Mariza De Andrade

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Mariza De Andrade, PhD

1991 …2024

Research activity per year

Search results

  • 2024

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

    Trans-Omics for Precision Medicine (TOPMed) program & INVENT Consortium, 2024, (Accepted/In press) In: Blood.

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

    Open Access
  • 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

  • Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection (Scientific Reports, (2023), 13, 1, (18532), 10.1038/s41598-023-45649-4)

    Ferar, K., Hall, T. O., Crawford, D. C., Rowley, R., Satterfield, B. A., Li, R., Gragert, L., Karlson, E. W., de Andrade, M., Kullo, I. J., McCarty, C. A., Kho, A., Hayes, M. G., Ritchie, M. D., Crane, P. K., Mirel, D. B., Carlson, C., Connolly, J. J., Hakonarson, H., Crenshaw, A. T., & 6 othersCarrell, D., Luo, Y., Dikilitas, O., Denny, J. C., Jarvik, G. P. & Crosslin, D. R., Dec 2023, In: Scientific reports. 13, 1, 19972.

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

  • Author Correction: Clonal haematopoiesis and risk of chronic liver disease (Nature, (2023), 616, 7958, (747-754), 10.1038/s41586-023-05857-4)

    NHLBI TOPMed Hematology Working Group, Jul 20 2023, In: Nature. 619, 7970, p. E47

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

  • 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

  • Corrigendum to: “An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs” [J Hepatol 75 (2021) 572-581, (S0168827821003342), (10.1016/j.jhep.2021.04.055)]

    US PBC Consortium, UK-PBC Consortium, for the Canadian PBC Consortium, Chinese PBC Consortium, Italian PBC Study Group & Japan PBC-GWAS Consortium, Apr 2023, In: Journal of hepatology. 78, 4, p. 883 1 p.

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

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

    NHLBI Trans-Omics in Precision Medicine (TOPMed) Consortium, Sep 2023, In: EBioMedicine. 95, 104758.

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

    Open Access

  • Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants

    Einson, J., Glinos, D., Boerwinkle, E., Castaldi, P., Darbar, D., De Andrade, M., Ellinor, P., Fornage, M., Gabriel, S., Germer, S., Gibbs, R., Hersh, C. P., Johnsen, J., Kaplan, R., Konkle, B. A., Kooperberg, C., Nassir, R., Loos, R. J. F., Meyers, D. A., Mitchell, B. D., & 13 othersPsaty, B., Vasan, R. S., Rich, S. S., Rienstra, M., Rotter, J. I., Saferali, A., Shoemaker, M. B., Silverman, E., Smith, A. V., Mohammadi, P., Castel, S. E., Iossifov, I. & Lappalainen, T., Aug 2023, In: Genetics. 224, 4, iyad115.

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

    Open Access

  • Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

    Ferar, K., Hall, T. O., Crawford, D. C., Rowley, R., Satterfield, B. A., Li, R., Gragert, L., Karlson, E. W., de Andrade, M., Kullo, I. J., McCarty, C. A., Kho, A., Hayes, M. G., Ritchie, M. D., Crane, P. K., Mirel, D. B., Carlson, C., Connolly, J. J., Hakonarson, H., Crenshaw, A. T., & 6 othersCarrell, D., Luo, Y., Dikilitas, O., Denny, J. C., Jarvik, G. P. & Crosslin, D. R., Dec 2023, In: Scientific reports. 13, 1, 18532.

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

    Open Access

  • Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm

    Joo, Y. Y., Pacheco, J. A., Thompson, W. K., Rasmussen-Torvik, L. J., Rasmussen, L. V., Lin, F. T. J., de Andrade, M., Borthwick, K. M., Bottinger, E., Cagan, A., Carrell, D. S., Denny, J. C., Ellis, S. B., Gottesman, O., Linneman, J. G., Pathak, J., Peissig, P. L., Shang, N., Tromp, G., Veerappan, A., & 5 othersSmith, M. E., Chisholm, R. L., Gawron, A. J., Hayes, M. G. & Kho, A. N., May 2023, In: PloS one. 18, 5 MAY, e0283553.

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

    Open Access

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

    Li, X., Quick, C., Zhou, H., Gaynor, S. M., Liu, Y., Chen, H., Selvaraj, M. S., Sun, R., Dey, R., Arnett, D. K., Bielak, L. F., Bis, J. C., Blangero, J., Boerwinkle, E., Bowden, D. W., Brody, J. A., Cade, B. E., Correa, A., Cupples, L. A., Curran, J. E., & 404 othersde Vries, P. S., Duggirala, R., Freedman, B. I., Göring, H. H. H., Guo, X., Haessler, J., Kalyani, R. R., Kooperberg, C., Kral, B. G., Lange, L. A., Manichaikul, A., Martin, L. W., McGarvey, S. T., Mitchell, B. D., Montasser, M. E., Morrison, A. C., Naseri, T., O’Connell, J. R., Palmer, N. D., Peyser, P. A., Psaty, B. M., Raffield, L. M., Redline, S., Reiner, A. P., Reupena, M. S., Rice, K. M., Rich, S. S., Sitlani, C. M., Smith, J. A., Taylor, K. D., Vasan, R. S., Willer, C. J., Wilson, J. G., Yanek, L. R., Zhao, W., Rotter, J. I., Natarajan, P., Peloso, G. M., Li, Z., Lin, X., Abe, N., Abecasis, G., Aguet, F., Albert, C., Almasy, L., Alonso, A., Ament, S., Anderson, P., Anugu, P., Applebaum-Bowden, D., Ardlie, K., Dan Arking, A., 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., Blackwell, T., Blue, N., Bowler, R., Broeckel, U., Broome, J., Brown, D., Bunting, K., Burchard, E., Bustamante, C., Buth, E., Cardwell, J., Carey, V., Carrier, J., Carson, A., 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., Chen, Y. D. I., Cho, M., Choi, S. H., Chuang, L. M., Chung, M., Chung, R. H., Clish, C., Comhair, S., Conomos, M., Cornell, E., Crandall, C., Crapo, J., Curtis, J., Custer, B., Damcott, C., Darbar, D., David, S., Davis, C., Daya, M., de Andrade, M., de las Fuentes, L., DeBaun, M., Deka, R., DeMeo, D., Devine, S., Dinh, H., Doddapaneni, H., Duan, Q., Dugan-Perez, S., 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., Graw, S., Gray, K. J., Grine, D., Gross, C., Gu, C. C., Guan, Y., Gupta, N., Hall, M., Han, Y., Hanly, P., Harris, D., Hawley, N. L., He, J., Ben Heavner, H., 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., Kimoff, J., Kinney, G., Konkle, B., Kramer, H., Lange, C., Lange, E., Laurie, C., Laurie, C., LeBoff, M., Lee, J., Lee, S., Lee, W. J., LeFaive, J., Levine, D., Levy, D., Lewis, J., Li, X., Li, Y., Lin, H., Lin, H., Liu, S., Liu, Y., Liu, Y., Loos, R. J. F., Lubitz, S., Lunetta, K., Luo, J., Magalang, U., Mahaney, M., Make, B., Manning, A., Manson, J. A., Marton, M., Mathai, S., Mathias, R., May, S., McArdle, P., McDonald, M. L., McFarland, S., McGoldrick, D., McHugh, C., McNeil, B., Mei, H., Meigs, J., Menon, V., Mestroni, L., Metcalf, G., Meyers, D. A., Mignot, E., Mikulla, J., Min, N., Minear, M., Minster, R. L., Moll, M., Momin, Z., Montgomery, C., Muzny, D., Mychaleckyj, J. C., Nadkarni, G., Naik, R., Nekhai, S., Nelson, S. C., Neltner, B., Nessner, C., Nickerson, D., Nkechinyere, O., North, K., O’Connor, T., Ochs-Balcom, H., Okwuonu, G., Pack, A., Paik, D. T., Pankow, J., Papanicolaou, G., Parker, C., Peralta, J. M., Perez, M., Perry, J., Peters, U., Phillips, L. S., Pleiness, J., Pollin, T., Post, W., Becker, J. P., Boorgula, M. P., Preuss, M., Qasba, P., Qiao, D., Qin, Z., Rafaels, N., Rajendran, M., Rao, D. C., Rasmussen-Torvik, L., Ratan, A., Reed, R., Reeves, C., Regan, E., Robillard, R., Robine, N., Dan Roden, R., Roselli, C., Ruczinski, I., Runnels, A., Russell, P., Ruuska, S., Ryan, K., Sabino, E. C., Saleheen, D., Salimi, S., Salvi, S., Salzberg, S., Sandow, K., Sankaran, V. G., Santibanez, J., Schwander, K., Schwartz, D., Sciurba, F., Seidman, C., Seidman, J., Sériès, F., Sheehan, V., Sherman, S. L., Shetty, A., Shetty, A., Sheu, W. H. H., Shoemaker, M. B., Silver, B., Silverman, E., Skomro, R., Smith, A. V., 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., Tracy, R., 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., Williams, K., Williams, L. K., Wilson, C., Winterkorn, L., Wong, Q., Wu, J., Xu, H., Yang, I., Yu, K., Zekavat, S. M., Zhang, Y., Zhao, S. X., Zhu, X., Ziv, E., Zody, M. & Zoellner, S., Jan 2023, In: Nature Genetics. 55, 1, p. 154-164 11 p.

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

    Open Access

  • The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

    NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Apr 2023, In: Science Advances. 9, 17, eabm4945.

    Research output: Contribution to journal › Review article › peer-review

    Open Access

  • Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

    Young, K. L., Fisher, V., Deng, X., Brody, J. A., Graff, M., Lim, E., Lin, B. M., Xu, H., Amin, N., An, P., Aslibekyan, S., Fohner, A. E., Hidalgo, B., Lenzini, P., Kraaij, R., Medina-Gomez, C., Prokić, I., Rivadeneira, F., Sitlani, C., Tao, R., & 42 othersvan Rooij, J., Zhang, D., Broome, J. G., Buth, E. J., Heavner, B. D., Jain, D., Smith, A. V., Barnes, K., Boorgula, M. P., Chavan, S., Darbar, D., De Andrade, M., Guo, X., Haessler, J., Irvin, M. R., Kalyani, R. R., Kardia, S. L. R., Kooperberg, C., Kim, W., Mathias, R. A., McDonald, M. L., Mitchell, B. D., Peyser, P. A., Regan, E. A., Redline, S., Reiner, A. P., Rich, S. S., Rotter, J. I., Smith, J. A., Weiss, S., Wiggins, K. L., Yanek, L. R., Arnett, D., Heard-Costa, N. L., Leal, S., Lin, D., McKnight, B., Province, M., van Duijn, C. M., North, K. E., Cupples, L. A. & Liu, C. T., Jan 12 2023, In: Human Genetics and Genomics Advances. 4, 1, 100163.

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

    Open Access

  • Whole Genome Analysis of Venous Thromboembolism: The Trans-Omics for Precision Medicine Program

    Seyerle, A. A., Laurie, C. A., Coombes, B. J., Jain, D., Conomos, M. P., Brody, J., Chen, M. H., Gogarten, S. M., Beutel, K. M., Gupta, N., Heckbert, S. R., Jackson, R. D., Johnson, A. D., Ko, D., Manson, J. E., McKnight, B., Metcalf, G. A., Morrison, A. C., Reiner, A. P., Sofer, T., & 14 othersTang, W., Wiggins, K. L., Boerwinkle, E., De Andrade, M., Gabriel, S. B., Gibbs, R. A., Laurie, C. C., Psaty, B. M., Vasan, R. S., Rice, K., Kooperberg, C., Pankow, J. S., Smith, N. L. & Pankratz, N., Apr 1 2023, In: Circulation: Genomic and Precision Medicine. 16, 2, p. E003532

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

    Open Access
  • 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, 2022, (Accepted/In press) In: Nature Methods.

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

    Open Access

  • 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

  • Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055))

    PBC Consortia, Canadian PBC Consortium, Chinese PBC Consortium, Italian PBC Study Group, Japan PBC-GWAS Consortium, US PBC Consortium & UK-PBC Consortium, Feb 2022, In: Journal of hepatology. 76, 2, p. 489 1 p.

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

  • Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer

    Byun, J., Han, Y., Li, Y., Xia, J., Long, E., Choi, J., Xiao, X., Zhu, M., Zhou, W., Sun, R., Bossé, Y., Song, Z., Schwartz, A., Lusk, C., Rafnar, T., Stefansson, K., Zhang, T., Zhao, W., Pettit, R. W., Liu, Y., & 65 othersLi, X., Zhou, H., Walsh, K. M., Gorlov, I., Gorlova, O., Zhu, D., Rosenberg, S. M., Pinney, S., Bailey-Wilson, J. E., Mandal, D., de Andrade, M., Gaba, C., Willey, J. C., You, M., Anderson, M., Wiencke, J. K., Albanes, D., Lam, S., Tardon, A., Chen, C., Goodman, G., Bojeson, S., Brenner, H., Landi, M. T., Chanock, S. J., Johansson, M., Muley, T., Risch, A., Wichmann, H. E., Bickeböller, H., Christiani, D. C., Rennert, G., Arnold, S., Field, J. K., Shete, S., Le Marchand, L., Melander, O., Brunnstrom, H., Liu, G., Andrew, A. S., Kiemeney, L. A., Shen, H., Zienolddiny, S., Grankvist, K., Johansson, M., Caporaso, N., Cox, A., Hong, Y. C., Yuan, J. M., Lazarus, P., Schabath, M. B., Aldrich, M. C., Patel, A., Lan, Q., Rothman, N., Taylor, F., Kachuri, L., Witte, J. S., Sakoda, L. C., Spitz, M., Brennan, P., Lin, X., McKay, J., Hung, R. J. & Amos, C. I., Aug 2022, In: Nature Genetics. 54, 8, p. 1167-1177 11 p.

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

    Open Access

  • Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

    Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group, Oct 18 2022, In: Circulation. 146, 16, p. 1225-1242 18 p.

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

    Open Access

  • Genetically predicted cortisol levels and risk of venous thromboembolism

    INVENT Consortium, Aug 2022, In: PloS one. 17, 8 August, e0272807.

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

    Open Access

  • Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

    Fernando D. Martinez on behalf of the NHLBI CARE Network, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Hematology and Hemostasis Working Group & TOPMed Structural Variation Working Group, Jan 12 2022, In: Cell Genomics. 2, 1, 100084.

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

    Open Access

  • Genetic diversity fuels gene discovery for tobacco and alcohol use

    23andMe Research Team & The Biobank Japan Project, Dec 22 2022, In: Nature. 612, 7941, p. 720-724 5 p.

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

    Open Access

  • Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

    The Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Apr 2022, In: Science Advances. 8, 14, eabl6579.

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

    Open Access

  • Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

    Temprano-Sagrera, G., Sitlani, C. M., Bone, W. P., Martin-Bornez, M., Voight, B. F., Morrison, A. C., Damrauer, S. M., de Vries, P. S., Smith, N. L., Sabater-Lleal, M., Dehghan, A., Heath, A. S., Morrison, A. C., Reiner, A. P., Johnson, A., Richmond, A., Peters, A., van Hylckama Vlieg, A., McKnight, B., Psaty, B. M., & 363 othersHayward, C., Ward-Caviness, C., O’Donnell, C., Chasman, D., Strachan, D. P., Tregouet, D. A., Mook-Kanamori, D., Gill, D., Thibord, F., Asselbergs, F. W., Leebeek, F. W. G., Rosendaal, F. R., Davies, G., Homuth, G., Temprano, G., Campbell, H., Taylor, H. A., Bressler, J., Huffman, J. E., Rotter, J. I., Yao, J., Wilson, J. F., Bis, J. C., Hahn, J. M., Desch, K. C., Wiggins, K. L., Raffield, L. M., Bielak, L. F., Yanek, L. R., Kleber, M. E., Mueller, M., Kavousi, M., Mangino, M., Liu, M., Brown, M. R., Conomos, M. P., Jhun, M. A., Chen, M. H., de Maat, M. P. M., Pankratz, N., Smith, N. L., Peyser, P. A., Elliot, P., Wei, P., Wild, P. S., Morange, P. E., van der Harst, P., Yang, Q., Le, N. Q., Marioni, R., Li, R., Damrauer, S. M., Cox, S. R., Trompet, S., Felix, S. B., Völker, U., Tang, W., Koenig, W., Jukema, J. W., Guo, X., Lindstrom, S., Wang, L., Smith, E. N., Gordon, W., van Hylckama Vlieg, A., de Andrade, M., Brody, J. A., Pattee, J. W., Haessler, J., Brumpton, B. M., Suchon, P., Chen, M. H., Turman, C., Germain, M., Wiggins, K. L., MacDonald, J., Braekkan, S. K., Armasu, S. M., Pankratz, N., Jackson, R. D., Nielsen, J. B., Giulianini, F., Puurunen, M. K., Ibrahim, M., Heckbert, S. R., Bammler, T. K., Frazer, K. A., McCauley, B. M., Taylor, K., Pankow, J. S., Reiner, A. P., Gabrielsen, M. E., Deleuze, J. F., O’Donnell, C. J., Kim, J., McKnight, B., Kraft, P., Hansen, J. B., Rosendaal, F. R., Heit, J. A., Psaty, B. M., Tang, W., Kooperberg, C., Hveem, K., Ridker, P. M., Morange, P. E., Johnson, A. D., Kabrhel, C., Trégouët, D. A., Smith, N. L., Malik, R., Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Mishra, A., Rutten-Jacobs, L., Giese, A. K., van der Laan, S. W., Gretarsdottir, S., Anderson, C. D., Chong, M., Adams, H. H. H., Ago, T., Almgren, P., Amouyel, P., Ay, H., Bartz, T. M., Benavente, O. R., Bevan, S., Boncoraglio, G. B., Brown, R. D., Butterworth, A. S., Carrera, C., Carty, C. L., Chen, W. M., Cole, J. W., Correa, A., Cotlarciuc, I., Cruchaga, C., Danesh, J., de Bakker, P. I. W., DeStefano, A. L., den Hoed, M., Duan, Q., Engelter, S. T., Falcone, G. J., Gottesman, R. F., Grewal, R. P., Gudnason, V., Gustafsson, S., Haessler, J., Harris, T. B., Hassan, A., Havulinna, A. S., Heckbert, S. R., Holliday, E. G., Howard, G., Hsu, F. C., Hyacinth, H. I., Arfan Ikram, M., Ingelsson, E., Irvin, M. R., Jian, X., Jiménez-Conde, J., Johnson, J. A., Jukema, J. W., Kanai, M., Keene, K. L., Kissela, B. M., Kleindorfer, D. O., Kooperberg, C., Kubo, M., Lange, L. A., Langefeld, C. D., Langenberg, C., Launer, L. J., Lee, J. M., Lemmens, R., Leys, D., Lewis, C. M., Lin, W. Y., Lindgren, A. G., Lorentzen, E., Magnusson, P. K., Maguire, J., Manichaikul, A., McArdle, P. F., Meschia, J. F., Mitchell, B. D., Mosley, T. H., Nalls, M. A., Ninomiya, T., O’Donnell, M. J., Psaty, B. M., Pulit, S. L., Rannikmäe, K., Reiner, A. P., Rexrode, K. M., Rice, K., Rich, S. S., Ridker, P. M., Rost, N. S., Rothwell, P. M., Rotter, J. I., Rundek, T., Sacco, R. L., Sakaue, S., Sale, M. M., Salomaa, V., Sapkota, B. R., Schmidt, R., Schmidt, C. O., Schminke, U., Sharma, P., Slowik, A., Sudlow, C. L. M., Tanislav, C., Tatlisumak, T., Taylor, K. D., Thijs, V. N. S., Thorleifsson, G., Thorsteinsdottir, U., Tiedt, S., Trompet, S., Tzourio, C., van Duijn, C. M., Walters, M., Wareham, N. J., Wassertheil-Smoller, S., Wilson, J. G., Wiggins, K. L., Yang, Q., Yusuf, S., Amin, N., Aparicio, H. S., Arnett, D. K., Attia, J., Beiser, A. S., Berr, C., Buring, J. E., Bustamante, M., Caso, V., Cheng, Y. C., Hoan Choi, S., Chowhan, A., Cullell, N., Dartigues, J. F., Delavaran, H., Delgado, P., Dörr, M., Engström, G., Ford, I., Gurpreet, W. S., Hamsten, A., Heitsch, L., Hozawa, A., Ibanez, L., Ilinca, A., Ingelsson, M., Iwasaki, M., Jackson, R. D., Jood, K., Jousilahti, P., Kaffashian, S., Kalra, L., Kamouchi, M., Kitazono, T., Kjartansson, O., Kloss, M., Koudstaal, P. J., Krupinski, J., Labovitz, D. L., Laurie, C. C., Levi, C. R., Li, L., Lind, L., Lindgren, C. M., Lioutas, V., Mei Liu, Y., Lopez, O. L., Makoto, H., Martinez-Majander, N., Matsuda, K., Minegishi, N., Montaner, J., Morris, A. P., Muiño, E., Müller-Nurasyid, M., Norrving, B., Ogishima, S., Parati, E. A., Reddy Peddareddygari, L., Pedersen, N. L., Pera, J., Perola, M., Pezzini, A., Pileggi, S., Rabionet, R., Riba-Llena, I., Ribasés, M., Romero, J. R., Roquer, J., Rudd, A. G., Sarin, A. P., Sarju, R., Sarnowski, C., Sasaki, M., Satizabal, C. L., Satoh, M., Sattar, N., Sawada, N., Sibolt, G., Sigurdsson, Á., Smith, A., Sobue, K., Soriano-Tárraga, C., Stanne, T., Colin Stine, O., Stott, D. J., Strauch, K., Takai, T., Tanaka, H., Tanno, K., Teumer, A., Tomppo, L., Torres-Aguila, N. P., Touze, E., Tsugane, S., Uitterlinden, A. G., Valdimarsson, E. M., van der Lee, S. J., Völzke, H., Wakai, K., Weir, D., Williams, S. R., Wolfe, C. D. A., Wong, Q., Xu, H., Yamaji, T., Sanghera, D. K., Melander, O., Jern, C., Strbian, D., Fernandez-Cadenas, I., Longstreth, W. T., Rolfs, A., Hata, J., Woo, D., Rosand, J., Pare, G., Hopewell, J. C., Saleheen, D., Stefansson, K., Worrall, B. B., Kittner, S. J., Seshadri, S., Fornage, M., Markus, H. S., Howson, J. M. M., Kamatani, Y., Debette, S. & Dichgans, M., Jun 1 2022, In: Journal of Thrombosis and Haemostasis. 20, 6, p. 1331-1349 19 p.

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

    Open Access

  • Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (Nature, (2022), 611, 7934, (115-123), 10.1038/s41586-022-05165-3)

    The COMPASS Consortium, the INVENT consortium, The Dutch Parelsnoer Initiative (PSI) Cerebrovascular Disease Study Group, The Estonian Biobank, The PRECISE4Q Consortium, The FinnGen Consortium, The NINDS Stroke Genetics Network (SiGN), The MEGASTROKE Consortium, The SIREN Consortium, The China Kadoorie Biobank Collaborative Group, The VA Million Veteran Program, The International Stroke Genetics Consortium (ISGC), The Biobank Japan, The CHARGE Consortium, The GIGASTROKE Consortium, Regeneron Genetics Center, The ODYSSEY Study, HUNT All-In Stroke, The SICFAIL Study, The Generacion Study, & 6 othersThe Copenhagen City Heart Study, The SMART Study, Clinical Research Collaboration for Stroke in Korea (CRCS-K) and Korea Biobank Array (KBA) Project, Helsinki Stroke Project, Follow-up Studies & EPIC-CVD, Dec 1 2022, In: Nature. 612, 7938, p. E7

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

  • Rare genetic variants explain missing heritability in smoking

    Jang, S. K., Evans, L., Fialkowski, A., Arnett, D. K., Ashley-Koch, A. E., Barnes, K. C., Becker, D. M., Bis, J. C., Blangero, J., Bleecker, E. R., Boorgula, M. P., Bowden, D. W., Brody, J. A., Cade, B. E., Jenkins, B. W. C., Carson, A. P., Chavan, S., Cupples, L. A., Custer, B., Damrauer, S. M., & 70 othersDavid, S. P., de Andrade, M., Dinardo, C. L., Fingerlin, T. E., Fornage, M., Freedman, B. I., Garrett, M. E., Gharib, S. A., Glahn, D. C., Haessler, J., Heckbert, S. R., Hokanson, J. E., Hou, L., Hwang, S. J., Hyman, M. C., Judy, R., Justice, A. E., Kaplan, R. C., Kardia, S. L. R., Kelly, S., Kim, W., Kooperberg, C., Levy, D., Lloyd-Jones, D. M., Loos, R. J. F., Manichaikul, A. W., Gladwin, M. T., Martin, L. W., Nouraie, M., Melander, O., Meyers, D. A., Montgomery, C. G., North, K. E., Oelsner, E. C., Palmer, N. D., Payton, M., Peljto, A. L., Peyser, P. A., Preuss, M., Psaty, B. M., Qiao, D., Rader, D. J., Rafaels, N., Redline, S., Reed, R. M., Reiner, A. P., Rich, S. S., Rotter, J. I., Schwartz, D. A., Shadyab, A. H., Silverman, E. K., Smith, N. L., Smith, J. G., Smith, A. V., Smith, J. A., Tang, W., Taylor, K. D., Telen, M. J., Vasan, R. S., Gordeuk, V. R., Wang, Z., Wiggins, K. L., Yanek, L. R., Yang, I. V., Young, K. A., Young, K. L., Zhang, Y., Liu, D. J., Keller, M. C. & Vrieze, S., Nov 2022, In: Nature Human Behaviour. 6, 11, p. 1577-1586 10 p.

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

    Open Access

  • Stroke genetics informs drug discovery and risk prediction across ancestries

    The COMPASS Consortium, the INVENT consortium, The Dutch Parelsnoer Initiative (PSI) Cerebrovascular Disease Study Group, The Estonian Biobank, The PRECISEQ Consortium, The FinnGen Consortium, The NINDS Stroke Genetics Network (SiGN), The MEGASTROKE Consortium, The SIREN Consortium, The China Kadoorie Biobank Collaborative Group, The VA Million Veteran Program, The International Stroke Genetics Consortium (ISGC), The Biobank Japan, The CHARGE Consortium, The GIGASTROKE Consortium, Regeneron Genetics Center, The ODYSSEY Study, HUNT All-In Stroke, The SICFAIL Study, The Generacion Study, & 6 othersThe Copenhagen City Heart Study, The SMART Study, Clinical Research Collaboration for Stroke in Korea (CRCS-K) and Korea Biobank Array (KBA) Project, Helsinki Stroke Project, Follow-up Studies & EPIC-CVD, Nov 3 2022, In: Nature. 611, 7934, p. 115-123 9 p.

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

    Open Access

  • The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

    Wang, Z., Choi, S. W., Chami, N., Boerwinkle, E., Fornage, M., Redline, S., Bis, J. C., Brody, J. A., Psaty, B. M., Kim, W., McDonald, M. L. N., Regan, E. A., Silverman, E. K., Liu, C. T., Vasan, R. S., Kalyani, R. R., Mathias, R. A., Yanek, L. R., Arnett, D. K., Justice, A. E., & 21 othersNorth, K. E., Kaplan, R., Heckbert, SR., de Andrade, M., Guo, X., Lange, L. A., Rich, SS., Rotter, J. I., Ellinor, P. T., Lubitz, S. A., Blangero, J., Shoemaker, M. B., Darbar, D., Gladwin, M. T., Albert, C. M., Chasman, D. I., Jackson, R. D., Kooperberg, C., Reiner, A. P., O’Reilly, P. F. & Loos, R. J. F., May 3 2022, In: Frontiers in Endocrinology. 13, 863893.

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

    Open Access

  • 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
  • 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

  • An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

    PBC Consortia, Canadian PBC Consortium, Chinese PBC Consortium, Italian PBC Study Group, Japan PBC-GWAS Consortium, US PBC Consortium & UK-PBC Consortium, Sep 2021, In: Journal of hepatology. 75, 3, p. 572-581 10 p.

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

    Open Access

  • Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry

    Satterfield, B. A., Dikilitas, O., Safarova, M. S., Clarke, S. L., Tcheandjieu, C., Zhu, X., Bastarache, L., Larson, E. B., Justice, A. E., Shang, N., Rosenthal, E. A., Shah, A. S., Namjou-Khales, B., Urbina, E. M., Wei, W. Q., Feng, Q. P., Jarvik, G. P., Hebbring, S. J., De Andrade, M., Manolio, T. A., & 2 othersAssimes, T. L. & Kullo, I. J., Aug 1 2021, In: Circulation: Genomic and Precision Medicine. 14, 4, p. E003354

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

    Open Access

  • A system for phenotype harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) program

    Stilp, A. M., Emery, L. S., Broome, J. G., Buth, E. J., Khan, A. T., Laurie, C. A., Wang, F. F., Wong, Q., Chen, D., D’Augustine, C. M., Heard-Costa, N. L., Hohensee, C. R., Johnson, W. C., Juarez, L. D., Liu, J., Mutalik, K. M., Raffield, L. M., Wiggins, K. L., de Vries, P. S., Kelly, T. N., & 52 othersKooperberg, C., Natarajan, P., Peloso, G. M., Peyser, P. A., Reiner, A. P., Arnett, D. K., Aslibekyan, S., Barnes, K. C., Bielak, L. F., Bis, J. C., Cade, B. E., Chen, M. H., Correa, A., Adrienne Cupples, L., de Andrade, M., Ellinor, P. T., Fornage, M., Franceschini, N., Gan, W., Ganesh, S. K., Graffelman, J., Grove, M. L., Guo, X., Hawley, N. L., Hsu, W. L., Jackson, R. D., Jaquish, C. E., Johnson, A. D., Kardia, S. L. R., Kelly, S., Lee, J., Mathias, R. A., McGarvey, S. T., Mitchell, B. D., Montasser, M. E., Morrison, A. C., North, K. E., Nouraie, S. M., Oelsner, E. C., Pankratz, N., Rich, S. S., Rotter, J. I., Smith, J. A., Taylor, K. D., Vasan, R. S., Weeks, D. E., Weiss, S. T., Wilson, C. G., Yanek, L. R., Psaty, B. M., Heckbert, S. R. & Laurie, C. C., 2021, In: American journal of epidemiology. 190, 10, p. 1977-1992 16 p.

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

    Open Access

  • Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (Nature, (2020), 586, 7831, (763-768), 10.1038/s41586-020-2819-2)

    NHLBI Trans-Omics for Precision Medicine Consortium, Mar 25 2021, In: Nature. 591, 7851, p. E27

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

  • Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response (Nature Genetics, (2021), 53, 10, (1504-1516), 10.1038/s41588-021-00935-7)

    NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 2021, In: Nature Genetics. 53, 12, p. 1722 1 p.

    Research output: Contribution to journal › Comment/debate › peer-review

    Open Access

  • 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

  • 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

  • Genetic variation and recurrent haplotypes on chromosome 6q23-25 risk locus in familial lung cancer

    Musolf, A. M., Simpson, C. L., Moiz, B. A., Pikielny, C. W., Middlebrooks, C. D., Mandal, D., De Andrade, M., Cole, M. D., Gaba, C., Yang, P., You, M., Li, Y., Kupert, E. Y., Anderson, M. W., Schwartz, A. G., Pinney, S. M., Amos, C. I. & Bailey-Wilson, J. E., Jun 2021, In: Cancer research. 81, 12, p. 3162-3173 12 p.

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

    Open Access

  • 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

  • Genome-Wide Association Study of Peripheral Artery Disease

    Van Zuydam, N. R., Stiby, A., Abdalla, M., Austin, E., Dahlström, E. H., McLachlan, S., Vlachopoulou, E., Ahlqvist, E., Di Liao, C., Sandholm, N., Forsblom, C., Mahajan, A., Robertson, N. R., Rayner, N. W., Lindholm, E., Sinisalo, J., Perola, M., Kallio, M., Weiss, E., Price, J., & 12 othersPaterson, A., Klein, B., Salomaa, V., Palmer, C. N. A., Groop, P. H., Groop, L., McCarthy, M. I., De Andrade, M., Morris, A. P., Hopewell, J. C., Colhoun, H. M. & Kullo, I. J., Oct 1 2021, In: Circulation: Genomic and Precision Medicine. 14, 5, p. E002862

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

    Open Access

  • Neptune: an environment for the delivery of genomic medicine

    eMERGE Consortium, Oct 2021, In: Genetics in Medicine. 23, 10, p. 1838-1846 9 p.

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

    Open Access

  • Outcomes of COVID-19 in patients with cancer: A closer look at pre-emptive routine screening strategies

    Xie, Z., Saliba, A. N., Abeykoon, J., Majeed, U., Almquist, D. R., Wiedmeier-Nutor, J. E., Bezerra, E., Andrade-Gonzalez, X., Hickman, A., Sorenson, K., Rakshit, S., Wee, C., Tella, S. H., Kommalapati, A., Abdallah, N., Pritchett, J., de Andrade, M., Uprety, D., Badley, A., Manochakian, R., & 9 othersAilawadhi, S., Bryce, A. H., Hubbard, J. M., Gangat, N., Thompson, C. A., Witzig, T. E., McWilliams, R. R., Leventakos, K. & Halfdanarson, T. R., Sep 1 2021, In: JCO Oncology Practice. 17, 9, p. E1382-E1393

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

    Open Access

  • Rare deleterious germline variants and risk of lung cancer

    Liu, Y., Xia, J., McKay, J., Tsavachidis, S., Xiao, X., Spitz, M. R., Cheng, C., Byun, J., Hong, W., Li, Y., Zhu, D., Song, Z., Rosenberg, S. M., Scheurer, M. E., Kheradmand, F., Pikielny, C. W., Lusk, C. M., Schwartz, A. G., Wistuba, I. I., Cho, M. H., & 27 othersSilverman, E. K., Bailey-Wilson, J., Pinney, S. M., Anderson, M., Kupert, E., Gaba, C., Mandal, D., You, M., de Andrade, M., Yang, P., Liloglou, T., Davies, M. P. A., Lissowska, J., Swiatkowska, B., Zaridze, D., Mukeria, A., Janout, V., Holcatova, I., Mates, D., Stojsic, J., Scelo, G., Brennan, P., Liu, G., Field, J. K., Hung, R. J., Christiani, D. C. & Amos, C. I., Dec 2021, In: npj Precision Oncology. 5, 1, 12.

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

    Open Access

  • Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries

    NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, May 2021, In: Genetics. 218, 1, iyab044.

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

    Open Access

  • 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
    20 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

  • 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
  • 2020

    A digital health weight-loss intervention in severe obesity

    Senecal, C., Collazo-Clavell, M., Larrabee, B. R., de Andrade, M., Lin, W., Chen, B., Lerman, L. O., Lerman, A. & Lopez-Jimenez, F., 2020, In: Digital Health. 6

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

    Open Access
    1 Scopus citations

  • A Digital Health Weight Loss Program in 250,000 Individuals

    Senecal, C., Widmer, R. J., Larrabee, B. R., De Andrade, M., Lerman, L. O., Lerman, A. & Lopez-Jimenez, F., 2020, In: Journal of Obesity. 2020, 9497164.

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

    Open Access

  • Bivariate traits association analysis using generalized estimating equations in family data

    de Andrade, M., Mazo Lopera, M. A. & Duarte, N. E., Apr 1 2020, In: Statistical Applications in Genetics and Molecular Biology. 19, 2, 20190030.

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

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