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Plos Genetics|July 23, 2013
ENU-induced mutation in the DNA-binding domain of KLF3 reveals important roles for KLF3 in cardiovascular development and function in miceLois Kelsey, Ann M Flenniken, Dawei Qu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2024
Large-scale genomic investigation of pediatric cholestasis reveals a novel hepatorenal ciliopathy caused by PSKH1 mutationsSateesh Maddirevula, Mohammad Shagrani, Ae-Ri Ji, et al.
Conservation Genetics (Print)|August 14, 2018
The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservationVioleta Muñoz-Fuentes, Pilar Cacheiro, Terrence F Meehan, et al.
Neuroscience Applied|July 14, 2025
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brainLillian Garrett, Dietrich Trümbach, Donghyung Lee, et al.
Genome Medicine|October 13, 2022
Mendelian gene identification through mouse embryo viability screeningPilar Cacheiro, Carl Henrik Westerberg, Jesse Mager, et al.
BMC Biology|February 4, 2023
Genome-wide screening reveals the genetic basis of mammalian embryonic eye developmentJustine M Chee, Louise Lanoue, Dave Clary, et al.
Scientific Reports|December 1, 2022
Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genesKendall Higgins, Bret A Moore, Zorana Berberovic, et al.
Development (Cambridge, England)|September 13, 2005
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasiaAnn M Flenniken, Lucy R Osborne, Nicole Anderson, et al.
Plos Genetics|January 14, 2020
High-throughput discovery of genetic determinants of circadian misalignmentTao Zhang, Pancheng Xie, Yingying Dong, et al.
American Journal of Ophthalmology|June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROMEAla Moshiri, Niusha Kasiri, Michael Shea, et al.
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