Transcriptome Sequencing of a Large Human Family Identifies the Impact of Rare Noncoding Variants

Por Li, Xin, Battle, Alexis, Karczewski, Konrad J., Zappala, Zach, Knowles, David A., Smith, Kevin S., Kukurba, Kim R., Wu, Eric, Simon, Noah, Montgomery, Stephen B.
Publicado em 2014

Genome-Wide Profiling of Cap-Independent Translation Enhancing Elements in the Human Genome

Por Wellensiek, Brian P., Larsen, Andrew C., Stephens, Bret, Kukurba, Kim, Waern, Karl, Briones, Natalia, Liu, Li, Snyder, Michael, Jacobs, Bertram L., Kumar, Sudhir, Chaput, John C.
Publicado em 2013

PATH-SCAN: A REPORTING TOOL FOR IDENTIFYING CLINICALLY ACTIONABLE VARIANTS

Por DANESHJOU, ROXANA, ZAPPALA, ZACHARY, KUKURBA, KIM, BOYLE, SEAN M, ORMOND, KELLY E, KLEIN, TERI E, SNYDER, MICHAEL, BUSTAMANTE, CARLOS D, ALTMAN, RUSS B, MONTGOMERY, STEPHEN B
Publicado em 2014

Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse

Por Babak, Tomas, DeVeale, Brian, Tsang, Emily K., Zhou, Yiqi, Li, Xin, Smith, Kevin S., Kukurba, Kim R., Zhang, Rui, Li, Jin Billy, van der Kooy, Derek, Montgomery, Stephen B., Fraser, Hunter B.
Publicado no Nat Genet (2015)

The landscape of genomic imprinting across diverse adult human tissues

Por Baran, Yael, Subramaniam, Meena, Biton, Anne, Tukiainen, Taru, Tsang, Emily K., Rivas, Manuel A., Pirinen, Matti, Gutierrez-Arcelus, Maria, Smith, Kevin S., Kukurba, Kim R., Zhang, Rui, Eng, Celeste, Torgerson, Dara G., Urbanek, Cydney, Li, Jin Billy, Rodriguez-Santana, Jose R., Burchard, Esteban G., Seibold, Max A., MacArthur, Daniel G., Montgomery, Stephen B., Zaitlen, Noah A., Lappalainen, Tuuli
Publicado no Genome Res (2015)