Angeline Lai

1.3k total citations
31 papers, 349 citations indexed

About

Angeline Lai is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Angeline Lai has authored 31 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 7 papers in Surgery. Recurrent topics in Angeline Lai's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Connective tissue disorders research (4 papers). Angeline Lai is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Connective tissue disorders research (4 papers). Angeline Lai collaborates with scholars based in Singapore, United States and New Zealand. Angeline Lai's co-authors include Saumya Shekhar Jamuar, Ene‐Choo Tan, Maggie Brett, Ivy Ng, A. S. Jacobsen, Ah Moy Tan, Stephen P. Robertson, Eileen C.P. Lim, Tim Morgan and Henricus P. M. Kunst and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Gene.

In The Last Decade

Angeline Lai

29 papers receiving 340 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Angeline Lai Singapore 10 152 133 67 40 28 31 349
Azmy M. Al-Hadidy Jordan 9 94 0.6× 89 0.7× 49 0.7× 33 0.8× 22 0.8× 21 274
Pietro Sirleto Italy 12 221 1.5× 137 1.0× 30 0.4× 40 1.0× 31 1.1× 25 399
Ken L. Jones United States 6 154 1.0× 96 0.7× 38 0.6× 31 0.8× 22 0.8× 7 284
Prajnya Ranganath India 11 150 1.0× 115 0.9× 40 0.6× 23 0.6× 41 1.5× 56 367
Johanna Lundin Sweden 9 216 1.4× 91 0.7× 65 1.0× 20 0.5× 21 0.8× 20 397
Katherine Neas New Zealand 12 214 1.4× 103 0.8× 26 0.4× 49 1.2× 14 0.5× 22 430
J.G. Dauwerse Netherlands 6 211 1.4× 129 1.0× 21 0.3× 23 0.6× 16 0.6× 7 307
Tahir Naeem Khan Pakistan 11 118 0.8× 59 0.4× 26 0.4× 47 1.2× 9 0.3× 32 308
Özge Özalp Yüreğir Türkiye 8 137 0.9× 133 1.0× 27 0.4× 35 0.9× 10 0.4× 20 288
Stefano Petrocchi Italy 8 84 0.6× 129 1.0× 31 0.5× 15 0.4× 18 0.6× 15 236

Countries citing papers authored by Angeline Lai

Since Specialization
Citations

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

Fields of papers citing papers by Angeline Lai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angeline Lai

This figure shows the co-authorship network connecting the top 25 collaborators of Angeline Lai. A scholar is included among the top collaborators of Angeline Lai 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 Angeline Lai. Angeline Lai 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.
Lim, Weng Khong, et al.. (2025). National Thalassemia Registry: a 30 year journey of implementing carrier screening in Singapore. The Lancet Regional Health - Western Pacific. 55. 101471–101471. 1 indexed citations
2.
Koh, Mark Jean Aan, Angeline Lai, C. C. Tchoyoson Lim, et al.. (2021). Speckled brain lesions in Incontinentia Pigmenti patients with acquired brain syndromes. European Journal of Paediatric Neurology. 33. 106–111. 3 indexed citations
3.
Haag, Natja, Ene‐Choo Tan, Matthias Begemann, et al.. (2021). Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. European Journal of Human Genetics. 29(11). 1663–1668. 6 indexed citations
4.
Lai, Angeline, et al.. (2020). Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene. Journal of the Neurological Sciences. 414. 116819–116819. 4 indexed citations
5.
Jamuar, Saumya Shekhar, et al.. (2020). Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disorders. Gene. 731. 144360–144360. 8 indexed citations
6.
Wei, Heming, Angeline Lai, Ee Shien Tan, et al.. (2020). Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes. Archives of Disease in Childhood. 106(1). 38–43. 5 indexed citations
7.
Brett, Maggie, et al.. (2017). Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event. Journal of Human Genetics. 62(7). 711–715. 7 indexed citations
8.
Cham, Breana & Angeline Lai. (2017). AB019. Clinical chromosomal microarray analysis in Singapore. Annals of Translational Medicine. 5(S2). AB019–AB019.
9.
Jamuar, Saumya Shekhar, Jyn Ling Kuan, Maggie Brett, et al.. (2016). Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?. EBioMedicine. 5. 211–216. 17 indexed citations
10.
O’Neill, Adam C., Sophia Cameron‐Christie, Tim Morgan, et al.. (2015). Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome. The American Journal of Human Genetics. 96(4). 623–630. 54 indexed citations
11.
Lim, Eileen C.P., Maggie Brett, Angeline Lai, et al.. (2015). Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients. Human Genomics. 9(1). 33–33. 27 indexed citations
12.
Jamuar, Saumya Shekhar, Ee Shien Tan, Breana Cham, et al.. (2015). Left Ventricular Non-compaction: Is It Genetic?. Pediatric Cardiology. 36(8). 1565–1572. 9 indexed citations
13.
Lai, Angeline, et al.. (2014). An osteosclerotic form of Robinow syndrome. American Journal of Medical Genetics Part A. 164(10). 2638–2642. 7 indexed citations
14.
Lai, Angeline, et al.. (2014). Asymptomatic proteinuria, renal cysts and dorsal pancreas agenesis. Clinical Kidney Journal. 7(4). 411–412. 2 indexed citations
15.
Lai, Angeline, et al.. (2013). Loeys–Dietz syndrome in a Southeast Asian Hospital: a case series. European Journal of Pediatrics. 173(3). 387–391. 2 indexed citations
16.
Lai, Angeline, et al.. (2013). Association of trisomy 18 with hepatoblastoma and its implications. European Journal of Pediatrics. 173(12). 1595–1598. 24 indexed citations
17.
Jamuar, Saumya Shekhar, Angeline Lai, Sheila Unger, & Gen Nishimura. (2012). Clinical and radiological findings in Pallister–Killian syndrome. European Journal of Medical Genetics. 55(3). 167–172. 11 indexed citations
18.
Jamuar, Saumya Shekhar, et al.. (2011). Use of deferiprone for iron chelation in patients with transfusion‐dependent thalassaemia. Journal of Paediatrics and Child Health. 47(11). 812–817. 11 indexed citations
19.
Lai, Angeline, et al.. (2008). A mutation in FGFR2 in a child with Pfeiffer syndrome and a sacral appendage. Clinical Dysmorphology. 17(1). 73–74. 7 indexed citations
20.
Lai, Angeline, et al.. (2002). Intussusception: A Three-Year Review. Annals of the Academy of Medicine Singapore. 31(1). 81–85. 34 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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