Ho‐Ming Luk
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 40
- Genomics and Rare Diseases 13
- Genetic Syndromes and Imprinting 12
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 7
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- Congenital heart defects research 7
- RNA modifications and cancer 6
- Co-authors
- Ivan F. M. Lo (47 shared papers)Brian Hon‐Yin Chung (22 shared papers)Kelvin Y.K. Chan (7 shared papers)Anita Sik Yau Kan (9 shared papers)Kwong Wai Choy (6 shared papers)Cheuk Wing Fung (4 shared papers)Wilson Chong (1 shared paper)Chi Chiu Wang (1 shared paper)
- Journals
- European Journal of Medical Genetics (6 papers)Scientific Reports (3 papers)American Journal of Medical Genetics Part A (21 papers)Prenatal Diagnosis (2 papers)Frontiers in Pediatrics (2 papers)
- Partner nations
- ChinaHong KongUnited States
In The Last Decade
Ho‐Ming Luk
61 papers receiving 483 citations
Peers
Comparison fields: 5 of 53
- Genetics 241
- Pediatrics, Perinatology and Child Health 75
- Developmental Biology 7
- Molecular Biology 206
- Clinical Biochemistry 16
Countries citing papers authored by Ho‐Ming Luk
This map shows the geographic impact of Ho‐Ming Luk'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 Ho‐Ming Luk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ho‐Ming Luk more than expected).
Fields of papers citing papers by Ho‐Ming Luk
This network shows the impact of papers produced by Ho‐Ming Luk. 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 Ho‐Ming Luk. The network helps show where Ho‐Ming Luk may publish in the future.
Co-authors
The 25 scholars most cited alongside Ho‐Ming Luk, 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 71 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 30 | |
| 2 | 2016 | 29 | |
| 3 | 2012 | 29 | |
| 4 | 2019 | 28 | |
| 5 | 2018 | 22 | |
| 6 | 2018 | 19 | |
| 7 | 2018 | 16 | |
| 8 | 2017 | 16 | |
| 9 | 2020 | 15 | |
| 10 | 2019 | 14 | |
| 11 | 2020 | 14 | |
| 12 | 2020 | 14 | |
| 13 | 2021 | 13 | |
| 14 | 2014 | 12 | |
| 15 | 2016 | 12 | |
| 16 | 2020 | 10 | |
| 17 | 2014 | 10 | |
| 18 | 2021 | 9 | |
| 19 | 2020 | 9 | |
| 20 | 2018 | 9 |
About Ho‐Ming Luk
Ho‐Ming Luk is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Pathology and Forensic Medicine, having authored 71 papers that have together received 488 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genetic Syndromes and Imprinting (12 papers), Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (8 papers), Congenital heart defects research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), RNA modifications and cancer (6 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Genetics (241 citations), Pediatrics, Perinatology and Child Health (75 citations), Developmental Biology (7 citations), Molecular Biology (206 citations) and Clinical Biochemistry (16 citations). Ho‐Ming Luk has collaborated with scholars based in China, Hong Kong and United States. Frequent co-authors include Ivan F. M. Lo, Brian Hon‐Yin Chung, Kelvin Y.K. Chan, Anita Sik Yau Kan, Kwong Wai Choy, Cheuk Wing Fung, Wilson Chong, Chi Chiu Wang, Christopher Chun Yu Mak and Tak Yeung Leung. Their work appears in journals such as European Journal of Medical Genetics, Scientific Reports, American Journal of Medical Genetics Part A, Prenatal Diagnosis and Frontiers in Pediatrics.
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.