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A structural variation reference for medical and population genetics.

R. Collins, H. Brand, K. Karczewski, X. Zhao, J. Alföldi, L. Francioli, A. Khera, C. Lowther, L. Gauthier, H. Wang, N. Watts, M. Solomonson, A. Baumann, R. Munshi, M. Walker, C. Whelan, Y. Huang, T. Brookings, T. Sharpe, M. Stone, E. Valkanas, J. Fu, G. Tiao, K. Laricchia, V. Ruano-Rubio, C. Stevens, N. Gupta, C. Cusick, L. Margolin, I. Armean, E. Banks, L. Bergelson, K. Cibulskis, K. Connolly, M. Covarrubias, B. Cummings, M. Daly, S. Donnelly, Y. Farjoun, S. Ferriera, S. Gabriel, J. Gentry, T. Jeandet, D. Kaplan, C. Llanwarne, E. Minikel, B. Neale, S. Novod, A. O'Donnell-Luria, N. Petrillo, T. Poterba, D. Roazen, A. Saltzman, K. Samocha, M. Schleicher, C. Seed, J. Soto, K. Tibbetts, C. Tolonen, C. Vittal, G. Wade, A. Wang, Q. Wang, J. Ware, B. Weisburd, N. Whiffin, C. Salinas, T. Ahmad, C. Albert, D. Ardissino, G. Atzmon, J. Barnard, L. Beaugerie, E. Benjamin, M. Boehnke, L. Bonnycastle, E. Bottinger, D. Bowden, M. Bown, J. Chambers, J. Chan, D. Chasman, J. Cho, M. Chung, B. Cohen, A. Correa, D. Dabelea, D. Darbar, R. Duggirala, J. Dupuis, P. Ellinor, R. Elosua, J. Erdmann, T. Esko, M. Färkkilä, J. Florez, A. Franke, G. Getz, B. Glaser, S. Glatt, D. Goldstein, C. Gonzalez, L. Groop, C. Haiman, C. Hanis, M. Harms, M. Hiltunen, M. Holi, C. Hultman, M. Kallela, J. Kaprio, S. Kathiresan, B. Kim, Y. Kim, G. Kirov, J. Kooner, S. Koskinen, H. Krumholz, S. Kugathasan, S. Kwak, M. Laakso, T. Lehtimäki, R. Loos, S. Lubitz, R. Ma, D. MacArthur, J. Marrugat, K. Mattila, S. McCarroll, M. McCarthy, D. McGovern, R. McPherson, J. Meigs, O. Melander, A. Metspalu, P. Nilsson, M. O'Donovan, D. Öngür, L. Orozco, M. Owen, C. Palmer, A. Palotie, K. Park, C. Pato, A. Pulver, N. Rahman, A. Remes, J. Rioux, S. Ripatti, D. Roden, D. Saleheen, V. Salomaa, N. Samani, J. Scharf, H. Schunkert, M. Shoemaker, P. Sklar, H. Soininen, H. Sokol, T. Spector, P. Sullivan, J. Suvisaari, E. Tai, Y. Teo, T. Tiinamaija, M. Tsuang, D. Turner, T. Tusie-Luna, E. Vartiainen, H. Watkins, R. Weersma, M. Wessman, J. Wilson, R. Xavier, K. Taylor, H. Lin, S. Rich, W. Post, Y. Chen, J. Rotter, C. Nusbaum, A. Philippakis, E. Lander, and M. Talkowski. Nat., 581 (7809): 444-451 (2020)

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Klaus Roden

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Harald Roden

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Improving the phenotype risk score as a scalable approach to identifying patients with Mendelian disease.L. Bastarache, J. Hughey, J. Goldstein, J. Bastraache, S. Das, N. Zaki, C. Zeng, L. Tang, D. Roden, and J. Denny. J. Am. Medical Informatics Assoc., 26 (12): 1437-1447 (2019)An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.J. Schildcrout, M. Basford, J. Pulley, D. Masys, D. Roden, D. Wang, C. Chute, I. Kullo, D. Carrell, P. Peissig and 2 other author(s). J. Biomed. Informatics, 43 (6): 914-923 (2010)The All of Us Research Program Researcher Workbench Phenotype Library: Five Disease Implementations.I. Humes, R. Loperena-Cortes, M. Basford, K. Mayo, J. DiPaolo, D. Schlueter, J. Qian, W. Wei, R. Carroll, D. Glazer and 4 other author(s). AMIA, AMIA, (2020)Visual Integration of Results from a Large Dna Biobank (Biovu) Using Synthesis-View.S. Pendergrass, S. Dudek, D. Roden, D. Crawford, and M. Ritchie. Pacific Symposium on Biocomputing, page 265-275. World Scientific Publishing, (2011)PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.N. Zheng, Q. Feng, V. Kerchberger, J. Zhao, T. Edwards, N. Cox, C. Stein, D. Roden, J. Denny, and W. Wei. J. Am. Medical Informatics Assoc., 27 (11): 1675-1687 (2020)Real-time Clinical Note Monitoring to Detect Conditions for Follow-up: a Case Study of Clinical Trial Enrollment in Drug-induced Torsades de Pointes and Stevens-Johnson Syndrome.S. DeLozier, P. Speltz, J. Brito, L. Tang, J. Wang, J. Smith, D. Giuse, E. Phillips, K. Williams, T. Strickland and 3 other author(s). AMIA, AMIA, (2020)The All of Us Research Program Researcher Workbench: Cloud based access and analytics to advance precision medicine.A. Ramirez, K. Mayo, R. Carroll, K. Muthuraman, M. Basford, D. Glazer, P. Harris, A. Philippakis, and D. Roden. AMIA, AMIA, (2020)PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.J. Kirby, P. Speltz, L. Rasmussen, M. Basford, O. Gottesman, P. Peissig, J. Pacheco, G. Tromp, J. Pathak, D. Carrell and 8 other author(s). JAMIA, 23 (6): 1046-1052 (2016)The mutational constraint spectrum quantified from variation in 141,456 humansK. Karczewski, L. Francioli, G. Tiao, B. Cummings, J. Alföldi, Q. Wang, R. Collins, K. Laricchia, A. Ganna, D. Birnbaum and 167 other author(s). Nature, 581 (7809): 434--443 (2020)A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19.N. Zheng, J. Warner, T. Osterman, Q. Wells, X. Shu, S. Deppen, S. Karp, S. Dwyer, Q. Feng, N. Cox and 5 other author(s). J. Biomed. Informatics, (2021)

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Disambiguation of "Roden, Dan M."

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A structural variation reference for medical and population genetics.

Please choose a person to relate this publication to

Klaus Roden

Gabriele Roden

Jan Roden

Günter Roden

Harald Roden

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Roden, Dan M."

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML A structural variation reference for medical and population genetics.

Please choose a person to relate this publication to

Klaus Roden

Gabriele Roden

Jan Roden

Günter Roden

Harald Roden

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
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history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
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MSOffice XML

A structural variation reference for medical and population genetics.