Minh Bui

8.4k total citations
131 papers, 2.9k citations indexed

About

Minh Bui is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Minh Bui has authored 131 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Genetics, 42 papers in Cognitive Neuroscience and 41 papers in Molecular Biology. Recurrent topics in Minh Bui's work include Genetics and Neurodevelopmental Disorders (49 papers), Autism Spectrum Disorder Research (42 papers) and Bone health and osteoporosis research (18 papers). Minh Bui is often cited by papers focused on Genetics and Neurodevelopmental Disorders (49 papers), Autism Spectrum Disorder Research (42 papers) and Bone health and osteoporosis research (18 papers). Minh Bui collaborates with scholars based in Australia, United States and United Kingdom. Minh Bui's co-authors include Danuta Z. Loesch, Richard Huggins, Annette K. Taylor, John L. Hopper, Ego Seeman, Cheryl Dissanayake, Roger Zebaze, Sally Clifford, Ali Ghasemzadeh and Xiaofang Wang and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Minh Bui

127 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Minh Bui Australia 32 1.4k 1.1k 920 440 277 131 2.9k
F. John Meaney United States 29 865 0.6× 585 0.5× 1.0k 1.1× 67 0.2× 480 1.7× 84 3.2k
Margaret Zacharin Australia 36 879 0.6× 90 0.1× 944 1.0× 394 0.9× 179 0.6× 174 4.1k
Nikolaus C. Netzer Germany 28 500 0.4× 676 0.6× 549 0.6× 70 0.2× 2.7k 9.8× 98 5.0k
Vincent Pialoux France 35 1.2k 0.9× 127 0.1× 449 0.5× 423 1.0× 1.1k 4.1× 137 3.8k
Tadao Tsuboyama Japan 39 344 0.2× 139 0.1× 887 1.0× 533 1.2× 761 2.7× 146 4.3k
Naoakira Niino Japan 29 228 0.2× 144 0.1× 318 0.3× 255 0.6× 473 1.7× 76 2.5k
Jean Ouellet Canada 36 349 0.2× 291 0.3× 391 0.4× 182 0.4× 539 1.9× 163 4.2k
Deborah A. Hall United States 33 1.8k 1.2× 908 0.9× 1.4k 1.5× 13 0.0× 239 0.9× 136 4.2k
Alessandro Cicognani Italy 37 1.0k 0.7× 184 0.2× 1.4k 1.5× 40 0.1× 290 1.0× 113 4.0k
Stephen D. R. Harridge United Kingdom 39 316 0.2× 126 0.1× 1.7k 1.8× 947 2.2× 1.8k 6.5× 111 5.1k

Countries citing papers authored by Minh Bui

Since Specialization
Citations

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

Fields of papers citing papers by Minh Bui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Minh Bui

This figure shows the co-authorship network connecting the top 25 collaborators of Minh Bui. A scholar is included among the top collaborators of Minh 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 Minh Bui. Minh 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.
Champion, G. David, Minh Bui, Phillip Aouad, et al.. (2025). Associations Between Lifetime Histories of Iron Deficiency, Anxiety, Depression and Multiple Pain Conditions: An Observational Study Using a Large-Scale National Database. Journal of Pain Research. Volume 18. 3781–3792. 1 indexed citations
2.
Li, Shuai, Gillian S. Dite, Robert J. MacInnis, et al.. (2024). Causation and familial confounding as explanations for the associations of polygenic risk scores with breast cancer: Evidence from innovative ICE FALCON and ICE CRISTAL analyses. Genetic Epidemiology. 48(8). 401–413. 3 indexed citations
3.
Alshawsh, Mohammed Abdullah, Melissa Wake, Jozef Gécz, et al.. (2024). Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns. Epigenomics. 16(18). 1203–1214. 2 indexed citations
4.
Bui, Minh, et al.. (2023). Is There a Causal Relationship between Physical Activity and Bone Microarchitecture? A Study of Adult Female Twin Pairs. Journal of Bone and Mineral Research. 38(7). 951–957. 3 indexed citations
5.
Kraan, Claudine M., Minh Bui, Alison D. Archibald, et al.. (2023). Social and physical predictors of mental health impact in adult women who have an FMR1 premutation. SHILAP Revista de lepidopterología. 1(1). 100829–100829. 1 indexed citations
6.
Larsen, Søren Vinther, et al.. (2023). Population-based cohort study of oral contraceptive use and risk of depression. Epidemiology and Psychiatric Sciences. 32. e39–e39. 32 indexed citations
7.
Wang, Fang, Carra A. Simpson, Cali E. Willet, et al.. (2023). Development of the oral resistome during the first decade of life. Nature Communications. 14(1). 1291–1291. 19 indexed citations
8.
9.
Champion, G. David, et al.. (2022). Improved definition of growing pains: A common familial primary pain disorder of early childhood. SHILAP Revista de lepidopterología. 4(2). 78–86. 3 indexed citations
10.
Champion, G. David, et al.. (2021). Familial and Genetic Influences on the Common Pediatric Primary Pain Disorders: A Twin Family Study. Children. 8(2). 89–89. 7 indexed citations
11.
Kraan, Claudine M., Emma K. Baker, Marta Arpone, et al.. (2020). DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome. International Journal of Molecular Sciences. 21(20). 7735–7735. 12 indexed citations
12.
Champion, G. David, et al.. (2020). Contrasting painless and painful phenotypes of pediatric restless legs syndrome: a twin family study. Sleep Medicine. 75. 361–367. 11 indexed citations
13.
Baker, Emma K., Merlin G. Butler, Ling Ling, et al.. (2020). Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders. Translational Psychiatry. 10(1). 362–362. 11 indexed citations
14.
Zebaze, Roger, Minh Bui, Marko Lukic, et al.. (2019). Adding Marrow Adiposity and Cortical Porosity to Femoral Neck Areal Bone Mineral Density Improves the Discrimination of Women With Nonvertebral Fractures From Controls. Journal of Bone and Mineral Research. 34(8). 1451–1460. 16 indexed citations
15.
Chapurlat, Roland, Minh Bui, Elisabeth Sornay‐Rendu, et al.. (2019). Deterioration of Cortical and Trabecular Microstructure Identifies Women With Osteopenia or Normal Bone Mineral Density at Imminent and Long-Term Risk for Fragility Fracture: A Prospective Study. Journal of Bone and Mineral Research. 35(5). 833–844. 41 indexed citations
16.
MacInnis, Robert J., Daniel F. Schmidt, Enes Makalic, et al.. (2016). Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk. Cancer Epidemiology Biomarkers & Prevention. 25(12). 1619–1624. 3 indexed citations
17.
Hopper, John L., Tuong L. Nguyen, Jennifer Stone, et al.. (2016). Childhood body mass index and adult mammographic density measures that predict breast cancer risk. Breast Cancer Research and Treatment. 156(1). 163–170. 21 indexed citations
18.
Lam, Freddy Man Hin, et al.. (2015). Chronic effects of stroke on hip bone density and tibial morphology: a longitudinal study. Osteoporosis International. 27(2). 591–603. 17 indexed citations
19.
Loesch, Danuta Z., David E. Godler, Andrew Evans, et al.. (2011). Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism. Genetics in Medicine. 13(5). 392–399. 65 indexed citations
20.
Loesch, Danuta Z., et al.. (2006). Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats. Journal of Medical Genetics. 44(3). 200–204. 70 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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