Henry M. Colecraft

4.9k total citations
83 papers, 3.5k citations indexed

About

Henry M. Colecraft is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Henry M. Colecraft has authored 83 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 48 papers in Cardiology and Cardiovascular Medicine and 26 papers in Cellular and Molecular Neuroscience. Recurrent topics in Henry M. Colecraft's work include Ion channel regulation and function (59 papers), Cardiac electrophysiology and arrhythmias (45 papers) and Neuroscience and Neuropharmacology Research (17 papers). Henry M. Colecraft is often cited by papers focused on Ion channel regulation and function (59 papers), Cardiac electrophysiology and arrhythmias (45 papers) and Neuroscience and Neuropharmacology Research (17 papers). Henry M. Colecraft collaborates with scholars based in United States, Italy and China. Henry M. Colecraft's co-authors include David T. Yue, Tingting Yang, Prakash Subramanyam, Robin M. Shaw, Badr A. Alseikhan, Jayalakshmi Miriyala, Scott Mittman, Kun Fang, Carla D. DeMaria and Xianghua Xu and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Henry M. Colecraft

81 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Henry M. Colecraft United States	36	2.8k	1.7k	1.2k	296	254	83	3.5k
Jean‐François Desaphy Italy	31	1.9k 0.7×	765 0.5×	895 0.8×	326 1.1×	565 2.2×	118	2.7k
Patricia McDonald United States	23	2.7k 1.0×	437 0.3×	1.2k 1.1×	356 1.2×	226 0.9×	52	3.4k
Marco Mongillo Italy	31	3.2k 1.1×	1.6k 0.9×	778 0.7×	568 1.9×	768 3.0×	70	4.6k
Finn Olav Levy Norway	36	2.5k 0.9×	794 0.5×	1.1k 1.0×	301 1.0×	382 1.5×	131	4.1k
Barbara A. Wible United States	32	3.6k 1.3×	2.8k 1.7×	1.5k 1.3×	151 0.5×	153 0.6×	48	4.2k
Hugues Abriel Switzerland	45	4.8k 1.7×	3.5k 2.1×	1.3k 1.1×	317 1.1×	382 1.5×	140	6.2k
Nora Rosemblit United States	10	2.9k 1.0×	2.1k 1.3×	693 0.6×	118 0.4×	165 0.6×	11	3.8k
Daniel C. Devor United States	33	2.2k 0.8×	735 0.4×	609 0.5×	260 0.9×	492 1.9×	70	3.6k
Robert D. Harvey United States	33	2.5k 0.9×	1.6k 0.9×	863 0.7×	161 0.5×	302 1.2×	74	3.0k
Joshua I. Goldhaber United States	42	3.6k 1.3×	3.1k 1.9×	1.1k 0.9×	189 0.6×	391 1.5×	113	5.3k

Countries citing papers authored by Henry M. Colecraft

Since Specialization

Citations

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

Fields of papers citing papers by Henry M. Colecraft

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Henry M. Colecraft. 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 Henry M. Colecraft. The network helps show where Henry M. Colecraft may publish in the future.

Co-authorship network of co-authors of Henry M. Colecraft

This figure shows the co-authorship network connecting the top 25 collaborators of Henry M. Colecraft. A scholar is included among the top collaborators of Henry M. Colecraft 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 Henry M. Colecraft. Henry M. Colecraft 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

Morgenstern, Travis J., Papiya Choudhury, Meera J. Desai, et al.. (2025). Ion channel inhibition by targeted recruitment of NEDD4-2 with divalent nanobodies. Nature Communications. 17(1). 378–378.

Choudhury, Papiya, et al.. (2025). Decoding polyubiquitin regulation of KV7. 1 (KCNQ1) surface expression with engineered linkage-selective deubiquitinases. Nature Communications. 16(1). 5805–5805. 2 indexed citations

Yang, Lin, Henry M. Colecraft, X. Shawn Liu, et al.. (2024). A genetically encoded actuator selectively boosts L-type calcium channels in diverse physiological settings. Biophysical Journal. 123(3). 534a–534a. 1 indexed citations

Yang, Lin, Petronel Tuluc, Henry M. Colecraft, et al.. (2024). A genetically encoded actuator boosts L-type calcium channel function in diverse physiological settings. Science Advances. 10(44). eadq3374–eadq3374. 1 indexed citations

Morgenstern, Travis J., et al.. (2024). Inhibition of ion channel functional expression by targeted recruitment of NEDD4-2 with divalent nanobodies. Biophysical Journal. 123(3). 28a–28a. 1 indexed citations

Xie, Bing, Chuanyun Xu, Jacqueline Niu, et al.. (2023). Multiplex epigenome editing of MECP2 to rescue Rett syndrome neurons. Science Translational Medicine. 15(679). eadd4666–eadd4666. 49 indexed citations

Sampson, Kevin J., et al.. (2023). Divergent regulation of KCNQ1/E1 by targeted recruitment of protein kinase A to distinct sites on the channel complex. eLife. 12. 6 indexed citations

Wu, Xiaoan, et al.. (2022). Pharmacological rescue of specific long QT variants of KCNQ1/KCNE1 channels. Frontiers in Physiology. 13. 902224–902224. 6 indexed citations

González, Bryan J., Haoquan Zhao, Jacqueline Niu, et al.. (2022). Reduced calcium levels and accumulation of abnormal insulin granules in stem cell models of HNF1A deficiency. Communications Biology. 5(1). 779–779. 16 indexed citations

10.

Morgenstern, Travis J., Erick O. Hernández‐Ochoa, Papiya Choudhury, et al.. (2022). Selective posttranslational inhibition of CaVβ1-associated voltage-dependent calcium channels with a functionalized nanobody. Nature Communications. 13(1). 7556–7556. 11 indexed citations

11.

Bauer, Daniel, Brigitte Hertel, Henry M. Colecraft, et al.. (2020). The mutation L69P in the PAS domain of the hERG potassium channel results in LQTS by trafficking deficiency. Channels. 14(1). 163–174. 4 indexed citations

12.

Khanna, Rajesh, Jie Yu, Xiaofang Yang, et al.. (2019). Targeting the CaVα–CaVβ interaction yields an antagonist of the N-type CaV2.2 channel with broad antinociceptive efficacy. Pain. 160(7). 1644–1661. 35 indexed citations

13.

Hu, Zhenyu, Guang Li, Jiong‐Wei Wang, et al.. (2018). Regulation of Blood Pressure by Targeting Ca _V 1.2-Galectin-1 Protein Interaction. Circulation. 138(14). 1431–1445. 29 indexed citations

14.

Yang, Lin, Alexander N. Katchman, Jared Kushner, et al.. (2018). Cardiac CaV1.2 channels require β subunits for β-adrenergic–mediated modulation but not trafficking. Journal of Clinical Investigation. 129(2). 647–658. 44 indexed citations

15.

Katchman, Alexander N., Lin Yang, Sergey I. Zakharov, et al.. (2017). Proteolytic cleavage and PKA phosphorylation of α _1C subunit are not required for adrenergic regulation of Ca _V 1.2 in the heart. Proceedings of the National Academy of Sciences. 114(34). 9194–9199. 31 indexed citations

16.

Joseph, Leroy C., Grace J. Kim, Emanuele Barca, et al.. (2017). Inhibition of NADPH oxidase 2 (NOX2) prevents sepsis-induced cardiomyopathy by improving calcium handling and mitochondrial function. JCI Insight. 2(17). 132 indexed citations

17.

Grandi, Eleonora, Michael C. Sanguinetti, Daniel C. Bartos, et al.. (2016). Potassium channels in the heart: structure, function and regulation. The Journal of Physiology. 595(7). 2209–2228. 83 indexed citations

18.

Chang, Donald D. & Henry M. Colecraft. (2015). Rad and Rem are non‐canonical G‐proteins with respect to the regulatory role of guanine nucleotide binding in Ca _V 1.2 channel regulation. The Journal of Physiology. 593(23). 5075–5090. 11 indexed citations

19.

Subramanyam, Prakash, Donald D. Chang, Kun Fang, et al.. (2013). Manipulating L-type calcium channels in cardiomyocytes using split-intein protein transsplicing. Proceedings of the National Academy of Sciences. 110(38). 15461–15466. 28 indexed citations

20.

Alseikhan, Badr A., Carla D. DeMaria, Henry M. Colecraft, & David T. Yue. (2002). Engineered calmodulins reveal the unexpected eminence of Ca ²⁺ channel inactivation in controlling heart excitation. Proceedings of the National Academy of Sciences. 99(26). 17185–17190. 156 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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