Reach Banner
Last name


Search Results to Andrew Paterson

This is a "connection" page, showing the details of why an item matched the keywords from your search.


One or more keywords matched the following items that are connected to Paterson, Andrew

Item TypeName
Concept Genotype
Academic Article Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism.
Academic Article Umbilical vein and placental vessels from newborns with hereditary haemorrhagic telangiectasia type 1 genotype are normal despite reduced expression of endoglin.
Academic Article Transmission ratio distortion in families from the Framingham Heart Study.
Academic Article HLA class II haplotypes in Mexican systemic lupus erythematosus patients.
Academic Article Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population.
Academic Article A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1.
Academic Article Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics Study.
Academic Article To: Biason-Lauber A, Boehm B, Lang-Muritano M et al. (2005) association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity. Diabetologia 48:900-905.
Academic Article Evaluating outlier loci and their effect on the identification of pedigree errors.
Academic Article LDL composition in E2/2 subjects and LDL distribution by Apo E genotype in type 1 diabetes.
Academic Article Multiple variants in vascular endothelial growth factor (VEGFA) are risk factors for time to severe retinopathy in type 1 diabetes: the DCCT/EDIC genetics study.
Academic Article Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study.
Academic Article IL5RA and TNFRSF6B gene variants are associated with sporadic IgA nephropathy.
Academic Article Identification of LTBP2 on chromosome 14q as a novel candidate gene for bone mineral density variation and fracture risk association.
Academic Article Association between IGF1 CA microsatellites and mammographic density, anthropometric measures, and circulating IGF-I levels in premenopausal Caucasian women.
Academic Article Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
Academic Article Unified criteria for ultrasonographic diagnosis of ADPKD.
Academic Article STrengthening the REporting of Genetic Association Studies (STREGA)--an extension of the STROBE statement.
Academic Article Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.
Academic Article The associations of apolipoprotein E and angiotensin-converting enzyme polymorphisms and cognitive function in Type 1 diabetes based on an 18-year follow-up of the DCCT cohort.
Academic Article Family-based association study of IGF1 microsatellites and height, weight, and body mass index.
Academic Article Genetic variation of DKK3 may modify renal disease severity in ADPKD.
Academic Article A genome-wide scan for common alleles affecting risk for autism.
Academic Article Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.
Academic Article Individual common variants exert weak effects on the risk for autism spectrum disorders.
Academic Article The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels.
Academic Article Haptoglobin genotype and the rate of renal function decline in the diabetes control and complications trial/epidemiology of diabetes interventions and complications study.
Academic Article Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes.
Academic Article Iddm30 controls pancreatic expression of Ccl11 (Eotaxin) and the Th1/Th2 balance within the insulitic lesions.
Academic Article GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescence.
Academic Article Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Academic Article Drinking from the Holy Grail: analysis of whole-genome sequencing from the Genetic Analysis Workshop 18.
Academic Article OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.
Academic Article Determinants of intestinal permeability in healthy first-degree relatives of individuals with Crohn's disease.
Academic Article Caffeine Consumption Contributes to Skin Intrinsic Fluorescence in Type 1 Diabetes.
Academic Article Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event.
Academic Article Refining Genotype-Phenotype Correlation in Autosomal Dominant Polycystic Kidney Disease.
Academic Article IBD Genetic Risk Profile in Healthy First-Degree Relatives of Crohn's Disease Patients.
Academic Article New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins.
Academic Article Association of host genome with intestinal microbial composition in a large healthy cohort.
Academic Article Genetic determinants of impaired awareness of hypoglycemia in type 1 diabetes.
Academic Article Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes.
Academic Article FUT2 genotype and secretory status are not associated with fecal microbial composition and inferred function in healthy subjects.
Academic Article A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) gene.
Academic Article Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.
Academic Article Is there a third gene for autosomal dominant polycystic kidney disease?
Academic Article Association of the MscI polymorphism of the dopamine D3 receptor gene with tardive dyskinesia in schizophrenia.
Academic Article The analysis of parental origin of alleles may detect susceptibility loci for complex disorders.
Academic Article Haplotype analysis in the Collaborative Study on the Genetics of Alcoholism data: double recombinants.
Academic Article Long repeat tracts at SCA8 in major psychosis.
Academic Article Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease.
Academic Article Sex- and age-of-onset-based locus heterogeneity in asthma.
Academic Article Recurrent fetal loss associated with bilineal inheritance of type 1 autosomal dominant polycystic kidney disease.
Academic Article Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.
Academic Article Association of systemic lupus erythematosus (SLE) genetic susceptibility loci with lupus nephritis in childhood-onset and adult-onset SLE.
Academic Article Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population.
Academic Article Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes.
Academic Article Genome-wide association study of emotional empathy in children.
Academic Article Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
Academic Article Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects.
Academic Article Validation of QTLs for Fiber Quality Introgressed from Gossypium mustelinum by Selective Genotyping.

Search criteria
  • Genotype