Jun-Wei Su

1.1k citations

75 papers · 658 indexed · h-index 14

Impact in

Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Assisted Reproductive Technology and Twin Pregnancy
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting

Papers in ⓘ

Pediatrics, Perinatology and Child Health 48
- Prenatal Screening and Diagnostics 45
Genetics 52
- Genomic variations and chromosomal abnormalities 38
- Genetic Syndromes and Imprinting 8
- Connective tissue disorders research 7

Co-authors: Chih‐Ping Chen (72 shared papers)Wayseen Wang (72 shared papers)Schu‐Rern Chern (64 shared papers)Peih-Shan Wu (36 shared papers)Yi‐Ning Su (28 shared papers)Yi‐Yung Chen (16 shared papers)Lifeng Chen (15 shared papers)Chen‐Chi Lee (17 shared papers)
Journals: Gene (17 papers)Taiwanese Journal of Obstetrics and Gynecology (51 papers)European Journal of Medical Genetics (1 paper)Medicine (1 paper)Genomics (1 paper)
Partner nations: Taiwan Canada United States

In The Last Decade

Jun-Wei Su

75 papers receiving 598 citations

Peers

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-authors

The 25 scholars most cited alongside Jun-Wei Su, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jun-Wei Su Line = papers co-authored together Jun-Wei Su links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 75 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review Gene ·Chih‐Ping Chen, Tung-Yao Chang, Wan‐Yuo Guo, Pei‐Chen Wu, Liang‐Kai Wang, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Lifeng Chen, Wayseen Wang	2013	31
2	Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Yi‐Yung Chen, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu‐Ting Chen, Chen‐Chi Lee, Lifeng Chen, Wayseen Wang	2013	27
3	Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysis Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Yi‐Ning Su, Schu‐Rern Chern, Yuting Chen, Peih-Shan Wu, Jun-Wei Su, Chen‐Wen Pan, Wayseen Wang	2012	25
4	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 ·Chih‐Ping Chen, Shuenn‐Dyh Chang, Tzu‐Hao Wang, Liang‐Kai Wang, Jeng-Daw Tsai, Yupeng Liu, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yuting Chen, Wayseen Wang	2013	20
5	Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Yi‐Ning Su, Jun-Wei Su, Schu‐Rern Chern, Yuting Chen, Lifeng Chen, Wayseen Wang	2013	19
6	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Yi‐Ning Su, Shuan‐Pei Lin, Schu‐Rern Chern, Jun-Wei Su, Yu-Ting Chen, Meng‐Shan Lee, Wayseen Wang	2013	19
7	Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Kuo-Gon Wang, Tsang‐Ming Ko, Schu‐Rern Chern, Jun-Wei Su, Dai‐Dyi Town, Wayseen Wang	2013	18
8	Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: Prenatal diagnosis and aCGH characterization using uncultured amniocytes Gene ·Chih‐Ping Chen, Jian‐Pei Huang, Yi‐Yung Chen, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen‐Wen Pan, Wayseen Wang	2013	18
9	Conjoined twins detected in the first trimester: A review Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Chin‐Yuan Hsu, Jun-Wei Su, Hsiao-En Cindy Chen, Alan Hsieh, Alex Hwa-Jiun Hsieh, Wayseen Wang	2011	18
10	Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review Gene ·Chih‐Ping Chen, Jian‐Pei Huang, Yi‐Yung Chen, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yuting Chen, Wenlin Chen, Wayseen Wang	2013	16
11	A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome European Journal of Medical Genetics ·Chih‐Ping Chen, Shuan‐Pei Lin, Schu‐Rern Chern, Peih-Shan Wu, Shuenn‐Dyh Chang, Shu‐Hang Ng, Yupeng Liu, Jun-Wei Su, Wayseen Wang	2012	15
12	Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20 Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Shuenn‐Dyh Chang, Ho‐Yen Chueh, Yi‐Ning Su, Schu‐Rern Chern, Jun-Wei Su, Yuting Chen, Wenlin Chen, Meng‐Shan Lee, Wayseen Wang	2013	14
13	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 ·Chih‐Ping Chen, Kwui-Shuai Hwang, Her‐Young Su, Shuan‐Pei Lin, Yi‐Ning Su, Schu‐Rern Chern, Jun-Wei Su, Yu-Ting Chen, Wenlin Chen, Wayseen Wang	2013	14
14	Prenatal diagnosis of trisomy 8 mosaicism Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Yi‐Ning Su, Schu‐Rern Chern, Yuting Chen, Jun-Wei Su, Chen‐Wen Pan, Wayseen Wang	2012	14
15	Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review Gene ·Chih‐Ping Chen, Ming Chen, Yi‐Ning Su, Jian‐Pei Huang, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Shun‐Ping Chang, Yuting Chen, Chen‐Chi Lee, Lifeng Chen, Chen‐Wen Pan, Wayseen Wang	2013	13
16	3q26.31–q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: Prenatal diagnosis and aCGH characterization Gene ·Chih‐Ping Chen, Chen‐Ju Lin, Yi‐Yung Chen, Liang‐Kai Wang, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Lifeng Chen, Dai‐Dyi Town, Chen‐Wen Pan, Wayseen Wang	2013	13
17	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome Gene ·Chih‐Ping Chen, Tsang‐Ming Ko, Yi‐Yung Chen, Jun-Wei Su, Wayseen Wang	2013	13
18	Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Schu‐Rern Chern, Tung‐Yao Chang, Yi‐Ning Su, Yi‐Yung Chen, Jun-Wei Su, Wayseen Wang	2012	12
19	Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: Prenatal diagnosis and aCGH characterization using uncultured amniocytes Gene ·Chih‐Ping Chen, Ming‐Chao Huang, Yi‐Yung Chen, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Dai‐Dyi Town, Wayseen Wang	2013	12
20	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold Gene ·Chih‐Ping Chen, Yi‐Yung Chen, Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yuting Chen, Haiyong Chen, Wayseen Wang	2012	11

About Jun-Wei Su

Jun-Wei Su is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Developmental Biology, Urology and Surgery, having authored 75 papers that have together received 658 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (45 papers), Genomic variations and chromosomal abnormalities (38 papers), Chromosomal and Genetic Variations (12 papers), Congenital Anomalies and Fetal Surgery (12 papers), Congenital heart defects research (10 papers), Genetic Syndromes and Imprinting (8 papers), Connective tissue disorders research (7 papers) and RNA modifications and cancer (7 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (353 citations), Genetics (472 citations), Developmental Biology (22 citations), Molecular Biology (197 citations) and Plant Science (99 citations). Jun-Wei Su has collaborated with scholars based in Taiwan, Canada and United States. Frequent co-authors include Chih‐Ping Chen, Wayseen Wang, Schu‐Rern Chern, Peih-Shan Wu, Yi‐Ning Su, Yi‐Yung Chen, Lifeng Chen, Chen‐Chi Lee, Chen‐Wen Pan and Wenlin Chen. Their work appears in journals such as Gene, Taiwanese Journal of Obstetrics and Gynecology, European Journal of Medical Genetics, Medicine and Genomics.

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