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
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- dental development and anomalies
Papers in
- Genetics 26
- Cleft Lip and Palate Research 11
- Craniofacial Disorders and Treatments 8
- Congenital Ear and Nasal Anomalies 8
- Genomic variations and chromosomal abnormalities 4
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- Congenital heart defects research 3
- Hedgehog Signaling Pathway Studies 3
- Co-authors
- R M Winter (4 shared papers)S Malcolm (1 shared paper)Natalie J. Prescott (1 shared paper)Robin M. Winter (3 shared papers)Brian C. Sommerlad (4 shared papers)Lyn S. Chitty (2 shared papers)Debbie Sell (3 shared papers)Howard M. Saal (1 shared paper)
- Journals
- Clinical Genetics (3 papers)European Journal of Medical Genetics (2 papers)Journal of Dental Research (2 papers)Prenatal Diagnosis (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Melissa Lees
35 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 84
- Genetics 673
- Genetics 164
- Molecular Biology 511
- Reproductive Medicine 51
- Neurology 68
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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 112 | |
| 2 | 2009 | 93 | |
| 3 | 2018 | 91 | |
| 4 | 2011 | 80 | |
| 5 | 2004 | 76 | |
| 6 | 2017 | 60 | |
| 7 | 2005 | 59 | |
| 8 | 2011 | 54 | |
| 9 | 1999 | 50 | |
| 10 | 2003 | 46 | |
| 11 | 2013 | 37 | |
| 12 | 2016 | 37 | |
| 13 | 2011 | 36 | |
| 14 | 2008 | 31 | |
| 15 | 1998 | 26 | |
| 16 | 1998 | 26 | |
| 17 | 2011 | 24 | |
| 18 | 2022 | 20 | |
| 19 | 2016 | 20 | |
| 20 | 2012 | 20 |
About Melissa Lees
Melissa Lees is a scholar working on Genetics, Molecular Biology, Genetics, Surgery and Pulmonary and Respiratory Medicine, having authored 37 papers that have together received 1.1k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (11 papers), Craniofacial Disorders and Treatments (8 papers), Congenital Ear and Nasal Anomalies (8 papers), Genomic variations and chromosomal abnormalities (4 papers), Tracheal and airway disorders (3 papers), Congenital heart defects research (3 papers), Hedgehog Signaling Pathway Studies (3 papers) and Congenital Anomalies and Fetal Surgery (3 papers). The work is most often cited by research in Genetics (673 citations), Genetics (164 citations), Molecular Biology (511 citations), Reproductive Medicine (51 citations) and Neurology (68 citations). Melissa Lees has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include R M Winter, S Malcolm, Natalie J. Prescott, Robin M. Winter, Brian C. Sommerlad, Lyn S. Chitty, Debbie Sell, Howard M. Saal, William Reardon and S Malcolm. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Journal of Dental Research, Prenatal Diagnosis and Journal of Medical 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.