Mei‐Chyn Chao

1.0k total citations
52 papers, 804 citations indexed

About

Mei‐Chyn Chao is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mei‐Chyn Chao has authored 52 papers receiving a total of 804 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mei‐Chyn Chao's work include Genetic Syndromes and Imprinting (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Mei‐Chyn Chao is often cited by papers focused on Genetic Syndromes and Imprinting (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Mei‐Chyn Chao collaborates with scholars based in Taiwan, United States and France. Mei‐Chyn Chao's co-authors include Wuh‐Liang Hwu, Li‐Ping Tsai, Bai‐Hsiun Chen, Jiunn‐Ren Wu, Chia‐Fang Wu, Fuu‐Jen Tsai, Hsiang‐Yu Lin, Ming‐Tsang Wu, Chih‐Kuang Chuang and Dau‐Ming Niu and has published in prestigious journals such as Environmental Science & Technology, PLoS ONE and Analytical Biochemistry.

In The Last Decade

Mei‐Chyn Chao

49 papers receiving 782 citations

Peers

Mei‐Chyn Chao

PHYSI

GENET

HTM

EPIDE

Daoyin Dong United States

Mariarosaria Negri Italy

Jogi V. Pattisapu United States

Lauren A. Vanderlinden United States

Junko Nishioka Japan

Timothy M. Barrow United Kingdom

Cheng‐Hui Lin Taiwan

Nancy L. Parmalee United States

Dandan Zong China

Elisabete Silva Portugal

Daoyin Dong United States

Mei‐Chyn Chao

373 ×1.3

73 ×0.4

PHYSI

85 ×0.5

GENET

38 ×0.2

HTM

132 ×1.3

EPIDE

Citations per year, relative to Mei‐Chyn Chao Mei‐Chyn Chao (= 1×) peers Daoyin Dong

Countries citing papers authored by Mei‐Chyn Chao

Since Specialization

Citations

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

Fields of papers citing papers by Mei‐Chyn Chao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mei‐Chyn Chao. 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 Mei‐Chyn Chao. The network helps show where Mei‐Chyn Chao may publish in the future.

Co-authorship network of co-authors of Mei‐Chyn Chao

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

All Works

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20 of 20 papers shown

Chen, Kuan‐Jung, Mei‐Chyn Chao, Tung‐Ming Chang, et al.. (2021). Genotype and phenotype studies of Lowe syndrome in three families in Taiwan. Pediatrics & Neonatology. 62(3). 327–328.

Lin, Hsiang‐Yu, Chung‐Lin Lee, Chia-Ying Chang, et al.. (2020). Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019). Orphanet Journal of Rare Diseases. 15(1). 314–314. 17 indexed citations

Chien, Yin‐Hsiu, et al.. (2013). Fatty Acid Oxidation Disorders in a Chinese Population in Taiwan. JIMD Reports. 11. 165–172. 28 indexed citations

Hsiao, Hui‐Pin, et al.. (2010). Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus. International Journal of Pediatric Endocrinology. 2010. 1–4. 4 indexed citations

Lin, Hsiang‐Yu, Chih‐Kuang Chuang, Dau‐Ming Niu, et al.. (2009). Incidence of the mucopolysaccharidoses in Taiwan, 1984–2004. American Journal of Medical Genetics Part A. 149A(5). 960–964. 150 indexed citations

Chao, Mei‐Chyn, et al.. (2009). Ischemic Stroke in Williams‐Beuren Syndrome: A Case Report. The Kaohsiung Journal of Medical Sciences. 25(4). 212–216. 3 indexed citations

Hwa, Hsiao‐Lin, Chien‐Hao Huang, Chung‐Hsiung Chen, et al.. (2008). Small Mutations of the DMD Gene in Taiwanese Families. Journal of the Formosan Medical Association. 107(6). 463–469. 6 indexed citations

Lo, Fu‐Sung, Pao‐Chin Chiu, San‐Ging Shu, et al.. (2008). Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature. European Journal of Pediatrics. 168(8). 919–923. 24 indexed citations

Hwa, Hsiao‐Lin, et al.. (2007). Multiplex Ligation-dependent Probe Amplification Identification of Deletions and Duplications of the Duchenne Muscular Dystrophy Gene in Taiwanese Subjects. Journal of the Formosan Medical Association. 106(5). 339–346. 33 indexed citations

10.

Chao, Mei‐Chyn, et al.. (2007). A sensitive liquid chromatographic method for the analysis of isovaleric and valeric acids in urine as fluorescent derivatives. Journal of Chromatography A. 1156(1-2). 259–263. 3 indexed citations

11.

Lee, Yann‐Jinn, et al.. (2007). Mutational Analysis of PTPN11 Gene in Taiwanese Children with Noonan Syndrome. Journal of the Formosan Medical Association. 106(2). 169–172. 23 indexed citations

12.

Lin, Hsiang‐Yu, Han‐Yang Hung, Hsin‐An Kao, et al.. (2007). Prader–Willi syndrome in Taiwan. Pediatrics International. 49(3). 375–379. 15 indexed citations

13.

Tzeng, Ching‐Cherng, Li‐Ping Tsai, Wuh‐Liang Hwu, et al.. (2005). Prevalence of theFMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype. American Journal of Medical Genetics Part A. 133A(1). 37–43. 48 indexed citations

14.

Hsiao, Hui‐Hua, Ming‐Yu Yang, Yi‐Chang Liu, et al.. (2005). RBM15-MKL1 (OTT-MAL) fusion transcript in an adult acute myeloid leukemia patient. American Journal of Hematology. 79(1). 43–45. 13 indexed citations

15.

Hsiao, Hui‐Hua, Hui‐Pin Hsiao, Hui‐Jen Tsai, et al.. (2004). Case of Chronic Lymphocytic Leukemia with Unusual Chromosome Aberrations. International Journal of Hematology. 80(4). 351–353. 4 indexed citations

16.

Tung, Yi‐Ching, et al.. (2004). Comparison of Nucleotide Sequence of P2C Region in Diabetogenic and Non‐Diabetogenic Coxsackie Virus B5 Isolates. The Kaohsiung Journal of Medical Sciences. 20(11). 525–532. 1 indexed citations

17.

Liu, Yichun, Ming‐Liang Lee, Chih‐Ping Chen, et al.. (1997). Inversion and Enlargement of the Heterochromatin Region of Chromosome No.9 among Taiwanese. 9(3). 159–167. 2 indexed citations

18.

Tsai, Wen–Yu, et al.. (1995). Prevalence of permanent primary congenital hypothyroidism in Taiwan.. PubMed. 94(5). 271–3. 9 indexed citations

19.

Chang, Chao‐Sung, Sheng‐Fung Lin, Tyen‐Po Chen, et al.. (1992). Leukemic manifestation in a case of alpha‐chain disease with multiple polypoid intestinal lymphocytic lymphoma. American Journal of Hematology. 41(3). 209–214. 6 indexed citations

20.

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

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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