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High SHBG and Low Bioavailable Testosterone are Strongly Causally Associated with Increased Forearm Fracture Risk in Women: An MR Study Leveraging Novel Female-Specific Data.
- Published in:
- Calcified Tissue International, 2024, v. 115, n. 5, p. 648, doi. 10.1007/s00223-024-01301-5
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- Article
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-022-32936-3
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- Publication type:
- Article
Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34461-9
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- Publication type:
- Article
Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31188-5
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- Publication type:
- Article
Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease.
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- BMC Research Notes, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13104-019-4807-x
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- Publication type:
- Article
Polygenic risk scores for cervical HPV infection, neoplasia and cancer show potential for personalised screening: comparison of two methods.
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- Infectious Agents & Cancer, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13027-023-00561-4
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- Publication type:
- Article
MARV: a tool for genome-wide multiphenotype analysis of rare variants.
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- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-017-1530-2
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- Publication type:
- Article
SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes.
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- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-016-1437-3
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- Publication type:
- Article
Comparison of variation in frequency for SNPs associated with asthma or liver disease between Estonia, HapMap populations and the 1000 genome project populations.
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- International Journal of Immunogenetics, 2019, v. 46, n. 2, p. 49, doi. 10.1111/iji.12413
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- Article
Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
- Published in:
- 2019
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- Correction Notice
Causal relationships between obesity and the leading causes of death in women and men.
- Published in:
- PLoS Genetics, 2019, v. 15, n. 10, p. 1, doi. 10.1371/journal.pgen.1008405
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- Publication type:
- Article
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
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- PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007813
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- Publication type:
- Article
Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays.
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- Nucleic Acids Research, 2008, v. 36, n. 12, p. e75, doi. 10.1093/nar/gkn357
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- Publication type:
- Article
Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27258-9
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- Publication type:
- Article
Genome-wide association study identifies five risk loci for pernicious anemia.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24051-6
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- Publication type:
- Article
Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22538-w
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- Publication type:
- Article
Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population.
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- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 7, p. 974, doi. 10.1515/CCLM.2008.187
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- Publication type:
- Article
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index.
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- Nature Genetics, 2015, v. 47, n. 10, p. 1114, doi. 10.1038/ng.3390
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- Publication type:
- Article
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
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- Nature Genetics, 2013, v. 45, n. 5, p. 501, doi. 10.1038/ng.2606
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- Publication type:
- Article
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.
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- Nature Genetics, 2012, v. 44, n. 9, p. 991, doi. 10.1038/ng.2385
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- Publication type:
- Article
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
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- 2011
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- Correction Notice
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
- Published in:
- Nature Genetics, 2010, v. 42, n. 11, p. 949, doi. 10.1038/ng.685
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- Publication type:
- Article
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
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- Nature Genetics, 2010, v. 42, n. 11, p. 937, doi. 10.1038/ng.686
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- Publication type:
- Article
Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior.
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- Nature Genetics, 2010, v. 42, n. 5, p. 448, doi. 10.1038/ng.573
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- Publication type:
- Article
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.
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- Nature Genetics, 2010, v. 42, n. 5, p. 430, doi. 10.1038/ng.567
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- Article
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
- Published in:
- 2010
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- Publication type:
- Correction Notice
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
- Published in:
- Nature Genetics, 2010, v. 42, n. 2, p. 105, doi. 10.1038/ng.520
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- Publication type:
- Article
Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH.
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- Diabetologia, 2023, v. 66, n. 7, p. 1260, doi. 10.1007/s00125-023-05922-7
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- Publication type:
- Article
Selective sweep on human amylase genes postdates the split with Neanderthals.
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- Scientific Reports, 2016, p. 37198, doi. 10.1038/srep37198
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- Publication type:
- Article
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41180-2
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- Publication type:
- Article
Rare copy-number variants as modulators of common disease susceptibility.
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- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-023-01265-5
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- Article
Mapping the Genetic Architecture of Gene Regulation in Whole Blood.
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- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0093844
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- Article
Contribution of 32 GWAS-Identified Common Variants to Severe Obesity in European Adults Referred for Bariatric Surgery.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070735
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- Publication type:
- Article
Genetic Structure of Europeans: A View from the North-East.
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- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005472
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- Publication type:
- Article
Estimation of recurrent atherosclerotic cardiovascular event risk in patients with established cardiovascular disease: the updated SMART2 algorithm.
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- European Heart Journal, 2022, v. 43, n. 18, p. 1715, doi. 10.1093/eurheartj/ehac056
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- Article
Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02196-2
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- Article
Improved polygenic prediction by Bayesian multiple regression on summary statistics.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-12653-0
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- Publication type:
- Article
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12522-w
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- Publication type:
- Article
Polygenic Risk Score Predicts Modified Risk in BRCA1 Pathogenic Variant c.4035del and c.5266dup Carriers in Breast Cancer Patients.
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- Cancers, 2023, v. 15, n. 11, p. 2957, doi. 10.3390/cancers15112957
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- Article
Genomic inflation factors under polygenic inheritance.
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- European Journal of Human Genetics, 2011, v. 19, n. 7, p. 807, doi. 10.1038/ejhg.2011.39
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- Article
Haplotypes in the human Foxo1a and Foxo3a genes; impact on disease and mortality at old age.
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- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 294, doi. 10.1038/sj.ejhg.5201766
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- Article
Uncovering the shared genetic components of thyroid disorders and reproductive health.
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- European Journal of Endocrinology, 2024, v. 191, n. 2, p. 211, doi. 10.1093/ejendo/lvae094
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- Publication type:
- Article
Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation.
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- BMC Genomics, 2007, v. 8, p. 159, doi. 10.1186/1471-2164-8-159
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- Publication type:
- Article
GWAMA: software for genome-wide associationmeta-analysis.
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- BMC Bioinformatics, 2010, v. 11, p. 288, doi. 10.1186/1471-2105-11-288
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- Publication type:
- Article
Circulating anti-Müllerian hormone levels in pre-menopausal women: novel genetic insights from a genome-wide association meta-analysis.
- Published in:
- Human Reproduction, 2024, v. 39, n. 7, p. 1564, doi. 10.1093/humrep/deae117
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- Publication type:
- Article
Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancy.
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- Human Reproduction, 2023, v. 38, n. 12, p. 2516, doi. 10.1093/humrep/dead217
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- Article
Endometrial receptivity revisited: endometrial transcriptome adjusted for tissue cellular heterogeneity.
- Published in:
- 2018
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- Publication type:
- journal article
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry.
- Published in:
- BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-09990-w
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- Publication type:
- Article
RegScan: a GWAS tool for quick estimation of allele effects on continuous traits and their combinations.
- Published in:
- Briefings in Bioinformatics, 2015, v. 16, n. 1, p. 39, doi. 10.1093/bib/bbt066
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- Publication type:
- Article
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 12, p. 2103, doi. 10.1093/hmg/ddad043
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- Publication type:
- Article