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Evaluating empirical bounds on complex disease genetic architecture.

Evaluating empirical bounds on complex disease genetic architecture.

http://www.wikidata.org/entity/Q39329664

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Rare-variant association analysis: study designs and statistical tests Understanding rare and common diseases in the context of human evolution Strategies for Imputing and Analyzing Rare Variants in Association Studies Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate The genetic architecture of type 2 diabetes Exposing the exposures responsible for type 2 diabetes and obesity.Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Variant association tools for quality control and analysis of large-scale sequence and genotyping array data The role of functional data in interpreting the effects of genetic variation The impact of rare and low-frequency genetic variants in common disease The impact of population demography and selection on the genetic architecture of complex traits.Most genetic risk for autism resides with common variation.Genetic simulation tools for post-genome wide association studies of complex diseases Jumping on the Train of Personalized Medicine: A Primer for Non- Geneticist Clinicians: Part 3. Clinical Applications in the Personalized Medicine Area.A joint history of the nature of genetic variation and the nature of schizophrenia.The effect of paternal age on offspring intelligence and personality when controlling for paternal trait level Rare variant association studies: considerations, challenges and opportunities.A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study Genetics of type 2 diabetes-pitfalls and possibilities.The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease Contrasting genetic architectures in different mouse reference populations used for studying complex traits.Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17.Recent advances in understanding the genetic architecture of type 2 diabetes Type 2 Diabetes Risk Allele Loci in the Qatari Population.A Model of Compound Heterozygous, Loss-of-Function Alleles Is Broadly Consistent with Observations from Complex-Disease GWAS Datasets.Explaining additional genetic variation in complex traits A rare-variant test for high-dimensional data.Linkage Analysis of Urine Arsenic Species Patterns in the Strong Heart Family Study Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory Estimating the mutation load in human genomes Common variants explain a large fraction of the variability in the liability to psoriasis in a Han Chinese population.Considerations for rare variants in drug metabolism genes and the clinical implications.Genetic susceptibility to type 2 diabetes and obesity: from genome-wide association studies to rare variants and beyond.How important are rare variants in common disease?An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases.Whole-genome sequencing approaches for conservation biology: advantages, limitations, and practical recommendations.An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes.The genetics of anxiety-related negative valence system traits.

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P2860

Evaluating empirical bounds on complex disease genetic architecture.

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Evaluating empirical bounds on complex disease genetic architecture.

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Evaluating empirical bounds on complex disease genetic architecture.

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Evaluating empirical bounds on complex disease genetic architecture.

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Evaluating empirical bounds on complex disease genetic architecture.

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A high-resolution map of human evolutionary constraint using 29 mammals

Finding the missing heritability of complex diseases

The allelic architecture of human disease genes: common disease-common variant... or not?

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

A map of human genome variation from population-scale sequencing

Genetic risk prediction in complex disease

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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Genetic heterogeneity in human disease

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