Dũng Chí Vũ

1.4k total citations
35 papers, 857 citations indexed

About

Dũng Chí Vũ is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Dũng Chí Vũ has authored 35 papers receiving a total of 857 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Physiology, 11 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Dũng Chí Vũ's work include Blood properties and coagulation (8 papers), Pancreatic function and diabetes (8 papers) and Erythrocyte Function and Pathophysiology (7 papers). Dũng Chí Vũ is often cited by papers focused on Blood properties and coagulation (8 papers), Pancreatic function and diabetes (8 papers) and Erythrocyte Function and Pathophysiology (7 papers). Dũng Chí Vũ collaborates with scholars based in Vietnam, Switzerland and United States. Dũng Chí Vũ's co-authors include Marguerite Neerman‐Arbez, Pål R. Njølstad, Andrew T. Hattersley, Sian Ellard, Aviva Must, Hélène Cyr, William H. Dietz, Wojciech Młynarski, Oscar Rubio‐Cabezas and Neil H. White and has published in prestigious journals such as Nature Communications, Blood and Scientific Reports.

In The Last Decade

Dũng Chí Vũ

35 papers receiving 827 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dũng Chí Vũ Vietnam 16 316 247 222 187 181 35 857
Nurgün Kandemir Türkiye 18 180 0.6× 366 1.5× 106 0.5× 78 0.4× 65 0.4× 53 842
Maria Soller Sweden 20 267 0.8× 359 1.5× 60 0.3× 128 0.7× 153 0.8× 46 884
Jayesh Sheth India 18 243 0.8× 277 1.1× 318 1.4× 81 0.4× 29 0.2× 111 938
Yardena Tenenbaum‐Rakover Israel 20 395 1.3× 609 2.5× 66 0.3× 135 0.7× 138 0.8× 52 1.3k
David Kronn United States 15 270 0.9× 362 1.5× 195 0.9× 72 0.4× 79 0.4× 35 1.0k
Wendy K. Chung United States 18 447 1.4× 415 1.7× 197 0.9× 130 0.7× 311 1.7× 28 1.3k
K Zuppinger Switzerland 18 294 0.9× 299 1.2× 84 0.4× 171 0.9× 67 0.4× 75 957
Felix Schreiner Germany 13 215 0.7× 215 0.9× 66 0.3× 43 0.2× 54 0.3× 35 546
Catherine DeVile United Kingdom 17 224 0.7× 274 1.1× 236 1.1× 110 0.6× 46 0.3× 36 1.1k
Urs Zumsteg Switzerland 15 334 1.1× 169 0.7× 83 0.4× 286 1.5× 54 0.3× 35 910

Countries citing papers authored by Dũng Chí Vũ

Since Specialization
Citations

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

Fields of papers citing papers by Dũng Chí Vũ

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dũng Chí Vũ. 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 Dũng Chí Vũ. The network helps show where Dũng Chí Vũ may publish in the future.

Co-authorship network of co-authors of Dũng Chí Vũ

This figure shows the co-authorship network connecting the top 25 collaborators of Dũng Chí Vũ. A scholar is included among the top collaborators of Dũng Chí Vũ 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 Dũng Chí Vũ. Dũng Chí Vũ 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.
Trần, Văn Khanh, Phuong Thi Le, Hai Anh Tran, et al.. (2024). A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients. Frontiers in Pediatrics. 12. 1165492–1165492. 2 indexed citations
2.
Greeley, Siri Atma W., Michel Polak, Pål R. Njølstad, et al.. (2022). ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents. Pediatric Diabetes. 23(8). 1188–1211. 63 indexed citations
3.
Germain, Dominique P., Sergey Moiseev, Fernando Suárez‐Obando, et al.. (2021). The benefits and challenges of family genetic testing in rare genetic diseases—lessons from Fabry disease. Molecular Genetics & Genomic Medicine. 9(5). e1666–e1666. 30 indexed citations
4.
Vũ, Dũng Chí, Shaukat Khan, Hironori Kobayashi, et al.. (2021). Diagnosis of Mucopolysaccharidoses and Mucolipidosis by Assaying Multiplex Enzymes and Glycosaminoglycans. Diagnostics. 11(8). 1347–1347. 11 indexed citations
5.
Tomatsu, Shunji, Kenji E. Orii, Toshiyuki Fukao, et al.. (2020). Validation of Liquid Chromatography-Tandem Mass Spectrometry-Based 5-Plex Assay for Mucopolysaccharidoses. International Journal of Molecular Sciences. 21(6). 2025–2025. 4 indexed citations
6.
Trần, Văn Khanh, Phuong Thi Le, Anh Duy Nguyen, et al.. (2019). Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy. Taiwanese Journal of Obstetrics and Gynecology. 58(5). 645–649. 4 indexed citations
7.
Croft, Brittany, Thomas Ohnesorg, Jacqueline Hewitt, et al.. (2018). Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9. Nature Communications. 9(1). 5319–5319. 117 indexed citations
8.
Vũ, Dũng Chí, et al.. (2015). AB125. Neonatal diabetes mellitus due to insulin gene mutation.. Annals of Translational Medicine. 3(2). 126–126. 2 indexed citations
9.
Vũ, Dũng Chí, Sarah E. Flanagan, Sian Ellard, et al.. (2015). AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome. Annals of Translational Medicine. 4(2). 129–129. 1 indexed citations
10.
Vũ, Dũng Chí, et al.. (2015). AB132. Neonatal diabetes in Wolcott-Rallison syndrome: a case report. Annals of Translational Medicine. 3(2). 133–133. 1 indexed citations
11.
Niba, Emma Tabe Eko, Văn Khanh Trần, Dũng Chí Vũ, et al.. (2014). Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene. Clinica Chimica Acta. 436. 155–159. 11 indexed citations
12.
Rubio‐Cabezas, Oscar, Andrew T. Hattersley, Pål R. Njølstad, et al.. (2014). The diagnosis and management of monogenic diabetes in children and adolescents. Pediatric Diabetes. 15(S20). 47–64. 144 indexed citations
13.
Stroka, Deborah, Adrian Keogh, Dũng Chí Vũ, et al.. (2014). In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes. Journal of Thrombosis and Haemostasis. 12(11). 1874–1879. 4 indexed citations
14.
Vũ, Dũng Chí, Hoan Nguyen, Khanh P. Nguyen, et al.. (2011). Glycaemic control in children with neonatal diabetes and type 1 diabetes in Vietnam. International Health. 3(3). 188–192. 2 indexed citations
15.
Fukao, Toshiyuki, Dũng Chí Vũ, Hironori Kobayashi, et al.. (2010). A common mutation, R208X, identified in Vietnamese patients with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency. Molecular Genetics and Metabolism. 100(1). 37–41. 21 indexed citations
16.
17.
Vũ, Dũng Chí, Dorothée Caille, Philippe de Moerloose, et al.. (2005). Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia. Human Molecular Genetics. 14(21). 3271–3280. 33 indexed citations
18.
Vũ, Dũng Chí, et al.. (2005). Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the γ chain globular domain impairing fibrinogen secretion. Journal of Medical Genetics. 42(9). e57–e57. 18 indexed citations
19.
Vũ, Dũng Chí, Claude Walzer, Estelle N. Bianchi, et al.. (2003). Transcription regulator LMO4 interferes with neuritogenesis in human SH-SY5Y neuroblastoma cells. Molecular Brain Research. 115(2). 93–103. 23 indexed citations
20.
Leuba, G., André Vernay, Dũng Chí Vũ, et al.. (2003). Differential expression of LMO4 protein in Alzheimer's disease. Neuropathology and Applied Neurobiology. 30(1). 57–69. 20 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Nurgün Kandemir Breakdown of academic impact, for papers by Maria Soller Breakdown of academic impact, for papers by Jayesh Sheth Breakdown of academic impact, for papers by Yardena Tenenbaum‐Rakover Breakdown of academic impact, for papers by David Kronn Breakdown of academic impact, for papers by Wendy K. Chung Breakdown of academic impact, for papers by K Zuppinger Breakdown of academic impact, for papers by Felix Schreiner Breakdown of academic impact, for papers by Catherine DeVile Breakdown of academic impact, for papers by Urs Zumsteg
Rankless by CCL
2026