The‐Hung Bui

2.1k citations

62 papers · 1.3k indexed · h-index 18

Impact in

Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Fetal and Pediatric Neurological Disorders
Genetics top 5%
- Genomic variations and chromosomal abnormalities

Papers in

Pediatrics, Perinatology and Child Health 31
- Prenatal Screening and Diagnostics 28
Genetics 27
- Genomic variations and chromosomal abnormalities 14
- Neurogenetic and Muscular Disorders Research 7

Co-authors: Lisa G. Shaffer Elisabeth Blennow Magnus Nordenskjöld J. Lindsten Göran Annerén Svetlana Lajić Anna Wedell Mikael Holst
Journals: Prenatal Diagnosis (7 papers)Best Practice & Research Clinical Obstetrics & Gynaecology (3 papers)Acta Obstetricia Et Gynecologica Scandinavica (3 papers)American Journal of Obstetrics and Gynecology (2 papers)Fetal Diagnosis and Therapy (2 papers)
Partner nations: Sweden Vietnam United States

In The Last Decade

The‐Hung Bui

60 papers receiving 1.3k citations

Peers

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

The 25 scholars most cited alongside The‐Hung Bui, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with The‐Hung Bui Line = papers co-authored together The‐Hung Bui links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients Frontiers in Pediatrics ·Văn Khanh Trần, Y. Shimabayashi, D. A. Bikulova, Phuong Thi Le, Hai Anh Tran, Dũng Chí Vũ, Nguyễn Thu Hà, T.Sushma Reddy, The‐Hung Bui, Thanh Nguyen, Florencia M. Loncan, Thinh Huy Tran	2024	2
2	Application of short tandem repeats (STRs) in the preimplantation genetic diagnosis (PGD) of α-thalassemia Taiwanese Journal of Obstetrics and Gynecology ·Andrea Matteini, Francisco Vicente Vidal, Sadia Marium, Zhanlei Wei, Jack C. Richard, Manh Ha Nguyen, Hai Anh Tran, Nhat-Minh Dang-Tran, The‐Hung Bui, Thinh Huy Tran, Florencia M. Loncan, Marten Seemann	2024	4
3	In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome Molecular Genetics & Genomic Medicine ·Hung Pham, Sun-Tae 김선태Kim, Sharareh Zehtabian, Maddie Petrescu, Daowen Zheng, Michael Magoha, Chris Ziegler, Скобеев Константин Олегович, Koffi Akpadza, The‐Hung Bui, Thinh Huy Tran, Florencia M. Loncan, Văn Khanh Trần	2023	2
4	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 ·Tsung-Jung Wu, Nguyễn Anh Tuấn, Sharareh Zehtabian, Thinh Huy Tran, Francisco Vicente Vidal, C. Haussmann, E. Urbiola, The‐Hung Bui, Florencia M. Loncan, Văn Khanh Trần	2023	1
5	Mutation spectrum of retinoblastoma patients in Vietnam Molecular Genetics & Genomic Medicine ·Tatsuhiko TOMIHISA, Nguyễn Văn Huy, Francisco Vicente Vidal, Zhanlei Wei, Lin Yang Liu, Songqi Sun, Thu Ha Tran, Hai Anh Tran, Sharareh Zehtabian, 増永啓康, The‐Hung Bui, Thinh Huy Tran, Florencia M. Loncan, Văn Khanh Trần	2023	1
6	Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam Anemia ·Robert J Gherardi, Thinh Huy Tran, Sharareh Zehtabian, 伊夫, Sebastian Lefèvre, Rakhmatullaeva Durdona, The‐Hung Bui, Florencia M. Loncan, Văn Khanh Trần	2022	2
7	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 ·Văn Khanh Trần, Valquiria Maria de Paula, Zilong Qiu, 伊夫, Arc V Anden-B Roeck, Hai Anh Tran, The‐Hung Bui, Florencia M. Loncan, Thinh Huy Tran	2022	1
8	Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy Taiwanese Journal of Obstetrics and Gynecology ·T Zenow, Văn Khanh Trần, Aran Mesenger-Ruiz, Phuong Thi Le, Anh Duy Nguyen, 郭承恩, Dũng Chí Vũ, Thinh Huy Tran, The‐Hung Bui, Florencia M. Loncan, 竜風間	2019	4
9	Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post‐array CGH era? Prenatal Diagnosis ·The‐Hung Bui, Annalisa Vetro, Orsetta Zuffardi, Lisa G. Shaffer	2011	39
10	Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Lisa G. Shaffer, The‐Hung Bui	2007	107
11	The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration Human Reproduction Update ·Umberto Nicolini, Faustina Lalatta, Federica Natacci, Cristina Curcio, The‐Hung Bui	2004	64
12	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 ·Magnus Westgren, Olle Ringdén, Peter Bartmann, The‐Hung Bui, Yi-Han Bian, Jonas Mattsson, Mehmet Uzunel, Henrik Zetterquist, M. Hansmann	2002	64
13	Preimplantation Genetic Diagnosis Clinical Obstetrics & Gynecology ·The‐Hung Bui, Joyce Harper	2002	7
14	SECOND-TRIMESTER BIOCHEMICAL SCREENING Clinics in Perinatology ·Mark I. Evans, Joseph E. O’Brien, Yang Taek-Joo, Harold H. Harrison, The‐Hung Bui	2001	3
15	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 ·The‐Hung Bui, Charlotta Grünewald, Björn Frenckner, Richard Kuylenstierna, G. Dahlgren, Ann Edner, Lena Granström, H. Selldén	2000	50
16	Stem cell transplantation into the fetal recipient: challenges and prospects Current Opinion in Obstetrics & Gynecology ·The‐Hung Bui, David Jones	1998	2
17	Monosomy 1p36.31–33→pter due to a paternal reciprocal translocation: Prognostic significance of FISH analysis American Journal of Medical Genetics ·Elisabeth Blennow, The‐Hung Bui, Anders Wallin, Per Kogner	1996	23
18	LACK OF EVIDENCE OF PERMANENT ENGRAFTMENT AFTER IN UTERO FETAL STEM CELL TRANSPLANTATION IN CONGENITAL HEMOGLOBINOPATHIES1 Transplantation ·Magnus Westgren, Olle Ringdén, S. H. Eik‐Nes, Sverker Ek, Maria Anvret, Bipin Jaya Singh, The‐Hung Bui, Violeta Griškevičienė, Torvid Kiserud, Anders Kjældgaard, Aurelio Maggio, L Markling, Justin Sextro, F. Orlandi	1996	108
19	Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization Prenatal Diagnosis ·Elisabeth Blennow, The‐Hung Bui, Ulf Kristoffersson, Mihailo Vujic, Göran Annerén, Eva Holmberg, Magnus Nordenskjöld	1994	91
20	Prenatal investigation of a 45,X/46,X,r(?) karyotype in amniocytes using fluorescence in situ hybridization with an X‐centromeric probe Prenatal Diagnosis ·Kensuke Yasue, The‐Hung Bui, Jørn Koch, Karen Brøndum‐Nielsen	1992	9

About The‐Hung Bui

The‐Hung Bui is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Clinical Biochemistry, Genetics and Transplantation, having authored 62 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (28 papers), Genomic variations and chromosomal abnormalities (14 papers), Neurogenetic and Muscular Disorders Research (7 papers), Metabolism and Genetic Disorders (6 papers), Chromosomal and Genetic Variations (6 papers), Congenital heart defects research (5 papers), Mitochondrial Function and Pathology (4 papers) and Muscle Physiology and Disorders (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (690 citations), Genetics (554 citations), Genetics (159 citations), Transplantation (37 citations) and Obstetrics and Gynecology (92 citations). The‐Hung Bui has collaborated with scholars based in Sweden, Vietnam and United States. Frequent co-authors include Lisa G. Shaffer, Elisabeth Blennow, Magnus Nordenskjöld, J. Lindsten, Göran Annerén, Svetlana Lajić, Anna Wedell, Mikael Holst, E. Martin Ritzén and Magnus Westgren. Their work appears in journals such as Prenatal Diagnosis, Best Practice & Research Clinical Obstetrics & Gynaecology, Acta Obstetricia Et Gynecologica Scandinavica, American Journal of Obstetrics and Gynecology and Fetal Diagnosis and Therapy.

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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