Shun‐Ping Chang

421 total citations
41 papers, 278 citations indexed

About

Shun‐Ping Chang is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Shun‐Ping Chang has authored 41 papers receiving a total of 278 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 22 papers in Pediatrics, Perinatology and Child Health and 13 papers in Plant Science. Recurrent topics in Shun‐Ping Chang's work include Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (20 papers) and Chromosomal and Genetic Variations (13 papers). Shun‐Ping Chang is often cited by papers focused on Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (20 papers) and Chromosomal and Genetic Variations (13 papers). Shun‐Ping Chang collaborates with scholars based in Taiwan, United States and Switzerland. Shun‐Ping Chang's co-authors include Ming Chen, Gwo‐Chin Ma, Shou‐Jen Kuo, Chin‐San Liu, Chih‐Ping Chen, Ming‐Ching Shen, Wayseen Wang, Jin‐Chung Shih, Kun‐Tu Yeh and Peih-Shan Wu and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Shun‐Ping Chang

37 papers receiving 265 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shun‐Ping Chang Taiwan	10	96	94	89	49	47	41	278
Kyra E. Stuurman Netherlands	8	137 1.4×	72 0.8×	76 0.9×	10 0.2×	64 1.4×	18	274
Steven Schonberg United States	13	247 2.6×	147 1.6×	111 1.2×	21 0.4×	20 0.4×	19	422
R.N. Simmers Australia	9	205 2.1×	158 1.7×	70 0.8×	37 0.8×	31 0.7×	10	389
C. R. Greenberg Canada	8	72 0.8×	88 0.9×	31 0.3×	13 0.3×	22 0.5×	13	218
Thomas R. W. Oliver United Kingdom	5	119 1.2×	70 0.7×	73 0.8×	20 0.4×	11 0.2×	9	252
Kristen S. Jahn United States	5	440 4.6×	52 0.6×	37 0.4×	72 1.5×	20 0.4×	5	530
M. Elizabeth McCready Canada	10	80 0.8×	120 1.3×	39 0.4×	15 0.3×	7 0.1×	25	254
Houda Hamdi‐Rozé France	10	107 1.1×	71 0.8×	27 0.3×	72 1.5×	14 0.3×	14	228
Manoussos N. Papadakis Greece	10	105 1.1×	85 0.9×	76 0.9×	139 2.8×	13 0.3×	22	301
Georgia R. Kafer Australia	7	317 3.3×	32 0.3×	34 0.4×	13 0.3×	18 0.4×	13	407

Countries citing papers authored by Shun‐Ping Chang

Since Specialization

Citations

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

Fields of papers citing papers by Shun‐Ping Chang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shun‐Ping Chang. 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 Shun‐Ping Chang. The network helps show where Shun‐Ping Chang may publish in the future.

Co-authorship network of co-authors of Shun‐Ping Chang

This figure shows the co-authorship network connecting the top 25 collaborators of Shun‐Ping Chang. A scholar is included among the top collaborators of Shun‐Ping Chang 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 Shun‐Ping Chang. Shun‐Ping Chang 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

Chang, Shun‐Ping, et al.. (2025). Utility of long-read sequencing to delineate a rare large deletion of beta-globin gene which escaped Sanger sequencing at prenatal diagnosis in a family clustered with hereditary persistence of fetal hemoglobin. Taiwanese Journal of Obstetrics and Gynecology. 64(6). 1080–1084.

Chang, Ting‐Yu, Wan‐Ju Wu, Mei‐Hui Lee, et al.. (2025). Genetic investigations of autosomal recessive inherited ichthyosis impressed by fetal ultrasound: Exome sequencing and haplotype linkage analysis. Taiwanese Journal of Obstetrics and Gynecology. 64(1). 53–60.

Chen, Ming, et al.. (2022). Origin and timing of de novo variants implicated in type 2 von Willebrand disease. Journal of Cellular and Molecular Medicine. 26(21). 5403–5413. 4 indexed citations

Chen, Chih‐Ping, Ming Chen, Gwo‐Chin Ma, et al.. (2022). Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22. Taiwanese Journal of Obstetrics and Gynecology. 61(2). 364–367.

Ma, Gwo‐Chin, Ying-Chung Chen, Wan‐Ju Wu, et al.. (2019). Prenatal Diagnosis of Autosomal Recessive Renal Tubular Dysgenesis with Anhydramnios Caused by a Mutation in the AGT Gene. Diagnostics. 9(4). 185–185. 5 indexed citations

Chen, Chih‐Ping, Ming Chen, Shun‐Ping Chang, et al.. (2017). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2. Taiwanese Journal of Obstetrics and Gynecology. 56(2). 234–237. 2 indexed citations

Shen, Ming‐Ching, et al.. (2016). De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD. Thrombosis Journal. 14(S1). 36–36. 6 indexed citations

Chen, Ming, Shun‐Ping Chang, Gwo‐Chin Ma, et al.. (2016). Preimplantation genetic diagnosis of hemophilia A. Thrombosis Journal. 14(S1). 33–33. 11 indexed citations

Chen, Chih‐Ping, Kung‐Liahng Wang, Ming Chen, et al.. (2016). Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay. Taiwanese Journal of Obstetrics and Gynecology. 55(3). 419–422. 2 indexed citations

10.

Yang, Yu‐Shih, Shun‐Ping Chang, Hsin‐Fu Chen, et al.. (2015). Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. Molecular Cytogenetics. 8(1). 49–49. 9 indexed citations

11.

Chen, Chih‐Ping, Ming Chen, Yi‐Ning Su, et al.. (2014). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15. Taiwanese Journal of Obstetrics and Gynecology. 53(1). 129–132. 4 indexed citations

12.

Chen, Hsin‐Fu, Shun‐Ping Chang, Sheng-Hai Wu, et al.. (2014). Validating a rapid, real-time, PCR-based direct mutation detection assay for preimplantation genetic diagnosis. Gene. 548(2). 299–305. 14 indexed citations

13.

Chen, Chih‐Ping, Ming Chen, Yi‐Ning Su, et al.. (2013). Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review. Gene. 529(1). 169–175. 13 indexed citations

14.

Yeang, Chen-Hsiang, Gwo‐Chin Ma, Jin‐Chung Shih, et al.. (2012). Genome-Wide Gene Expression Analysis Implicates the Immune Response and Lymphangiogenesis in the Pathogenesis of Fetal Chylothorax. PLoS ONE. 7(4). e34901–e34901. 10 indexed citations

15.

Chen, Chih‐Ping, Ming Chen, Schu‐Rern Chern, et al.. (2012). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2. Taiwanese Journal of Obstetrics and Gynecology. 51(3). 411–417. 8 indexed citations

16.

Chen, Chih‐Ping, Ming Chen, Yi‐Ning Su, et al.. (2012). Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. Taiwanese Journal of Obstetrics and Gynecology. 51(2). 245–252. 3 indexed citations

17.

Chen, Chih‐Ping, Ming Chen, Gwo‐Chin Ma, et al.. (2011). Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome. Taiwanese Journal of Obstetrics and Gynecology. 50(2). 253–257. 1 indexed citations

18.

Lee, Ni‐Chung, Shun‐Ping Chang, Cheng‐Shyong Chang, et al.. (2009). Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding. Prenatal Diagnosis. 29(11). 1058–1060. 3 indexed citations

19.

Chen, Ling‐Yun, Tze-Ho Chen, Chia‐Hung Chou, et al.. (2009). Differential Expression of NUDT9 at Different Phases of The Menstrual Cycle and in Different Components of Normal and Neoplastic Human Endometrium. Taiwanese Journal of Obstetrics and Gynecology. 48(2). 96–107. 2 indexed citations

20.

Ma, Gwo‐Chin, Shuenn‐Dyh Chang, Yu Chang, et al.. (2008). Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography. Fertility and Sterility. 90(4). 1279–1282. 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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