Sheng Chih Jin

8.2k total citations
60 papers, 1.4k citations indexed

About

Sheng Chih Jin is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sheng Chih Jin has authored 60 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 27 papers in Molecular Biology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sheng Chih Jin's work include Genomics and Rare Diseases (12 papers), Fetal and Pediatric Neurological Disorders (11 papers) and Congenital heart defects research (8 papers). Sheng Chih Jin is often cited by papers focused on Genomics and Rare Diseases (12 papers), Fetal and Pediatric Neurological Disorders (11 papers) and Congenital heart defects research (8 papers). Sheng Chih Jin collaborates with scholars based in United States, China and South Korea. Sheng Chih Jin's co-authors include Bruno A. Benítez, Breanna Cooper, Carlos Cruchaga, Kristopher T. Kahle, Pau Pástor, Alison Goate, Sebastián Cervantes, Rudolph E. Tanzi, Marina Cella and Kristina Mullin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and PLoS ONE.

In The Last Decade

Sheng Chih Jin

54 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sheng Chih Jin United States 18 516 471 426 304 280 60 1.4k
Sophie Lebon France 24 1.0k 1.9× 489 1.0× 148 0.3× 252 0.8× 111 0.4× 40 2.0k
Laura Ghezzi Italy 22 697 1.4× 464 1.0× 727 1.7× 306 1.0× 87 0.3× 57 1.9k
Sara Cipriani Italy 21 438 0.8× 447 0.9× 124 0.3× 119 0.4× 88 0.3× 28 1.7k
Isaías Glezer Brazil 20 388 0.8× 460 1.0× 253 0.6× 256 0.8× 49 0.2× 37 1.3k
Shongshan Fan United States 20 522 1.0× 345 0.7× 120 0.3× 198 0.7× 85 0.3× 26 1.4k
Kévin Baranger France 24 516 1.0× 326 0.7× 813 1.9× 164 0.5× 53 0.2× 42 1.8k
Christina Fenger Denmark 16 288 0.6× 605 1.3× 130 0.3× 354 1.2× 71 0.3× 30 1.2k
Christian Barbato Italy 26 1.1k 2.1× 171 0.4× 507 1.2× 81 0.3× 122 0.4× 79 1.9k
Fang He China 20 623 1.2× 180 0.4× 98 0.2× 107 0.4× 410 1.5× 59 1.3k

Countries citing papers authored by Sheng Chih Jin

Since Specialization
Citations

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

Fields of papers citing papers by Sheng Chih Jin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sheng Chih Jin. 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 Sheng Chih Jin. The network helps show where Sheng Chih Jin may publish in the future.

Co-authorship network of co-authors of Sheng Chih Jin

This figure shows the co-authorship network connecting the top 25 collaborators of Sheng Chih Jin. A scholar is included among the top collaborators of Sheng Chih Jin 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 Sheng Chih Jin. Sheng Chih Jin 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.
Thủy, Lê Thị Thanh, Sheng Chih Jin, Sun-Ae Shin, et al.. (2025). Injectable polyplex-loaded glycol chitosan thermogel for efficient and safe inner ear gene delivery. Journal of Controlled Release. 380. 1095–1108. 3 indexed citations
2.
Choi, Julie, et al.. (2025). Unleashing the Power of Multiomics: Unraveling the Molecular Landscape of Peripheral Neuropathy. Annals of Clinical and Translational Neurology. 12(4). 674–685.
3.
Allington, Garrett, Neel H. Mehta, Evan Dennis, et al.. (2024). De novo variants disrupt an LDB1 -regulated transcriptional network in congenital ventriculomegaly. Brain. 148(5). 1817–1828.
4.
Lewis, Sara A., et al.. (2024). Potential clinical applications of advanced genomic analysis in cerebral palsy. EBioMedicine. 106. 105229–105229. 2 indexed citations
5.
Mehta, Neel H., et al.. (2023). Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus. JAMA Network Open. 6(11). e2343384–e2343384. 7 indexed citations
6.
Timberlake, Andrew T., Garrett Allington, Emre Kiziltug, et al.. (2023). De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis. The American Journal of Human Genetics. 110(5). 846–862. 11 indexed citations
7.
Jiang, Wei, Weilai Dong, Hongyu Li, et al.. (2022). Network assisted analysis of de novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease. PLoS Genetics. 18(6). e1010252–e1010252. 2 indexed citations
8.
Jin, Sheng Chih, Rainelli Koumangoye, Stephanie M. Robert, et al.. (2021). Protein kinase D1 variant associated with human epilepsy and peripheral nerve hypermyelination. Clinical Genetics. 100(2). 176–186. 4 indexed citations
9.
Fazeli, Walid, Somayeh Bakhtiari, Abbas Tafakhori, et al.. (2021). The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature. European Journal of Paediatric Neurology. 36. 7–13. 5 indexed citations
10.
Tang, Clara Sze-Man, Sheng Chih Jin, Xuehan Zhuang, et al.. (2021). Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors. JCI Insight. 7(2). 11 indexed citations
11.
Škorvánek, Matěj, Petra Pavelekova, Chen Zhao, et al.. (2021). Variant recurrence confirms the existence of a FBXO31‐related spastic‐dystonic cerebral palsy syndrome. Annals of Clinical and Translational Neurology. 8(4). 951–955. 7 indexed citations
12.
Robson, Andrew, Svetlana Makova, Samir Zaidi, et al.. (2019). Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility. Proceedings of the National Academy of Sciences. 116(28). 14049–14054. 29 indexed citations
13.
Furey, Charuta G., Xue Zeng, Weilai Dong, et al.. (2018). Human Genetics and Molecular Mechanisms of Congenital Hydrocephalus. World Neurosurgery. 119. 441–443. 9 indexed citations
14.
Antwi, Prince, Christopher S. Hong, Daniel Durán, et al.. (2018). A novel association of campomelic dysplasia and hydrocephalus with an unbalanced chromosomal translocation upstream of SOX9. Molecular Case Studies. 4(3). a002766–a002766. 6 indexed citations
15.
Durán, Daniel, Sheng Chih Jin, Tyrone DeSpenza, et al.. (2016). Digenic mutations of human OCRL paralogs in Dent’s disease type 2 associated with Chiari I malformation. Human Genome Variation. 3(1). 16042–16042. 9 indexed citations
16.
Jin, Sheng Chih, Bruno A. Benítez, Yuetiva Deming, & Carlos Cruchaga. (2015). Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer’s Disease. Methods in molecular biology. 1303. 299–314. 2 indexed citations
17.
Jin, Sheng Chih, Bruno A. Benítez, Celeste M. Karch, et al.. (2014). Coding variants in TREM2 increase risk for Alzheimer's disease. Human Molecular Genetics. 23(21). 5838–5846. 237 indexed citations
18.
Benítez, Bruno A., Celeste M. Karch, Yefei Cai, et al.. (2013). The PSEN1, p.E318G Variant Increases the Risk of Alzheimer's Disease in APOE-ε4 Carriers. PLoS Genetics. 9(8). e1003685–e1003685. 52 indexed citations
19.
Jin, Sheng Chih, et al.. (2011). Identification of MC1R gene polymorphisms for plumage color variation in Korean native chicken. 72–74.
20.
Caporaso, Neil E., Fangyi Gu, Nilanjan Chatterjee, et al.. (2009). Genome-Wide and Candidate Gene Association Study of Cigarette Smoking Behaviors. PLoS ONE. 4(2). e4653–e4653. 184 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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