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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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Stacey Jeffery

Gabriel Grün

Katharina Gabriel

Gabriel Eikenberg

Oscar Gabriel

Other publications of authors with the same name

An immunogenic personal neoantigen vaccine for patients with melanomaP. Ott, Z. Hu, D. Keskin, S. Shukla, J. Sun, D. Bozym, W. Zhang, A. Luoma, A. Giobbie-Hurder, L. Peter and 30 other author(s). Nature, 547 (7662): 217--221 (July 2017)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)Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA, IDH1, EGFR, and NF1R. Verhaak, K. Hoadley, E. Purdom, V. Wang, Y. Qi, M. Wilkerson, C. Miller, L. Ding, T. Golub, J. Mesirov and 23 other author(s). Cancer Cell, 17 (1): 98--110 (2010)Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA, IDH1, EGFR, and NF1R. Verhaak, K. Hoadley, E. Purdom, V. Wang, Y. Qi, M. Wilkerson, C. Miller, L. Ding, T. Golub, J. Mesirov and 23 other author(s). Cancer Cell, 17 (1): 98 - 110 (2010)Advances in understanding cancer genomes through second-generation sequencing.M. Meyerson, S. Gabriel, and G. Getz. Nature reviews. Genetics, 11 (10): 685--696 (Oct 17, 2010)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)Comprehensive genomic characterization defines human glioblastoma genes and core pathwaysT. Network, R. McLendon, A. Friedman, D. Bigner, E. Van Meir, D. Brat, G. M. Mastrogianakis, J. Olson, T. Mikkelsen, N. Lehman and 222 other author(s). Nature, (September 2008)Sensitive detection of somatic point mutations in impure and heterogeneous cancer samplesK. Cibulskis, M. Lawrence, S. Carter, A. Sivachenko, D. Jaffe, C. Sougnez, S. Gabriel, M. Meyerson, E. Lander, and G. Getz. Nature Biotechnology, 31 (3): 213--219 (2013)Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic PipelinesK. Ellrott, M. Bailey, G. Saksena, K. Covington, C. Kandoth, C. Stewart, J. Hess, S. Ma, K. Chiotti, M. McLellan and 730 other author(s). Cell Systems, 6 (3): 271--281.e7 (March 2018)Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 PatientsA. Kahles, K. Lehmann, N. Toussaint, M. Hüser, S. Stark, T. Sachsenberg, O. Stegle, O. Kohlbacher, C. Sander, S. Caesar-Johnson and 725 other author(s). Cancer Cell, 34 (2): 211--224.e6 (August 2018)

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Disambiguation of "Gabriel, Stacey"

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A structural variation reference for medical and population genetics.

Please choose a person to relate this publication to

Stacey Jeffery

Gabriel Grün

Katharina Gabriel

Gabriel Eikenberg

Oscar Gabriel

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Gabriel, Stacey"

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

Stacey Jeffery

Gabriel Grün

Katharina Gabriel

Gabriel Eikenberg

Oscar Gabriel

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
community post
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.