Achih Chen

715 total citations
7 papers, 514 citations indexed

About

Achih Chen is a scholar working on Sensory Systems, Molecular Biology and Surgery. According to data from OpenAlex, Achih Chen has authored 7 papers receiving a total of 514 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Sensory Systems, 4 papers in Molecular Biology and 1 paper in Surgery. Recurrent topics in Achih Chen's work include Hearing, Cochlea, Tinnitus, Genetics (5 papers), RNA regulation and disease (4 papers) and Congenital heart defects research (2 papers). Achih Chen is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (5 papers), RNA regulation and disease (4 papers) and Congenital heart defects research (2 papers). Achih Chen collaborates with scholars based in United States, India and Belgium. Achih Chen's co-authors include Richard J. Smith, Guy Van Camp, Li Ni, Peter Van Hauwe, Paul Coucke, Isabelle Schatteman, Yutaka Satō, David C. Hughes, Kristien Verhoeven and F. Erwin Offeciers and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Genomics.

In The Last Decade

Achih Chen

6 papers receiving 503 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Achih Chen United States	6	355	221	154	99	93	7	514
Sigrid Wayne United States	11	364 1.0×	344 1.6×	115 0.7×	40 0.4×	74 0.8×	19	543
Martijn H. Kemperman Netherlands	13	275 0.8×	126 0.6×	156 1.0×	59 0.6×	92 1.0×	16	385
Suoqiang Zhai China	17	441 1.2×	411 1.9×	146 0.9×	43 0.4×	115 1.2×	42	781
Tomonori Takasaka Japan	9	270 0.8×	224 1.0×	82 0.5×	37 0.4×	60 0.6×	11	450
Steven J. H. Bom Netherlands	12	268 0.8×	125 0.6×	172 1.1×	40 0.4×	107 1.2×	20	392
Atsushi Namba Japan	10	469 1.3×	208 0.9×	258 1.7×	54 0.5×	107 1.2×	18	605
Hong-Joon Park South Korea	16	374 1.1×	303 1.4×	143 0.9×	23 0.2×	85 0.9×	28	553
PJ Willems Greece	5	271 0.8×	356 1.6×	124 0.8×	27 0.3×	63 0.7×	8	590
Yongchuan Chai China	16	481 1.4×	295 1.3×	206 1.3×	35 0.4×	138 1.5×	50	707
Elona Cama Italy	11	288 0.8×	158 0.7×	125 0.8×	32 0.3×	128 1.4×	18	404

Countries citing papers authored by Achih Chen

Since Specialization

Citations

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

Fields of papers citing papers by Achih Chen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Achih Chen

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

All Works

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7 of 7 papers shown

1.

Chen, Achih, et al.. (2018). The Dimpleplasty: A New Streamlined Approach to Surgical Creation of Dynamic Facial Dimples, Our Experience, and Results. The American Journal of Cosmetic Surgery. 36(3). 138–142.

2.

Jain, Pawan Kumar, Anil K. Lalwani, Tenesha N. Smith, et al.. (1998). A Gene for Recessive Nonsyndromic Sensorineural Deafness (DFNB18) Maps to the Chromosomal Region 11p14–p15.1 Containing the Usher Syndrome Type 1C Gene. Genomics. 50(2). 290–292. 34 indexed citations

3.

Verhoeven, Kristien, Karin Kirschhofer, P. Kevin Legan, et al.. (1998). Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nature Genetics. 19(1). 60–62. 253 indexed citations

4.

Chen, Achih, Sigrid Wayne, Adam Bell, et al.. (1997). New gene for autosomal recessive non‐syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics. 71(4). 467–471. 7 indexed citations

5.

Chen, Achih, Sigrid Wayne, Arabandi Ramesh, et al.. (1997). New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics. 71(4). 467–471. 39 indexed citations

6.

Chen, Achih, Mary C. Francis, Li Ni, et al.. (1995). Phenotypic manifestations of branchiootorenal syndrome. American Journal of Medical Genetics. 58(4). 365–370. 140 indexed citations

7.

Fukushima, Kunihiro, Arabandi Ramesh, C. R. Srikumari Srisailapathy, et al.. (1995). Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q. Human Molecular Genetics. 4(9). 1643–1648. 41 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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