Lista de obras - Kathryn Roeder - Dominio Público Uruguay

A Graphical Technique for Determining the Number of Components in a Mixture of Normals

A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

artículo científico publicado en 2016

A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories

article

A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY.

artículo científico publicado en 2010

A Semiparametric Mixture Approach to Case-Control Studies with Errors in Covariables

article published in 1996

A Unified Treatment of Integer Parameter Models

A framework for the interpretation of de novo mutation in human disease

artículo científico publicado en 2014

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

scientific journal article

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

artículo científico publicado en 2020

A statistical model for locating regulatory regions in genomic DNA.

artículo científico publicado en 1997

African ancestry and lung function in Puerto Rican children

artículo científico publicado en 2012

Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis

artículo científico publicado en 2011

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.

artículo científico publicado en 2018

Analysis of multilocus models of association

artículo científico publicado en 2003

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

artículo científico publicado en 2013

Analysis of single-locus tests to detect gene/disease associations

article

Association studies for quantitative traits in structured populations

Binning Clones by Hybridization with Complex Probes: Statistical Refinement of an Inner Product Mapping Method

Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men.

artículo científico publicado en 2010

Characterization of multilocus linkage disequilibrium

artículo científico publicado en 2005

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate

artículo científico publicado en 2014

Cladistic analysis of human apolipoprotein a4 polymorphisms in relation to quantitative plasma lipid risk factors of coronary heart disease

artículo científico publicado en 2003

Clustering and alignment of polymorphic sequences for HLA-DRB1 genotyping

artículo científico publicado en 2013

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

artículo científico publicado en 2013

Comment

2006 article by Tzeng & Roeder

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

artículo científico publicado en 2012

Common genetic variants, acting additively, are a major source of risk for autism

artículo científico publicado en 2012

Common risk variants identified in autism spectrum disorder

Constructing local cell-specific networks from single-cell data

artículo científico publicado en 2021

Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees

artículo científico publicado en 2011

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

artículo científico publicado en 2014

DNA Fingerprinting: A Review of the Controversy

article

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder

artículo científico publicado en 2014

De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

artículo científico publicado en 2020

De novo mutations revealed by whole-exome sequencing are strongly associated with autism ⬇️

artículo científico publicado el 4 de abril de 2012

Density Estimation with Confidence Sets Exemplified by Superclusters and Voids in the Galaxies

Depression and mental health help-seeking behaviors in a predominantly African American population of children and adolescents with epilepsy

artículo científico publicado en 2009

Discovering genetic ancestry using spectral graph theory

artículo científico publicado en 2010

Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens

artículo científico publicado en 2023

Disequilibrium Mapping: Composite Likelihood for Pairwise Disequilibrium

article by B. Devlin et al published August 1996 in Genomics

Do common variants play a role in risk for autism? Evidence and theoretical musings

artículo científico publicado en 2010

Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

scholarly article published in Nature Genetics

Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci

scholarly article published in Nature Genetics

Evolutionary-based association analysis using haplotype data

artículo científico publicado en 2003

False discovery control with p-value weighting

Forensic Inference from DNA Fingerprints

Fractional paternity assignment: theoretical development and comparison to other methods

artículo científico publicado en 1988

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

artículo científico publicado en 2010

Gene expression elucidates functional impact of polygenic risk for schizophrenia

artículo científico publicado en 2016

Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men.

artículo científico publicado en 2010

Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation

artículo científico publicado en 2007

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

artículo científico publicado en 2013

Genome-Wide Significance Levels and Weighted Hypothesis Testing

artículo científico publicado en 2009

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

artículo científico publicado en 2010

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

artículo científico publicado en 2018

Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania.

artículo científico publicado en 2001

Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau

Genomic Control to the extreme

Genomic control, a new approach to genetic-based association studies

artículo científico publicado en 2001

HIGH DIMENSIONAL VARIABLE SELECTION.

artículo científico publicado en 2009

Haplotype fine mapping by evolutionary trees

artículo científico publicado en 2000

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

artículo científico publicado en 2017

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men

artículo científico publicado en 2009

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Improving power in genome-wide association studies: weights tip the scale

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

scientific journal article

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

artículo científico publicado en 2015

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

artículo científico publicado en 2013

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

scientific article published on 23 January 2020

MIRA: mutual information-based reporter algorithm for metabolic networks

artículo científico publicado en 2014

MIRA: mutual information-based reporter algorithm for metabolic networks

artículo científico publicado en 2015

Mixture models for linkage analysis of affected sibling pairs and covariates

artículo científico publicado en 2002

Modeling Uncertainty in Latent Class Membership: A Case Study in Criminology

article

Most genetic risk for autism resides with common variation ⬇️

artículo científico publicado en 2014

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

artículo científico publicado en 2011

NETWORK ASSISTED ANALYSIS TO REVEAL THE GENETIC BASIS OF AUTISM. ⬇️

artículo científico publicado en 2015

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

artículo científico publicado en 2011

Not All Autism Genes Are Created Equal: A Response to Myers et al

artículo científico publicado en 2020

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.

artículo científico publicado en 2003

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

artículo científico publicado en 2008

Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching

article

Overdispersion Diagnostics for Generalized Linear Models

Patterns and rates of exonic de novo mutations in autism spectrum disorders

artículo científico publicado en 2012

Pleiotropy and principal components of heritability combine to increase power for association analysis

article

Positive Semidefinite Rank-based Correlation Matrix Estimation with Application to Semiparametric Graph Estimation

artículo científico publicado en 2014

Practical Bayesian Density Estimation Using Mixtures of Normals

REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.

artículo científico publicado en 2013

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

artículo científico publicado en 2013

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

artículo científico publicado en 2017

Residual Diagnostics for Mixture Models

article

SNP-based analysis of genetic substructure in the German population.

artículo científico publicado en 2006

STRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCE.

artículo científico publicado en 2011

Screen and clean: a tool for identifying interactions in genome-wide association studies

artículo científico publicado en 2010

Searching for disease susceptibility variants in structured populations

scientific article published on 02 June 2008

Statistical Genetics: False discovery or missed discovery?

article

Synaptic, transcriptional and chromatin genes disrupted in autism

artículo científico publicado en 2014

TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease.

artículo científico publicado en 2011

Testing for an unusual distribution of rare variants

artículo científico publicado en 2011

Testing for association based on excess allele sharing in a sample of related cases and controls

artículo científico publicado en 2007

The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability

artículo científico publicado en 2017

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders

artículo científico publicado en 2012

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

artículo científico publicado en 2015

The heritability of IQ

artículo científico publicado en 1997

The power of genomic control

artículo científico publicado en 2000

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families

artículo científico publicado en 2014

Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes

artículo científico publicado en 2001

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

artículo científico publicado en 2009

Unbiased methods for population-based association studies

artículo científico publicado en 2001

Uniqueness of estimation and identifiability in mixture models

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies

artículo científico publicado en 2010

Using linkage genome scans to improve power of association in genome scans

artículo científico publicado en 2006

Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children

artículo científico publicado en 2012

Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.

artículo científico publicado en 2013

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

scientific article published on 01 April 2020

Lista de obras de Kathryn Roeder

A Graphical Technique for Determining the Number of Components in a Mixture of Normals

A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories

A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY.

A Semiparametric Mixture Approach to Case-Control Studies with Errors in Covariables

A Unified Treatment of Integer Parameter Models

A framework for the interpretation of de novo mutation in human disease

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

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

A statistical model for locating regulatory regions in genomic DNA.

African ancestry and lung function in Puerto Rican children

Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.

Analysis of multilocus models of association

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

Analysis of single-locus tests to detect gene/disease associations

Association studies for quantitative traits in structured populations

Binning Clones by Hybridization with Complex Probes: Statistical Refinement of an Inner Product Mapping Method

Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men.

Characterization of multilocus linkage disequilibrium

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate

Cladistic analysis of human apolipoprotein a4 polymorphisms in relation to quantitative plasma lipid risk factors of coronary heart disease

Clustering and alignment of polymorphic sequences for HLA-DRB1 genotyping

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

Comment

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Common genetic variants, acting additively, are a major source of risk for autism

Common risk variants identified in autism spectrum disorder

Constructing local cell-specific networks from single-cell data

Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

DNA Fingerprinting: A Review of the Controversy

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder

De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

De novo mutations revealed by whole-exome sequencing are strongly associated with autism ⬇️

Density Estimation with Confidence Sets Exemplified by Superclusters and Voids in the Galaxies

Depression and mental health help-seeking behaviors in a predominantly African American population of children and adolescents with epilepsy

Discovering genetic ancestry using spectral graph theory

Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens

Disequilibrium Mapping: Composite Likelihood for Pairwise Disequilibrium

Do common variants play a role in risk for autism? Evidence and theoretical musings

Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci

Evolutionary-based association analysis using haplotype data

False discovery control with p-value weighting

Forensic Inference from DNA Fingerprints

Fractional paternity assignment: theoretical development and comparison to other methods

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

Gene expression elucidates functional impact of polygenic risk for schizophrenia

Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men.

Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation

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

Genome-Wide Significance Levels and Weighted Hypothesis Testing

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania.

Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau

Genomic Control to the extreme

Genomic control, a new approach to genetic-based association studies

HIGH DIMENSIONAL VARIABLE SELECTION.

Haplotype fine mapping by evolutionary trees

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men

Identification of common genetic risk variants for autism spectrum disorder

Improving power in genome-wide association studies: weights tip the scale

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

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

MIRA: mutual information-based reporter algorithm for metabolic networks

MIRA: mutual information-based reporter algorithm for metabolic networks

Mixture models for linkage analysis of affected sibling pairs and covariates

Modeling Uncertainty in Latent Class Membership: A Case Study in Criminology

Most genetic risk for autism resides with common variation ⬇️

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

NETWORK ASSISTED ANALYSIS TO REVEAL THE GENETIC BASIS OF AUTISM. ⬇️

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

Not All Autism Genes Are Created Equal: A Response to Myers et al

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk