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Nature Communications|February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discoveryPilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
Pain|May 13, 2022
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screenJanine M Wotton, Emma Peterson, Ann M Flenniken, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 9, 2023
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in miceManuela A Oestereicher, Janine M Wotton, Shinya Ayabe, et al.
American Journal of Human Genetics|August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delayRonit Marom, Lindsay C Burrage, Rossella Venditti, et al.
American Journal of Human Genetics|February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia PhenotypesLindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Plos Genetics|December 28, 2020
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral densityAnna L Swan, Christine Schütt, Jan Rozman, et al.
Bioinformatics (Oxford, England)|October 9, 2019
Soft windowing application to improve analysis of high-throughput phenotyping dataHamed Haselimashhadi, Jeremy C Mason, Violeta Munoz-Fuentes, et al.
Communications Biology|December 28, 2018
Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Communications Biology|March 12, 2019
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Nature|April 8, 2021
The NIH Somatic Cell Genome Editing programKrishanu Saha, Erik J Sontheimer, P J Brooks, et al.
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