Pleiotropic Effects and Compensation Mechanisms Determine Tissue Specificity in Mitochondrial Myopathy and Sideroblastic Anemia (MLASA)

Por Bykhovskaya, Yelena, Mengesha, Emebet, Fischel-Ghodsian, Nathan
Publicado em 2007

Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins

Por Bykhovskaya, Yelena, Mengesha, Emebet, Fischel-Ghodsian, Nathan
Publicado em 2009

Missense Mutation in Pseudouridine Synthase 1 (PUS1) Causes Mitochondrial Myopathy and Sideroblastic Anemia (MLASA)

Por Bykhovskaya, Yelena, Casas, Kari, Mengesha, Emebet, Inbal, Aida, Fischel-Ghodsian, Nathan
Publicado em 2004

IL23R Haplotypes Provide A Large Population Attributable Risk for Crohn’s Disease

Por Taylor, Kent D., Targan, Stephan R., Mei, Ling, Ippoliti, Andrew F., McGovern, Dermot, Mengesha, Emebet, King, Lily, Rotter, Jerome I.
Publicado em 2008

The TNF family member TL1A induces IL‐22 secretion in committed human T(h)17 cells via IL‐9 induction

Por Thomas, Lisa S., Targan, Stephan R., Tsuda, Masato, Yu, Qi T., Salumbides, Brenda C., Haritunians, Talin, Mengesha, Emebet, McGovern, Dermot P.B., Michelsen, Kathrin S.
Publicado no J Leukoc Biol (2016)

Systems Genetics Reveals the Functional Context of PCOS Loci and Identifies Genetic and Molecular Mechanisms of Disease Heterogeneity

Por Jones, Michelle R., Brower, Meredith A., Xu, Ning, Cui, Jinrui, Mengesha, Emebet, Chen, Yii-Der I., Taylor, Kent D., Azziz, Ricardo, Goodarzi, Mark O.
Publicado no PLoS Genet (2015)

Metabolic and cardiovascular genes in polycystic ovary syndrome: A candidate-wide association study (CWAS)

Por Jones, Michelle R., Chua, Angela K., Mengesha, Emebet A., Taylor, Kent D., Chen, Yii-Der I., Li, Xiaohui, Krauss, Ronald M., Rotter, Jerome I., Legro, Richard S., Azziz, Ricardo, Goodarzi, Mark O.
Publicado em 2011

IL-23 Receptor (IL-23R) Gene Protects Against Pediatric Crohn’s Disease

Por Dubinsky, Marla C., Wang, Dai, Picornell, Yoana, Wrobel, Iwona, Katzir, Lirona, Quiros, Antonio, Dutridge, Debra, Wahbeh, Ghassan, Silber, Gary, Bahar, Ron, Mengesha, Emebet, Targan, Stephan R., Taylor, Kent D., Rotter, Jerome I.
Publicado em 2007

MAGI2 genetic variation and inflammatory bowel disease (IBD)

Por McGovern, Dermot P.B., Taylor, Kent D., Landers, Carol, Derkowski, Carrie, Dutridge, Deb, Dubinsky, Marla, Ippoliti, Andy, Vasiliauskas, Eric, Mei, Ling, Mengesha, Emebet, King, Lily, Pressman, Sheila, Targan, Stephan R., Rotter, Jerome I.
Publicado em 2009

Genetic epistasis of IL23/IL17 pathway genes in Crohn’s disease

Por McGovern, Dermot P.B., Rotter, Jerome I., Mei, Ling, Haritunians, Talin, Landers, Carol, Derkowski, Carrie, Dutridge, Deb, Dubinsky, Marla, Ippoliti, Andy, Vasiliauskas, Eric, Mengesha, Emebet, King, Lily, Pressman, Sheila, Targan, Stephan R., Taylor, Kent D.
Publicado em 2009

Genetic Predictors of Medically Refractory Ulcerative Colitis

Por Haritunians, Talin, Taylor, Kent D., Targan, Stephan R., Dubinsky, Marla, Ippoliti, Andrew, Kwon, Soonil, Guo, Xiuqing, Melmed, Gil Y., Berel, Dror, Mengesha, Emebet, Psaty, Bruce M., Glazer, Nicole L., Vasiliauskas, Eric A., Rotter, Jerome I., Fleshner, Phillip R., McGovern, Dermot P.B.
Publicado em 2010

Steroidogenic Regulatory Factor FOS Is Underexpressed in Polycystic Ovary Syndrome (PCOS) Adipose Tissue and Genetically Associated with PCOS Susceptibility

Por Jones, Michelle R., Chazenbalk, Gregorio, Xu, Ning, Chua, Angela K., Eigler, Tamar, Mengesha, Emebet, Chen, Yen-Hao, Lee, Jung-Min, Pall, Marita, Li, Xiaohui, Chen, Yii-Der I., Taylor, Kent D., Mathur, Ruchi, Krauss, Ronald M., Rotter, Jerome I., Legro, Richard S., Azziz, Ricardo, Goodarzi, Mark O.
Publicado em 2012

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Por Guan, Min-Xin, Yan, Qingfeng, Li, Xiaoming, Bykhovskaya, Yelena, Gallo-Teran, Jaime, Hajek, Petr, Umeda, Noriko, Zhao, Hui, Garrido, Gema, Mengesha, Emebet, Suzuki, Tsutomu, Castillo, Ignacio del, Peters, Jennifer Lynne, Li, Ronghua, Qian, Yaping, Wang, Xinjian, Ballana, Ester, Shohat, Mordechai, Lu, Jianxin, Estivill, Xavier, Watanabe, Kimitsuna, Fischel-Ghodsian, Nathan
Publicado em 2006

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease

Por McGovern, Dermot P.B., Jones, Michelle R., Taylor, Kent D., Marciante, Kristin, Yan, Xiaofei, Dubinsky, Marla, Ippoliti, Andy, Vasiliauskas, Eric, Berel, Dror, Derkowski, Carrie, Dutridge, Deb, Fleshner, Phil, Shih, David Q., Melmed, Gil, Mengesha, Emebet, King, Lily, Pressman, Sheila, Haritunians, Talin, Guo, Xiuqing, Targan, Stephan R., Rotter, Jerome I.
Publicado em 2010

Variants in ZNF365 isoform D are associated with Crohn’s Disease

Por Haritunians, Talin, Jones, Michelle R., McGovern, Dermot P.B., Shih, David Q., Barrett, Robert J., Derkowski, Carrie, Dubinsky, Marla C., Dutridge, Debra, Fleshner, Phillip R., Ippoliti, Andrew, King, Lily, Leshinsky-Silver, Esther, Levine, Arie, Melmed, Gil Y., Mengesha, Emebet, Vasilauskas, Eric A., Ziaee, Shabnam, Rotter, Jerome I., Targan, Stephan R., Taylor, Kent D.
Publicado em 2011