Lista de obras - Rachel L Kember - Dominio Público Uruguay

A B2 SINE insertion in the Comt1 gene (Comt1(B2i)) results in an overexpressing, behavior modifying allele present in classical inbred mouse strains

artículo científico publicado en 2010

A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes

scientific article published on 06 August 2019

A population-specific reference panel empowers genetic studies of Anabaptist populations

artículo científico publicado en 2017

Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: implications for neuropsychiatric disease.

artículo científico publicado en 2012

Advancing paternal age is associated with deficits in social and exploratory behaviors in the offspring: a mouse model

artículo científico publicado en 2009

Association of Inherited Pathogenic Variants in Checkpoint Kinase 2 (CHEK2) With Susceptibility to Testicular Germ Cell Tumors

scientific article published on 01 April 2019

Author Correction: A population-specific reference panel empowers genetic studies of Anabaptist populations.

artículo científico publicado en 2018

Author Correction: Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

artículo científico publicado en 2019

Behavioural battery testing: evaluation and behavioural outcomes in 8 inbred mouse strains

artículo científico publicado en 2009

Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

artículo científico publicado en 2015

Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree

Genetically Determined Birthweight Associates with Atrial Fibrillation: A Mendelian Randomization Study

scientific article published on 27 April 2020

Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci

artículo científico publicado en 2022

Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

artículo científico publicado en 2019

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

artículo científico publicado en 2020

Genomic Risk Stratification Predicts All-Cause Mortality After Cardiac Catheterization

scientific article published on 01 November 2018

Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate

artículo científico publicado en 2014

Identifying and Reducing Bias in Genome-Wide Association Studies of Alcohol-Related Traits

artículo científico publicado en 2022

Increased burden of deleterious variants in essential genes in autism spectrum disorder

artículo científico publicado en 2016

Integrating human brain proteomic data with genome-wide association study findings identifies novel brain proteins in substance use traits

artículo científico publicado en 2022

Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease

scientific article published on 01 June 2020

Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction

artículo científico publicado en 2021

Promising 2-Pronged Approach to Genetic Basis of Bipolar Disorder

artículo científico publicado en 2016

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

artículo científico publicado en 2018

The power of genetic diversity in genome-wide association studies of lipids

Transcriptomic changes in the frontal cortex associated with paternal age.

artículo científico publicado en 2014

Transcriptomic signatures across human tissues identify functional rare genetic variation

artículo científico publicado en 2020

Lista de obras de Rachel L Kember

A B2 SINE insertion in the Comt1 gene (Comt1(B2i)) results in an overexpressing, behavior modifying allele present in classical inbred mouse strains

A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes

A population-specific reference panel empowers genetic studies of Anabaptist populations

Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: implications for neuropsychiatric disease.

Advancing paternal age is associated with deficits in social and exploratory behaviors in the offspring: a mouse model

Association of Inherited Pathogenic Variants in Checkpoint Kinase 2 (CHEK2) With Susceptibility to Testicular Germ Cell Tumors

Author Correction: A population-specific reference panel empowers genetic studies of Anabaptist populations.

Author Correction: Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

Behavioural battery testing: evaluation and behavioural outcomes in 8 inbred mouse strains

Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree

Genetically Determined Birthweight Associates with Atrial Fibrillation: A Mendelian Randomization Study

Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci

Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

Genomic Risk Stratification Predicts All-Cause Mortality After Cardiac Catheterization

Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate

Identifying and Reducing Bias in Genome-Wide Association Studies of Alcohol-Related Traits

Increased burden of deleterious variants in essential genes in autism spectrum disorder

Integrating human brain proteomic data with genome-wide association study findings identifies novel brain proteins in substance use traits

Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease

Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction

Promising 2-Pronged Approach to Genetic Basis of Bipolar Disorder

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

The power of genetic diversity in genome-wide association studies of lipids

Transcriptomic changes in the frontal cortex associated with paternal age.

Transcriptomic signatures across human tissues identify functional rare genetic variation