Jacob Shujui Hsu

816 total citations
33 papers, 316 citations indexed

About

Jacob Shujui Hsu is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Jacob Shujui Hsu has authored 33 papers receiving a total of 316 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Sensory Systems and 9 papers in Genetics. Recurrent topics in Jacob Shujui Hsu's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Genomics and Rare Diseases (7 papers) and Ear Surgery and Otitis Media (4 papers). Jacob Shujui Hsu is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), Genomics and Rare Diseases (7 papers) and Ear Surgery and Otitis Media (4 papers). Jacob Shujui Hsu collaborates with scholars based in Taiwan, Hong Kong and China. Jacob Shujui Hsu's co-authors include Miaoxin Li, Pak C. Sham, Pei‐Lung Chen, Shu‐Leong Ho, Pak-Chung Sham, María-Mercé García-Barceló, Shirley Yin-Yu Pang, Kay Cheong Teo, Clara Sze-Man Tang and Chen‐Chi Wu and has published in prestigious journals such as Nucleic Acids Research, Bioinformatics and PLoS ONE.

In The Last Decade

Jacob Shujui Hsu

29 papers receiving 313 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacob Shujui Hsu Taiwan 10 105 89 80 45 43 33 316
Adam Mp 6 180 1.7× 36 0.4× 113 1.4× 30 0.7× 27 0.6× 286 388
A Amemiya Japan 6 173 1.6× 41 0.5× 104 1.3× 29 0.6× 23 0.5× 269 377
Ardinger Hh United States 6 192 1.8× 37 0.4× 124 1.6× 30 0.7× 27 0.6× 287 402
Bean Ljh 6 180 1.7× 35 0.4× 113 1.4× 29 0.6× 27 0.6× 285 386
Asma I. Tahir Saudi Arabia 11 129 1.2× 21 0.2× 90 1.1× 34 0.8× 16 0.4× 19 294
Maddalena Martella Italy 11 215 2.0× 54 0.6× 26 0.3× 31 0.7× 21 0.5× 21 372
Bird Td United States 6 162 1.5× 29 0.3× 90 1.1× 25 0.6× 26 0.6× 244 342
Mefford Hc 6 163 1.6× 28 0.3× 90 1.1× 24 0.5× 25 0.6× 239 337
Ami V. Patel United States 10 108 1.0× 20 0.2× 35 0.4× 90 2.0× 47 1.1× 18 299
Emmanuelle Ranza Switzerland 12 137 1.3× 15 0.2× 103 1.3× 18 0.4× 12 0.3× 22 295

Countries citing papers authored by Jacob Shujui Hsu

Since Specialization
Citations

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

Fields of papers citing papers by Jacob Shujui Hsu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jacob Shujui Hsu. 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 Jacob Shujui Hsu. The network helps show where Jacob Shujui Hsu may publish in the future.

Co-authorship network of co-authors of Jacob Shujui Hsu

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

All Works

20 of 20 papers shown
1.
Duan, Demin, et al.. (2025). Comparisons of performances of structural variants detection algorithms in solitary or combination strategy. PLoS ONE. 20(2). e0314982–e0314982. 2 indexed citations
2.
Chien, Po‐Hsiu, Chin-Yi Cheng, Yubin Wang, et al.. (2025). Evaluating Discordant Somatic Calls Across Mutation Discovery Approaches to Minimize False-Negative Drug-Resistant Findings. Journal of Molecular Diagnostics. 27(8). 768–782.
3.
4.
Feng, Yen‐Chen Anne, Wei J. Chen, Mei‐Chen Lin, et al.. (2025). Paternal age, de novo mutation, and age at onset among co-affected schizophrenia sib-pairs: whole-genome sequencing in multiplex families. Molecular Psychiatry. 30(8). 3560–3567. 2 indexed citations
5.
Lin, Pei‐Hsuan, Cheng‐Yu Tsai, Yu‐Ting Chiang, et al.. (2025). Unraveling the complex genetic landscape of OTOF-related hearing loss: a deep dive into cryptic variants and haplotype phasing. Molecular Medicine. 31(1). 181–181.
6.
7.
Tsai, Cheng‐Yu, Pei‐Hsuan Lin, Yu‐Jen Wu, et al.. (2024). Machine learning-based longitudinal prediction for GJB2-related sensorineural hearing loss. Computers in Biology and Medicine. 176. 108597–108597. 3 indexed citations
8.
Hsu, Chia‐Lang, et al.. (2024). Genetic complexity of killer-cell immunoglobulin-like receptor genes in human pangenome assemblies. Genome Research. 34(8). 1211–1223. 3 indexed citations
9.
Chang, Fang‐Yu, Chang‐Hao Yang, Chung‐May Yang, et al.. (2024). Genetics in neovascular age‐related macular degeneration susceptibility and treatment response to anti‐VEGF intravitreal injection: A case series study. Clinical and Experimental Ophthalmology. 52(6). 655–664. 3 indexed citations
10.
Chiang, Yu‐Ting, Pei‐Hsuan Lin, Cheng‐Yu Tsai, et al.. (2023). Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment. Journal of Molecular Diagnostics. 25(11). 827–837. 5 indexed citations
11.
Tsai, Cheng‐Yu, Pei‐Hsuan Lin, Yu‐Ting Chiang, et al.. (2023). Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population. Genes. 14(4). 880–880. 2 indexed citations
12.
Hsu, Jacob Shujui, Pei‐Lung Chen, Jia‐Feng Wu, et al.. (2023). Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases. The Journal of Pediatrics. 258. 113408–113408. 8 indexed citations
13.
Lin, Pei‐Hsuan, Hung‐Pin Wu, Che‐Ming Wu, et al.. (2022). Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study. Biomedicines. 10(7). 1523–1523. 16 indexed citations
14.
Chen, Nae-Chyun, Chia‐Lang Hsu, Jacob Shujui Hsu, et al.. (2022). Profiling genes encoding the adaptive immune receptor repertoire with gAIRR Suite. Frontiers in Immunology. 13. 922513–922513. 8 indexed citations
15.
Tang, Clara Sze-Man, Man‐Ting So, Haibing Yue, et al.. (2021). Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism. EBioMedicine. 71. 103530–103530. 45 indexed citations
16.
Zhang, Yamin, Mingli Li, Qiang Wang, et al.. (2019). A joint study of whole exome sequencing and structural MRI analysis in major depressive disorder. Psychological Medicine. 50(3). 384–395. 20 indexed citations
17.
Hsu, Jacob Shujui, Ruizhong Zhang, Fanny Yeung, et al.. (2019). Cancer gene mutations in congenital pulmonary airway malformation patients. ERJ Open Research. 5(1). 196–2018. 15 indexed citations
18.
Tang, Clara Sze-Man, Xuehan Zhuang, Esw Ngan, et al.. (2018). Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing. European Journal of Human Genetics. 26(6). 818–826. 17 indexed citations
19.
Pang, Shirley Yin-Yu, Kay Cheong Teo, Jacob Shujui Hsu, et al.. (2017). The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a review. Translational Neurodegeneration. 6(1). 27–27. 19 indexed citations
20.
Hsu, Jacob Shujui, Johnny S. H. Kwan, Zhicheng Pan, et al.. (2016). Inheritance-mode specific pathogenicity prioritization (ISPP) for human protein coding genes. Bioinformatics. 32(20). 3065–3071. 10 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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