concept study
99. Comparative Effectiveness and Safety of Low-Dose Oral Anticoagulants in Patients With Atrial Fibrillation
100. Pharmacogenomic markers of metoprolol and α-OH-metoprolol concentrations: a genome-wide association study
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