Suh-Jen Chen

417 total citations
37 papers, 288 citations indexed

About

Suh-Jen Chen is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Suh-Jen Chen has authored 37 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 8 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Suh-Jen Chen's work include Genomic variations and chromosomal abnormalities (9 papers), Craniofacial Disorders and Treatments (6 papers) and Prenatal Screening and Diagnostics (5 papers). Suh-Jen Chen is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Craniofacial Disorders and Treatments (6 papers) and Prenatal Screening and Diagnostics (5 papers). Suh-Jen Chen collaborates with scholars based in Taiwan and United States. Suh-Jen Chen's co-authors include Pen‐Hua Su, Jia‐Yuh Chen, Yan‐Yan Ng, Soo‐Cheen Ng, Teng‐Fu Tsao, Trang‐Tiau Wu, Shu‐Li Wang, Shun‐Fa Yang, Jiayu Chen and Chiu‐Yueh Hsiao and has published in prestigious journals such as Pediatric Research, Human Genetics and Early Human Development.

In The Last Decade

Suh-Jen Chen

36 papers receiving 276 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suh-Jen Chen Taiwan 10 110 69 60 50 46 37 288
Jaime Kulak Brazil 11 72 0.7× 47 0.7× 40 0.7× 121 2.4× 53 1.2× 28 398
Maria Elfving Sweden 8 115 1.0× 88 1.3× 47 0.8× 53 1.1× 38 0.8× 14 300
İbrahim Şahin Türkiye 11 54 0.5× 98 1.4× 33 0.6× 49 1.0× 36 0.8× 51 338
H. G. Dörr Germany 10 112 1.0× 100 1.4× 89 1.5× 28 0.6× 52 1.1× 19 302
O. Vérier‐Mine France 8 80 0.7× 77 1.1× 69 1.1× 71 1.4× 121 2.6× 18 396
A. Amante Italy 10 62 0.6× 90 1.3× 77 1.3× 11 0.2× 28 0.6× 36 311
Iva Gueorguieva France 8 77 0.7× 101 1.5× 24 0.4× 13 0.3× 22 0.5× 20 296
L Benso Italy 14 79 0.7× 106 1.5× 94 1.6× 66 1.3× 30 0.7× 41 464
Gloria Queipo Mexico 12 184 1.7× 192 2.8× 32 0.5× 53 1.1× 90 2.0× 37 434
Shigenori Iwagaki Japan 10 64 0.6× 28 0.4× 101 1.7× 71 1.4× 41 0.9× 44 309

Countries citing papers authored by Suh-Jen Chen

Since Specialization
Citations

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

Fields of papers citing papers by Suh-Jen Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suh-Jen Chen

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

All Works

20 of 20 papers shown
1.
Wu, Trang‐Tiau, Yan‐Yan Ng, Soo‐Cheen Ng, et al.. (2012). Herlyn-Werner-Wunderlich Syndrome Consisting of Uterine Didelphys, Obstructed Hemivagina and Ipsilateral Renal Agenesis in a Newborn. Pediatrics & Neonatology. 53(1). 68–71. 47 indexed citations
2.
Hsiao, Chiu‐Yueh, et al.. (2012). Perceived knowledge and clinical comfort with genetics among Taiwanese nurses enrolled in a RN-to-BSN program. Nurse Education Today. 33(8). 802–807. 12 indexed citations
3.
4.
Su, Pen‐Hua, Jia‐Yuh Chen, & Suh-Jen Chen. (2011). Siblings With Deletion 22q13.3 and Trisomy 15q26 Inherited From a Maternally Balanced Translocation. Pediatrics & Neonatology. 52(5). 287–289. 4 indexed citations
5.
Su, Pen‐Hua, et al.. (2011). Interstitial Deletions of the Short Arm of Chromosome 4 in a Patient With Mental Retardation and Focal Seizure. Pediatrics & Neonatology. 52(3). 165–168. 2 indexed citations
6.
Su, Pen‐Hua, Jia‐Yuh Chen, Teng‐Fu Tsao, & Suh-Jen Chen. (2011). De Novo Interstitial Deletion of Chromosome 2 (p23p24). Pediatrics & Neonatology. 52(1). 46–50. 8 indexed citations
7.
Su, Pen‐Hua, et al.. (2011). Leptin expression and leptin receptor gene polymorphisms in growth hormone deficiency patients. Human Genetics. 129(4). 455–462. 5 indexed citations
8.
Ng, Yan‐Yan, et al.. (2010). Ocular Findings in a Case of Trisomy 18 With Variant of Dandy-Walker Syndrome. Pediatrics & Neonatology. 51(5). 292–295. 5 indexed citations
9.
Su, Pen‐Hua, et al.. (2010). Exclusion of MYF5, GSC, RUNX2, and TCOF1 mutation in a case of cerebro-costo-mandibular syndrome. Clinical Dysmorphology. 19(2). 51–55. 7 indexed citations
10.
Ng, Yan‐Yan, et al.. (2010). Successful Weaning of a Laryngeal Mask Airway After a Tongue-lip Adhesion Operation in a Case With Cerebro-costo-mandibular Syndrome. Pediatrics & Neonatology. 51(1). 57–60. 5 indexed citations
11.
Su, Pen‐Hua, et al.. (2010). Persistent falcine sinus and unilateral renal agenesis in a girl with Sotos syndrome. Clinical Dysmorphology. 20(1). 42–46. 1 indexed citations
12.
Su, Pen‐Hua, et al.. (2009). Pfeiffer-like Syndrome With Holoprosencephaly: A Newborn With Maternal Smoking and Alcohol Exposure. Pediatrics & Neonatology. 50(5). 234–238. 6 indexed citations
13.
Su, Pen‐Hua, et al.. (2008). Identification of a novel mutation and polymorphic change in the NIPBL gene of subjects with Cornelia de Lange syndrome. Genes & Genomics. 30(3). 253–260. 1 indexed citations
14.
Su, Pen‐Hua, et al.. (2008). Transthyretin levels are not related to Apgar score in low birth weight and very low birth weight infants. Early Human Development. 84(8). 533–538. 6 indexed citations
15.
Su, Pen‐Hua, Jia‐Yuh Chen, Suh-Jen Chen, Teng‐Fu Tsao, & Yujie Lai. (2008). Sacral Dysgenesis Associated with Terminal Deletion of Chromosome 7 (q36-qter). Pediatrics & Neonatology. 49(5). 189–192. 8 indexed citations
16.
Su, Pen‐Hua, et al.. (2008). Hydranencephaly Associated with Interruption of Bilateral Internal Carotid Arteries. Pediatrics & Neonatology. 49(2). 43–47. 22 indexed citations
17.
Su, Pen‐Hua, et al.. (2008). Terminal Deletion of Chromosome 6q. Pediatrics & Neonatology. 49(3). 88–93. 7 indexed citations
18.
Su, Pen‐Hua, et al.. (2006). Treacher Collins Syndrome with a de Novo 5-bp Deletion in the TCOF1 Gene. Journal of the Formosan Medical Association. 105(6). 518–521. 16 indexed citations
19.
Su, Pen‐Hua, et al.. (2006). Basilar artery dolichoectasia in a boy with a combination of partial monosomy 18p and partial trisomy 20q. Clinical Dysmorphology. 15(4). 225–228. 3 indexed citations
20.
Su, Pen‐Hua, et al.. (2002). Multiple congenital anomalies in association with supernumerary chromosome 47 inherited from a maternal balanced translocation.. PubMed. 101(4). 301–3. 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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