Steven M. Reppert

5.4k total citations · 2 hit papers
27 papers, 4.4k citations indexed

About

Steven M. Reppert is a scholar working on Endocrine and Autonomic Systems, Cellular and Molecular Neuroscience and Social Psychology. According to data from OpenAlex, Steven M. Reppert has authored 27 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Endocrine and Autonomic Systems, 11 papers in Cellular and Molecular Neuroscience and 10 papers in Social Psychology. Recurrent topics in Steven M. Reppert's work include Circadian rhythm and melatonin (23 papers), Neuroendocrine regulation and behavior (10 papers) and Photoreceptor and optogenetics research (6 papers). Steven M. Reppert is often cited by papers focused on Circadian rhythm and melatonin (23 papers), Neuroendocrine regulation and behavior (10 papers) and Photoreceptor and optogenetics research (6 papers). Steven M. Reppert collaborates with scholars based in United States and United Kingdom. Steven M. Reppert's co-authors include David R. Weaver, Diomedes E. Logothetis, David K. Welsh, Markus Meister, James F. Gusella, Susan A. Slaugenhaupt, Catherine Godson, C.D. Mahle, Scott A. Rivkees and Ivo Šauman and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Steven M. Reppert

27 papers receiving 4.3k citations

Hit Papers

Individual neurons dissoc... 1995 2026 2005 2015 1995 1995 250 500 750 1000

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Steven M. Reppert United States 25 3.5k 1.7k 884 875 705 27 4.4k
Takahiro Moriya Japan 30 3.4k 1.0× 1.5k 0.8× 1.1k 1.2× 1.4k 1.6× 685 1.0× 76 4.3k
Jörg H. Stehle Germany 37 3.4k 1.0× 1.7k 1.0× 1.2k 1.3× 852 1.0× 334 0.5× 73 4.9k
Helena Illnerová Czechia 37 3.6k 1.0× 1.2k 0.7× 918 1.0× 1.4k 1.6× 480 0.7× 102 4.1k
Douglas G. McMahon United States 45 3.6k 1.0× 3.2k 1.8× 1.3k 1.4× 897 1.0× 426 0.6× 108 6.0k
Martin R. Ralph Canada 34 5.0k 1.4× 2.1k 1.2× 1.7k 1.9× 1.8k 2.1× 869 1.2× 90 6.3k
Yasufumi Shigeyoshi Japan 36 4.7k 1.3× 1.6k 0.9× 810 0.9× 1.7k 2.0× 1.5k 2.1× 103 6.1k
Mireille Masson‐Pévet France 35 2.3k 0.7× 1.1k 0.6× 527 0.6× 712 0.8× 150 0.2× 83 3.5k
Fred C. Davis United States 32 5.8k 1.6× 1.8k 1.1× 1.2k 1.3× 2.3k 2.7× 1.3k 1.8× 52 7.4k
Hugh D. Piggins United Kingdom 43 4.7k 1.3× 2.5k 1.5× 2.0k 2.3× 1.4k 1.6× 500 0.7× 119 5.7k
Brooke H. Miller United States 16 2.6k 0.7× 817 0.5× 428 0.5× 1.4k 1.6× 613 0.9× 19 4.3k

Countries citing papers authored by Steven M. Reppert

Since Specialization
Citations

This map shows the geographic impact of Steven M. Reppert's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Steven M. Reppert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steven M. Reppert more than expected).

Fields of papers citing papers by Steven M. Reppert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven M. Reppert. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Steven M. Reppert. The network helps show where Steven M. Reppert may publish in the future.

Co-authorship network of co-authors of Steven M. Reppert

This figure shows the co-authorship network connecting the top 25 collaborators of Steven M. Reppert. A scholar is included among the top collaborators of Steven M. Reppert based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Steven M. Reppert. Steven M. Reppert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Chang, D.C. & Steven M. Reppert. (2001). The Circadian Clocks of Mice and Men. Neuron. 29(3). 555–558. 51 indexed citations
2.
Clayton, Jonathan D., Charalambos P. Kyriacou, & Steven M. Reppert. (2001). Keeping time with the human genome. Nature. 409(6822). 829–831. 67 indexed citations
3.
4.
Reppert, Steven M.. (1998). A Clockwork Explosion!. Neuron. 21(1). 1–4. 154 indexed citations
5.
Liu, Chen, David R. Weaver, Steven H. Strogatz, & Steven M. Reppert. (1997). Cellular Construction of a Circadian Clock: Period Determination in the Suprachiasmatic Nuclei. Cell. 91(6). 855–860. 394 indexed citations
6.
Reppert, Steven M. & David R. Weaver. (1997). Forward Genetic Approach Strikes Gold: Cloning of a Mammalian Clock Gene. Cell. 89(4). 487–490. 41 indexed citations
7.
Šauman, Ivo & Steven M. Reppert. (1996). Circadian Clock Neurons in the Silkmoth Antheraea pernyi: Novel Mechanisms of Period Protein Regulation. Neuron. 17(5). 889–900. 196 indexed citations
8.
Weaver, David R. & Steven M. Reppert. (1995). Definition of the developmental transition from dopaminergic to photic regulation of c-fos gene expression in the rat suprachiasmatic nucleus. Molecular Brain Research. 33(1). 136–148. 80 indexed citations
9.
Slaugenhaupt, Susan A., Alfred L. Roca, Christopher B. Liebert, et al.. (1995). Mapping of the Gene for the Mel1a-Melatonin Receptor to Human Chromosome 4 (MTNR1A) and Mouse Chromosome 8 (Mtnr1a). Genomics. 27(2). 355–357. 72 indexed citations
10.
Reppert, Steven M. & Ivo Šauman. (1995). period and timeless Tango: A dance of two clock genes. Neuron. 15(5). 983–986. 36 indexed citations
11.
Welsh, David K., Diomedes E. Logothetis, Markus Meister, & Steven M. Reppert. (1995). Individual neurons dissociated from rat suprachiasmatic nucleus express independently phased circadian firing rhythms. Neuron. 14(4). 697–706. 1117 indexed citations breakdown →
12.
Weaver, David R., Scott A. Rivkees, & Steven M. Reppert. (1992). D1-dopamine receptors activate c-fos expression in the fetal suprachiasmatic nuclei.. Proceedings of the National Academy of Sciences. 89(19). 9201–9204. 83 indexed citations
13.
Rivkees, Scott A. & Steven M. Reppert. (1991). Appearance of melatonin receptors during embryonic life in Siberian hamsters (Phodopus sungorous). Brain Research. 568(1-2). 345–349. 30 indexed citations
14.
Reppert, Steven M., David R. Weaver, Jörg H. Stehle, & Scott A. Rivkees. (1991). Molecular Cloning and Characterization of a Rat A1-Adenosine Receptor that is Widely Expressed in Brain and Spinal Cord. Molecular Endocrinology. 5(8). 1037–1048. 282 indexed citations
15.
Weaver, David R., et al.. (1991). Melatonin receptors and signal transduction during development in Siberian hamsters (Phodopus sungorus). Developmental Brain Research. 59(1). 83–88. 37 indexed citations
16.
Weaver, David R. & Steven M. Reppert. (1990). MELATONIN RECEPTORS ARE PRESENT IN THE FERRET PARS TUBERALIS AND PARS DISTALIS, BUT NOT IN BRAIN. Endocrinology. 127(5). 2607–2609. 85 indexed citations
17.
Reppert, Steven M.. (1988). Maternal communication of circadian phase to the developing mammal. Psychoneuroendocrinology. 13(1-2). 63–78. 40 indexed citations
18.
Beitins, Inese Z., Ariel L. Barkan, Anne Klibanski, et al.. (1985). Hormonal Responses to Short Term Fasting in Postmenopausal Women*. The Journal of Clinical Endocrinology & Metabolism. 60(6). 1120–1126. 37 indexed citations
19.
Bullen, Beverly A., Gary S. Skrinar, I. Z. Beitins, et al.. (1984). Endurance training effects on plasma hormonal responsiveness and sex hormone excretion. Journal of Applied Physiology. 56(6). 1453–1463. 83 indexed citations
20.
Reppert, Steven M., et al.. (1982). Circadian properties of vasopressin and melatonin rhythms in cat cerebrospinal fluid. American Journal of Physiology-Endocrinology and Metabolism. 243(6). E489–E498. 44 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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