Chun Hao Wong

618 total citations
5 papers, 119 citations indexed

About

Chun Hao Wong is a scholar working on Neurology, Genetics and Neurology. According to data from OpenAlex, Chun Hao Wong has authored 5 papers receiving a total of 119 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Neurology, 3 papers in Genetics and 2 papers in Neurology. Recurrent topics in Chun Hao Wong's work include Amyotrophic Lateral Sclerosis Research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Neurological diseases and metabolism (2 papers). Chun Hao Wong is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Neurological diseases and metabolism (2 papers). Chun Hao Wong collaborates with scholars based in United Kingdom, United States and Saudi Arabia. Chun Hao Wong's co-authors include Bradley Smith, Caroline Vance, Christopher E. Shaw, Simon Topp, Emma L. Scotter, Satomi Maekawa, Jacqueline C. Mitchell, Peter C. Sapp, Ammar Al‐Chalabi and Robert H. Brown and has published in prestigious journals such as The Journal of Cell Biology and Neurobiology of Aging.

In The Last Decade

Chun Hao Wong

5 papers receiving 119 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chun Hao Wong United Kingdom	4	97	56	53	25	25	5	119
Sarah Ryan United Kingdom	6	103 1.1×	76 1.4×	75 1.4×	13 0.5×	13 0.5×	8	151
J Clark Australia	6	119 1.2×	70 1.3×	75 1.4×	21 0.8×	27 1.1×	7	188
Katharine Y. Zhang Australia	6	144 1.5×	87 1.6×	111 2.1×	39 1.6×	26 1.0×	8	210
Julie Steele United States	3	106 1.1×	38 0.7×	32 0.6×	19 0.8×	12 0.5×	3	135
Cinzia Tiloca Italy	5	112 1.2×	57 1.0×	35 0.7×	61 2.4×	9 0.4×	5	138
Fahri Küçükali Belgium	3	55 0.6×	27 0.5×	62 1.2×	31 1.2×	11 0.4×	8	123
Silvia De Pasqua Italy	7	109 1.1×	55 1.0×	26 0.5×	29 1.2×	8 0.3×	9	146
Vincent Anquetil France	7	53 0.5×	20 0.4×	96 1.8×	29 1.2×	11 0.4×	14	165
Daniela Bernardo Italy	6	68 0.7×	31 0.6×	72 1.4×	22 0.9×	14 0.6×	13	146
Francesca Avemaria Italy	7	102 1.1×	70 1.3×	40 0.8×	27 1.1×	5 0.2×	15	139

Countries citing papers authored by Chun Hao Wong

Since Specialization

Citations

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

Fields of papers citing papers by Chun Hao Wong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chun Hao Wong. 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 Chun Hao Wong. The network helps show where Chun Hao Wong may publish in the future.

Co-authorship network of co-authors of Chun Hao Wong

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

All Works

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5 of 5 papers shown

1.

Wong, Chun Hao, Steven Wingett, Qian Chen, et al.. (2024). Genome-scale requirements for dynein-based transport revealed by a high-content arrayed CRISPR screen. The Journal of Cell Biology. 223(5). 2 indexed citations

2.

Gotkine, Marc, Martina de Majo, Chun Hao Wong, et al.. (2021). A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay. Neurobiology of Aging. 106. 1–6. 5 indexed citations

3.

Scotter, Emma L., Leon Smyth, Chun Hao Wong, et al.. (2016). C9ORF72 and UBQLN2 mutations are causes of amyotrophic lateral sclerosis in New Zealand: a genetic and pathologic study using banked human brain tissue. Neurobiology of Aging. 49. 214.e1–214.e5. 17 indexed citations

4.

Wong, Chun Hao, Simon Topp, Soragia Athina Gkazi, et al.. (2015). The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients. Neurobiology of Aging. 36(10). 2908.e17–2908.e18. 14 indexed citations

5.

Smith, Bradley, Caroline Vance, Emma L. Scotter, et al.. (2014). Novel mutations support a role for Profilin 1 in the pathogenesis of ALS. Neurobiology of Aging. 36(3). 1602.e17–1602.e27. 81 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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