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1. Full Text Efficacy and Safety of Low-Dose Colchicine after Myocardial Infarction
by Tardif, Jean-Claude and Kouz, Simon and Waters, David D and Bertrand, Olivier F and Diaz, Rafael and Maggioni, Aldo P and Pinto, Fausto J and Ibrahim, Reda and Gamra, Habib and Kiwan, Ghassan S and Berry, Colin and López-Sendón, José and Ostadal, Petr and Koenig, Wolfgang and Angoulvant, Denis and Grégoire, Jean C and Lavoie, Marc-André and Dubé, Marie-Pierre and Rhainds, David and Provencher, Mylène and Blondeau, Lucie and Orfanos, Andreas and L’Allier, Philippe L and Guertin, Marie-Claude and Roubille, François
The New England journal of medicine, ISSN 0028-4793, 12/2019, Volume 381, Issue 26, pp. 2497 - 2505
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Recurrence | Double-Blind Method | Humans | Middle Aged | Kaplan-Meier Estimate | Proportional Hazards Models | Colchicine - administration & dosage | Male | Biomarkers - blood | Colchicine - adverse effects | Incidence | Myocardial Infarction - therapy | Anti-Inflammatory Agents - adverse effects | Myocardial Infarction - drug therapy | Intention to Treat Analysis | Cardiovascular Diseases - epidemiology | Cardiovascular Diseases - mortality | Angina Pectoris - epidemiology | Anti-Inflammatory Agents - administration & dosage | Female | Stroke - epidemiology | Aged | C-Reactive Protein - analysis | Percutaneous Coronary Intervention | Heart | Heart failure | Myocardial infarction | Cerebral infarction | Cardiac arrhythmia | Pericarditis | Stroke | Heart attacks | Gout | Oral administration | Clinical trials | Diarrhea | Cardiovascular disease | Inflammation | Angina | Thrombosis | Patients | Manuscripts | Ischemia | Consent | Arteriosclerosis | Colchicine | Cardiovascular diseases | Index Medicus | Abridged Index Medicus | Life Sciences
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2. Full Text DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions
by Buscarlet, Manuel and Provost, Sylvie and Zada, Yassamin Feroz and Barhdadi, Amina and Bourgoin, Vincent and Lépine, Guylaine and Mollica, Luigina and Szuber, Natasha and Dubé, Marie-Pierre and Busque, Lambert
Blood, ISSN 0006-4971, 08/2017, Volume 130, Issue 6, pp. 753 - 762
Life Sciences & Biomedicine | Hematology | Science & Technology | 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 | Index Medicus | Abridged Index Medicus
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3. Full Text DNA methylation signature of human fetal alcohol spectrum disorder
by Portales-Casamar, Elodie and Lussier, Alexandre A and Jones, Meaghan J and MacIsaac, Julia L and Edgar, Rachel D and Mah, Sarah M and Barhdadi, Amina and Provost, Sylvie and Lemieux-Perreault, Louis-Philippe and Cynader, Max S and Chudley, Albert E and Dubé, Marie-Pierre and Reynolds, James N and Pavlidis, Paul and Kobor, Michael S
Epigenetics & chromatin, ISSN 1756-8935, 06/2016, Volume 9, Issue 1, pp. 25 - 25
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fetal alcohol syndrome | Epigenetic inheritance | Analysis | Genomics | Effect of alcohol on | Fetus | Genetic aspects | Research | Diagnosis
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4. Full Text The Genetics of Congenital Amusia (Tone Deafness): A Family-Aggregation Study
by Peretz, Isabelle and Cummings, Stéphanie and Dubé, Marie-Pierre
American journal of human genetics, ISSN 0002-9297, 2007, Volume 81, Issue 3, pp. 582 - 588
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Otorhinolaryngology. Stomatology | Non tumoral diseases | Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Deafness - genetics | Genetic Testing | Humans | Middle Aged | Male | Auditory Perception - genetics | Pedigree | Music | Adolescent | Adult | Female | Aged | Child | Gene expression | Genetic disorders | Research | Genetics | Ears & hearing | Hearing impairment | Genes | Index Medicus | Report
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5. Full Text Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits
by Auer, Paul L and Teumer, Alexander and Schick, Ursula and O'Shaughnessy, Andrew and Lo, Ken Sin and Chami, Nathalie and Carlson, Chris and De Denus, Simon and Dubé, Marie-Pierre and Haessler, Jeff and Jackson, Rebecca D and Kooperberg, Charles and Perreault, Louis-Philippe Lemieux and Nauck, Matthias and Peters, Ulrike and Rioux, John D and Schmidt, Frank and Turcot, Valérie and Völker, Uwe and Völzke, Henry and Greinacher, Andreas and Hsu, Li and Tardif, Jean-Claude and Diaz, George A and Reiner, Alexander P and Lettre, Guillaume
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 6, pp. 629 - 634
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genome-Wide Association Study | Frameshift Mutation | Humans | Middle Aged | Hematocrit | Janus Kinase 2 - genetics | Genotype | Hemoglobins - genetics | Male | Mutation, Missense | Chemotaxis | Neutropenia - congenital | Exome | Platelet Count | Hematopoiesis | Pedigree | Receptors, Interleukin-8B - genetics | Adult | Female | Aged | Leukocyte Count | Neutropenia - genetics | Genetic aspects | Genetic variation | Identification and classification | Chemokine receptors | Proteins | Medicine | Studies | Blood platelets | Education | Womens health | Genes | Genomics | Mutation | Grants | Binding sites | Index Medicus
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6. Full Text Polygenic determinants in extremes of high-density lipoprotein cholesterol
by Dron, Jacqueline S and Wang, Jian and Low-Kam, Cécile and Khetarpal, Sumeet A and Robinson, John F and McIntyre, Adam D and Ban, Matthew R and Cao, Henian and Rhainds, David and Dubé, Marie-Pierre and Rader, Daniel J and Lettre, Guillaume and Tardif, Jean-Claude and Hegele, Robert A
Journal of lipid research, ISSN 0022-2275, 2017, Volume 58, Issue 11, pp. 2162 - 2170
Polygenic risk score | Next-generation sequencing | Dyslipidemias | Genomics | Rare variants | Complex trait | Genetics | Common variants | Genes in lipid dysfunction | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Genetic Variation | Humans | Middle Aged | Cholesterol, HDL - blood | Adult | Female | Genotype | Male | Aged | High-Throughput Nucleotide Sequencing | Cholesterol, HDL - genetics | Genetic variance | Lipoproteins (high density) | Polygenic inheritance | Low density lipoprotein | Cholesterol | Dyslipidemia | Index Medicus | rare variants | Patient-Oriented and Epidemiological Research | genetics | next-generation sequencing | complex trait | genomics | genes in lipid dysfunction | dyslipidemias | polygenic risk score | common variants
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7. 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
mutation | cholesterol, LDL | sequence analysis, DNA | hypercholesterolemia type IIA | hyperlipoproteinemias | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | 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 | Index Medicus
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8. Full Text Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts
by Awadalla, Philip and Gauthier, Julie and Myers, Rachel A and Casals, Ferran and Hamdan, Fadi F and Griffing, Alexander R and Côté, Mélanie and Henrion, Edouard and Spiegelman, Dan and Tarabeux, Julien and Piton, Amélie and Yang, Yan and Boyko, Adam and Bustamante, Carlos and Xiong, Lan and Rapoport, Judith L and Addington, Anjené M and DeLisi, J. Lynn E and Krebs, Marie-Odile and Joober, Ridha and Millet, Bruno and Fombonne, Éric and Mottron, Laurent and Zilversmit, Martine and Keebler, Jon and Daoud, Hussein and Marineau, Claude and Roy-Gagnon, Marie-Hélène and Dubé, Marie-Pierre and Eyre-Walker, Adam and Drapeau, Pierre and Stone, Eric A and Lafrenière, Ronald G and Rouleau, Guy A
American journal of human genetics, ISSN 0002-9297, 09/2010, Volume 87, Issue 3, pp. 316 - 324
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Medical genetics | Developmental disorders | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Child clinical studies | Autistic Disorder - genetics | Cell Line | Humans | Gene Expression Regulation | Mutagenesis - genetics | Male | DNA Mutational Analysis - methods | Mutation - genetics | Schizophrenia - genetics | Base Pairing - genetics | Family | Female | Chromosome Segregation - genetics | Cohort Studies | Autism | Gene mutations | Analysis | Schizophrenia | Genetic aspects | Research | Population genetics | Genetics | Mutation | Deoxyribonucleic acid--DNA | Index Medicus
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9. Full Text A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura
by Marcinkiewicz, Martin M and Sequeiros, Jorge and Tucker, Stephen J and Poulin, Jean-François and Ramagopalan, Sreeram and Cader, M Zameel and McLaughlan, Shannon and Boisvert, Karine and Griffiths, Lyn R and Dubé, Marie-Pierre and Lafrenière, François and Pereira-Monteiro, Jose Maria and Ebers, George and Simoneau, Maryse and Brais, Bernard and Rouleau, Guy A and Ansorge, Olaf and Andres-Enguix, Isabelle and Gupta, Namrata and Lafrenière, Ronald G
Nature medicine, ISSN 1078-8956, 10/2010, Volume 16, Issue 10, pp. 1157 - 1160
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Cell Biology | Research & Experimental Medicine | Animals | Humans | Potassium Channels - physiology | Mice | Polymorphism, Single Nucleotide | Migraine with Aura - genetics | Mutation | Genetic Linkage | Potassium Channels - genetics | Gene mutations | Migraine | Physiological aspects | Genetic aspects | Potassium channels | Properties | Gene expression | Identification and classification | Neurology | Genetics | Potassium | Index Medicus
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