Lista de obras -

A New Method for Computing the Multipoint Posterior Probability of Linkage

scientific article published on 01 January 2004

A case of autism and uniparental disomy of chromosome 1.

artículo científico publicado en 2005

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.

artículo científico publicado en 2018

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

scientific journal article

A major susceptibility locus for specific language impairment is located on 13q21.

artículo científico publicado en 2002

A model-integrated multipoint Bayesian analysis of hypertension in the Framingham Heart Study data finds little evidence of linkage

artículo científico publicado en 2003

A molecular genetic study of autism and related phenotypes in extended pedigrees

artículo científico publicado en 2013

A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications

artículo científico publicado en 2008

A new linear regression-like residual for survival analysis, with application to genome wide association studies of time-to-event data

scientific article published on 04 May 2020

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

artículo científico publicado en 2011

A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia

artículo científico publicado en 2015

Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage

artículo científico publicado en 2007

Ascertainment bias in linkage analysis: comments on Ginsburg et al

scientific article published on 01 April 2005

Association statistics under the PPL framework ⬇️

artículo científico publicado el 1 de diciembre de 2010

Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7.

artículo científico publicado en 2003

Calculation of multipoint likelihoods using flanking marker data: a simulation study

artículo científico publicado en 2005

Cell responses only partially shape cell-to-cell variations in protein abundances in Escherichia coli chemotaxis

artículo científico publicado en 2013

Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci ⬇️

artículo científico publicado el 12 de octubre de 2010

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

artículo científico publicado en 2014

Correction: In Silico Modeling of Itk Activation Kinetics in Thymocytes Suggests Competing Positive and Negative IP4 Mediated Feedbacks Increase Robustness

artículo científico publicado en 2014

Data-driven quantification of the robustness and sensitivity of cell signaling networks

artículo científico publicado en 2013

Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky

artículo científico publicado en 2007

Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.

artículo científico publicado en 2005

Employing MCMC under the PPL framework to analyze sequence data in large pedigrees ⬇️

artículo científico publicado el 19 de abril de 2013

Evaluation of FOXP2 as an autism susceptibility gene

artículo científico publicado en 2002

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene

artículo científico publicado en 2005

Evidence, temperature, and the laws of thermodynamics.

artículo científico publicado en 2014

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment

artículo científico publicado en 2004

Expected Monotonicity – A Desirable Property for Evidence Measures? ⬇️

artículo científico publicado el 21 de julio de 2010

Exploiting gene x gene interaction in linkage analysis

artículo científico publicado en 2007

Fast and accurate calculation of a computationally intensive statistic for mapping disease genes

artículo científico publicado en 2009

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

artículo científico publicado en 2010

Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans

artículo científico publicado en 2005

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

artículo científico publicado en 2007

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

artículo científico publicado en 2013

Genome-wide linkage analysis of blood pressure under locus heterogeneity

artículo científico publicado en 2003

HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity

artículo científico publicado en 2002

HLODs, Trait Models, and Ascertainment: Implications of Admixture for Parameter Estimation and Linkage Detection

scientific article published on 01 January 2002

Heterogeneity: GAW Group 15

scientific article published on 01 January 2005

Host-to-host variation of ecological interactions in polymicrobial infections

artículo científico publicado en 2014

Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

artículo científico publicado en 2009

In silico modeling of Itk activation kinetics in thymocytes suggests competing positive and negative IP4 mediated feedbacks increase robustness

artículo científico publicado en 2013

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

scientific journal article

Is schizophrenia linked to chromosome 1q?

artículo científico publicado en 2002

KELVIN: a software package for rigorous measurement of statistical evidence in human genetics.

artículo científico publicado en 2011

Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy

artículo científico publicado en 2018

MLIP: using multiple processors to compute the posterior probability of linkage

artículo científico publicado en 2008

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

artículo científico publicado en 2007

Measurement of Evidence and Evidence of Measurement

artículo científico publicado en 2011

Meta-analysis of repository data: impact of data regularization on NIMH schizophrenia linkage results

artículo científico publicado en 2014

Next-generation linkage analysis.

artículo científico publicado en 2011

Next-generation linkage and association methods applied to hypertension: a multifaceted approach to the analysis of sequence data

artículo científico publicado en 2014

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

artículo científico publicado en 2011

PEDSnet: a National Pediatric Learning Health System

artículo científico publicado en 2014

Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations

artículo científico publicado en 2005

Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.

artículo científico publicado en 2008

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

artículo científico publicado en 2011

Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies

artículo científico publicado en 2014

SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility

artículo científico publicado en 2013

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

artículo científico publicado en 2020

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

artículo científico publicado en 2014

The Posterior Probability of Linkage Allowing for Linkage Disequilibrium and a New Estimate of Disequilibrium between a Trait and a Marker

article

The emperor's new methods

artículo científico publicado en 2003

The incorporation of prior genomic information does not necessarily improve the performance of Bayesian linkage methods: an example involving sex-specific recombination and the two-point PPL.

artículo científico publicado en 2005

The value of regenotyping older linkage data sets with denser marker panels

artículo científico publicado en 2014

Thermometers: something for statistical geneticists to think about

artículo científico publicado en 2006

Two novel quantitative trait linkage analysis statistics based on the posterior probability of linkage: application to the COGA families

artículo científico publicado en 2005

Two-locus heterogeneity cannot be distinguished from two-locus epistasis on the basis of affected-sib-pair data

artículo científico publicado en 2003

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

artículo científico publicado en 2014

Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype

artículo científico publicado en 2018

Where’s the Evidence? ⬇️

artículo científico publicado el 22 de marzo de 2011

Lista de obras de

A New Method for Computing the Multipoint Posterior Probability of Linkage

A case of autism and uniparental disomy of chromosome 1.

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.

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

A major susceptibility locus for specific language impairment is located on 13q21.

A model-integrated multipoint Bayesian analysis of hypertension in the Framingham Heart Study data finds little evidence of linkage

A molecular genetic study of autism and related phenotypes in extended pedigrees

A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications

A new linear regression-like residual for survival analysis, with application to genome wide association studies of time-to-event data

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

A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia

Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage

Ascertainment bias in linkage analysis: comments on Ginsburg et al

Association statistics under the PPL framework ⬇️

Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7.

Calculation of multipoint likelihoods using flanking marker data: a simulation study

Cell responses only partially shape cell-to-cell variations in protein abundances in Escherichia coli chemotaxis

Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci ⬇️

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Correction: In Silico Modeling of Itk Activation Kinetics in Thymocytes Suggests Competing Positive and Negative IP4 Mediated Feedbacks Increase Robustness

Data-driven quantification of the robustness and sensitivity of cell signaling networks

Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky

Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.

Employing MCMC under the PPL framework to analyze sequence data in large pedigrees ⬇️

Evaluation of FOXP2 as an autism susceptibility gene

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene

Evidence, temperature, and the laws of thermodynamics.

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment

Expected Monotonicity – A Desirable Property for Evidence Measures? ⬇️

Exploiting gene x gene interaction in linkage analysis

Fast and accurate calculation of a computationally intensive statistic for mapping disease genes

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

Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans

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

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

Genome-wide linkage analysis of blood pressure under locus heterogeneity

HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity

HLODs, Trait Models, and Ascertainment: Implications of Admixture for Parameter Estimation and Linkage Detection

Heterogeneity: GAW Group 15

Host-to-host variation of ecological interactions in polymicrobial infections

Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

In silico modeling of Itk activation kinetics in thymocytes suggests competing positive and negative IP4 mediated feedbacks increase robustness

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

Is schizophrenia linked to chromosome 1q?

KELVIN: a software package for rigorous measurement of statistical evidence in human genetics.

Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy

MLIP: using multiple processors to compute the posterior probability of linkage

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Measurement of Evidence and Evidence of Measurement

Meta-analysis of repository data: impact of data regularization on NIMH schizophrenia linkage results

Next-generation linkage analysis.

Next-generation linkage and association methods applied to hypertension: a multifaceted approach to the analysis of sequence data

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

PEDSnet: a National Pediatric Learning Health System

Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations

Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies

SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

The Posterior Probability of Linkage Allowing for Linkage Disequilibrium and a New Estimate of Disequilibrium between a Trait and a Marker

The emperor's new methods

The incorporation of prior genomic information does not necessarily improve the performance of Bayesian linkage methods: an example involving sex-specific recombination and the two-point PPL.

The value of regenotyping older linkage data sets with denser marker panels

Thermometers: something for statistical geneticists to think about

Two novel quantitative trait linkage analysis statistics based on the posterior probability of linkage: application to the COGA families

Two-locus heterogeneity cannot be distinguished from two-locus epistasis on the basis of affected-sib-pair data

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype

Where’s the Evidence? ⬇️