Kit San Yeung

1.3k total citations
29 papers, 529 citations indexed

About

Kit San Yeung is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kit San Yeung has authored 29 papers receiving a total of 529 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kit San Yeung's work include Genomics and Rare Diseases (11 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetic Syndromes and Imprinting (4 papers). Kit San Yeung is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetic Syndromes and Imprinting (4 papers). Kit San Yeung collaborates with scholars based in Hong Kong, China and Canada. Kit San Yeung's co-authors include Brian Hon‐Yin Chung, Christopher Chun Yu Mak, Wanling Yang, Steven Lim Cho Pei, Mullin H.C. Yu, Adrian H. Koh, Eranga N. Vithana, Tin Aung, Victor H. K. Yong and Gordon Leung and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and American Journal of Kidney Diseases.

In The Last Decade

Kit San Yeung

29 papers receiving 509 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kit San Yeung Hong Kong	13	252	245	65	57	50	29	529
Nisha Patel Saudi Arabia	17	428 1.7×	267 1.1×	37 0.6×	53 0.9×	72 1.4×	39	727
Gülen Eda Ütine Türkiye	14	367 1.5×	373 1.5×	77 1.2×	66 1.2×	19 0.4×	114	715
Go Hun Seo South Korea	11	256 1.0×	204 0.8×	26 0.4×	36 0.6×	21 0.4×	82	527
Pelin Özlem Şimşek‐Kiper Türkiye	14	377 1.5×	326 1.3×	35 0.5×	57 1.0×	21 0.4×	99	662
Soo‐Mi Park United Kingdom	15	464 1.8×	258 1.1×	46 0.7×	74 1.3×	13 0.3×	39	794
Deborah Morrogh United Kingdom	9	247 1.0×	299 1.2×	29 0.4×	34 0.6×	21 0.4×	13	542
Hamad Alzaidan Saudi Arabia	14	283 1.1×	173 0.7×	66 1.0×	67 1.2×	12 0.2×	39	578
Ke-Yu Deng China	6	354 1.4×	120 0.5×	34 0.5×	32 0.6×	34 0.7×	8	527
Francesco Benedicenti Italy	10	165 0.7×	123 0.5×	43 0.7×	66 1.2×	27 0.5×	21	417
Maree Flaherty Australia	14	286 1.1×	257 1.0×	40 0.6×	46 0.8×	153 3.1×	30	566

Countries citing papers authored by Kit San Yeung

Since Specialization

Citations

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

Fields of papers citing papers by Kit San Yeung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kit San Yeung. 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 Kit San Yeung. The network helps show where Kit San Yeung may publish in the future.

Co-authorship network of co-authors of Kit San Yeung

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

All Works

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20 of 20 papers shown

Yu, Mullin H.C., Jasmine Lee Fong Fung, Christopher Chun Yu Mak, et al.. (2022). Functional Evaluation and Genetic Landscape of Children and Young Adults Referred for Assessment of Bronchiectasis. Frontiers in Genetics. 13. 933381–933381. 1 indexed citations

Yu, Mullin H.C., Kit San Yeung, Jasmine Lee Fong Fung, et al.. (2021). Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis. Frontiers in Genetics. 11. 620162–620162. 6 indexed citations

Yeung, Kit San, Cheuk Wing Fung, Han‐Chih Hencher Lee, et al.. (2020). The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes. Molecular Genetics & Genomic Medicine. 8(7). e1229–e1229. 11 indexed citations

Yeung, Kit San, et al.. (2020). A case of G1013R FBN1 mutation: A potential genotype–phenotype correlation in severe Marfan syndrome. American Journal of Medical Genetics Part A. 182(6). 1329–1335. 4 indexed citations

Tung, Joanna Yuet‐ling, Kit San Yeung, Anita Sik Yau Kan, et al.. (2020). Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism. International Journal of Pediatric Endocrinology. 2020(1). 13–13. 5 indexed citations

Yu, Mullin H.C., Christopher Chun Yu Mak, Jasmine Lee Fong Fung, et al.. (2020). Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data. Journal of Human Genetics. 66(6). 637–641. 4 indexed citations

Fung, Jasmine Lee Fong, Mullin H.C. Yu, Shushu Huang, et al.. (2020). A three-year follow-up study evaluating clinical utility of exome sequencing and diagnostic potential of reanalysis. npj Genomic Medicine. 5(1). 37–37. 48 indexed citations

Chiu, Annie Ting Gee, Rui Liang, Mullin H.C. Yu, et al.. (2020). Diagnostic value of whole‐exome sequencing in Chinese pediatric‐onset neuromuscular patients. Molecular Genetics & Genomic Medicine. 8(5). e1205–e1205. 16 indexed citations

Leung, Gordon, Kit San Yeung, Christopher Chun Yu Mak, et al.. (2019). A significant inflation in TGM6 genetic risk casts doubt in its causation in spinocerebellar ataxia type 35. Parkinsonism & Related Disorders. 63. 42–45. 10 indexed citations

10.

Mok, Gary, Kit San Yeung, Wanling Yang, et al.. (2018). Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey. npj Genomic Medicine. 3(1). 19–19. 8 indexed citations

11.

Mak, Christopher Chun Yu, Jasmine Lee Fong Fung, Wilfred Hing Sang Wong, et al.. (2018). Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES). BMC Medical Genomics. 11(1). 93–93. 34 indexed citations

12.

Yeung, Kit San, Matthew Ho, So Lun Lee, et al.. (2018). Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay. Journal of Medical Genetics. 55(12). 847–852. 2 indexed citations

13.

Yeung, Kit San, Winnie W. Y. Tso, Christopher Chun Yu Mak, et al.. (2017). Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism. Molecular Autism. 8(1). 66–66. 86 indexed citations

14.

Yeung, Kit San, et al.. (2017). Somatic PIK3CA mutations in seven patients with PIK3CA‐related overgrowth spectrum. American Journal of Medical Genetics Part A. 173(4). 978–984. 26 indexed citations

15.

Yeung, Kit San, Brian Hon‐Yin Chung, Sanaa Choufani, et al.. (2017). Genome-Wide DNA Methylation Analysis of Chinese Patients with Systemic Lupus Erythematosus Identified Hypomethylation in Genes Related to the Type I Interferon Pathway. PLoS ONE. 12(1). e0169553–e0169553. 36 indexed citations

16.

Mak, Christopher Chun Yu, Pak‐cheong Chow, Anthony P. Y. Liu, et al.. (2016). De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients. npj Genomic Medicine. 1(1). 16033–16033. 7 indexed citations

17.

Yeung, Kit San, et al.. (2016). Silver-Russell syndrome in Hong Kong. Hong Kong Medical Journal. 22(6). 526–33. 6 indexed citations

18.

Lee, Kelvin Y. C., Adrian H. Koh, Tin Aung, et al.. (2005). Characterization of Bietti Crystalline Dystrophy Patients withCYP4V2Mutations. Investigative Ophthalmology & Visual Science. 46(10). 3812–3812. 62 indexed citations

19.

Yeung, Kit San, et al.. (2003). Collapsing glomerulopathy coexisting with membranous glomerulonephritis in native kidney biopsies: a report of 3 HIV-negative patients. American Journal of Kidney Diseases. 42(3). 591–595. 6 indexed citations

20.

Jones, Christopher, Brian L. Bleau, N Buskard, et al.. (1994). Simultaneous Development of Diffuse Immunoblastic Lymphoma in Recipients of Renal Transplants From a Single Cadaver Donor: Transmission of Epstein-Barr Virus and Triggering by OKT3. American Journal of Kidney Diseases. 23(1). 130–134. 10 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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