Man‐Ting So

1.5k total citations
29 papers, 666 citations indexed

About

Man‐Ting So is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Man‐Ting So has authored 29 papers receiving a total of 666 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Surgery, 14 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Man‐Ting So's work include Congenital gastrointestinal and neural anomalies (17 papers), Digestive system and related health (8 papers) and Congenital Anomalies and Fetal Surgery (4 papers). Man‐Ting So is often cited by papers focused on Congenital gastrointestinal and neural anomalies (17 papers), Digestive system and related health (8 papers) and Congenital Anomalies and Fetal Surgery (4 papers). Man‐Ting So collaborates with scholars based in Hong Kong, China and Vietnam. Man‐Ting So's co-authors include Esw Ngan, Pak C. Sham, María-Mercé García-Barceló, Xiaoping Miao, Stacey S. Cherny, Vincent Chi‐Hang Lui, Clara Sze-Man Tang, Kenneth Kak‐Yuen Wong, Thomas Y.Y. Leon and Paul Kwong Hang Tam and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Schizophrenia Bulletin.

In The Last Decade

Man‐Ting So

29 papers receiving 658 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Man‐Ting So Hong Kong 15 439 225 163 85 42 29 666
María-Mercé García-Barceló Hong Kong 14 307 0.7× 180 0.8× 155 1.0× 56 0.7× 38 0.9× 27 526
Paola Griseri Italy 19 330 0.8× 188 0.8× 351 2.2× 73 0.9× 101 2.4× 32 772
Maria‐Mercè Garcia‐Barceló Hong Kong 11 257 0.6× 119 0.5× 132 0.8× 42 0.5× 27 0.6× 15 407
Silvia Borghini Italy 11 113 0.3× 87 0.4× 286 1.8× 112 1.3× 36 0.9× 18 491
Naoko Amano Japan 12 64 0.1× 180 0.8× 281 1.7× 40 0.5× 26 0.6× 41 507
Michael Muchow United States 9 219 0.5× 67 0.3× 112 0.7× 227 2.7× 105 2.5× 9 594
Toshiaki Tsujimura Japan 14 581 1.3× 226 1.0× 126 0.8× 23 0.3× 6 0.1× 22 701
Wee Teik Keng Malaysia 11 100 0.2× 183 0.8× 183 1.1× 50 0.6× 19 0.5× 20 420
Hae Joung Sul South Korea 12 52 0.1× 130 0.6× 187 1.1× 83 1.0× 49 1.2× 24 382
Nikolaos Settas United States 9 107 0.2× 63 0.3× 111 0.7× 28 0.3× 41 1.0× 19 302

Countries citing papers authored by Man‐Ting So

Since Specialization
Citations

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

Fields of papers citing papers by Man‐Ting So

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Man‐Ting So. 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 Man‐Ting So. The network helps show where Man‐Ting So may publish in the future.

Co-authorship network of co-authors of Man‐Ting So

This figure shows the co-authorship network connecting the top 25 collaborators of Man‐Ting So. A scholar is included among the top collaborators of Man‐Ting So 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 Man‐Ting So. Man‐Ting So 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.
Tang, Clara Sze-Man, Man‐Ting So, Haibing Yue, et al.. (2021). Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism. EBioMedicine. 71. 103530–103530. 45 indexed citations
2.
Hsu, Jacob Shujui, Ruizhong Zhang, Fanny Yeung, et al.. (2019). Cancer gene mutations in congenital pulmonary airway malformation patients. ERJ Open Research. 5(1). 196–2018. 15 indexed citations
3.
So, Man‐Ting, Clara Sze-Man Tang, Kenneth K. Wong, et al.. (2018). Epidemiological characteristics of Hirschsprung’s disease (HSCR): Results of a case series of fifty patients from Bangladesh. Journal of Pediatric Surgery. 53(10). 1955–1959. 6 indexed citations
4.
Tang, Clara Sze-Man, Man‐Ting So, Stacey S. Cherny, et al.. (2017). Actionable secondary findings from whole-genome sequencing of 954 East Asians. Human Genetics. 137(1). 31–37. 37 indexed citations
5.
Hsu, Jacob Shujui, Man‐Ting So, Clara Sze-Man Tang, et al.. (2017). De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca. Human Molecular Genetics. 27(2). 351–358. 5 indexed citations
6.
Porsch, Robert M., Elisa Merello, Patrizia De Marco, et al.. (2016). Sacral agenesis: a pilot whole exome sequencing and copy number study. BMC Medical Genetics. 17(1). 98–98. 13 indexed citations
7.
Tang, Clara Sze-Man, Hongsheng Gui, Man‐Ting So, et al.. (2015). Depletion of theIKBKAPortholog in zebrafish leads to hirschsprung disease-like phenotype. World Journal of Gastroenterology. 21(7). 2040–2046. 13 indexed citations
8.
Wong, Emily, Hon‐Cheong So, Miaoxin Li, et al.. (2013). Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese. Schizophrenia Bulletin. 40(4). 777–786. 47 indexed citations
9.
Leon, Thomas Y.Y., Man‐Ting So, Vincent Chi Hang Lui, et al.. (2011). Functional analyses of RET mutations in Chinese hirschsprung disease patients. Birth Defects Research Part A Clinical and Molecular Teratology. 94(1). 47–51. 3 indexed citations
10.
Tang, Clara Sze-Man, Esw Ngan, Man‐Ting So, et al.. (2011). Mutations in the NRG1 gene are associated with Hirschsprung disease. Human Genetics. 131(1). 67–76. 43 indexed citations
11.
Tang, Clara Sze-Man, Yunia Sribudiani, Xiaoping Miao, et al.. (2010). Fine mapping of the 9q31 Hirschsprung’s disease locus. Human Genetics. 127(6). 675–683. 17 indexed citations
12.
Cornes, Belinda K., Clara Sze-Man Tang, Thomas Y.Y. Leon, et al.. (2010). Haplotype Analysis Reveals a Possible Founder Effect of RET Mutation R114H for Hirschsprung's Disease in the Chinese Population. PLoS ONE. 5(6). e10918–e10918. 17 indexed citations
13.
García-Barceló, María-Mercé, Xiaoping Miao, Clara Sze-Man Tang, et al.. (2010). No NRG1 V266L in Chinese patients with schizophrenia. Psychiatric Genetics. 21(1). 47–49. 2 indexed citations
14.
García-Barceló, María-Mercé, Vincent Chi‐Hang Lui, Man‐Ting So, et al.. (2009). MNX1 (HLXB9) mutations in Currarino patients. Journal of Pediatric Surgery. 44(10). 1892–1898. 30 indexed citations
15.
Leon, Thomas Y.Y., et al.. (2009). Transcriptional regulation of RET by Nkx2-1, Phox2b, Sox10, and Pax3. Journal of Pediatric Surgery. 44(10). 1904–1912. 45 indexed citations
16.
Garcia‐Barceló, Maria‐Mercè, Kenneth Kak‐Yuen Wong, Vincent Chi‐Hang Lui, et al.. (2008). Identification of a HOXD13 mutation in a VACTERL patient. American Journal of Medical Genetics Part A. 146A(24). 3181–3185. 70 indexed citations
17.
García-Barceló, María-Mercé, Clara Sze-Man Tang, Xiaoping Miao, et al.. (2008). Mapping of a Hirschsprung's disease locus in 3p21. European Journal of Human Genetics. 16(7). 833–840. 14 indexed citations
18.
Garcia-Barceló, Mercè, Sebastian K. King, Xiaoping Miao, et al.. (2007). Application of HapMap data to the evaluation of 8 candidate genes for pediatric slow transit constipation. Journal of Pediatric Surgery. 42(4). 666–671. 8 indexed citations
19.
Garcia‐Barceló, Maria‐Mercè, Esw Ngan, Thomas Yuk-Yu Leon, et al.. (2007). Evaluation of the Thyroid Transcription Factor‐1 Gene (TITF1) as a Hirschsprung's Disease Locus. Annals of Human Genetics. 71(6). 746–754. 12 indexed citations
20.
Garcia-Barceló, Mercè, Raymond W. Ganster, Vincent Chi Hang Lui, et al.. (2004). TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease. Human Molecular Genetics. 14(2). 191–204. 77 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 María-Mercé García-Barceló Breakdown of academic impact, for papers by Paola Griseri Breakdown of academic impact, for papers by Maria‐Mercè Garcia‐Barceló Breakdown of academic impact, for papers by Silvia Borghini Breakdown of academic impact, for papers by Naoko Amano Breakdown of academic impact, for papers by Michael Muchow Breakdown of academic impact, for papers by Toshiaki Tsujimura Breakdown of academic impact, for papers by Wee Teik Keng Breakdown of academic impact, for papers by Hae Joung Sul Breakdown of academic impact, for papers by Nikolaos Settas
Rankless by CCL
2026