Jyh‐Feng Lu

2.6k total citations
63 papers, 2.1k citations indexed

About

Jyh‐Feng Lu is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Jyh‐Feng Lu has authored 63 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 9 papers in Genetics. Recurrent topics in Jyh‐Feng Lu's work include Peroxisome Proliferator-Activated Receptors (12 papers), Metabolism and Genetic Disorders (10 papers) and Genomics and Rare Diseases (5 papers). Jyh‐Feng Lu is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (12 papers), Metabolism and Genetic Disorders (10 papers) and Genomics and Rare Diseases (5 papers). Jyh‐Feng Lu collaborates with scholars based in Taiwan, United States and China. Jyh‐Feng Lu's co-authors include Kirby D. Smith, Paul A. Watkins, Bing‐Huei Chen, Lelita T. Braiterman, Ann B. Moser, Baskaran Stephen Inbaraj, Fu‐Yuan Siao, Jinn‐Shyan Wang, Stephan Kemp and Martina C. McGuinness and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Jyh‐Feng Lu

60 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jyh‐Feng Lu Taiwan 23 1.4k 325 320 184 170 63 2.1k
Shadi Moghaddas United States 22 2.2k 1.6× 170 0.5× 600 1.9× 168 0.9× 360 2.1× 34 3.5k
Xingguo Liu China 29 1.5k 1.1× 229 0.7× 238 0.7× 81 0.4× 241 1.4× 120 2.6k
Gian Franco Gaetani Italy 19 789 0.6× 122 0.4× 335 1.0× 96 0.5× 123 0.7× 45 1.9k
John E. Dominy United States 24 1.6k 1.1× 106 0.3× 770 2.4× 554 3.0× 318 1.9× 32 3.3k
Russell C. Scaduto United States 21 1.3k 1.0× 158 0.5× 360 1.1× 133 0.7× 118 0.7× 36 2.4k
Ashok K. Srivastava Canada 28 1.4k 1.0× 89 0.3× 571 1.8× 88 0.5× 178 1.0× 87 2.7k
Hirokazu Hara Japan 32 1.1k 0.8× 49 0.2× 254 0.8× 151 0.8× 285 1.7× 154 3.3k
Bülent Mutus Canada 32 1.2k 0.8× 137 0.4× 809 2.5× 621 3.4× 63 0.4× 106 3.1k
Sumiko Inoue Japan 34 1.1k 0.8× 53 0.2× 217 0.7× 121 0.7× 293 1.7× 58 3.3k
Arun K. Das United States 24 1.0k 0.8× 164 0.5× 380 1.2× 289 1.6× 38 0.2× 73 1.8k

Countries citing papers authored by Jyh‐Feng Lu

Since Specialization
Citations

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

Fields of papers citing papers by Jyh‐Feng Lu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jyh‐Feng Lu. 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 Jyh‐Feng Lu. The network helps show where Jyh‐Feng Lu may publish in the future.

Co-authorship network of co-authors of Jyh‐Feng Lu

This figure shows the co-authorship network connecting the top 25 collaborators of Jyh‐Feng Lu. A scholar is included among the top collaborators of Jyh‐Feng Lu 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 Jyh‐Feng Lu. Jyh‐Feng Lu 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.
2.
Liang, Jao‐Shwann, Kun‐Long Hung, Li‐Ju Lin, et al.. (2023). Novel PEX1 mutations in fibroblasts from children with Zellweger spectrum disorders exhibit temperature sensitive characteristics. Epilepsy & Behavior. 145. 109266–109266. 1 indexed citations
3.
Huang, Kang-Chieh, Mong‐Lien Wang, Shih‐Jen Chen, et al.. (2019). Morphological and Molecular Defects in Human Three-Dimensional Retinal Organoid Model of X-Linked Juvenile Retinoschisis. Stem Cell Reports. 13(5). 906–923. 75 indexed citations
4.
Liang, Jao‐Shwann, et al.. (2019). Phenotypic manifestations between male and female children with CDKL5 mutations. Brain and Development. 41(9). 783–789. 19 indexed citations
5.
Liang, Jao‐Shwann, Jinn‐Shyan Wang, Li‐Ju Lin, et al.. (2018). Genetic Diagnosis in Children with Epilepsy and Developmental Delay/Mental Retardation Using Targeted Gene Panel Analysis. Neuropsychiatry. 8(5). 4 indexed citations
6.
Huang, Kang-Chieh, Aliaksandr A. Yarmishyn, Jyh‐Feng Lu, et al.. (2018). Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis. Stem Cell Research. 29. 152–156. 5 indexed citations
7.
Lu, Jyh‐Feng, et al.. (2018). SCN2A mutation in an infant presenting with migrating focal seizures and infantile spasm responsive to a ketogenic diet. Brain and Development. 40(8). 724–727. 21 indexed citations
8.
Chao, Wei‐Chih, Li‐Ju Lin, Jyh‐Feng Lu, et al.. (2017). Unveiling the water-associated conformational mobility in the active site of ascorbate peroxidase. Biochimica et Biophysica Acta (BBA) - General Subjects. 1862(3). 451–459. 4 indexed citations
9.
Liang, Jao‐Shwann, Li‐Ju Lin, Ming‐Tao Yang, Jinn‐Shyan Wang, & Jyh‐Feng Lu. (2017). The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features. Brain and Development. 39(10). 877–881. 12 indexed citations
10.
Chao, Wei‐Chih, Jiun‐Yi Shen, Cheng‐Han Yang, et al.. (2016). The In Situ Tryptophan Analogue Probes the Conformational Dynamics in Asparaginase Isozymes. Biophysical Journal. 110(8). 1732–1743. 15 indexed citations
11.
Lv, Qiang, et al.. (2013). Association of the methylenetetrahydrofolate reductase gene A1298C polymorphism with stroke risk based on a meta-analysis. Genetics and Molecular Research. 12(4). 6882–6894. 13 indexed citations
12.
Shen, Jiun‐Yi, Wei‐Chih Chao, Chun Liu, et al.. (2013). Probing water micro-solvation in proteins by water catalysed proton-transfer tautomerism. Nature Communications. 4(1). 2611–2611. 61 indexed citations
13.
Claret, Laurent, et al.. (2012). Simulations Using a Drug–Disease Modeling Framework and Phase II Data Predict Phase III Survival Outcome in First-Line Non–Small-Cell Lung Cancer. Clinical Pharmacology & Therapeutics. 92(5). 631–634. 29 indexed citations
14.
Chao, Wei‐Chih, Jyh‐Feng Lu, Jinn‐Shyan Wang, et al.. (2011). Probing the Interaction between Prostacyclin Synthase and Prostaglandin H2 Analogues or Inhibitors via a Combination of Resonance Raman Spectroscopy and Molecular Dynamics Simulation Approaches. Journal of the American Chemical Society. 133(46). 18870–18879. 10 indexed citations
15.
Lu, Jyh‐Feng, et al.. (2009). CFTR (TG)m(T)n polymorphism in patients with CBAVD in a population expressing low incidence of cystic fibrosis. Clinical Genetics. 76(3). 282–286. 17 indexed citations
16.
Chiang, Han‐Sun, et al.. (2008). CFTR Mutation Analysis of a Caucasian Father with Congenital Bilateral Absence of Vas Deferens, a Taiwanese Mother, and Twins Resulting from ICSI Procedure. Journal of the Formosan Medical Association. 107(9). 736–740. 7 indexed citations
17.
Inbaraj, Baskaran Stephen, et al.. (2008). Adsorption of toxic mercury(II) by an extracellular biopolymer poly(γ-glutamic acid). Bioresource Technology. 100(1). 200–207. 205 indexed citations
18.
Pai, Pei‐Jing, et al.. (2007). Rapid protein identification using a disposable on‐line clean‐up/concentrating device and electrospray ionization mass spectrometry. Rapid Communications in Mass Spectrometry. 21(4). 459–465. 3 indexed citations
19.
Wong, Lee-Jun, et al.. (2006). AIB1 gene amplification and the instability of polyQ encoding sequence in breast cancer cell lines. BMC Cancer. 6(1). 111–111. 11 indexed citations
20.
Heinzer, Ann K., Martina C. McGuinness, Jyh‐Feng Lu, et al.. (2003). Mouse Models and Genetic Modifiers in X-Linked Adrenoleukodystrophy. Advances in experimental medicine and biology. 544. 75–93. 18 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Shadi Moghaddas Breakdown of academic impact, for papers by Xingguo Liu Breakdown of academic impact, for papers by Gian Franco Gaetani Breakdown of academic impact, for papers by John E. Dominy Breakdown of academic impact, for papers by Russell C. Scaduto Breakdown of academic impact, for papers by Ashok K. Srivastava Breakdown of academic impact, for papers by Hirokazu Hara Breakdown of academic impact, for papers by Bülent Mutus Breakdown of academic impact, for papers by Sumiko Inoue Breakdown of academic impact, for papers by Arun K. Das
Rankless by CCL
2026