Angeline Lai
Impact in
-
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Hemoglobinopathies and Related Disorders
- Connective tissue disorders research
Papers in
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- Congenital heart defects research 4
- Renal and related cancers 2
- Genetics 15
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 4
- Connective tissue disorders research 4
- Genetics and Neurodevelopmental Disorders 3
- Hemoglobinopathies and Related Disorders 3
- Co-authors
- Saumya Shekhar Jamuar (13 shared papers)Ene‐Choo Tan (14 shared papers)Maggie Brett (12 shared papers)Ivy Ng (7 shared papers)Ee‐Shien Tan (5 shared papers)A. S. Jacobsen (1 shared paper)Ah Moy Tan (2 shared papers)Eileen C.P. Lim (4 shared papers)
- Journals
- European Journal of Pediatrics (3 papers)Gene (3 papers)Prenatal Diagnosis (1 paper)Clinical Kidney Journal (1 paper)Human Genomics (1 paper)
- Partner nations
- SingaporeUnited StatesSwitzerland
In The Last Decade
Angeline Lai
29 papers receiving 342 citations
Peers
Comparison fields: 5 of 62
- Developmental Biology 10
- Genetics 122
- Genetics 36
- Molecular Biology 136
- Hematology 21
Countries citing papers authored by Angeline Lai
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
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-authors
The 25 scholars most cited alongside Angeline Lai, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 56 | |
| 2 | 2002 | 34 | |
| 3 | 2012 | 32 | |
| 4 | 2014 | 28 | |
| 5 | 2015 | 27 | |
| 6 | 2013 | 24 | |
| 7 | 2016 | 17 | |
| 8 | 2015 | 14 | |
| 9 | 2011 | 11 | |
| 10 | 2012 | 11 | |
| 11 | 2019 | 9 | |
| 12 | 2015 | 9 | |
| 13 | 2020 | 8 | |
| 14 | 2014 | 7 | |
| 15 | 2008 | 7 | |
| 16 | 2017 | 7 | |
| 17 | 2021 | 6 | |
| 18 | Loeys-Dietz syndrome: a Marfan-like syndrome associated with aggressive vasculopathy. | 2009 | 6 |
| 19 | 2019 | 5 | |
| 20 | 2015 | 5 |
About Angeline Lai
Angeline Lai is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Cardiology and Cardiovascular Medicine, having authored 32 papers that have together received 351 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Connective tissue disorders research (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Hemoglobinopathies and Related Disorders (3 papers), Urological Disorders and Treatments (2 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Developmental Biology (10 citations), Genetics (122 citations), Genetics (36 citations), Molecular Biology (136 citations) and Hematology (21 citations). Angeline Lai has collaborated with scholars based in Singapore, United States and Switzerland. Frequent co-authors include Saumya Shekhar Jamuar, Ene‐Choo Tan, Maggie Brett, Ivy Ng, Ee‐Shien Tan, A. S. Jacobsen, Ah Moy Tan, Eileen C.P. Lim, Stephen P. Robertson and David Markie. Their work appears in journals such as European Journal of Pediatrics, Gene, Prenatal Diagnosis, Clinical Kidney Journal and Human Genomics.
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.