Thuong Ha

822 total citations
13 papers, 136 citations indexed

About

Thuong Ha is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Thuong Ha has authored 13 papers receiving a total of 136 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Oncology. Recurrent topics in Thuong Ha's work include Genomics and Rare Diseases (3 papers), Renal and related cancers (3 papers) and Genetics, Aging, and Longevity in Model Organisms (2 papers). Thuong Ha is often cited by papers focused on Genomics and Rare Diseases (3 papers), Renal and related cancers (3 papers) and Genetics, Aging, and Longevity in Model Organisms (2 papers). Thuong Ha collaborates with scholars based in Australia, United States and Canada. Thuong Ha's co-authors include Jozef Gécz, Nigel J. O’Neil, David L. Baillie, Greg Vatcher, Erin J. Gilchrist, Mark Corbett, Helen Chamberlin, Marie Shaw, Jean‐Louis Mandel and Jamel Chelly and has published in prestigious journals such as Gene, Human Mutation and The Medical Journal of Australia.

In The Last Decade

Thuong Ha

13 papers receiving 136 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thuong Ha Australia	6	77	47	33	20	16	13	136
Yetki Aslan France	3	112 1.5×	29 0.6×	30 0.9×	6 0.3×	6 0.4×	4	264
Marianna Yusupova United States	8	100 1.3×	31 0.7×	5 0.2×	16 0.8×	32 2.0×	10	276
N.O. Hadziselimovic Switzerland	8	127 1.6×	50 1.1×	32 1.0×	20 1.0×	7 0.4×	8	273
Leire Abalde-Atristain United States	6	211 2.7×	47 1.0×	11 0.3×	10 0.5×	26 1.6×	10	267
Yushi Redhead United Kingdom	7	59 0.8×	18 0.4×	10 0.3×	7 0.3×	9 0.6×	8	200
Mika H. Martikainen Finland	13	205 2.7×	47 1.0×	6 0.2×	16 0.8×	13 0.8×	34	418
Laura C. Murphy United Kingdom	8	116 1.5×	64 1.4×	4 0.1×	44 2.2×	36 2.3×	14	197
Adélaïde Bernard United States	3	215 2.8×	111 2.4×	8 0.2×	9 0.5×	14 0.9×	4	289
Jamie B. Littleboy Australia	5	144 1.9×	50 1.1×	6 0.2×	37 1.9×	6 0.4×	5	225
Jeff Aaronson United States	4	164 2.1×	47 1.0×	20 0.6×	6 0.3×	2 0.1×	4	183

Countries citing papers authored by Thuong Ha

Since Specialization

Citations

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

Fields of papers citing papers by Thuong Ha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thuong Ha

This figure shows the co-authorship network connecting the top 25 collaborators of Thuong Ha. A scholar is included among the top collaborators of Thuong Ha 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 Thuong Ha. Thuong Ha is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Ha, Thuong, et al.. (2023). Relationship between BMI and prognosis of chronic heart failure outpatients in Vietnam: a single-center study. Frontiers in Nutrition. 10. 1251601–1251601. 5 indexed citations

Ghaoui, Roula, Thuong Ha, Jennifer Kerkhof, et al.. (2023). Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis. Neuromuscular Disorders. 33(6). 484–489. 3 indexed citations

Karolak, Justyna A., Przemysław Szafrański, Tomasz Gambin, et al.. (2022). Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant. European Journal of Human Genetics. 30(10). 1182–1186. 2 indexed citations

Scott, Hamish S., Alex Brown, Karin S. Kassahn, et al.. (2022). The clinical and genetic features of hereditary pancreatitis in South Australia. The Medical Journal of Australia. 216(11). 578–582. 3 indexed citations

Byrne, Alicia B., Jinghua Feng, Thuong Ha, et al.. (2021). Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia. BMC Medical Genomics. 14(1). 64–64. 5 indexed citations

Arts, Peer, Alicia B. Byrne, Tristan Hardy, et al.. (2020). Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome. American Journal of Medical Genetics Part A. 182(5). 1273–1277. 11 indexed citations

Quartier, Angélique, Thuong Ha, George McGillivray, et al.. (2019). Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment. Human Mutation. 40(11). 2021–2032. 39 indexed citations

Corbett, Mark, Samantha J. Turner, Alison Gardner, et al.. (2017). Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations. European Journal of Medical Genetics. 60(8). 437–443. 8 indexed citations

Kumar, Raman, Thuong Ha, Duyen Pham, et al.. (2016). A non-coding variant in the 5ʹ UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability. European Journal of Human Genetics. 24(11). 1612–1616. 8 indexed citations

10.

Ha, Thuong, Lynette G. Sadleir, Simone Mandelstam, et al.. (2015). A mutation in COL4A2 causes autosomal dominant porencephaly with cataracts. American Journal of Medical Genetics Part A. 170(4). 1059–1063. 13 indexed citations

11.

Vatcher, Greg, W. Brad Barbazuk, Nigel J. O’Neil, et al.. (1999). Identification and characterization of a serine hydroxymethyltransferase isoform in Caenorhabditis briggsae. Gene. 230(2). 137–144. 3 indexed citations

12.

O’Neil, Nigel J., Helen Chamberlin, Erin J. Gilchrist, et al.. (1998). Lethal mutations defining 112 complementation groups in a 4.5 Mb sequenced region of Caenorhabditis elegans chromosome III. Molecular and General Genetics MGG. 260(2-3). 280–288. 35 indexed citations

13.

O’Neil, Nigel J., Helen Chamberlin, Erin J. Gilchrist, et al.. (1998). Lethal mutations defining 112 complementation groups in a 4.5 Mb sequenced region of. Molecular and General Genetics MGG. 260(2). 280–280. 1 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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