Search Results - "Roden, Dan"

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  1. 1
    Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

    Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

    Roselli, CarolinaAff1, Aff2, Surakka, IdaAff3, Olesen, Morten S.Aff4, Sveinbjornsson, GardarAff5, Marston, Nicholas A.Aff6, Aff7, Choi, Seung Hoan, Holm, Hilma, Chaffin, Mark, Gudbjartsson, DanielAff5, Aff8, Hill, Matthew C.Aff1, Aff9, Aegisdottir, Hildur, Albert, Christine M.Aff10, Aff11, Alonso, Alvaro, Anderson, Christopher D.Aff13, Aff14, Arking, Dan E.Aff15, Arnar, David O.Aff5, Aff16, Aff17, Barnard, John, Benjamin, Emelia J.Aff19, Aff20, Aff21, Braunwald, EugeneAff6, Aff7, Brumpton, BenAff22, Aff23, Campbell, Archie, Chami, NathalieAff25, Aff26, Chasman, Daniel I.Aff11, Aff27, Cho, KellyAff28, Aff29, Choi, Eue-Keun, Christophersen, Ingrid E.Aff31, Aff32, Chung, Mina K., Conen, David, Crijns, Harry J., Cutler, Michael J., Czuba, TomaszAff37, Aff38, Damrauer, Scott M.Aff39, Aff40, Aff41, Dichgans, MartinAff42, Aff43, Dörr, MarcusAff44, Aff45, Dudink, Elton, Duong, ThuyVy, Erikstrup, ChristianAff46, Aff47, Esko, Tõnu, Fatkin, DianeAff49, Aff50, Aff51, Faul, Jessica D., Ferreira, Manuel, Freitag, Daniel F., Ganesh, Santhi K.Aff55, Aff56, Gaziano, J. MichaelAff57, Aff58, Geelhoed, Bastiaan, Ghouse, JonasAff4, Aff59, Gieger, Christian, Giulianini, Franco, Graham, Sarah E., Gudnason, VilmundurAff16, Aff61, Guo, XiuqingAff62, Aff63, Haggerty, Christopher, Hayward, Caroline, Heckbert, Susan R.Aff66, Aff67, Hveem, Kristian, Ito, Kaoru, Johnson, ReneeAff49, Aff50, Jukema, J. WouterAff69, Aff70, Jurgens, Sean J.Aff1, Aff71, Kääb, StefanAff72, Aff73, Kane, John P., Kany, ShinwanAff1, Aff75, Aff76, Kardia, Sharon L. R., Kavousi, Maryam, Khurshid, ShaanAff1, Aff79, Kamanu, Frederick K.Aff6, Aff7, Kirchhof, PaulusAff75, Aff76, Aff80, Aff81, Kleber, Marcus E.Aff82, Aff83, Knight, StaceyAff36, Aff84, Komuro, IsseiAff85, Aff86, Krieger, Jose E., Launer, Lenore J., Li, Dadong, Lin, Honghuang, Lin, Henry J.Aff62, Aff63, Loos, Ruth J. F.Aff25, Aff90, Lotta, Luca, Lubitz, Steven A.Aff1, Aff79, Lunetta, Kathryn L., Macfarlane, Peter W.Aff92, Aff93, Magnusson, Patrik K. E., Malik, RainerAff42, Aff43, Mantineo, Helene, Marcus, Gregory M., März, WinfriedAff83, Aff97, McManus, David D., Melander, Olle, Melloni, Giorgio E. M., Meyre, Pascal B., Miyazawa, Kazuo, Mohanty, Sanghamitra, Monfort, Laia M.Aff4, Aff59, Müller-Nurasyid, MartinaAff102, Aff103, Nafissi, Navid A., Natale, AndreaAff101, Aff105, Nazarian, Saman, Ostrowski, Sisse R.Aff107, Aff108, Pak, Hui-Nam, Pang, Shichao, Pedersen, Ole B., Pedersen, Nancy L., Pereira, Alexandre C., Pirruccello, James P., Preuss, Michael, Psaty, Bruce M., Pullinger, Clive R., Rader, Daniel J., Rämö, Joel T.Aff1, Aff9, Aff115, Ridker, Paul M.Aff11, Aff27, Rienstra, Michiel, Risch, LorenzAff116, Aff117, Roden, Dan M., Rotter, Jerome I.Aff62, Aff119, Sabatine, Marc S.Aff6, Aff7, Schunkert, HeribertAff110, Aff120, Shah, Svati H., Shim, Jaemin, Shoemaker, M. Benjamin, Simonson, Bridget, Sinner, Moritz F.Aff72, Aff73, Smit, Roelof A. J., Smith, Jennifer A.Aff52, Aff77, Smith, Nicholas L.Aff66, Aff67, Aff123, Smith, J. GustavAff37, Aff38, Soliman, Elsayed Z., Sørensen, Erik, Sotoodehnia, Nona, Strbian, Daniel, Stricker, Bruno H., Teder-Laving, Maris, Sun, Yan V.Aff12, Aff127, Thériault, SébastienAff34, Aff128, Thorolfsdottir, Rosa B., Thorsteinsdottir, UnnurAff5, Aff16, Tveit, ArnljotAff31, Aff129, van der Harst, Pim, van Meurs, JoyceAff78, Aff131, Wang, Biqi, Weiss, StefanAff45, Aff132, Wells, Quinn S., Weng, Lu-ChenAff1, Aff133, Aff134, Wilson, Peter W.Aff12, Aff135, Aff136, Xiao, LingAff1, Aff9, Yang, Pil-Sung, Yao, Jie, Yoneda, Zachary T., Zeller, TanjaAff76, Aff138, Zeng, Lingyao, Zhao, WeiAff52, Aff77, Zhou, Xiang, Zöllner, Sebastian, Ruff, Christian T.Aff6, Aff7, Bundgaard, HenningAff59, Aff108, Willer, CristenAff3, Aff141, Stefansson, KariAff5, Aff16, Ellinor, Patrick T.Aff1, Aff79, Aff142, IDs41588024020723_cor1

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  2. 2
    Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

    Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

    Choi, Seung HoanAff1, Aff2, Jurgens, Sean J.Aff1, Aff3, Xiao, LingAff1, Aff4, Hill, Matthew C.Aff1, Aff4, Haggerty, Christopher M., Sveinbjörnsson, Garðar, Morrill, Valerie N., Marston, Nicholas A.Aff7, Aff8, Weng, Lu-ChenAff1, Aff4, Pirruccello, James P.Aff1, Aff4, Aff9, Arnar, David O.Aff6, Aff10, Aff11, Gudbjartsson, Daniel FannarAff6, Aff12, Mantineo, Helene, von Falkenhausen, Aenne S.Aff13, Aff14, Natale, Andrea, Tveit, Arnljot, Geelhoed, Bastiaan, Roselli, Carolina, Van Wagoner, David R., Darbar, Dawood, Haase, Doreen, Soliman, Elsayed Z., Davogustto, Giovanni E., Jun, Goo, Calkins, Hugh, Anderson, Jeffrey L.Aff25, Aff26, Brody, Jennifer A., Halford, Jennifer L.Aff1, Aff4, Barnard, John, Hokanson, John E., Smith, Jonathan D., Bis, Joshua C., Young, Kendra, Johnson, Linda S. B., Risch, LorenzAff31, Aff32, Gula, Lorne J., Kwee, Lydia Coulter, Chaffin, Mark D., Kühne, Michael, Preuss, Michael, Gupta, Namrata, Nafissi, Navid A., Smith, Nicholas L.Aff39, Aff40, Nilsson, Peter M.Aff41, Aff42, van der Harst, PimAff17, Aff43, Wells, Quinn S.Aff22, Aff44, Judy, Renae L.Aff45, Aff46, Schnabel, Renate B.Aff20, Aff47, Aff48, Johnson, ReneeAff49, Aff50, Smit, Roelof A. J., Gabriel, Stacey, Knight, StaceyAff25, Aff51, Furukawa, Tetsushi, Blackwell, Thomas W., Nauffal, VictorAff1, Aff4, Wang, XinAff1, Aff4, Min, Yuan-I, Yoneda, Zachary T., Laksman, Zachary W. M., Bezzina, Connie R., Alonso, Alvaro, Psaty, Bruce M.Aff27, Aff39, Albert, Christine M., Arking, Dan E., Roden, Dan M., Chasman, Daniel I.Aff37, Aff59, Rader, Daniel J., Conen, David, McManus, David D., Fatkin, DianeAff49, Aff50, Aff63, Benjamin, Emelia J.Aff64, Aff65, Boerwinkle, Eric, Marcus, Gregory M., Christophersen, Ingrid E.Aff16, Aff67, Smith, J. GustavAff68, Aff69, Roberts, Jason D.Aff33, Aff70, Raffield, Laura M., Shoemaker, M. Benjamin, Cho, Michael H., Cutler, Michael J., Rienstra, Michiel, Chung, Mina K., S. Olesen, MortenAff74, Aff75, Sinner, Moritz F.Aff13, Aff14, Sotoodehnia, Nona, Kirchhof, PaulusAff20, Aff47, Aff48, Aff76, Loos, Ruth J. F.Aff36, Aff77, Nazarian, Saman, Mohanty, SanghamitraAff15, Aff79, Damrauer, Scott M.Aff45, Aff46, Aff60, Kaab, StefanAff13, Aff14, Heckbert, Susan R.Aff40, Aff80, Redline, Susan, Shah, Svati H., Tanaka, ToshihiroAff82, Aff83, Ebana, Yusuke, Holm, Hilma, Stefansson, KariAff6, Aff11, Ruff, Christian T.Aff7, Aff8, Sabatine, Marc S.Aff7, Aff8, Lunetta, Kathryn L.Aff2, Aff64, Lubitz, Steven A.Aff1, Aff4, Aff85, Ellinor, Patrick T.Aff1, Aff4, Aff85, IDs41588025020749_cor1

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  3. 3
    The impact of common and rare genetic variants on bradyarrhythmia development

    The impact of common and rare genetic variants on bradyarrhythmia development

    Weng, Lu-ChenAff1, Aff2, Aff3, Rämö, Joel T.Aff4, Aff5, Jurgens, Sean J.Aff2, Aff6, Khurshid, ShaanAff1, Aff2, Aff7, Chaffin, Mark, Hall, Amelia Weber, Morrill, Valerie N., Wang, Xin, Nauffal, VictorAff2, Aff3, Aff9, Sun, Yan V.Aff10, Aff11, Beer, Dominik, Lee, Simon, Nadkarni, Girish N., Duong, ThuyVy, Wang, Biqi, Czuba, TomaszAff16, Aff17, Austin, Thomas R.Aff18, Aff19, Yoneda, Zachary T., Friedman, Daniel J., Clayton, Anne, Hyman, Matthew C., Judy, Renae L., Skanes, Allan C., Orland, Kate M., Treu, Timothy M., Oetjens, Matthew T., Alonso, Alvaro, Soliman, Elsayed Z., Lin, Honghuang, Lunetta, Kathryn L., van der Pals, Jesper, Issa, Tariq Z., Nafissi, Navid A., May, Heidi T., Leong-Sit, Peter, Roselli, CarolinaAff2, Aff33, Choi, Seung Hoan, Khan, Habib R., Knight, StaceyAff22, Aff35, Karlsson Linnér, RichardAff27, Aff36, Bezzina, Connie R., Ripatti, Samuli, Heckbert, Susan R.Aff18, Aff19, Gaziano, J. MichaelAff3, Aff39, Aff40, Loos, Ruth J. F.Aff41, Aff42, Psaty, Bruce M.Aff18, Aff43, Smith, J. GustavAff16, Aff17, Aff31, Aff44, Benjamin, Emelia J.Aff45, Aff46, Aff47, Arking, Dan E., Rader, Daniel J., Shah, Svati H.Aff21, Aff49, Roden, Dan M., Damrauer, Scott M.Aff24, Aff51, Eckhardt, Lee L., Roberts, Jason D., Cutler, Michael J., Shoemaker, M. Benjamin, Haggerty, Christopher M.Aff12, Aff52, Cho, KellyAff3, Aff39, Aff40, Palotie, AarnoAff4, Aff53, Aff54, Wilson, Peter W. F.Aff10, Aff55, Ellinor, Patrick T.Aff2, Aff7, Lubitz, Steven A.Aff7, IDs41588024019782_cor1

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  4. 4
    Invasive Assessment of Coronary Artery Disease in Clonal Hematopoiesis of Indeterminate Potential.

    Invasive Assessment of Coronary Artery Disease in Clonal Hematopoiesis of Indeterminate Potential.

    Heimlich, J Brett, Raddatz, Michael A, Wells, John, Vlasschaert, Caitlyn, Olson, Sydney, Threadcraft, Marcus, Foster, Kristoff, Boateng, Emmanuel, Umbarger, Kelsey, Su, Yan Ru, Roden, Dan M, Barker, Colin M, Bick, Alexander G

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  5. 5
    Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

    Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

    Mack, Taralynn M, Raddatz, Michael A, Pershad, Yash, Nachun, Daniel C, Taylor, Kent D, Guo, Xiuqing, Shuldiner, Alan R, O’Connell, Jeffrey R, Kenny, Eimear E, Loos, Ruth JF, Redline, Susan, Cade, Brian E, Psaty, Bruce M, Bis, Joshua C, Brody, Jennifer A, Silverman, Edwin K, Yun, Jeong H, Cho, Michael H, DeMeo, Dawn L, Levy, Daniel, Johnson, Andrew D, Mathias, Rasika A, Yanek, Lisa R, Heckbert, Susan R, Smith, Nicholas L, Wiggins, Kerri L, Raffield, Laura M, Carson, April P, Rotter, Jerome I, Rich, Stephen S, Manichaikul, Ani W, Gu, C Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Shoemaker, M Benjamin, Roden, Dan M, Kooperberg, Charles, Auer, Paul L, Desai, Pinkal, Blackwell, Thomas W, Smith, Albert V, Reiner, Alexander P, Jaiswal, Siddhartha, Weinstock, Joshua S, Bick, Alexander G

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  6. 6
    Determinants of mosaic chromosomal alteration fitness.

    Determinants of mosaic chromosomal alteration fitness.

    Pershad, Yash, Mack, Taralynn, Poisner, Hannah, Jakubek, Yasminka, Stilp, Adrienne, Mitchell, Braxton, Lewis, Joshua, Boerwinkle, Eric, Loos, Ruth, Chami, Nathalie, Wang, Zhe, Barnes, Kathleen, Pankratz, Nathan, Fornage, Myriam, Redline, Susan, Psaty, Bruce, Bis, Joshua, Shojaie, Ali, Silverman, Edwin, Cho, Michael, Yun, Jeong, DeMeo, Dawn, Levy, Daniel, Johnson, Andrew, Mathias, Rasika, Taub, Margaret, Arnett, Donna, North, Kari, Raffield, Laura, Carson, April, Doyle, Margaret, Rich, Stephen, Guo, Xiuqing, Cox, Nancy, Roden, Dan, Franceschini, Nora, Desai, Pinkal, Reiner, Alex, Auer, Paul, Scheet, Paul, Jaiswal, Siddhartha, Weinstock, Joshua, Bick, Alexander, Rotter, Jerome

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  7. 7
    Comparison of HLA allelic imputation programs

    Comparison of HLA allelic imputation programs

    Karnes, Jason H., Shaffer, Christian M., Bastarache, Lisa, Gaudieri, Silvana, Glazer, Andrew M., Steiner, Heidi E., Mosley, Jonathan D., Mallal, Simon, Denny, Joshua C., Phillips, Elizabeth J., Roden, Dan M.

    Univ Arizona, Coll Pharm, Dept Pharm Practice & Sci

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  8. 8
    Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

    Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

    Keener, Rebecca, Chhetri, Surya B, Connelly, Carla J, Taub, Margaret A, Conomos, Matthew P, Weinstock, Joshua, Ni, Bohan, Strober, Benjamin, Aslibekyan, Stella, Auer, Paul L, Barwick, Lucas, Becker, Lewis C, Blangero, John, Bleecker, Eugene R, Brody, Jennifer A, Cade, Brian E, Celedon, Juan C, Chang, Yi-Cheng, Cupples, L Adrienne, Custer, Brian, Freedman, Barry I, Gladwin, Mark T, Heckbert, Susan R, Hou, Lifang, Irvin, Marguerite R, Isasi, Carmen R, Johnsen, Jill M, Kenny, Eimear E, Kooperberg, Charles, Minster, Ryan L, Naseri, Take, Viali, Satupa’itea, Nekhai, Sergei, Pankratz, Nathan, Peyser, Patricia A, Taylor, Kent D, Telen, Marilyn J, Wu, Baojun, Yanek, Lisa R, Yang, Ivana V, Albert, Christine, Arnett, Donna K, Ashley-Koch, Allison E, Barnes, Kathleen C, Bis, Joshua C, Blackwell, Thomas W, Boerwinkle, Eric, Burchard, Esteban G, Carson, April P, Chen, Zhanghua, Chen, Yii-Der Ida, Darbar, Dawood, de Andrade, Mariza, Ellinor, Patrick T, Fornage, Myriam, Gelb, Bruce D, Gilliland, Frank D, He, Jiang, Islam, Talat, Kaab, Stefan, Kardia, Sharon LR, Kelly, Shannon, Konkle, Barbara A, Kumar, Rajesh, Loos, Ruth JF, Martinez, Fernando D, McGarvey, Stephen T, Meyers, Deborah A, Mitchell, Braxton D, Montgomery, Courtney G, North, Kari E, Palmer, Nicholette D, Peralta, Juan M, Raby, Benjamin A, Redline, Susan, Rich, Stephen S, Roden, Dan, Rotter, Jerome I, Ruczinski, Ingo, Schwartz, David, Sciurba, Frank, Shoemaker, M Benjamin, Silverman, Edwin K, Sinner, Moritz F, Smith, Nicholas L, Smith, Albert V, Tiwari, Hemant K, Vasan, Ramachandran S, Weiss, Scott T, Williams, L Keoki, Zhang, Yingze, Ziv, Elad, Raffield, Laura M, Reiner, Alexander P, Arvanitis, Marios, Greider, Carol W, Mathias, Rasika A, Battle, Alexis

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  9. 9

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  10. 10

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  11. 11

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  12. 12

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  13. 13
    Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

    Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

    Mack, Taralynn M., Raddatz, Michael A.Aff1, Aff2, Pershad, Yash, Nachun, Daniel C., Taylor, Kent D., Guo, Xiuqing, Shuldiner, Alan R., O’Connell, Jeffrey R., Kenny, Eimear E., Loos, Ruth J. F.Aff7, Aff8, Redline, SusanAff9, Aff10, Cade, Brian E.Aff9, Aff10, Aff11, Psaty, Bruce M.Aff12, Aff13, Aff14, Aff15, Bis, Joshua C., Brody, Jennifer A., Silverman, Edwin K., Yun, Jeong H., Cho, Michael H., DeMeo, Dawn L., Levy, Daniel, Johnson, Andrew D., Mathias, Rasika A., Yanek, Lisa R., Heckbert, Susan R.Aff13, Aff19, Smith, Nicholas L.Aff13, Aff19, Aff20, Wiggins, Kerri L., Raffield, Laura M., Carson, April P., Rotter, Jerome I., Rich, Stephen S., Manichaikul, Ani W., Gu, C. Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Shoemaker, M. Benjamin, Roden, Dan M., Kooperberg, Charles, Auer, Paul L., Desai, PinkalAff31, Aff32, Blackwell, Thomas W., Smith, Albert V., Reiner, Alexander P., Jaiswal, Siddhartha, Weinstock, Joshua S., Bick, Alexander G.Aff1, Aff34, IDs43587024006477_cor45

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  14. 14
    ParSE-seq: a calibrated multiplexed assay to facilitate the clinical classification of putative splice-altering variants

    ParSE-seq: a calibrated multiplexed assay to facilitate the clinical classification of putative splice-altering variants

    O’Neill, Matthew J., Yang, Tao, Laudeman, Julie, Calandranis, Maria E., Harvey, M. Lorena, Solus, Joseph F., Roden, Dan M.Aff2, Aff3, Aff4, IDs41467024524744_cor7, Glazer, Andrew M.Aff2, IDs41467024524744_cor8

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  15. 15
    Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome

    Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome

    Lancaster, Megan C., Chen, Hung-HsinAff2, Aff3, Shoemaker, M. Benjamin, Fleming, Matthew R., Strickland, Teresa L., Baker, James T., Evans, Grahame F., Polikowsky, Hannah G., Samuels, David C., Huff, Chad D., Roden, Dan M.Aff1, Aff4, Below, Jennifer E.Aff2, IDs41467024519774_cor12

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  16. 16
    Benchmarking computational variant effect predictors by their ability to infer human traits

    Benchmarking computational variant effect predictors by their ability to infer human traits

    Tabet, Daniel R.Aff1, Aff2, Aff3, Aff4, Kuang, DaAff1, Aff2, Aff3, Aff4, Lancaster, Megan C., Li, RoujiaAff1, Aff2, Aff3, Aff4, Liu, KarenAff1, Aff2, Aff3, Aff4, Weile, JochenAff1, Aff2, Aff3, Aff4, Coté, Atina G.Aff1, Aff2, Aff3, Aff4, Wu, YingzhouAff1, Aff2, Aff3, Aff4, Hegele, Robert A., Roden, Dan M.Aff5, Aff6, Aff7, Roth, Frederick P.Aff1, Aff2, Aff3, Aff4, Aff9, IDs13059024033147_cor11

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  17. 17
    High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology

    High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology

    Muhammad, AyeshaAff1, Aff2, Calandranis, Maria E., Li, BianAff3, Aff4, Yang, Tao, Blackwell, Daniel J., Harvey, M. Lorena, Smith, Jeremy E., Daniel, Zerubabell A., Chew, Ashli E., Capra, John A., Matreyek, Kenneth A., Fowler, Douglas M., Roden, Dan M.Aff1, Aff3, Aff8, Aff9, Glazer, Andrew M.Aff1, Aff3, IDs13073024013405_cor14

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  18. 18
    Clinical associations with a polygenic predisposition to benign lower white blood cell counts

    Clinical associations with a polygenic predisposition to benign lower white blood cell counts

    Mosley, Jonathan D.Aff1, Aff2, IDs41467024478045_cor1, Shelley, John P., Dickson, Alyson L., Zanussi, Jacy, Daniel, Laura L., Zheng, Neil S.Aff1, Aff3, Bastarache, Lisa, Wei, Wei-Qi, Shi, Mingjian, Jarvik, Gail P.Aff4, Aff5, Rosenthal, Elisabeth A., Khan, Atlas, Sherafati, Alborz, Kullo, Iftikhar J., Walunas, Theresa L., Glessner, Joseph, Hakonarson, Hakon, Cox, Nancy J., Roden, Dan M.Aff1, Aff2, Aff11, Frangakis, Stephan G., Vanderwerff, Brett, Stein, C. MichaelAff1, Aff11, Van Driest, Sara L.Aff1, Aff14, Borinstein, Scott C., Shu, Xiao-OuAff1, Aff15, Zawistowski, Matthew, Chung, Cecilia P., Kawai, Vivian K.

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  19. 19
    Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer’s disease with real-world clinical validation

    Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer’s disease with real-world clinical validation

    Yan, Chao, Grabowska, Monika E., Dickson, Alyson L., Li, BingshanAff3, Aff4, Wen, ZhexingAff5, Aff6, Roden, Dan M., Michael Stein, C., Embí, Peter J.Aff1, Aff2, Peterson, Josh F.Aff1, Aff2, Feng, QiPing, Malin, Bradley A.Aff1, Aff7, Aff8, Wei, Wei-QiAff1, Aff7, IDs41746024010383_cor12

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  20. 20
    The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

    The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

    Puckelwartz, Megan J.Aff1, Aff2, IDs1307302401284w_cor1, Pesce, Lorenzo L.Aff1, Aff2, Hernandez, Edgar J., Webster, Gregory, Dellefave-Castillo, Lisa M., Russell, Mark W., Geisler, Sarah S., Kearns, Samuel D., Karthik, Felix, Etheridge, Susan P., Monroe, Tanner O., Pottinger, Tess D., Kannankeril, Prince J., Shoemaker, M. Benjamin, Fountain, Darlene, Roden, Dan M., Faulkner, Meghan, MacLeod, Heather M., Burns, Kristin M., Yandell, Mark, Tristani-Firouzi, Martin, George, Jr., Alfred L., McNally, Elizabeth M.

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