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A multi-omics study of circulating phospholipid markers of blood pressure.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04446-7
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- Publication type:
- Article
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.
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- PLoS Genetics, 2019, v. 15, n. 11, p. 1, doi. 10.1371/journal.pgen.1008480
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- Publication type:
- Article
Evidence for a role in growth and salt resistance of a plasma membrane H<sup>+</sup>-ATPase in the root endodermis.
- Published in:
- Plant Journal, 2001, v. 27, n. 3, p. 191, doi. 10.1046/j.1365-313X.2001.01081.x
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- Publication type:
- Article
Genome-wide linkage analysis of serum creatinine in three isolated European populations.
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- Kidney International, 2009, v. 76, n. 3, p. 297, doi. 10.1038/ki.2009.135
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- Publication type:
- Article
Genome-Wide Association Study (GWAS) of plasma Aß levels in the dalmatian islands of Vis and korcula
- Published in:
- 2009
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- Publication type:
- Abstract
Genome-wide association analysis identifies six new loci associated with forced vital capacity.
- Published in:
- Nature Genetics, 2014, v. 46, n. 7, p. 669, doi. 10.1038/ng.3011
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- Publication type:
- Article
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
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- Nature Genetics, 2013, v. 45, n. 2, p. 145, doi. 10.1038/ng.2500
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- Publication type:
- Article
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
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- Nature Genetics, 2013, v. 45, n. 2, p. 155, doi. 10.1038/ng.2506
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- Publication type:
- Article
Genome-wide association study identifies five loci associated with lung function.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 36, doi. 10.1038/ng.501
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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
Variants in STAT5B associate with serum TC and LDL-C levels.
- Published in:
- 2011
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- Publication type:
- journal article
Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson's Disease.
- Published in:
- Journal of Molecular Neuroscience, 2011, v. 43, n. 3, p. 246, doi. 10.1007/s12031-010-9409-y
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- Publication type:
- Article
A phenome-wide association and factorial Mendelian randomization study on the repurposing of uric acid-lowering drugs for cardiovascular outcomes.
- Published in:
- European Journal of Epidemiology, 2024, v. 39, n. 8, p. 869, doi. 10.1007/s10654-024-01138-0
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- Publication type:
- Article
Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 Loci.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107110
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- Publication type:
- Article
Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068604
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- Publication type:
- Article
Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping.
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- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046501
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- Publication type:
- Article
Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates.
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- 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
A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample.
- Published in:
- PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0019382
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- Publication type:
- Article
Concordant Association of Insulin Degrading Enzyme Gene (IDE) Variants with IDE mRNA, Aß, and Alzheimer's Disease.
- Published in:
- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008764
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- Publication type:
- Article
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits.
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- PLoS Genetics, 2020, v. 16, n. 7, p. 1, doi. 10.1371/journal.pgen.1008785
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- Publication type:
- Article
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium.
- Published in:
- Human Genetics, 2012, v. 131, n. 9, p. 1467, doi. 10.1007/s00439-012-1176-0
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- Publication type:
- Article
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-07819-1
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- Publication type:
- Article
Inference of identity by descent in population isolates and optimal sequencing studies.
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- 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
Genome-wide analysis of epistasis in body mass index using multiple human populations.
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- 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
Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits.
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- 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
Genes predict village of origin in rural Europe.
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- European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1269, doi. 10.1038/ejhg.2010.92
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- Publication type:
- Article
Quantifying the increase in average human heterozygosity due to urbanisation.
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- 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
3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 478, doi. 10.1038/sj.ejhg.5201589
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- Publication type:
- Article
Individual multi-locus heterozygosity is associated with lower morning plasma cortisol concentrations.
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- European Journal of Endocrinology, 2013, v. 169, n. 1, p. 59, doi. 10.1530/EJE-12-0916
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- Publication type:
- Article
Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants.
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- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-01497-w
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- Publication type:
- Article
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
- Published in:
- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0802-y
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- Publication type:
- Article
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
- Published in:
- Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0634-9
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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
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
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.
- Published in:
- Nature Communications, 2016, v. 7, n. 3, p. 11008, doi. 10.1038/ncomms11008
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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
Genomics Meets Glycomics--The First GWAS Study of Human N-Glycome Identifies HNF1α as a Master Regulator of Plasma Protein Fucosylation.
- Published in:
- PLoS Pathogens, 2011, v. 7, n. 2, p. 1, doi. 10.1371/journal.pgen.1001256
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- Publication type:
- Article
Insights into the genetic basis of retinal detachment.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 4, p. 689, doi. 10.1093/hmg/ddz294
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- Publication type:
- Article
Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 14, p. 4167, doi. 10.1093/hmg/ddv145
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- Publication type:
- Article
Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 20, p. 5527, doi. 10.1093/hmg/ddu253
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- Publication type:
- Article
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 23, p. 4857, doi. 10.1093/hmg/ddt336
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- Publication type:
- Article
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 13, p. 2754
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- Publication type:
- Article
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 24, p. 5000, doi. 10.1093/hmg/ddr414
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- Publication type:
- Article
The long and short‐'sightedness' of BMP3 in eye development.
- Published in:
- Acta Ophthalmologica (1755375X), 2022, v. 100, p. N.PAG, doi. 10.1111/j.1755-3768.2022.0670
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- Publication type:
- Article
A mouse model of brittle cornea syndrome type 2.
- Published in:
- Acta Ophthalmologica (1755375X), 2022, v. 100, p. N.PAG, doi. 10.1111/j.1755-3768.2022.0383
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- Publication type:
- Article
Investigating the use of translational readthrough inducing drugs in keratocytes from a mouse model of brittle cornea syndrome.
- Published in:
- Acta Ophthalmologica (1755375X), 2022, v. 100, p. N.PAG, doi. 10.1111/j.1755-3768.2022.0381
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- Publication type:
- Article
Directional dominance on stature and cognition in diverse human populations.
- Published in:
- Nature, 2015, v. 523, n. 7561, p. 459, doi. 10.1038/nature14618
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- Publication type:
- Article
FTO genotype is associated with phenotypic variability of body mass index.
- Published in:
- Nature, 2012, v. 490, n. 7419, p. 267, doi. 10.1038/nature11401
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- Publication type:
- Article
Regional variation in health is predominantly driven by lifestyle rather than genetics.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00497-5
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- Publication type:
- Article