Patrick Yap
Impact in
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
Papers in
- Genetics 7
- Genomics and Rare Diseases 3
- Connective tissue disorders research 3
- Genetic Syndromes and Imprinting 1
- Neurogenetic and Muscular Disorders Research 1
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- Epigenetics and DNA Methylation 1
- Co-authors
- Tiong Yang Tan (4 shared papers)Naomi L. Baker (1 shared paper)Peter G. Farlie (1 shared paper)Ravi Savarirayan (2 shared papers)Natasha J. Brown (2 shared papers)Naomichi Matsumoto (1 shared paper)Noriko Miyake (1 shared paper)Yoshinori Tsurusaki (1 shared paper)
- Journals
- Bone (1 paper)Journal of the Royal Society of New Zealand (1 paper)The Lancet Child & Adolescent Health (1 paper)Prenatal Diagnosis (1 paper)Clinical Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesNew Zealand
In The Last Decade
Patrick Yap
9 papers receiving 196 citations
Peers
Comparison fields: 5 of 43
- Genetics 125
- Anatomy 3
- Genetics 14
- Immunology and Allergy 7
- Molecular Biology 81
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 | 2015 | 61 | |
| 2 | 2020 | 47 | |
| 3 | 2016 | 40 | |
| 4 | 2018 | 12 | |
| 5 | 2015 | 11 | |
| 6 | 2024 | 10 | |
| 7 | 2016 | 9 | |
| 8 | 2015 | 7 | |
| 9 | 2018 | 4 |
About Patrick Yap
Patrick Yap is a scholar working on Genetics, Molecular Biology, Surgery, Pulmonary and Respiratory Medicine and Genetics, having authored 9 papers that have together received 201 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Connective tissue disorders research (3 papers), Sarcoma Diagnosis and Treatment (1 paper), Epigenetics and DNA Methylation (1 paper), Cancer Genomics and Diagnostics (1 paper), Genetic Syndromes and Imprinting (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Neurofibromatosis and Schwannoma Cases (1 paper). The work is most often cited by research in Genetics (125 citations), Anatomy (3 citations), Genetics (14 citations), Immunology and Allergy (7 citations) and Molecular Biology (81 citations). Patrick Yap has collaborated with scholars based in Australia, United States and New Zealand. Frequent co-authors include Tiong Yang Tan, Naomi L. Baker, Peter G. Farlie, Ravi Savarirayan, Natasha J. Brown, Naomichi Matsumoto, Noriko Miyake, Yoshinori Tsurusaki, Eriko Koshimizu and Toshiro Nagai. Their work appears in journals such as Bone, Journal of the Royal Society of New Zealand, The Lancet Child & Adolescent Health, Prenatal Diagnosis 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.