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Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes.
- Published in:
- Human Genetics, 2003, v. 113, n. 2, p. 99, doi. 10.1007/s00439-003-0940-6
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- Publication type:
- Article
No Evidence That Genetic Variation at the Klotho Locus Is Associated With Longevity in Caucasians from the Newcastle 85+ Study and the UK Biobank.
- Published in:
- 2022
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- Publication type:
- journal article
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36678-8
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- Publication type:
- Article
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
- Published in:
- Clinical Infectious Diseases, 2021, v. 73, n. 10, p. 1860, doi. 10.1093/cid/ciab216
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- Publication type:
- Article
A Genome-wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1, and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis in Brazil.
- Published in:
- Clinical Infectious Diseases, 2021, v. 72, n. 10, p. e515, doi. 10.1093/cid/ciaa1230
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- Publication type:
- Article
DNA methylation abnormalities at gene promoters are extensive and variable in the elderly and phenocopy cancer cells.
- Published in:
- FASEB Journal, 2014, v. 28, n. 7, p. 3261, doi. 10.1096/fj.13-246173
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- Publication type:
- Article
Heterogeneity in the magnitude of the insulin gene effect on HLA risk in type 1 diabetes.
- Published in:
- 2004
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- Publication type:
- journal article
Remapping the insulin gene/IDDM2 locus in type 1 diabetes.
- Published in:
- 2004
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- Publication type:
- journal article
Maternal-Fetal Interactions and Birth Order Influence Insulin Variable Number of Tandem Repeats Allele Class Associations with Head Size at Birth and Childhood Weight Gain.
- Published in:
- Diabetes, 2004, v. 53, n. 4, p. 1128, doi. 10.2337/diabetes.53.4.1128
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- Publication type:
- Article
Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases.
- Published in:
- 2001
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- Publication type:
- journal article
Machine learning in genome-wide association studies.
- Published in:
- Genetic Epidemiology, 2009, v. 33, n. S1, p. S51, doi. 10.1002/gepi.20473
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- Publication type:
- Article
Quantitative trait association in parent offspring trios: Extension of case/pseudocontrol method and comparison of prospective and retrospective approaches.
- Published in:
- Genetic Epidemiology, 2007, v. 31, n. 8, p. 813, doi. 10.1002/gepi.20243
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- Publication type:
- Article
Exploring causality via identification of SNPs or haplotypes responsible for a linkage signal.
- Published in:
- Genetic Epidemiology, 2007, v. 31, n. 7, p. 727, doi. 10.1002/gepi.20236
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- Publication type:
- Article
Introduction to Genetic Analysis Workshop 15 summaries.
- Published in:
- Genetic Epidemiology, 2007, v. 31, n. S1, p. S1, doi. 10.1002/gepi.20274
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- Publication type:
- Article
Explorative two?locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures?related photosensitivity loci.
- Published in:
- Genetic Epidemiology, 2007, v. 31, n. 1, p. 42, doi. 10.1002/gepi.20190
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- Publication type:
- Article
Perils and pitfalls of permutation tests for distinguishing the effects of neighbouring polymorphisms.
- Published in:
- Genetic Epidemiology, 2006, v. 30, n. 7, p. 582, doi. 10.1002/gepi.20167
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- Publication type:
- Article
A multimarker regression‐based test of linkage for affected sib‐pairs at two linked loci.
- Published in:
- Genetic Epidemiology, 2006, v. 30, n. 3, p. 191, doi. 10.1002/gepi.20137
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- Publication type:
- Article
Estimation and testing of genotype and haplotype effects in case‐control studies: comparison of weighted regression and multiple imputation procedures.
- Published in:
- Genetic Epidemiology, 2006, v. 30, n. 3, p. 259, doi. 10.1002/gepi.20142
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- Publication type:
- Article
Summary of contributions to GAW Group 5: Linkage mapping methods, Problem 2.
- Published in:
- Genetic Epidemiology, 2005, v. 29, n. S1, p. S35, doi. 10.1002/gepi.20108
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- Publication type:
- Article
Comparison of population- and family-based methods for genetic association analysis in the presence of interacting loci.
- Published in:
- Genetic Epidemiology, 2005, v. 29, n. 1, p. 51, doi. 10.1002/gepi.20077
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- Publication type:
- Article
A conditional-on-exchangeable-parental-genotypes likelihood that remains unbiased at the causal locus under multiple-affected-sibling ascertainment.
- Published in:
- Genetic Epidemiology, 2005, v. 29, n. 1, p. 87, doi. 10.1002/gepi.20069
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- Publication type:
- Article
Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.
- Published in:
- Genetic Epidemiology, 2004, v. 26, n. 3, p. 167, doi. 10.1002/gepi.10307
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- Publication type:
- Article
Properties of case/pseudocontrol analysis for genetic association studies: Effects of recombination, ascertainment, and multiple affected offspring.
- Published in:
- Genetic Epidemiology, 2004, v. 26, n. 3, p. 186, doi. 10.1002/gepi.10306
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- Publication type:
- Article
Gamma regression improves Haseman-Elston and variance components linkage analysis for sib-pairs.
- Published in:
- Genetic Epidemiology, 2004, v. 26, n. 2, p. 97, doi. 10.1002/gepi.10299
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- Publication type:
- Article
Association mapping of complex diseases in linked regions: estimation of genetic effects and feasibility of testing rare variants.
- Published in:
- Genetic Epidemiology, 2003, v. 24, n. 1, p. 36, doi. 10.1002/gepi.10216
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- Publication type:
- Article
Linkage Analysis of Genetic Analysis Workshop 12 Simulated Data Based on Affected Individuals Only.
- Published in:
- Genetic Epidemiology, 2001, v. 21, p. S510, doi. 10.1002/gepi.2001.21.s1.s510
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- Publication type:
- Article
Correcting for ascertainment bias of relative-risk estimates obtained using affected-sib-pair linkage data.
- Published in:
- Genetic Epidemiology, 2000, v. 18, n. 4, p. 307, doi. 10.1002/(SICI)1098-2272(200004)18:4<307::AID-GEPI4>3.0.CO;2-3
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- Publication type:
- Article
Ascertainment bias in the estimation of sibling genetic risk parameters.
- Published in:
- Genetic Epidemiology, 2000, v. 18, n. 3, p. 217, doi. 10.1002/(SICI)1098-2272(200003)18:3<217::AID-GEPI3>3.0.CO;2-8
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- Publication type:
- Article
Bootstrap confidence intervals for relative risk parameters in affected-sib-pair data.
- Published in:
- Genetic Epidemiology, 2000, v. 18, n. 2, p. 157, doi. 10.1002/(SICI)1098-2272(200002)18:2<157::AID-GEPI5>3.0.CO;2-W
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- Publication type:
- Article
Fieller's theorem and linkage disequilibrium mapping.
- Published in:
- Genetic Epidemiology, 1999, v. 17, n. 4, p. 237, doi. 10.1002/(SICI)1098-2272(199911)17:4<237::AID-GEPI1>3.0.CO;2-P
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- Publication type:
- Article
Improving the power for disease locus detection in affected-sib-pair studies by using two-locus analysis and multiple regression methods.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. S521, doi. 10.1002/gepi.1370170784
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- Publication type:
- Article
Confidence intervals for relative risk estimates from affected-sib-pair data.
- Published in:
- Genetic Epidemiology, 1997, v. 14, n. 6, p. 593, doi. 10.1002/(SICI)1098-2272(1997)14:6<593::AID-GEPI7>3.0.CO;2-0
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- Publication type:
- Article
Dealing with Missing Data in Family-Based Association Studies: A Multiple Imputation Approach.
- Published in:
- Human Heredity, 2007, v. 63, n. 3/4, p. 229, doi. 10.1159/000100481
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- Publication type:
- Article
Detecting gene-gene interactions that underlie human diseases.
- Published in:
- 2009
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- Publication type:
- journal article
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 16, p. 4420, doi. 10.1093/hmg/ddu139
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- Publication type:
- Article
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 7, p. 1473, doi. 10.1093/hmg/dds552
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- Publication type:
- Article
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.
- Published in:
- Nature Communications, 2015, v. 6, n. 9, p. 8019, doi. 10.1038/ncomms9019
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- Publication type:
- Article
Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis.
- Published in:
- Science Translational Medicine, 2020, v. 12, n. 572, p. 1, doi. 10.1126/scitranslmed.aba4448
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- Publication type:
- Article
PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling.
- Published in:
- BMC Bioinformatics, 2012, v. 13, n. 1, p. 149, doi. 10.1186/1471-2105-13-149
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- Publication type:
- Article
Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 3, p. 333, doi. 10.1002/acn3.532
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- Publication type:
- Article
Genetic variants associated with leaf spot disease resistance in oil palm (Elaeis guineensis): A genome‐wide association study.
- Published in:
- Plant Pathology, 2023, v. 72, n. 9, p. 1626, doi. 10.1111/ppa.13774
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- Publication type:
- Article
The Application of Genetic Risk Scores in Rheumatic Diseases: A Perspective.
- Published in:
- Genes, 2023, v. 14, n. 12, p. 2167, doi. 10.3390/genes14122167
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- Publication type:
- Article
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart Disease.
- Published in:
- Genes, 2019, v. 10, n. 9, p. 663, doi. 10.3390/genes10090663
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- Publication type:
- Article
A composite-likelihood approach for identifying polymorphisms that are potentially directly associated with disease.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 5, p. 644, doi. 10.1038/ejhg.2008.242
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- Publication type:
- Article
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
- Published in:
- Nature Genetics, 2013, v. 45, n. 7, p. 822, doi. 10.1038/ng.2637
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- Publication type:
- Article
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.
- Published in:
- Nature Genetics, 2013, v. 45, n. 2, p. 208, doi. 10.1038/ng.2518
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- Publication type:
- Article
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
- Published in:
- Nature Genetics, 2012, v. 44, n. 10, p. 1137, doi. 10.1038/ng.2395
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- Publication type:
- Article
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
- Published in:
- 2011
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- Publication type:
- Correction notice
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
- Published in:
- Nature Genetics, 2011, v. 43, n. 4, p. 329, doi. 10.1038/ng.789
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- Publication type:
- Article
Reply to “Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent”.
- Published in:
- 2010
- By:
- Publication type:
- Letter