Pages that link to "Q34651283"
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The following pages link to A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene (Q34651283):
Displayed 50 items.
- The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature (Q21261502) (← links)
- Prevalence in the United States of selected candidate gene variants. Third National Health and Nutrition Examination Survey, 1991- 1994 (Q23917519) (← links)
- Genome-wide association studies for complex traits: consensus, uncertainty and challenges (Q24550632) (← links)
- Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients (Q24600432) (← links)
- Common variants at five new loci associated with early-onset inflammatory bowel disease (Q24600801) (← links)
- Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (Q24605530) (← links)
- Rare structural variation of synapse and neurotransmission genes in autism (Q24608775) (← links)
- A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis (Q24609382) (← links)
- Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects (Q24631241) (← links)
- The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI (Q24631490) (← links)
- Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes (Q24632382) (← links)
- A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis (Q24634112) (← links)
- A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3 (Q24644978) (← links)
- Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease (Q24646902) (← links)
- Neuroimaging of the Philadelphia neurodevelopmental cohort (Q26863642) (← links)
- Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13 (Q27335170) (← links)
- Recent advances in the genetics of autoimmune disease (Q28238782) (← links)
- Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritis (Q28262855) (← links)
- Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases (Q28394008) (← links)
- Liver sinusoidal endothelial cell lectin, LSECtin, negatively regulates hepatic T-cell immune response (Q28508006) (← links)
- The diabetes susceptibility gene Clec16a regulates mitophagy (Q28511990) (← links)
- Association of CD247 (CD3ζ) gene polymorphisms with T1D and AITD in the population of northern Sweden (Q28597963) (← links)
- Genome-wide association analysis of milk yield traits in Nordic Red Cattle using imputed whole genome sequence variants (Q28602117) (← links)
- Integrated enrichment analysis of variants and pathways in genome-wide association studies indicates central role for IL-2 signaling genes in type 1 diabetes, and cytokine signaling genes in Crohn's disease (Q28677042) (← links)
- Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes (Q28730163) (← links)
- Novel associations for hypothyroidism include known autoimmune risk loci (Q28730714) (← links)
- A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci (Q28943424) (← links)
- Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes (Q29417127) (← links)
- A HapMap harvest of insights into the genetics of common disease (Q29614875) (← links)
- Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes (Q30277972) (← links)
- Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes (Q30301272) (← links)
- Meet me halfway: when genomics meets structural bioinformatics (Q30400158) (← links)
- Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes (Q30411328) (← links)
- Evidence for two independent associations with type 1 diabetes at the 12q13 locus (Q30426203) (← links)
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions (Q30434949) (← links)
- Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium (Q30436570) (← links)
- A generalized family-based association test for dichotomous traits (Q30436785) (← links)
- Current status and the future for the genetics of type I diabetes. (Q30437395) (← links)
- PUMA: a unified framework for penalized multiple regression analysis of GWAS data (Q30653367) (← links)
- Human CLEC16A regulates autophagy through modulating mTOR activity (Q30981879) (← links)
- Proceedings of the Tenth Annual UT-ORNL-KBRIN Bioinformatics Summit 2011. (Q31038696) (← links)
- Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP. (Q33323357) (← links)
- Detection of genome-wide polymorphisms in the AT-rich Plasmodium falciparum genome using a high-density microarray (Q33362971) (← links)
- Tracing sub-structure in the European American population with PCA-informative markers (Q33370082) (← links)
- Genomic landscape of a three-generation pedigree segregating affective disorder (Q33408823) (← links)
- Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry. (Q33455772) (← links)
- High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. (Q33480832) (← links)
- From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes. (Q33509503) (← links)
- Genetic heterogeneity in latent autoimmune diabetes is linked to various degrees of autoimmune activity: results from the Nord-Trøndelag Health Study (Q33556625) (← links)
- No association of the IRS1 and PAX4 genes with type I diabetes. (Q33581622) (← links)