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Search Results to Andrew Paterson

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

Item TypeName
Concept Aged, 80 and over
Concept Aged
Concept Middle Aged
Academic Article Transmission ratio distortion in families from the Framingham Heart Study.
Academic Article Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene.
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 Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney disease.
Academic Article Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population.
Academic Article ANKH variants associated with ankylosing spondylitis: gender differences.
Academic Article Assessment of linkage and association of 13 genetic loci with bone mineral density.
Academic Article Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study.
Academic Article LDL composition in E2/2 subjects and LDL distribution by Apo E genotype in type 1 diabetes.
Academic Article Effect of environmental factors and gender on the heritability of bone mineral density and bone size.
Academic Article Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.
Academic Article Molecular diagnostics in autosomal dominant polycystic kidney disease: utility and limitations.
Academic Article IL5RA and TNFRSF6B gene variants are associated with sporadic IgA nephropathy.
Academic Article Association between IGF1 CA microsatellites and mammographic density, anthropometric measures, and circulating IGF-I levels in premenopausal Caucasian women.
Academic Article Unified criteria for ultrasonographic diagnosis of ADPKD.
Academic Article Evidence for pathogenicity of atypical splice mutations in autosomal dominant polycystic kidney disease.
Academic Article Family history of renal disease severity predicts the mutated gene in ADPKD.
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 Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer.
Academic Article High resolution mapping in the major histocompatibility complex region identifies multiple independent novel loci for psoriatic arthritis.
Academic Article Common variants in ZNF365 are associated with both mammographic density and breast cancer risk.
Academic Article A genome-wide linkage study of mammographic density, a risk factor for breast cancer.
Academic Article Identification of a novel percent mammographic density locus at 12q24.
Academic Article Common genetic determinants of intraocular pressure and primary open-angle glaucoma.
Academic Article Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
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 Mammographic density and breast cancer: a comparison of related and unrelated controls in the Breast Cancer Family Registry.
Academic Article Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.
Academic Article Evaluating the role of epigenetic histone modifications in the metabolic memory of type 1 diabetes.
Academic Article Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes.
Academic Article GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescence.
Academic Article Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency.
Academic Article Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Academic Article Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.
Academic Article OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.
Academic Article Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.
Academic Article The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
Academic Article Oxidized Low-Density Lipoprotein and the Incidence of Proliferative Diabetic Retinopathy and Clinically Significant Macular Edema Determined From Fundus Photographs.
Academic Article Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.
Academic Article Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes.
Academic Article Lifestyle and clinical determinants of skin autofluorescence in a population-based cohort study.
Academic Article Albuminuria Changes and Cardiovascular and Renal Outcomes in Type 1 Diabetes: The DCCT/EDIC Study.
Academic Article Genetic Variants Associated with Circulating Parathyroid Hormone.
Academic Article Bayesian latent variable models for hierarchical clustered count outcomes with repeated measures in microbiome studies.
Academic Article Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation.
Academic Article Polycystic Kidney Disease without an Apparent Family History.
Academic Article Genetic determinants of impaired awareness of hypoglycemia in type 1 diabetes.
Academic Article The origins of breast cancer associated with mammographic density: a testable biological hypothesis.
Academic Article Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer disease.
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 DNA methylation at the putative promoter region of the human dopamine D2 receptor gene.
Academic Article Association of the MscI polymorphism of the dopamine D3 receptor gene with tardive dyskinesia in schizophrenia.
Academic Article Genetic anticipation and breast cancer: a prospective follow-up study.
Academic Article A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.
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 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.
Academic Article The Genetic Landscape of Renal Complications in Type 1 Diabetes.
Academic Article A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.
Academic Article Phenotypic and genetic analysis of an adult cohort with extreme obesity.
Academic Article Skin autofluorescence predicts incident type 2 diabetes, cardiovascular disease and mortality in the general population.
Academic Article Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS.
Academic Article Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population.
Academic Article Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease.
Academic Article Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of Glycemia.
Academic Article Skin autofluorescence predicts new cardiovascular disease and mortality in people with type 2 diabetes.
Academic Article Residual ß cell function in long-term type 1 diabetes associates with reduced incidence of hypoglycemia.
Academic Article Conservative and operative management for cerebrospinal-fluid leakage after closed head injury.

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