Yen-Ni Chen

548 citations

41 papers · 301 indexed · h-index 10

Genetics top 10%
Pediatrics, Perinatology and Child Health top 10%
Molecular Biology
Surgery
Plant Science

Co-authors: Chih‐Ping Chen Shin-Wen Chen Wayseen Wang Schu‐Rern Chern Peih-Shan Wu Chien-Wen Yang Chen‐Ju Lin Meng‐Shan Lee
Topics: Genomic variations and chromosomal abnormalities (26 papers)Prenatal Screening and Diagnostics (23 papers)Chromosomal and Genetic Variations (9 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Developmental Biology
Journals: Taiwanese Journal of Obstetrics and GynecologyJournal of Medical Ultrasound
Partner nations: Taiwan

In The Last Decade

Yen-Ni Chen

38 papers receiving 251 citations

Peers

Countries citing papers authored by Yen-Ni Chen

Since Specialization

Citations

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

Fields of papers citing papers by Yen-Ni Chen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yen-Ni Chen. 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 Yen-Ni Chen. The network helps show where Yen-Ni Chen may publish in the future.

Co-authorship network of co-authors of Yen-Ni Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Yen-Ni Chen. A scholar is included among the top collaborators of Yen-Ni Chen 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 Yen-Ni Chen. Yen-Ni Chen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound 2018 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Sui‐Yuan Chang,Yen-Ni Chen,Schu‐Rern Chern,Peih-Shan Wu,Shin-Wen Chen,(unknown),(unknown),Chien-Wen Yang,Lifeng Chen,Wayseen Wang	8
2	Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome 2017 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Chen‐Ju Lin,Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen‐Wen Pan,Chien-Wen Yang,Wayseen Wang	11
3	Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound 2017 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Liang‐Kai Wang,Pei‐Chen Wu,Tung‐Yao Chang,Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen‐Chi Lee,Chien-Wen Yang,Wayseen Wang	4
4	Prenatal Ultrasound Evaluation and Outcome of Pregnancy with Fetal Cystic Hygromas and Lymphangiomas 2017 ·Journal of Medical Ultrasound ·Yen-Ni Chen,Chih‐Ping Chen,Chen‐Ju Lin,Shin-Wen Chen	30
5	Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency 2017 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Chen‐Ju Lin,Yen-Ni Chen,Schu‐Rern Chern,Shin-Wen Chen,(unknown),Peih-Shan Wu,Lifeng Chen,Wayseen Wang	4
6	An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus 2017 ·Journal of Medical Ultrasound ·(unknown),Chih‐Ping Chen,Chen‐Ju Lin,Yen-Ni Chen,Shin-Wen Chen	0
7	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2 2017 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Ming Chen,Shun‐Ping Chang,(unknown),(unknown),Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen‐Chi Lee,Dai‐Dyi Town,Wenlin Chen,Wayseen Wang	2
8	Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,(unknown),(unknown),Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen‐Chi Lee,Dai‐Dyi Town,Meng‐Shan Lee,Chien-Wen Yang,Wayseen Wang	17
9	Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Chen‐Yu Chen,(unknown),(unknown),Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Haiyong Chen,Chien-Wen Yang,Wayseen Wang	5
10	Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Shuan‐Pei Lin,Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen‐Chi Lee,Dai‐Dyi Town,Chien-Wen Yang,Wayseen Wang	9
11	Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,(unknown),Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Meng‐Shan Lee,Chien-Wen Yang,Wayseen Wang	19
12	Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Shuan‐Pei Lin,Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chien-Wen Yang,Meng‐Shan Lee,Wayseen Wang	4
13	Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Chen‐Yu Chen,Tung‐Yao Chang,(unknown),Yen-Ni Chen,Shin-Wen Chen,Wayseen Wang	1
14	Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Chen‐Ju Lin,Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen‐Chi Lee,Lifeng Chen,Chien-Wen Yang,Wayseen Wang	4
15	Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Schu‐Rern Chern,Nan‐Chang Chiu,(unknown),Yen-Ni Chen,Shin-Wen Chen,Wayseen Wang	2
16	Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Schu‐Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen‐Chi Lee,Chien-Wen Yang,Wayseen Wang	8
17	Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature 2015 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Ming‐Chao Huang,Schu‐Rern Chern,(unknown),Yen-Ni Chen,Peih-Shan Wu,Lifeng Chen,Chen‐Wen Pan,Wayseen Wang	4
18	Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result 2015 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Shuan‐Pei Lin,(unknown),Yen-Ni Chen,Wayseen Wang	4
19	Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly 2015 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,(unknown),Tung‐Yao Chang,Wan‐Yuo Guo,Yen-Ni Chen,Peih-Shan Wu,Dai‐Dyi Town,Wayseen Wang	2
20	Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2–q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome 2014 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen,Chen‐Ju Lin,Schu‐Rern Chern,Yu-Peng Liu,(unknown),Yen-Ni Chen,Peih-Shan Wu,Dai‐Dyi Town,Lifeng Chen,Chien-Wen Yang,Wayseen Wang	10

About Yen-Ni Chen

Yen-Ni Chen is a scholar working on Developmental Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 41 papers that have together received 301 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (23 papers) and Chromosomal and Genetic Variations (9 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (180 citations), Genetics (210 citations) and Developmental Biology (10 citations). Yen-Ni Chen has collaborated with scholars based in Taiwan. Frequent co-authors include Chih‐Ping Chen, Shin-Wen Chen, Wayseen Wang, Schu‐Rern Chern, Peih-Shan Wu, Chien-Wen Yang, Chen‐Ju Lin, Meng‐Shan Lee, Chen‐Wen Pan and Lifeng Chen. Their work appears in journals such as Taiwanese Journal of Obstetrics and Gynecology and Journal of Medical Ultrasound.

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.

Explore authors with similar magnitude of impact