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Lista de obras de Ellen M Wijsman

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

artículo científico publicado en 2003

A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk

artículo científico publicado en 2008

A genome-wide linkage and association scan reveals novel loci for autism

artículo científico publicado en 2009

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

A macrophage sterol-responsive network linked to atherogenesis

artículo científico publicado en 2010

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

artículo científico publicado en 2011

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

artículo científico publicado en 2003

A score for Bayesian genome screening

artículo científico publicado en 2003

APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation

artículo científico publicado en 2005

Accounting for Epistasis in Linkage Analysis of General Pedigrees

article

Accounting for Linkage Disequilibrium among Markers in Linkage Analysis: Impact of Haplotype Frequency Estimation and Molecular Haplotypes for a Gene in a Candidate Region for Alzheimer’s Disease

article

Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

artículo científico publicado en 2012

Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP

artículo científico publicado en 2018

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Approaches to mapping genetically correlated complex traits

artículo científico publicado en 2003

Case-control association testing in the presence of unknown relationships

artículo científico publicado en 2009

Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers

article

Cholesterol accumulation regulates expression of macrophage proteins implicated in proteolysis and complement activation

artículo científico publicado en 2012

Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees

artículo científico publicado en 2014

Combining information from linkage and association methods

artículo científico publicado en 2009

Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees

scientific article published on 04 December 2018

Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data

artículo científico publicado en 2005

Comparison of multipoint linkage analyses for quantitative traits in the CEPH data: parametric LOD scores, variance components LOD scores, and Bayes factors

artículo científico publicado en 2007

Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3.

artículo científico publicado en 2005

Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association

artículo científico publicado en 2007

Contrasting identity-by-descent estimators, association studies, and linkage analyses using the Framingham Heart Study data

artículo científico publicado en 2009

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

artículo científico publicado en 2014

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

artículo científico publicado en 2019

Detection of Mendelian consistent genotyping errors in pedigrees

artículo científico publicado en 2014

Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis

artículo científico publicado en 2008

Estimating relationships between phenotypes and subjects drawn from admixed families

artículo científico publicado en 2016

Estimation and visualization of identity-by-descent within pedigrees simplifies interpretation of complex trait analysis

artículo científico publicado en 2011

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

artículo científico publicado en 2007

Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2.

artículo científico publicado en 2004

Evidence for genetic linkage of autism to chromosomes 7 and 4

Evidence for involvement of GNB1L in autism

artículo científico publicado en 2011

Evidence for multiple loci from a genome scan of autism kindreds.

artículo científico publicado en 2006

Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families

artículo científico publicado en 2010

Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment

artículo científico publicado en 2003

Extended intermarker linkage disequilibrium in the Afrikaners

artículo científico publicado en 2002

Familial aggregation of dyslexia phenotypes. II: paired correlated measures

artículo científico publicado en 2002

Familial aggregation patterns in mathematical ability

artículo científico publicado en 2004

Functional impact of global rare copy number variation in autism spectrum disorders

artículo científico publicado en 2010

GIGI-Quick: A Fast Approach to Impute Missing Genotypes in Genome-Wide Association Family Data

artículo científico publicado en 2017

GIGI: an approach to effective imputation of dense genotypes on large pedigrees

artículo científico publicado en 2013

Gender differences in severity of writing and reading disabilities

article

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

artículo científico publicado en 2011

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci

artículo científico publicado en 2007

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

artículo científico publicado en 2016

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

artículo científico publicado en 2018

Genetic and nongenetic sources of variation in phospholipid transfer protein activity

artículo científico publicado en 2009

Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment

artículo científico publicado en 2004

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

artículo científico publicado en 2002

Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia

artículo científico publicado en 2005

Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization

artículo científico publicado en 2010

Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset

artículo científico publicado en 2013

Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci

artículo científico publicado en 2008

Genome scan of age-at-onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneity

artículo científico publicado en 2011

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16

artículo científico publicado en 2010

Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

artículo científico publicado en 2011

Genome-wide linkage analyses of quantitative and categorical autism subphenotypes

artículo científico publicado en 2008

Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity

artículo científico publicado en 2006

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins

artículo científico publicado en 2002

Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders

artículo científico publicado en 2011

Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates

artículo científico publicado en 2009

Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data.

artículo científico publicado en 2016

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Inheritance model introduces differential bias in CNV calls between parents and offspring

artículo científico publicado en 2012

Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia

artículo científico publicado en 2013

Joint linkage and segregation analysis under multiallelic trait inheritance: simplifying interpretations for complex traits

artículo científico publicado en 2010

Joint linkage and segregation analysis using Markov chain Monte Carlo methods

artículo científico publicado en 2002

Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods

artículo científico publicado en 2004

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

artículo científico publicado en 2004

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families

artículo científico publicado en 2010

Linkage and association of phospholipid transfer protein activity to LASS4

artículo científico publicado en 2011

Low clusterin levels in high-density lipoprotein associate with insulin resistance, obesity, and dyslipoproteinemia

artículo científico publicado en 2010

Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan

artículo científico publicado en 2004

MCMC multilocus lod scores: application of a new approach

artículo científico publicado en 2005

MCMC-based linkage analysis for complex traits on general pedigrees: multipoint analysis with a two-locus model and a polygenic component

article

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

artículo científico publicado en 2007

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

artículo científico publicado en 2016

Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees

artículo científico publicado en 2006

Neurocognitive and electrophysiological evidence of altered face processing in parents of children with autism: implications for a model of abnormal development of social brain circuitry in autism

artículo científico publicado en 2005

Oligogenic segregation analysis of hereditary prostate cancer pedigrees: evidence for multiple loci affecting age at onset

artículo científico publicado en 2003

PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers

artículo científico publicado en 2015

Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes

artículo científico publicado en 2013

Presence of large deletions in kindreds with autism

artículo científico publicado en 2002

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

article

Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease

Relationship inference from trios of individuals, in the presence of typing error

artículo científico publicado en 2001

Replicating genotype-phenotype associations

artículo científico publicado en 2007

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

artículo científico publicado en 2010

Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder

scholarly article by N. H. Chapman et al published 1 October 2018 in Human Genetics

Segregation analysis of a complex quantitative trait: approaches for identifying influential data points

artículo científico publicado en 2006

Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding

artículo científico publicado en 2003

Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data

artículo científico publicado en 2007

Summary of Group 8: Development and extension of linkage methods

artículo científico publicado en 2003

The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer disease

artículo científico publicado en 2010

The role of large pedigrees in an era of high-throughput sequencing

artículo científico publicado en 2012

Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia

artículo científico publicado en 2006

Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.

artículo científico publicado en 2017

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes

artículo científico publicado en 2015

Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.

artículo científico publicado en 2018

Writing problems in developmental dyslexia: under-recognized and under-treated

artículo científico publicado en 2008

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