Zuoming Deng

Active 1998–2025

22
Papers
24,819
Citations
18
h-index
20
i10-index

Citations

Citations per year for Zuoming Deng1877: 1 citations1930: 1 citations1966: 2 citations1973: 1 citations1991: 1 citations1993: 1 citations1997: 1 citations1998: 4 citations1999: 7 citations2000: 136 citations2001: 504 citations2002: 642 citations2003: 530 citations2004: 462 citations2005: 344 citations2006: 253 citations2007: 260 citations2008: 225 citations2009: 213 citations2010: 211 citations2011: 188 citations2012: 126 citations2013: 139 citations2014: 139 citations2015: 190 citations2016: 155 citations2017: 183 citations2018: 155 citations2019: 384 citations2020: 391 citations2021: 504 citations2022: 415 citations2023: 332 citations2024: 452 citations2025: 205 citations2026: 10 citations1878–1929: no citations, so these years are not shown1931–1965: no citations, so these years are not shown1967–1972: no citations, so these years are not shown1974–1990: no citations, so these years are not shown1992: no citations, so this year is not shown1994–1996: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,829 citing papers, 34.6% of this breakdownUnited Kingdom: 848 citing papers, 7.6% of this breakdownGermany: 689 citing papers, 6.2% of this breakdownChina: 682 citing papers, 6.2% of this breakdownFrance: 539 citing papers, 4.9% of this breakdownCanada: 417 citing papers, 3.8% of this breakdownJapan: 405 citing papers, 3.6% of this breakdownItaly: 320 citing papers, 2.9% of this breakdownAustralia: 288 citing papers, 2.6% of this breakdownSpain: 277 citing papers, 2.5% of this breakdownSwitzerland: 257 citing papers, 2.3% of this breakdownSweden: 209 citing papers, 1.9% of this breakdown
0%34.6%Other 20.9%

Fields

  • Biochemistry, Genetics and Molecular Biology55.6%
  • Medicine14.6%
  • Immunology and Microbiology10%
  • Neuroscience5.7%
  • Agricultural and Biological Sciences5.7%
  • Computer Science2.7%
  • Other5.7%

Topics

  • Genomics and Phylogenetic Studies5.4%
  • RNA and protein synthesis mechanisms4.2%
  • Chromosomal and Genetic Variations3%
  • interferon and immune responses2.8%
  • Inflammasome and immune disorders2.8%
  • Genomics and Chromatin Dynamics2.4%
  • Other79.4%

Coauthors

All papers

Open in search
  1. The Sequence of the Human Genome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Arnold J. Levine, Richard J. Roberts, Mel I. Simon, Carolyn W. Slayman, Michael W. Hunkapiller, Randall Bolanos, Arthur L. Delcher, Ian Dew, Daniel Fasulo, Michael J. Flanigan, Liliana Florea, Aaron L. Halpern, Sridhar Hannenhalli, Saul Kravitz, Samuel Lévy, Clark Mobarry, Knut Reinert, Karin Remington, Jane Abu-Threideh, Ellen M. Beasley, Kendra Biddick, Vivien Bonazzi, Rhonda Brandon, Michele Cargill, Ishwar Chandramouliswaran, Rosane Charlab, Kabir Chaturvedi, Zuoming Deng, Valentina Di Francesco, Patrick Dunn, Karen Eilbeck, Carlos Evangelista, Andrei Gabrielian, Weiniu Gan, Wangmao Ge, Fangcheng Gong, Zhiping Gu, Ping Guan, Thomas J. Heiman, Maureen E. Higgins, Rui‐Ru Ji, Zhaoxi Ke, Karen A. Ketchum, Zhongwu Lai, Yiding Lei, Zhenya Li, Jiayin Li, Yong Liang, Xiaoying Lin, Fu Lu, Gennady V. Merkulov, Natalia V. Milshina, Helen M. Moore, Ashwinikumar K. Naik, Vaibhav A. Narayan, Beena Neelam, Deborah Nusskern, Douglas B. Rusch, Steven L. Salzberg, Wei Shao, Bixiong Chris Shue, Jing‐Tao Sun, Zhen Yuan Wang, Aihui Wang, Xin Wang, Jian Wang, Ming-Hui Wei, Ron Wides, Chunlin Xiao, Chunhua Yan and 173 more - Science 2001 cited by 13,699

  2. Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Natalie Deuitch, Dorota Rowczenio, Emily Rominger, Kristina V Wells, Chyi‐Chia Richard Lee, Weixin Wang, Megan Trick, James C. Mullikin, Gustaf Wigerblad, Stephen R. Brooks, Stefania Dell’Orso, Zuoming Deng, Jae Jin Chae, Alina Dulau‐Florea, May Christine V. Malicdan, Danica Novacic, Robert A. Colbert, Mariana J. Kaplan, Massimo Gadina, Sinisa Savic, Helen J. Lachmann, Mones Abu‐Asab, Benjamin D. Solomon, Kyle Retterer, William A. Gahl, Shawn M. Burgess, Ivona Aksentijevich, Neal S. Young, Katherine R. Calvo, Achim Werner, Daniel L. Kastner, Peter C. Grayson - New England Journal of Medicine 2020 cited by 1,154

  3. Activated STING in a Vascular and Pulmonary Syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrei Barysenka, Fabio Candotti, Steven M. Holland, Jason D. Hughes, Huseyin Mehmet, Andrew C. Issekutz, M Raffeld, Joshua McElwee, JÉRǑMe Fontana, Caterina P. Minniti, Susan Moir, Daniel L. Kastner, Massimo Gadina, A.C. Steven, Paul T. Wingfield, Stephen R. Brooks, Sergio D. Rosenzweig, Thomas A. Fleisher, Zuoming Deng, Manfred Boehm, Amy S. Paller, Raphaela Goldbach‐Mansky - New England Journal of Medicine 2014 cited by 1,387

  4. The Genome Sequence of Drosophila melanogaster

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , George L. Gabor, Miklós, Josep F. Abril, Anna Agbayani, Hui-Jin An, Cynthia Andrews‐Pfannkoch, Danita Baldwin, Richard M. Ballew, Anand Basu, James Baxendale, Leyla Bayraktaroglu, Ellen M. Beasley, Karen Beeson, Panayiotis V. Benos, Benjamin P. Berman, Deepali Bhandari, Slava Bolshakov, Dana Borkova, Michael R. Botchan, John Bouck, Peter Brokstein, Phillipe Brottier, Kenneth C. Burtis, Dana Busam, H. Butler, Édouard Cadieu, Ishwar Chandra, J. Michael Cherry, Simon Cawley, Carl Dahlke, Lionel B. Davenport, Peter L. Davies, Beatriz de Pablos, Arthur L. Delcher, Zuoming Deng, Anne Deslattes Mays, Ian Dew, Suzanne M. Dietz, Kristina Dodson, Lisa Doup, Michael Downes, Shannon Dugan-Rocha, Boris C. Dunkov, Patrick Dunn, Kenneth J. Durbin, Carlos Evangelista, Concepción Ferraz, Steven Ferriera, Wolfgang Fleischmann, Carl Fosler, Andrei Gabrielian, Neha Garg, William M Gelbart, Ken Glasser, Anna Glodek, Fangcheng Gong, James H. Gorrell, Zhiping Gu, Ping Guan, Michael A. Harris, Nomi L. Harris, Damon A. Harvey, Thomas J. Heiman, Judith Hernandez, Jarrett Houck, Damon Hostin, Kathryn A. Houston, Timothy J. Howland, Ming-Hui Wei, Chinyere Ibegwam and 95 more - Science 2000 cited by 6,042

  5. An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2014 cited by 735

  6. Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sinisa Savic, Daniel L. Kastner, Amanda K. Ombrello, David B. Beck, Peter C. Grayson - Arthritis & Rheumatology 2021 cited by 238

  7. Distinct interferon signatures and cytokine patterns define additional systemic autoinflammatory diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ian Ferguson, Polly J. Ferguson, Laura S. Finn, Marco Gattorno, Alexei A. Grom, Eric P. Hanson, Philip J. Hashkes, Christian M. Hedrich, Ronit Herzog, Gerd Horneff, Rita Jerath, Elizabeth A. Kessler, Hanna Kim, D. Kingsbury, Ronald M. Laxer, Pui Y. Lee, Min Ae Lee‐Kirsch, Laura B. Lewandowski, Suzanne C. Li, Vibke Lilleby, Vafa Mammadova, Lakshmi N. Moorthy, Gulnara Nasrullayeva, Kathleen M. O’Neil, Karen Onel, Seza Özen, Nancy Pan, Pascal Pillet, Daniela Gerent Petry Piotto, Marilynn Punaro, Andreas Reiff, Adam Reinhardt, Lisa G. Rider, Rafael Rivas‐Chacon, Tova Ronis, Angela Rösen‐Wolff, Johannes Roth, Natasha M. Ruth, Marite Rygg, Heinrike Schmeling, Grant S. Schulert, Christiaan Scott, Gisella Seminario, Andrew Shulman, Vidya Sivaraman, Mary Beth F. Son, Yuriy Stepanovskiy, Elizabeth Stringer, Sara Mansfield Taber, Maria Teresa Terreri, Cynthia J. Tifft, Troy R. Torgerson, Laura L. Tosi, Annet van Royen‐Kerkhof, Theresa Wampler Muskardin, Scott Canna, Raphaela Goldbach‐Mansky - Journal of Clinical Investigation 2019 cited by 239

  8. Novel proteasome assembly chaperone mutations in PSMG2/PAC2 cause the autoinflammatory interferonopathy CANDLE/PRAAS4

    Authors: , , , , , , , , , - Journal of Allergy and Clinical Immunology 2019 cited by 113

  9. Implications of combined NOD2 and other gene mutations in autoinflammatory diseases

    Authors: , , , , , , , , - Frontiers in Immunology 2023 cited by 25

  10. Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Danielle Fink, Radana Kotalová, Zuzana Paračková, Lucie Peterková, Daniela Kužílková, Vít Campr, Lucie Šrámková, Angélique Biancotto, Stephen R. Brooks, Cameron Manes, Eric Meffre, Rebecca L. Harper, Hye Sun Kuehn, Mariana J. Kaplan, Paul Brogan, Sergio D. Rosenzweig, Melinda S. Merchant, Zuoming Deng, Anna Huttenlocher, Susan Moir, Douglas B. Kuhns, Manfred Boehm, Karolina Škvárová Kramarzová, Raphaela Goldbach‐Mansky - Nature Communications 2023 cited by 35

  11. Genetically programmed alternative splicing of NEMO mediates an autoinflammatory disease phenotype

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Journal of Clinical Investigation 2022 cited by 42

  12. Somatic activating mutations in MAP2K1 cause melorheostosis

    Authors: , , , , , , , , , , , , , , , - Nature Communications 2018 cited by 82

  13. Inactivating Mutation in IRF8 Promotes Osteoclast Transcriptional Programs and Increases Susceptibility to Tooth Root Resorption

    Authors: , , , , , , , , , , , , - Journal of Bone and Mineral Research 2019 cited by 35

  14. Enrichment of Rare Variants of Hemophagocytic Lymphohistiocytosis Genes in Systemic Juvenile Idiopathic Arthritis

    Authors: , , , , , , , , , , , , , , , , , , , , , - Arthritis & Rheumatology 2024 cited by 11

  15. Familial Mediterranean Fever at the Millennium Clinical Spectrum, Ancient Mutations, and a Survey of 100 American Referrals to the National Institutes of Health

    Authors: , , , , , , - Medicine 1998 cited by 357

  16. Somatic SMAD3-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathway

    Authors: , , , , , , , , , , , , , , , , - The Journal of Experimental Medicine 2020 cited by 48

  17. A Comparison of Whole-Genome Shotgun-Derived Mouse Chromosome 16 and the Human Genome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jane J. Ye, Shibu Yooseph, Qi Zhao, Liansheng Zheng, Shiaoping C. Zhu, Kendra Biddick, Randall Bolanos, Arthur L. Delcher, Ian Dew, Daniel Fasulo, Michael J. Flanigan, Daniel H. Huson, Saul Kravitz, Jason Miller, Clark Mobarry, Knut Reinert, Karin Remington, Qing Zhang, Xiangqun Zheng-Bradley, Deborah Nusskern, Zhongwu Lai, Yiding Lei, Wenyan Zhong, Alison Yao, Ping Guan, Rui‐Ru Ji, Zhiping Gu, Zhenyuan Wang, Fei Zhong, Chunlin Xiao, Chia-Chien Chiang, Mark Yandell, Jennifer R. Wortman, Peter G. Amanatides, Suzanne L. Hladun, Eric C. Pratts, Jeffery E. Johnson, Kristina Dodson, Kerry J. Woodford, Cheryl Evans, Barry Gropman, Douglas B. Rusch, Eli Venter, Mei Wang, Thomas J. Smith, Jarrett Houck, Donald E. Tompkins, Charles A. Haynes, Debbie Jacob, Soo Chin, David R. Allen, Carl Dahlke, Robert D. Sanders, Kelvin Li, Xiangjun Liu, Alexander A. Levitsky, William H. Majoros, Quan Chen, Ashley C. Xia, John Lopez, Michael Donnelly, Matthew Newman, Anna Glodek, Cheryl Kraft, Marc Nodell, Feroze Ali, Hui-Jin An, Danita Baldwin-Pitts, Karen Beeson, Shuang Cai and 76 more - Science 2002 cited by 370

  18. Genetic variations in NLRP3 and NLRP12 genes in adult-onset patients with autoinflammatory diseases: a comparative study

    Authors: , , , , , , , , - Frontiers in Immunology 2024 cited by 9

  19. Next generation sequencing analysis reveals complex genetic architecture of childhood-onset systemic lupus erythematosus

    Authors: , , , , , , , , , , , , , , , , , - Lupus Science & Medicine 2025 cited by 6

  20. Diagnosis of Familial Mediterranean Fever by a Molecular Genetics Method

    Authors: , , , , - Annals of Internal Medicine 1998 cited by 97

  21. Gene and alternative splicing annotation with AIR

    Authors: , , , , , , , , , , , , , , - Genome Research 2005 cited by 78

  22. Melorheostotic Bone Lesions Caused by Somatic Mutations in MAP2K1 Have Deteriorated Microarchitecture and Periosteal Reaction

    Authors: , , , , , , , , , , , , , , - Journal of Bone and Mineral Research 2019 cited by 17

All 22 papers shown.