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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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Stephan Karczewski

Roman Karczewski

Konrad J Rögner

Konrad J Kuhn

Stephan Karczewski

Other publications of authors with the same name

Bioinformatics challenges for personalized medicine.G. Fernald, E. Capriotti, R. Daneshjou, K. Karczewski, and R. Altman. Bioinform., 27 (16): 2323 (2011)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)Interpretome: A Freely Available, Modular, and Secure Personal Genome Interpretation Engine.K. Karczewski, R. Tirrell, P. Cordero, N. Tatonetti, J. Dudley, K. Salari, M. Snyder, R. Altman, and S. Kim. Pacific Symposium on Biocomputing, page 339-350. World Scientific Publishing, (2012)Efficient genotype compression and analysis of large genetic variation datasetsR. Layer, N. Kindlon, K. Karczewski, E. ExAC, and A. Quinlan. bioRxiv, (Jun 5, 2015)Efficient genotype compression and analysis of large genetic-variation data setsR. Layer, N. Kindlon, K. Karczewski, and A. Quinlan. Nature Methods, 13 (1): 63--65 (Nov 9, 2015)The ExAC browser: displaying reference data information from over 60 000 exomes.K. Karczewski, B. Weisburd, B. Thomas, M. Solomonson, D. Ruderfer, D. Kavanagh, T. Hamamsy, M. Lek, K. Samocha, B. Cummings and 4 other author(s). Nucleic Acids Res., 45 (Database-Issue): D840-D845 (2017)Ten Simple Rules to Enable Multi-site Collaborations through Data Sharing.M. Boland, K. Karczewski, and N. Tatonetti. PLoS Comput. Biol., (2017)Session Introduction.K. Karczewski, N. Tatonetti, C. Patel, A. Manrai, C. Brown, and J. Ioannidis. PSB, page 117-119. (2017)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 and 174 other author(s). Nat., 581 (7809): 444-451 (2020)LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genes.A. Alasiri, K. Karczewski, B. Cole, B. Loza, J. Moore, S. der Laan, F. Asselbergs, B. Keating, and J. van Setten. BioData Min., (January 2023)

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Disambiguation of "Karczewski, Konrad J."

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A structural variation reference for medical and population genetics.

Please choose a person to relate this publication to

Stephan Karczewski

Roman Karczewski

Konrad J Rögner

Konrad J Kuhn

Stephan Karczewski

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Karczewski, Konrad J."

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

Stephan Karczewski

Roman Karczewski

Konrad J Rögner

Konrad J Kuhn

Stephan Karczewski

Other publications of authors with the same name

Disambiguation

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history of this post
URL
DOI
BibTeX
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A structural variation reference for medical and population genetics.