Works matching AU Hayward, Caroline
Results: 182
N-Glycan Profile and Kidney Disease in Type 1 Diabetes.
- Published in:
- 2018
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- Publication type:
- journal article
Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level.
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- Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0018-5
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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.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47436-6
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- Publication type:
- Article
Genome-wide characterization of 54 urinary metabolites reveals molecular impact of kidney function.
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- Nature Communications, 2025, v. 16, p. 1, doi. 10.1038/s41467-024-55182-1
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- Publication type:
- Article
Validation of Surrogates of Urine Osmolality in Population Studies.
- Published in:
- 2017
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- Publication type:
- journal article
Genomics Meets Glycomics--The First GWAS Study of Human N-Glycome Identifies HNF1α as a Master Regulator of Plasma Protein Fucosylation.
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- PLoS Pathogens, 2011, v. 7, n. 2, p. 1, doi. 10.1371/journal.pgen.1001256
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- Publication type:
- Article
Blood-based epigenome-wide analyses of 19 common disease states: A longitudinal, population-based linked cohort study of 18,413 Scottish individuals.
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- PLoS Medicine, 2023, v. 20, n. 7, p. 1, doi. 10.1371/journal.pmed.1004247
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- Publication type:
- Article
Amniotic fluid microvillar enzyme activities in the early detection of fetal abnormalities.
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- Prenatal Diagnosis, 1984, v. 4, n. 4, p. 261, doi. 10.1002/pd.1970040405
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- Publication type:
- Article
Prenatal diagnosis of cystic fibrosis by methylumbelliferylguanidinobenzoate protease titration in amniotic fluid.
- Published in:
- 1983
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- Publication type:
- journal article
Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies.
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- Human Mutation, 1997, v. 10, n. 6, p. 415, doi. 10.1002/(SICI)1098-1004(1997)10:6<415::AID-HUMU1>3.0.CO;2-C
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- Publication type:
- Article
Mutation screening of all 65 exons of the fibrillin-1 gene in 60 patients with Marfan syndrome: Report of 12 novel mutations.
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- Human Mutation, 1997, v. 10, n. 4, p. 280, doi. 10.1002/(SICI)1098-1004(1997)10:4<280::AID-HUMU3>3.0.CO;2-L
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- Publication type:
- Article
Identification of a novel nonsense mutation in the fibrillin gene (FBN1) using nonisotopic techniques.
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- Human Mutation, 1994, v. 3, n. 2, p. 159, doi. 10.1002/humu.1380030212
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- Publication type:
- Article
Fabrillin (FBN1) mutations in Marfan syndrome.
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- Human Mutation, 1992, v. 1, n. 1, p. 79, doi. 10.1002/humu.1380010115
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- Publication type:
- Article
Using tree-based methods for detection of gene–gene interactions in the presence of a polygenic signal: simulation study with application to educational attainment in the Generation Scotland Cohort Study.
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- Bioinformatics, 2019, v. 35, n. 2, p. 181, doi. 10.1093/bioinformatics/bty462
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- Publication type:
- Article
Association of low-frequency and rare coding variants with information processing speed.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01736-6
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- Publication type:
- Article
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB–FKBPL–NOTCH4 region of chromosome 6p21.3.
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- Human Molecular Genetics, 2012, v. 21, n. 18, p. 4138, doi. 10.1093/hmg/dds225
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- Publication type:
- Article
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.
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- Human Molecular Genetics, 2011, v. 20, n. 5, p. 1042, doi. 10.1093/hmg/ddq538
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- Publication type:
- Article
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.
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- Human Molecular Genetics, 2010, v. 19, n. 21, p. 4304, doi. 10.1093/hmg/ddq349
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- Publication type:
- Article
Variation in the uric acid transporter gene (SLC2A9) and memory performance.
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- Human Molecular Genetics, 2010, v. 19, n. 11, p. 2321, doi. 10.1093/hmg/ddq097
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- Publication type:
- Article
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.
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- Human Molecular Genetics, 2009, v. 18, n. 2, p. 373, doi. 10.1093/hmg/ddn350
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- Publication type:
- Article
Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits.
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- Human Molecular Genetics, 2007, v. 16, n. 2, p. 233, doi. 10.1093/hmg/ddl473
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- Publication type:
- Article
Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1680, doi. 10.1093/hmg/ddl091
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- Publication type:
- Article
Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration.
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- Human Molecular Genetics, 2003, v. 12, n. 20, p. 2657, doi. 10.1093/hmg/ddg289
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- Publication type:
- Article
Identification of SATB2 as the cleft palate gene on 2q32–q33.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2491, doi. 10.1093/hmg/ddg248
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- Publication type:
- Article
Genetic Variants in the ST6GAL1 Gene Are Associated with Thyroglobulin Plasma Level in Healthy Individuals.
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- Thyroid, 2019, v. 29, n. 6, p. 886, doi. 10.1089/thy.2018.0661
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- Publication type:
- Article
Genetic regulation of post-translational modification of two distinct proteins.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29189-5
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- Publication type:
- Article
Epigenetic measures of ageing predict the prevalence and incidence of leading causes of death and disease burden.
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- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00905-6
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- Publication type:
- Article
Characterisation of an inflammation-related epigenetic score and its association with cognitive ability.
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- Clinical Epigenetics, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13148-020-00903-8
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- Publication type:
- Article
Recent genomic heritage in Scotland.
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- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1605-2
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- Publication type:
- Article
Genome-wide methylation data improves dissection of the effect of smoking on body mass index.
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- PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009750
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- Publication type:
- Article
An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group.
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- Genetic Epidemiology, 2016, v. 40, n. 5, p. 404, doi. 10.1002/gepi.21978
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- Publication type:
- Article
General Framework for Meta-Analysis of Haplotype Association Tests.
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- Genetic Epidemiology, 2016, v. 40, n. 3, p. 244, doi. 10.1002/gepi.21959
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- Publication type:
- Article
Genetic comparison of a Croatian isolate and CEPH European founders.
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- Genetic Epidemiology, 2010, v. 34, n. 2, p. 140, doi. 10.1002/gepi.20443
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- Publication type:
- Article
Immunoreactive trypsin and the prenatal diagnosis of cystic fibrosis.
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- BJOG: An International Journal of Obstetrics & Gynaecology, 1984, v. 91, n. 5, p. 449, doi. 10.1111/j.1471-0528.1984.tb04782.x
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- Publication type:
- Article
Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01525-0
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- Publication type:
- Article
Regional variation in health is predominantly driven by lifestyle rather than genetics.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00497-5
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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
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.
- Published in:
- Nature Communications, 2016, v. 7, n. 11, p. 13357, doi. 10.1038/ncomms13357
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- Publication type:
- Article
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.
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- Nature Communications, 2015, v. 6, n. 3, p. 6689, doi. 10.1038/ncomms7689
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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
No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0111156
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- Publication type:
- Article
Genome-Wide Association Study of Executive Function
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Genome-Wide Association Study of Brain Gene Expression Levels (eGWAS)
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Genome-wide association study of memory performance
- Published in:
- 2011
- By:
- Publication type:
- Abstract
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
P4-167: Investigation of mitochondrial DNA damage in late-onset Alzheimer's disease
- Published in:
- 2008
- By:
- Publication type:
- Abstract
The PediGFR consortium: studying the genetics of complex kidney traits in children.
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- Nephrology Dialysis Transplantation, 2016, v. 31, n. 2, p. 173, doi. 10.1093/ndt/gfv356
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- Publication type:
- Article
Association of Genetic Variant at Chromosome 12q23.1 With Neuropathic Pain Susceptibility.
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- JAMA Network Open, 2021, v. 4, n. 12, p. e2136560, doi. 10.1001/jamanetworkopen.2021.36560
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- Publication type:
- Article
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
Association between Thyroid Function and Ocular Parameters.
- Published in:
- Biology (2079-7737), 2022, v. 11, n. 12, p. 1847, doi. 10.3390/biology11121847
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- Publication type:
- Article