Found: 21
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Cigarette Smoking and the Risk of Cutaneous Melanoma: A Case-Control Study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Semi-Quantitative Multiplex Profiling of the Complement System Identifies Associations of Complement Proteins with Genetic Variants and Metabolites in Age-Related Macular Degeneration.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 12, p. 1256, doi. 10.3390/jpm11121256
- By:
- Publication type:
- Article
The Effects of Common Genetic Variation in 96 Genes Involved in Thyroid Hormone Regulation on TSH and FT4 Concentrations.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 6, p. e2276, doi. 10.1210/clinem/dgac136
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- Publication type:
- Article
Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6 -Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 3, p. 1917, doi. 10.3390/ijms23031917
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- Publication type:
- Article
Genomics Research of Lifetime Depression in the Netherlands: The BIObanks Netherlands Internet Collaboration (BIONIC) Project.
- Published in:
- Twin Research & Human Genetics, 2024, v. 27, n. 1, p. 1, doi. 10.1017/thg.2024.4
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- Publication type:
- Article
Underestimation of hepcidin concentration by time of flight mass spectrometry and competitive ELISA in hepcidin p.Gly71Asp heterozygotes.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 5, p. e173, doi. 10.1515/cclm-2015-0757
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- Publication type:
- Article
A Comparison of Multivariate Genome-Wide Association Methods.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0095923
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- Publication type:
- Article
Candidate Gene Sequencing of SLC11A2 and TMPRSS6 in a Family with Severe Anaemia: Common SNPs, Rare Haplotypes, No Causative Mutation.
- Published in:
- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035015
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- Publication type:
- Article
Towards Personalized TSH Reference Ranges: A Genetic and Population-Based Approach in Three Independent Cohorts.
- Published in:
- Thyroid, 2024, v. 34, n. 8, p. 969, doi. 10.1089/thy.2024.0045
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- Publication type:
- Article
Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?
- Published in:
- BMC Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12863-015-0246-4
- By:
- Publication type:
- Article
Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?
- Published in:
- BMC Genetics, 2015, v. 16, n. 1, p. 79, doi. 10.1186/s12863-015-0246-4
- By:
- Publication type:
- Article
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.
- Published in:
- Nature Communications, 2017, v. 8, n. 3, p. 14694, doi. 10.1038/ncomms14694
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- Publication type:
- Article
Known Susceptibility SNPs for Sporadic Prostate Cancer Show a Similar Association With "Hereditary" Prostate Cancer.
- Published in:
- Prostate, 2015, v. 75, n. 5, p. 474, doi. 10.1002/pros.22933
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- Publication type:
- Article
Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.
- Published in:
- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0166628
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- Publication type:
- Article
Standardized serum hepcidin values in Dutch children: Set point relative to body iron changes during childhood.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Polygenic risk scores for schizophrenia and bipolar disorder predict creativity.
- Published in:
- Nature Neuroscience, 2015, v. 18, n. 7, p. 953, doi. 10.1038/nn.4040
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- Publication type:
- Article
Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomization analysis.
- Published in:
- International Journal of Epidemiology, 2024, v. 53, n. 1, p. 1, doi. 10.1093/ije/dyad170
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- Publication type:
- Article
Cohort Profile: The Nijmegen Biomedical Study (NBS).
- Published in:
- 2017
- By:
- Publication type:
- journal article
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene.
- Published in:
- Genes, 2019, v. 10, n. 12, p. 1023, doi. 10.3390/genes10121023
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- Publication type:
- Article
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations.
- Published in:
- PLoS ONE, 2019, v. 14, n. 5, p. 1, doi. 10.1371/journal.pone.0217477
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- Publication type:
- Article
Fast and accurate recurrent event analysis for genome‐wide association studies.
- Published in:
- Genetic Epidemiology, 2023, v. 47, n. 5, p. 365, doi. 10.1002/gepi.22525
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- Publication type:
- Article