Aaron M. Wenger

2010–2025 年に発表

53
論文数
19,931
被引用数
39
h 指数
48
i10 指数

被引用数

Aaron M. Wenger の年別被引用数1976 年: 被引用 1 件1987 年: 被引用 2 件1993 年: 被引用 1 件1996 年: 被引用 1 件2000 年: 被引用 1 件2001 年: 被引用 1 件2006 年: 被引用 1 件2007 年: 被引用 1 件2009 年: 被引用 2 件2010 年: 被引用 3 件2011 年: 被引用 21 件2012 年: 被引用 63 件2013 年: 被引用 96 件2014 年: 被引用 111 件2015 年: 被引用 111 件2016 年: 被引用 118 件2017 年: 被引用 152 件2018 年: 被引用 208 件2019 年: 被引用 671 件2020 年: 被引用 749 件2021 年: 被引用 1,000 件2022 年: 被引用 1,083 件2023 年: 被引用 1,068 件2024 年: 被引用 1,470 件2025 年: 被引用 746 件2026 年: 被引用 47 件1977〜1986 年は被引用が無いため表示していません1988〜1992 年は被引用が無いため表示していません1994〜1995 年は被引用が無いため表示していません1997〜1999 年は被引用が無いため表示していません2002〜2005 年は被引用が無いため表示していません2008 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 3,466 件、この内訳の 28.8%中国: 引用元論文 1,082 件、この内訳の 9%イギリス: 引用元論文 836 件、この内訳の 6.9%ドイツ: 引用元論文 829 件、この内訳の 6.9%カナダ: 引用元論文 467 件、この内訳の 3.9%オーストラリア: 引用元論文 396 件、この内訳の 3.3%フランス: 引用元論文 393 件、この内訳の 3.3%オランダ: 引用元論文 353 件、この内訳の 2.9%スペイン: 引用元論文 341 件、この内訳の 2.8%イタリア: 引用元論文 334 件、この内訳の 2.8%日本: 引用元論文 309 件、この内訳の 2.6%スイス: 引用元論文 232 件、この内訳の 1.9%
0%28.8%その他 24.9%

分野

  • Biochemistry, Genetics and Molecular Biology70.6%
  • Medicine13.1%
  • Agricultural and Biological Sciences5.6%
  • Immunology and Microbiology3.9%
  • Neuroscience3.1%
  • Computer Science1%
  • その他2.7%

トピック

  • Genomics and Phylogenetic Studies7.6%
  • Genomics and Chromatin Dynamics5.3%
  • Genomics and Rare Diseases5.1%
  • Epigenetics and DNA Methylation5%
  • Chromosomal and Genetic Variations3.8%
  • RNA modifications and cancer3%
  • その他70.2%

共著者

全論文

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  1. The complete sequence of a human genome

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Robert S. Fulton, Arkarachai Fungtammasan, Erik Garrison, Patrick G. S. Grady, Tina A. Graves-Lindsay, Ira M. Hall, Nancy F. Hansen, Gabrielle A. Hartley, Marina Haukness, Kerstin Howe, Michael W. Hunkapiller, Chirag Jain, Miten Jain, Erich D. Jarvis, Peter Kerpedjiev, Melanie Kirsche, Mikhail Kolmogorov, Jonas Korlach, Milinn Kremitzki, Heng Li, Valerie V. Maduro, Tobias Marschall, Ann M. Mc Cartney, Jennifer McDaniel, Danny E. Miller, James C. Mullikin, Eugene W. Myers, Nathan D. Olson, Benedict Paten, Paul Peluso, Pavel A. Pevzner, David Porubskỳ, Tamara Potapova, Е. И. Рогаев, Jeffrey Rosenfeld, Steven L. Salzberg, Valérie Schneider, Fritz J. Sedlazeck, Kishwar Shafin, Colin J. Shew, Alaina Shumate, Ying Sims, Arian F. A. Smit, Daniela C. Soto, Ivan Sović, Jessica M. Storer, Aaron Streets, Beth A. Sullivan, Françoise Thibaud‐Nissen, James Torrance, Justin Wagner, Brian P. Walenz, Aaron M. Wenger, Jonathan Wood, Chunlin Xiao, Stephanie M. Yan, Alice Young, Samantha Zarate, Urvashi Surti, Rajiv C. McCoy, Megan Y. Dennis, Ivan A. Alexandrov, Jennifer L. Gerton, Rachel J. O’Neill, Winston Timp, Justin M. Zook, Michael C. Schatz, Evan E. Eichler, Karen H. Miga, Adam M. Phillippy - Science 2022 被引用: 3,421

  2. GREAT improves functional interpretation of cis-regulatory regions

    著者: , , , , , , , - Nature Biotechnology 2010 被引用: 5,003

  3. Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Biotechnology 2019 被引用: 1,944

  4. Haplotype-resolved diverse human genomes and integrated analysis of structural variation

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marta Byrska-Bishop, André Corvelo, Uday S. Evani, Tsung-Yu Lu, Mark Chaisson, Junjie Chen, Chong Li, Harrison Brand, Aaron M. Wenger, Maryam Ghareghani, William T. Harvey, Benjamin Raeder, Patrick Hasenfeld, Allison Regier, Haley Abel, Ira M. Hall, Paul Flicek, Oliver Stegle, Mark Gerstein, José M. C. Tubío, Zepeng Mu, Yang Li, Xinghua Shi, Alex Hastie, Kai Ye, Zechen Chong, Ashley D. Sanders, Michael C. Zody, Michael E. Talkowski, Ryan E. Mills, Scott E. Devine, Charles Lee, Jan O. Korbel, Tobias Marschall, Evan E. Eichler - Science 2021 被引用: 816

  5. Multi-platform discovery of haplotype-resolved structural variation in human genomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zechen Chong, Nelson T. Chuang, Christine Lambert, Deanna M. Church, Laura Clarke, Andrew Farrell, Joey Flores, Timur R. Galeev, David U. Gorkin, Madhusudan Gujral, Victor Guryev, Haynes Heaton, Jonas Korlach, Sushant Kumar, Jee Young Kwon, Ernest T. Lam, Jong Eun Lee, Joyce Lee, Wan-Ping Lee, Sau Peng Lee, Shantao Li, Patrick Marks, Karine A. Viaud‐Martinez, Sascha Meiers, Katherine M. Munson, Fábio C. P. Navarro, Bradley J. Nelson, Conor Nodzak, Amina Noor, Sofia Kyriazopoulou-Panagiotopoulou, Andy Wing Chun Pang, Yunjiang Qiu, Gabriel Rosanio, Mallory Ryan, Adrian M. Stütz, Diana C.J. Spierings, Alistair Ward, AnneMarie E. Welch, Ming Xiao, Wei Xu, Chengsheng Zhang, Qihui Zhu, Xiangqun Zheng-Bradley, Ernesto Lowy, Sergei Yakneen, Steven A. McCarroll, Goo Jun, Li Ding, Chong‐Lek Koh, Bing Ren, Paul Flicek, Ken Chen, Mark Gerstein, Pui–Yan Kwok, Peter M. Lansdorp, Gábor Marth, Jonathan Sebat, Xinghua Shi, Ali Bashir, Kai Ye, Scott E. Devine, Michael E. Talkowski, Ryan E. Mills, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Charles Lee - Nature Communications 2019 被引用: 1,040

  6. Variant Review with the Integrative Genomics Viewer

    著者: , , , , - Cancer Research 2017 被引用: 1,251

  7. A robust benchmark for detection of germline large deletions and insertions

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Arda Söylev, Michael C. Schatz, Shilpa Garg, George M. Church, Tobias Marschall, Ken Chen, Xian Fan, Adam C. English, Jeffrey Rosenfeld, Weichen Zhou, Ryan E. Mills, Jay M. Sage, Jennifer R. Davis, Michael D. Kaiser, John S. Oliver, Anthony P. Catalano, Mark Chaisson, Noah Spies, Fritz J. Sedlazeck, Marc Salit - Nature Biotechnology 2020 被引用: 483

  8. M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity

    著者: , , , , , , , - Nature Genetics 2016 被引用: 917

  9. Curated variation benchmarks for challenging medically relevant autosomal genes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Karen H. Miga, Mark Ebbert, Alaina Shumate, Heng Li, Chen-Shan Chin, Justin M. Zook, Fritz J. Sedlazeck - Nature Biotechnology 2022 被引用: 252

  10. Characterization and visualization of tandem repeats at genome scale

    著者: , , , , , , , , , , , , , , , , , , , , , , - Nature Biotechnology 2024 被引用: 125

  11. DeepConsensus improves the accuracy of sequences with a gap-aware sequence transformer

    著者: , , , , , , , , , , , , , , , , , , - Nature Biotechnology 2022 被引用: 153

  12. Semi-automated assembly of high-quality diploid human reference genomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alex Hastie, Marina Haukness, Erich Jaeger, Miten Jain, Melanie Kirsche, Mikhail Kolmogorov, Jan O. Korbel, Sergey Koren, Jonas Korlach, Joyce Lee, Daofeng Li, Tina Lindsay, Julian Lucas, Feng Luo, Tobias Marschall, Matthew W. Mitchell, Jennifer McDaniel, Fan Nie, Hugh E. Olsen, Nathan D. Olson, Trevor Pesout, Tamara Potapova, Daniela Puiu, Allison Regier, Jue Ruan, Steven L. Salzberg, Ashley D. Sanders, Michael C. Schatz, Anthony D. Schmitt, Valérie Schneider, Siddarth Selvaraj, Kishwar Shafin, Alaina Shumate, Nathan O. Stitziel, Catherine Stober, James Torrance, Justin Wagner, Jianxin Wang, Aaron M. Wenger, Chuan‐Le Xiao, Aleksey V. Zimin, Guojie Zhang, Ting Wang, Heng Li, Erik Garrison, David Haussler, Ira M. Hall, Justin M. Zook, Evan E. Eichler, Adam M. Phillippy, Benedict Paten, Kerstin Howe, Karen H. Miga - Nature 2022 被引用: 229

  13. Benchmarking challenging small variants with linked and long reads

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Álvaro Martínez Barrio, Ian T. Fiddes, Chunlin Xiao, Arkarachai Fungtammasan, Chen-Shan Chin, Aaron M. Wenger, William J. Rowell, Fritz J. Sedlazeck, Andrew Carroll, Marc Salit, Justin M. Zook - Cell Genomics 2022 被引用: 209

  14. Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Margaret Gibson, Jeffrey A. Goldstein, Elin Grundberg, Kelsee Halpin, Brian S. Harvey, Bryce A. Heese, Wendy Hein, Suzanne Herd, Susan Hughes, Mohammed Ilyas, Jill D. Jacobson, Janda Jenkins, Jiang Shao, Jeffrey Johnston, Kathryn Keeler, Jonas Korlach, Jennifer Kussmann, Christine Lambert, Caitlin E. Lawson, Jean‐Baptiste Le Pichon, J. Steven Leeder, Vicki C. Little, Daniel Louiselle, Michael Lypka, Brittany McDonald, Neil Miller, Ann Modrcin, Annapoorna Nair, Shelby H. Neal, Christopher M. Oermann, Donna Pacicca, Kailash Pawar, Nyshele Posey, Nigel Price, Laura Puckett, Julio Quezada, Nikita Raje, William J. Rowell, Eric T. Rush, Venkatesh Sampath, Carol Saunders, Caitlin Schwager, Richard M. Schwend, Elizabeth Shaffer, Craig Smail, Sarah Soden, Meghan E. Strenk, Bonnie Sullivan, Brooke Sweeney, Jade Tam‐Williams, Adam M. Walter, Holly Welsh, Aaron M. Wenger, Laurel K. Willig, Yun Yan, Scott T. Younger, Dihong Zhou, Tricia Zion, Isabelle Thiffault, Tomi Pastinen - Genetics in Medicine 2022 被引用: 98

  15. AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature

    著者: , , , , , , , , , , , , , , - Science Translational Medicine 2020 被引用: 125

  16. Systematic reanalysis of clinical exome data yields additional diagnoses: implications for providers

    著者: , , , - Genetics in Medicine 2016 被引用: 329

  17. Human-specific tandem repeat expansion and differential gene expression during primate evolution

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Danny Antaki, Thomas Anantharaman, Peter A. Audano, Harrison Brand, Stuart Cantsilieris, Han Cao, Eliza Cerveira, Chong Chen, Xintong Chen, Chen-Shan Chin, Zechen Chong, Nelson T. Chuang, Christine Lambert, Deanna M. Church, Laura Clarke, Andrew Farrell, Joey Flores, Timur Galeey, David U. Gorkin, Madhusudan Gujral, Victor Guryev, Haynes Heaton, Jonas Korlach, Sushant Kumar, Jee Young Kwon, Ernest T. Lam, Jong Eun Lee, Joyce Lee, Wan‐Ping Lee, Sau Peng Lee, Shantao Li, Patrick Marks, Karine A. Viaud-Martinez, Sascha Meiers, Katherine M. Munson, Fábio C. P. Navarro, Bradley J. Nelson, Conor Nodzak, Amina Noor, Sofia Kyriazopoulou-Panagiotopoulou, Andy Wing Chun Pang, Yunjiang Qiu, Gabriel Rosanio, Mallory Ryan, Adrian M. Stütz, Diana C.J. Spierings, Alistair Ward, AnneMarie E. Welch, Ming Xiao, Wei Xu, Chengsheng Zhang, Qihui Zhu, Xiangqun Zheng-Bradley, Ernesto Lowy, Sergei Yakneen, Steven A. McCarroll, Goo Jun, Li Ding, Chong‐Lek Koh, Bing Ren, Paul Flicek, Ken Chen, Mark Gerstein, Pui–Yan Kwok, Peter M. Lansdorp, Gábor Marth, Jonathan Sebat, Xinghua Shi, Ali Bashir, Kai Ye ほか 7 名 - National Academy of Sciences, Proceedings of the National Academy of Sciences 2019 被引用: 158

  18. Long-read genome sequencing identifies causal structural variation in a Mendelian disease

    著者: , , , , , , , , , , , , , , , , , , - Genetics in Medicine 2017 被引用: 275

  19. Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort

    著者: , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2023 被引用: 43

  20. Human-specific loss of regulatory DNA and the evolution of human-specific traits

    著者: , , , , , , , , , , , , - Nature 2011 被引用: 562

  21. HiPhase: jointly phasing small, structural, and tandem repeat variants from HiFi sequencing

    著者: , , , , , - Bioinformatics, Bioinform. 2024 被引用: 43

  22. Approaches to long-read sequencing in a clinical setting to improve diagnostic rate

    著者: , , , , , , , , , , , , - Scientific Reports 2022 被引用: 55

  23. Comprehensive de novo mutation discovery with HiFi long-read sequencing

    著者: , , , , , , , , , , , , , - Genome Medicine 2023 被引用: 58

  24. Microbiota modulate transcription in the intestinal epithelium without remodeling the accessible chromatin landscape

    著者: , , , , , , , , , - Genome Research 2014 被引用: 166