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Sex Chromosomal Transposable Element Accumulation and Male-Driven Substitutional Evolution in Humans.
- Published in:
- Molecular Biology & Evolution, 2000, v. 17, n. 5, p. 804, doi. 10.1093/oxfordjournals.molbev.a026359
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- Publication type:
- Article
Retinal arteriolar tortuosity and fractal dimension are associated with long-term cardiovascular outcomes in people with type 2 diabetes.
- Published in:
- Diabetologia, 2021, v. 64, n. 10, p. 2215, doi. 10.1007/s00125-021-05499-z
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- Publication type:
- Article
Correction to: Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes.
- Published in:
- 2018
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- Publication type:
- Erratum
Prevalence and clinical prediction of osteoporosis in a contemporary cohort of patients with rheumatoid arthritis.
- Published in:
- 2014
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- Publication type:
- Journal Article
Prevalence and clinical prediction of osteoporosis in a contemporary cohort of patients with rheumatoid arthritis.
- Published in:
- Rheumatology, 2014, v. 53, n. 10, p. 1759, doi. 10.1093/rheumatology/keu162
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- Publication type:
- Article
Large scale phenotype imputation and in vivo functional validation implicate ADAMTS14 as an adiposity gene.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-022-35563-0
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- Publication type:
- Article
Weighted functional linear regression models for gene-based association analysis.
- Published in:
- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0190486
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- Publication type:
- Article
Recent genomic heritage in Scotland.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1605-2
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- Publication type:
- Article
Validity of the DIAL-R for Identifying Children with Special Education Needs and Predicting Early Reading Achievement.
- Published in:
- Journal of Psychoeducational Assessment, 1988, v. 6, n. 3, p. 289, doi. 10.1177/073428298800600312
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- Publication type:
- Article
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 21, p. 4304, doi. 10.1093/hmg/ddq349
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- Publication type:
- Article
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01490-8
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- Publication type:
- Article
Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00453-3
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- Publication type:
- Article
Bayesian association scan reveals loci associated with human lifespan and linked biomarkers.
- Published in:
- Nature Communications, 2017, v. 8, n. 7, p. 15842, doi. 10.1038/ncomms15842
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- Publication type:
- Article
Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan.
- Published in:
- Nature Communications, 2016, v. 7, n. 3, p. 11174, doi. 10.1038/ncomms11174
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- Publication type:
- Article
Multicohort analysis of the maternal age effect on recombination.
- Published in:
- Nature Communications, 2015, v. 6, n. 8, p. 7846, doi. 10.1038/ncomms8846
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- Publication type:
- Article
Inference of identity by descent in population isolates and optimal sequencing studies.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1140, doi. 10.1038/ejhg.2012.307
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- Publication type:
- Article
Serum metabolomic profiles associated with subclinical and clinical cardiovascular phenotypes in people with type 2 diabetes.
- Published in:
- Cardiovascular Diabetology, 2022, v. 21, n. 1, p. 1, doi. 10.1186/s12933-022-01493-w
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- Publication type:
- Article
Comparative assessment of methods for estimatingindividual genome-wide homozygosity-by-descentfrom human genomic data.
- Published in:
- BMC Genomics, 2010, v. 11, p. 139, doi. 10.1186/1471-2164-11-139
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- Publication type:
- Article
Genome-wide analysis of epistasis in body mass index using multiple human populations.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 8, p. 857, doi. 10.1038/ejhg.2012.17
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- Publication type:
- Article
Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 2, p. 198, doi. 10.1038/ejhg.2011.170
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- Publication type:
- Article
Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 1, p. 77, doi. 10.1038/ejhg.2011.138
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- Publication type:
- Article
Population structure and genome-wide patterns of variation in Ireland and Britain.
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- European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1248, doi. 10.1038/ejhg.2010.87
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- Publication type:
- Article
Comparison of participant information and informed consent forms of five European studies in genetic isolated populations.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 296, doi. 10.1038/ejhg.2009.155
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- Publication type:
- Article
Quantifying the increase in average human heterozygosity due to urbanisation.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1097, doi. 10.1038/ejhg.2008.48
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- Publication type:
- Article
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 47, doi. 10.1038/ng.269
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- Publication type:
- Article
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout.
- Published in:
- Nature Genetics, 2008, v. 40, n. 4, p. 437, doi. 10.1038/ng.106
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- Publication type:
- Article
Mendelian randomisation identifies priority groups for prophylactic EBV vaccination.
- Published in:
- BMC Infectious Diseases, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12879-023-08031-3
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- Publication type:
- Article
Genome Wide Association Identifies Common Variants at the <i>SERPINA6/SERPINA1</i> Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 7, p. 1, doi. 10.1371/journal.pgen.1004474
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- Publication type:
- Article
Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002490
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- Publication type:
- Article
Modeling of Environmental Effects in Genome-Wide Association Studies Identifies SLC2A2 and HP as Novel Loci Influencing Serum Cholesterol Levels.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 1, p. 1, doi. 10.1371/journal.pgen.1000798
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- Publication type:
- Article
Comparative analysis of transferrin and IgG N-glycosylation in two human populations.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-04685-6
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- Publication type:
- Article
Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene.
- Published in:
- Obesity (19307381), 2010, v. 18, n. 4, p. 803, doi. 10.1038/oby.2009.359
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- Publication type:
- Article
A NEW INCOMPATIBILITY LOCUS IN NEUROSPORA CRASSA.
- Published in:
- Genetics, 1966, v. 53, n. 3, p. 621
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- Publication type:
- Article
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.
- Published in:
- eLife, 2019, p. 1, doi. 10.7554/eLife.39856
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- Publication type:
- Article
Nontrivial Replication of Loci Detected by Multi-Trait Methods.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.627989
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- Publication type:
- Article
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09301-y
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- Publication type:
- Article
Author Correction: GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04857-7
- By:
- Publication type:
- Article
Reply to ‘Misestimation of heritability and prediction accuracy of male-pattern baldness’.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04808-2
- By:
- Publication type:
- Article
The TCF7L2 Diabetes Risk Variant is Associated with HbA<sub>1C</sub> Levels: a Genome-Wide Association Meta-Analysis.
- Published in:
- Annals of Human Genetics, 2010, v. 74, n. 6, p. 471, doi. 10.1111/j.1469-1809.2010.00607.x
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- Publication type:
- Article
Regional variation in the incidence rate and sex ratio of multiple sclerosis in Scotland 2010–2017: findings from the Scottish Multiple Sclerosis Register.
- Published in:
- Journal of Neurology, 2019, v. 266, n. 10, p. 2376, doi. 10.1007/s00415-019-09413-x
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- Publication type:
- Article
A combined long-range phasing and long haplotype imputation method to impute phase for SNP genotypes.
- Published in:
- Genetics Selection Evolution, 2011, v. 43, n. 3, p. 1, doi. 10.1186/1297-9686-43-12
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- Publication type:
- Article
Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-67001-w
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- Publication type:
- Article
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47436-6
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- Publication type:
- Article
Autozygosity influences cardiometabolic disease-associated traits in the AWI-Gen sub-Saharan African study.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-19595-y
- By:
- Publication type:
- Article
Evaluation of Bioelectrical Impedance Analysis for Identifying Overweight Individuals at Increased Cardiometabolic Risk: A Cross-Sectional Study.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106134
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- Publication type:
- Article
Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068604
- By:
- Publication type:
- Article
Improvement in Prediction of Coronary Heart Disease Risk over Conventional Risk Factors Using SNPs Identified in Genome-Wide Association Studies.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057310
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- Publication type:
- Article
Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023836
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- Publication type:
- Article
Copy Number Variation across European Populations.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023087
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- Publication type:
- Article