Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D

Journal: PLoS Genet

Publication date: 2023

Journal: PLoS Genet

Publication Year: 2023

Authors & Co-authors: 

A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program

Journal: PLoS Genet

Publication date: 2022

Journal: PLoS Genet

Publication Year: 2022

Authors & Co-authors: 

A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?

Journal: PLoS genetics

Publication date: 2017

Journal: PLoS genetics

Publication Year: 2017

Authors & Co-authors:  Zhao Xiao-Nan XN Lokanga Rachel R Allette Kimaada K Gazy Inbal I Wu Di D Usdin Karen K

Heterozygosity for a hypomorphic Polβ mutation reduces the expansion frequency in a mouse model of the Fragile X-related disorders.

Journal: PLoS genetics

Publication date: 2016

Journal: PLoS genetics

Publication Year: 2016

Authors & Co-authors:  Lokanga Rachel Adihe RA Senejani Alireza Ghodsi AG Sweasy Joann Balazs JB Usdin Karen K

Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.

Journal: PLoS genetics

Publication date: 2015

Journal: PLoS genetics

Publication Year: 2015

Authors & Co-authors:  Prescott Natalie J NJ Lehne Benjamin B Stone Kristina K Lee James C JC Taylor Kirstin K Knight Jo J Papouli Efterpi E Mirza Muddassar M MM Simpson Michael A MA Spain Sarah L SL