The impact of common and rare genetic variants on bradyarrhythmia development
- DOI
- 10.1038/s41588-024-01978-2
- Published
- 2025-01
- Container
- Nature Genetics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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BibTeX
@article{allodium:10.1038/s41588-024-01978-2,
title = {The impact of common and rare genetic variants on bradyarrhythmia development},
author = {Lu-Chen Weng and Joel T. Rämö and Sean J. Jurgens and Shaan Khurshid and Mark Chaffin and Amelia Weber Hall and Valerie N. Morrill and Xin Wang and Victor Nauffal and Yan V. Sun and Dominik Beer and Simon Lee and Girish N. Nadkarni and ThuyVy Duong and Biqi Wang and Tomasz Czuba and Thomas R. Austin and Zachary T. Yoneda and Daniel J. Friedman and Anne Clayton and Matthew C. Hyman and Renae L. Judy and Allan C. Skanes and Kate M. Orland and Timothy M. Treu and Matthew T. Oetjens and Alvaro Alonso and Elsayed Z. Soliman and Honghuang Lin and Kathryn L. Lunetta and Jesper van der Pals and Tariq Z. Issa and Navid A. Nafissi and Heidi T. May and Peter Leong-Sit and Carolina Roselli and Seung Hoan Choi and Unknown and Unknown and Unknown and Goncalo Abecasis and Aris Baras and Michael Cantor and Giovanni Coppola and Aris Economides and Luca A. Lotta and John D. Overton and Jeffrey G. Reid and Alan Shuldiner and Christina Beechert and Caitlin Forsythe and Erin D. Fuller and Zhenhua Gu and Michael Lattari and Alexander Lopez and Thomas D. Schleicher and Maria Sotiropoulos Padilla and Louis Widom and Sarah E. Wolf and Manasi Pradhan and Kia Manoochehri and Ricardo H. Ulloa and Xiaodong Bai and Suganthi Balasubramanian and Andrew Blumenfeld and Boris Boutkov and Gisu Eom and Lukas Habegger and Alicia Hawes and Shareef Khalid and Olga Krasheninina and Rouel Lanche and Adam J. Mansfield and Evan K. Maxwell and Mrunali Nafde and Sean O’Keeffe and Max Orelus and Razvan Panea and Tommy Polanco and Ayesha Rasool and William Salerno and Jeffrey C. Staples and Marcus B. Jones and Lyndon J. Mitnaul and Habib R. Khan and Stacey Knight and Richard Karlsson Linnér and Connie R. Bezzina and Samuli Ripatti and Susan R. Heckbert and J. Michael Gaziano and Ruth J. F. Loos and Bruce M. Psaty and J. Gustav Smith and Emelia J. Benjamin and Dan E. Arking and Daniel J. Rader and Svati H. Shah and Dan M. Roden and Scott M. Damrauer and Lee L. Eckhardt and Jason D. Roberts and Michael J. Cutler and M. Benjamin Shoemaker and Christopher M. Haggerty and Kelly Cho and Aarno Palotie and Peter W. F. Wilson and Patrick T. Ellinor and Steven A. Lubitz},
year = {2025},
journal = {Nature Genetics},
doi = {10.1038/s41588-024-01978-2},
url = {https://doi.org/10.1038/s41588-024-01978-2}
}RIS
TY - JOUR TI - The impact of common and rare genetic variants on bradyarrhythmia development AU - Lu-Chen Weng AU - Joel T. Rämö AU - Sean J. Jurgens AU - Shaan Khurshid AU - Mark Chaffin AU - Amelia Weber Hall AU - Valerie N. Morrill AU - Xin Wang AU - Victor Nauffal AU - Yan V. Sun AU - Dominik Beer AU - Simon Lee AU - Girish N. Nadkarni AU - ThuyVy Duong AU - Biqi Wang AU - Tomasz Czuba AU - Thomas R. Austin AU - Zachary T. Yoneda AU - Daniel J. Friedman AU - Anne Clayton AU - Matthew C. Hyman AU - Renae L. Judy AU - Allan C. Skanes AU - Kate M. Orland AU - Timothy M. Treu AU - Matthew T. Oetjens AU - Alvaro Alonso AU - Elsayed Z. Soliman AU - Honghuang Lin AU - Kathryn L. Lunetta AU - Jesper van der Pals AU - Tariq Z. Issa AU - Navid A. Nafissi AU - Heidi T. May AU - Peter Leong-Sit AU - Carolina Roselli AU - Seung Hoan Choi AU - Unknown AU - Unknown AU - Unknown AU - Goncalo Abecasis AU - Aris Baras AU - Michael Cantor AU - Giovanni Coppola AU - Aris Economides AU - Luca A. Lotta AU - John D. Overton AU - Jeffrey G. Reid AU - Alan Shuldiner AU - Christina Beechert AU - Caitlin Forsythe AU - Erin D. Fuller AU - Zhenhua Gu AU - Michael Lattari AU - Alexander Lopez AU - Thomas D. Schleicher AU - Maria Sotiropoulos Padilla AU - Louis Widom AU - Sarah E. Wolf AU - Manasi Pradhan AU - Kia Manoochehri AU - Ricardo H. Ulloa AU - Xiaodong Bai AU - Suganthi Balasubramanian AU - Andrew Blumenfeld AU - Boris Boutkov AU - Gisu Eom AU - Lukas Habegger AU - Alicia Hawes AU - Shareef Khalid AU - Olga Krasheninina AU - Rouel Lanche AU - Adam J. Mansfield AU - Evan K. Maxwell AU - Mrunali Nafde AU - Sean O’Keeffe AU - Max Orelus AU - Razvan Panea AU - Tommy Polanco AU - Ayesha Rasool AU - William Salerno AU - Jeffrey C. Staples AU - Marcus B. Jones AU - Lyndon J. Mitnaul AU - Habib R. Khan AU - Stacey Knight AU - Richard Karlsson Linnér AU - Connie R. Bezzina AU - Samuli Ripatti AU - Susan R. Heckbert AU - J. Michael Gaziano AU - Ruth J. F. Loos AU - Bruce M. Psaty AU - J. Gustav Smith AU - Emelia J. Benjamin AU - Dan E. Arking AU - Daniel J. Rader AU - Svati H. Shah AU - Dan M. Roden AU - Scott M. Damrauer AU - Lee L. Eckhardt AU - Jason D. Roberts AU - Michael J. Cutler AU - M. Benjamin Shoemaker AU - Christopher M. Haggerty AU - Kelly Cho AU - Aarno Palotie AU - Peter W. F. Wilson AU - Patrick T. Ellinor AU - Steven A. Lubitz PY - 2025 JO - Nature Genetics DO - 10.1038/s41588-024-01978-2 UR - https://doi.org/10.1038/s41588-024-01978-2 ER -
APA
Weng, L., Rämö, J. T., Jurgens, S. J., Khurshid, S., Chaffin, M., Hall, A. W., Morrill, V. N., Wang, X., Nauffal, V., Sun, Y. V., Beer, D., Lee, S., Nadkarni, G. N., Duong, T., Wang, B., Czuba, T., Austin, T. R., Yoneda, Z. T., Friedman, D. J., Clayton, A., Hyman, M. C., Judy, R. L., Skanes, A. C., Orland, K. M., Treu, T. M., Oetjens, M. T., Alonso, A., Soliman, E. Z., Lin, H., Lunetta, K. L., Pals, J. V. D., Issa, T. Z., Nafissi, N. A., May, H. T., Leong-Sit, P., Roselli, C., Choi, S. H., Unknown, Unknown, Unknown, Abecasis, G., Baras, A., Cantor, M., Coppola, G., Economides, A., Lotta, L. A., Overton, J. D., Reid, J. G., Shuldiner, A., Beechert, C., Forsythe, C., Fuller, E. D., Gu, Z., Lattari, M., Lopez, A., Schleicher, T. D., Padilla, M. S., Widom, L., Wolf, S. E., Pradhan, M., Manoochehri, K., Ulloa, R. H., Bai, X., Balasubramanian, S., Blumenfeld, A., Boutkov, B., Eom, G., Habegger, L., Hawes, A., Khalid, S., Krasheninina, O., Lanche, R., Mansfield, A. J., Maxwell, E. K., Nafde, M., O’Keeffe, S., Orelus, M., Panea, R., Polanco, T., Rasool, A., Salerno, W., Staples, J. C., Jones, M. B., Mitnaul, L. J., Khan, H. R., Knight, S., Linnér, R. K., Bezzina, C. R., Ripatti, S., Heckbert, S. R., Gaziano, J. M., Loos, R. J. F., Psaty, B. M., Smith, J. G., Benjamin, E. J., Arking, D. E., Rader, D. J., Shah, S. H., Roden, D. M., Damrauer, S. M., Eckhardt, L. L., Roberts, J. D., Cutler, M. J., Shoemaker, M. B., Haggerty, C. M., Cho, K., Palotie, A., Wilson, P. W. F., Ellinor, P. T., & Lubitz, S. A. (2025). The impact of common and rare genetic variants on bradyarrhythmia development. Nature Genetics. https://doi.org/10.1038/s41588-024-01978-2
Source records
- crossref · retrieved 2026-09-26T06:47:11.732Z