Ellen M. Wijsman
educated at: University of Wisconsin–Madison
occupation: geneticist, statistician
official website: faculty.washington.edu/wijsman
Articles 105
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Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation
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Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees
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Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project
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Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP
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Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease
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Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
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Analysis of shared heritability in common disorders of the brain
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Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.
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Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder
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GIGI-Quick: A Fast Approach to Impute Missing Genotypes in Genome-Wide Association Family Data.
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Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.
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Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.
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Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data.
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Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech
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Estimating relationships between phenotypes and subjects drawn from admixed families
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PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers
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Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes
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Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees
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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
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Detection of Mendelian consistent genotyping errors in pedigrees
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
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Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset
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Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia
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GIGI: an approach to effective imputation of dense genotypes on large pedigrees
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Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes
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Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
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The role of large pedigrees in an era of high-throughput sequencing
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Individual common variants exert weak effects on the risk for autism spectrum disorders
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Inheritance model introduces differential bias in CNV calls between parents and offspring
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Cholesterol accumulation regulates expression of macrophage proteins implicated in proteolysis and complement activation
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Genome scan of age-at-onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneity
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Evidence for involvement of GNB1L in autism
Human - wd:Q37369759