DC Rao

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DC Rao

Professor of Biostatistics, Professor of Biostatistics in Genetics, Professor of Mathematics, Professor of Biostatistics in Psychiatry

 https://orcid.org/0009-0006-8538-2141

    Willing to Mentor

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    PhD/MSTP Students

    • 41327
      Citations
    1970 …2025

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    • 2025

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

      Regeneron Genetics Center & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Mar 2025, In: Nature Genetics. 57, 3, p. 548-562 15 p., e020163.

      Research output: Contribution to journal › Article › peer-review

      2 Scopus citations
    • 2024

      A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

      Trans-Omics for Precision Medicine (TOPMed) program, The INVENT Consortium, de Vries, P. S., Reventun, P., Brown, M. R., Heath, A. S., Huffman, J. E., Le, N. Q., Bebo, A., Brody, J. A., Temprano-Sagrera, G., Raffield, L. M., Ozel, A. B., Thibord, F., Jain, D., Lewis, J. P., Rodriguez, B. A. T., Pankratz, N., Taylor, K. D. & Polasek, O. & 182 others, Chen, M. H., Yanek, L. R., Carrasquilla, G. D., Marioni, R. E., Kleber, M. E., Trégouët, D. A., Yao, J., Li-Gao, R., Joshi, P. K., Trompet, S., Martinez-Perez, A., Ghanbari, M., Howard, T. E., Reiner, A. P., Arvanitis, M., Ryan, K. A., Bartz, T. M., Rudan, I., Faraday, N., Linneberg, A., Ekunwe, L., Davies, G., Delgado, G. E., Suchon, P., Guo, X., Rosendaal, F. R., Klaric, L., Noordam, R., van Rooij, F., Curran, J. E., Wheeler, M. M., Osburn, W. O., O'Connell, J. R., Boerwinkle, E., Beswick, A., Psaty, B. M., Kolcic, I., Souto, J. C., Becker, L. C., Hansen, T., Doyle, M. F., Harris, S. E., Moissl, A. P., Deleuze, J. F., Rich, S. S., van Hylckama Vlieg, A., Campbell, H., Stott, D. J., Soria, J. M., de Maat, M. P. M., Almasy, L., Brody, L. C., Auer, P. L., Abe, N., Abecasis, G., Aguet, F., Albert, C., Alonso, A., Ament, S., Anderson, P., Anugu, P., Applebaum-Bowden, D., Ardlie, K., Arking, D., Arnett, D. K., Ashley-Koch, A., Aslibekyan, S., Assimes, T., Auer, P., Avramopoulos, D., Ayas, N., Balasubramanian, A., Barnard, J., Barnes, K., Barr, R. G., Barron-Casella, E., Barwick, L., Beaty, T., Beck, G., Becker, D., Becker, L., Beer, R., Beitelshees, A., Benjamin, E., Benos, T., Bezerra, M., Bielak, L., Bis, J., Blackwell, T., Blangero, J., Blue, N., Bowden, D. W., Bowler, R., Brody, J., Broeckel, U., Broome, J., Brown, D., Bunting, K., Burchard, E., Bustamante, C., Buth, E., Cade, B., Cardwell, J., Carey, V., Carrier, J., Carson, A. P., Carty, C., Casaburi, R., Casas Romero, J. P., Casella, J., Castaldi, P., Chaffin, M., Chang, C., Chang, Y. C., Chasman, D., Chavan, S., Chen, B. J., Chen, W. M., Ida Chen, Y. D., Cho, M., Choi, S. H., Chuang, L. M., Chung, M., Chung, R. H., Clish, C., Comhair, S., Conomos, M., Cornell, E., Correa, A., Crandall, C., Crapo, J., Cupples, L. A., Curran, J., Curtis, J., Custer, B., Damcott, C., Darbar, D., David, S., Davis, C., Daya, M., de Andrade, M., de las Fuentes, L., de Vries, P., DeBaun, M., Deka, R., DeMeo, D., Devine, S., Dinh, H., Doddapaneni, H., Duan, Q., Dugan-Perez, S., Duggirala, R., Durda, J. P., Dutcher, S. K., Eaton, C., El Boueiz, A., Ellinor, P., Emery, L., Erzurum, S., Farber, C., Farek, J., Fingerlin, T., Flickinger, M., Fornage, M., Franceschini, N., Frazar, C., Fu, M., Fullerton, S. M., Fulton, L., Gabriel, S., Gan, W., Gao, S., Gao, Y., Gass, M., Geiger, H., Gelb, B., Geraci, M., Germer, S., Gerszten, R., Gu, C. C., Rao, D. C. & Sung, Y. J., May 2 2024, In: Blood. 143, 18, p. 1845-1855 11 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      3 Scopus citations

    • An approach to identify gene-environment interactions and reveal new biological insight in complex traits

      Zhu, X., Yang, Y., Lorincz-Comi, N., Li, G., Bentley, A. R., de Vries, P. S., Brown, M., Morrison, A. C., Rotimi, C. N., Gauderman, W. J., Rao, D. C. & Aschard, H., Dec 2024, In: Nature communications. 15, 1, 3385.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      7 Scopus citations

    • Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure

      Guirette, M., Lan, J., McKeown, N. M., Brown, M. R., Chen, H., De Vries, P. S., Kim, H., Rebholz, C. M., Morrison, A. C., Bartz, T. M., Fretts, A. M., Guo, X., Lemaitre, R. N., Liu, C. T., Noordam, R., De Mutsert, R., Rosendaal, F. R., Wang, C. A., Beilin, L. J. & Mori, T. A. & 26 others, Oddy, W. H., Pennell, C. E., Chai, J. F., Whitton, C., Van Dam, R. M., Liu, J., Tai, E. S., Sim, X., Neuhouser, M. L., Kooperberg, C., Tinker, L. F., Franceschini, N., Huan, T. X., Winkler, T. W., Bentley, A. R., Gauderman, W. J., Heerkens, L., Tanaka, T., Van Rooij, J., Munroe, P. B., Warren, H. R., Voortman, T., Chen, H., Rao, D. C., Levy, D. & Ma, J., Mar 1 2024, In: Hypertension. 81, 3, p. 552-560 9 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      4 Scopus citations
    • 2023

      Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Apr 27 2023, In: Nature. 616, 7958, p. 755-763 9 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      43 Scopus citations

    • A Brief History behind the journal Genetic Epidemiology and the International Genetic Epidemiology Society

      Rao, D. C., Jul 2023, In: Genetic Epidemiology. 47, 5, p. 361-364 4 p.

      Research output: Contribution to journal › Article › peer-review

    • Clonal haematopoiesis and risk of chronic liver disease

      NHLBI TOPMed Hematology Working Group, Apr 27 2023, In: Nature. 616, 7958, p. 747-754 8 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      93 Scopus citations

    • Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

      NHLBI Trans-Omics in Precision Medicine (TOPMed) Consortium, Recto, K., Kachroo, P., Huan, T., Van Den Berg, D., Lee, G. Y., Bui, H., Lee, D. H., Gereige, J., Yao, C., Hwang, S. J., Joehanes, R., Weiss, S. T., Abe, N., Abecasis, G., Aguet, F., Albert, C., Almasy, L., Alonso, A. & Ament, S. & 181 others, Anderson, P., Anugu, P., Applebaum-Bowden, D., Ardlie, K., Arking, D., Arnett, D. K., Ashley-Koch, A., Aslibekyan, S., Assimes, T., Auer, P., Avramopoulos, D., Ayas, N., Balasubramanian, A., Barnard, J., Barnes, K., Barr, R. G., Barron-Casella, E., Barwick, L., Beaty, T., Beck, G., Becker, D., Becker, L., Beer, R., Beitelshees, A., Benjamin, E., Benos, T., Bezerra, M., Bielak, L., Bis, J., Blackwell, T., Blangero, J., Blue, N., Boerwinkle, E., Bowden, D. W., Bowler, R., Brody, J., Broeckel, U., Broome, J., Brown, D., Bunting, K., Burchard, E., Bustamante, C., Buth, E., Cade, B., Cardwell, J., Carey, V., Carrier, J., Carson, A. P., Carty, C., Casaburi, R., Casas Romero, J. P., Casella, J., Castaldi, P., Chaffin, M., Chang, C., Chang, Y. C., Chasman, D., Chavan, S., Chen, B. J., Chen, W. M., Ida Chen, Y. D., Cho, M., Choi, S. H., Chuang, L. M., Chung, M., Chung, R. H., Clish, C., Comhair, S., Conomos, M., Cornell, E., Correa, A., Crandall, C., Crapo, J., Cupples, L. A., Curran, J., Curtis, J., Custer, B., Damcott, C., Darbar, D., David, S., Davis, C., Daya, M., de Andrade, M., de las Fuentes, L., de Vries, P., DeBaun, M., Deka, R., DeMeo, D., Devine, S., Dinh, H., Doddapaneni, H., Duan, Q., Dugan-Perez, S., Duggirala, R., Durda, J. P., Dutcher, S. K., Eaton, C., Ekunwe, L., El Boueiz, A., Ellinor, P., Emery, L., Erzurum, S., Farber, C., Farek, J., Fingerlin, T., Flickinger, M., Fornage, M., Franceschini, N., Frazar, C., Fu, M., Fullerton, S. M., Fulton, L., Gabriel, S., Gan, W., Gao, S., Gao, Y., Gass, M., Geiger, H., Gelb, B., Geraci, M., Germer, S., Gerszten, R., Ghosh, A., Gibbs, R., Gignoux, C., Gladwin, M., Glahn, D., Gogarten, S., Gong, D. W., Goring, H., Graw, S., Gray, K. J., Grine, D., Gross, C., Gu, C. C., Guan, Y., Guo, X., Gupta, N., Haessler, J., Hall, M., Han, Y., Hanly, P., Harris, D., Hawley, N. L., He, J., Heavner, B., Heckbert, S., Hernandez, R., Herrington, D., Hersh, C., Hidalgo, B., Hixson, J., Hobbs, B., Hokanson, J., Hong, E., Hoth, K., Hsiung, C., Hu, J., Hung, Y. J., Huston, H., Hwu, C. M., Irvin, M. R., Jackson, R., Jain, D., Jaquish, C., Johnsen, J., Johnson, A., Johnson, C., Johnston, R., Jones, K., Kang, H. M., Kaplan, R., Kardia, S., Kelly, S., Kenny, E., Kessler, M., Khan, A., Khan, Z., Kim, W., Rao, D. C. & Sung, Y. J., Sep 2023, In: EBioMedicine. 95, 104758.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      6 Scopus citations

    • Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci

      de las Fuentes, L., Schwander, K. L., Brown, M. R., Bentley, A. R., Winkler, T. W., Sung, Y. J., Munroe, P. B., Miller, C. L., Aschard, H., Aslibekyan, S., Bartz, T. M., Bielak, L. F., Chai, J. F., Cheng, C. Y., Dorajoo, R., Feitosa, M. F., Guo, X., Hartwig, F. P., Horimoto, A. & Kolčić, I. & 178 others, Lim, E., Liu, Y., Manning, A. K., Marten, J., Musani, S. K., Noordam, R., Padmanabhan, S., Rankinen, T., Richard, M. A., Ridker, P. M., Smith, A. V., Vojinovic, D., Zonderman, A. B., Alver, M., Boissel, M., Christensen, K., Freedman, B. I., Gao, C., Giulianini, F., Harris, S. E., He, M., Hsu, F. C., Kühnel, B., Laguzzi, F., Li, X., Lyytikäinen, L. P., Nolte, I. M., Poveda, A., Rauramaa, R., Riaz, M., Robino, A., Sofer, T., Takeuchi, F., Tayo, B. O., van der Most, P. J., Verweij, N., Ware, E. B., Weiss, S., Wen, W., Yanek, L. R., Zhan, Y., Amin, N., Arking, D. E., Ballantyne, C., Boerwinkle, E., Brody, J. A., Broeckel, U., Campbell, A., Canouil, M., Chai, X., Chen, Y. D. I., Chen, X., Chitrala, K. N., Concas, M. P., de Faire, U., de Mutsert, R., de Silva, H. J., de Vries, P. S., Do, A., Faul, J. D., Fisher, V., Floyd, J. S., Forrester, T., Friedlander, Y., Girotto, G., Gu, C. C., Hallmans, G., Heikkinen, S., Heng, C. K., Homuth, G., Hunt, S., Ikram, M. A., Jacobs, D. R., Kavousi, M., Khor, C. C., Kilpeläinen, T. O., Koh, W. P., Komulainen, P., Langefeld, C. D., Liang, J., Liu, K., Liu, J., Lohman, K., Mägi, R., Manichaikul, A. W., McKenzie, C. A., Meitinger, T., Milaneschi, Y., Nauck, M., Nelson, C. P., O’Connell, J. R., Palmer, N. D., Pereira, A. C., Perls, T., Peters, A., Polašek, O., Raitakari, O. T., Rice, K., Rice, T. K., Rich, S. S., Sabanayagam, C., Schreiner, P. J., Shu, X. O., Sidney, S., Sims, M., Smith, J. A., Starr, J. M., Strauch, K., Tai, E. S., Taylor, K. D., Tsai, M. Y., Uitterlinden, A. G., van Heemst, D., Waldenberger, M., Wang, Y. X., Wei, W. B., Wilson, G., Xuan, D., Yao, J., Yu, C., Yuan, J. M., Zhao, W., Becker, D. M., Bonnefond, A., Bowden, D. W., Cooper, R. S., Deary, I. J., Divers, J., Esko, T., Franks, P. W., Froguel, P., Gieger, C., Jonas, J. B., Kato, N., Lakka, T. A., Leander, K., Lehtimäki, T., Magnusson, P. K. E., North, K. E., Ntalla, I., Penninx, B., Samani, N. J., Snieder, H., Spedicati, B., van der Harst, P., Völzke, H., Wagenknecht, L. E., Weir, D. R., Wojczynski, M. K., Wu, T., Zheng, W., Zhu, X., Bouchard, C., Chasman, D. I., Evans, M. K., Fox, E. R., Gudnason, V., Hayward, C., Horta, B. L., Kardia, S. L. R., Krieger, J. E., Mook-Kanamori, D. O., Peyser, P. A., Province, M. M., Psaty, B. M., Rudan, I., Sim, X., Smith, B. H., van Dam, R. M., van Duijn, C. M., Wong, T. Y., Arnett, D. K., Rao, D. C., Gauderman, J., Liu, C. T., Morrison, A. C., Rotter, J. I. & Fornage, M., 2023, In: Frontiers in Genetics. 14, 1235337.

      Research output: Contribution to journal › Article › peer-review

      Open Access

    • Genetic insights into resting heart rate and its role in cardiovascular disease

      the DCCT/EDIC Research Group, Dec 2023, In: Nature communications. 14, 1, 4646.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      14 Scopus citations

    • Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Lipids Working Group, Jan 2023, In: Nature Genetics. 55, 1, p. 154-164 11 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      19 Scopus citations

    • Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Wang, Y., Selvaraj, M. S., Li, X., Li, Z., Holdcraft, J. A., Arnett, D. K., Bis, J. C., Blangero, J., Boerwinkle, E., Bowden, D. W., Cade, B. E., Carlson, J. C., Carson, A. P., Chen, Y. D. I., Curran, J. E., de Vries, P. S., Dutcher, S. K., Ellinor, P. T. & Floyd, J. S. & 55 others, Fornage, M., Freedman, B. I., Gabriel, S., Germer, S., Gibbs, R. A., Guo, X., He, J., Heard-Costa, N., Hildalgo, B., Hou, L., Irvin, M. R., Joehanes, R., Kaplan, R. C., Kardia, S. L., Kelly, T. N., Kim, R., Kooperberg, C., Kral, B. G., Levy, D., Li, C., Liu, C., Lloyd-Jone, D., Loos, R. J., Mahaney, M. C., Martin, L. W., Mathias, R. A., Minster, R. L., Mitchell, B. D., Montasser, M. E., Morrison, A. C., Murabito, J. M., Naseri, T., O'Connell, J. R., Palmer, N. D., Preuss, M. H., Psaty, B. M., Raffield, L. M., Rao, D. C., Redline, S., Reiner, A. P., Rich, S. S., Ruepena, M. S., Sheu, W. H. H., Smith, J. A., Smith, A., Tiwari, H. K., Tsai, M. Y., Viaud-Martinez, K. A., Wang, Z., Yanek, L. R., Zhao, W., Rotter, J. I., Lin, X., Natarajan, P. & Peloso, G. M., Oct 5 2023, In: American journal of human genetics. 110, 10, p. 1704-1717 14 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      2 Scopus citations

    • Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program

      Armstrong, N. D., Srinivasasainagendra, V., Ammous, F., Assimes, T. L., Beitelshees, A. L., Brody, J., Cade, B. E., Ida Chen, Y. D., Chen, H., de Vries, P. S., Floyd, J. S., Franceschini, N., Guo, X., Hellwege, J. N., House, J. S., Hwu, C. M., Kardia, S. L. R., Lange, E. M., Lange, L. A. & McDonough, C. W. & 24 others, Montasser, M. E., O’Connell, J. R., Shuey, M. M., Sun, X., Tanner, R. M., Wang, Z., Zhao, W., Carson, A. P., Edwards, T. L., Kelly, T. N., Kenny, E. E., Kooperberg, C., Loos, R. J. F., Morrison, A. C., Motsinger-Reif, A., Psaty, B. M., Rao, D. C., Redline, S., Rich, S. S., Rotter, J. I., Smith, J. A., Smith, A. V., Irvin, M. R. & Arnett, D. K., 2023, In: Frontiers in Genetics. 14, 1278215.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      1 Scopus citations
    • 2022

      A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & TOPMed Lipids Working Group, Dec 2022, In: Nature Methods. 19, 12, p. 1599-1611 13 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      47 Scopus citations

    • A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

      Million Veterans Program, Global Lipids Genetics Consortium, Locke, A. E., Wojczynski, M. K., Sung, Y. J., Rao, D. C. & Province, M. A., Aug 4 2022, In: American journal of human genetics. 109, 8, p. 1366-1387 22 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      21 Scopus citations

    • A saturated map of common genetic variants associated with human height

      23andMe Research Team, VA Million Veteran Program, DiscovEHR (DiscovEHR and MyCode Community Health Initiative), eMERGE (Electronic Medical Records and Genomics Network), Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific group, Oct 27 2022, In: Nature. 610, 7933, p. 704-712 9 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      295 Scopus citations

    • Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

      TOPMed Anthropometry Working Group & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Mar 2022, In: Nature Genetics. 54, 3, p. 263-273 11 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      162 Scopus citations

    • Gene-lifestyle interactions in the genomics of human complex traits

      the CHARGE Gene-Lifestyle Interactions Working Group, Jun 2022, In: European Journal of Human Genetics. 30, 6, p. 730-739 10 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      18 Scopus citations

    • Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

      Kanoni, S., Graham, S. E., Wang, Y., Surakka, I., Ramdas, S., Zhu, X., Clarke, S. L., Bhatti, K. F., Vedantam, S., Winkler, T. W., Locke, A. E., Marouli, E., Zajac, G. J. M., Wu, K. H. H., Ntalla, I., Hui, Q., Klarin, D., Hilliard, A. T., Wang, Z. & Xue, C. & 519 others, Thorleifsson, G., Helgadottir, A., Gudbjartsson, D. F., Holm, H., Olafsson, I., Hwang, M. Y., Han, S., Akiyama, M., Sakaue, S., Terao, C., Kanai, M., Zhou, W., Brumpton, B. M., Rasheed, H., Havulinna, A. S., Veturi, Y., Pacheco, J. A., Rosenthal, E. A., Lingren, T., Feng, Q. P., Kullo, I. J., Narita, A., Takayama, J., Martin, H. C., Hunt, K. A., Trivedi, B., Haessler, J., Giulianini, F., Bradford, Y., Miller, J. E., Campbell, A., Lin, K., Millwood, I. Y., Rasheed, A., Hindy, G., Faul, J. D., Zhao, W., Weir, D. R., Turman, C., Huang, H., Graff, M., Choudhury, A., Sengupta, D., Mahajan, A., Brown, M. R., Zhang, W., Yu, K., Schmidt, E. M., Pandit, A., Gustafsson, S., Yin, X., Luan, J., Zhao, J. H., Matsuda, F., Jang, H. M., Yoon, K., Medina-Gomez, C., Pitsillides, A., Hottenga, J. J., Wood, A. R., Ji, Y., Gao, Z., Haworth, S., Yousri, N. A., Mitchell, R. E., Chai, J. F., Aadahl, M., Bjerregaard, A. A., Yao, J., Manichaikul, A., Hwu, C. M., Hung, Y. J., Warren, H. R., Ramirez, J., Bork-Jensen, J., Kårhus, L. L., Goel, A., Sabater-Lleal, M., Noordam, R., Mauro, P., Matteo, F., McDaid, A. F., Marques-Vidal, P., Wielscher, M., Trompet, S., Sattar, N., Møllehave, L. T., Munz, M., Zeng, L., Huang, J., Yang, B., Poveda, A., Kurbasic, A., Lamina, C., Forer, L., Scholz, M., Galesloot, T. E., Bradfield, J. P., Ruotsalainen, S. E., Daw, E. W., Zmuda, J. M., Mitchell, J. S., Fuchsberger, C., Christensen, H., Brody, J. A., Vazquez-Moreno, M., Feitosa, M. F., Wojczynski, M. K., Wang, Z., Preuss, M. H., Mangino, M., Christofidou, P., Verweij, N., Benjamins, J. W., Engmann, J., Tsao, N. L., Verma, A., Slieker, R. C., Lo, K. S., Zilhao, N. R., Le, P., Kleber, M. E., Delgado, G. E., Huo, S., Ikeda, D. D., Iha, H., Yang, J., Liu, J., Demirkan, A., Leonard, H. L., Marten, J., Frank, M., Schmidt, B., Smyth, L. J., Cañadas-Garre, M., Wang, C., Nakatochi, M., Wong, A., Hutri-Kähönen, N., Sim, X., Xia, R., Huerta-Chagoya, A., Fernandez-Lopez, J. C., Lyssenko, V., Nongmaithem, S. S., Bayyana, S., Stringham, H. M., Irvin, M. R., Oldmeadow, C., Kim, H. N., Ryu, S., Timmers, P. R. H. J., Arbeeva, L., Dorajoo, R., Lange, L. A., Prasad, G., Lorés-Motta, L., Pauper, M., Long, J., Li, X., Theusch, E., Takeuchi, F., Spracklen, C. N., Loukola, A., Bollepalli, S., Warner, S. C., Wang, Y. X., Wei, W. B., Nutile, T., Ruggiero, D., Sung, Y. J., Chen, S., Liu, F., Yang, J., Kentistou, K. A., Banas, B., Nardone, G. G., Meidtner, K., Bielak, L. F., Smith, J. A., Hebbar, P., Farmaki, A. E., Hofer, E., Lin, M., Concas, M. P., Vaccargiu, S., van der Most, P. J., Pitkänen, N., Cade, B. E., van der Laan, S. W., Chitrala, K. N., Weiss, S., Bentley, A. R., Doumatey, A. P., Adeyemo, A. 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      Research output: Contribution to journal › Article › peer-review

      Open Access
      28 Scopus citations

    • Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

      Kelly, T. N., Sun, X., He, K. Y., Brown, M. R., Taliun, S. A. G., Hellwege, J. N., Irvin, M. R., Mi, X., Brody, J. A., Franceschini, N., Guo, X., Hwang, S. J., De Vries, P. S., Gao, Y., Moscati, A., Nadkarni, G. N., Yanek, L. R., Elfassy, T., Smith, J. A. & Chung, R. H. & 85 others, Beitelshees, A. L., Patki, A., Aslibekyan, S., Blobner, B. M., Peralta, J. M., Assimes, T. L., Palmas, W. R., Liu, C., Bress, A. P., Huang, Z., Becker, L. C., Hwa, C. M., O'connell, J. R., Carlson, J. C., Warren, H. R., Das, S., Giri, A., Martin, L. W., Craig Johnson, W., Fox, E. R., Bottinger, E. P., Razavi, A. C., Vaidya, D., Chuang, L. M., Chang, Y. P. C., Naseri, T., Jain, D., Kang, H. M., Hung, A. M., Srinivasasainagendra, V., Snively, B. M., Gu, D., Montasser, M. E., Reupena, M. S., Heavner, B. D., Lefaive, J., Hixson, J. E., Rice, K. M., Wang, F. F., Nielsen, J. B., Huang, J., Khan, A. T., Zhou, W., Nierenberg, J. L., Laurie, C. C., Armstrong, N. D., Shi, M., Pan, Y., Stilp, A. M., Emery, L., Wong, Q., Hawley, N. L., Minster, R. L., Curran, J. E., Munroe, P. B., Weeks, D. E., North, K. E., Tracy, R. P., Kenny, E. E., Shimbo, D., Chakravarti, A., Rich, S. S., Reiner, A. P., Blangero, J., Redline, S., Mitchell, B. D., Rao, D. C., Ida Chen, Y. D., Kardia, S. L. R., Kaplan, R. C., Mathias, R. A., He, J., Psaty, B. M., Fornage, M., Loos, R. J. F., Correa, A., Boerwinkle, E., Rotter, J. I., Kooperberg, C., Edwards, T. L., Abecasis, G. R., Zhu, X., Levy, D., Arnett, D. K. & Morrison, A. C., Aug 1 2022, In: Hypertension. 79, 8, p. 1656-1667 12 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      17 Scopus citations

    • Multi-omics insights into the biological mechanisms underlying statistical gene-by-lifestyle interactions with smoking and alcohol consumption

      on behalf of the CHARGE Gene-Lifestyle Interactions Working Group, Dec 5 2022, In: Frontiers in Genetics. 13, 954713.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      2 Scopus citations

    • Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

      AMP-T2D-GENES, Myocardial Infarction Genetics Consortium, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & NHLBI TOPMed Lipids Working Group, Jan 6 2022, In: American journal of human genetics. 109, 1, p. 81-96 16 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      22 Scopus citations

    • Rare coding variants in RCN3 are associated with blood pressure

      The Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2022, In: BMC genomics. 23, 1, 148.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      2 Scopus citations

    • Regular exercise and patterns of response across multiple cardiometabolic traits: The HERITAGE family study

      Barber, J. L., Ruiz-Ramie, J. J., Robbins, J. M., Gerszten, R. E., Leon, A. S., Rao, D. C., Skinner, J. S., Bouchard, C. & Sarzynski, M. A., Jan 1 2022, In: British journal of sports medicine. 56, 2, p. 95-100 6 p.

      Research output: Contribution to journal › Article › peer-review

      13 Scopus citations

    • Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

      Tahir, U. A., Katz, D. H., Avila-Pachecho, J., Bick, A. G., Pampana, A., Robbins, J. M., Yu, Z., Chen, Z. Z., Benson, M. D., Cruz, D. E., Ngo, D., Deng, S., Shi, X., Zheng, S., Eisman, A. S., Farrell, L., Hall, M. E., Correa, A., Tracy, R. P. & Durda, P. & 410 others, Taylor, K. D., Liu, Y., Johnson, W. C., Guo, X., Yao, J., Chen, Y. D. I., Manichaikul, A. W., Ruberg, F. L., Blaner, W. S., Jain, D., Bouchard, C., Sarzynski, M. A., Rich, S. S., Rotter, J. I., Wang, T. J., Wilson, J. G., Clish, C. B., Natarajan, P., Gerszten, R. E., Abe, N., Abecasis, G., Aguet, F., Albert, C., Almasy, L., Alonso, A., Ament, S., Anderson, P., Anugu, P., Applebaum-Bowden, D., Ardlie, K., Arking, D., Arnett, D. K., Ashley-Koch, A., Aslibekyan, S., Assimes, T., Auer, P., Avramopoulos, D., Ayas, N., Balasubramanian, A., Barnard, J., Barnes, K., Barr, R. 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B., Silver, B., Silverman, E., Skomro, R., Smith, A. V., Smith, J., Smith, J., Smith, N., Smith, T., Smoller, S., Snively, B., Snyder, M., Sofer, T., Sotoodehnia, N., Stilp, A. M., Storm, G., Streeten, E., Su, J. L., Sung, Y. J., Sylvia, J., Szpiro, A., Taliun, D., Tang, H., Taub, M., Taylor, M., Taylor, S., Telen, M., Thornton, T. A., Threlkeld, M., Tinker, L., Tirschwell, D., Tishkoff, S., Tiwari, H., Tong, C., Tsai, M., Vaidya, D., Van Den Berg, D., VandeHaar, P., Vrieze, S., Walker, T., Wallace, R., Walts, A., Wang, F. F., Wang, H., Wang, J., Watson, K., Watt, J., Weeks, D. E., Weinstock, J., Weir, B., Weiss, S. T., Weng, L. C., Wessel, J., Willer, C., Williams, K., Williams, L. K., Wilson, C., Winterkorn, L., Wong, Q., Wu, J., Xu, H., Yanek, L., Yang, I., Yu, K., Zekavat, S. M., Zhang, Y., Zhao, S. X., Zhao, W., Zhu, X., Ziv, E., Zody, M. & Zoellner, S., Dec 2022, In: Nature communications. 13, 1, 4923.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      23 Scopus citations

    • Whole genome sequence analysis of blood lipid levels in >66,000 individuals

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2022, In: Nature communications. 13, 1, 5995.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      32 Scopus citations
    • 2021

      A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Oct 2021, In: Nature Genetics. 53, 10, p. 1504-1516 13 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      83 Scopus citations

    • Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & FinnGen, Dec 1 2021, In: Nature communications. 12, 1, 2182.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      14 Scopus citations

    • Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

      Graff, M., Justice, A. E., Young, K. L., Marouli, E., Zhang, X., Fine, R. S., Lim, E., Buchanan, V., Rand, K., Feitosa, M. F., Wojczynski, M. K., Yanek, L. R., Shao, Y., Rohde, R., Adeyemo, A. A., Aldrich, M. C., Allison, M. A., Ambrosone, C. B., Ambs, S. & Amos, C. & 205 others, Arnett, D. K., Atwood, L., Bandera, E. V., Bartz, T., Becker, D. M., Berndt, S. I., Bernstein, L., Bielak, L. F., Blot, W. J., Bottinger, E. P., Bowden, D. W., Bradfield, J. P., Brody, J. A., Broeckel, U., Burke, G., Cade, B. E., Cai, Q., Caporaso, N., Carlson, C., Carpten, J., Casey, G., Chanock, S. J., Chen, G., Chen, M., Chen, Y. D. I., Chen, W. M., Chesi, A., Chiang, C. W. K., Chu, L., Coetzee, G. A., Conti, D. V., Cooper, R. S., Cushman, M., Demerath, E., Deming, S. L., Dimitrov, L., Ding, J., Diver, W. R., Duan, Q., Evans, M. K., Falusi, A. G., Faul, J. D., Fornage, M., Fox, C., Freedman, B. I., Garcia, M., Gillanders, E. M., Goodman, P., Gottesman, O., Grant, S. F. A., Guo, X., Hakonarson, H., Haritunians, T., Harris, T. B., Harris, C. C., Henderson, B. E., Hennis, A., Hernandez, D. G., Hirschhorn, J. N., McNeill, L. H., Howard, T. D., Howard, B., Hsing, A. W., Hsu, Y. H. H., Hu, J. J., Huff, C. D., Huo, D., Ingles, S. A., Irvin, M. R., John, E. M., Johnson, K. C., Jordan, J. M., Kabagambe, E. K., Kang, S. J., Kardia, S. L., Keating, B. J., Kittles, R. A., Klein, E. A., Kolb, S., Kolonel, L. N., Kooperberg, C., Kuller, L., Kutlar, A., Lange, L., Langefeld, C. D., Le Marchand, L., Leonard, H., Lettre, G., Levin, A. M., Li, Y., Li, J., Liu, Y., Liu, Y., Liu, S., Lohman, K., Lotay, V., Lu, Y., Maixner, W., Manson, J. A. E., McKnight, B., Meng, Y., Monda, K. L., Monroe, K., Moore, J. H., Mosley, T. H., Mudgal, P., Murphy, A. B., Nadukuru, R., Nalls, M. A., Nathanson, K. L., Nayak, U., N'Diaye, A., Nemesure, B., Neslund-Dudas, C., Neuhouser, M. L., Nyante, S., Ochs-Balcom, H., Ogundiran, T. O., Ogunniyi, A., Ojengbede, O., Okut, H., Olopade, O. I., Olshan, A., Padhukasahasram, B., Palmer, J., Palmer, C. D., Palmer, N. D., Papanicolaou, G., Patel, S. R., Pettaway, C. A., Peyser, P. A., Press, M. F., Rao, D. C., Rasmussen-Torvik, L. J., Redline, S., Reiner, A. P., Rhie, S. K., Rodriguez-Gil, J. L., Rotimi, C. N., Rotter, J. I., Ruiz-Narvaez, E. A., Rybicki, B. A., Salako, B., Sale, M. M., Sanderson, M., Schadt, E., Schreiner, P. J., Schurmann, C., Schwartz, A. G., Shriner, D. A., Signorello, L. B., Singleton, A. B., Siscovick, D. S., Smith, J. A., Smith, S., Speliotes, E., Spitz, M., Stanford, J. L., Stevens, V. L., Stram, A., Strom, S. S., Sucheston, L., Sun, Y. V., Tajuddin, S. M., Taylor, H., Taylor, K., Tayo, B. O., Thun, M. J., Tucker, M. A., Vaidya, D., Van Den Berg, D. J., Vedantam, S., Vitolins, M., Wang, Z., Ware, E. B., Wassertheil-Smoller, S., Weir, D. R., Wiencke, J. K., Williams, S. M., Williams, L. K., Wilson, J. G., Witte, J. S., Wrensch, M., Wu, X., Yao, J., Zakai, N., Zanetti, K., Zemel, B. S., Zhao, W., Zhao, J. H., Zheng, W., Zhi, D., Zhou, J., Zhu, X., Ziegler, R. G., Zmuda, J., Zonderman, A. B., Psaty, B. M., Borecki, I. B., Cupples, L. A., Liu, C. T., Haiman, C. A., Loos, R., Ng, M. C. Y. & North, K. E., Apr 1 2021, In: American journal of human genetics. 108, 4, p. 564-582 19 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      19 Scopus citations

    • Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

      Lifelines Cohort Study, Jun 2021, In: Molecular Psychiatry. 26, 6, p. 2111-2125 15 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      18 Scopus citations

    • Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium

      NHLBI SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS), Dec 2021, In: Genome medicine. 13, 1, 66.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      25 Scopus citations

    • Genome sequencing unveils a regulatory landscape of platelet reactivity

      NHLBI Trans-Omics for Precision (TOPMed) Consortium, Dec 1 2021, In: Nature communications. 12, 1, 3626.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      36 Scopus citations

    • Lifestyle Risk Score: handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions

      Xu, H., Schwander, K., Brown, M. R., Wang, W., Waken, R. J., Boerwinkle, E., Cupples, L. A., de las Fuentes, L., van Heemst, D., Osazuwa-Peters, O., de Vries, P. S., van Dijk, K. W., Sung, Y. J., Zhang, X., Morrison, A. C., Rao, D. C., Noordam, R. & Liu, C. T., May 2021, In: European Journal of Human Genetics. 29, 5, p. 839-850 12 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      1 Scopus citations

    • Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

      Lifelines Cohort Study, Jan 14 2021, In: Human Genetics and Genomics Advances. 2, 1, 100013.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      7 Scopus citations

    • Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

      Wang, H., Noordam, R., Cade, B. E., Schwander, K., Winkler, T. W., Lee, J., Sung, Y. J., Bentley, A. R., Manning, A. K., Aschard, H., Kilpeläinen, T. O., Ilkov, M., Brown, M. R., Horimoto, A. R., Richard, M., Bartz, T. M., Vojinovic, D., Lim, E., Nierenberg, J. L. & Liu, Y. & 105 others, Chitrala, K., Rankinen, T., Musani, S. K., Franceschini, N., Rauramaa, R., Alver, M., Zee, P. C., Harris, S. E., van der Most, P. J., Nolte, I. M., Munroe, P. B., Palmer, N. D., Kühnel, B., Weiss, S., Wen, W., Hall, K. A., Lyytikäinen, L. P., O’Connell, J., Eiriksdottir, G., Launer, L. J., de Vries, P. S., Arking, D. E., Chen, H., Boerwinkle, E., Krieger, J. E., Schreiner, P. J., Sidney, S., Shikany, J. M., Rice, K., Chen, Y. D. I., Gharib, S. A., Bis, J. C., Luik, A. I., Ikram, M. A., Uitterlinden, A. G., Amin, N., Xu, H., Levy, D., He, J., Lohman, K. K., Zonderman, A. B., Rice, T. K., Sims, M., Wilson, G., Sofer, T., Rich, S. S., Palmas, W., Yao, J., Guo, X., Rotter, J. I., Biermasz, N. R., Mook-Kanamori, D. O., Martin, L. W., Barac, A., Wallace, R. B., Gottlieb, D. J., Komulainen, P., Heikkinen, S., Mägi, R., Milani, L., Metspalu, A., Starr, J. M., Milaneschi, Y., Waken, R. J., Gao, C., Waldenberger, M., Peters, A., Strauch, K., Meitinger, T., Roenneberg, T., Völker, U., Dörr, M., Shu, X. O., Mukherjee, S., Hillman, D. R., Kähönen, M., Wagenknecht, L. E., Gieger, C., Grabe, H. J., Zheng, W., Palmer, L. J., Lehtimäki, T., Gudnason, V., Morrison, A. C., Pereira, A. C., Fornage, M., Psaty, B. M., van Duijn, C. M., Liu, C. T., Kelly, T. N., Evans, M. K., Bouchard, C., Fox, E. R., Kooperberg, C., Zhu, X., Lakka, T. A., Esko, T., North, K. E., Deary, I. J., Snieder, H., Penninx, B. W. J. H., Gauderman, W. J., Rao, D. C., Redline, S. & van Heemst, D., Nov 2021, In: Molecular Psychiatry. 26, 11, p. 6293-6304 12 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      14 Scopus citations

    • Population sequencing data reveal a compendium of mutational processes in the human germ line

      Seplyarskiy, V. B., Soldatov, R. A., Koch, E., McGinty, R. J., Goldmann, J. M., Hernandez, R. D., Barnes, K., Correa, A., Burchard, E. G., Ellinor, P. T., McGarvey, S. T., Mitchell, B. D., Vasan, R. S., Redline, S., Silverman, E., Weiss, S. T., Arnett, D. K., Blangero, J., Boerwinkle, E. & He, J. & 22 others, Montgomery, C., Rao, D. C., Rotter, J. I., Taylor, K. D., Brody, J. A., Ida Chen, Y. D., De Las Fuentes, L., Hwu, C. M., Rich, S. S., Manichaikul, A. W., Mychaleckyj, J. C., Palmer, N. D., Smith, J. A., Kardia, S. L. R., Peyser, P. A., Bielak, L. F., O'Connor, T. D., Emery, L. S., Gilissen, C., Wong, W. S. W., Kharchenko, P. V. & Sunyaev, S., Aug 27 2021, In: Science. 373, 6558, p. 1030-1035 6 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      30 Scopus citations

    • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Feb 11 2021, In: Nature. 590, 7845, p. 290-299 10 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      1014 Scopus citations

    • The power of genetic diversity in genome-wide association studies of lipids

      VA Million Veteran Program & Global Lipids Genetics Consortium*, Dec 23 2021, In: Nature. 600, 7890, p. 675-679 5 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      438 Scopus citations

    • Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 1 2021, In: Nature communications. 12, 1, 3506.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      7 Scopus citations

    • Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population

      Irvin, M. R., Aggarwal, P., Claas, S. A., de las Fuentes, L., Do, A. N., Gu, C. C., Matter, A., Olson, B. S., Patki, A., Schwander, K., Smith, J. D., Srinivasasainagendra, V., Tiwari, H. K., Turner, A. J., Nickerson, D. A., Rao, D. C., Broeckel, U. & Arnett, D. K., Feb 19 2021, In: Frontiers in Genetics. 12, 588452.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      7 Scopus citations

    • Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

      TOPMed Sleep Working Group & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2021, In: Genome medicine. 13, 1, 136.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      21 Scopus citations
    • 2020

      Deriving stratified effects from joint models investigating gene-environment interactions

      Laville, V., Majarian, T., De Vries, P. S., Bentley, A. R., Feitosa, M. F., Sung, Y. J., Rao, D. C., Manning, A., Manning, A., Aschard, H. & Aschard, H., Jun 18 2020, In: BMC bioinformatics. 21, 1, 251.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      3 Scopus citations

    • Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

      NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium & TOPMed Lipids Working Group, Sep 1 2020, In: Nature Genetics. 52, 9, p. 969-983 15 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      130 Scopus citations

    • Efficient gene–environment interaction tests for large biobank-scale sequencing studies

      Wang, X., Lim, E., Liu, C. T., Sung, Y. J., Rao, D. C., Morrison, A. C., Boerwinkle, E., Manning, A. K. & Chen, H., Nov 2020, In: Genetic Epidemiology. 44, 8, p. 908-923 16 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      15 Scopus citations

    • Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry

      de las Fuentes, L., Sung, Y. J., Sitlani, C. M., Avery, C. L., Bartz, T. M., Keyser, C. D., Evans, D. S., Li, X., Musani, S. K., Ruiter, R., Smith, A. V., Sun, F., Trompet, S., Xu, H., Arnett, D. K., Bis, J. C., Broeckel, U., Busch, E. L., Chen, Y. D. I. & Correa, A. & 30 others, Cummings, S. R., Floyd, J. S., Ford, I., Guo, X., Harris, T. B., Ikram, M. A., Lange, L., Launer, L. J., Reiner, A. P., Schwander, K., Smith, N. L., Sotoodehnia, N., Stewart, J. D., Stott, D. J., Stürmer, T., Taylor, K. D., Uitterlinden, A., Vasan, R. S., Wiggins, K. L., Cupples, L. A., Gudnason, V., Heckbert, S. R., Jukema, J. W., Liu, Y., Psaty, B. M., Rao, D. C., Rotter, J. I., Stricker, B., Wilson, J. G. & Whitsel, E. A., Jun 1 2020, In: Pharmacogenomics Journal. 20, 3, p. 482-493 12 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      4 Scopus citations

    • Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures

      Osazuwa-Peters, O. L., Waken, R. J., Schwander, K. L., Sung, Y. J., de Vries, P. S., Hartz, S. M., Chasman, D. I., Morrison, A. C., Bierut, L. J., Xiong, C., de las Fuentes, L. & Rao, D. C., Sep 1 2020, In: Genetic Epidemiology. 44, 6, p. 629-641 13 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      6 Scopus citations

    • Inherited causes of clonal haematopoiesis in 97,691 whole genomes

      NHLBI Trans-Omics for Precision Medicine Consortium, Oct 29 2020, In: Nature. 586, 7831, p. 763-768 6 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      441 Scopus citations

    • Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

      Wu, P., Rybin, D., Bielak, L. F., Feitosa, M. F., Franceschini, N., Li, Y., Lu, Y., Marten, J., Musani, S. K., Noordam, R., Raghavan, S., Rose, L. M., Schwander, K., Smith, A. V., Tajuddin, S. M., Vojinovic, D., Amin, N., Arnett, D. K., Bottinger, E. P. & Demirkan, A. & 38 others, Florez, J. C., Ghanbari, M., Harris, T. B., Launer, L. J., Liu, J., Liu, J., Mook-Kanamori, D. O., Murray, A. D., Nalls, M. A., Peyser, P. A., Uitterlinden, A. G., Voortman, T., Bouchard, C., Chasman, D., Correa, A., de Mutsert, R., Evans, M. K., Gudnason, V., Hayward, C., Kao, L., Kardia, S. L. R., Kooperberg, C., Loos, R. J. F., Province, M. M., Rankinen, T., Redline, S., Ridker, P. M., Rotter, J. I., Siscovick, D., Smith, B. H., van Duijn, C., Zonderman, A. B., Rao, D. C., Wilson, J. G., Dupuis, J., Meigs, J. B., Liu, C. T. & Vassy, J. L., May 2020, In: PloS one. 15, 5, e0230815.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      11 Scopus citations
    • 2019

      A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

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      Research output: Contribution to journal › Article › peer-review

      Open Access
      28 Scopus citations

    • Associations of autozygosity with a broad range of human phenotypes

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