Jun-Wei Su

1.1k total citations
75 papers, 658 citations indexed

About

Jun-Wei Su is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Jun-Wei Su has authored 75 papers receiving a total of 658 indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 48 papers in Pediatrics, Perinatology and Child Health and 26 papers in Molecular Biology. Recurrent topics in Jun-Wei Su's work include Prenatal Screening and Diagnostics (45 papers), Genomic variations and chromosomal abnormalities (38 papers) and Congenital Anomalies and Fetal Surgery (12 papers). Jun-Wei Su is often cited by papers focused on Prenatal Screening and Diagnostics (45 papers), Genomic variations and chromosomal abnormalities (38 papers) and Congenital Anomalies and Fetal Surgery (12 papers). Jun-Wei Su collaborates with scholars based in Taiwan, Canada and United States. Jun-Wei Su's co-authors include Wayseen Wang, Chih‐Ping Chen, Schu‐Rern Chern, Peih-Shan Wu, Yi‐Ning Su, Yi‐Yung Chen, Lifeng Chen, Chen‐Chi Lee, Chen‐Wen Pan and Wenlin Chen and has published in prestigious journals such as Gene, Medicine and Genomics.

In The Last Decade

Jun-Wei Su

75 papers receiving 598 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jun-Wei Su Taiwan	14	472	353	197	106	99	75	658
Chen‐Wen Pan Taiwan	14	438 0.9×	418 1.2×	136 0.7×	124 1.2×	98 1.0×	68	593
Chen‐Chi Lee Taiwan	17	673 1.4×	550 1.6×	285 1.4×	185 1.7×	176 1.8×	116	929
Judy Chernos Canada	15	521 1.1×	286 0.8×	375 1.9×	97 0.9×	132 1.3×	38	859
Shin-Wen Chen Taiwan	12	511 1.1×	548 1.6×	180 0.9×	166 1.6×	77 0.8×	152	747
Koh‐ichiro Yoshiura Japan	14	170 0.4×	185 0.5×	181 0.9×	58 0.5×	32 0.3×	35	549
Anna Baroncini Italy	13	256 0.5×	128 0.4×	149 0.8×	61 0.6×	101 1.0×	29	458
Nathalie Leporrier France	15	167 0.4×	251 0.7×	153 0.8×	94 0.9×	34 0.3×	24	478
I. López Pajares Spain	12	316 0.7×	106 0.3×	286 1.5×	76 0.7×	94 0.9×	27	493
Daniele De Brasi Italy	14	256 0.5×	86 0.2×	224 1.1×	73 0.7×	48 0.5×	44	478
N. Morichon-Delvallez France	12	320 0.7×	143 0.4×	173 0.9×	66 0.6×	74 0.7×	26	418

Countries citing papers authored by Jun-Wei Su

Since Specialization

Citations

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

Fields of papers citing papers by Jun-Wei Su

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jun-Wei Su

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

Chen, Chih‐Ping, Chen‐Ju Lin, Schu‐Rern Chern, et al.. (2013). Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta. Taiwanese Journal of Obstetrics and Gynecology. 52(2). 303–305. 3 indexed citations

Chen, Chih‐Ping, Tung‐Yao Chang, Wan‐Yuo Guo, et al.. (2013). Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of maternal epilepsy. Taiwanese Journal of Obstetrics and Gynecology. 52(3). 415–419. 9 indexed citations

Chen, Chih‐Ping, et al.. (2013). Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis. Taiwanese Journal of Obstetrics and Gynecology. 52(4). 607–610. 4 indexed citations

Chen, Chih‐Ping, Chen‐Yu Chen, Jun-Wei Su, & Wayseen Wang. (2013). Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios. Taiwanese Journal of Obstetrics and Gynecology. 52(4). 571–574. 1 indexed citations

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2013). Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review. Genomics. 102(4). 265–269. 7 indexed citations

Chen, Chih‐Ping, Shuenn‐Dyh Chang, Ho‐Yen Chueh, et al.. (2013). Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20. Taiwanese Journal of Obstetrics and Gynecology. 52(1). 145–146. 14 indexed citations

Chen, Chih‐Ping, Her‐Young Su, Shuan‐Pei Lin, et al.. (2013). Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry. Taiwanese Journal of Obstetrics and Gynecology. 52(1). 125–128. 14 indexed citations

Chen, Chih‐Ping, Shuenn‐Dyh Chang, Tzu‐Hao Wang, et al.. (2013). Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family. Taiwanese Journal of Obstetrics and Gynecology. 52(4). 551–557. 20 indexed citations

Chen, Chih‐Ping, Tsang‐Ming Ko, Schu‐Rern Chern, et al.. (2013). Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review. Taiwanese Journal of Obstetrics and Gynecology. 52(3). 446–449. 18 indexed citations

10.

Chen, Chih‐Ping, Yi‐Ning Su, Tung‐Yao Chang, et al.. (2013). Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst, and Apert syndrome. Taiwanese Journal of Obstetrics and Gynecology. 52(2). 273–277. 1 indexed citations

11.

Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2013). Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 52(3). 450–453. 5 indexed citations

12.

Chen, Chih‐Ping, Yi‐Ning Su, Jun-Wei Su, et al.. (2013). Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis. Taiwanese Journal of Obstetrics and Gynecology. 52(1). 97–105. 19 indexed citations

13.

Chen, Chih‐Ping, Shuan‐Pei Lin, Yi‐Ning Su, et al.. (2013). Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 52(1). 152–153. 1 indexed citations

14.

Chen, Chih‐Ping, et al.. (2013). VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer. Taiwanese Journal of Obstetrics and Gynecology. 52(4). 575–579. 8 indexed citations

15.

Chen, Chih‐Ping, Yi‐Ning Su, Tung‐Yao Chang, et al.. (2012). Osteogenesis imperfecta type I: Second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father. Taiwanese Journal of Obstetrics and Gynecology. 51(2). 276–279. 2 indexed citations

16.

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

17.

Chen, Chih‐Ping, Shuenn‐Dyh Chang, Yuting Chen, et al.. (2012). Mosaic isochromosome 20q detected at amniocentesis: A likely cell culture artifact. Taiwanese Journal of Obstetrics and Gynecology. 51(4). 663–665. 4 indexed citations

18.

Chen, Chih‐Ping, Yi‐Ning Su, Yi‐Yung Chen, et al.. (2012). Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly. Taiwanese Journal of Obstetrics and Gynecology. 51(3). 471–474. 4 indexed citations

19.

Chen, Chih‐Ping, Shuan‐Pei Lin, Yi‐Ning Su, et al.. (2012). Osteogenesis imperfecta type IV: Prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 51(2). 271–275. 7 indexed citations

20.

Chen, Chih‐Ping, Yi‐Yung Chen, Jun-Wei Su, & Wayseen Wang. (2011). First-trimester two-dimensional and three-dimensional ultrasound demonstration of craniofacial defects, abdominal wall defects and upper limb deficiency associated with limb–body wall complex. Taiwanese Journal of Obstetrics and Gynecology. 50(4). 558–560. 2 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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