Alex Magee
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Genomics and Rare Diseases
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- Epigenetics and DNA Methylation
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
- Genetics 11
- Congenital Ear and Nasal Anomalies 5
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Cleft Lip and Palate Research 2
- Craniofacial Disorders and Treatments 2
- Co-authors
- Hilde Van Esch (1 shared paper)N. C. Nevin (6 shared papers)Ben C.J. Hamel (1 shared paper)Bert B.A. de Vries (1 shared paper)David Geneviève (1 shared paper)Jean‐Pierre Fryns (1 shared paper)Tjitske Kleefstra (1 shared paper)Hans van Bokhoven (1 shared paper)
- Journals
- Human Molecular Genetics (3 papers)Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (2 papers)Archives of Disease in Childhood Fetal & Neonatal (1 paper)Clinical Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Alex Magee
21 papers receiving 927 citations
Peers
Comparison fields: 5 of 72
- Genetics 507
- Genetics 137
- Molecular Biology 471
- Cellular and Molecular Neuroscience 78
- Pulmonary and Respiratory Medicine 81
Countries citing papers authored by Alex Magee
This map shows the geographic impact of Alex Magee'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 Alex Magee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alex Magee more than expected).
Fields of papers citing papers by Alex Magee
This network shows the impact of papers produced by Alex Magee. 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 Alex Magee. The network helps show where Alex Magee may publish in the future.
Co-authors
The 25 scholars most cited alongside Alex Magee, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 279 | |
| 2 | 2006 | 160 | |
| 3 | 2015 | 82 | |
| 4 | 1995 | 77 | |
| 5 | 2014 | 72 | |
| 6 | 2007 | 65 | |
| 7 | 2016 | 44 | |
| 8 | 2016 | 28 | |
| 9 | 1998 | 24 | |
| 10 | 1998 | 24 | |
| 11 | 2017 | 22 | |
| 12 | 1998 | 16 | |
| 13 | 1999 | 15 | |
| 14 | 2016 | 8 | |
| 15 | 2002 | 8 | |
| 16 | 2006 | 7 | |
| 17 | 1994 | 7 | |
| 18 | 2008 | 6 | |
| 19 | 1992 | 6 | |
| 20 | 2002 | 1 |
About Alex Magee
Alex Magee is a scholar working on Genetics, Molecular Biology, Genetics, Surgery and Cellular and Molecular Neuroscience, having authored 21 papers that have together received 952 indexed citations. Recurring topics across this work include Congenital Ear and Nasal Anomalies (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic Neurodegenerative Diseases (2 papers), Cleft Lip and Palate Research (2 papers), Herpesvirus Infections and Treatments (2 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (507 citations), Genetics (137 citations), Molecular Biology (471 citations), Cellular and Molecular Neuroscience (78 citations) and Pulmonary and Respiratory Medicine (81 citations). Alex Magee has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Hilde Van Esch, N. C. Nevin, Ben C.J. Hamel, Bert B.A. de Vries, David Geneviève, Jean‐Pierre Fryns, Tjitske Kleefstra, Hans van Bokhoven, Han G. Brunner and Jeanne Amiel. Their work appears in journals such as Human Molecular Genetics, Journal of Medical Genetics, The American Journal of Human Genetics, Archives of Disease in Childhood Fetal & Neonatal 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.