Reduced body mass, food intake, and testis size in response to short photoperiod in adult F344 rats

por Shoemaker, M Benjamin, Heideman, Paul D
Publicado 2002

Genomic contributors to atrial electroanatomical remodeling and atrial fibrillation progression: Pathway enrichment analysis of GWAS data

por Husser, Daniela, Ueberham, Laura, Dinov, Borislav, Kosiuk, Jedrzej, Kornej, Jelena, Hindricks, Gerhard, Shoemaker, M. Benjamin, Roden, Dan M., Bollmann, Andreas, Büttner, Petra
Publicado 2016

Cardiac Sarcoidosis and a Likely Pathogenic TTN Variant in a Patient Presenting With Ventricular Tachycardia

por Virk, Zain M., Richardson, T. Lee, Nowatzke, Joseph F., Ullah, Asad, Pedrotty, Dawn M., Shoemaker, M. Benjamin, Kanagasundram, Arvindh, Roden, Dan M., Stevenson, William G.
Publicado 2023

Rare variants in genes encoding the cardiac sodium channel and associated compounds and their impact on outcome of catheter ablation of atrial fibrillation

por Husser, Daniela, Ueberham, Laura, Hindricks, Gerhard, Büttner, Petra, Ingram, Christie, Weeke, Peter, Shoemaker, M. Benjamin, Adams, Volker, Arya, Arash, Sommer, Philipp, Darbar, Dawood, Roden, Dan M., Bollmann, Andreas
Publicado 2017

Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome

por Lancaster, Megan C., Chen, Hung-Hsin, Shoemaker, M. Benjamin, Fleming, Matthew R., Baker, James T., Polikowsky, Hannah G., Samuels, David C., Huff, Chad D., Roden, Dan M., Below, Jennifer E.
Publicado 2023

Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT Syndrome

por Lancaster, Megan C., Chen, Hung-Hsin, Shoemaker, M. Benjamin, Fleming, Matthew R., Baker, James T., Evans, Grahame, Polikowsky, Hannah G., Samuels, David C., Huff, Chad D., Roden, Dan M., Below, Jennifer E.
Publicado 2023

2-Hydroxybenzylamine (2-HOBA) to prevent early recurrence of atrial fibrillation after catheter ablation: protocol for a randomized controlled trial including detection of AF using...

por O’Neill, Matthew J., Yoneda, Zachary T., Crawford, Diane M., Ye, Fei, Ao, Mingfang, Pitchford, Lisa M., Rathmacher, John A., Murray, Katherine T., Akers, Wendell S., Roden, Dan M., Michaud, Gregory F., Shoemaker, M. Benjamin
Publicado 2021

Functional modeling in zebrafish demonstrates that the atrial-fibrillation-associated gene GREM2 regulates cardiac laterality, cardiomyocyte differentiation and atrial rhythm

por Müller, Iris I., Melville, David B., Tanwar, Vineeta, Rybski, Witold M., Mukherjee, Amrita, Shoemaker, M. Benjamin, Wang, Wan-Der, Schoenhard, John A., Roden, Dan M., Darbar, Dawood, Knapik, Ela W., Hatzopoulos, Antonis K.
Publicado 2013

Safety, tolerability, and pharmacokinetics of repeated oral doses of 2-hydroxybenzylamine acetate in healthy volunteers: a double-blind, randomized, placebo-controlled clinical tri...

por Pitchford, Lisa M., Driver, Patricia M., Fuller, John C., Akers, Wendell S., Abumrad, Naji N., Amarnath, Venkataraman, Milne, Ginger L., Chen, Sheau-Chiann, Ye, Fei, Roberts, L. Jackson, Shoemaker, M. Benjamin, Oates, John A., Rathmacher, John A., Boutaud, Olivier
Publicado 2020

Measurement of diffuse ventricular fibrosis with myocardial T1 in patients with atrial fibrillation

por Montgomery, Jay A., Abdallah, Wissam, Yoneda, Zachary T., Brittain, Evan, Aznaurov, Sam G., Parvez, Babar, Adkins, Keith, Whalen, S. Patrick, Estrada, J.C., Shen, Sharon, Crossley, George H., Kanagasundram, Arvindh, Saavedra, Pablo, Ellis, Christopher R., Lawson, Mark, Darbar, Dawood, Shoemaker, M. Benjamin
Publicado 2016

Non-pulmonary vein mediated atrial fibrillation: A novel sub-phenotype

por Farrell, Maureen, Yoneda, Zachary, Montgomery, Jay, Crawford, Diane, Wray, Lauren Lee, Xu, Meng, Kolek, Matthew J., Richardson, Travis, Lugo, Ricardo, Metawee, Mohamed, Michaud, Greg, Estrada, Juan Carlos, Saavedra, Pablo, Shen, Sharon, Kanagasundram, Arvindh, Ellis, Christopher R., Crossley, George, Roden, Dan, Shoemaker, M. Benjamin
Publicado 2017

Disruption of Z-Disc Function Promotes Mechanical Dysfunction in Human Myocardium: Evidence for a Dual Myofilament Modulatory Role by Alpha-Actinin 2

por Rodriguez Garcia, Michelle, Schmeckpeper, Jeffrey, Landim-Vieira, Maicon, Coscarella, Isabella Leite, Fang, Xuan, Ma, Weikang, Spran, Payton A., Yuan, Shengyao, Qi, Lin, Kahmini, Aida Rahimi, Shoemaker, M. Benjamin, Atkinson, James B., Kekenes-Huskey, Peter M., Irving, Thomas C., Chase, Prescott Bryant, Knollmann, Björn C., Pinto, Jose Renato
Publicado 2023

Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes

por Yoneda, Zachary T., Anderson, Katherine C., Quintana, Joseph A., O’Neill, Matthew J., Sims, Richard A., Glazer, Andrew M., Shaffer, Christian M., Crawford, Diane M., Stricker, Thomas, Ye, Fei, Wells, Quinn, Stevenson, Lynne W., Michaud, Gregory F., Darbar, Dawood, Lubitz, Steven A., Ellinor, Patrick T., Roden, Dan M., Shoemaker, M. Benjamin
Publicado 2021

Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes

por Yoneda, Zachary T., Anderson, Katherine C., Ye, Fei, Quintana, Joseph A., O’Neill, Matthew J., Sims, Richard A., Sun, Lili, Glazer, Andrew M., Davogustto, Giovanni, El-Harasis, Majd, Laws, James L., Saldivar, Brittany N., Crawford, Diane M., Stricker, Thomas, Wells, Quinn, Darbar, Dawood, Michaud, Gregory F., Stevenson, Lynne W., Lubitz, Steven A., Ellinor, Patrick T., Roden, Dan M., Shoemaker, M. Benjamin
Publicado 2022

Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants

por Einson, Jonah, Glinos, Dafni, Boerwinkle, Eric, Castaldi, Peter, Darbar, Dawood, de Andrade, Mariza, Ellinor, Patrick, Fornage, Myriam, Gabriel, Stacey, Germer, Soren, Gibbs, Richard, Hersh, Craig P., Johnsen, Jill, Kaplan, Robert, Konkle, Barbara A., Kooperberg, Charles, Nassir, Rami, Loos, Ruth J.F., Meyers, Deborah A, Mitchell, Braxton D., Psaty, Bruce, Vasan, Ramachandran S., Rich, Stephen S., Rienstra, Michael, Rotter, Jerome I., Saferali, Aabida, Shoemaker, M. Benjamin, Silverman, Edwin, Smith, Albert Vernon, Mohammadi, Pejman, Castel, Stephane E., Iossifov, Ivan, Lappalainen, Tuuli
Publicado 2023

The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

por Wang, Zhe, Choi, Shing Wan, Chami, Nathalie, Boerwinkle, Eric, Fornage, Myriam, Redline, Susan, Bis, Joshua C., Brody, Jennifer A., Psaty, Bruce M., Kim, Wonji, McDonald, Merry-Lynn N., Regan, Elizabeth A., Silverman, Edwin K., Liu, Ching-Ti, Vasan, Ramachandran S., Kalyani, Rita R., Mathias, Rasika A., Yanek, Lisa R., Arnett, Donna K., Justice, Anne E., North, Kari E., Kaplan, Robert, Heckbert, Susan R., de Andrade, Mariza, Guo, Xiuqing, Lange, Leslie A., Rich, Stephen S., Rotter, Jerome I., Ellinor, Patrick T., Lubitz, Steven A., Blangero, John, Shoemaker, M. Benjamin, Darbar, Dawood, Gladwin, Mark T., Albert, Christine M., Chasman, Daniel I., Jackson, Rebecca D., Kooperberg, Charles, Reiner, Alexander P., O’Reilly, Paul F., Loos, Ruth J. F.
Publicado 2022

Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

por Weng, Lu-Chen, Lunetta, Kathryn L., Müller-Nurasyid, Martina, Smith, Albert Vernon, Thériault, Sébastien, Weeke, Peter E., Barnard, John, Bis, Joshua C., Lyytikäinen, Leo-Pekka, Kleber, Marcus E., Martinsson, Andreas, Lin, Henry J., Rienstra, Michiel, Trompet, Stella, Krijthe, Bouwe P., Dörr, Marcus, Klarin, Derek, Chasman, Daniel I., Sinner, Moritz F., Waldenberger, Melanie, Launer, Lenore J., Harris, Tamara B., Soliman, Elsayed Z., Alonso, Alvaro, Paré, Guillaume, Teixeira, Pedro L., Denny, Joshua C., Shoemaker, M. Benjamin, Van Wagoner, David R., Smith, Jonathan D., Psaty, Bruce M., Sotoodehnia, Nona, Taylor, Kent D., Kähönen, Mika, Nikus, Kjell, Delgado, Graciela E., Melander, Olle, Engström, Gunnar, Yao, Jie, Guo, Xiuqing, Christophersen, Ingrid E., Ellinor, Patrick T., Geelhoed, Bastiaan, Verweij, Niek, Macfarlane, Peter, Ford, Ian, Heeringa, Jan, Franco, Oscar H., Uitterlinden, André G., Völker, Uwe, Teumer, Alexander, Rose, Lynda M., Kääb, Stefan, Gudnason, Vilmundur, Arking, Dan E., Conen, David, Roden, Dan M., Chung, Mina K., Heckbert, Susan R., Benjamin, Emelia J., Lehtimäki, Terho, März, Winfried, Smith, J. Gustav, Rotter, Jerome I., van der Harst, Pim, Jukema, J. Wouter, Stricker, Bruno H., Felix, Stephan B., Albert, Christine M., Lubitz, Steven A.
Publicado 2017

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

por Weinstock, Joshua S., Laurie, Cecelia A., Broome, Jai G., Taylor, Kent D., Guo, Xiuqing, Shuldiner, Alan R., O’Connell, Jeffrey R., Lewis, Joshua P., Boerwinkle, Eric, Barnes, Kathleen C., Chami, Nathalie, Kenny, Eimear E., Loos, Ruth J. F., Fornage, Myriam, Redline, Susan, Cade, Brian E., Gilliland, Frank D., Chen, Zhanghua, Gauderman, W. James, Kumar, Rajesh, Grammer, Leslie, Schleimer, Robert P., Psaty, Bruce M., Bis, Joshua C., Brody, Jennifer A., Silverman, Edwin K., Yun, Jeong H., Qiao, Dandi, Weiss, Scott T., Lasky-Su, Jessica, DeMeo, Dawn L., Palmer, Nicholette D., Freedman, Barry I., Bowden, Donald W., Cho, Michael H., Vasan, Ramachandran S., Johnson, Andrew D., Yanek, Lisa R., Becker, Lewis C., Kardia, Sharon, He, Jiang, Kaplan, Robert, Heckbert, Susan R., Smith, Nicholas L., Wiggins, Kerri L., Arnett, Donna K., Irvin, Marguerite R., Tiwari, Hemant, Correa, Adolfo, Raffield, Laura M., Gao, Yan, de Andrade, Mariza, Rotter, Jerome I., Rich, Stephen S., Manichaikul, Ani W., Konkle, Barbara A., Johnsen, Jill M., Wheeler, Marsha M., Custer, Brian S., Duggirala, Ravindranath, Curran, Joanne E., Blangero, John, Gui, Hongsheng, Xiao, Shujie, Williams, L. Keoki, Meyers, Deborah A., Li, Xingnan, Ortega, Victor, McGarvey, Stephen, Gu, C. Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Shoemaker, M. Benjamin, Darbar, Dawood, Roden, Dan, Albert, Christine, Kooperberg, Charles, Desai, Pinkal, Blackwell, Thomas W., Abecasis, Goncalo R., Smith, Albert V., Kang, Hyun M., Mathias, Rasika, Natarajan, Pradeep, Jaiswal, Siddhartha, Reiner, Alexander P., Bick, Alexander G.
Publicado 2023

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

por Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, Charlotte, Postema, Pieter G., Amin, Ahmad S., Nannenberg, Eline A., Ware, James S., Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt M., Bézieau, Stéphane, Bos, J. Martijn, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Celen, Candan, Clauss, Sebastian, Corveleyn, Anniek, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Dittmann, Sven, Ellinor, Patrick T., Ortuño, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen K., Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P. C., Kurabayashi, Masahiko, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart L., Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphaël P., Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Molina, Maria Sabater, Sacher, Frédéric, Sahin, Hatice, Sarquella-Brugada, Georgia, Sebastiano, Regina, Sharma, Sanjay, Sheppard, Mary N., Shimamoto, Keiko, Shoemaker, M. Benjamin, Stallmeyer, Birgit, Steinfurt, Johannes, Tanaka, Yuji, Tester, David J., Usuda, Keisuke, van der Zwaag, Paul A., Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Winkel, Bo G., Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G. A., Lubitz, Steven A., Antzelevitch, Charles, Platonov, Pyotr G., Odening, Katja E., Roden, Dan M., Roberts, Jason D., Skinner, Jonathan R., Tfelt-Hansen, Jacob, van den Berg, Maarten P., Olesen, Morten S., Lambiase, Pier D., Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B., Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F., Ackerman, Michael J., Brugada, Ramon, Brugada, Josep, Gimeno, Juan R., Hasdemir, Can, Guicheney, Pascale, Priori, Silvia G., Schulze-Bahr, Eric, Makita, Naomasa, Schwartz, Peter J., Shimizu, Wataru, Aiba, Takeshi, Schott, Jean-Jacques, Redon, Richard, Ohno, Seiko, Probst, Vincent, Behr, Elijah R., Barc, Julien, Bezzina, Connie R.
Publicado 2020

WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

por Zhang, Xinruo, Brody, Jennifer A., Graff, Mariaelisa, Highland, Heather M., Chami, Nathalie, Xu, Hanfei, Wang, Zhe, Ferrier, Kendra, Chittoor, Geetha, Josyula, Navya S., Li, Xihao, Li, Zilin, Allison, Matthew A., Becker, Diane M., Bielak, Lawrence F., Bis, Joshua C., Boorgula, Meher Preethi, Bowden, Donald W., Broome, Jai G., Buth, Erin J., Carlson, Christopher S., Chang, Kyong-Mi, Chavan, Sameer, Chiu, Yen-Feng, Chuang, Lee-Ming, Conomos, Matthew P., DeMeo, Dawn L., Du, Margaret, Duggirala, Ravindranath, Eng, Celeste, Fohner, Alison E., Freedman, Barry I., Garrett, Melanie E., Guo, Xiuqing, Haiman, Chris, Heavner, Benjamin D., Hidalgo, Bertha, Hixson, James E., Ho, Yuk-Lam, Hobbs, Brian D., Hu, Donglei, Hui, Qin, Hwu, Chii-Min, Jackson, Rebecca D., Jain, Deepti, Kalyani, Rita R., Kardia, Sharon L.R., Kelly, Tanika N., Lange, Ethan M., LeNoir, Michael, Li, Changwei, Marchand, Loic Le., McDonald, Merry-Lynn N., McHugh, Caitlin P., Morrison, Alanna C., Naseri, Take, O’Connell, Jeffrey, O’Donnell, Christopher J., Palmer, Nicholette D., Pankow, James S., Perry, James A., Peters, Ulrike, Preuss, Michael H., Rao, D.C., Regan, Elizabeth A., Reupena, Sefuiva M., Roden, Dan M., Rodriguez-Santana, Jose, Sitlani, Colleen M., Smith, Jennifer A., Tiwari, Hemant K., Vasan, Ramachandran S., Wang, Zeyuan, Weeks, Daniel E., Wessel, Jennifer, Wiggins, Kerri L., Wilkens, Lynne R., Wilson, Peter W.F., Yanek, Lisa R., Yoneda, Zachary T., Zhao, Wei, Zöllner, Sebastian, Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Blangero, John, Boerwinkle, Eric, Burchard, Esteban G., Carson, April P., Chasman, Daniel I., Chen, Yii-Der Ida, Curran, Joanne E., Fornage, Myriam, Gordeuk, Victor R., He, Jiang, Heckbert, Susan R., Hou, Lifang, Irvin, Marguerite R., Kooperberg, Charles, Minster, Ryan L., Mitchell, Braxton D., Nouraie, Mehdi, Psaty, Bruce M., Raffield, Laura M., Reiner, Alexander P., Rich, Stephen S., Rotter, Jerome I., Shoemaker, M. Benjamin, Smith, Nicholas L., Taylor, Kent D., Telen, Marilyn J., Weiss, Scott T., Zhang, Yingze, Heard-Costa, Nancy, Sun, Yan V., Lin, Xihong, Adrienne Cupples, L., Lange, Leslie A., Liu, Ching-Ti, Loos, Ruth J.F., North, Kari E., Justice, Anne E.
Publicado 2023