Shio‐Jean Lin

972 total citations
20 papers, 733 citations indexed

About

Shio‐Jean Lin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shio‐Jean Lin has authored 20 papers receiving a total of 733 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shio‐Jean Lin's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Congenital limb and hand anomalies (2 papers). Shio‐Jean Lin is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Congenital limb and hand anomalies (2 papers). Shio‐Jean Lin collaborates with scholars based in Taiwan, United States and India. Shio‐Jean Lin's co-authors include Chao Huang, Wuh‐Liang Hwu, Ching‐Chuan Liu, Tsu‐Fuh Yeh, Yao‐Jong Yang, Jen‐Ren Wang, Shih‐Min Wang, Yin‐Hsiu Chien, Ni‐Chung Lee and Hui-Ying Yeh and has published in prestigious journals such as Clinical Infectious Diseases, Epidemiology and Urology.

In The Last Decade

Shio‐Jean Lin

20 papers receiving 714 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shio‐Jean Lin Taiwan 10 277 249 214 178 171 20 733
Hiroyuki Torisu Japan 17 59 0.2× 58 0.2× 113 0.5× 150 0.8× 193 1.1× 57 804
R Arana Argentina 7 243 0.9× 65 0.3× 74 0.3× 42 0.2× 107 0.6× 12 570
E. Kinnunen Finland 17 46 0.2× 166 0.7× 111 0.5× 150 0.8× 98 0.6× 37 928
Esther Picillo Italy 17 81 0.3× 162 0.7× 164 0.8× 24 0.1× 458 2.7× 32 817
George R. Noren United States 16 40 0.1× 289 1.2× 192 0.9× 48 0.3× 67 0.4× 43 720
Samuel H. Tucker United States 12 68 0.2× 60 0.2× 53 0.2× 58 0.3× 127 0.7× 16 415
Tommy Stödberg Sweden 14 56 0.2× 39 0.2× 138 0.6× 118 0.7× 169 1.0× 22 625
Quentin Pascal France 10 102 0.4× 41 0.2× 84 0.4× 83 0.5× 417 2.4× 23 748
Yuan Lü China 11 114 0.4× 18 0.1× 158 0.7× 128 0.7× 119 0.7× 40 579
S. K. Shankar India 19 56 0.2× 38 0.2× 144 0.7× 132 0.7× 149 0.9× 40 797

Countries citing papers authored by Shio‐Jean Lin

Since Specialization
Citations

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

Fields of papers citing papers by Shio‐Jean Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shio‐Jean Lin. 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 Shio‐Jean Lin. The network helps show where Shio‐Jean Lin may publish in the future.

Co-authorship network of co-authors of Shio‐Jean Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Shio‐Jean Lin. A scholar is included among the top collaborators of Shio‐Jean Lin 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 Shio‐Jean Lin. Shio‐Jean Lin 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.
Chow, Julie Chi, et al.. (2014). Genetic Evaluation of Children with Global Developmental Delay—Current Status of Network Systems in Taiwan. Pediatrics & Neonatology. 56(4). 213–219. 3 indexed citations
2.
Tsai, Meng‐Che, Yen‐Yin Chou, Shio‐Jean Lin, & Li‐Ping Tsai. (2012). A novel SRD5A2 mutation in a Taiwanese newborn with ambiguous genitalia. The Kaohsiung Journal of Medical Sciences. 28(4). 231–235. 6 indexed citations
3.
Lin, Hsiang‐Yu, Ming‐Ren Chen, Chih‐Kuang Chuang, et al.. (2010). Enzyme replacement therapy for mucopolysaccharidosis VI—experience in Taiwan. Journal of Inherited Metabolic Disease. 33(S3). 421–427. 23 indexed citations
4.
Chou, Yen‐Yin, et al.. (2010). Complex Chromosome Rearrangement 46,XY, der(9)t(Y;9)(q12;p23) in a Girl With Sex Reversal and Mental Retardation. Urology. 77(5). 1213–1216. 5 indexed citations
5.
Chen, Chung‐Yu, Yumin Wu, Yen‐Yin Chou, Shio‐Jean Lin, & Ching-Chang Lee. (2010). Phthalate Exposure May Affect Girl Puberty Via Stimulation of Kisspeptin-54 Secretion. Epidemiology. 22. S127–S128. 1 indexed citations
6.
Hwu, Wuh‐Liang, Yin‐Hsiu Chien, Ni‐Chung Lee, et al.. (2009). Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onsetGLAmutation c.936+919G>A (IVS4+919G>A). Human Mutation. 30(10). 1397–1405. 263 indexed citations
7.
Hung, Chia‐Cheng, Yi‐Ning Su, Po‐Nien Tsao, et al.. (2007). Unequal crossover recombination – population screening for PHOX2B gene polyalanine polymorphism using CE. Electrophoresis. 28(6). 894–899. 22 indexed citations
8.
Chen, Pau‐Chung, Suh‐Fang Jeng, Chia‐Jung Hsieh, et al.. (2007). High perinatal seroprevalence of cytomegalovirus in northern Taiwan. Journal of Paediatrics and Child Health. 44(4). 166–169. 42 indexed citations
9.
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
10.
Chou, Yen‐Yin, et al.. (2005). Hypophosphatasia in Taiwan: Report of Two Cases. The Kaohsiung Journal of Medical Sciences. 21(3). 134–137. 3 indexed citations
11.
Chien, Yin‐Hsiu, Hui-Ying Yeh, Shio‐Jean Lin, et al.. (2003). Phenotype and genotype analyses of ornithine transcarbamylase deficiency in Taiwanese.. PubMed. 102(12). 851–6. 2 indexed citations
12.
Tzeng, Ching‐Cherng, et al.. (2000). Implication of Screening for FMR1 and FMR2 Gene Mutation in Individuals With Nonspecific Mental Retardation in Taiwan. Diagnostic Molecular Pathology. 9(2). 75–80. 14 indexed citations
13.
Wang, Shih‐Min, Ching‐Chuan Liu, Jen‐Ren Wang, et al.. (1999). Clinical Spectrum of Enterovirus 71 Infection in Children in Southern Taiwan, with an Emphasis on Neurological Complications. Clinical Infectious Diseases. 29(1). 184–190. 248 indexed citations
14.
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
15.
Wu, Meng‐Hsing, Pao‐Lin Kuo, & Shio‐Jean Lin. (1995). Prenatal diagnosis of recurrence of short rib‐polydactyly syndrome. American Journal of Medical Genetics. 55(3). 279–284. 14 indexed citations
16.
Huang, Chao, et al.. (1992). X‐linked recessive inheritance of dysgenesis of corpus callosum in a chinese family. American Journal of Medical Genetics. 44(5). 619–623. 12 indexed citations
17.
Chang, Chen‐Lin, et al.. (1991). 15‐Hydroxyprostaglandin Dehydrogenase Activity in the Lower Genitourinary Tract A Preliminary Report. British Journal of Urology. 68(6). 579–581. 5 indexed citations
18.
Wu, Jing‐Ming, et al.. (1991). Unusual cardiac malformations in Holt-Oram syndrome: report of two cases.. PubMed. 32(2). 100–4. 7 indexed citations
19.
Lin, Shio‐Jean, Tso‐Ren Wang, & Sou‐Ming Chuang. (1990). Partial trisomy 13q: report of a case.. PubMed. 29(4). 270–3. 1 indexed citations
20.
Wang, Tso‐Ren, Shio‐Jean Lin, John M. Opitz, & James F. Reynolds. (1987). Further evidence for genetic heterogeneity of whistling face or Freeman‐Sheldon syndrome in a Chinese family. American Journal of Medical Genetics. 28(2). 471–475. 12 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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