Found: 12
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Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 9, p. 1, doi. 10.1371/journal.pgen.1002903
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- Article
A genetic model of ivabradine recapitulates results from randomized clinical trials.
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- PLoS ONE, 2020, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0236193
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- 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
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- 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
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- Article
Methylomic changes in individuals with psychosis, prenatally exposed to endocrine disrupting compounds: Lessons from diethylstilbestrol.
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- PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0174783
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- 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
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- 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
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- Article
Study of effect modifiers of genetically predicted CETP reduction.
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- Genetic Epidemiology, 2023, v. 47, n. 2, p. 198, doi. 10.1002/gepi.22514
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- Article
Construction of a femininity score in the UK Biobank and its association with angina diagnosis prior to myocardial infarction.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05713-x
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- Article
A Genome-Wide Association Study of Oxypurinol Concentrations in Patients Treated with Allopurinol.
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- Journal of Personalized Medicine, 2024, v. 14, n. 6, p. 649, doi. 10.3390/jpm14060649
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- Article
DNA methylation signature of human fetal alcohol spectrum disorder.
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- Epigenetics & Chromatin, 2016, v. 9, p. 1, doi. 10.1186/s13072-016-0074-4
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- Article
Comparison of Sequencing Based CNV Discovery Methods Using Monozygotic Twin Quartets.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0122287
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- Article