APA

Kowalski M. H., Qian H., Hou Z., Rosen J. D., Tapia A. L., Shan Y., Jain D., Argos M., Arnett D. K., Avery C., Barnes K. C., Becker L. C., Bien S. A., Bis J. C., Blangero J., Boerwinkle E., Bowden D. W., Buyske S., Cai J., Cho M. H., Choi S. H., Choquet H., Cupples L. A., Cushman M., Daya M., de Vries P. S., Ellinor P. T., Faraday N., Fornage M., Gabriel S., Ganesh S. K., Graff M., Gupta N., He J., Heckbert S. R., Hidalgo B., Hodonsky C. J., Irvin M. R., Johnson A. D., Jorgenson E., Kaplan R., Kardia S. L. R., Kelly T. N., Kooperberg C., Lasky-Su J. A., Loos R. J. F., Lubitz S. A., Mathias R. A., McHugh C. P., Montgomery C., Moon J., Morrison A. C., Palmer N. D., Pankratz N., Papanicolaou G. J., Peralta J. M., Peyser P. A., Rich S. S., Rotter J. I., Silverman E. K., Smith J. A., Smith N. L., Taylor K. D., Thornton T. A., Tiwari H. K., Tracy R. P., Wang T., Weiss S. T., Weng L., Wiggins K. L., Wilson J. G., Yanek L. R., Zöllner S., North K. E., Auer P. L., Raffield L. M., Reiner A. P. & Li Y. (20200303). Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. : PLoS genetics.

Chicago

Kowalski Madeline H, Qian Huijun, Hou Ziyi, Rosen Jonathan D, Tapia Amanda L, Shan Yue, Jain Deepti, Argos Maria, Arnett Donna K, Avery Christy, Barnes Kathleen C, Becker Lewis C, Bien Stephanie A, Bis Joshua C, Blangero John, Boerwinkle Eric, Bowden Donald W, Buyske Steve, Cai Jianwen, Cho Michael H, Choi Seung Hoan, Choquet Hélène, Cupples L Adrienne, Cushman Mary, Daya Michelle, de Vries Paul S, Ellinor Patrick T, Faraday Nauder, Fornage Myriam, Gabriel Stacey, Ganesh Santhi K, Graff Misa, Gupta Namrata, He Jiang, Heckbert Susan R, Hidalgo Bertha, Hodonsky Chani J, Irvin Marguerite R, Johnson Andrew D, Jorgenson Eric, Kaplan Robert, Kardia Sharon L R, Kelly Tanika N, Kooperberg Charles, Lasky-Su Jessica A, Loos Ruth J F, Lubitz Steven A, Mathias Rasika A, McHugh Caitlin P, Montgomery Courtney, Moon Jee-Young, Morrison Alanna C, Palmer Nicholette D, Pankratz Nathan, Papanicolaou George J, Peralta Juan M, Peyser Patricia A, Rich Stephen S, Rotter Jerome I, Silverman Edwin K, Smith Jennifer A, Smith Nicholas L, Taylor Kent D, Thornton Timothy A, Tiwari Hemant K, Tracy Russell P, Wang Tao, Weiss Scott T, Weng Lu-Chen, Wiggins Kerri L, Wilson James G, Yanek Lisa R, Zöllner Sebastian, North Kari E, Auer Paul L, Raffield Laura M, Reiner Alexander P and Li Yun. 20200303. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. : PLoS genetics.

Harvard

Kowalski M. H., Qian H., Hou Z., Rosen J. D., Tapia A. L., Shan Y., Jain D., Argos M., Arnett D. K., Avery C., Barnes K. C., Becker L. C., Bien S. A., Bis J. C., Blangero J., Boerwinkle E., Bowden D. W., Buyske S., Cai J., Cho M. H., Choi S. H., Choquet H., Cupples L. A., Cushman M., Daya M., de Vries P. S., Ellinor P. T., Faraday N., Fornage M., Gabriel S., Ganesh S. K., Graff M., Gupta N., He J., Heckbert S. R., Hidalgo B., Hodonsky C. J., Irvin M. R., Johnson A. D., Jorgenson E., Kaplan R., Kardia S. L. R., Kelly T. N., Kooperberg C., Lasky-Su J. A., Loos R. J. F., Lubitz S. A., Mathias R. A., McHugh C. P., Montgomery C., Moon J., Morrison A. C., Palmer N. D., Pankratz N., Papanicolaou G. J., Peralta J. M., Peyser P. A., Rich S. S., Rotter J. I., Silverman E. K., Smith J. A., Smith N. L., Taylor K. D., Thornton T. A., Tiwari H. K., Tracy R. P., Wang T., Weiss S. T., Weng L., Wiggins K. L., Wilson J. G., Yanek L. R., Zöllner S., North K. E., Auer P. L., Raffield L. M., Reiner A. P. and Li Y. (20200303). Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. : PLoS genetics.

MLA

Kowalski Madeline H, Qian Huijun, Hou Ziyi, Rosen Jonathan D, Tapia Amanda L, Shan Yue, Jain Deepti, Argos Maria, Arnett Donna K, Avery Christy, Barnes Kathleen C, Becker Lewis C, Bien Stephanie A, Bis Joshua C, Blangero John, Boerwinkle Eric, Bowden Donald W, Buyske Steve, Cai Jianwen, Cho Michael H, Choi Seung Hoan, Choquet Hélène, Cupples L Adrienne, Cushman Mary, Daya Michelle, de Vries Paul S, Ellinor Patrick T, Faraday Nauder, Fornage Myriam, Gabriel Stacey, Ganesh Santhi K, Graff Misa, Gupta Namrata, He Jiang, Heckbert Susan R, Hidalgo Bertha, Hodonsky Chani J, Irvin Marguerite R, Johnson Andrew D, Jorgenson Eric, Kaplan Robert, Kardia Sharon L R, Kelly Tanika N, Kooperberg Charles, Lasky-Su Jessica A, Loos Ruth J F, Lubitz Steven A, Mathias Rasika A, McHugh Caitlin P, Montgomery Courtney, Moon Jee-Young, Morrison Alanna C, Palmer Nicholette D, Pankratz Nathan, Papanicolaou George J, Peralta Juan M, Peyser Patricia A, Rich Stephen S, Rotter Jerome I, Silverman Edwin K, Smith Jennifer A, Smith Nicholas L, Taylor Kent D, Thornton Timothy A, Tiwari Hemant K, Tracy Russell P, Wang Tao, Weiss Scott T, Weng Lu-Chen, Wiggins Kerri L, Wilson James G, Yanek Lisa R, Zöllner Sebastian, North Kari E, Auer Paul L, Raffield Laura M, Reiner Alexander P and Li Yun. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. : PLoS genetics. 20200303.