Established Genetic Risk Factors Do Not Distinguish Early and Later Onset Crohn’s Disease

le Essers, Jonah B., Lee, Jessica J., Kugathasan, Subra, Stevens, Christine R., Grand, Richard J., Daly, Mark J.
Foilsithe 2009

Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis

le Fernando, Michelle M. A., Stevens, Christine R., Walsh, Emily C., De Jager, Philip L., Goyette, Philippe, Plenge, Robert M., Vyse, Timothy J., Rioux, John D.
Foilsithe 2008

SMAD3 gene variant is a risk factor for recurrent surgery in patients with Crohn’s disease

le Fowler, Sharyle A, Ananthakrishnan, Ashwin N, Gardet, Agnes, Stevens, Christine R, Korzenik, Joshua R, Sands, Bruce E, Daly, Mark J, Xavier, Ramnik J, Yajnik, Vijay
Foilsithe in J Crohns Colitis (2014)

Identification of Two Independent Risk Factors for Lupus within the MHC in United Kingdom Families

le Fernando, Michelle M. A, Stevens, Christine R, Sabeti, Pardis C, Walsh, Emily C, McWhinnie, Alasdair J. M, Shah, Anila, Green, Todd, Rioux, John D, Vyse, Timothy J
Foilsithe 2007

Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism

le Chahrour, Maria H., Yu, Timothy W., Lim, Elaine T., Ataman, Bulent, Coulter, Michael E., Hill, R. Sean, Stevens, Christine R., Schubert, Christian R., Greenberg, Michael E., Gabriel, Stacey B., Walsh, Christopher A.
Foilsithe 2012

PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features

le Khalil, Raida, Kenny, Connor, Hill, R. Sean, Mochida, Ganeshwaran H., Nasir, Ramzi H., Partlow, Jennifer N., Barry, Brenda J., Al-Saffar, Muna, Egan, Chloe, Stevens, Christine R., Gabriel, Stacey B., Barkovich, A. James, Ellison, Jay W., Al-Gazali, Lihadh, Walsh, Christopher A., Chahrour, Maria H.
Foilsithe in Am J Med Genet B Neuropsychiatr Genet (2018)

Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome

le Manzini, M. Chiara, Tambunan, Dimira E., Hill, R. Sean, Yu, Tim W., Maynard, Thomas M., Heinzen, Erin L., Shianna, Kevin V., Stevens, Christine R., Partlow, Jennifer N., Barry, Brenda J., Rodriguez, Jacqueline, Gupta, Vandana A., Al-Qudah, Abdel-Karim, Eyaid, Wafaa M., Friedman, Jan M., Salih, Mustafa A., Clark, Robin, Moroni, Isabella, Mora, Marina, Beggs, Alan H., Gabriel, Stacey B., Walsh, Christopher A.
Foilsithe 2012

Evolution of Osteocrin as an activity-regulated factor in the primate brain

le Ataman, Bulent, Boulting, Gabriella L., Harmin, David A., Yang, Marty G., Baker-Salisbury, Mollie, Yap, Ee-Lynn, Malik, Athar N., Mei, Kevin, Rubin, Alex A., Spiegel, Ivo, Durresi, Ershela, Sharma, Nikhil, Hu, Linda S., Pletikos, Mihovil, Griffith, Eric C., Partlow, Jennifer N., Stevens, Christine R., Adli, Mazhar, Chahrour, Maria, Sestan, Nenad, Walsh, Christopher A., Berezovskii, Vladimir K., Livingstone, Margaret S., Greenberg, Michael E.
Foilsithe in Nature (2016)

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

le McGovern, Dermot P.B., Gardet, Agnès, Törkvist, Leif, Goyette, Philippe, Essers, Jonah, Taylor, Kent D., Neale, Benjamin M., Ong, Rick T.H., Lagacé, Caroline, Li, Chun, Green, Todd, Stevens, Christine R., Beauchamp, Claudine, Fleshner, Phillip R., Carlson, Marie, D'Amato, Mauro, Halfvarson, Jonas, Hibberd, Martin L., Lördal, Mikael, Padyukov, Leonid, Andriulli, Angelo, Colombo, Elisabetta, Latiano, Anna, Palmieri, Orazio, Bernard, Edmond-Jean, Deslandres, Colette, Hommes, Daan W., de Jong, Dirk J, Stokkers, Pieter C., Weersma, Rinse K., Sharma, Yashoda, Silverberg, Mark, Cho, Judy H., Wu, Jing, Roeder, Kathryn, Brant, Steven R., Schumm, L. Phillip, Duerr, Richard H., Dubinsky, Marla C., Glazer, Nicole L., Haritunians, Talin, Ippoliti, Andy, Melmed, Gil Y., Siscovick, David S., Vasiliauskas, Eric A., Targan, Stephan R., Annese, Vito, Wijmenga, Cisca, Pettersson, Sven, Rotter, Jerome I., Xavier, Ramnik J., Daly, Mark J., Rioux, John D., Seielstad, Mark
Foilsithe 2010

Identification of common genetic risk variants for autism spectrum disorder

le Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Poterba, Timothy, Poulsen, Jesper Buchhave, St Pourcain, Beate, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Smith, George Davey, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.
Foilsithe in Nat Genet (2019)