Copy number variation in African Americans

Por McElroy, Joseph P, Nelson, Matthew R, Caillier, Stacy J, Oksenberg, Jorge R
Publicado em 2009

SNP imputation bias reduces effect size determination

Por Khankhanian, Pouya, Din, Lennox, Caillier, Stacy J., Gourraud, Pierre-Antoine, Baranzini, Sergio E.
Publicado no Front Genet (2015)

The killer immunoglobulin-like receptor KIR3DL1 combination with HLA-Bw4 is protective against multiple sclerosis in African Americans

Por Hollenbach, Jill A., Pando, Marcelo J., Caillier, Stacy J., Gourraud, Pierre-Antoine, Oksenberg, Jorge R.
Publicado no Genes Immun (2016)

Synergy or Independence? Deciphering the Interaction of HLA Class I and NK Cell KIR Alleles in Early HIV-1 Disease Progression

Por Barbour, Jason D, Sriram, Uma, Caillier, Stacy J, Levy, Jay A, Hecht, Frederick M, Oksenberg, Jorge R
Publicado em 2007

Correction: Synergy or Independence? Deciphering the Interaction of HLA Class I and NK Cell KIR Alleles in Early HIV-1 Disease Progression

Por Barbour, Jason D, Sriram, Uma, Caillier, Stacy J, Levy, Jay A, Hecht, Frederick M, Oksenberg, Jorge R
Publicado em 2007

Genetic variation in the odorant receptors family 13 and the mhc loci influence mate selection in a multiple sclerosis dataset

Por Khankhanian, Pouya, Gourraud, Pierre-Antoine, Caillier, Stacy J, Santaniello, Adam, Hauser, Stephen L, Baranzini, Sergio E, Oksenberg, Jorge R
Publicado em 2010

Mitochondrial DNA sequence variation in multiple sclerosis

Por Tranah, Gregory J., Santaniello, Adam, Caillier, Stacy J., D'Alfonso, Sandra, Martinelli Boneschi, Filippo, Hauser, Stephen L., Oksenberg, Jorge R.
Publicado no Neurology (2015)

The R620W Polymorphism of the Protein Tyrosine Phosphatase PTPN22 Is Not Associated with Multiple Sclerosis

Por Begovich, Ann B., Caillier, Stacy J., Alexander, Heather C., Penko, Joanne M., Hauser, Stephen L., Barcellos, Lisa F., Oksenberg, Jorge R.
Publicado em 2005

Aggregation of MS genetic risk variants in multiple and single case families

Por Gourraud, Pierre-Antoine, McElroy, Joseph P., Caillier, Stacy J., Johnson, Britt A., Santaniello, Adam, Hauser, Stephen L., Oksenberg, Jorge. R.
Publicado em 2011

A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome

Por Didonna, Alessandro, Isobe, Noriko, Caillier, Stacy J., Li, Kathy H., Burlingame, Alma L., Hauser, Stephen L., Baranzini, Sergio E., Patsopoulos, Nikolaos A., Oksenberg, Jorge R.
Publicado no Hum Mol Genet (2015)

Abrogation of T cell quiescence characterizes patients at high risk for multiple sclerosis after the initial neurological event

Por Corvol, Jean-Christophe, Pelletier, Daniel, Henry, Roland G., Caillier, Stacy J., Wang, Joanne, Pappas, Derek, Casazza, Simona, Okuda, Darin T., Hauser, Stephen L., Oksenberg, Jorge R., Baranzini, Sergio E.
Publicado em 2008

Transcription-Based Prediction of Response to IFNβ Using Supervised Computational Methods

Por Baranzini, Sergio E, Mousavi, Parvin, Rio, Jordi, Caillier, Stacy J, Stillman, Althea, Villoslada, Pablo, Wyatt, Matthew M, Comabella, Manuel, Greller, Larry D, Somogyi, Roland, Montalban, Xavier, Oksenberg, Jorge R
Publicado em 2005

Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis

Por Barcellos, Lisa F., Ramsay, Patricia P., Caillier, Stacy J., Sawcer, Stephen, Haines, Jonathan, Schmidt, Silke, Pericak-Vance, Margaret, Compston, D. Alastair S., Gabatto, Pablo, Hauser, Stephen L., Oksenberg, Jorge R.
Publicado em 2008

Uncoupling the Roles of HLA-DRB1 and HLA-DRB5 Genes in Multiple Sclerosis()

Por Caillier, Stacy J., Briggs, Farren, Cree, Bruce A. C., Baranzini, Sergio E., Fernandez-Viña, Marcelo, Ramsay, Patricia P., Khan, Omar, Royal, Walter, Hauser, Stephen L., Barcellos, Lisa F., Oksenberg, Jorge R.
Publicado no J Immunol (2008)

Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls

Por Nickles, Dorothee, Chen, Hsuan P., Li, Michael M., Khankhanian, Pouya, Madireddy, Lohith, Caillier, Stacy J., Santaniello, Adam, Cree, Bruce A.C., Pelletier, Daniel, Hauser, Stephen L., Oksenberg, Jorge R., Baranzini, Sergio E.
Publicado em 2013

Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis

Por Harbo, Hanne F, Isobe, Noriko, Berg-Hansen, Pål, Bos, Steffan D, Caillier, Stacy J, Gustavsen, Marte W, Mero, Inger-Lise, Celius, Elisabeth Gulowsen, Hauser, Stephen L, Oksenberg, Jorge R, Gourraud, Pierre-Antoine
Publicado em 2013

Refining the association of MHC with multiple sclerosis in African Americans

Por McElroy, Joseph P., Cree, Bruce A. C., Caillier, Stacy J., Gregersen, Peter K., Herbert, Joseph, Khan, Omar A., Freudenberg, Jan, Lee, Annette, Bridges, S. Louis, Hauser, Stephen L., Oksenberg, Jorge R., Gourraud, Pierre-Antoine
Publicado em 2010

Multiple sclerosis susceptibility alleles in African Americans

Por Johnson, Britt A., Wang, Joanne, Taylor, Elise M., Caillier, Stacy J., Herbert, Joseph, Khan, Omar A., Cross, Anne H., De Jager, Philip L., Gourraud, Pierre-Antoine F., Cree, Bruce C.A., Hauser, Stephen L., Oksenberg, Jorge R.
Publicado em 2009

Association of HLA Genetic Risk Burden With Disease Phenotypes in Multiple Sclerosis

Por Isobe, Noriko, Keshavan, Anisha, Gourraud, Pierre-Antoine, Zhu, Alyssa H., Datta, Esha, Schlaeger, Regina, Caillier, Stacy J., Santaniello, Adam, Lizée, Antoine, Himmelstein, Daniel S., Baranzini, Sergio E., Hollenbach, Jill, Cree, Bruce A. C., Hauser, Stephen L., Oksenberg, Jorge R., Henry, Roland G.
Publicado no JAMA Neurol (2016)

Genetic risk variants in African Americans with multiple sclerosis

Por Isobe, Noriko, Gourraud, Pierre-Antoine, Harbo, Hanne F., Caillier, Stacy J., Santaniello, Adam, Khankhanian, Pouya, Maiers, Martin, Spellman, Stephen, Cereb, Nezih, Yang, SooYoung, Pando, Marcelo J., Piccio, Laura, Cross, Anne H., De Jager, Philip L., Cree, Bruce A.C., Hauser, Stephen L., Oksenberg, Jorge R.
Publicado em 2013