Michael H. Hastings

Active 1985–2025

Also published as
Michael H Hastings
115
Papers
25,135
Citations
85
h-index
112
i10-index

Citations

Citations per year for Michael H. Hastings1962: 2 citations1982: 2 citations1987: 2 citations1988: 2 citations1989: 3 citations1991: 6 citations1992: 11 citations1993: 25 citations1994: 21 citations1995: 21 citations1996: 32 citations1997: 19 citations1998: 39 citations1999: 49 citations2000: 154 citations2001: 202 citations2002: 233 citations2003: 260 citations2004: 177 citations2005: 239 citations2006: 246 citations2007: 347 citations2008: 248 citations2009: 272 citations2010: 355 citations2011: 257 citations2012: 253 citations2013: 350 citations2014: 296 citations2015: 217 citations2016: 230 citations2017: 212 citations2018: 213 citations2019: 711 citations2020: 771 citations2021: 770 citations2022: 527 citations2023: 515 citations2024: 676 citations2025: 343 citations2026: 4 citations1963–1981: no citations, so these years are not shown1983–1986: no citations, so these years are not shown1990: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,485 citing papers, 31.7% of this breakdownUnited Kingdom: 769 citing papers, 9.8% of this breakdownChina: 597 citing papers, 7.6% of this breakdownGermany: 486 citing papers, 6.2% of this breakdownJapan: 446 citing papers, 5.7% of this breakdownFrance: 333 citing papers, 4.3% of this breakdownCanada: 279 citing papers, 3.6% of this breakdownSwitzerland: 227 citing papers, 2.9% of this breakdownNetherlands: 215 citing papers, 2.7% of this breakdownItaly: 184 citing papers, 2.3% of this breakdownAustralia: 155 citing papers, 2% of this breakdownSpain: 152 citing papers, 1.9% of this breakdown
0%31.7%Other 19.3%

Fields

  • Neuroscience73.6%
  • Biochemistry, Genetics and Molecular Biology9.6%
  • Medicine9%
  • Agricultural and Biological Sciences2.8%
  • Psychology2.3%
  • Environmental Science0.7%
  • Other2%

Topics

  • Circadian rhythm and melatonin24.3%
  • Light effects on plants5.4%
  • Sleep and Wakefulness Research5.2%
  • Dietary Effects on Health4.5%
  • Photoreceptor and optogenetics research4.2%
  • Spaceflight effects on biology4%
  • Other52.4%

Coauthors

All papers

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  1. Generation of circadian rhythms in the suprachiasmatic nucleus

    Authors: , , - Nature reviews. Neuroscience 2018 cited by 1,058

  2. Behaviorally consequential astrocytic regulation of neural circuits

    Authors: , , , , , , , , , , - Neuron 2020 cited by 317

  3. Peroxiredoxins are conserved markers of circadian rhythms

    Authors: , , , , , , , , , , , , , , , , , , - Nature 2012 cited by 934

  4. Medicine in the Fourth Dimension

    Authors: , , , , , , , , , , , , , , , , , - Cell Metabolism 2019 cited by 367

  5. mCRY1 and mCRY2 Are Essential Components of the Negative Limb of the Circadian Clock Feedback Loop

    Authors: , , , , , , , , - Cell 1999 cited by 1,622

  6. Astrocytes Control Circadian Timekeeping in the Suprachiasmatic Nucleus via Glutamatergic Signaling

    Authors: , , , , - Neuron 2017 cited by 433

  7. Cell-autonomous clock of astrocytes drives circadian behavior in mammals

    Authors: , , , , , , - Science 2019 cited by 328

  8. A clockwork web: circadian timing in brain and periphery, in health and disease

    Authors: , , - Nature reviews. Neuroscience 2003 cited by 1,195

  9. Guidelines for Genome-Scale Analysis of Biological Rhythms

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Paul de Goede, Susan S. Golden, Carla A. Green, John Harer, Stacey L. Harmer, Jeff Haspel, Michael H. Hastings, Hanspeter Herzel, Erik D. Herzog, Christy M. Hoffmann, Christian I. Hong, Jacob Hughey, Jennifer Hurley, Horacio O. de la Iglesia, Carl Hirschie Johnson, Steve A. Kay, Nobuya Koike, Karl Kornacker, Achim Kramer, Katja Lamia, Tanya Leise, Scott A. Lewis, Jiajia Li, Xiaodong Li, Andrew C. Liu, Jennifer Loros, Tami A. Martino, Jérôme S. Menet, Martha Merrow, Andrew J. Millar, Todd C. Mockler, Félix Naef, Emi Nagoshi, Michael N. Nitabach, María Olmedo, Dmitri A. Nusinow, Louis J. Ptáček, D.A.J. Rand, Akhilesh B. Reddy, María S. Robles, Till Roenneberg, Michael Rosbash, Marc D. Ruben, Samuel S. C. Rund, Aziz Sancar, Paolo Sassone‐Corsi, Amita Sehgal, Scott Sherrill-Mix, Debra J. Skene, Kai‐Florian Storch, Joseph S. Takahashi, Hiroki R. Ueda, Han Wang, Charles J. Weitz, Pål O. Westermark, Herman Wijnen, Ying Xu, Gang Wu, Seung Hee Yoo, Michael W. Young, Eric Erquan Zhang, T. Zieliński, John B. Hogenesch - Journal of Biological Rhythms 2017 cited by 303

  10. Regulating the Suprachiasmatic Nucleus (SCN) Circadian Clockwork: Interplay between Cell-Autonomous and Circuit-Level Mechanisms

    Authors: , , , - Cold Spring Harbor Perspectives in Biology 2017 cited by 272

  11. Interacting Molecular Loops in the Mammalian Circadian Clock

    Authors: , , , , , , , , , , , - Science 2000 cited by 1,367

  12. Differential Functions of mPer1, mPer2, and mPer3 in the SCN Circadian Clock

    Authors: , , , , , - Neuron 2001 cited by 896

  13. The Mammalian Circadian Timing System and the Suprachiasmatic Nucleus as Its Pacemaker

    Authors: , , - Biology 2019 cited by 199

  14. Astrocytic control of extracellular GABA drives circadian timekeeping in the suprachiasmatic nucleus

    Authors: , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2023 cited by 52

  15. Circadian Orchestration of the Hepatic Proteome

    Authors: , , , , , , , , , , , - Current Biology 2006 cited by 553

  16. The After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period

    Authors: , , , , , , , , , , , , , , , - Science 2007 cited by 482

  17. A diversity of paracrine signals sustains molecular circadian cycling in suprachiasmatic nucleus circuits

    Authors: , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2011 cited by 289

  18. Genetic code expansion in the mouse brain

    Authors: , , , , , , , , - Nature Chemical Biology 2016 cited by 135

  19. Circadian VIPergic Neurons of the Suprachiasmatic Nuclei Sculpt the Sleep-Wake Cycle

    Authors: , , , , , , , , , , , , , , , , - Neuron 2020 cited by 104

  20. cAMP-Dependent Signaling as a Core Component of the Mammalian Circadian Pacemaker

    Authors: , , , , - Science 2008 cited by 418

  21. Entrainment of disrupted circadian behavior through inhibition of casein kinase 1 (CK1) enzymes

    Authors: , , , , , , , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2010 cited by 262

  22. Single‐cell transcriptomics of suprachiasmatic nuclei reveal a Prokineticin‐driven circadian network

    Authors: , , , , , - The EMBO Journal 2021 cited by 86

  23. The VPAC2 Receptor Is Essential for Circadian Function in the Mouse Suprachiasmatic Nuclei

    Authors: , , , , , , , , , , , , - Cell 2002 cited by 560

  24. Disintegration of the Sleep-Wake Cycle and Circadian Timing in Huntington's Disease

    Authors: , , , , , - Journal of Neuroscience 2005 cited by 406