Lista de obras - Eric M. Sobel - Dominio Público Uruguay

A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus).

artículo científico publicado en 2007

A hierarchical model for estimating significance levels of non-parametric linkage statistics for large pedigrees

article

A random walk method for computing genetic location scores.

artículo científico publicado en 1991

A susceptibility locus for migraine with aura, on chromosome 4q24.

scientific article published on 08 February 2002

Association testing with Mendel.

artículo científico publicado en 2005

Breast Cancer Risk and Insulin Resistance: Post Genome-Wide Gene-Environment Interaction Study Using a Random Survival Forest

scientific article published on 01 April 2019

Chromosome 1 loci in Finnish schizophrenia families

artículo científico publicado en 2001

Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal women

artículo científico publicado en 2013

Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families

artículo científico publicado en 2007

Detection and integration of genotyping errors in statistical genetics

artículo científico publicado en 2002

Detection of intergenerational genetic effects with application to HLA-B matching as a risk factor for schizophrenia

artículo científico publicado en 2011

Effect of genetic variants and traits related to glucose metabolism and their interaction with obesity on breast and colorectal cancer risk among postmenopausal women

artículo científico publicado en 2017

Efficient simulation of P values for linkage analysis

artículo científico publicado en 2004

Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval

artículo científico publicado en 2009

Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data

artículo científico publicado en 2016

Fast genome-wide pedigree quantitative trait loci analysis using MENDEL

artículo científico publicado en 2014

Fine mapping of the multiple sclerosis susceptibility locus on 5p14–p12

artículo científico publicado en 2005

Genome-wide QTL and eQTL analyses using Mendel

artículo científico publicado en 2016

Genome-wide association analysis by lasso penalized logistic regression

scientific article published on 28 January 2009

Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study

scientific article published on 14 September 2020

Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women

article

Genome-wide ultraconserved elements exhibit higher phylogenetic informativeness than traditional gene markers in percomorph fishes

artículo científico publicado en 2015

Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes

artículo científico publicado en 2017

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

artículo científico publicado en 2001

Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome

artículo científico publicado en 2008

Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex

artículo científico publicado en 2010

Interaction of insulin-like growth factor-I and insulin resistance-related genetic variants with lifestyle factors on postmenopausal breast cancer risk

artículo científico publicado en 2017

Linkage analysis without defined pedigrees

artículo científico publicado en 2011

Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.

artículo científico publicado en 2010

Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia

artículo científico publicado en 2004

Measured Haplotype Analysis of the Angiotensin-I Converting Enzyme Gene

article

Mendel-GPU: haplotyping and genotype imputation on graphics processing units

artículo científico publicado en 2012

Mendel: the Swiss army knife of genetic analysis programs

artículo científico publicado en 2013

Merging microsatellite data

artículo científico publicado en 2006

Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis

artículo científico publicado en 2008

Mixed effects models for quantitative trait loci mapping with inbred strains

artículo científico publicado en 2008

Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees

artículo científico publicado en 2001

Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data

artículo científico publicado en 2014

Obesity and associated lifestyles modify the effect of glucose metabolism-related genetic variants on impaired glucose homeostasis among postmenopausal women ⬇️

artículo científico publicado en 2016

Penalized regression for genome-wide association screening of sequence data ⬇️

artículo científico publicado el 1 de enero de 2011

Post Genome-Wide Gene-Environment Interaction Study Using Random Survival Forest: Insulin Resistance, Lifestyle Factors, and Colorectal Cancer Risk

scientific article published on 25 September 2019

Quantitative trait Loci association mapping by imputation of strain origins in multifounder crosses

artículo científico publicado en 2011

Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20.

artículo científico publicado en 2007

Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3.

artículo científico publicado en 2012

Shared molecular pathways and gene networks for cardiovascular disease and type 2 diabetes mellitus in women across diverse ethnicities.

artículo científico publicado en 2014

The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions

artículo científico publicado en 2015

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

scholarly article

The systems genetics resource: a web application to mine global data for complex disease traits

artículo científico publicado en 2013

Trait components provide tools to dissect the genetic susceptibility of migraine

artículo científico publicado en 2006

Unifying ideas for non-parametric linkage analysis

artículo científico publicado en 2011

Variance component models for X-linked QTLs

artículo científico publicado en 2006

WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels

artículo científico publicado en 2008

Lista de obras de Eric M. Sobel

A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus).

A hierarchical model for estimating significance levels of non-parametric linkage statistics for large pedigrees

A random walk method for computing genetic location scores.

A susceptibility locus for migraine with aura, on chromosome 4q24.

Association testing with Mendel.

Breast Cancer Risk and Insulin Resistance: Post Genome-Wide Gene-Environment Interaction Study Using a Random Survival Forest

Chromosome 1 loci in Finnish schizophrenia families

Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal women

Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families

Detection and integration of genotyping errors in statistical genetics

Detection of intergenerational genetic effects with application to HLA-B matching as a risk factor for schizophrenia

Effect of genetic variants and traits related to glucose metabolism and their interaction with obesity on breast and colorectal cancer risk among postmenopausal women

Efficient simulation of P values for linkage analysis

Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval

Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data

Fast genome-wide pedigree quantitative trait loci analysis using MENDEL

Fine mapping of the multiple sclerosis susceptibility locus on 5p14–p12

Genome-wide QTL and eQTL analyses using Mendel

Genome-wide association analysis by lasso penalized logistic regression

Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study

Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women

Genome-wide ultraconserved elements exhibit higher phylogenetic informativeness than traditional gene markers in percomorph fishes

Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome

Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex

Interaction of insulin-like growth factor-I and insulin resistance-related genetic variants with lifestyle factors on postmenopausal breast cancer risk

Linkage analysis without defined pedigrees

Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.

Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia

Measured Haplotype Analysis of the Angiotensin-I Converting Enzyme Gene

Mendel-GPU: haplotyping and genotype imputation on graphics processing units

Mendel: the Swiss army knife of genetic analysis programs

Merging microsatellite data

Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis

Mixed effects models for quantitative trait loci mapping with inbred strains

Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees

Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data

Obesity and associated lifestyles modify the effect of glucose metabolism-related genetic variants on impaired glucose homeostasis among postmenopausal women ⬇️

Penalized regression for genome-wide association screening of sequence data ⬇️

Post Genome-Wide Gene-Environment Interaction Study Using Random Survival Forest: Insulin Resistance, Lifestyle Factors, and Colorectal Cancer Risk

Quantitative trait Loci association mapping by imputation of strain origins in multifounder crosses

Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20.

Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3.

Shared molecular pathways and gene networks for cardiovascular disease and type 2 diabetes mellitus in women across diverse ethnicities.

The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

The systems genetics resource: a web application to mine global data for complex disease traits

Trait components provide tools to dissect the genetic susceptibility of migraine

Unifying ideas for non-parametric linkage analysis

Variance component models for X-linked QTLs

WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels