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Spironolactone metabolite concentrations in decompensated heart failure: insights from the ATHENA-HF trial.
- Published in:
- 2020
- By:
- Publication type:
- journal article
No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Older adults with heart failure treated with carvedilol, bisoprolol, or metoprolol tartrate: risk of mortality.
- Published in:
- Pharmacoepidemiology & Drug Safety, 2017, v. 26, n. 1, p. 81, doi. 10.1002/pds.4132
- By:
- Publication type:
- Article
Validation of patient-reported warfarin dose in a prospective incident cohort study.
- Published in:
- 2014
- By:
- Publication type:
- Other
Autosomal-dominant locus for restless legs syndrome in French-Canadians on chromosome 16p12.1.
- Published in:
- Movement Disorders, 2009, v. 24, n. 1, p. 40, doi. 10.1002/mds.22263
- By:
- Publication type:
- Article
Sex, drugs, and heart failure: a sex‐sensitive review of the evidence base behind current heart failure clinical guidelines.
- Published in:
- ESC Heart Failure, 2018, v. 5, n. 5, p. 745, doi. 10.1002/ehf2.12307
- By:
- Publication type:
- Article
Impact of amiodarone use on metoprolol concentrations, α‐OH‐metoprolol concentrations, metoprolol dosing and heart rate: A cross‐sectional study.
- Published in:
- Pharmacology Research & Perspectives, 2023, v. 11, n. 5, p. 1, doi. 10.1002/prp2.1137
- By:
- Publication type:
- Article
Risk of congenital heart defects is influenced by genetic variation in folate metabolism.
- Published in:
- Cardiology in the Young, 2013, v. 23, n. 1, p. 89, doi. 10.1017/S1047951112000431
- By:
- Publication type:
- Article
Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in Quebec.
- Published in:
- Cardiology in the Young, 2011, v. 21, n. 6, p. 654, doi. 10.1017/S1047951111000813
- By:
- Publication type:
- Article
A Discrete Event Simulation Model to Assess the Economic Value of a Hypothetical Pharmacogenomics Test for Statin-Induced Myopathy in Patients Initiating a Statin in Secondary Cardiovascular Prevention.
- Published in:
- Molecular Diagnosis & Therapy, 2018, v. 22, n. 2, p. 241, doi. 10.1007/s40291-018-0323-2
- By:
- Publication type:
- Article
The challenge of detecting epistasis (G×G Interactions): Genetic Analysis Workshop 16.
- Published in:
- Genetic Epidemiology, 2009, v. 33, n. S1, p. S58, doi. 10.1002/gepi.20474
- By:
- Publication type:
- Article
Multistage designs in the genomic era: Providing balance in complex disease studies.
- Published in:
- Genetic Epidemiology, 2007, v. 31, n. S1, p. S118, doi. 10.1002/gepi.20288
- By:
- Publication type:
- Article
Loss-of-function genetic diseases and the concept of pharmaceutical targets.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Human monogenic disorders — a source of novel drug targets.
- Published in:
- Nature Reviews Genetics, 2006, v. 7, n. 4, p. 249, doi. 10.1038/nrg1828
- By:
- Publication type:
- Article
Mutations in the calcium-related gene IL1RAPL1 are associated with autism.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 24, p. 3965
- By:
- Publication type:
- Article
Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve.
- Published in:
- Nature Communications, 2017, v. 8, n. 5, p. 15481, doi. 10.1038/ncomms15481
- By:
- Publication type:
- Article
Pharmacogenetics of Lipid-Lowering Agents: an Update Review on Genotype-Dependent Effects of HDL-Targetingand Statin Therapies.
- Published in:
- Current Atherosclerosis Reports, 2017, v. 19, n. 11, p. 1, doi. 10.1007/s11883-017-0679-5
- By:
- Publication type:
- Article
Comparison of genotype clustering tools with rare variants.
- Published in:
- BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-52
- By:
- Publication type:
- Article
Partitioning of copy-number genotypes in pedigrees.
- Published in:
- BMC Bioinformatics, 2010, v. 11, p. 226, doi. 10.1186/1471-2105-11-226
- By:
- Publication type:
- Article
A sex-specific evolutionary interaction between ADCY9 and CETP.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.69198
- By:
- Publication type:
- Article
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 372, doi. 10.1038/sj.ejhg.5200471
- By:
- Publication type:
- Article
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
- Published in:
- Nature Genetics, 2014, v. 46, n. 6, p. 629, doi. 10.1038/ng.2962
- By:
- Publication type:
- Article
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.
- Published in:
- Nature Genetics, 2013, v. 45, n. 5, p. 578, doi. 10.1038/ng.0513-578
- By:
- Publication type:
- Article
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.
- Published in:
- Nature Genetics, 2009, v. 41, n. 12, p. 1345, doi. 10.1038/ng.478
- By:
- Publication type:
- Article
Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis.
- Published in:
- 2004
- By:
- Publication type:
- Letter
DNA methylation changes in fetal alcohol spectrum disorder.
- Published in:
- International Journal of Developmental Neuroscience, 2015, v. 47, p. 126, doi. 10.1016/j.ijdevneu.2015.04.336
- By:
- Publication type:
- Article
Pharmacogenetics-guided dalcetrapib therapy after an acute coronary syndrome.
- Published in:
- European Heart Journal, 2022, v. 43, n. 48, p. 5062, doi. 10.1093/eurheartj/ehac644
- By:
- Publication type:
- Article
Pharmacogenetics-guided dalcetrapib therapy after an acute coronary syndrome: the dal-GenE trial.
- Published in:
- European Heart Journal, 2022, v. 43, n. 39, p. 3947, doi. 10.1093/eurheartj/ehac374
- By:
- Publication type:
- Article
Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?
- Published in:
- Annals of the New York Academy of Sciences, 2022, v. 1517, n. 1, p. 279, doi. 10.1111/nyas.14883
- By:
- Publication type:
- Article
Comparative effectiveness and safety of high‐dose rivaroxaban and apixaban for atrial fibrillation: A propensity score‐matched cohort study.
- Published in:
- Pharmacotherapy, 2021, v. 41, n. 4, p. 379, doi. 10.1002/phar.2509
- By:
- Publication type:
- Article
Oral Anticoagulant Prescription Trends, Profile Use, and Determinants of Adherence in Patients with Atrial Fibrillation.
- Published in:
- Pharmacotherapy, 2020, v. 40, n. 1, p. 40, doi. 10.1002/phar.2350
- By:
- Publication type:
- Article
Pharmacogenomics to Revive Drug Development in Cardiovascular Disease.
- Published in:
- Cardiovascular Drugs & Therapy, 2016, v. 30, n. 1, p. 59, doi. 10.1007/s10557-015-6637-y
- By:
- Publication type:
- Article
Segregation of LIPG, CETP, and GALNT2 Mutations in Caucasian Families with Extremely High HDL Cholesterol.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0037437
- By:
- Publication type:
- Article
Application of Homozygosity Haplotype Analysis to Genetic Mapping with High-Density SNP Genotype Data.
- Published in:
- PLoS ONE, 2009, v. 4, n. 4, p. 1, doi. 10.1371/journal.pone.0005280
- By:
- Publication type:
- Article
Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.
- Published in:
- Nature Genetics, 2002, v. 32, n. 2, p. 326, doi. 10.1038/ng957
- By:
- Publication type:
- Article
Whole-genome sequencing in French Canadians from Quebec.
- Published in:
- Human Genetics, 2016, v. 135, n. 11, p. 1213, doi. 10.1007/s00439-016-1702-6
- By:
- Publication type:
- Article
Modifiers of (CAG) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes.
- Published in:
- Human Genetics, 2014, v. 133, n. 10, p. 1311, doi. 10.1007/s00439-014-1467-8
- By:
- Publication type:
- Article
Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30875-7
- By:
- Publication type:
- Article
A genetic model of ivabradine recapitulates results from randomized clinical trials.
- Published in:
- PLoS ONE, 2020, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0236193
- By:
- Publication type:
- Article
Impact of regular physical activity on weekly warfarin dose requirement.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2016, v. 41, n. 2, p. 328, doi. 10.1007/s11239-015-1248-9
- By:
- Publication type:
- Article
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme.
- Published in:
- ESC Heart Failure, 2022, v. 9, n. 5, p. 2997, doi. 10.1002/ehf2.14026
- By:
- Publication type:
- Article
A genetic association study of heart failure: more evidence for the role of BAG3 in idiopathic dilated cardiomyopathy.
- Published in:
- ESC Heart Failure, 2020, v. 7, n. 6, p. 4384, doi. 10.1002/ehf2.12934
- By:
- Publication type:
- Article
Genetics of symptom remission in outpatients with COVID-19.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-90365-6
- By:
- Publication type:
- Article
Comparative Effectiveness and Safety of Low-Dose Oral Anticoagulants in Patients With Atrial Fibrillation.
- Published in:
- Frontiers in Pharmacology, 2022, v. 12, p. 1, doi. 10.3389/fphar.2021.812018
- By:
- Publication type:
- Article
Ten renin-angiotensin system-related gene polymorphisms in maximally treated Canadian Caucasian patients with heart failure.
- Published in:
- British Journal of Clinical Pharmacology, 2008, v. 65, n. 5, p. 742, doi. 10.1111/j.1365-2125.2007.03091.x
- By:
- Publication type:
- Article
ExPheWas: a platform for cis-Mendelian randomization and gene-based association scans.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. W1, p. W305, doi. 10.1093/nar/gkac289
- By:
- Publication type:
- Article
Methylomic changes in individuals with psychosis, prenatally exposed to endocrine disrupting compounds: Lessons from diethylstilbestrol.
- Published in:
- PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0174783
- By:
- Publication type:
- Article
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals.
- Published in:
- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164212
- By:
- Publication type:
- Article
Females present higher dose‐adjusted drug concentrations of metoprolol and allopurinol/oxypurinol than males.
- Published in:
- CTS: Clinical & Translational Science, 2023, v. 16, n. 5, p. 872, doi. 10.1111/cts.13497
- By:
- Publication type:
- Article
pyGenClean: efficient tool for genetic data clean up before association testing.
- Published in:
- Bioinformatics, 2013, v. 29, n. 13, p. 1704, doi. 10.1093/bioinformatics/btt261
- By:
- Publication type:
- Article