Clinical translation of genetic predictors for type 2 diabetes

por Majithia, Amit R., Florez, Jose C.
Publicado 2009

Key events of pancreas formation are triggered in gut endoderm by ectopic expression of pancreatic regulatory genes

por Grapin-Botton, Anne, Majithia, Amit R., Melton, Douglas A.
Publicado 2001

Thousands of missing variants in the UK Biobank are recoverable by genome realignment

por Jia, Tongqiu, Munson, Brenton, Allen, Hana Lango, Ideker, Trey, Majithia, Amit R.
Publicado en Ann Hum Genet (2020)

Rate of Change of Premeal Glucose Measured by Continuous Glucose Monitoring Predicts Postmeal Glycemic Excursions in Patients With Type 1 Diabetes: Implications for Therapy

por Majithia, Amit R., Wiltschko, Alexander B., Zheng, Hui, Walford, Geoffrey A., Nathan, David M.
Publicado en J Diabetes Sci Technol (2017)

Multiplex detection of four pathogenic retroviruses using molecular beacons

por Vet, Jacqueline A. M., Majithia, Amit R., Marras, Salvatore A. E., Tyagi, Sanjay, Dube, Syamalima, Poiesz, Bernard J., Kramer, Fred Russell
Publicado 1999

Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

por Majithia, Amit R., Flannick, Jason, Shahinian, Peter, Guo, Michael, Bray, Mark-Anthony, Fontanillas, Pierre, Gabriel, Stacey B., Rosen, Evan D., Altshuler, David
Publicado en Proc Natl Acad Sci U S A (2014)

A Virtual Type 2 Diabetes Clinic Using Continuous Glucose Monitoring and Endocrinology Visits

por Dixon, Ronald F., Zisser, Howard, Layne, Jennifer E., Barleen, Nathan A., Miller, David P., Moloney, Daniel P., Majithia, Amit R., Gabbay, Robert A., Riff, Josh
Publicado en J Diabetes Sci Technol (2019)

Remote Application and Use of Real-Time Continuous Glucose Monitoring by Adults with Type 2 Diabetes in a Virtual Diabetes Clinic

por Bergenstal, Richard M., Layne, Jennifer E., Zisser, Howard, Gabbay, Robert A., Barleen, Nathan A., Lee, Amy Armento, Majithia, Amit R., Parkin, Christopher G., Dixon, Ronald F.
Publicado en Diabetes Technol Ther (2021)

Glycemic Outcomes in Adults With Type 2 Diabetes Participating in a Continuous Glucose Monitor–Driven Virtual Diabetes Clinic: Prospective Trial

por Majithia, Amit R, Kusiak, Coco M, Armento Lee, Amy, Colangelo, Francis R, Romanelli, Robert J, Robertson, Scott, Miller, David P, Erani, David M, Layne, Jennifer E, Dixon, Ronald F, Zisser, Howard
Publicado en J Med Internet Res (2020)

A pharmacogenetic approach to the treatment of patients with PPARG mutations

por Agostini, Maura, Schoenmakers, Erik, Beig, Junaid, Fairall, Louise, Szatmari, Istvan, Rajanayagam, Odelia, Muskett, Fred, Adams, Claire, Marais, A. David, O’Rahilly, Stephen, Semple, Robert K., Nagy, Laszlo, Majithia, Amit R., Schwabe, John, Blom, Dirk J., Murphy, Rinki, Chatterjee, Krishna, Savage, David B.
Publicado en Diabetes (2018)

Natural helix 9 mutants of PPARγ differently affect its transcriptional activity

por Broekema, Marjoleine F., Massink, Maarten P.G., Donato, Cinzia, de Ligt, Joep, Schaarschmidt, Joerg, Borgman, Anouska, Schooneman, Marieke G., Melchers, Diana, Gerding, Martin N., Houtman, René, Bonvin, Alexandre M.J.J., Majithia, Amit R., Monajemi, Houshang, van Haaften, Gijs W., Soeters, Maarten R., Kalkhoven, Eric
Publicado en Mol Metab (2018)

Prospective functional classification of all possible missense variants in PPARG

por Majithia, Amit R., Tsuda, Ben, Agostini, Maura, Gnanapradeepan, Keerthana, Rice, Robert, Peloso, Gina, Patel, Kashyap A., Zhang, Xiaolan, Broekema, Marjoleine F., Patterson, Nick, Duby, Marc, Sharpe, Ted, Kalkhoven, Eric, Rosen, Evan D., Barroso, Inês, Ellard, Sian, Kathiresan, Sekar, O’Rahilly, Stephen, Chatterjee, Krishna, Florez, Jose C., Mikkelsen, Tarjei, Savage, David B., Altshuler, David
Publicado en Nat Genet (2016)

Discovering metabolic disease gene interactions by correlated effects on cellular morphology

por Jiao, Yang, Ahmed, Umer, Sim, M.F. Michelle, Bejar, Andrea, Zhang, Xiaolan, Talukder, M. Mesbah Uddin, Rice, Robert, Flannick, Jason, Podgornaia, Anna I., Reilly, Dermot F., Engreitz, Jesse M., Kost-Alimova, Maria, Hartland, Kate, Mercader, Josep-Maria, Georges, Sara, Wagh, Vilas, Tadin-Strapps, Marija, Doench, John G., Edwardson, J. Michael, Rochford, Justin J., Rosen, Evan D., Majithia, Amit R.
Publicado en Mol Metab (2019)

Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders

por Lal, Dennis, May, Patrick, Perez-Palma, Eduardo, Samocha, Kaitlin E., Kosmicki, Jack A., Robinson, Elise B., Møller, Rikke S., Krause, Roland, Nürnberg, Peter, Weckhuysen, Sarah, De Jonghe, Peter, Guerrini, Renzo, Niestroj, Lisa M., Du, Juliana, Marini, Carla, Ware, James S., Kurki, Mitja, Gormley, Padhraig, Tang, Sha, Wu, Sitao, Biskup, Saskia, Poduri, Annapurna, Neubauer, Bernd A., Koeleman, Bobby P. C., Helbig, Katherine L., Weber, Yvonne G., Helbig, Ingo, Majithia, Amit R., Palotie, Aarno, Daly, Mark J.
Publicado en Genome Med (2020)