Serotonin 2c receptor RNA editing in major depression and suicide

Por Lyddon, Rebecca, Dwork, Andrew J., Keddache, Mehdi, Siever, Larry J., Dracheva, Stella
Publicado em 2012

Compound heterozygosity for two novel mutations in the erythrocyte protein 4.2 gene causing spherocytosis in a Caucasian patient

Por Hammill, Adrienne M., Risinger, Mary A., Joiner, Clinton H., Keddache, Mehdi, Kalfa, Theodosia A.
Publicado em 2011

From single-SNP to wide-locus: genome-wide association studies identifying functionally related genes and intragenic regions in small sample studies

Por Wittkowski, Knut M, Sonakya, Vikas, Song, Tingting, Seybold, Martin P, Keddache, Mehdi, Durner, Martina
Publicado em 2013

Analysis of Immune Regulatory Genes' Copy Number Variants in Graves' Disease

Por Huber, Amanda K., Concepcion, Erlinda S., Gandhi, Alisha, Menconi, Francesca, Smith, Eric P., Keddache, Mehdi, Tomer, Yaron
Publicado em 2011

INTERFERON-ALPHA MEDIATES THE DEVELOPMENT OF AUTOIMMUNITY BOTH BY DIRECT TISSUE TOXICITY AND THROUGH IMMUNE-CELL RECRUITMENT MECHANISMS

Por Akeno, Nagako, Smith, Eric P., Stefan, Mihaela, Huber, Amanda K., Zhang, Weijia, Keddache, Mehdi, Tomer, Yaron
Publicado em 2011

Fine Mapping of Loci Linked to Autoimmune Thyroid Disease Identifies Novel Susceptibility Genes

Por Tomer, Yaron, Hasham, Alia, Davies, Terry F., Stefan, Mihaela, Concepcion, Erlinda, Keddache, Mehdi, Greenberg, David A.
Publicado em 2013

Gaucher Disease: Transcriptome Analyses Using Microarray or mRNA Sequencing in a Gba1 Mutant Mouse Model Treated with Velaglucerase alfa or Imiglucerase

Por Dasgupta, Nupur, Xu, You-Hai, Oh, Sunghee, Sun, Ying, Jia, Li, Keddache, Mehdi, Grabowski, Gregory A
Publicado em 2013

Lampe1: An ENU-Germline Mutation Causing Spontaneous Hepatosteatosis Identified through Targeted Exon-Enrichment and Next-Generation Sequencing

Por Sheridan, Rachel, Lampe, Kristin, Shanmukhappa, Shiva Kumar, Putnam, Patrick, Keddache, Mehdi, Divanovic, Senad, Bezerra, Jorge, Hoebe, Kasper
Publicado em 2011

Dissecting the Genetic Susceptibility to Graves’ Disease in a Cohort of Patients of Italian Origin

Por Lombardi, Angela, Menconi, Francesca, Greenberg, David, Concepcion, Erlinda, Leo, Marenza, Rocchi, Roberto, Marinó, Michele, Keddache, Mehdi, Tomer, Yaron
Publicado no Front Endocrinol (Lausanne) (2016)

Novel variations in the adiponectin gene (ADIPOQ) may affect distribution of oligomeric complexes

Por Kottyan, Leah C, Woo, Jessica G, Keddache, Mehdi, Banach, Walter, Crimmins, Nancy A, Dolan, Lawrence M, Martin, Lisa J
Publicado em 2012

Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy

Por Holland, Katherine D., Kearney, Jennifer A., Glauser, Tracy A., Buck, Gerri, Keddache, Mehdi, Blankston, John, Glaaser, Ian, Kass., Robert S., Meisler, Miriam H
Publicado em 2008

Genetically-driven target tissue over-expression of CD40: A novel mechanism in autoimmune disease

Por Huber, Amanda K., Finkelman, Fred D., Li, Cheuk Wun, Concepcion, Erlinda, Smith, Eric, Jacobson, Eric, Latif, Rauf, Keddache, Mehdi, Zhang, Weijia, Tomer, Yaron
Publicado em 2012

Fucosyltransferase 2 non-secretor and low secretor status predicts severe outcomes in premature infants

Por Morrow, Ardythe L., Meinzen-Derr, Jareen, Huang, Pengwei, Schibler, Kurt R., Cahill, Tanya, Keddache, Mehdi, Kallapur, Suhas G., Newburg, David S., Tabangin, Meredith, Warner, Barbara B., Jiang, Xi
Publicado em 2011

Multiple interactions between the alpha(2C)- and beta(1)-adrenergic receptors influence heart failure survival

Por Kardia, Sharon LR, Kelly, Reagan J, Keddache, Mehdi A, Aronow, Bruce J, Grabowski, Gregory A, Hahn, Harvey S, Case, Karen L, Wagoner, Lynne E, Dorn, Gerald W, Liggett, Stephen B
Publicado em 2008

Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiency

Por Namjou, Bahram, Keddache, Mehdi, Fletcher, David, Dillon, Skyler, Kottyan, Leah, Wiley, Graham, Gaffney, Patrick M., Wakeland, Benjamin E., Liang, Chaoying, Wakeland, Edward K., Scofield, Hal, Kaufman, Kenneth, Harley, John B.
Publicado em 2012

Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse model

Por Dasgupta, Nupur, Xu, You-hai, Li, Ronghua, Peng, Yanyan, Pandey, Manoj K., Tinch, Stuart L., Liou, Benjamin, Inskeep, Venette, Zhang, Wujuan, Setchell, Kenneth D.R., Keddache, Mehdi, Grabowski, Gregory A., Sun, Ying
Publicado no Hum Mol Genet (2015)

EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children

Por Namjou, Bahram, Keddache, Mehdi, Marsolo, Keith, Wagner, Michael, Lingren, Todd, Cobb, Beth, Perry, Cassandra, Kennebeck, Stephanie, Holm, Ingrid A., Li, Rongling, Crimmins, Nancy A., Martin, Lisa, Solti, Imre, Kohane, Isaac S., Harley, John B.
Publicado em 2013

Assessing impacts of unconventional natural gas extraction on microbial communities in headwater stream ecosystems in Northwestern Pennsylvania

Por Trexler, Ryan, Solomon, Caroline, Brislawn, Colin J., Wright, Justin R., Rosenberger, Abigail, McClure, Erin E., Grube, Alyssa M., Peterson, Mark P., Keddache, Mehdi, Mason, Olivia U., Hazen, Terry C., Grant, Christopher J., Lamendella, Regina
Publicado no Front Microbiol (2014)

Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy

Por Greenberg, David A., Durner, Martina, Keddache, Mehdi, Shinnar, Shlomo, Resor, Stanley R., Moshe, Solomon L., Rosenbaum, David, Cohen, Jeffrey, Harden, Cynthia, Kang, Harriet, Wallace, Sibylle, Luciano, Daniel, Ballaban-Gil, Karen, Tomasini, Livia, Zhou, Guilian, Klotz, Irene, Dicker, Elisa
Publicado em 2000

The susceptibility loci Juvenile Idiopathic Arthritis shares with other autoimmune diseases extend to PTPN2, COG6 and ANGPT1

Por Thompson, Susan D., Sudman, Marc, Ramos, Paula S., Marion, Miranda C., Ryan, Mary, Tsoras, Monica, Weiler, Tracey, Wagner, Michael, Keddache, Mehdi, Haas, J. Peter, Mueller, Cornelia, Prahalad, Sampath, Bohnsack, John, Wise, Carol A., Punaro, Marilynn, Zhang, Dongping, Rosé, Carlos D., Comeau, Mary E., Divers, Jasmin, Glass, David N., Langefeld, Carl D.
Publicado em 2010