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List of works by 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

scientific article

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

scientific article

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

scientific article published on 26 June 2012

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

scientific article

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.

scientific article published on 25 April 2018

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

scientific article published on 17 May 2019

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

scientific article published on 2 December 2009

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

scientific article

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

scientific article published in 2022

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

scientific article published on 02 April 2019

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

scientific article published on 25 May 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

scientific article (publication date: March 2014)

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

scientific article published in 2022

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

scientific article published on 12 December 2016

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

scientific article published in 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

scientific article published on 26 August 2021

Promising 2-Pronged Approach to Genetic Basis of Bipolar Disorder

scientific article published on 01 June 2016

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

scientific article published on 7 September 2018

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

Transcriptomic changes in the frontal cortex associated with paternal age.

scientific article published on 23 March 2014

Transcriptomic signatures across human tissues identify functional rare genetic variation

scientific article

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