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Investigation of the human ANP gene in type 1 diabetic nephropathy: case-control and follow-up studies.
- Published in:
- 2004
- By:
- Publication type:
- journal article
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.
- Published in:
- Diabetologia, 2019, v. 62, n. 2, p. 292, doi. 10.1007/s00125-018-4783-z
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- Publication type:
- Article
Environmental and genetic factors associated with morphine response in the postoperative period.
- Published in:
- Clinical Pharmacology & Therapeutics, 2006, v. 79, n. 4, p. 316, doi. 10.1016/j.clpt.2006.01.007
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- Publication type:
- Article
CYP3A5 and MDR1 Genetic Polymorphisms and Cyclosporine Pharmacokinetics After Renal Transplantation.
- Published in:
- Clinical Pharmacology & Therapeutics, 2004, v. 75, n. 5, p. 422, doi. 10.1016/j.clpt.2004.01.009
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- Publication type:
- Article
Pharmacogenetics of Acenocoumarol Pharmacodynamics<sup>*</sup>.
- Published in:
- Clinical Pharmacology & Therapeutics, 2004, v. 75, n. 5, p. 403, doi. 10.1016/j.clpt.2004.01.008
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- Publication type:
- Article
Combined effects of genetic and environmental factors on insulin resistance associated with reduced fetal growth.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Combines Effects of Genetic and Environmental Factors on Insulin Resistance Associated With Reduced Fetal Growth.
- Published in:
- Diabetes, 2002, v. 51, n. 12, p. 3473, doi. 10.2337/diabetes.51.12.3473
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- Publication type:
- Article
Bivariate familial correlation analysis of quantitative traits by use of estimating equations: Application to a familial analysis of the insulin resistance syndrome.
- Published in:
- Genetic Epidemiology, 1999, v. 16, n. 1, p. 69, doi. 10.1002/(SICI)1098-2272(1999)16:1<69::AID-GEPI6>3.0.CO;2-H
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- Publication type:
- Article
A systems-approach reveals human nestin is an endothelial-enriched, angiogenesis-independent intermediate filament protein.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-32859-4
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- Publication type:
- Article
High prevalence of laminopathies among patients with metabolic syndrome.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 19, p. 3779, doi. 10.1093/hmg/ddr294
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- Publication type:
- Article
Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 15, p. 1587, doi. 10.1093/hmg/ddh168
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- Publication type:
- Article
Platelet-activating factor-acetylhydrolase and PAF-receptor gene haplotypes in relation to future cardiovascular event in patients with coronary artery disease.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 13, p. 1341, doi. 10.1093/hmg/ddh145
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- Publication type:
- Article
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02306-5
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- Publication type:
- Article
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02306-5
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- Publication type:
- Article
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci.
- Published in:
- Nature Communications, 2015, v. 6, n. 2, p. 6326, doi. 10.1038/ncomms7326
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- Publication type:
- Article
Human thymopoiesis is influenced by a common genetic variant within the TCRA-TCRD locus.
- Published in:
- Science Translational Medicine, 2018, v. 10, n. 457, p. 1, doi. 10.1126/scitranslmed.aao2966
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- Publication type:
- Article
G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes.
- Published in:
- Diabetes, 2008, v. 57, n. 10, p. 2843, doi. 10.2337/db08-0073
- By:
- Publication type:
- Article
Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations.
- Published in:
- Diabetes, 2006, v. 55, n. 11, p. 3166, doi. 10.2337/db06-0271
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- Publication type:
- Article
Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans.
- Published in:
- G3: Genes | Genomes | Genetics, 2016, v. 6, n. 10, p. 3361, doi. 10.1534/g3.116.033894
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- Publication type:
- Article
Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM Project.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 12, p. 1512, doi. 10.1038/ejhg.2008.127
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- Publication type:
- Article
Serum myeloperoxidase concentration in a healthy population: biological variations, familial resemblance and new genetic polymorphisms.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 10, p. 780, doi. 10.1038/sj.ejhg.5200702
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- Publication type:
- Article
EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension.
- Published in:
- Nature Genetics, 2014, v. 46, n. 1, p. 65, doi. 10.1038/ng.2844
- By:
- Publication type:
- Article
Impaired balance between neutrophil extracellular trap formation and degradation by DNases in COVID-19 disease.
- Published in:
- Journal of Translational Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12967-024-05044-7
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- Publication type:
- Article
GUESS-ing Polygenic Associations with Multiple Phenotypes Using a GPU-Based Evolutionary Stochastic Search Algorithm.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 8, p. 1, doi. 10.1371/journal.pgen.1003657
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- Publication type:
- Article
Genome-Wide Haplotype Analysis of Cis Expression Quantitative Trait Loci in Monocytes.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003240
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- Publication type:
- Article
Effect of cytochrome P450 2C19 genotype on voriconazole exposure in cystic fibrosis lung transplant patients.
- Published in:
- European Journal of Clinical Pharmacology, 2011, v. 67, n. 3, p. 253, doi. 10.1007/s00228-010-0914-2
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- Publication type:
- Article
Plasma levels of hsa-miR-152-3p are associated with diabetic nephropathy in patients with type 2 diabetes.
- Published in:
- Nephrology Dialysis Transplantation, 2018, v. 33, n. 12, p. 2201, doi. 10.1093/ndt/gfx367
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- Publication type:
- Article
Gender-Specific Association of a Perilipin Gene Haplotype with Obesity Risk in a White Population<sup>**</sup>.
- Published in:
- Obesity (19307381), 2004, v. 12, n. 11, p. 1758, doi. 10.1038/oby.2004.218
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- Publication type:
- Article
DNA‐pools targeted‐sequencing as a robust cost‐effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis.
- Published in:
- Clinical Genetics, 2024, v. 105, n. 2, p. 185, doi. 10.1111/cge.14427
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- Publication type:
- Article
Targeted panel sequencing in adult patients with left ventricular non‐compaction reveals a large genetic heterogeneity.
- Published in:
- Clinical Genetics, 2019, v. 95, n. 3, p. 356, doi. 10.1111/cge.13484
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- Publication type:
- Article
Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.
- Published in:
- British Journal of Haematology, 2012, v. 157, n. 2, p. 230, doi. 10.1111/j.1365-2141.2011.09025.x
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- Publication type:
- Article
Deciphering the molecular basis of venous thromboembolism: where are we and where should we go?
- Published in:
- British Journal of Haematology, 2010, v. 148, n. 4, p. 495, doi. 10.1111/j.1365-2141.2009.07975.x
- By:
- Publication type:
- Article
MACARON: a python framework to identify and re-annotate multi-base affected codons in whole genome/exome sequence data.
- Published in:
- Bioinformatics, 2018, v. 34, n. 19, p. 3396, doi. 10.1093/bioinformatics/bty382
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- Publication type:
- Article
Anti-integrin αv therapy improves cardiac fibrosis after myocardial infarction by blunting cardiac PW1+ stromal cells.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-68223-8
- By:
- Publication type:
- Article
Genome-Wide Investigation of DNA Methylation Marks Associated with FV Leiden Mutation.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0108087
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- Publication type:
- Article
Graphical Modeling of Gene Expression in Monocytes Suggests Molecular Mechanisms Explaining Increased Atherosclerosis in Smokers.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0050888
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- Publication type:
- Article
Comprehensive Exploration of the Effects of miRNA SNPs on Monocyte Gene Expression.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045863
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- Publication type:
- Article
miR-421 and miR-30c Inhibit SERPINE 1 Gene Expression in Human Endothelial Cells.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0044532
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- Publication type:
- Article
Genetic Markers Enhance Coronary Risk Prediction in Men: The MORGAM Prospective Cohorts.
- Published in:
- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040922
- By:
- Publication type:
- Article
Caution in Interpreting Results from Imputation Analysis When Linkage Disequilibrium Extends over a Large Distance: A Case Study on Venous Thrombosis.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038538
- By:
- Publication type:
- Article
MFGE8 Does Not Influence Chorio-Retinal Homeostasis or Choroidal Neovascularization in vivo.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033244
- By:
- Publication type:
- Article
Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study.
- Published in:
- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0025581
- By:
- Publication type:
- Article
The Choice of the Filtering Method in Microarrays Affects the Inference Regarding Dosage Compensation of the Active X-Chromosome.
- Published in:
- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0023956
- By:
- Publication type:
- Article
What is currently known about the genetics of venous thromboembolism at the dawn of next generation sequencing technologies.
- Published in:
- British Journal of Haematology, 2018, v. 180, n. 3, p. 335, doi. 10.1111/bjh.15004
- By:
- Publication type:
- Article
Genetic Variations at the Endocannabinoid Type 1 Receptor Gene (CNR1) Are Associated with Obesity Phenotypes in Men.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 6, p. 2382, doi. 10.1210/jc.2006-2523
- By:
- Publication type:
- Article
Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study.
- Published in:
- Human Genetics, 2017, v. 136, n. 7, p. 897, doi. 10.1007/s00439-017-1811-x
- By:
- Publication type:
- Article
Design and Rationale of the ERA-CVD Consortium PREMED-CAD-Precision Medicine in Coronary Artery Disease.
- Published in:
- Biomolecules (2218-273X), 2020, v. 10, n. 1, p. 1, doi. 10.3390/biom10010125
- By:
- Publication type:
- Article
Small Open Reading Frames, How to Find Them and Determine Their Function.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2021.796060
- By:
- Publication type:
- Article
PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations.
- Published in:
- Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01117-2
- By:
- Publication type:
- Article