Eva R. Chin

4.8k total citations · 1 hit paper
62 papers, 3.7k citations indexed

About

Eva R. Chin is a scholar working on Molecular Biology, Physiology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Eva R. Chin has authored 62 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 16 papers in Physiology and 15 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Eva R. Chin's work include Muscle Physiology and Disorders (28 papers), Cardiomyopathy and Myosin Studies (13 papers) and Adipose Tissue and Metabolism (11 papers). Eva R. Chin is often cited by papers focused on Muscle Physiology and Disorders (28 papers), Cardiomyopathy and Myosin Studies (13 papers) and Adipose Tissue and Metabolism (11 papers). Eva R. Chin collaborates with scholars based in United States, Canada and Australia. Eva R. Chin's co-authors include David G. Allen, R. Sanders Williams, Rhonda Bassel‐Duby, Robin N. Michel, Caroline G. Humphries, John M. Shelton, James A. Richardson, Quan Yang, Haiyan Wu and Eric N. Olson and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Genes & Development.

In The Last Decade

Eva R. Chin

60 papers receiving 3.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type

1998 839 citations Eva R. Chin, Caroline G. Humphries et al. profile →

Peers

Eva R. Chin

PHYSI

CCM

REHAB

Christopher W. Ward United States

Mitchell J. Anderson Australia

G. Salviati Italy

Dominique Mornet France

Joseph M. Metzger United States

Matthias Vorgerd Germany

Brian Glancy United States

Marco Mongillo Italy

Mark A. Anderson United States

Creed M. Stary United States

Christopher W. Ward United States

Eva R. Chin

4.2k ×1.8

1.2k ×1.1

PHYSI

925 ×1.1

2.0k ×3.3

CCM

613 ×1.3

REHAB

Citations per year, relative to Eva R. Chin Eva R. Chin (= 1×) peers Christopher W. Ward

Countries citing papers authored by Eva R. Chin

Since Specialization

Citations

This map shows the geographic impact of Eva R. Chin'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 Eva R. Chin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva R. Chin more than expected).

Fields of papers citing papers by Eva R. Chin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eva R. Chin. 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 Eva R. Chin. The network helps show where Eva R. Chin may publish in the future.

Co-authorship network of co-authors of Eva R. Chin

This figure shows the co-authorship network connecting the top 25 collaborators of Eva R. Chin. A scholar is included among the top collaborators of Eva R. Chin 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 Eva R. Chin. Eva R. Chin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Pugsley, Michael K., et al.. (2025). A characterization of aficamten, a cardiac myosin inhibitor, in core battery safety pharmacology studies. Journal of Pharmacological and Toxicological Methods. 133. 107611–107611. 1 indexed citations

Heuberger, Jules A. A. C., John B. Hutchison, Klaus Gjervig Jensen, et al.. (2024). Safety, Pharmacokinetics, and Pharmacodynamics of a First‐in‐Class ClC‐1 Inhibitor to Enhance Muscle Excitability: Phase I Randomized Controlled Trial. Clinical Pharmacology & Therapeutics. 117(3). 768–778. 1 indexed citations

Hartman, James J., Darren T. Hwee, Jingying Wang, et al.. (2020). Characterization of the Cardiac Myosin Inhibitor CK-3773274: a Potential Therapeutic Approach for Hypertrophic Cardiomyopathy. Biophysical Journal. 118(3). 596a–596a. 8 indexed citations

Amici, David R., Iago Pinal‐Fernandez, Davi A. G. Mázala, et al.. (2017). Calcium dysregulation, functional calpainopathy, and endoplasmic reticulum stress in sporadic inclusion body myositis. Acta Neuropathologica Communications. 5(1). 24–24. 36 indexed citations

Mázala, Davi A. G., et al.. (2016). The SH3 and cysteine-rich domain 3 (Stac3) gene is important to growth, fiber composition, and calcium release from the sarcoplasmic reticulum in postnatal skeletal muscle. Skeletal Muscle. 6(1). 17–17. 17 indexed citations

Mázala, Davi A. G., Stephen J. P. Pratt, Dapeng Chen, et al.. (2015). SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models. American Journal of Physiology-Cell Physiology. 308(9). C699–C709. 51 indexed citations

Bamman, Marcas M., Dan M. Cooper, Frank W. Booth, et al.. (2014). Exercise Biology and Medicine: Innovative Research to Improve Global Health. Mayo Clinic Proceedings. 89(2). 148–153. 31 indexed citations

Chin, Eva R.. (2010). Intracellular Ca2+ Signaling in Skeletal Muscle. Exercise and Sport Sciences Reviews. 38(2). 76–85. 37 indexed citations

Cairns, Simeon P., Eva R. Chin, & Jean‐Marc Renaud. (2007). Stimulation pulse characteristics and electrode configuration determine site of excitation in isolated mammalian skeletal muscle: implications for fatigue. Journal of Applied Physiology. 103(1). 359–368. 37 indexed citations

10.

Chakkalakal, Joe V., et al.. (2006). Targeted inhibition of Ca2+/calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle. Human Molecular Genetics. 15(9). 1423–1435. 53 indexed citations

11.

Angus, Lindsay, Joe V. Chakkalakal, Alexandre Méjat, et al.. (2005). Calcineurin-NFAT signaling, together with GABP and peroxisome PGC-1α, drives utrophin gene expression at the neuromuscular junction. American Journal of Physiology-Cell Physiology. 289(4). C908–C917. 71 indexed citations

12.

Hornberger, Troy A., Ryan D. Mateja, Eva R. Chin, Jessica L. Andrews, & Karyn A. Esser. (2004). Aging does not alter the mechanosensitivity of the p38, p70^S6k, and JNK2 signaling pathways in skeletal muscle. Journal of Applied Physiology. 98(4). 1562–1566. 44 indexed citations

13.

Michel, Robin N., Shannon E. Dunn, & Eva R. Chin. (2004). Calcineurin and skeletal muscle growth. Proceedings of The Nutrition Society. 63(2). 341–349. 89 indexed citations

14.

Chin, Eva R., Robert W. Grange, Alain R. Simard, et al.. (2003). Alterations in Slow‐Twitch Muscle Phenotype in Transgenic Mice Overexpressing the Ca²⁺ Buffering Protein Parvalbumin. The Journal of Physiology. 547(2). 649–663. 43 indexed citations

15.

Thurston, Lisa, et al.. (2002). EXPRESSION OF 11B-HYDROXYSTEROID DEHYDROGENASE (11BHSD) PROTEINS IN LUTEINIZING HUMAN GRANULOSA-LUTEIN CELLS; EVIDENCE FOR PRODUCTION OF A PARACRINE/AUTOCRINE OVARIAN INHIBITOR OF 11BHSD1 ACTIVITY. 4(2). 37–45. 1 indexed citations

16.

Garry, Daniel J., George A. Ordway, John N. Lorenz, et al.. (1998). Mice without myoglobin. Nature. 395(6705). 905–908. 224 indexed citations

17.

Chin, Eva R. & David G. Allen. (1997). Effects of reduced muscle glycogen concentration on force, Ca2+ release and contractile protein function in intact mouse skeletal muscle.. The Journal of Physiology. 498(1). 17–29. 160 indexed citations

18.

Green, H., et al.. (1995). Failure of short term stimulation to reduce sarcoplasmic reticulum Ca2+-ATPase function in homogenates of rat gastrocnemius. Molecular and Cellular Biochemistry. 146(1). 23–33. 10 indexed citations

19.

Green, H. J., et al.. (1994). Preservation of sarcoplasmic reticulum Ca²⁺-sequestering function in homogenates of different fibre type composition following sprint activity. Canadian Journal of Physiology and Pharmacology. 72(10). 1231–1237. 11 indexed citations

20.

Green, H.J., et al.. (1992). Time‐dependoent increases in Na⁺,K⁺‐ATPase content of low‐frequency‐stimulated rabbit muscle. FEBS Letters. 310(2). 129–131. 20 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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