Circadian-based Treatment Strategy Effective in the BACHD Mouse Model of Huntington’s Disease von Whittaker, Daniel S., Loh, Dawn H., Wang, Huei-Bin, Tahara, Yu, Kuljis, Dika, Cutler, Tamara, Ghiani, Cristina A., Shibata, Shigenobu, Block, Gene D., Colwell, Christopher S.

Volltext

Time-Restricted Feeding Improves Circadian Dysfunction as well as Motor Symptoms in the Q175 Mouse Model of Huntington's Disease von Wang, Huei-Bin, Loh, Dawn H, Whittaker, Daniel S, Cutler, Tamara, Howland, David, Colwell, Christopher S

Volltext

Neurocardiovascular deficits in the Q175 mouse model of Huntington's disease von Cutler, Tamara S., Park, Saemi, Loh, Dawn H., Jordan, Maria C., Yokota, Tomohiro, Roos, Kenneth P., Ghiani, Cristina A., Colwell, Christopher S.

Volltext

Age-related decline in circadian output von Nakamura, Takahiro J, Nakamura, Wataru, Yamazaki, Shin, Kudo, Takashi, Cutler, Tamara, Colwell, Christopher S, Block, Gene D

Volltext

Circadian dysfunction in the Q175 model of Huntington's disease: Network analysis von Smarr, Benjamin, Cutler, Tamara, Loh, Dawn H., Kudo, Takashi, Kuljis, Dika, Kriegsfeld, Lance, Ghiani, Cristina A., Colwell, Christopher S.

Volltext

Multi-ethnic genome-wide association study for atrial fibrillation von Roselli, Carolina, Chaffin, Mark D., Weng, Lu-Chen, Aeschbacher, Stefanie, Ahlberg, Gustav, Albert, Christine M., Alonso, Alvaro, Anderson, Christopher D., Arking, Dan E., Bartz, Traci M., Benjamin, Emelia J., Bihlmeyer, Nathan A., Bis, Joshua C., Bloom, Heather L., Brody, Jennifer A., Chen, Lin Y., Choi, Eue-Keun, Christophersen, Ingrid E., Conen, David, Cook, James, Damrauer, Scott M., Denny, Joshua C., Dudley, Samuel C., Esko, Tonu, Felix, Stephan B., Franco, Oscar H., Geelhoed, Bastiaan, Grewal, Raji P., Gutmann, Rebecca, Harris, Tamara B., Hofman, Albert, Huang, Jie, Huang, Paul L., Ito, Kaoru, Johnson, Renee, Kääb, Stefan, Kamatani, Yoichiro, Kastrati, Adnan, Katschnig-Winter, Petra, Kessler, Thorsten, Kirchhof, Paulus, Kleber, Marcus E., Kubo, Michiaki, Lin, Henry J., Lindgren, Cecilia M., Loos, Ruth J. F., Lu, Yingchang, Lyytikäinen, Leo-Pekka, Magnusson, Patrik K., Malik, Rainer, Mansur, Alfredo J., Marcus, Gregory M., März, Winfried, Melander, Olle, Müller-Nurasyid, Martina, Nazarian, Saman, Neumann, Benjamin, Newton-Cheh, Christopher, Nilsson, Peter, Noordam, Raymond, Oellers, Heidi, Pak, Hui-Nam, Pedersen, Nancy L., Psaty, Bruce M., Pulit, Sara L., Pullinger, Clive R., Ribasés, Marta, Rienstra, Michiel, Rosand, Jonathan, Rost, Natalia, Saba, Samir, Schramm, Katharina, Schurman, Claudia, Scott, Stuart A., Shaffer, Christian, Shah, Svati, Shalaby, Alaa A., Shim, Jaemin, Shoemaker, M. Benjamin, Sinner, Moritz F., Smith, Albert V., Smith, Blair H., Sun, Han, Tanaka, Toshihiro, Tanriverdi, Kahraman, Taylor, Kent D., Thériault, Sébastien, Trompet, Stella, Tucker, Nathan R., Tveit, Arnljot, Uitterlinden, Andre G., Van Der Harst, Pim, Van Wagoner, David R., Wang, Biqi, Wong, Jorge A., Woo, Daniel, Yoneda, Zachary T., Zeller, Tanja, Zeng, Lingyao, Lubitz, Steven A.

Volltext

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction von Ntalla, Ioanna, Cartwright, James H., Hall, Amelia Weber, Tucker, Nathan R., Choi, Seung Hoan, Barnes, Michael R., Warren, Helen R., Hayward, Caroline, Marten, Jonathan, Concas, Maria Pina, Boutin, Thibaud, Lima-Costa, Maria Fernanda, Souza, Renan P., Tarazona-Santos, Eduardo, Giedraitis, Vilmantas, Foco, Luisa, Gögele, Martin, Hicks, Andrew A., Cook, James P., Lindgren, Cecilia M., Riaz, Muhammad B., Sinagra, Gianfranco, Ulivi, Sheila, Kähönen, Mika, Mishra, Pashupati P., Nikus, Kjell, Padmanabhan, Sandosh, O’Connell, Jeff R., Aeschbacher, Stefanie, Risch, Lorenz, Thériault, Sébastien, Hutri-Kähönen, Nina, Lehtimäki, Terho, Barnes, Catriona L. K., Joshi, Peter K., Isaacs, Aaron, van Duijn, Cornelia M., Gudnason, Vilmundur, Harris, Tamara B., Nadkarni, Girish N., Correa, Adolfo, Mei, Hao, Wilson, James, Müller-Nurasyid, Martina, Waldenberger, Melanie, Mangino, Massimo, Kääb, Stefan, Schramm, Katharina, Strauch, Konstantin, Cutler, Michael J., Fatkin, Diane, Olesen, Morten, Roden, Dan M., Gustav Smith, J., Biggs, Mary L., Bis, Joshua C., Sotoodehnia, Nona, Pramstaller, Peter P., Ford, Ian, Wouter Jukema, J., Macfarlane, Peter W., Trompet, Stella, Dörr, Marcus, Felix, Stephan B., Weiss, Stefan, Havulinna, Aki S., Jula, Antti, Sääksjärvi, Katri, Rotter, Jerome I., Yao, Jie, Maan, Arie C., Mook-Kanamori, Dennis O., Cucca, Francesco, Lakatta, Edward G., Qian, Yong, Lin, Honghuang, Newton-Cheh, Christopher H., Lunetta, Kathryn L., Murray, Alison D., Stricker, Bruno H., Uitterlinden, André, van den Berg, Marten E., Haessler, Jeffrey, Kooperberg, Charles, Peters, Ulrike, Reiner, Alexander P., Arking, Dan E., Boerwinkle, Eric, Soliman, Elsayed Z., Gogarten, Stephanie M., Kerr, Kathleen F., Laurie, Cathy C., Abdullah Said, M., Yldau van der Ende, M., Ramirez, Julia, Van Duijvenboden, Stefan, Arnar, David O., Thorolfsdottir, Rosa B., Ellinor, Patrick T., Lubitz, Steven A.

Volltext

Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome von Elias-Mas, Andrea, Potrony, Miriam, Bague, Jaume, Cutler, David J, Alvarez-Mora, Maria Isabel, Torres, Teresa, Barcos, Tamara, Puig-Butille, Joan Anton, Rubio, Marta, Madrigal, Irene, Puig, Susana, Allen, Emily G, Rodriguez-Revenga, Laia

Volltext

SeqAnt: a web service to rapidly identify and annotate DNA sequence variations von Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E

Volltext

Perturbation of sphingolipid metabolism and ceramide production in HIV-dementia von Haughey, Norman J., Cutler, Roy G., Tamara, Anita, McArthur, Justin C., Vargas, Diana L., Pardo, Carlos A., Turchan, Jadwiga, Nath, Avindra, Mattson, Mark P.

Volltext

Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care von Sanchez Russo, Rossana, Gambello, Michael J., Murphy, Melissa M., Aberizk, Katrina, Black, Emily, Burrell, T. Lindsey, Carlock, Grace, Cubells, Joseph F., Epstein, Michael T., Espana, Roberto, Goines, Katrina, Guest, Ryan M., Klaiman, Cheryl, Koh, Sookyong, Leslie, Elizabeth J., Li, Longchuan, Novacek, Derek M., Saulnier, Celine A., Sefik, Esra, Shultz, Sarah, Walker, Elaine, White, Stormi Pulver, Mulle, Jennifer Gladys

Volltext

Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome von Sefik, Esra, Purcell, Ryan H., Walker, Elaine F., Bassell, Gary J., Mulle, Jennifer G.

Volltext

Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report von Murphy, Melissa M., Burrell, T. Lindsey, Cubells, Joseph F., Epstein, Michael T., Espana, Roberto, Gambello, Michael J., Goines, Katrina, Klaiman, Cheryl, Koh, Sookyong, Russo, Rossana Sanchez, Saulnier, Celine A., Walker, Elaine, Mulle, Jennifer Gladys

Volltext

Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry von Pollak, Rebecca M, Murphy, Melissa M, Epstein, Michael P, Zwick, Michael E, Klaiman, Cheryl, Saulnier, Celine A, Mulle, Jennifer G

Volltext

Novel markers of oxidative stress in actively progressive HIV dementia von Sacktor, Ned, Haughey, Norman, Cutler, Roy, Tamara, Anita, Turchan, Jadwiga, Pardo, Carlos, Vargas, Diana, Nath, Avindra

Volltext

Developmental Outcomes After Pediatric Heart Transplantation von Chinnock, Richard E., MD, Freier, M. Catherin, PhD, Ashwal, Stephen, MD, Pivonka-Jones, Jamie, PhD, Shankel, Tamara, MD, Cutler, Drew, MD, Bailey, Leonard, MD

Volltext

Does breast density affect the ability of MRI to detect mammographically occult cancers? von Freedman, Beth Cutler, Luongo, Jocelyn, Gillego, Alyssa, Fulop, Tamara, Boolbol, Susan K.

Volltext

Calcineurin inhibitor minimization using sirolimus leads to improved renal function in pediatric heart transplant recipients von Chinnock, Timothy J., Shankel, Tamara, Deming, Douglas, Cutler, Drew, Sahney, Shobha, Fitts, James, Chinnock, Richard E.

Volltext

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse von Sun, Miao, Mondal, Kajari, Patel, Viren, Horner, Vanessa L, Long, Alyssa B, Cutler, David J, Caspary, Tamara, Zwick, Michael E

Volltext

Shifting Resources and Focus to Meet the Goals of the National HIV/AIDS Strategy: The Enhanced Comprehensive HIV Prevention Planning Project, 2010-2013 von Flores, Stephen A., Purcell, David W., Fisher, Holly H., Belcher, Lisa, Carey, James W., Courtenay-Quirk, Cari, Dunbar, Erica, Eke, Agatha N., Galindo, Carla A., Glassman, Marlene, Margolis, Andrew D., Neumann, Mary Spink, Prather, Cynthia, Stratford, Dale, Taylor, Raekiela D., Mermin, Jonathan

Volltext