Impact of exome sequencing in inflammatory bowel disease

Por Cardinale, Christopher J, Kelsen, Judith R, Baldassano, Robert N, Hakonarson, Hakon
Publicado em 2013

Termination Factor Rho and Its Cofactors NusA and NusG Silence Foreign DNA in E. coli

Por Cardinale, Christopher J., Washburn, Robert S., Tadigotla, Vasisht R., Brown, Lewis M., Gottesman, Max E., Nudler, Evgeny
Publicado em 2008

Transcriptome Profiling of Human Ulcerative Colitis Mucosa Reveals Altered Expression of Pathways Enriched in Genetic Susceptibility Loci

Por Cardinale, Christopher J., Wei, Zhi, Li, Jin, Zhu, Junfei, Gu, Mengnan, Baldassano, Robert N., Grant, Struan F. A., Hakonarson, Hakon
Publicado em 2014

CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations

Por Dajani, Rana, Li, Jin, Wei, Zhi, Glessner, Joseph T., Chang, Xiao, Cardinale, Christopher J., Pellegrino, Renata, Wang, Tiancheng, Hakooz, Nancy, Khader, Yousef, Sheshani, Amina, Zandaki, Duaa, Hakonarson, Hakon
Publicado no Sci Rep (2015)

A Novel BHLHE41 Variant is Associated with Short Sleep and Resistance to Sleep Deprivation in Humans

Por Pellegrino, Renata, Kavakli, Ibrahim Halil, Goel, Namni, Cardinale, Christopher J., Dinges, David F., Kuna, Samuel T., Maislin, Greg, Van Dongen, Hans P.A., Tufik, Sergio, Hogenesch, John B., Hakonarson, Hakon, Pack, Allan I.
Publicado em 2014

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study

Por Cardinale, Christopher J., Li, Dong, Tian, Lifeng, Connolly, John J., March, Michael E., Hou, Cuiping, Wang, Fengxiang, Snyder, James, Kim, Cecilia E., Chiavacci, Rosetta M., Sleiman, Patrick M., Burnham, Jon M., Hakonarson, Hakon
Publicado no BMC Musculoskelet Disord (2016)

Extended haplotype association study in Crohn’s disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3

Por Zhang, Wei, Hui, Ken Y., Gusev, Alexander, Warner, Neil, Evelyn Ng, Sok Meng, Ferguson, John, Choi, Murim, Burberry, Aaron, Abraham, Clara, Mayer, Lloyd, Desnick, Robert J., Cardinale, Christopher J., Hakonarson, Hakon, Waterman, Matti, Chowers, Yehuda, Karban, Amir, Brant, Steven R., Silverberg, Mark S., Gregersen, Peter K., Katz, Seymour, Lifton, Richard P., Zhao, Hongyu, Nuñez, Gabriel, Pe’er, Itsik, Peter, Inga, Cho, Judy H.
Publicado em 2013

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Por Li, Yun R., Zhao, Sihai D., Li, Jin, Bradfield, Jonathan P., Mohebnasab, Maede, Steel, Laura, Kobie, Julie, Abrams, Debra J., Mentch, Frank D., Glessner, Joseph T., Guo, Yiran, Wei, Zhi, Connolly, John J., Cardinale, Christopher J., Bakay, Marina, Li, Dong, Maggadottir, S. Melkorka, Thomas, Kelly A., Qui, Haijun, Chiavacci, Rosetta M., Kim, Cecilia E., Wang, Fengxiang, Snyder, James, Flatø, Berit, Førre, Øystein, Denson, Lee A., Thompson, Susan D., Becker, Mara L., Guthery, Stephen L., Latiano, Anna, Perez, Elena, Resnick, Elena, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Silverberg, Mark S., Lie, Benedicte A., Punaro, Marilynn, Russell, Richard K., Wilson, David C., Dubinsky, Marla C., Monos, Dimitri S., Annese, Vito, Munro, Jane E., Wise, Carol, Chapel, Helen, Cunningham-Rundles, Charlotte, Orange, Jordan S., Behrens, Edward M., Sullivan, Kathleen E., Kugathasan, Subra, Griffiths, Anne M., Satsangi, Jack, Grant, Struan F. A., Sleiman, Patrick M. A., Finkel, Terri H., Polychronakos, Constantin, Baldassano, Robert N., Luning Prak, Eline T., Ellis, Justine A., Li, Hongzhe, Keating, Brendan J., Hakonarson, Hakon
Publicado no Nat Commun (2015)

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Por Li, Yun R, Li, Jin, Zhao, Sihai D, Bradfield, Jonathan P, Mentch, Frank D, Maggadottir, S Melkorka, Hou, Cuiping, Abrams, Debra J, Chang, Diana, Gao, Feng, Guo, Yiran, Wei, Zhi, Connolly, John J, Cardinale, Christopher J, Bakay, Marina, Glessner, Joseph T, Li, Dong, Kao, Charlly, Thomas, Kelly A, Qiu, Haijun, Chiavacci, Rosetta M, Kim, Cecilia E, Wang, Fengxiang, Snyder, James, Richie, Marylyn D, Flatø, Berit, Førre, Øystein, Denson, Lee A, Thompson, Susan D, Becker, Mara L, Guthery, Stephen L, Latiano, Anna, Perez, Elena, Resnick, Elena, Russell, Richard K, Wilson, David C, Silverberg, Mark S, Annese, Vito, Lie, Benedicte A, Punaro, Marilynn, Dubinsky, Marla C, Monos, Dimitri S, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Kugathasan, Subra, Ellis, Justine A, Munro, Jane E, Sullivan, Kathleen E, Wise, Carol A, Chapel, Helen, Cunningham-Rundles, Charlotte, Grant, Struan F A, Orange, Jordan S, Sleiman, Patrick M A, Behrens, Edward M, Griffiths, Anne M, Satsangi, Jack, Finkel, Terri H, Keinan, Alon, Prak, Eline T Luning, Polychronakos, Constantin, Baldassano, Robert N, Li, Hongzhe, Keating, Brendan J, Hakonarson, Hakon
Publicado no Nat Med (2015)