May–Jen Huang

601 total citations
18 papers, 466 citations indexed

About

May–Jen Huang is a scholar working on Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, May–Jen Huang has authored 18 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Pediatrics, Perinatology and Child Health, 8 papers in Pulmonary and Respiratory Medicine and 6 papers in Molecular Biology. Recurrent topics in May–Jen Huang's work include Neonatal Health and Biochemistry (17 papers), Methemoglobinemia and Tumor Lysis Syndrome (8 papers) and Heme Oxygenase-1 and Carbon Monoxide (5 papers). May–Jen Huang is often cited by papers focused on Neonatal Health and Biochemistry (17 papers), Methemoglobinemia and Tumor Lysis Syndrome (8 papers) and Heme Oxygenase-1 and Carbon Monoxide (5 papers). May–Jen Huang collaborates with scholars based in Taiwan, United States and Singapore. May–Jen Huang's co-authors include Ching‐Shan Huang, Hsiu‐Chen Teng, Kung-Sheng Tang, Hui-Wen Weng, Pi‐Feng Chang, Sien‐Sing Yang, Kuo‐Inn Tsou Yau, Kun‐Long Hung, Tang K. Tang and Hua‐Ling Chen and has published in prestigious journals such as Gastroenterology, Biochemical and Biophysical Research Communications and World Journal of Gastroenterology.

In The Last Decade

May–Jen Huang

18 papers receiving 446 citations

Peers

May–Jen Huang
Andrew D. Johnson United States
David Roper United Kingdom
L Schalm Netherlands
M Tasso Spain
Donald B. Rolfes United States
May–Jen Huang
Citations per year, relative to May–Jen Huang May–Jen Huang (= 1×) peers E Salvidio

Countries citing papers authored by May–Jen Huang

Since Specialization
Citations

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

Fields of papers citing papers by May–Jen Huang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by May–Jen Huang. 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 May–Jen Huang. The network helps show where May–Jen Huang may publish in the future.

Co-authorship network of co-authors of May–Jen Huang

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

All Works

18 of 18 papers shown
1.
Huang, May–Jen, Yu‐Cheng Lin, Kevin Liu, Pi‐Feng Chang, & Ching‐Shan Huang. (2020). Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia. Pediatrics & Neonatology. 61(5). 506–512. 5 indexed citations
2.
Huang, May–Jen, et al.. (2014). Multiple variants in UGT1A1 gene are factors to develop indirect hyper-bilirubinemia.. PubMed. 3(4). 194–8. 6 indexed citations
3.
Huang, Yangyang, et al.. (2011). Bilirubin concentrations in thalassemia heterozygotes in university students. European Journal Of Haematology. 86(4). 317–323. 4 indexed citations
4.
Huang, Yangyang, et al.. (2008). Variations in the UDP-Glucuronosyltransferase 1A1 Gene for the Development of Unconjugated Hyperbilirubinemia in Taiwanese. Pharmacogenomics. 9(9). 1229–1235. 15 indexed citations
5.
Tang, Kung-Sheng, Chuan–Mo Lee, Hsiu‐Chen Teng, May–Jen Huang, & Ching‐Shan Huang. (2007). UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis. Biochemical and Biophysical Research Communications. 366(3). 643–648. 10 indexed citations
6.
Huang, Ching‐Shan, et al.. (2006). Crigler-Najjar Syndrome Type 2. Journal of the Formosan Medical Association. 105(11). 950–953. 8 indexed citations
7.
Huang, Ching‐Shan, et al.. (2005). Genetic factors related to unconjugated hyperbilirubinemia amongst adults. Pharmacogenetics and Genomics. 15(1). 43–50. 46 indexed citations
8.
Huang, May–Jen. (2005). Polymorphisms of uridine-diphosphoglucuronosyltransferase 1A7 gene in Taiwan Chinese. World Journal of Gastroenterology. 11(6). 797–797. 18 indexed citations
9.
Huang, May–Jen, et al.. (2004). Risk Factors for Severe Hyperbilirubinemia in Neonates. Pediatric Research. 56(5). 682–689. 178 indexed citations
10.
11.
Huang, Ching‐Shan, et al.. (2002). Relationship Between Bilirubin UDP-Glucuronosyl Transferase 1A1 Gene and Neonatal Hyperbilirubinemia. Pediatric Research. 52(4). 601–605. 60 indexed citations
12.
Huang, Ching‐Shan, et al.. (2002). Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia. Gastroenterology. 123(1). 127–133. 68 indexed citations
13.
Huang, Ching‐Shan, et al.. (2001). A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A 1 gene that causes Crigler‐Najjar syndrome type II. Pharmacogenetics. 11(7). 639–642. 11 indexed citations
14.
Huang, May–Jen, et al.. (2001). Genetic variations of randomly amplified polymorphic DNA polymorphisms in Taoyuan and Duroc pigs. 118(2). 111–118. 1 indexed citations
15.
Chen, Hua‐Ling, May–Jen Huang, Ching‐Shan Huang, & Tang K. Tang. (1996). G6PD IManKang (517 T→C; 173 Phe→Leu): A New Chinese G6PD Variant Associated with Neonatal Jaundice. Human Heredity. 46(4). 201–204. 17 indexed citations
16.
Huang, Ching‐Shan, et al.. (1992). Molecular Diagnosis of Glucose-6-Phosphate Dehydrogenase (G6PD) Mutations. 3(4). 47–59. 3 indexed citations
17.
Huang, Ching‐Shan, Chieh-Ju C. Tang, May–Jen Huang, & Tang K. Tang. (1992). Diagnosis of Glucose-6-Phosphate Dehydrogenase (G6PD) Mutations by DNA Amplification and Allele-Specific Oligonucleotide Probes. Acta Haematologica. 88(2-3). 92–95. 2 indexed citations
18.
Tang, Tang, et al.. (1992). Molecular diagnosis of G6PD mutations. 3. 47–59. 3 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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