The‐Hung Bui

2.1k total citations
62 papers, 1.3k citations indexed

About

The‐Hung Bui is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, The‐Hung Bui has authored 62 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Pediatrics, Perinatology and Child Health, 27 papers in Genetics and 23 papers in Molecular Biology. Recurrent topics in The‐Hung Bui's work include Prenatal Screening and Diagnostics (28 papers), Genomic variations and chromosomal abnormalities (14 papers) and Neurogenetic and Muscular Disorders Research (7 papers). The‐Hung Bui is often cited by papers focused on Prenatal Screening and Diagnostics (28 papers), Genomic variations and chromosomal abnormalities (14 papers) and Neurogenetic and Muscular Disorders Research (7 papers). The‐Hung Bui collaborates with scholars based in Sweden, Vietnam and United States. The‐Hung Bui's co-authors include Lisa G. Shaffer, Elisabeth Blennow, Magnus Nordenskjöld, J. Lindsten, Göran Annerén, Anna Wedell, Svetlana Lajić, E. Martin Ritzén, Mikael Holst and Magnus Westgren and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

The‐Hung Bui

60 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
The‐Hung Bui Sweden 18 690 554 416 188 159 62 1.3k
Y. Gillerot Belgium 22 426 0.6× 616 1.1× 740 1.8× 64 0.3× 102 0.6× 74 1.8k
Carmen Morales Spain 23 449 0.7× 337 0.6× 284 0.7× 75 0.4× 182 1.1× 69 1.4k
Gioacchino Scarano Italy 25 396 0.6× 838 1.5× 1.2k 2.8× 79 0.4× 70 0.4× 83 2.3k
S A Al-Awadi Kuwait 17 239 0.3× 424 0.8× 294 0.7× 45 0.2× 161 1.0× 66 899
Karin E. M. Diderich Netherlands 21 560 0.8× 563 1.0× 822 2.0× 56 0.3× 54 0.3× 60 1.6k
Nicos Skordis Cyprus 24 370 0.5× 569 1.0× 664 1.6× 64 0.3× 634 4.0× 109 1.9k
María Luisa Martínez‐Frías Spain 22 453 0.7× 577 1.0× 445 1.1× 40 0.2× 96 0.6× 51 1.7k
Yoshikazu Kuroki Japan 26 400 0.6× 1.4k 2.6× 835 2.0× 159 0.8× 111 0.7× 106 2.2k
M. H. K. Shokeir Canada 19 178 0.3× 355 0.6× 557 1.3× 49 0.3× 175 1.1× 48 1.3k
Reuven Sharony Israel 20 474 0.7× 254 0.5× 215 0.5× 32 0.2× 45 0.3× 79 1.0k

Countries citing papers authored by The‐Hung Bui

Since Specialization
Citations

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

Fields of papers citing papers by The‐Hung Bui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by The‐Hung Bui. 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 The‐Hung Bui. The network helps show where The‐Hung Bui may publish in the future.

Co-authorship network of co-authors of The‐Hung Bui

This figure shows the co-authorship network connecting the top 25 collaborators of The‐Hung Bui. A scholar is included among the top collaborators of The‐Hung Bui 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 The‐Hung Bui. The‐Hung Bui 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.
Pham, Hung, et al.. (2023). In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome. Molecular Genetics & Genomic Medicine. 11(12). e2263–e2263. 2 indexed citations
3.
Tuấn, Nguyễn Anh, et al.. (2023). Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report. SHILAP Revista de lepidopterología. 11(3). e7025–e7025. 1 indexed citations
4.
5.
Trần, Văn Khanh, et al.. (2022). Whole exome sequencing analysis in a couple with three children who died prematurely due to carnitine-acylcarnitine translocase deficiency. Taiwanese Journal of Obstetrics and Gynecology. 61(1). 153–156. 1 indexed citations
6.
Tran, Thinh Huy, et al.. (2021). Microcephaly primary hereditary (MCPH): Report of novel ASPM variants and prenatal diagnosis in a Vietnamese family. Taiwanese Journal of Obstetrics and Gynecology. 60(5). 907–910. 3 indexed citations
7.
Tran, Thinh Huy, et al.. (2020). A case of self‐improving collodion ichthyosis in Vietnam. Pediatric Dermatology. 37(3). 574–575. 4 indexed citations
8.
Bui, The‐Hung, Annalisa Vetro, Orsetta Zuffardi, & Lisa G. Shaffer. (2011). Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post‐array CGH era?. Prenatal Diagnosis. 31(3). 235–243. 39 indexed citations
9.
Soysal, Yasemin, Sevim Balcı, Thomas Liehr, et al.. (2009). Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. American Journal of Medical Genetics Part A. 149A(12). 2782–2787. 13 indexed citations
10.
Nicolini, Umberto, Faustina Lalatta, Federica Natacci, Cristina Curcio, & The‐Hung Bui. (2004). The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration. Human Reproduction Update. 10(6). 541–548. 64 indexed citations
11.
Westgren, Magnus, Olle Ringdén, Peter Bartmann, et al.. (2002). Prenatal T-cell reconstitution after in utero transplantation with fetal liver cells in a patient with X-linked severe combined immunodeficiency. American Journal of Obstetrics and Gynecology. 187(2). 475–482. 64 indexed citations
12.
Bui, The‐Hung, Charlotta Grünewald, Björn Frenckner, et al.. (2000). Successful EXIT (Ex Utero Intrapartum Treatment) Procedure in a Fetus Diagnosed Prenatally with Congenital High-Airway Obstruction Syndrome Due to Laryngeal Atresia. European Journal of Pediatric Surgery. 10(5). 328–333. 50 indexed citations
13.
Bui, The‐Hung, et al.. (2000). Early prenatal diagnosis of the ICF syndrome. Prenatal Diagnosis. 20(10). 828–831. 5 indexed citations
14.
Bui, The‐Hung & David Jones. (1998). Stem cell transplantation into the fetal recipient: challenges and prospects. Current Opinion in Obstetrics & Gynecology. 10(2). 105–108. 2 indexed citations
15.
Saade, George R., David L. Berry, The‐Hung Bui, et al.. (1998). Amniotic Septostomy for the Treatment of Twin Oligohydramnios-Polyhydramnios Sequence. Fetal Diagnosis and Therapy. 13(2). 86–93. 90 indexed citations
16.
Westgren, Magnus, Sverker Ek, The‐Hung Bui, et al.. (1997). Tissue distribution of transplanted fetal liver cells in the human fetal recipient. American Journal of Obstetrics and Gynecology. 176(1). 49–53. 17 indexed citations
17.
Westgren, Magnus, Olle Ringdén, S. H. Eik‐Nes, et al.. (1996). LACK OF EVIDENCE OF PERMANENT ENGRAFTMENT AFTER IN UTERO FETAL STEM CELL TRANSPLANTATION IN CONGENITAL HEMOGLOBINOPATHIES1. Transplantation. 61(8). 1176–1179. 108 indexed citations
18.
Ek, Sverker, Magnus Westgren, Helmut Pschera, et al.. (1994). Screening of Fetal Stem Cells for Infection and Cytogenetic Abnormalities. Fetal Diagnosis and Therapy. 9(6). 357–361. 9 indexed citations
19.
Han, Fei‐Yu, et al.. (1994). Direct and inverted reciprocal chromosome insertions between chromosomes 7 and 14 in a woman with recurrent miscarriages. American Journal of Medical Genetics. 52(3). 349–351. 7 indexed citations
20.
Lambert, B., et al.. (1976). DNA repair and frequency of X‐ray and u.v.‐light induced chromosome aberrations in leukocytes from patients with Down's syndrome. Annals of Human Genetics. 39(3). 293–303. 55 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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