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Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.
- Published in:
- 2022
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- Publication type:
- Correction Notice
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32009-5
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- Publication type:
- Article
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32009-5
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- Publication type:
- Article
LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancer.
- Published in:
- BMC Bioinformatics, 2016, v. 17, p. 1, doi. 10.1186/s12859-016-0935-7
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- Publication type:
- Article
Extended Overnight Monitoring of Respiratory Events after Bariatric Surgery.
- Published in:
- Surgeries (2673-4095), 2023, v. 4, n. 3, p. 483, doi. 10.3390/surgeries4030047
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- Publication type:
- Article
The origins and genetic interactions of KRAS mutations are allele- and tissue-specific.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22125-z
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- Publication type:
- Article
Clinical and morphological effects of hyperbaric oxygen therapy in patients with interstitial cystitis associated with fibromyalgia.
- Published in:
- 2019
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- Publication type:
- journal article
Risk of new‐onset diabetes and efficacy of pharmacological weight loss therapy.
- Published in:
- Diabetes, Obesity & Metabolism, 2024, v. 26, n. 10, p. 4441, doi. 10.1111/dom.15798
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- Publication type:
- Article
A polygenic risk score predicts atrial fibrillation in cardiovascular disease.
- Published in:
- European Heart Journal, 2023, v. 44, n. 3, p. 221, doi. 10.1093/eurheartj/ehac460
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- Publication type:
- Article
Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07730-9
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- Publication type:
- Article
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07070-8
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- Publication type:
- Article
A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data.
- Published in:
- 2017
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- Publication type:
- journal article
Organizational aspects of pediatric anesthesia and surgery between two waves of Covid‐19.
- Published in:
- Acta Anaesthesiologica Scandinavica, 2021, v. 65, n. 6, p. 755, doi. 10.1111/aas.13802
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- Publication type:
- Article
Estimating and presenting hazard ratios and absolute risks from a Cox model with complex nonlinear interactions.
- Published in:
- American Journal of Epidemiology, 2024, v. 193, n. 8, p. 1155, doi. 10.1093/aje/kwae037
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- Publication type:
- Article
DOTS-Finder: a comprehensive tool for assessing driver genes in cancer genomes.
- Published in:
- Genome Medicine, 2014, v. 6, n. 6, p. 1, doi. 10.1186/gm563
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- Publication type:
- Article
Very low-depth whole-genome sequencing in complex trait association studies.
- Published in:
- Bioinformatics, 2019, v. 35, n. 15, p. 2555, doi. 10.1093/bioinformatics/bty1032
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- Publication type:
- Article
INSPEcT: a computational tool to infer mRNA synthesis, processing and degradation dynamics from RNA- and 4sU-seq time course experiments.
- Published in:
- Bioinformatics, 2015, v. 31, n. 17, p. 2829, doi. 10.1093/bioinformatics/btv288
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- Publication type:
- Article