Pages that link to "Q6217960"
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The following pages link to John A. Todd (Q6217960):
Displaying 50 items.
- Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history (Q21145273) (← links)
- Common genetic determinants of vitamin D insufficiency: a genome-wide association study (Q24602058) (← links)
- An allele of IKZF1 (Ikaros) conferring susceptibility to childhood acute lymphoblastic leukemia protects against type 1 diabetes (Q24612348) (← links)
- Shared and distinct genetic variants in type 1 diabetes and celiac disease (Q24623113) (← links)
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (Q24628710) (← links)
- Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes (Q24632382) (← links)
- Identification of Cd101 as a susceptibility gene for Novosphingobium aromaticivorans-induced liver autoimmunity (Q24633643) (← links)
- A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3 (Q24644978) (← links)
- Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (Q24646663) (← links)
- Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project (Q24649206) (← links)
- Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes (Q24651119) (← links)
- Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes (Q24652324) (← links)
- Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci (Q24658255) (← links)
- T1DBase, a community web-based resource for type 1 diabetes research (Q24796182) (← links)
- Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes (Q24797435) (← links)
- Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray genotyping (Q24802893) (← links)
- Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans (Q24810018) (← links)
- Polymorphism discovery and association analyses of the interferon genes in type 1 diabetes (Q25256966) (← links)
- Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease (Q28201947) (← links)
- Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus (Q28289699) (← links)
- Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes (Q28304750) (← links)
- Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer (Q28388006) (← links)
- Evidence that Cd101 is an autoimmune diabetes gene in nonobese diabetic mice (Q28509117) (← links)
- Regulatory T Cell Responses in Participants with Type 1 Diabetes after a Single Dose of Interleukin-2: A Non-Randomised, Open Label, Adaptive Dose-Finding Trial (Q28554636) (← links)
- Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters (Q28592966) (← links)
- Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. (Q29417005) (← links)
- Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk (Q30279028) (← links)
- Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping (Q30279124) (← links)
- Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers (Q30300404) (← links)
- Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes (Q30301272) (← links)
- HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: analysis of the type 1 diabetes genetics consortium families (Q30411842) (← links)
- Next generation sequencing reveals the association of DRB3*02:02 with type 1 diabetes (Q30412114) (← links)
- A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes (Q30412627) (← links)
- A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples (Q30412638) (← links)
- Negligible impact of rare autoimmune-locus coding-region variants on missing heritability (Q30415780) (← links)
- Evidence of gene-gene interaction and age-at-diagnosis effects in type 1 diabetes (Q30416530) (← links)
- Functional IL6R 358Ala allele impairs classical IL-6 receptor signaling and influences risk of diverse inflammatory diseases (Q30419941) (← links)
- Seven newly identified loci for autoimmune thyroid disease (Q30424090) (← links)
- Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry (Q30426245) (← links)
- Tests for genetic interactions in type 1 diabetes: linkage and stratification analyses of 4,422 affected sib-pairs (Q30428049) (← links)
- Pervasive sharing of genetic effects in autoimmune disease (Q30431030) (← links)
- Genetics of type 1 diabetes: what's next? (Q30431554) (← links)
- Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium (Q30436570) (← links)
- Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship. (Q30564668) (← links)
- Limitations of stratifying sib-pair data in common disease linkage studies: an example using chromosome 10p14-10q11 in type 1 diabetes (Q30743224) (← links)
- Genome-wide end-sequenced BAC resources for the NOD/MrkTac() and NOD/ShiLtJ() mouse genomes (Q30883833) (← links)
- Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases (Q30904970) (← links)
- Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics (Q30978583) (← links)
- T1DBase: integration and presentation of complex data for type 1 diabetes research (Q31085600) (← links)
- Mouse microsatellites from a flow-sorted 4:6 Robertsonian chromosome (Q33193213) (← links)