Melissa Lees
Impact in
- Genetics top 5%
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Congenital Ear and Nasal Anomalies
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- dental development and anomalies
- Congenital heart defects research
Papers in
- Genetics 24
- Cleft Lip and Palate Research 11
- Congenital Ear and Nasal Anomalies 8
- Craniofacial Disorders and Treatments 6
- Genomic variations and chromosomal abnormalities 4
- Genetic and rare skin diseases. 3
- Genetics and Neurodevelopmental Disorders 2
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- Hedgehog Signaling Pathway Studies 3
- Co-authors
- R M Winter (4 shared papers)Natalie J. Prescott (1 shared paper)S Malcolm (1 shared paper)Robin M. Winter (3 shared papers)Brian C. Sommerlad (4 shared papers)Lyn S. Chitty (2 shared papers)Adrian Barnett (1 shared paper)Raoul C. M. Hennekam (3 shared papers)
- Journals
- Clinical Genetics (3 papers)European Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)Journal of Dental Research (2 papers)The Cleft Palate-Craniofacial Journal (2 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Melissa Lees
36 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 80
- Genetics 633
- Genetics 148
- Molecular Biology 458
- Neurology 82
- Reproductive Medicine 44
Countries citing papers authored by Melissa Lees
This map shows the geographic impact of Melissa Lees'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 Melissa Lees with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Melissa Lees more than expected).
Fields of papers citing papers by Melissa Lees
This network shows the impact of papers produced by Melissa Lees. 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 Melissa Lees. The network helps show where Melissa Lees may publish in the future.
Co-authors
The 25 scholars most cited alongside Melissa Lees, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 112 | |
| 2 | 2009 | 96 | |
| 3 | 2018 | 91 | |
| 4 | 2011 | 81 | |
| 5 | 2004 | 76 | |
| 6 | 2017 | 60 | |
| 7 | 2005 | 59 | |
| 8 | 2011 | 54 | |
| 9 | 1999 | 50 | |
| 10 | 2003 | 46 | |
| 11 | 2016 | 39 | |
| 12 | 2013 | 38 | |
| 13 | 2011 | 36 | |
| 14 | 2008 | 31 | |
| 15 | 2011 | 27 | |
| 16 | 1998 | 26 | |
| 17 | 1998 | 26 | |
| 18 | 2011 | 24 | |
| 19 | 2022 | 23 | |
| 20 | 2012 | 21 |
About Melissa Lees
Melissa Lees is a scholar working on Genetics, Molecular Biology, Genetics, Surgery and Pulmonary and Respiratory Medicine, having authored 38 papers that have together received 1.2k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (11 papers), Congenital Ear and Nasal Anomalies (8 papers), Craniofacial Disorders and Treatments (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetic and rare skin diseases. (3 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (633 citations), Genetics (148 citations), Molecular Biology (458 citations), Neurology (82 citations) and Reproductive Medicine (44 citations). Melissa Lees has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include R M Winter, Natalie J. Prescott, S Malcolm, Robin M. Winter, Brian C. Sommerlad, Lyn S. Chitty, Adrian Barnett, Raoul C. M. Hennekam, S Malcolm and Kim Harland. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Prenatal Diagnosis, Journal of Dental Research and The Cleft Palate-Craniofacial Journal.
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.