Mariza De Andrade

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Mariza De Andrade, PhD

1991 …2023

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  • 2023

    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
  • 2022

    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

  • 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

  • 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

  • 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 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

  • 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

  • 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, 2022, (Accepted/In press) In: Nature Genetics.

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

  • 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

  • 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

  • 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

  • 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

  • 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

    TOPMed Analysis Working Group & NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, May 17 2021, In: Genetics. 218, 1

    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

  • Cerebral small vessel disease genomics and its implications across the lifespan

    International Network against Thrombosis (INVENT) Consortium & International Headache Genomics Consortium (IHGC), Dec 2020, In: Nature communications. 11, 1, 6285.

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

    Open Access
    2 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

    5 Scopus citations

  • Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection

    Turley, T. N., O'Byrne, M. M., Kosel, M. L., De Andrade, M., Gulati, R., Hayes, S. N., Tweet, M. S. & Olson, T. M., Aug 2020, In: JAMA cardiology. 5, 8, p. 929-938 10 p.

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

    Open Access
    10 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

    34 Scopus citations

  • Whole exome sequencing of highly aggregated lung cancer families reveals linked loci for increased cancer risk on chromosomes 12q, 7p, and 4q

    Musolf, A. M., Moiz, B. A., Sun, H., Pikielny, C. W., Bosse, Y., Mandal, D., De Andrade, M., Gaba, C., Yang, P., Li, Y., You, M., Govindan, R., Wilson, R. K., Kupert, E. Y., Anderson, M. W., Schwartz, A. G., Pinney, S. M., Amos, C. I. & Bailey-Wilson, J. E., Feb 1 2020, In: Cancer Epidemiology Biomarkers and Prevention. 29, 2, p. 434-442 9 p.

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

    1 Scopus citations
  • 2019

    A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR

    Safarova, M. S., Satterfield, B. A., Fan, X., Austin, E. E., Ye, Z., Bastarache, L., Zheng, N., Ritchie, M. D., Borthwick, K. M., Williams, M. S., Larson, E. B., Scrol, A., Jarvik, G. P., Crosslin, D. R., Leppig, K., Rasmussen-Torvik, L. J., Pendergrass, S. A., Sturm, A. C., Namjou, B., Shah, A. S., & 12 othersCarroll, R. J., Chung, W. K., Wei, W. Q., Feng, Q. P., Stein, C. M., Roden, D. M., Manolio, T. A., Schaid, D. J., Denny, J. C., Hebbring, S. J., de Andrade, M. & Kullo, I. J., Dec 1 2019, In: npj Genomic Medicine. 4, 1, 3.

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

    Open Access
    7 Scopus citations

  • Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

    DISCO Consortium & CARDIoGRAMPlusC4D Study Group, Jan 8 2019, In: Journal of the American College of Cardiology. 73, 1, p. 58-66 9 p.

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

    Open Access
    62 Scopus citations

  • Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

    Kraja, A. T., Liu, C., Fetterman, J. L., Graff, M., Have, C. T., Gu, C., Yanek, L. R., Feitosa, M. F., Arking, D. E., Chasman, D. I., Young, K., Ligthart, S., Hill, W. D., Weiss, S., Luan, J., Giulianini, F., Li-Gao, R., Hartwig, F. P., Lin, S. J., Wang, L., & 132 othersRichardson, T. G., Yao, J., Fernandez, E. P., Ghanbari, M., Wojczynski, M. K., Lee, W. J., Argos, M., Armasu, S. M., Barve, R. A., Ryan, K. A., An, P., Baranski, T. J., Bielinski, S. J., Bowden, D. W., Broeckel, U., Christensen, K., Chu, A. Y., Corley, J., Cox, S. R., Uitterlinden, A. G., Rivadeneira, F., Cropp, C. D., Daw, E. W., van Heemst, D., de las Fuentes, L., Gao, H., Tzoulaki, I., Ahluwalia, T. S., de Mutsert, R., Emery, L. S., Erzurumluoglu, A. M., Perry, J. A., Fu, M., Forouhi, N. G., Gu, Z., Hai, Y., Harris, S. E., Hemani, G., Hunt, S. C., Irvin, M. R., Jonsson, A. E., Justice, A. E., Kerrison, N. D., Larson, N. B., Lin, K. H., Love-Gregory, L. D., Mathias, R. A., Lee, J. H., Nauck, M., Noordam, R., Ong, K. K., Pankow, J., Patki, A., Pattie, A., Petersmann, A., Qi, Q., Ribel-Madsen, R., Rohde, R., Sandow, K., Schnurr, T. M., Sofer, T., Starr, J. M., Taylor, A. M., Teumer, A., Timpson, N. J., de Haan, H. G., Wang, Y., Weeke, P. E., Williams, C., Wu, H., Yang, W., Zeng, D., Witte, D. R., Weir, B. S., Wareham, N. J., Vestergaard, H., Turner, S. T., Torp-Pedersen, C., Stergiakouli, E., Sheu, W. H. H., Rosendaal, F. R., Ikram, M. A., Franco, O. H., Ridker, P. M., Perls, T. T., Pedersen, O., Nohr, E. A., Newman, A. B., Linneberg, A., Langenberg, C., Kilpeläinen, T. O., Kardia, S. L. R., Jørgensen, M. E., Jørgensen, T., Sørensen, T. I. A., Homuth, G., Hansen, T., Goodarzi, M. O., Deary, I. J., Christensen, C., Chen, Y. D. I., Chakravarti, A., Brandslund, I., Bonnelykke, K., Taylor, K. D., Wilson, J. G., Rodriguez, S., Davies, G., Horta, B. L., Thyagarajan, B., Rao, D. C., Grarup, N., Davila-Roman, V. G., Hudson, G., Guo, X., Arnett, D. K., Hayward, C., Vaidya, D., Mook-Kanamori, D. O., Tiwari, H. K., Levy, D., Loos, R. J. F., Dehghan, A., Elliott, P., Malik, A. N., Scott, R. A., Becker, D. M., de Andrade, M., Province, M. A., Meigs, J. B., Rotter, J. I. & North, K. E., Jan 3 2019, In: American journal of human genetics. 104, 1, p. 112-138 27 p.

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

    Open Access
    36 Scopus citations

  • Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

    Chiang, T., Liu, X., Wu, T. J., Hu, J., Sedlazeck, F. J., White, S., Schaid, D., Andrade, M. D., Jarvik, G. P., Crosslin, D., Stanaway, I., Carrell, D. S., Connolly, J. J., Hakonarson, H., Groopman, E. E., Gharavi, A. G., Fedotov, A., Bi, W., Leduc, M. S., Murdock, D. R., & 10 othersJiang, Y., Meng, L., Eng, C. M., Wen, S., Yang, Y., Muzny, D. M., Boerwinkle, E., Salerno, W., Venner, E. & Gibbs, R. A., Sep 1 2019, In: Genetics in Medicine. 21, 9, p. 2135-2144 10 p.

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

    Open Access
    6 Scopus citations

  • Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

    Lindström, 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., Chasman, D. I., Suchon, P., Chen, M. H., Turman, C., Germain, M., Wiggins, K. L., MacDonald, J., Braekkan, S. K., Armasu, S. M., Pankratz, N., & 37 othersJackson, R. D., Nielsen, J. B., Giulianini, F., Puurunen, M. K., Ibrahim, M., Heckbert, S. R., Damrauer, S. M., Natarajan, P., Klarin, D., De Vries, P. S., Sabater-Lleal, M., Huffman, J. E., 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., Nov 7 2019, In: Blood. 134, 19, p. 1645-1657 13 p.

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

    Open Access
    31 Scopus citations

  • Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

    the eMERGE Consortium, Sep 5 2019, In: American journal of human genetics. 105, 3, p. 588-605 18 p.

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

    Open Access
    31 Scopus citations

  • Immune Cell Infiltration May Be a Key Determinant of Long-Term Survival in Small Cell Lung Cancer

    Muppa, P., Parrilha Terra, S. B. S., Sharma, A., Mansfield, A. S., Aubry, M. C., Bhinge, K., Asiedu, M. K., de Andrade, M., Janaki, N., Murphy, S. J., Nasir, A., Van Keulen, V., Vasmatzis, G., Wigle, D. A., Yang, P., Yi, E. S., Peikert, T. & Kosari, F., Jul 2019, In: Journal of Thoracic Oncology. 14, 7, p. 1286-1295 10 p.

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

    Open Access
    23 Scopus citations

  • Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region

    Hung, R. J., Spitz, M. R., Houlston, R. S., Schwartz, A. G., Field, J. K., Ying, J., Li, Y., Han, Y., Ji, X., Chen, W., Wu, X., Gorlov, I. P., Na, J., de Andrade, M., Liu, G., Brhane, Y., Diao, N., Wenzlaff, A., Davies, M. P. A., Liloglou, T., & 46 othersTimofeeva, M., Muley, T., Rennert, H., Saliba, W., Ryan, B. M., Bowman, E., Barros-Dios, J. M., Pérez-Ríos, M., Morgenstern, H., Zienolddiny, S., Skaug, V., Ugolini, D., Bonassi, S., van der Heijden, E. H. F. M., Tardon, A., Bojesen, S. E., Landi, M. T., Johansson, M., Bickeböller, H., Arnold, S., Le Marchand, L., Melander, O., Andrew, A., Grankvist, K., Caporaso, N., Teare, M. D., Schabath, M. B., Aldrich, M. C., Kiemeney, L. A., Wichmann, H. E., Lazarus, P., Mayordomo, J., Neri, M., Haugen, A., Zhang, Z. F., Ruano-Raviña, A., Brenner, H., Harris, C. C., Orlow, I., Rennert, G., Risch, A., Brennan, P., Christiani, D. C., Amos, C. I., Yang, P. & Gorlova, O. Y., Aug 2019, In: Journal of Thoracic Oncology. 14, 8, p. 1360-1369 10 p.

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

    Open Access
    8 Scopus citations

  • Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

    Schmidt, A. F., Holmes, M. V., Preiss, D., Swerdlow, D. I., Denaxas, S., Fatemifar, G., Faraway, R., Finan, C., Valentine, D., Fairhurst-Hunter, Z., Hartwig, F. P., Horta, B. L., Hypponen, E., Power, C., Moldovan, M., Van Iperen, E., Hovingh, K., Demuth, I., Norman, K., Steinhagen-Thiessen, E., & 145 othersDemuth, J., Bertram, L., Lill, C. M., Coassin, S., Willeit, J., Kiechl, S., Willeit, K., Mason, D., Wright, J., Morris, R., Wanamethee, G., Whincup, P., Ben-Shlomo, Y., McLachlan, S., Price, J. F., Kivimaki, M., Welch, C., Sanchez-Galvez, A., Marques-Vidal, P., Nicolaides, A., Panayiotou, A. G., Onland-Moret, N. C., Van Der Schouw, Y. T., Matullo, G., Fiorito, G., Guarrera, S., Sacerdote, C., Wareham, N. J., Langenberg, C., Scott, R. A., Luan, JA., Bobak, M., Malyutina, S., Pajak, A., Kubinova, R., Tamosiunas, A., Pikhart, H., Grarup, N., Pedersen, O., Hansen, T., Linneberg, A., Jess, T., Cooper, J., Humphries, S. E., Brilliant, M., Kitchner, T., Hakonarson, H., Carrell, D. S., McCarty, C. A., Lester, K. H., Larson, E. B., Crosslin, D. R., De Andrade, M., Roden, D. M., Denny, J. C., Carty, C., Hancock, S., Attia, J., Holliday, E., Scott, R., Schofield, P., O'Donnell, M., Yusuf, S., Chong, M., Pare, G., Van Der Harst, P., Said, M. A., Eppinga, R. N., Verweij, N., Snieder, H., Christen, T., Mook-Kanamori, D. O., Gustafsson, S., Lind, L., Ingelsson, E., Pazoki, R., Franco, O., Hofman, A., Uitterlinden, A., Dehghan, A., Teumer, A., Baumeister, S., Dörr, M., Lerch, M. M., Völker, U., Völzke, H., Ward, J., Pell, J. P., Meade, T., Christophersen, I. E., Maitland-Van Der Zee, A. H., Baranova, E. V., Young, R., Ford, I., Campbell, A., Padmanabhan, S., Bots, M. L., Grobbee, D. E., Froguel, P., Thuillier, D., Roussel, R., Bonnefond, A., Cariou, B., Smart, M., Bao, Y., Kumari, M., Mahajan, A., Hopewell, J. C., Seshadri, S., Dale, C., Costa, R. P. E., Ridker, P. M., Chasman, D. I., Reiner, A. P., Ritchie, M. D., Lange, L. A., Cornish, A. J., Dobbins, S. E., Hemminki, K., Kinnersley, B., Sanson, M., Labreche, K., Simon, M., Bondy, M., Law, P., Speedy, H., Allan, J., Li, N., Went, M., Weinhold, N., Morgan, G., Sonneveld, P., Nilsson, B., Goldschmidt, H., Sud, A., Engert, A., Hansson, M., Hemingway, H., Asselbergs, F. W., Patel, R. S., Keating, B. J., Sattar, N., Houlston, R., Casas, J. P. & Hingorani, A. D., 2019, In: BMC cardiovascular disorders. 19, 1, 240.

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

    Open Access
    2 Scopus citations

  • The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype

    The eMERGE Network, Feb 2019, In: Genetic epidemiology. 43, 1, p. 63-81 19 p.

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

    16 Scopus citations

  • Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

    National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium, Dec 1 2019, In: Chest. 156, 6, p. 1068-1079 12 p.

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

    Open Access
    3 Scopus citations
  • 2018

    Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

    NHLBI TOPMed Lipids Working Group, Dec 1 2018, In: Nature communications. 9, 1, 3391.

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

    Open Access
    63 Scopus citations

  • Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

    Zekavat, S. M., Ruotsalainen, S., Handsaker, R. E., Alver, M., Bloom, J., Poterba, T., Seed, C., Ernst, J., Chaffin, M., Engreitz, J., Peloso, G. M., Manichaikul, A., Yang, C., Ryan, K. A., Fu, M., Johnson, W. C., Tsai, M., Budoff, M., Ramachandran, V. S., Cupples, L. A., & 323 othersRotter, J. I., Rich, S. S., Post, W., Mitchell, B. D., Correa, A., Metspalu, A., Wilson, J. G., Salomaa, V., Kellis, M., Daly, M. J., Neale, B. M., McCarroll, S., Surakka, I., Esko, T., Ganna, A., Ripatti, S., Kathiresan, S., Natarajan, P., Abe, N., Abecasis, G., Albert, C., Allred, N. P., Almasy, L., Alonso, A., Ament, S., Anderson, P., Anugu, P., Applebaum-Bowden, D., Arking, D., Arnett, D. K., Ashley-Koch, A., Aslibekyan, S., Assimes, T., Auer, P., Avramopoulos, D., Barnard, J., Barnes, K., Barr, R. G., Barron-Casella, E., Beaty, T., Becker, D., Becker, L., Beer, R., Begum, F., Beitelshees, A., Benjamin, E., Bezerra, M., Bielak, L., Bis, J., Blackwell, T., Blangero, J., Boerwinkle, E., Borecki, I., Bowler, R., Brody, J., Broeckel, U., Broome, J., Bunting, K., Burchard, E., Cardwell, J., Carty, C., Casaburi, R., Casella, J., Chang, 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., Cornell, E., Crandall, C., Crapo, J., Curran, J., Curtis, J., Custer, B., Damcott, C., Darbar, D., Das, S., David, S., Davis, C., Daya, M., Andrade, M. D., Debaun, M., Deka, R., Demeo, D., Devine, S., Do, R., Duan, Q., Duggirala, R., Durda, P., Dutcher, S., Eaton, C., Ekunwe, L., Ellinor, P., Emery, L., Farber, C., Farnam, L., Fingerlin, T., Flickinger, M., Fornage, M., Franceschini, N., Fullerton, S. M., Fulton, L., Gabriel, S., Gan, W., Gao, Y., Gass, M., Gelb, B., Geng, X., Germer, S., Gignoux, C., Gladwin, M., Glahn, D., Gogarten, S., Gong, D. W., Goring, H., Gu, C. C., Guan, Y., Guo, X., Haessler, J., Hall, M., Harris, D., Hawley, N., He, J., Heavner, B., Heckbert, S., Hernandez, R., Herrington, D., Hersh, C., Hidalgo, B., Hixson, J., Hokanson, J., Hong, E., Hoth, K., Hsiung, C., Huston, H., Hwu, C. M., Irvin, M. R., Jackson, R., Jain, D., Jaquish, C., Jhun, M. A., Johnsen, J., Johnson, A., Johnston, R., Jones, K., Kang, H. M., Kaplan, R., Kardia, S., Kaufman, L., Kelly, S., Kenny, E., Kessler, M., Khan, A., Kinney, G., Konkle, B., Kooperberg, C., Kramer, H., Krauter, S., Lange, C., Lange, E., Lange, L., Laurie, C., Laurie, C., Leboff, M., Lee, S. S., Lee, W. J., Lefaive, J., Levine, D., Levy, D., Lewis, J., Li, Y., Lin, H., Lin, K. H., Liu, S., Liu, Y., Loos, R., Lubitz, S., Lunetta, K., Luo, J., Mahaney, M., Make, B., Manson, J. A., Margolin, L., Martin, L., Mathai, S., Mathias, R., McArdle, P., McDonald, M. L., McFarland, S., McGarvey, S., Mei, H., Meyers, D. A., Mikulla, J., Min, N., Minear, M., Minster, R. L., Montasser, M. E., Musani, S., Mwasongwe, S., Mychaleckyj, J. C., Nadkarni, G., Naik, R., Nekhai, S., Nickerson, D., North, K., O'connell, J., O'connor, T., Ochs-Balcom, H., Pankow, J., Papanicolaou, G., Parker, M., Parsa, A., Penchev, S., Peralta, J. M., Perez, M., Perry, J., Peters, U., Peyser, P., Phillips, L., Phillips, S., Pollin, T., Becker, J. P., Boorgula, M. P., Preuss, M., Prokopenko, D., Psaty, B., Qasba, P., Qiao, D., Qin, Z., Rafaels, N., Raffield, L., Rao, D. C., Rasmussen-Torvik, L., Ratan, A., Redline, S., Reed, R., Regan, E., Reiner, A., Rice, K., Roden, D., Roselli, C., Ruczinski, I., Russell, P., Ruuska, S., Sakornsakolpat, P., Salimi, S., Salzberg, S., Sandow, K., Sankaran, V., Scheller, C., Schmidt, E., Schwander, K., Schwartz, D., Sciurba, F., Seidman, C., Sheehan, V., Shetty, A., Shetty, A., Sheu, W. H. H., Shoemaker, M. B., Silver, B., Silverman, E., Smith, J., Smith, J., Smith, N., Smith, T., Smoller, S., Snively, B., Sofer, T., Sotoodehnia, N., Stilp, A., Streeten, E., Sung, Y. J., Sylvia, J., Szpiro, A., Sztalryd, C., Taliun, D., Tang, H., Taub, M., Taylor, K., Taylor, S., Telen, M., Thornton, T. A., Tinker, L., Tirschwell, D., Tiwari, H., Tracy, R., Vaidya, D., Vandehaar, P., Vrieze, S., Walker, T., Wallace, R., Walts, A., Wan, E., Wang, F. F., Watson, K., Weeks, D. E., Weir, B., Weiss, S., Weng, L. C., Willer, C., Williams, K., Williams, L. K., Wilson, C., Wong, Q., Xu, H., Yanek, L., Yang, I., Yang, R., Zaghloul, N., Zhang, Y., Zhao, S. X., Zhao, W., Zheng, X., Zhi, D., Zhou, X., Zody, M. & Zoellner, S., Dec 1 2018, In: Nature communications. 9, 1, 2606.

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

    Open Access
    30 Scopus citations

  • External validation of the United Kingdom-primary biliary cholangitis risk scores of patients with primary biliary cholangitis treated with ursodeoxycholic acid

    Cheung, A. C., Gulamhusein, A. F., Juran, B. D., Schlicht, E. M., McCauley, B. M., de Andrade, M., Atkinson, E. J. & Lazaridis, K. N., Jun 2018, In: Hepatology Communications. 2, 6, p. 676-682 7 p.

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

    Open Access
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