Patrick Yap
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 11
- Genomics and Rare Diseases 7
- Connective tissue disorders research 3
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- RNA regulation and disease 2
- RNA modifications and cancer 1
- Co-authors
- Tiong Yang Tan (5 shared papers)Peter G. Farlie (1 shared paper)Naomi L. Baker (1 shared paper)Ravi Savarirayan (3 shared papers)Natasha J. Brown (2 shared papers)Zornitza Stark (3 shared papers)George McGillivray (3 shared papers)Hirotomo Saitsu (1 shared paper)
- Journals
- Genetics in Medicine (3 papers)Archives of Pediatrics and Adolescent Medicine (1 paper)The American Journal of Human Genetics (1 paper)Bone (1 paper)Clinical Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesNew Zealand
In The Last Decade
Patrick Yap
16 papers receiving 973 citations
Peers
Comparison fields: 5 of 66
- Genetics 671
- Cancer Research 83
- Molecular Biology 338
- Clinical Biochemistry 32
- Pediatrics, Perinatology and Child Health 77
Countries citing papers authored by Patrick Yap
This map shows the geographic impact of Patrick Yap'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 Patrick Yap with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Yap more than expected).
Fields of papers citing papers by Patrick Yap
This network shows the impact of papers produced by Patrick Yap. 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 Patrick Yap. The network helps show where Patrick Yap may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Yap, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 314 | |
| 2 | 2017 | 247 | |
| 3 | 2018 | 90 | |
| 4 | 2015 | 66 | |
| 5 | 2020 | 66 | |
| 6 | 2021 | 66 | |
| 7 | 2016 | 41 | |
| 8 | 2018 | 33 | |
| 9 | 2018 | 15 | |
| 10 | 2024 | 12 | |
| 11 | 2015 | 12 | |
| 12 | 2017 | 11 | |
| 13 | 2016 | 10 | |
| 14 | 2015 | 7 | |
| 15 | 2016 | 5 | |
| 16 | 2018 | 4 |
About Patrick Yap
Patrick Yap is a scholar working on Genetics, Molecular Biology, Cancer Research, Pulmonary and Respiratory Medicine and Genetics, having authored 16 papers that have together received 999 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Connective tissue disorders research (3 papers), RNA regulation and disease (2 papers), Sarcoma Diagnosis and Treatment (1 paper), Cancer Genomics and Diagnostics (1 paper), Pancreatic function and diabetes (1 paper), Congenital Diaphragmatic Hernia Studies (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (671 citations), Cancer Research (83 citations), Molecular Biology (338 citations), Clinical Biochemistry (32 citations) and Pediatrics, Perinatology and Child Health (77 citations). Patrick Yap has collaborated with scholars based in Australia, United States and New Zealand. Frequent co-authors include Tiong Yang Tan, Peter G. Farlie, Naomi L. Baker, Ravi Savarirayan, Natasha J. Brown, Zornitza Stark, George McGillivray, Hirotomo Saitsu, Nobuhiko Okamoto and Tomoki Kosho. Their work appears in journals such as Genetics in Medicine, Archives of Pediatrics and Adolescent Medicine, The American Journal of Human Genetics, Bone and Clinical Genetics.
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.