Qinghao Fu

518 total citations
8 papers, 403 citations indexed

About

Qinghao Fu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Qinghao Fu has authored 8 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Physiology. Recurrent topics in Qinghao Fu's work include Alzheimer's disease research and treatments (3 papers), Ion channel regulation and function (2 papers) and Inflammatory Myopathies and Dermatomyositis (2 papers). Qinghao Fu is often cited by papers focused on Alzheimer's disease research and treatments (3 papers), Ion channel regulation and function (2 papers) and Inflammatory Myopathies and Dermatomyositis (2 papers). Qinghao Fu collaborates with scholars based in United States and India. Qinghao Fu's co-authors include Henry Querfurth, Kenneth M. Rosen, Pravir Kumar, Hankyu Lee, Charbel Moussa, Jie Shen, Michael G. Schlossmacher, Tohru Kitada, Gangjian Qin and Matthew S. Goldberg and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neurophysiology and The FASEB Journal.

In The Last Decade

Qinghao Fu

8 papers receiving 401 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Qinghao Fu United States	7	194	182	122	92	91	8	403
Caterina Ferraina Italy	9	233 1.2×	155 0.9×	84 0.7×	76 0.8×	64 0.7×	10	404
Jung Hee Shim South Korea	6	152 0.8×	112 0.6×	76 0.6×	172 1.9×	99 1.1×	8	386
Adrián Martín‐Segura Spain	6	179 0.9×	117 0.6×	58 0.5×	172 1.9×	49 0.5×	9	424
Enji Zhang South Korea	11	132 0.7×	157 0.9×	107 0.9×	51 0.6×	46 0.5×	19	388
Sheue-Houy Tyan United States	7	132 0.7×	207 1.1×	99 0.8×	28 0.3×	76 0.8×	9	347
Laura R. Rodríguez Spain	7	150 0.8×	114 0.6×	89 0.7×	172 1.9×	114 1.3×	11	384
Karin Breu Switzerland	5	94 0.5×	192 1.1×	57 0.5×	92 1.0×	42 0.5×	6	345
Joanne Clark United States	12	383 2.0×	155 0.9×	170 1.4×	68 0.7×	154 1.7×	14	592
Nsikan Akpan United States	9	252 1.3×	92 0.5×	90 0.7×	65 0.7×	30 0.3×	10	416
Evgeniya I. Fedotova Russia	8	213 1.1×	94 0.5×	100 0.8×	43 0.5×	131 1.4×	22	411

Countries citing papers authored by Qinghao Fu

Since Specialization

Citations

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

Fields of papers citing papers by Qinghao Fu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Qinghao Fu. 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 Qinghao Fu. The network helps show where Qinghao Fu may publish in the future.

Co-authorship network of co-authors of Qinghao Fu

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Kwon, Bumsup, Pravir Kumar, Hankyu Lee, et al.. (2014). Aberrant cell cycle reentry in human and experimental inclusion body myositis and polymyositis. Human Molecular Genetics. 23(14). 3681–3694. 16 indexed citations

2.

Lee, Hankyu, Edward Rocnik, Qinghao Fu, et al.. (2012). Foxo/Atrogin induction in human and experimental myositis. Neurobiology of Disease. 46(2). 463–475. 15 indexed citations

3.

Lee, Hankyu, Pravir Kumar, Qinghao Fu, Kenneth M. Rosen, & Henry Querfurth. (2009). The Insulin/Akt Signaling Pathway Is Targeted by Intracellular β-Amyloid. Molecular Biology of the Cell. 20(5). 1533–1544. 179 indexed citations

4.

Rosen, Kenneth M., Charbel Moussa, Hankyu Lee, et al.. (2009). Parkin reverses intracellular β‐amyloid accumulation and its negative effects on proteasome function. Journal of Neuroscience Research. 88(1). 167–178. 72 indexed citations

5.

Moussa, Charbel, Qinghao Fu, Pravir Kumar, et al.. (2006). Transgenic expression of B‐APP in fast‐twitch skeletal muscle leads to calcium dyshomeostasis and IBM‐like pathology. The FASEB Journal. 20(12). 2165–2167. 32 indexed citations

6.

Rosen, Kenneth M., Charbel Moussa, Qinghao Fu, et al.. (2006). Parkin Protects against Mitochondrial Toxins and β-Amyloid Accumulation in Skeletal Muscle Cells. Journal of Biological Chemistry. 281(18). 12809–12816. 68 indexed citations

7.

Lin, Jen‐Wei, et al.. (2005). Probing the Endogenous Ca²⁺Buffers at the Presynaptic Terminals of the Crayfish Neuromuscular Junction. Journal of Neurophysiology. 94(1). 377–386. 15 indexed citations

8.

Lin, Jen‐Wei & Qinghao Fu. (2004). Modulation of available vesicles and release kinetics at the inhibitor of the crayfish neuromuscular junction. Neuroscience. 130(4). 889–895. 6 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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