World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
92
Citations
53553
World Ranking
2159
National Ranking
1167

Overview

John B. Hogenesch is affiliated with Cincinnati Children's Hospital Medical Center in the United States. Their research primarily spans the fields of Neuroscience and Medicine, with a focus on subfields such as Endocrine and Autonomic Systems, Physiology, Molecular Biology, Aging, and Experimental and Cognitive Psychology.

The scientist's work covers several main topics including Circadian rhythm and melatonin, Genetics, Aging, and Longevity in Model Organisms, Dietary Effects on Health, Sleep and related disorders, Sleep and Wakefulness Research, Blood Pressure and Hypertension Studies, and Spaceflight effects on biology.

Recent papers authored by John B. Hogenesch include:

  • Circadian disruption, clock genes, and metabolic health, 2024, Journal of Clinical Investigation
  • Adaptive Thermogenesis in Mice Is Enhanced by Opsin 3-Dependent Adipocyte Light Sensing, 2020, Cell Reports
  • The Circadian Clock Gene, Bmal1, Regulates Intestinal Stem Cell Signaling and Represses Tumor Initiation, 2021, Cellular and Molecular Gastroenterology and Hepatology
  • Toward Precision Medicine: Circadian Rhythm of Blood Pressure and Chronotherapy for Hypertension - 2021 NHLBI Workshop Report, 2022, Hypertension
  • NF-κB modifies the mammalian circadian clock through interaction with the core clock protein BMAL1, 2021, PLoS Genetics

Frequent co-authors collaborating with John B. Hogenesch include Gang Wu, Lauren J. Francey, David F. Smith, Marc D. Ruben, and Ron C. Anafi.

Their publications frequently appear in venues such as bioRxiv (Cold Spring Harbor Laboratory), Proceedings of the National Academy of Sciences, Transplantation and Cellular Therapy, Journal of Clinical Investigation, and Hypertension.

Best Publications

  • A gene atlas of the mouse and human protein-encoding transcriptomes

    Andrew I. Su;Tim Wiltshire;Serge Batalov;Hilmar Lapp

  • Coordinated transcription of key pathways in the mouse by the circadian clock.

    Satchidananda Panda;Marina P. Antoch;Brooke H. Miller;Andrew I. Su;Andrew I. Su

  • A circadian gene expression atlas in mammals: Implications for biology and medicine

    Ray Zhang;Nicholas F. Lahens;Heather I. Ballance;Michael E. Hughes

  • Orchestrated Transcription of Key Pathways in Arabidopsis by the Circadian Clock

    Stacey L. Harmer;John B. Hogenesch;Marty Straume;Hur-Song Chang

  • Mop3 Is an Essential Component of the Master Circadian Pacemaker in Mammals

    Maureen K. Bunger;Lisa D. Wilsbacher;Susan M. Moran;Cynthia Clendenin

  • Large-scale analysis of the human and mouse transcriptomes

    Andrew I. Su;Michael P. Cooke;Keith A. Ching;Yaron Hakak

  • The PAS Superfamily: Sensors of Environmental and Developmental Signals

    Yi-Zhong Gu;John B. Hogenesch;Christopher A. Bradfield

  • A Functional Genomics Strategy Reveals Rora as a Component of the Mammalian Circadian Clock

    Trey K. Sato;Trey K. Sato;Satchidananda Panda;Satchidananda Panda;Loren J. Miraglia;Teresa M. Reyes

  • Circadian rhythms from flies to human

    Satchidananda Panda;John B. Hogenesch;Steve A. Kay;Steve A. Kay

  • BMAL1 and CLOCK, Two Essential Components of the Circadian Clock, Are Involved in Glucose Homeostasis

    R. Daniel Rudic;Peter McNamara;Anne Maria Curtis;Raymond C. Boston

  • Genome-wide analysis of cAMP-response element binding protein occupancy, phosphorylation, and target gene activation in human tissues

    Xinmin Zhang;Duncan T. Odom;Seung Hoi Koo;Michael D. Conkright

  • A Heat-Sensitive TRP Channel Expressed in Keratinocytes

    Andrea M. Peier;Alison J. Reeve;David A. Andersson;Aziz Moqrich

  • JTK_CYCLE: an efficient nonparametric algorithm for detecting rhythmic components in genome-scale data sets.

    Michael E. Hughes;John B. Hogenesch;Karl Kornacker

  • Melanopsin (Opn4) Requirement for Normal Light-Induced Circadian Phase Shifting

    Satchidananda Panda;Trey K. Sato;Trey K. Sato;Ana Maria Castrucci;Mark D. Rollag

  • Urocortin II: a member of the corticotropin-releasing factor (CRF) neuropeptide family that is selectively bound by type 2 CRF receptors.

    T. M. Reyes;K. Lewis;M. H. Perrin;K. S. Kunitake

  • THE BASIC-HELIX-LOOP-HELIX-PAS ORPHAN MOP3 FORMS TRANSCRIPTIONALLY ACTIVE COMPLEXES WITH CIRCADIAN AND HYPOXIA FACTORS

    John B. Hogenesch;Yi-Zhong Gu;Sanjay Jain;Christopher A. Bradfield

  • A strategy for probing the function of noncoding RNAs finds a repressor of NFAT.

    A. T. Willingham;A. P. Orth;S. Batalov;E. C. Peters

  • Melanopsin Is Required for Non-Image-Forming Photic Responses in Blind Mice

    Satchidananda Panda;Ignacio Provencio;Daniel C. Tu;Susana S. Pires

  • Molecular characterization and chromosomal localization of a third alpha-class hypoxia inducible factor subunit, HIF3alpha.

    Gu Yz;Moran Sm;Hogenesch Jb;Wartman L

  • ESRP1 and ESRP2 Are Epithelial Cell-Type-Specific Regulators of FGFR2 Splicing

    Claude C. Warzecha;Trey K. Sato;Behnam Nabet;John B. Hogenesch

Frequent Co-Authors

Satchidananda Panda
Satchidananda Panda Salk Institute for Biological Studies
Steve A. Kay
Steve A. Kay University of Southern California
Garret A. FitzGerald
Garret A. FitzGerald University of Pennsylvania
Andrew I. Su
Andrew I. Su Scripps Research Institute
Joseph S. Takahashi
Joseph S. Takahashi The University of Texas Southwestern Medical Center
Peter G. Schultz
Peter G. Schultz Scripps Research Institute
Christopher A. Bradfield
Christopher A. Bradfield University of Wisconsin–Madison
Amita Sehgal
Amita Sehgal University of Pennsylvania
Reiner A. Veitia
Reiner A. Veitia Université Paris Cité
Peggy J. Farnham
Peggy J. Farnham University of Southern California

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