Found: 21
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The functional ACTN3 577X variant increases the risk of falling in older females: results from two large independent cohort studies.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
The Functional ACTN3 577X Variant Increases the Risk of Falling in Older Females: Results From Two Large Independent Cohort Studies.
- Published in:
- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2011, v. 66A, n. 1, p. 130, doi. 10.1093/gerona/glq189
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- Publication type:
- Article
Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Investigating Shared Aetiology Between Type 2 Diabetes and Major Depressive Disorder in a Population Based Cohort.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 3, p. 227, doi. 10.1002/ajmg.b.32478
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- Publication type:
- Article
Autophagy: A new player in skeletal maintenance?
- Published in:
- Journal of Bone & Mineral Research, 2012, v. 27, n. 7, p. 1439, doi. 10.1002/jbmr.1668
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- Publication type:
- Article
Identification of a Major Locus for Paget's Disease on Chromosome 10p13 in Families of British Descent.
- Published in:
- Journal of Bone & Mineral Research, 2008, v. 23, n. 1, p. 58, doi. 10.1359/JBMR.071004
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- Publication type:
- Article
Loss of Ubiquitin-Binding Associated With Paget's Disease of Bone p62 ( SQSTM1) Mutations.
- Published in:
- Journal of Bone & Mineral Research, 2005, v. 20, n. 4, p. 619, doi. 10.1359/JBMR.041205
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- Publication type:
- Article
Ubiquitin-Associated Domain Mutations of SQSTM1 in Paget's Disease of Bone: Evidence for a Founder Effect in Patients of British Descent.
- Published in:
- Journal of Bone & Mineral Research, 2005, v. 20, n. 2, p. 227, doi. 10.1359/JBMR.041106
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- Publication type:
- Article
Novel UBA Domain Mutations of SQSTM1 in Paget's Disease of Bone: Genotype Phenotype Correlation, Functional Analysis, and Structural Consequences.
- Published in:
- Journal of Bone & Mineral Research, 2004, v. 19, n. 7, p. 1122, doi. 10.1359/JBMR.0403015
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- Publication type:
- Article
Polymorphisms in the P2X7 receptor gene are associated with low lumbar spine bone mineral density and accelerated bone loss in post-menopausal women.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 5, p. 559, doi. 10.1038/ejhg.2011.245
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- Publication type:
- Article
Investigating the viability of genetic screening/testing for RA susceptibility using combinations of five confirmed risk loci.
- Published in:
- Rheumatology, 2009, v. 48, n. 11, p. 1369, doi. 10.1093/rheumatology/kep272
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- Publication type:
- Article
Quantifying the extent to which index event biases influence large genetic association studies.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 5, p. 1018, doi. 10.1093/hmg/ddw433
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- Publication type:
- Article
Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0170653
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- Publication type:
- Article
Novel Rheumatoid Arthritis Susceptibility Locus at 22q12 Identified in an Extended UK Genome-Wide Association Study.
- Published in:
- Arthritis & Rheumatology, 2014, v. 66, n. 1, p. 24, doi. 10.1002/art.38196
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- Publication type:
- Article
Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003808
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- Publication type:
- Article
Informed Conditioning on Clinical Covariates Increases Power in Case-Control Association Studies.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 11, p. 1, doi. 10.1371/journal.pgen.1003032
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- Publication type:
- Article
Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness.
- Published in:
- International Journal of Epidemiology, 2013, v. 42, n. 3, p. 689, doi. 10.1093/ije/dys084
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- Publication type:
- Article
Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 22, p. 4543
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- Publication type:
- Article
Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 13, p. 2518, doi. 10.1093/hmg/ddp177
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- Publication type:
- Article
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 22, p. 2735, doi. 10.1093/hmg/11.22.2735
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- Publication type:
- Article
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
- Published in:
- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0414-4
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- Publication type:
- Article