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Daniel C. Koboldt

2007–2024 年に発表

66
論文数
38,295
被引用数
44
h 指数
62
i10 指数

被引用数

Daniel C. Koboldt の年別被引用数1985 年: 被引用 1 件1989 年: 被引用 1 件1990 年: 被引用 1 件1992 年: 被引用 2 件1993 年: 被引用 1 件1995 年: 被引用 1 件1999 年: 被引用 2 件2002 年: 被引用 1 件2004 年: 被引用 4 件2006 年: 被引用 2 件2007 年: 被引用 5 件2008 年: 被引用 19 件2009 年: 被引用 236 件2010 年: 被引用 382 件2011 年: 被引用 602 件2012 年: 被引用 747 件2013 年: 被引用 958 件2014 年: 被引用 980 件2015 年: 被引用 860 件2016 年: 被引用 797 件2017 年: 被引用 722 件2018 年: 被引用 653 件2019 年: 被引用 1,598 件2020 年: 被引用 1,454 件2021 年: 被引用 1,325 件2022 年: 被引用 975 件2023 年: 被引用 708 件2024 年: 被引用 875 件2025 年: 被引用 431 件2026 年: 被引用 31 件1986〜1988 年は被引用が無いため表示していません1991 年は被引用が無いため表示していません1994 年は被引用が無いため表示していません1996〜1998 年は被引用が無いため表示していません2000〜2001 年は被引用が無いため表示していません2003 年は被引用が無いため表示していません2005 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 6,732 件、この内訳の 31.2%中国: 引用元論文 2,081 件、この内訳の 9.7%イギリス: 引用元論文 1,476 件、この内訳の 6.8%ドイツ: 引用元論文 1,114 件、この内訳の 5.2%カナダ: 引用元論文 815 件、この内訳の 3.8%イタリア: 引用元論文 760 件、この内訳の 3.5%フランス: 引用元論文 746 件、この内訳の 3.5%日本: 引用元論文 608 件、この内訳の 2.8%スペイン: 引用元論文 594 件、この内訳の 2.8%オランダ: 引用元論文 574 件、この内訳の 2.7%オーストラリア: 引用元論文 570 件、この内訳の 2.6%スイス: 引用元論文 441 件、この内訳の 2%
0%31.2%その他 23.4%

機関

分野

  • Biochemistry, Genetics and Molecular Biology48.7%
  • Medicine42%
  • Immunology and Microbiology3.3%
  • Agricultural and Biological Sciences1.4%
  • Neuroscience1.2%
  • Computer Science1.1%
  • その他2.3%

トピック

  • Cancer Genomics and Diagnostics7.5%
  • Glioma Diagnosis and Treatment3.8%
  • Acute Myeloid Leukemia Research3.7%
  • Epigenetics and DNA Methylation3.1%
  • RNA modifications and cancer2.2%
  • Genomics and Phylogenetic Studies2.1%
  • その他77.6%

共著者

全論文

検索で開く
  1. Comprehensive genomic characterization defines human glioblastoma genes and core pathways

    著者: Roger E. McLendon, D D Bigner, Allan H. Friedman, Erwin G. Van Meir, Gena M. Mastrogianakis, Jeffrey J. Olson, Daniel J. Brat, Tom Mikkelsen, Norman L. Lehman, Ken Aldape, W.K. Alfred Yung, Oliver Bögler, Scott Vandenberg, Mitchel S. Berger, Michael D. Prados, Donna M. Muzny, Margaret Morgan, Stephen W. Scherer, Aniko Sabo, Lynn Nazareth, Lora Lewis, Otis Hall, Yiming Zhu, Yanru Ren, Omar Alvi, Jiqiang Yao, Alicia Hawes, Shalini N. Jhangiani, Gerald Fowler, Anthony San Lucas, Christie Kovar, Andrew Cree, Huyen Dinh, Jireh Santibanez, Vandita Joshi, Manuel L. Gonzalez‐Garay, Christopher A. Miller, Aleksandar Milosavljevic, David A. Wheeler, Richard A. Gibbs, L A Donehower, Kristian Cibulskis, Carrie Sougnez, Tim Fennell, Scott Mahan, Jane Wilkinson, Liuda Ziaugra, Robert C. Onofrio, Toby Bloom, Robert Nicol, Kristin Ardlie, Jennifer Baldwin, Stacey Gabriel, Eric S. Lander, Gad Getz, Wendy Winckler, Roel G.W. Verhaak, Michael S. Lawrence, Michael O’Kelly, Jim Robinson, Gabriele Alexe, Rameen Beroukhim, Scott L. Carter, Derek Y. Chiang, Josh Gould, Supriya Gupta, Josh Korn, Craig H. Mermel, Jill P. Mesirov, Stefano Monti, Huy Nguyen, Melissa Parkin, Michael Reich, Nicolas Stransky, Barbara A. Weir, Levi A. Garraway, Todd R. Golub, Matthew Meyerson, Jun Li, Robert S. Fulton, Michael D. McLellan, John Wallis, David E. Larson, Xiaoqi Shi, Rachel M. Abbott, Lucinda Fulton, Ken Chen, Daniel C. Koboldt, Michael C. Wendl, Rick Meyer, Yuzhu Tang, Ling Lin, John R. Osborne, Brian H. Dunford-Shore, Tracie L. Miner, Kim D. Delehaunty, Chris Markovic, G.M. Swift, William Courtney, Craig Pohl - Nature 2008 被引用: 7,856

  2. VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing

    著者: Daniel C. Koboldt, Qunyuan Zhang, David E. Larson, Dong Shen, Michael D. McLellan, Ling Lin, Christopher A. Miller, Elaine R. Mardis, Li Ding, Richard K. Wilson - Genome Research 2012 被引用: 5,323

  3. Cancer exome analysis reveals a T-cell-dependent mechanism of cancer immunoediting

    著者: Hirokazu Matsushita, Matthew D. Vesely, Daniel C. Koboldt, Charles G. Rickert, Ravindra Uppaluri, Vincent Magrini, Cora D. Arthur, J. Michael White, Yee-Shiuan Chen, Lauren Shea, Jasreet Hundal, Michael C. Wendl, Ryan Demeter, Todd Wylie, James P. Allison, Mark J. Smyth, Lloyd J. Old, Elaine R. Mardis, Robert D. Schreiber - Nature 2012 被引用: 1,297

  4. Best practices for variant calling in clinical sequencing

    著者: Daniel C. Koboldt - Genome Medicine 2020 被引用: 411

  5. VarScan: variant detection in massively parallel sequencing of individual and pooled samples

    著者: Daniel C. Koboldt, Ken Chen, Todd Wylie, David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding - Bioinformatics, Bioinform. 2009 被引用: 1,427

  6. DNMT3A Mutations in Acute Myeloid Leukemia

    著者: Timothy J. Ley, Li Ding, Matthew J. Walter, Michael D. McLellan, Tamara Lamprecht, David E. Larson, Cyriac Kandoth, Jacqueline E. Payton, Jack Baty, John S. Welch, Christopher Harris, Cheryl F. Lichti, R. Reid Townsend, Robert S. Fulton, David J. Dooling, Daniel C. Koboldt, Heather K. Schmidt, Qunyuan Zhang, John R. Osborne, Ling Lin, Michelle D. O’Laughlin, Joshua F. McMichael, Kim D. Delehaunty, Sean McGrath, Lucinda A. Fulton, Vincent Magrini, Tammi L. Vickery, Jasreet Hundal, Lisa L. Cook, Joshua J. Conyers, Gary W. Swift, Jerry P. Reed, Patricia A. Alldredge, Todd Wylie, Jason Walker, Joelle Kalicki, Mark A. Watson, Sharon E. Heath, William D. Shannon, Nobish Varghese, Rakesh Nagarajan, Peter Westervelt, Michael H. Tomasson, Daniel C. Link, Timothy A. Graubert, John F. DiPersio, Elaine R. Mardis, Richard K. Wilson - New England Journal of Medicine 2010 被引用: 1,980

  7. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing

    著者: Li Ding, Timothy J. Ley, David E. Larson, Christopher A. Miller, Daniel C. Koboldt, John S. Welch, Julie Ritchey, Margaret A. Young, Tamara Lamprecht, Michael D. McLellan, Joshua F. McMichael, John W. Wallis, Charles Lu, Dong Shen, Christopher Harris, David J. Dooling, Robert S. Fulton, Lucinda Fulton, Ken Chen, Heather K. Schmidt, Joelle Kalicki-Veizer, Vincent Magrini, Lisa Cook, Sean McGrath, Tammi L. Vickery, Michael C. Wendl, Sharon E. Heath, Mark A. Watson, Daniel C. Link, Michael H. Tomasson, William D. Shannon, Jacqueline E. Payton, Shashikant Kulkarni, Peter Westervelt, Matthew J. Walter, Timothy A. Graubert, Elaine R. Mardis, Richard K. Wilson, John F. DiPersio - Nature 2012 被引用: 2,027

  8. Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome

    著者: Elaine R. Mardis, Li Ding, David J. Dooling, David E. Larson, Michael D. McLellan, Ken Chen, Daniel C. Koboldt, Robert S. Fulton, Kim D. Delehaunty, Sean McGrath, Lucinda A. Fulton, Devin P. Locke, Vincent Magrini, Rachel M. Abbott, Tammi L. Vickery, Jerry S. Reed, Jody S. Robinson, Todd Wylie, Scott M. Smith, Lynn K. Carmichael, James M. Eldred, Christopher Harris, Jason Walker, Joshua B. Peck, Feiyu Du, Adam F. Dukes, Gabriel E. Sanderson, Anthony M. Brummett, Eric M. Clark, Joshua F. McMichael, Rick Meyer, Jonathan K. Schindler, Craig Pohl, John W. Wallis, Xiaoqi Shi, Ling Lin, Heather K. Schmidt, Yuzhu Tang, Carrie A. Haipek, Madeline E. Wiechert, Jolynda V. Ivy, Joelle Kalicki, Glendoria Elliott, Rhonda E. Ries, Jacqueline E. Payton, Peter Westervelt, Michael H. Tomasson, Mark A. Watson, Jack Baty, Sharon E. Heath, William D. Shannon, Rakesh Nagarajan, Daniel C. Link, Matthew J. Walter, Timothy A. Graubert, John F. DiPersio, Richard K. Wilson, Timothy J. Ley - New England Journal of Medicine 2009 被引用: 2,226

  9. Activating HER2 Mutations in HER2 Gene Amplification Negative Breast Cancer

    著者: Ron Bose, Shyam M. Kavuri, Adam C. Searleman, Wei Shen, Dong Shen, Daniel C. Koboldt, John Monsey, Nicholas Goel, Adam B. Aronson, Shunqiang Li, X. Cynthia, Li Ding, Elaine R. Mardis, Matthew J. Ellis - Cancer Discovery 2012 被引用: 880

  10. Somatic mutations affect key pathways in lung adenocarcinoma

    著者: Li Ding, Gad Getz, David A. Wheeler, Elaine R. Mardis, Michael D. McLellan, Kristian Cibulskis, Carrie Sougnez, Heidi Greulich, Donna M. Muzny, Margaret Morgan, Lucinda Fulton, Robert S. Fulton, Qunyuan Zhang, Michael C. Wendl, Michael S. Lawrence, David E. Larson, Ken Chen, David J. Dooling, Aniko Sabo, Alicia Hawes, Hua Shen, Shalini N. Jhangiani, Lora Lewis, Otis Hall, Yiming Zhu, Tittu Mathew, Yanru Ren, Jiqiang Yao, Steven E. Scherer, Kerstin Clerc, Ginger Metcalf, Brian Ng, Aleksandar Milosavljevic, Manuel L. Gonzalez‐Garay, John R. Osborne, Rick Meyer, Xiaoqi Shi, Yuzhu Tang, Daniel C. Koboldt, Ling Lin, Rachel M. Abbott, Tracie L. Miner, Craig Pohl, Ginger Fewell, Carrie A. Haipek, Heather K. Schmidt, Brian H. Dunford-Shore, Aldi T. Kraja, Seth D. Crosby, Christopher S. Sawyer, Tammi L. Vickery, Sacha N Sander, Jody S. Robinson, Wendy Winckler, Jennifer Baldwin, Lucian R. Chirieac, Amit Dutt, Tim Fennell, Megan Hanna, Bruce E. Johnson, Robert C. Onofrio, Roman K. Thomas, Giovanni Tonon, Barbara A. Weir, Xiao‐Jun Zhao, Liuda Ziaugra, Michael C. Zody, Thomas J. Giordano, Mark B. Orringer, Jack A. Roth, Margaret R. Spitz, Ignacio I. Wistuba, Bradley A. Ozenberger, Peter J. Good, Andrew C. Chang, David G. Beer, Mark A. Watson, Marc Ladanyi, Stephen Broderick, Akihiko Yoshizawa, William D. Travis, William Pao, Michael A. Province, George M. Weinstock, Harold Varmus, Stacey Gabriel, Eric S. Lander, Richard A. Gibbs, Matthew Meyerson, Richard K. Wilson - Nature 2008 被引用: 2,750

  11. The Origin and Evolution of Mutations in Acute Myeloid Leukemia

    著者: John S. Welch, Timothy J. Ley, Daniel C. Link, Christopher A. Miller, David E. Larson, Daniel C. Koboldt, Lukas D. Wartman, Tamara Lamprecht, Fulu Liu, Jun Xia, Cyriac Kandoth, Robert S. Fulton, Michael D. McLellan, David J. Dooling, John W. Wallis, Ken Chen, Christopher Harris, Heather K. Schmidt, Joelle Kalicki-Veizer, Charles Lu, Qunyuan Zhang, Ling Lin, Michelle D. O’Laughlin, Joshua F. McMichael, Kim D. Delehaunty, Lucinda A. Fulton, Vincent Magrini, Sean McGrath, Ryan Demeter, Tammi L. Vickery, Jasreet Hundal, Lisa L. Cook, Gary W. Swift, Jerry P. Reed, Patricia A. Alldredge, Todd Wylie, Jason Walker, Mark A. Watson, Sharon E. Heath, William D. Shannon, Nobish Varghese, Rakesh Nagarajan, Jacqueline E. Payton, Jack Baty, Shashikant Kulkarni, Jeffery M. Klco, Michael H. Tomasson, Peter Westervelt, Matthew J. Walter, Timothy A. Graubert, John F. DiPersio, Li Ding, Elaine R. Mardis, Richard K. Wilson - Cell 2012 被引用: 1,576

  12. The Next-Generation Sequencing Revolution and Its Impact on Genomics

    著者: Daniel C. Koboldt, Karyn Meltz Steinberg, David E. Larson, Richard K. Wilson, Elaine R. Mardis - Cell 2013 被引用: 1,056

  13. SomaticSniper: identification of somatic point mutations in whole genome sequencing data

    著者: David E. Larson, Christopher C. Harris, Ken Chen, Daniel C. Koboldt, Travis E. Abbott, David J. Dooling, Timothy J. Ley, Elaine R. Mardis, Richard K. Wilson, Li Ding - Bioinformatics, Bioinform. 2011 被引用: 693

  14. MuSiC: Identifying mutational significance in cancer genomes

    著者: Nathan D. Dees, Qunyuan Zhang, Cyriac Kandoth, Michael C. Wendl, William Schierding, Daniel C. Koboldt, Thomas B. Mooney, Matthew B. Callaway, David J. Dooling, Elaine R. Mardis, Richard K. Wilson, Li Ding - Genome Research 2012 被引用: 740

  15. Whole-genome analysis informs breast cancer response to aromatase inhibition

    著者: Matthew J. Ellis, Li Ding, Dong Shen, Jingqin Luo, Vera J. Suman, John W. Wallis, Brian Andrew Van Tine, Jeremy Hoog, Reece Goiffon, Theodore C. Goldstein, Sam Ng, Lin Li, Robert J. Crowder, Jacqueline Snider, Karla V. Ballman, Jason D. Weber, Ken Chen, Daniel C. Koboldt, Cyriac Kandoth, William Schierding, Joshua F. McMichael, Christopher A. Miller, Charles Lu, Christopher Harris, Michael D. McLellan, Michael C. Wendl, Katherine DeSchryver, D. Craig Allred, Laura J. Esserman, Gary Unzeitig, Julie A. Margenthaler, Gildy V. Babiera, P. Kelly Marcom, J. Michael Guenther, Marilyn Leitch, Kelly K. Hunt, John A. Olson, Tao Yu, Christopher A. Maher, Lucinda Fulton, Robert S. Fulton, Michelle Harrison, Ben Oberkfell, Feiyu Du, Ryan Demeter, Tammi L. Vickery, Adnan Elhammali, Helen Piwnica‐Worms, Sandra McDonald, Mark A. Watson, David J. Dooling, David M. Ota, Li-Wei Chang, Ron Bose, Timothy J. Ley, David Piwnica‐Worms, Joshua M. Stuart, Richard K. Wilson, Elaine R. Mardis - Nature 2012 被引用: 1,035

  16. Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes

    著者: Timothy A. Graubert, Dong Shen, Li Ding, Theresa Okeyo-Owuor, Cara L Lunn, Jin Shao, Kilannin Krysiak, Christopher Harris, Daniel C. Koboldt, David E. Larson, Michael D. McLellan, David J. Dooling, Rachel M. Abbott, Robert S. Fulton, Heather K. Schmidt, Joelle Kalicki-Veizer, Michelle D. O’Laughlin, Marcus Grillot, Jack Baty, Sharon E. Heath, John L. Frater, Talat Nasim, Daniel C. Link, Michael H. Tomasson, Peter Westervelt, John F. DiPersio, Elaine R. Mardis, Timothy J. Ley, Richard K. Wilson, Matthew J. Walter - Nature Genetics 2011 被引用: 582

  17. The Alzheimer's Disease Sequencing Project: Study design and sample selection

    著者: Gary W. Beecham, Joshua C. Bis, Eden R. Martin, Seung Hoan Choi, Anita L. DeStefano, Cornelia M. van Duijn, Myriam Fornage, S.B. Gabriel, Daniel C. Koboldt, David E. Larson, A.C. Naj, Bruce M. Psaty, William Salerno, William S. Bush, Tatiana Foroud, Ellen M. Wijsman, Lindsay A. Farrer, Alison Goate, Jonathan L. Haines, Margaret A. Pericak‐Vance, Eric Boerwinkle, Richard Mayeux, Sudha Seshadri, Gerard D. Schellenberg - Neurology Genetics 2017 被引用: 237

  18. Patterns and functional implications of rare germline variants across 12 cancer types

    著者: Charles Lu, Mingchao Xie, Michael C. Wendl, Jiayin Wang, Michael D. McLellan, Mark D.M. Leiserson, Kuan‐lin Huang, Matthew A. Wyczalkowski, Reyka G. Jayasinghe, Tapahsama Banerjee, Jie Ning, Piyush Tripathi, Qunyuan Zhang, Beifang Niu, Kai Ye, Heather K. Schmidt, Robert S. Fulton, Joshua F. McMichael, Prag Batra, Cyriac Kandoth, Maheetha Bharadwaj, Daniel C. Koboldt, Christopher A. Miller, Krishna Kanchi, James M. Eldred, David E. Larson, John S. Welch, Ming You, Bradley A. Ozenberger, Ramaswamy Govindan, Matthew J. Walter, Matthew J. Ellis, Elaine R. Mardis, Timothy A. Graubert, John F. DiPersio, Timothy J. Ley, Richard K. Wilson, Paul J. Goodfellow, Benjamin J. Raphael, Feng Chen, Kimberly J. Johnson, Jeffrey D. Parvin, Li Ding - Nature Communications 2015 被引用: 313

  19. Genome remodelling in a basal-like breast cancer metastasis and xenograft

    著者: Li Ding, Matthew J. Ellis, Shunqiang Li, David E. Larson, Ken Chen, John W. Wallis, Christopher Harris, Michael D. McLellan, Robert S. Fulton, Lucinda Fulton, Rachel M. Abbott, Jeremy Hoog, David J. Dooling, Daniel C. Koboldt, Heather K. Schmidt, Joelle Kalicki, Qunyuan Zhang, Lei Chen, Ling Lin, Michael C. Wendl, Joshua F. McMichael, Vincent Magrini, Lisa Cook, Sean McGrath, Tammi L. Vickery, Elizabeth L. Appelbaum, Katherine DeSchryver, Sherri R. Davies, Therese Guintoli, Lin Li, Robert J. Crowder, Tao Yu, Jacqueline Snider, Scott M. Smith, Adam F. Dukes, Gabriel E. Sanderson, Craig Pohl, Kim D. Delehaunty, Catrina C. Fronick, Kimberley A. Pape, Jerry S. Reed, Jody S. Robinson, Jennifer S. Hodges, William Schierding, Nathan D. Dees, Dong Shen, Devin P. Locke, Madeline E. Wiechert, James M. Eldred, Josh B. Peck, Benjamin J. Oberkfell, Justin T. Lolofie, Feiyu Du, Amy Hawkins, Michelle D. O’Laughlin, Kelly E. Bernard, Mark Cunningham, Glendoria Elliott, Mark Mason, Dominic M. Thompson, Jennifer Ivanovich, Paul J. Goodfellow, Charles M. Perou, George M. Weinstock, Rebecca Aft, Mark A. Watson, Timothy J. Ley, Richard K. Wilson, Elaine R. Mardis - Nature 2010 被引用: 1,172

  20. Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection

    著者: Daniel C. Koboldt, David E. Larson, Richard K. Wilson - Current Protocols in Bioinformatics 2013 被引用: 225

  21. Detection of brain somatic variation in epilepsy‐associated developmental lesions

    著者: Tracy A. Bedrosian, Katherine E. Miller, Olivia Grischow, Kathleen M. Schieffer, Stephanie LaHaye, Hyojung Yoon, Anthony R. Miller, Jason B. Navarro, Jesse J. Westfall, Kristen Leraas, Samantha Choi, Rachel Williamson, James Fitch, Benjamin Kelly, Peter White, Kristy Lee, Sean McGrath, Catherine E. Cottrell, Vincent Magrini, Jeffrey R. Leonard, Jonathan Pindrik, Ammar Shaikhouni, Daniel R. Boué, Diana Thomas, Christopher R. Pierson, Richard K. Wilson, Adam P. Ostendorf, Elaine R. Mardis, Daniel C. Koboldt - Epilepsia 2022 被引用: 53

  22. Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domestication

    著者: Michael J. Montague, Gang Li, Barbara Gandolfi, Razib Khan, Bronwen Aken, S. Searle, Patrick Minx, LaDeana Hillier, Daniel C. Koboldt, Brian W. Davis, Carlos A. Driscoll, Christina S. Barr, Kevin Blackistone, Javier Quilez, Belén Lorente-Galdós, Tomàs Marquès‐Bonet, Can Alkan, Gregg W.C. Thomas, Matthew W. Hahn, Marilyn Menotti‐Raymond, Stephen J. O’Brien, Richard K. Wilson, Leslie A. Lyons, William J. Murphy, Wesley C. Warren - National Academy of Sciences, Proceedings of the National Academy of Sciences 2014 被引用: 360

  23. Clonal Architecture of Secondary Acute Myeloid Leukemia

    著者: Matthew J. Walter, Dong Shen, Li Ding, Jin Shao, Daniel C. Koboldt, Ken Chen, David E. Larson, Michael D. McLellan, David J. Dooling, Rachel M. Abbott, Robert S. Fulton, Vincent Magrini, Heather K. Schmidt, Joelle Kalicki-Veizer, Michelle D. O’Laughlin, Xian Fan, Marcus Grillot, Sarah Witowski, Sharon E. Heath, John L. Frater, William Eades, Michael H. Tomasson, Peter Westervelt, John F. DiPersio, Daniel C. Link, Elaine R. Mardis, Timothy J. Ley, Richard K. Wilson, Timothy A. Graubert - New England Journal of Medicine 2012 被引用: 771

  24. Exome sequencing of Finnish isolates enhances rare-variant association power

    著者: Adam E. Locke, Karyn Meltz Steinberg, Charleston W. K. Chiang, Susan K. Service, Aki S. Havulinna, Laurel Stell, Matti Pirinen, Haley Abel, Colby Chiang, Robert S. Fulton, Anne Jackson, Chul Joo Kang, Krishna Kanchi, Daniel C. Koboldt, David E. Larson, Joanne O. Nelson, Thomas J. Nicholas, Arto Pietilä, Vasily Ramensky, Debashree Ray, Laura J. Scott, Heather M. Stringham, Jagadish Vangipurapu, Ryan Welch, Pranav Yajnik, Xianyong Yin, Johan G. Eriksson, Mika Ala‐Korpela, Marjo‐Riitta Järvelin, Minna Männikkö, Hannele Laivuori, FinnGen Project, Susan K. Dutcher, Nathan O. Stitziel, Richard K. Wilson, Ira M. Hall, Chiara Sabatti, Aarno Palotie, Veikko Salomaa, Markku Laakso, Samuli Ripatti, Michael Boehnke, Nelson B. Freimer - Nature 2019 被引用: 217