Lista de obras - Alun Thomas - Dominio Público Uruguay

A Draft Sequence of the Rice Genome (Oryza sativa L. ssp. japonica)

artículo científico publicado en 2002

A Laboratory Information Management System (LIMS) for a high throughput genetic platform aimed at candidate gene mutation screening

artículo científico publicado en 2007

A candidate prostate cancer susceptibility gene at chromosome 17p

artículo científico publicado en 2001

A chromosome 16 quantitative trait locus regulates allogeneic bone marrow engraftment in nonmyeloablated mice.

artículo científico publicado en 2009

A linear time algorithm for calculation of multiple pairwise kinship coefficients and the genetic index of familiality

artículo científico publicado en 1994

A method and program for estimating graphical models for linkage disequilibrium that scale linearly with the number of loci, and their application to gene drop simulation

scientific article published on 16 March 2009

A multivariate time series approach to modeling and forecasting demand in the emergency department.

artículo científico publicado en 2008

A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease

artículo científico publicado en 2008

A primary genetic linkage map for human chromosome 12.

artículo científico publicado en 1987

A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

artículo científico publicado en 2011

Accelerated gene counting for haplotype frequency estimation

artículo científico publicado en 2003

Accuracy and computational efficiency of a graphical modeling approach to linkage disequilibrium estimation.

artículo científico publicado en 2011

An analysis of unclassified missense substitutions in human BRCA1

scientific article published on 01 January 2006

An application of the latent p value method to assess linkage in asthma pedigrees.

artículo científico publicado en 2010

Assessment of SNP streak statistics using gene drop simulation with linkage disequilibrium.

artículo científico publicado en 2010

Automated construction and testing of multi-locus gene–gene associations ⬇️

artículo científico publicado el 13 de noviembre de 2010

Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions

artículo científico publicado en 2012

Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses:ELAC2 and familial early-onset prostate cancer

artículo científico publicado en 2005

Characterizing allelic associations from unphased diploid data by graphical modeling.

artículo científico publicado en 2005

Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications.

artículo científico publicado en 2008

Classifying, identifying and enumerating arbitrary relationships

artículo científico publicado en 1988

Creation of a national resource with linked genealogy and phenotypic data: the Veterans Genealogy Project

artículo científico publicado en 2013

Detecting Pleiotropy and Epistasis Using Variance Components Linkage Analysis in jPAP ⬇️

artículo científico publicado el 23 de diciembre de 2011

Effect of linkage disequilibrium on the identification of functional variants

artículo científico publicado en 2011

Efficient parameter estimation for models of healthcare-associated pathogen transmission in discrete and continuous time

artículo científico publicado en 2013

Enumerating the decomposable neighbours of a decomposable graph under a simple perturbation scheme

artículo científico publicado en 2009

Enumerating the junction trees of a decomposable graph

artículo científico publicado en 2009

Estimating the parameters of a model for protein-protein interaction graphs

artículo científico publicado en 2006

Evaluation of record linkage between a large healthcare provider and the Utah Population Database.

artículo científico publicado en 2011

Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree

artículo científico publicado en 2005

Extending the Fellegi-Sunter probabilistic record linkage method for approximate field comparators

artículo científico publicado en 2009

Familial associations between cancer sites

artículo científico publicado en 1999

Fine mapping of the Bmgr5 quantitative trait locus for allogeneic bone marrow engraftment in mice

artículo científico publicado en 2013

GMCheck: Bayesian error checking for pedigree genotypes and phenotypes

artículo científico publicado en 2005

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

artículo científico publicado en 2016

Graphical modeling of the joint distribution of alleles at associated loci

artículo científico publicado en 2004

Haplotype association analyses in resources of mixed structure using Monte Carlo testing ⬇️

artículo científico publicado el 9 de diciembre de 2010

Identification and study of Utah pseudo-isolate populations—prospects for gene identification

article

Identification of a major susceptibility locus for lethal graft-versus-host disease in MHC-matched mice

artículo científico publicado en 2009

Identification of regions of positive selection using Shared Genomic Segment analysis

artículo científico publicado en 2011

Identification of specific Y chromosomes associated with increased prostate cancer risk

artículo científico publicado en 2014

Identifying rare variants from exome scans: the GAW17 experience

artículo científico publicado en 2011

Improved hidden Markov model for nosocomial infections

artículo científico publicado en 2013

Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.

artículo científico publicado en 2012

Linkage of body mass index to chromosome 20 in Utah pedigrees.

artículo científico publicado en 2001

Maximum likelihood estimates of allele frequencies and error rates from samples of related individuals by gene counting

artículo científico publicado en 2006

Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

artículo científico publicado en 2018

Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.

artículo científico publicado en 2011

Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees

artículo científico publicado en 2012

Pathways analysis of differential gene expression induced by engrafting doses of total body irradiation for allogeneic bone marrow transplantation in mice ⬇️

artículo científico publicado el 24 de mayo de 2013

Population-based risk assessment for other cancers in relatives of hereditary prostate cancer (HPC) cases

artículo científico publicado en 2005

Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer

artículo científico publicado en 2009

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

artículo científico publicado en 2011

Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study

artículo científico publicado en 2009

Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.

artículo científico publicado en 2007

Shared genomic segment analysis: the power to find rare disease variants

artículo científico publicado en 2012

Software trapping: a strategy for finding genes in large genomic regions

scientific article published on 01 April 1995

Tests of association for rare variants: case control mutation screening

artículo científico publicado en 2011

The conditional independences between variables derived from two independent identically distributed Markov random fields when pairwise order is ignored

artículo científico publicado en 2009

The predictive value of BRCA1 and BRCA2 mutation testing

artículo científico publicado en 2000

Towards linkage analysis with markers in linkage disequilibrium by graphical modelling.

artículo científico publicado en 2007

Use of strain typing data to estimate bacterial transmission rates in healthcare settings.

artículo científico publicado en 2005

Lista de obras de Alun Thomas

A Draft Sequence of the Rice Genome (Oryza sativa L. ssp. japonica)

A Laboratory Information Management System (LIMS) for a high throughput genetic platform aimed at candidate gene mutation screening

A candidate prostate cancer susceptibility gene at chromosome 17p

A chromosome 16 quantitative trait locus regulates allogeneic bone marrow engraftment in nonmyeloablated mice.

A linear time algorithm for calculation of multiple pairwise kinship coefficients and the genetic index of familiality

A method and program for estimating graphical models for linkage disequilibrium that scale linearly with the number of loci, and their application to gene drop simulation

A multivariate time series approach to modeling and forecasting demand in the emergency department.

A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease

A primary genetic linkage map for human chromosome 12.

A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

Accelerated gene counting for haplotype frequency estimation

Accuracy and computational efficiency of a graphical modeling approach to linkage disequilibrium estimation.

An analysis of unclassified missense substitutions in human BRCA1

An application of the latent p value method to assess linkage in asthma pedigrees.

Assessment of SNP streak statistics using gene drop simulation with linkage disequilibrium.

Automated construction and testing of multi-locus gene–gene associations ⬇️

Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions

Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses:ELAC2 and familial early-onset prostate cancer

Characterizing allelic associations from unphased diploid data by graphical modeling.

Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications.

Classifying, identifying and enumerating arbitrary relationships

Creation of a national resource with linked genealogy and phenotypic data: the Veterans Genealogy Project

Detecting Pleiotropy and Epistasis Using Variance Components Linkage Analysis in jPAP ⬇️

Effect of linkage disequilibrium on the identification of functional variants

Efficient parameter estimation for models of healthcare-associated pathogen transmission in discrete and continuous time

Enumerating the decomposable neighbours of a decomposable graph under a simple perturbation scheme

Enumerating the junction trees of a decomposable graph

Estimating the parameters of a model for protein-protein interaction graphs

Evaluation of record linkage between a large healthcare provider and the Utah Population Database.

Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree

Extending the Fellegi-Sunter probabilistic record linkage method for approximate field comparators

Familial associations between cancer sites

Fine mapping of the Bmgr5 quantitative trait locus for allogeneic bone marrow engraftment in mice

GMCheck: Bayesian error checking for pedigree genotypes and phenotypes

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

Graphical modeling of the joint distribution of alleles at associated loci

Haplotype association analyses in resources of mixed structure using Monte Carlo testing ⬇️

Identification and study of Utah pseudo-isolate populations—prospects for gene identification

Identification of a major susceptibility locus for lethal graft-versus-host disease in MHC-matched mice

Identification of regions of positive selection using Shared Genomic Segment analysis

Identification of specific Y chromosomes associated with increased prostate cancer risk

Identifying rare variants from exome scans: the GAW17 experience

Improved hidden Markov model for nosocomial infections

Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.

Linkage of body mass index to chromosome 20 in Utah pedigrees.

Maximum likelihood estimates of allele frequencies and error rates from samples of related individuals by gene counting

Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.

Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees

Pathways analysis of differential gene expression induced by engrafting doses of total body irradiation for allogeneic bone marrow transplantation in mice ⬇️

Population-based risk assessment for other cancers in relatives of hereditary prostate cancer (HPC) cases

Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study

Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.

Shared genomic segment analysis: the power to find rare disease variants

Software trapping: a strategy for finding genes in large genomic regions

Tests of association for rare variants: case control mutation screening

The conditional independences between variables derived from two independent identically distributed Markov random fields when pairwise order is ignored

The predictive value of BRCA1 and BRCA2 mutation testing

Towards linkage analysis with markers in linkage disequilibrium by graphical modelling.

Use of strain typing data to estimate bacterial transmission rates in healthcare settings.