基本信息
浏览量:6
职业迁徙
个人简介
I began my scientific career as a neuroscientist interested in how genes regulate behavior. A series of inspiring mentors propelled me to pursue those interests across industry and academia.
I've since worked with many scientists on projects in plants, flies, zebrafish, mice and people. This work has focused on the function of noncoding RNAs; building a Gene Atlas of the mouse, human and rat transcriptomes; and cell-based screening, among others.
I'm particularly interested in genome biology with a focus on the circadian clock. In my lab at Cincinnati Children’s Hospital Medical Center, we work to uncover the mechanisms of the circadian clock and apply that knowledge to medicine. For example, our lab has discovered several core clock genes and proven that they regulate physiology and behavior. This includes my discovery of the transcription factor Bmal1 — the master regulator of the mammalian clock — along with its paralog, Bmal2, and its partner, Npas2. Later, my lab characterized Rora/Rorb/Roc as key regulators of Bmal1 and circadian function. We also discovered Chrono as a non-canonical repressor of Bmal1/Clock, and Kpnb1 as a required transporter of the PER/CRY complex.
I've since worked with many scientists on projects in plants, flies, zebrafish, mice and people. This work has focused on the function of noncoding RNAs; building a Gene Atlas of the mouse, human and rat transcriptomes; and cell-based screening, among others.
I'm particularly interested in genome biology with a focus on the circadian clock. In my lab at Cincinnati Children’s Hospital Medical Center, we work to uncover the mechanisms of the circadian clock and apply that knowledge to medicine. For example, our lab has discovered several core clock genes and proven that they regulate physiology and behavior. This includes my discovery of the transcription factor Bmal1 — the master regulator of the mammalian clock — along with its paralog, Bmal2, and its partner, Npas2. Later, my lab characterized Rora/Rorb/Roc as key regulators of Bmal1 and circadian function. We also discovered Chrono as a non-canonical repressor of Bmal1/Clock, and Kpnb1 as a required transporter of the PER/CRY complex.
研究兴趣
论文共 270 篇作者统计合作学者相似作者
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Transplantation and Cellular Therapyno. 6 (2024): 632.e1-632.e5
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAno. 8 (2024)
Lauren A Schrader,Sean M Ronnekleiv-Kelly,John B Hogenesch, Christopher A Bradfield,Kristen Mc Malecki
The Journal of clinical investigationno. 14 (2024)
H. Craig Heller,Erik Herzog,Allison Brager,Gina Poe,Ravi Allada,Frank Scheer,Mary Carskadon,Horacio O. de la Iglesia, Rockelle Jang,Ashley Montero,Kenneth Wright, Philippe Mouraine,Matthew P. Walker,Namni Goel,John Hogenesch,Russell N. Van Gelder,Lance Kriegsfeld,Cheri Mah,Christopher Colwell,Jamie Zeitzer,Michael Grandner,Chandra L. Jackson,J. Roxanne Prichard,Steve A. Kay,Ketema Paul
Shi-Yang Li, Jan A. Hammarlund,Gang Wu, Jia-Wen Lian,Sacha J. Howell,Robert B. Clarke,Antony D. Adamson,Catia F. Goncalves,John B. Hogenesch,Ron C. Anafi,Qing-Jun Meng
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAno. 7 (2024)
Andrew C. Liu,Yang Shen,Carolyn R. Serbinski, Hongzhi He, Destino Roman,Mehari Endale,Lindsey Aschbacher-Smith, Katherine A. King,Jorge L. Granadillo, Isabel Lopez,Darcy A. Krueger,Thomas J. Dye,David F. Smith,John B. Hogenesch,Carlos E. Prada
HUMAN GENETICS AND GENOMICS ADVANCESno. 4 (2024)
JOURNAL OF CLINICAL INVESTIGATIONno. 4 (2023)
PLOS BIOLOGYno. 5 (2023)
Transplantation and Cellular Therapyno. 2 (2023): S135-S135
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作者统计
#Papers: 270
#Citation: 43564
H-Index: 83
G-Index: 190
Sociability: 7
Diversity: 3
Activity: 49
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