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

Choi SH, Jurgens SJ, Xiao L, Hill MC, Haggerty CM, Sveinbjörnsson G, Morrill VN, Marston NA, Weng LC, Pirruccello JP, Arnar DO, Gudbjartsson DF, Mantineo H, von Falkenhausen AS, Natale A, Tveit A, Geelhoed B, Roselli C, Van Wagoner DR, Darbar D, Haase D, Soliman EZ, Davogustto GE, Jun G, Calkins H, Anderson JL, Brody JA, Halford JL, Barnard J, Hokanson JE, Smith JD, Bis JC, Young K, Johnson LSB, Risch L, Gula LJ, Kwee LC, Chaffin MD, Kühne M, Preuss M, Gupta N, Nafissi NA, Smith NL, Nilsson PM, van der Harst P, Wells QS, Judy RL, Schnabel RB, Johnson R, Smit RAJ, Gabriel S, Knight S, Furukawa T, Blackwell TW, Nauffal V, Wang X, Min YI, Yoneda ZT, Laksman ZWM, Bezzina CR, Alonso A, Psaty BM, Albert CM, Arking DE, Roden DM, Chasman DI, Rader DJ, Conen D, McManus DD, Fatkin D, Benjamin EJ, Boerwinkle E, Marcus GM, Christophersen IE, Smith JG, Roberts JD, Raffield LM, Shoemaker MB, Cho MH, Cutler MJ, Rienstra M, Chung MK, S Olesen M, Sinner MF, Sotoodehnia N, Kirchhof P, Loos RJF, Nazarian S, Mohanty S, Damrauer SM, Kaab S, Heckbert SR, Redline S, Shah SH, Tanaka T, Ebana Y, Regeneron Genetics Center, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Holm H, Stefansson K, Ruff CT, Sabatine MS, Lunetta KL, Lubitz SA, Ellinor PT

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DOI: 10.1038/s41588-025-02074-9
Published: 2025 Mar
Container: Nature genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1038/s41588-025-02074-9,
  title = {Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.},
  author = {Choi SH and Jurgens SJ and Xiao L and Hill MC and Haggerty CM and Sveinbjörnsson G and Morrill VN and Marston NA and Weng LC and Pirruccello JP and Arnar DO and Gudbjartsson DF and Mantineo H and von Falkenhausen AS and Natale A and Tveit A and Geelhoed B and Roselli C and Van Wagoner DR and Darbar D and Haase D and Soliman EZ and Davogustto GE and Jun G and Calkins H and Anderson JL and Brody JA and Halford JL and Barnard J and Hokanson JE and Smith JD and Bis JC and Young K and Johnson LSB and Risch L and Gula LJ and Kwee LC and Chaffin MD and Kühne M and Preuss M and Gupta N and Nafissi NA and Smith NL and Nilsson PM and van der Harst P and Wells QS and Judy RL and Schnabel RB and Johnson R and Smit RAJ and Gabriel S and Knight S and Furukawa T and Blackwell TW and Nauffal V and Wang X and Min YI and Yoneda ZT and Laksman ZWM and Bezzina CR and Alonso A and Psaty BM and Albert CM and Arking DE and Roden DM and Chasman DI and Rader DJ and Conen D and McManus DD and Fatkin D and Benjamin EJ and Boerwinkle E and Marcus GM and Christophersen IE and Smith JG and Roberts JD and Raffield LM and Shoemaker MB and Cho MH and Cutler MJ and Rienstra M and Chung MK and S Olesen M and Sinner MF and Sotoodehnia N and Kirchhof P and Loos RJF and Nazarian S and Mohanty S and Damrauer SM and Kaab S and Heckbert SR and Redline S and Shah SH and Tanaka T and Ebana Y and Regeneron Genetics Center and NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium and Holm H and Stefansson K and Ruff CT and Sabatine MS and Lunetta KL and Lubitz SA and Ellinor PT},
  year = {2025},
  journal = {Nature genetics},
  doi = {10.1038/s41588-025-02074-9},
  url = {https://doi.org/10.1038/s41588-025-02074-9}
}

RIS

TY  - JOUR
TI  - Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.
AU  - Choi SH
AU  - Jurgens SJ
AU  - Xiao L
AU  - Hill MC
AU  - Haggerty CM
AU  - Sveinbjörnsson G
AU  - Morrill VN
AU  - Marston NA
AU  - Weng LC
AU  - Pirruccello JP
AU  - Arnar DO
AU  - Gudbjartsson DF
AU  - Mantineo H
AU  - von Falkenhausen AS
AU  - Natale A
AU  - Tveit A
AU  - Geelhoed B
AU  - Roselli C
AU  - Van Wagoner DR
AU  - Darbar D
AU  - Haase D
AU  - Soliman EZ
AU  - Davogustto GE
AU  - Jun G
AU  - Calkins H
AU  - Anderson JL
AU  - Brody JA
AU  - Halford JL
AU  - Barnard J
AU  - Hokanson JE
AU  - Smith JD
AU  - Bis JC
AU  - Young K
AU  - Johnson LSB
AU  - Risch L
AU  - Gula LJ
AU  - Kwee LC
AU  - Chaffin MD
AU  - Kühne M
AU  - Preuss M
AU  - Gupta N
AU  - Nafissi NA
AU  - Smith NL
AU  - Nilsson PM
AU  - van der Harst P
AU  - Wells QS
AU  - Judy RL
AU  - Schnabel RB
AU  - Johnson R
AU  - Smit RAJ
AU  - Gabriel S
AU  - Knight S
AU  - Furukawa T
AU  - Blackwell TW
AU  - Nauffal V
AU  - Wang X
AU  - Min YI
AU  - Yoneda ZT
AU  - Laksman ZWM
AU  - Bezzina CR
AU  - Alonso A
AU  - Psaty BM
AU  - Albert CM
AU  - Arking DE
AU  - Roden DM
AU  - Chasman DI
AU  - Rader DJ
AU  - Conen D
AU  - McManus DD
AU  - Fatkin D
AU  - Benjamin EJ
AU  - Boerwinkle E
AU  - Marcus GM
AU  - Christophersen IE
AU  - Smith JG
AU  - Roberts JD
AU  - Raffield LM
AU  - Shoemaker MB
AU  - Cho MH
AU  - Cutler MJ
AU  - Rienstra M
AU  - Chung MK
AU  - S Olesen M
AU  - Sinner MF
AU  - Sotoodehnia N
AU  - Kirchhof P
AU  - Loos RJF
AU  - Nazarian S
AU  - Mohanty S
AU  - Damrauer SM
AU  - Kaab S
AU  - Heckbert SR
AU  - Redline S
AU  - Shah SH
AU  - Tanaka T
AU  - Ebana Y
AU  - Regeneron Genetics Center
AU  - NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
AU  - Holm H
AU  - Stefansson K
AU  - Ruff CT
AU  - Sabatine MS
AU  - Lunetta KL
AU  - Lubitz SA
AU  - Ellinor PT
PY  - 2025
JO  - Nature genetics
DO  - 10.1038/s41588-025-02074-9
UR  - https://doi.org/10.1038/s41588-025-02074-9
ER  -

APA

SH, C., SJ, J., L, X., MC, H., CM, H., G, S., VN, M., NA, M., LC, W., JP, P., DO, A., DF, G., H, M., AS, V. F., A, N., A, T., B, G., C, R., DR, V. W., D, D., D, H., EZ, S., GE, D., G, J., H, C., JL, A., JA, B., JL, H., J, B., JE, H., JD, S., JC, B., K, Y., LSB, J., L, R., LJ, G., LC, K., MD, C., M, K., M, P., N, G., NA, N., NL, S., PM, N., P, V. D. H., QS, W., RL, J., RB, S., R, J., RAJ, S., S, G., S, K., T, F., TW, B., V, N., X, W., YI, M., ZT, Y., ZWM, L., CR, B., A, A., BM, P., CM, A., DE, A., DM, R., DI, C., DJ, R., D, C., DD, M., D, F., EJ, B., E, B., GM, M., IE, C., JG, S., JD, R., LM, R., MB, S., MH, C., MJ, C., M, R., MK, C., M, S. O., MF, S., N, S., P, K., RJF, L., S, N., S, M., SM, D., S, K., SR, H., S, R., SH, S., T, T., Y, E., Center, R. G., Consortium, N. T. F. P. M. (., H, H., K, S., CT, R., MS, S., KL, L., SA, L., & PT, E. (2025). Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.. Nature genetics. https://doi.org/10.1038/s41588-025-02074-9

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pubmed · retrieved 2026-09-25T17:26:56.586Z