about
A common variant of HMGA2 is associated with adult and childhood height in the general populationA landscape of driver mutations in melanomaMutational heterogeneity in cancer and the search for new cancer-associated genesTwelve type 2 diabetes susceptibility loci identified through large-scale association analysisMelanoma genome sequencing reveals frequent PREX2 mutationsExome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancerThe genomic complexity of primary human prostate cancerGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisCharacterization of single-nucleotide polymorphisms in coding regions of human genesNew genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskA genome-wide association search for type 2 diabetes genes in African AmericansGenetic variation in GIPR influences the glucose and insulin responses to an oral glucose challengeMeta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levelsThe Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivityThe mutational landscape of head and neck squamous cell carcinomaA high-density admixture scan in 1,670 African Americans with hypertension.Discerning the ancestry of European Americans in genetic association studiesAdmixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X.Genome-wide association of anthropometric traits in African- and African-derived populationsLower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion.The discovery of single-nucleotide polymorphisms--and inferences about human demographic history.Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records.Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men.RAS mutations are associated with the development of cutaneous squamous cell tumors in patients treated with RAF inhibitors.Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeA Novel Approach to High-Quality Postmortem Tissue Procurement: The GTEx Project.On the replication of genetic associations: timing can be everything!Punctuated evolution of prostate cancer genomes.Underlying genetic models of inheritance in established type 2 diabetes associations.Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design?Massively parallel single-nucleus RNA-seq with DroNc-seq.Multiple regions within 8q24 independently affect risk for prostate cancer.A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility.A common genetic variant is associated with adult and childhood obesity.Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysisErratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskLarge-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse
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P50
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Kristin Ardlie
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Kristin Ardlie
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P106
P1416
P21
P31
P6634
kristin-ardlie-b748406