A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations

Por Zhu, Xiaolin, Padmanabhan, Raghavendra, Copeland, Brett, Bridgers, Joshua, Ren, Zhong, Kamalakaran, Sitharthan, O'Driscoll-Collins, Ailbhe, Berkovic, Samuel F., Scheffer, Ingrid E., Poduri, Annapurna, Mei, Davide, Guerrini, Renzo, Lowenstein, Daniel H., Allen, Andrew S., Heinzen, Erin L., Goldstein, David B.
Publicado no PLoS Genet (2017)

Systems-Based Analysis of the Sarcocystis neurona Genome Identifies Pathways That Contribute to a Heteroxenous Life Cycle

Por Blazejewski, Tomasz, Nursimulu, Nirvana, Pszenny, Viviana, Dangoudoubiyam, Sriveny, Namasivayam, Sivaranjani, Chiasson, Melissa A., Chessman, Kyle, Tonkin, Michelle, Swapna, Lakshmipuram S., Hung, Stacy S., Bridgers, Joshua, Ricklefs, Stacy M., Boulanger, Martin J., Dubey, Jitender P., Porcella, Stephen F., Kissinger, Jessica C., Howe, Daniel K., Grigg, Michael E., Parkinson, John
Publicado no mBio (2015)

An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis

Por Petrovski, Slavé, Todd, Jamie L., Durheim, Michael T., Wang, Quanli, Chien, Jason W., Kelly, Fran L., Frankel, Courtney, Mebane, Caroline M., Ren, Zhong, Bridgers, Joshua, Urban, Thomas J., Malone, Colin D., Finlen Copeland, Ashley, Brinkley, Christie, Allen, Andrew S., O’Riordan, Thomas, McHutchison, John G., Palmer, Scott M., Goldstein, David B.
Publicado no Am J Respir Crit Care Med (2017)