Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (247) 247
Patent (65) 65
Publication (29) 29
Dissertation (6) 6
Book / eBook (2) 2
Magazine Article (2) 2
Book Chapter (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (127) 127
index medicus (98) 98
female (83) 83
male (78) 78
chemistry (63) 63
metallurgy (62) 62
biochemistry (58) 58
genetics & heredity (56) 56
beer (55) 55
compositions or test papers therefor (55) 55
condition-responsive control in microbiological orenzymological processes (55) 55
enzymology (55) 55
measuring or testing processes involving enzymes, nucleicacids or microorganisms (55) 55
microbiology (55) 55
mutation or genetic engineering (55) 55
processes of preparing such compositions (55) 55
spirits (55) 55
vinegar (55) 55
wine (55) 55
genetics (44) 44
middle aged (44) 44
aged (35) 35
genotype (35) 35
human necessities (35) 35
hygiene (35) 35
medical or veterinary science (35) 35
preparations for medical, dental, or toilet purposes (35) 35
adult (34) 34
mutation (32) 32
genetic aspects (30) 30
risk factors (29) 29
association (27) 27
pedigree (27) 27
polymorphism, single nucleotide (27) 27
organic chemistry (26) 26
pharmacogenetics (24) 24
article (23) 23
cardiac & cardiovascular systems (23) 23
research (23) 23
genetic variation (22) 22
phenotype (22) 22
risk (21) 21
genes (20) 20
pharmacology & pharmacy (20) 20
cohort studies (19) 19
genomes (18) 18
peptides (17) 17
pharmacogenomics (17) 17
cardiovascular disease (16) 16
genetic predisposition to disease (16) 16
genome-wide association study (16) 16
adolescent (15) 15
child (15) 15
genetic linkage (15) 15
medical and health sciences (15) 15
medicin och hälsovetenskap (15) 15
coronary artery disease (14) 14
gene expression (14) 14
gene frequency (14) 14
mutations (14) 14
aged, 80 and over (13) 13
analysis (13) 13
animals (13) 13
canada (13) 13
cholesterol (13) 13
alleles (12) 12
cardiovascular (12) 12
case-control studies (12) 12
disease (12) 12
genetic markers (12) 12
genomics (12) 12
medicine (12) 12
quebec (12) 12
studies (12) 12
biochemistry & molecular biology (11) 11
clinical medicine (11) 11
genome-wide association (11) 11
haplotypes (11) 11
linkage analysis (11) 11
lipids (11) 11
molecular sequence data (11) 11
nucleic acids (11) 11
population (11) 11
chromosome mapping (10) 10
derivatives thereof (10) 10
family (10) 10
health aspects (10) 10
hematology (10) 10
linkage disequilibrium (10) 10
medical research (10) 10
nucleosides (10) 10
nucleotides (10) 10
research article (10) 10
sugars (10) 10
warfarin (10) 10
amino acid sequence (9) 9
base sequence (9) 9
child, preschool (9) 9
compositions thereof (9) 9
culture media (9) 9
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (310) 310
French (35) 35
German (7) 7
Spanish (3) 3
Korean (2) 2
Portuguese (2) 2
Chinese (1) 1
Croatian (1) 1
Danish (1) 1
Estonian (1) 1
Hungarian (1) 1
Japanese (1) 1
Lithuanian (1) 1
Polish (1) 1
Serbian (1) 1
Slovenian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Lipoprotein (a), arterial inflammation, and PCSK9 inhibition
by Tardif, Jean-Claude and Rhéaume, Eric and Rhainds, David and Dubé, Marie-Pierre
European heart journal, ISSN 0195-668X, 09/2019, Volume 40, Issue 33, pp. 2782 - 2784
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Herbarium specimens as tools to assess the impact of large herbivores on plant species
by Marie-Pierre Beauvais and Stéphanie Pellerin and Jean Dubé and Claude Lavoie
Botany, ISSN 1916-2790, 02/2017, Volume 95, Issue 2, p. 153
  Herbarium specimens can be used to reconstruct spatiotemporal changes in plant morphology caused by environmental pressures. The reliability of... 
Morphology | Botany | Herbivores | Deer
Journal Article
Details down arrow
3. Full Text DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions
by Buscarlet, M and Provost, S and Zada, YF and Barhdadi, A and Bourgoin, V and Lepine, G and Mollica, L and Szuber, N and Dube, MP and Busque, L
BLOOD, ISSN 0006-4971, 08/2017, Volume 130, Issue 6, pp. 753 - 762
Age-associated clonal hematopoiesis caused by acquired mutations in myeloid cancer-associated genes is highly prevalent in the normal population. Its etiology,... 
CAPACITY | STEM-CELLS | HUMAN BONE-MARROW | AGE-RELATED-CHANGES | JAK2 HAPLOTYPE | CHROMOSOME INACTIVATION PATTERNS | SELF-RENEWAL | RISK | MUTATIONS | HEMATOLOGY | BLOOD | Genetic Predisposition to Disease | Age Factors | Humans | Middle Aged | Male | Proto-Oncogene Proteins - genetics | DNA-Binding Proteins - genetics | Telomere Homeostasis | Blood Cell Count | DNA (Cytosine-5-)-Methyltransferases - genetics | Hematopoiesis | Aged, 80 and over | Aging | Female | Aged | Clone Cells | Hematologic Neoplasms - genetics | High-Throughput Nucleotide Sequencing | Mutation | Cohort Studies | X Chromosome Inactivation
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text CETP: Pharmacogenomics-Based Response to the CETP Inhibitor Dalcetrapib
by Tardif, Jean-Claude and Rhainds, David and Rhéaume, Eric and Dubé, Marie-Pierre
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 03/2017, Volume 37, Issue 3, pp. 396 - 400
High-density lipoproteins are involved in reverse cholesterol transport and possess anti-inflammatory and antioxidative properties. Paradoxically, CETP... 
coronary artery disease | cholesterol | genetics | inflammation | pharmacology | ESTER TRANSFER PROTEIN | TORCETRAPIB | IDENTIFICATION | ACUTE CORONARY SYNDROME | HDL | HIGH-RISK | CHOLESTEROL EFFLUX | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | LIPOPROTEINS | CAMP | EVACETRAPIB | Cholesterol Ester Transfer Proteins - antagonists & inhibitors | Dyslipidemias - genetics | Predictive Value of Tests | Dyslipidemias - drug therapy | Pharmacogenetics | Humans | Treatment Outcome | Patient Selection | Homozygote | Dyslipidemias - blood | Phenotype | Anticholesteremic Agents - therapeutic use | Pharmacogenomic Variants | Heterozygote | Polymorphism, Single Nucleotide | Sulfhydryl Compounds - therapeutic use | Adenylyl Cyclases - genetics | Cholesterol Ester Transfer Proteins - metabolism | Precision Medicine
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Inherited chromosomally integrated HHV-6 demonstrates tissue-specific RNA expression in vivo that correlates with increased antibody immune response
by Peddu, Vikas and Dubuc, Isabelle and Gravel, Annie and Xie, Hong and Huang, Meei-Li and Tenenbaum, Dan and Jerome, Keith R and Tardif, Jean-Claude and Dubé, Marie-Pierre and Flamand, Louis and Greninger, Alexander L
Journal of Virology, ISSN 0022-538X, 10/2019
Human herpesvirus-6A and 6B (HHV-6A, HHV-6B) are human viruses capable of chromosomal integration. Approximately 1% of the human population carry one copy of... 
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text rs73185306 C/T is not a predisposing risk factor for inherited chromosomally-integrated human herpesvirus 6A/B
by Mouammine, Annabelle and Gravel, Annie and Dubuc, Isabelle and Feroz Zada, Yassamin and Provost, Sylvie and Busseuil, David and Tardif, Jean-Claude and Dubé, Marie-Pierre and Flamand, Louis
The Journal of Infectious Diseases, ISSN 0022-1899, 10/2019
Abstract Approximately 1% of the world population carry a copy of the human herpesvirus 6A or 6B (HHV-6A/B) in every cell of their body. This condition is... 
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Pharmacogenetics of Lipid-Lowering Agents: an Update Review on Genotype-Dependent Effects of HDL-Targetingand Statin Therapies
by Messas, Nathan and Dubé, Marie-Pierre and Tardif, Jean-Claude
Current Atherosclerosis Reports, ISSN 1523-3804, 11/2017, Volume 19, Issue 11, pp. 1 - 6
High-density lipoproteins (HDL) are involved in reverse cholesterol transport. Results from randomized trials of HDL-targeting therapies, including cholesteryl... 
High-density lipoproteins (HDL) | Pharmacogenetics | Medicine & Public Health | Cardiovascular disease | Angiology | Cardiology | Cholesteryl ester transfer protein (CETP) inhibitors | Statins | Analysis | Low density lipoproteins | Genetic aspects | Blood lipids | Trans fatty acids | Cardiovascular agents
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Cardiovascular pharmacogenomics; state of current knowledge and implementation in practice
by Shahabi, Payman and Dubé, Marie-Pierre
International Journal of Cardiology, ISSN 0167-5273, 2015, Volume 184, Issue 1, pp. 772 - 795
Abstract Pharmacogenomics (PGx) is the science that examines how an individual's genetic make-up affects the safety and efficacy of therapeutic drugs. PGx of... 
Cardiovascular | Pharmacogenetics | Implementation | Pharmacogenomics | INFLUENCING ANTIHYPERTENSIVE RESPONSE | CARDIAC & CARDIOVASCULAR SYSTEMS | LIPOPROTEIN CHOLESTEROL RESPONSE | WARFARIN DOSE REQUIREMENTS | ADVERSE DRUG-REACTIONS | ESTROGEN-RECEPTOR-ALPHA | CYTOCHROME-P450 2C19 GENOTYPE | TREATMENT PLATELET REACTIVITY | COMMON GENETIC-VARIATION | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Cardiovascular Agents - therapeutic use | Pharmacogenetics - methods | Cardiovascular Diseases - drug therapy | Humans | Genetic Association Studies - methods | Genome-Wide Association Study - methods | Cardiovascular Diseases - genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Lineage restriction analyses in CHIP indicate myeloid bias for TET2 and multipotent stem cell origin for DNMT3A
by Buscarlet, Manuel and Provost, Sylvie and Zada, Yassamin Feroz and Bourgoin, Vincent and Mollica, Luigina and Dubé, Marie-Pierre and Busque, Lambert
Blood, ISSN 0006-4971, 07/2018, Volume 132, Issue 3, pp. 277 - 280
We analyzed DNA from polymorphonuclear (PMN) cells, monocytes, B cells, and T cells of 107 individuals with clonal hematopoiesis of indeterminate potential... 
CLONAL HEMATOPOIESIS | RISK | MUTATIONS | HEMATOLOGY | MYELODYSPLASTIC SYNDROMES | AGE | HIERARCHY
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Meta-Analysis of Randomized Controlled Trials Assessing the Impact of Proprotein Convertase Subtilisin/Kexin Type 9 Antibodies on Mortality and Cardiovascular Outcomes
by AlTurki, Ahmed and Marafi, Mariam and Dawas, Ahmed and Dube, Marie-Pierre and Vieira, Lucy and Sherman, Mark H and Gregoire, Jean and Thanassoulis, George and Tardif, Jean-Claude and Huynh, Thao
The American Journal of Cardiology, ISSN 0002-9149, 09/2019
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically
by Wang, Jian and Dron, Jacqueline S and Ban, Matthew R and Robinson, John F and McIntyre, Adam D and Alazzam, Maher and Zhao, Pei Jun and Dilliott, Allison A and Cao, Henian and Huff, Murray W and Rhainds, David and Low-Kam, Cécile and Dubé, Marie-Pierre and Lettre, Guillaume and Tardif, Jean-Claude and Hegele, Robert A
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 12/2016, Volume 36, Issue 12, pp. 2439 - 2445
OBJECTIVE—Next-generation sequencing technology is transforming our understanding of heterozygous familial hypercholesterolemia, including revision of... 
mutation | cholesterol, LDL | sequence analysis, DNA | hypercholesterolemia type IIA | hyperlipoproteinemias | DIAGNOSIS | IMPROVE | FAMILIAL HYPERCHOLESTEROLEMIA | SCORE | CLINICIAN | PREVALENCE | GUIDANCE | GENERAL-POPULATION | LDL | DNA | cholesterol | PERIPHERAL VASCULAR DISEASE | sequence analysis | MUTATIONS | HEMATOLOGY | UTILITY | Predictive Value of Tests | Humans | Middle Aged | Hyperlipoproteinemia Type II - diagnosis | Male | Genetic Testing - methods | Multifactorial Inheritance | DNA Copy Number Variations | DNA Mutational Analysis | Adult | Cholesterol, LDL - blood | Female | Severity of Illness Index | Genetic Predisposition to Disease | Hyperlipoproteinemia Type II - blood | Risk Factors | Gene Dosage | Heredity | Biomarkers - blood | Genetic Markers | Phenotype | Heterozygote | Aged | High-Throughput Nucleotide Sequencing | Mutation | Ontario | Hyperlipoproteinemia Type II - genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text LONG-TERM RESIDUAL RISK AND PREDICTORS OF CARDIOVASCULAR DISEASE IN INDIVIDUALS TAKING STATINS FOR PRIMARY PREVENTION: INSIGHTS FROM THE CARTAGENE STUDY
by Robert-Halabi, Maxime and Ni, Jiayi and Nguyen, Anh and Dube, Marie-Pierre and AlTurki, Ahmed and Sherman, Mark and Thanassoulis, George and Gregoire, Jean and Tardif, Jean Claude and Huynh, Thao
Journal of the American College of Cardiology, ISSN 0735-1097, 03/2019, Volume 73, Issue 9, pp. 1773 - 1773
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Pharmacogenomic Prediction of Anthracycline-Induced Cardiotoxicity in Children
by Henk Visscher and Colin J.D. Ross and S. Rod Rassekh and Amina Barhdadi and Marie-Pierre Dubé and Hesham Al-Saloos and George S. Sandor and Huib N. Caron and Elvira C. van Dalen and Leontien C. Kremer and Helena J. van der Pal and Andrew M.K. Brown and Paul C. Rogers and Michael S. Phillips and Michael J. Rieder and Bruce C. Carleton and Michael R. Hayden and Canadian Pharmacogenomics Network for Drug Safety Consortium and Canadian Pharmacogenomics Network and Canadian Pharmacogenomics Network for Drug Safety Consortium
Journal of Clinical Oncology, ISSN 0732-183X, 05/2012, Volume 30, Issue 13, pp. 1422 - 1428
Purpose Anthracycline-induced cardiotoxicity (ACT) is a serious adverse drug reaction limiting anthracycline use and causing substantial morbidity and... 
LONG-TERM | RISK-FACTORS | GENETIC POLYMORPHISMS | ONCOLOGY | CLINICAL HEART-FAILURE | DOXORUBICIN | ADRIAMYCIN | IDENTIFICATION | CONCENTRATIVE NUCLEOSIDE TRANSPORTER-3 | ASSOCIATION | SINGLE NUCLEOTIDE POLYMORPHISMS | Anthracyclines - adverse effects | Age Factors | Humans | Antibiotics, Antineoplastic - adverse effects | Child, Preschool | Infant | Male | Netherlands | ATP-Binding Cassette Transporters - genetics | Membrane Transport Proteins - genetics | Biotransformation | ATP-Binding Cassette Transporters - metabolism | Anthracyclines - metabolism | Female | Membrane Transport Proteins - metabolism | Heart Diseases - chemically induced | Odds Ratio | Child | Infant, Newborn | Genetic Predisposition to Disease | Pharmacogenetics | Genetic Association Studies | Risk Assessment | Risk Factors | Kaplan-Meier Estimate | Neoplasms - drug therapy | Canada | Heart Diseases - etiology | Phenotype | Adolescent | Polymorphism, Single Nucleotide | Antibiotics, Antineoplastic - metabolism | Heart Diseases - genetics | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
14. Full Text Lipoprotein(a) levels, genotype, and incident aortic valve stenosis: a prospective mendelian randomization study and replication in a case-control cohort
by Arsenault, Benoit J and Boekholdt, S. Matthijs and Dubé, Marie-Pierre and Rhéaume, Eric and Wareham, Nicholas J and Khaw, Kay-Tee and Sandhu, Manjinder S and Tardif, Jean-Claude
Circulation. Cardiovascular genetics, ISSN 1942-325X, 2014, Volume 7, Issue 3, pp. 304 - 310
Although a previous study has suggested that a genetic variant in the LPA region was associated with the presence of aortic valve stenosis (AVS), no... 
Mendelian randomization analysis | Lipoproteins | Aortic valve stenosis | EPIC-NORFOLK | CORONARY | GENETICS & HEREDITY | aortic valve stenosis | LOW-DENSITY-LIPOPROTEIN | RISK | CALCIFICATION | GENETIC-VARIANTS | ASSOCIATION | lipoproteins | APOLIPOPROTEIN(A) | Aortic Valve Stenosis - genetics | Prospective Studies | Humans | Middle Aged | Aortic Valve Stenosis - blood | Male | Case-Control Studies | Incidence | Aortic Valve Stenosis - epidemiology | Mendelian Randomization Analysis | Adult | Female | Aged | Lipoprotein(a) - blood | Lipoprotein(a) - genetics | United Kingdom - epidemiology
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
15. Full Text Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy
by Carleton, Bruce C and Hayden, Michael R and Ross, Colin J D and Brooks, Beth and Phillips, Michael S and Rieder, Michael J and Rassekh, S Rod and Barhdadi, Amina and Visscher, Henk and Dubé, Marie-Pierre and Feroz-Zada, Yassamin and Brown, Andrew M K and Rogers, Paul C and Katzov-Eckert, Hagit and CPNDS Consortium and the CPNDS Consortium
Nature Genetics, ISSN 1061-4036, 12/2009, Volume 41, Issue 12, pp. 1345 - 1349
Cisplatin is a widely used and effective chemotherapeutic agent, although its use is restricted by the high incidence of irreversible ototoxicity associated... 
MERCAPTOPURINE | CATECHOL-O-METHYLTRANSFERASE | THERAPY | THIOPURINE S-METHYLTRANSFERASE | INDIVIDUAL SENSITIVITY | PHARMACOGENOMICS | GENETICS & HEREDITY | OTOTOXICITY | INTOLERANCE | CANCER | SINGLE-NUCLEOTIDE POLYMORPHISMS | Humans | Methyltransferases - genetics | Antineoplastic Agents - therapeutic use | Catechol O-Methyltransferase - genetics | Genetic Variation | Hearing Loss - genetics | Cisplatin - therapeutic use | Antineoplastic Agents - adverse effects | Cisplatin - adverse effects | Polymorphism, Single Nucleotide | Child | Hearing Loss - chemically induced | Cohort Studies | Complications and side effects | Methyltransferases | Genetic variation | Physiological aspects | Genetic aspects | Dosage and administration | Hearing disorders in children | Research | Risk factors | Cisplatin | Medical research | Chemotherapy | Oncology | Genetic testing | Pharmaceutical industry | Cancer therapies | Deoxyribonucleic acid--DNA | Clinical outcomes | Cancer | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
16. Full Text The Genetics of Congenital Amusia (Tone Deafness): A Family-Aggregation Study
by Peretz, Isabelle and Cummings, Stéphanie and Dubé, Marie-Pierre
The American Journal of Human Genetics, ISSN 0002-9297, 2007, Volume 81, Issue 3, pp. 582 - 588
Congenital amusia (commonly known as “tone deafness”) is a lifelong impairment of music perception that affects 4% of the population. To estimate whether... 
MUSIC | PERCEPTION | DYSLEXIA | GENES | GENETICS & HEREDITY | ABSOLUTE PITCH | DISORDERS | BRAIN | TUNE | Deafness - genetics | Genetic Testing | Humans | Middle Aged | Male | Auditory Perception - genetics | Pedigree | Music | Adolescent | Adult | Female | Aged | Child | Gene expression | Genetic disorders | Research | Report
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
17. Full Text Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
by Stitziel, Nathan O and Stirrups, Kathleen E and Masca, Nicholas G. D and Erdmann, Jeanette and Ferrario, Paola G and König, Inke R and Weeke, Peter E and Webb, Thomas R and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kanoni, Stavroula and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenborg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S. F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Piera A and Duga, Stefano and Marziliano, N