Lin-ya Tang

490 total citations
6 papers, 187 citations indexed

About

Lin-ya Tang is a scholar working on Molecular Biology, Clinical Biochemistry and Infectious Diseases. According to data from OpenAlex, Lin-ya Tang has authored 6 papers receiving a total of 187 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 1 paper in Infectious Diseases. Recurrent topics in Lin-ya Tang's work include Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and Genomics and Rare Diseases (1 paper). Lin-ya Tang is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and Genomics and Rare Diseases (1 paper). Lin-ya Tang collaborates with scholars based in United States, France and Taiwan. Lin-ya Tang's co-authors include Lee‐Jun C. Wong, David Dimmock, Eric Schmitt, Chad A. Shaw, A. Craig Chinault, Ellen K. Brundage, S. Lane Rutledge, Maria Descartes, Christine Reyes and Yasutoshi Koga and has published in prestigious journals such as Clinical Chemistry, Neuro-Oncology and Genetics in Medicine.

In The Last Decade

Lin-ya Tang

6 papers receiving 184 citations

Peers

Lin-ya Tang
Ping Chun Wu United States
William L. Macken United Kingdom
Rocío Rius Australia
Jose Carlo United States
William Lee Australia
Tom Hofste Netherlands
John W. Yarham United Kingdom
Lin-ya Tang
Citations per year, relative to Lin-ya Tang Lin-ya Tang (= 1×) peers Yukiko Yatsuka

Countries citing papers authored by Lin-ya Tang

Since Specialization
Citations

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

Fields of papers citing papers by Lin-ya Tang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lin-ya Tang. 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 Lin-ya Tang. The network helps show where Lin-ya Tang may publish in the future.

Co-authorship network of co-authors of Lin-ya Tang

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

All Works

6 of 6 papers shown
1.
Eterovic, Agda Karina, Nader Ezzeddine, Ping Song, et al.. (2019). HGG-09. A ROBUST CELL-FREE DNA (CFDNA) ASSAY TO DETECT MUTATIONS IN PLASMA SAMPLES OF PEDIATRIC HIGH GRADE GLIOMA PATIENTS DESPITE GENOMIC DNA (GDNA) CONTAMINATION. Neuro-Oncology. 21(Supplement_2). ii88–ii88. 1 indexed citations
2.
Dimmock, David, Lin-ya Tang, Eric Schmitt, & Lee‐Jun C. Wong. (2010). Quantitative Evaluation of the Mitochondrial DNA Depletion Syndrome. Clinical Chemistry. 56(7). 1119–1127. 101 indexed citations
3.
Nishigaki, Yutaka, Hitomi Ueno, Jorida Çoku, et al.. (2010). Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. Mitochondrion. 10(3). 300–308. 24 indexed citations
4.
Chinault, A. Craig, Chad A. Shaw, Ellen K. Brundage, Lin-ya Tang, & Lee‐Jun C. Wong. (2009). Application of dual-genome oligonucleotidearray-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes. Genetics in Medicine. 11(7). 518–526. 40 indexed citations
5.
Dimmock, David, Lin-ya Tang, Maria Descartes, et al.. (2009). A novel c.592-4_c.592-3delTT mutation in DGUOK gene causes exon skipping. Mitochondrion. 10(2). 188–191. 13 indexed citations
6.
Lutz, Richard E., David Dimmock, Eric Schmitt, et al.. (2009). De Novo Mutations in POLG Presenting with Acute Liver Failure or Encephalopathy. Journal of Pediatric Gastroenterology and Nutrition. 49(1). 126–129. 8 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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