Kwang‐Jen Hsiao

1.5k total citations
43 papers, 1.1k citations indexed

About

Kwang‐Jen Hsiao is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kwang‐Jen Hsiao has authored 43 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kwang‐Jen Hsiao's work include Metabolism and Genetic Disorders (16 papers), Neonatal Health and Biochemistry (8 papers) and Diet and metabolism studies (4 papers). Kwang‐Jen Hsiao is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Neonatal Health and Biochemistry (8 papers) and Diet and metabolism studies (4 papers). Kwang‐Jen Hsiao collaborates with scholars based in Taiwan, China and United States. Kwang‐Jen Hsiao's co-authors include Heng‐Chun Li, Wanda Chan, Fu‐Chuan Wei, Tsung‐Sheng Su, Pesus Chou, Wuh‐Liang Hwu, Pesus Chou, Dau‐Ming Niu, Hui‐Chen Ho and Yin‐Hsiu Chien and has published in prestigious journals such as PLoS ONE, American Journal of Psychiatry and Diabetes Care.

In The Last Decade

Kwang‐Jen Hsiao

41 papers receiving 1000 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kwang‐Jen Hsiao Taiwan 18 478 271 152 144 143 43 1.1k
V. Barash Israel 22 483 1.0× 229 0.8× 172 1.1× 163 1.1× 84 0.6× 49 1.1k
Karl S. Roth United States 20 583 1.2× 374 1.4× 66 0.4× 321 2.2× 34 0.2× 86 1.6k
C R Scriver Canada 18 485 1.0× 362 1.3× 161 1.1× 105 0.7× 59 0.4× 37 1.1k
Neslihan Önenli Mungan Türkiye 15 511 1.1× 139 0.5× 425 2.8× 75 0.5× 231 1.6× 97 1.4k
Jean Rey France 20 585 1.2× 692 2.6× 172 1.1× 114 0.8× 49 0.3× 45 1.1k
Uta Tacke Germany 13 329 0.7× 420 1.5× 124 0.8× 217 1.5× 55 0.4× 27 1.3k
Bénédicte Héron France 23 527 1.1× 263 1.0× 148 1.0× 102 0.7× 42 0.3× 65 1.6k
H Gröbe Germany 11 237 0.5× 143 0.5× 160 1.1× 69 0.5× 195 1.4× 30 680
G. F. Hoffmann Germany 17 561 1.2× 454 1.7× 82 0.5× 113 0.8× 22 0.2× 36 960
C. Meier Switzerland 17 467 1.0× 124 0.5× 91 0.6× 40 0.3× 40 0.3× 50 1.4k

Countries citing papers authored by Kwang‐Jen Hsiao

Since Specialization
Citations

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

Fields of papers citing papers by Kwang‐Jen Hsiao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kwang‐Jen Hsiao. 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 Kwang‐Jen Hsiao. The network helps show where Kwang‐Jen Hsiao may publish in the future.

Co-authorship network of co-authors of Kwang‐Jen Hsiao

This figure shows the co-authorship network connecting the top 25 collaborators of Kwang‐Jen Hsiao. A scholar is included among the top collaborators of Kwang‐Jen Hsiao 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 Kwang‐Jen Hsiao. Kwang‐Jen Hsiao 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.
Hsu, Ting‐Rong, Mei‐Ying Liu, I‐Jun Chou, et al.. (2025). Newborn screening facilitates early theranostics and improved spinal muscular atrophy outcome: five-year real-world evidence from Taiwan. Orphanet Journal of Rare Diseases. 20(1). 197–197.
2.
Tsao, Pei‐Chen, Hsing‐Yi Chen, Hui‐Chen Ho, et al.. (2023). Comparing Strategies for Critical Congenital Heart Disease Newborn Screening. PEDIATRICS. 151(3). 2 indexed citations
3.
Verma, Jyotsna, Divya C. Thomas, Kwang‐Jen Hsiao, et al.. (2015). Inherited metabolic disorders: Quality management for laboratory diagnosis. Clinica Chimica Acta. 447. 1–7. 7 indexed citations
4.
5.
Liu, Yi‐Chang, I‐Hsuan Lin, Wei‐Jen Chung, et al.. (2012). Proteomics Characterization of Cytoplasmic and Lipid-Associated Membrane Proteins of Human Pathogen Mycoplasma fermentans M64. PLoS ONE. 7(4). e35304–e35304. 18 indexed citations
6.
Lin, Sheng‐Chieh, et al.. (2008). Simultaneous assessment of the effects of exonic mutations on RNA splicing and protein functions. Biochemical and Biophysical Research Communications. 373(4). 515–520. 8 indexed citations
7.
Saheki, Takeyori, Keiko Kobayashi, Mikio Iijima, et al.. (2004). Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle. Molecular Genetics and Metabolism. 81. 20–26. 82 indexed citations
8.
Lan, Yu‐Ching, et al.. (2003). Antibody Reactivity to HIV-1 Vpu in HIV-1/AIDS Patients on Highly Active Antiretroviral Therapy. Journal of Biomedical Science. 10(2). 266–275. 1 indexed citations
9.
Liu, Xiaoqing, et al.. (2003). [Genotype and phenotype correlation in Chinese patients with Wilson's Disease].. PubMed. 41(1). 35–8. 3 indexed citations
10.
Chen, Kuan‐Ju, et al.. (2002). Identification and characterization of a novel liver-specific enhancer of the human phenylalanine hydroxylase gene. Human Genetics. 110(3). 235–243. 10 indexed citations
11.
Okano, Yoshiyuki, Minoru Asada, Akie Fujimoto, et al.. (2001). A Genetic Factor for Age-Related Cataract: Identification and Characterization of a Novel Galactokinase Variant, “Osaka,” in Asians. The American Journal of Human Genetics. 68(4). 1036–1042. 60 indexed citations
12.
Hsu, Hui‐Chi, Ching‐Fen Yang, Kwang‐Jen Hsiao, et al.. (2001). Detection of Kaposi sarcoma-associated herpesvirus in bone marrow biopsy samples from patients with multiple myeloma. Cancer. 91(8). 1409–1413. 14 indexed citations
13.
Hsiao, Kwang‐Jen, et al.. (2001). A silent mutation induces exon skipping in the phenylalanine hydroxylase gene in phenylketonuria. Human Genetics. 108(1). 14–19. 44 indexed citations
14.
Liu, Meiying, et al.. (2001). Mutation analysis of synapsin III gene in schizophrenia. American Journal of Medical Genetics. 114(1). 79–83. 17 indexed citations
15.
Lee, Yu-Ru, et al.. (1997). Association study of NlaIII and MspI genetic polymorphisms of catechol-O-methyltransferase gene and susceptibility to Schizophrenia. Biological Psychiatry. 41(9). 985–987. 28 indexed citations
16.
Wei, Fu‐Chuan, et al.. (1997). Association of TaqI A polymorphism of dopamine D2 receptor gene and tardive dyskinesia in schizophrenia. Biological Psychiatry. 41(7). 827–829. 80 indexed citations
17.
Chen, Chia‐Hsiang, Yu-Ru Lee, Mei‐Ying Liu, et al.. (1996). Identification of a BglI polymorphism of Catechol-O-methyltransferase (COMT) gene, and association study with schizophrenia. American Journal of Medical Genetics. 67(6). 556–559. 9 indexed citations
18.
Soong, Bing‐Wen, et al.. (1991). DNA polymorphisms and deletion analysis of the Duchenne–Becker muscular dystrophy gene in the chinese. American Journal of Medical Genetics. 38(4). 593–600. 15 indexed citations
19.
Wuu, Kuang-Dong, Shuan‐Yow Li, Jia‐Yuh Chen, et al.. (1991). Chromosomal and biochemical screening on mentally retarded school children in Taiwan. The Japanese Journal of Human Genetics. 36(3). 267–274. 13 indexed citations
20.
Wu, Jaw‐Ching, Shou‐Dong Lee, Kwang‐Jen Hsiao, et al.. (1988). Mass screening of primary hepatocellular carcinoma by alpha‐fetoprotein in a rural area of Taiwan – a dried blood spot method. Liver International. 8(2). 100–104. 19 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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