Lista de obras - Audrey E Hendricks - Dominio Público Uruguay

A comparison of gene region simulation methods

artículo científico publicado en 2012

Assessment of cortical and striatal involvement in 523 Huntington disease brains

artículo científico publicado en 2012

Comparison of statistical approaches to rare variant analysis for quantitative traits.

artículo científico publicado en 2011

Correction for multiple testing in a gene region

artículo científico publicado en 2013

Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxiety

artículo científico publicado en 2017

Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).

artículo científico publicado en 2009

Gene-gene Interaction Analyses for Atrial Fibrillation

artículo científico publicado en 2016

Genetic architecture of human thinness compared to severe obesity

artículo científico publicado en 2019

Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes

artículo científico publicado en 2013

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

artículo científico publicado en 2011

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

artículo científico publicado en 2008

High-throughput analysis suggests differences in journal false discovery rate by subject area and impact factor but not open access status

artículo científico publicado en 2020

Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes

artículo científico publicado en 2008

KSR2 mutations are associated with obesity, insulin resistance, and impaired cellular fuel oxidation

artículo científico publicado en 2013

Longitudinal Reduction in Diversity of Maternal Gut Microbiota During Pregnancy Is Observed in Multiple Low-Resource Settings: Results From the Women First Trial

scientific article published in 2022

Opportunities and challenges for the use of common controls in sequencing studies

artículo científico publicado en 2022

Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain

artículo científico publicado en 2012

Progress in methods for rare variant association

artículo científico publicado en 2016

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls

article

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

artículo científico publicado en 2018

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

artículo científico publicado en 2017

Replication of association between ELAVL4 and Parkinson disease: the GenePD study

artículo científico publicado en 2008

Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset

artículo científico publicado en 2009

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease

artículo científico publicado en 2012

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study

artículo científico publicado en 2008

The UK10K project identifies rare variants in health and disease

artículo científico publicado en 2015

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

artículo científico publicado en 2017

Whole-exome sequencing in an isolated population from the Dalmatian island of Vis

artículo científico publicado en 2016

Lista de obras de Audrey E Hendricks

A comparison of gene region simulation methods

Assessment of cortical and striatal involvement in 523 Huntington disease brains

Comparison of statistical approaches to rare variant analysis for quantitative traits.

Correction for multiple testing in a gene region

Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxiety

Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).

Gene-gene Interaction Analyses for Atrial Fibrillation

Genetic architecture of human thinness compared to severe obesity

Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

High-throughput analysis suggests differences in journal false discovery rate by subject area and impact factor but not open access status

Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes

KSR2 mutations are associated with obesity, insulin resistance, and impaired cellular fuel oxidation

Longitudinal Reduction in Diversity of Maternal Gut Microbiota During Pregnancy Is Observed in Multiple Low-Resource Settings: Results From the Women First Trial

Opportunities and challenges for the use of common controls in sequencing studies

Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain

Progress in methods for rare variant association

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

Replication of association between ELAVL4 and Parkinson disease: the GenePD study

Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study

The UK10K project identifies rare variants in health and disease

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

Whole-exome sequencing in an isolated population from the Dalmatian island of Vis