Jiasun Su

691 total citations
38 papers, 477 citations indexed

About

Jiasun Su is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jiasun Su has authored 38 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 15 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jiasun Su's work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Thyroid Disorders and Treatments (6 papers). Jiasun Su is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Thyroid Disorders and Treatments (6 papers). Jiasun Su collaborates with scholars based in China, United States and Taiwan. Jiasun Su's co-authors include Jingsi Luo, Shaoke Chen, Xin Fan, Chunyun Fu, Yiping Shen, Xuyun Hu, Shiyu Luo, Jin Wang, Bobo Xie and Shujie Zhang and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Jiasun Su

38 papers receiving 465 citations

Peers

Jiasun Su

EDM

GENET

PPCH

PRM

Chunyun Fu China

Débora Braslavsky Argentina

Erwin Lankes Germany

Ioanna Bouba Greece

Maria Kalina Poland

Rikke Søe Denmark

Attila Tar Hungary

Takahiro Tsushima United States

Keiichi Hara Japan

M C Postel-Vinay France

Chunyun Fu China

Jiasun Su

199 ×0.9

233 ×1.1

EDM

120 ×0.6

GENET

114 ×0.7

PPCH

42 ×1.0

PRM

Citations per year, relative to Jiasun Su Jiasun Su (= 1×) peers Chunyun Fu

Countries citing papers authored by Jiasun Su

Since Specialization

Citations

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

Fields of papers citing papers by Jiasun Su

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiasun Su

This figure shows the co-authorship network connecting the top 25 collaborators of Jiasun Su. A scholar is included among the top collaborators of Jiasun Su 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 Jiasun Su. Jiasun Su 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

Su, Jiasun, Shujie Zhang, Wei Li, et al.. (2025). Unmasking a Recessive Allele by a Rare Interstitial Deletion at 10q26.13q26.2: Prenatal Diagnosis of MMP21 ‐Related Disorder and Further Refine INSYN2A Involvement in the Postnatal Cognitive Phenotype. Molecular Genetics & Genomic Medicine. 13(2). e70082–e70082. 1 indexed citations

Su, Jiasun, et al.. (2024). Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control study. European Journal of Obstetrics & Gynecology and Reproductive Biology. 297. 91–95. 1 indexed citations

Zhang, Qiang, et al.. (2020). Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literature. BMC Medical Genomics. 13(1). 183–183. 3 indexed citations

Li, Qifei, Lifang Wang, Jiasun Su, et al.. (2019). Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 cases. Scientific Reports. 9(1). 10726–10726. 11 indexed citations

Hu, Xuyun, Chao Li, Jiasun Su, et al.. (2019). The first two Chinese Myhre syndrome patients with the recurrent SMAD4 pathogenic variants: Functional consequences and clinical diversity. Clinica Chimica Acta. 500. 128–134. 5 indexed citations

Fu, Chunyun, Shiyu Luo, Qifei Li, et al.. (2018). Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates. Scientific Reports. 8(1). 833–833. 33 indexed citations

Fu, Chunyun, Shiyu Luo, Yue Zhang, et al.. (2018). Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations. Clinica Chimica Acta. 489. 103–108. 10 indexed citations

Gui, Baoheng, Yanning Song, Xuyun Hu, et al.. (2018). Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome. Gene. 654. 110–115. 5 indexed citations

Fu, Chunyun, Shiyu Luo, Yingfeng Li, et al.. (2017). Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism. Clinica Chimica Acta. 476. 38–43. 16 indexed citations

10.

Hu, Xuyun, Baoheng Gui, Yufei Xu, et al.. (2017). Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants. Clinica Chimica Acta. 474. 159–164. 11 indexed citations

11.

Su, Jiasun, Jin Wang, Xin Fan, et al.. (2017). Mosaic UPD(7q)mat in a patient with silver Russell syndrome. Molecular Cytogenetics. 10(1). 36–36. 8 indexed citations

12.

Fan, Xin, Chunyun Fu, Yiping Shen, et al.. (2017). Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism. Clinica Chimica Acta. 468. 76–80. 41 indexed citations

13.

Fu, Chunyun, Bobo Xie, Shujie Zhang, et al.. (2016). Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism. BMJ Open. 6(5). e010719–e010719. 22 indexed citations

14.

Zhang, Shujie, Jin Wang, Shiyu Luo, et al.. (2016). Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability. Molecular Cytogenetics. 9(1). 66–66. 10 indexed citations

15.

Fu, Chunyun, Jin Wang, Shiyu Luo, et al.. (2016). Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients. Clinica Chimica Acta. 462. 127–132. 25 indexed citations

16.

Wang, Jin, Chunyun Fu, Shujie Zhang, et al.. (2016). A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33. Gene. 594(1). 59–65. 3 indexed citations

17.

Hu, Xuyun, Rongyu Chen, Chunyun Fu, et al.. (2016). Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism. Molecular and Cellular Endocrinology. 423. 60–66. 23 indexed citations

18.

Fu, Chunyun, Shiyu Luo, Shujie Zhang, et al.. (2016). Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients. Clinica Chimica Acta. 458. 30–34. 48 indexed citations

19.

Fu, Chunyun, Shujie Zhang, Yun Chen, et al.. (2016). Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism. Archives of Endocrinology and Metabolism. 60(4). 323–327. 12 indexed citations

20.

Shang, Lin, et al.. (2012). Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.. PubMed. 23(3). 405–13. 4 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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