Franklin Quan

995 total citations
25 papers, 740 citations indexed

About

Franklin Quan is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Franklin Quan has authored 25 papers receiving a total of 740 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Pulmonary and Respiratory Medicine and 6 papers in Genetics. Recurrent topics in Franklin Quan's work include Cystic Fibrosis Research Advances (8 papers), Congenital Ear and Nasal Anomalies (6 papers) and Mitochondrial Function and Pathology (3 papers). Franklin Quan is often cited by papers focused on Cystic Fibrosis Research Advances (8 papers), Congenital Ear and Nasal Anomalies (6 papers) and Mitochondrial Function and Pathology (3 papers). Franklin Quan collaborates with scholars based in United States, Canada and Poland. Franklin Quan's co-authors include Weimin Sun, Charles M. Strom, Joy B. Redman, Arlene Buller, Bradley W. Popovich, Mei Peng, Beryl Crossley, Nancy G. Kennaway, Roberto P. Anitori and Neil R.M. Buist and has published in prestigious journals such as Molecular and Cellular Biology, Development and Methods in enzymology on CD-ROM/Methods in enzymology.

In The Last Decade

Franklin Quan

24 papers receiving 713 citations

Peers

Franklin Quan
Xiangdong Bu United States
Marie Vincent France
Kinga Hadzsiev Hungary
Maria Descartes United States
Christine Reyes United States
Lindsay B. Henderson United States
Hisato Suzuki Japan
Naomi Hino‐Fukuyo Japan
Jiddeke M. van de Kamp Netherlands
Xiangdong Bu United States
Franklin Quan
Citations per year, relative to Franklin Quan Franklin Quan (= 1×) peers Xiangdong Bu

Countries citing papers authored by Franklin Quan

Since Specialization
Citations

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

Fields of papers citing papers by Franklin Quan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Franklin Quan. 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 Franklin Quan. The network helps show where Franklin Quan may publish in the future.

Co-authorship network of co-authors of Franklin Quan

This figure shows the co-authorship network connecting the top 25 collaborators of Franklin Quan. A scholar is included among the top collaborators of Franklin Quan 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 Franklin Quan. Franklin Quan 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.
Strom, Charles M., Beryl Crossley, Ke Zhang, et al.. (2012). Testing for variants in CYP2C19: population frequencies and testing experience in a clinical laboratory. Genetics in Medicine. 14(1). 95–100. 64 indexed citations
2.
Strom, Charles M., Beryl Crossley, Michael Jarvis, et al.. (2010). Cystic fibrosis testing 8 years on: Lessons learned from carrier screening and sequencing analysis. Genetics in Medicine. 13(2). 166–172. 37 indexed citations
3.
4.
Strom, Charles M., Beryl Crossley, Joy B. Redman, et al.. (2007). Molecular testing for Fragile X Syndrome: Lessons learned from 119,232 tests performed in a clinical laboratory. Genetics in Medicine. 9(1). 46–51. 42 indexed citations
5.
McGinniss, Matthew J., Rebecca Chen, Victoria M. Pratt, et al.. (2007). Development of a Web-Based Query Tool for Quality Assurance of Clinical Molecular Genetic Test Results. Journal of Molecular Diagnostics. 9(1). 95–98. 2 indexed citations
6.
7.
Sun, Weimin, Ben Anderson, Joy B. Redman, et al.. (2006). CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotype. Genetics in Medicine. 8(6). 339–345. 22 indexed citations
8.
Hantash, Feras, Joy B. Redman, Ben Anderson, et al.. (2006). Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening. Human Genetics. 119(3). 352–352. 1 indexed citations
9.
Brown, Nicholas M., Victoria M. Pratt, Arlene Buller, et al.. (2005). Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping results. Genetics in Medicine. 7(4). 278–282. 16 indexed citations
10.
Strom, Charles M., Richard Janeczko, Ben Anderson, et al.. (2005). Technical validation of a multiplex platform to detect thirty mutations in eight genetic diseases prevalent in individuals of Ashkenazi Jewish descent. Genetics in Medicine. 7(9). 633–639. 13 indexed citations
11.
Hantash, Feras, Joy B. Redman, Ben Anderson, et al.. (2005). Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening. Human Genetics. 119(1-2). 126–136. 37 indexed citations
12.
McGinniss, Matthew J., Christina Chen, Joy B. Redman, et al.. (2005). Extensive Sequencing of the CFTR gene: lessons learned from the first 157 patient samples. Human Genetics. 118(3-4). 331–338. 25 indexed citations
13.
Strom, Charles M., Beryl Crossley, Joy B. Redman, et al.. (2004). Cystic fibrosis screening: Lessons learned from the first 320,000 patients. Genetics in Medicine. 6(3). 136–140. 24 indexed citations
14.
Strom, Charles M., Beryl Crossley, Joy B. Redman, et al.. (2004). Molecular screening for diseases frequent in Ashkenazi Jews: Lessons learned from more than 100,000 tests performed in a commercial laboratory. Genetics in Medicine. 6(3). 145–152. 28 indexed citations
15.
Anitori, Roberto P., Franklin Quan, Richard G. Weleber, et al.. (2004). Contrasting phenotypes in three patients with novel mutations in mitochondrial tRNA genes. Molecular Genetics and Metabolism. 84(2). 176–188. 35 indexed citations
16.
Strom, Charles M., Donghui Huang, Christina Chen, et al.. (2003). Extensive sequencing of the cystic fibrosis transmembrane regulator gene: Assay validation and unexpected benefits of developing a comprehensive test. Genetics in Medicine. 5(1). 9–14. 44 indexed citations
17.
Keightley, J. Andrew, Roberto P. Anitori, Miriam D. Burton, et al.. (2000). Mitochondrial Encephalomyopathy and Complex III Deficiency Associated with a Stop-Codon Mutation in the Cytochrome b Gene. The American Journal of Human Genetics. 67(6). 1400–1410. 96 indexed citations
18.
Quan, Franklin, Markus Grompe, Petra Jakobs, & Bradley W. Popovich. (1995). Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism. Human Molecular Genetics. 4(9). 1681–1684. 43 indexed citations
19.
Quan, Franklin, et al.. (1995). A novel CAG repeat configuration in the SCA1 gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1. Human Molecular Genetics. 4(12). 2411–2413. 50 indexed citations
20.
Quan, Franklin, et al.. (1991). Human cytochrome c oxidase subunit VIb: characterization and mapping of a multigene family. Gene. 102(2). 229–236. 16 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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