Mark E. Nuñes
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
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- Alkaline Phosphatase Research Studies
Papers in ⓘ
- Genetics 12
- Connective tissue disorders research 3
- Genomics and Rare Diseases 3
- BRCA gene mutations in cancer 2
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- Genomics and Chromatin Dynamics 2
- Co-authors
- Peter H. Byers (2 shared papers)Anne-Sophie Lia-Baldini (3 shared papers)Deborah Krakow (1 shared paper)Melanie Pepin (1 shared paper)Brigitte Simon‐Bouy (2 shared papers)Frederick W. Luthardt (1 shared paper)Isabelle Brun‐Heath (2 shared papers)Jason P. Evans (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Human Genetics (2 papers)Mammalian Genome (2 papers)British Journal of Haematology (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United StatesFranceGermany
In The Last Decade
Mark E. Nuñes
24 papers receiving 628 citations
Peers
Comparison fields: 5 of 71
- Developmental Biology 95
- Endocrinology, Diabetes and Metabolism 237
- Rheumatology 183
- Genetics 211
- Orthopedics and Sports Medicine 64
Countries citing papers authored by Mark E. Nuñes
This map shows the geographic impact of Mark E. Nuñes'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 Mark E. Nuñes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark E. Nuñes more than expected).
Fields of papers citing papers by Mark E. Nuñes
This network shows the impact of papers produced by Mark E. Nuñes. 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 Mark E. Nuñes. The network helps show where Mark E. Nuñes may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark E. Nuñes, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 96 | |
| 2 | 2001 | 88 | |
| 3 | 2012 | 61 | |
| 4 | 1995 | 60 | |
| 5 | 2006 | 57 | |
| 6 | 1996 | 46 | |
| 7 | 2008 | 38 | |
| 8 | 2016 | 34 | |
| 9 | 2008 | 30 | |
| 10 | 2007 | 29 | |
| 11 | 1997 | 21 | |
| 12 | 1994 | 13 | |
| 13 | 1996 | 10 | |
| 14 | 2005 | 9 | |
| 15 | 2017 | 9 | |
| 16 | 1994 | 9 | |
| 17 | 1997 | 7 | |
| 18 | c-myc expression in the thyroid. I: Normal, adenomatous, and cancerous thyroid tissue. | 1987 | 7 |
| 19 | 2002 | 7 | |
| 20 | 2024 | 5 |
About Mark E. Nuñes
Mark E. Nuñes is a scholar working on Genetics, Molecular Biology, Developmental Biology, Endocrinology, Diabetes and Metabolism and Pediatrics, Perinatology and Child Health, having authored 24 papers that have together received 644 indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (5 papers), Alkaline Phosphatase Research Studies (4 papers), Connective tissue disorders research (3 papers), Prenatal Screening and Diagnostics (3 papers), Heterotopic Ossification and Related Conditions (3 papers), Genomics and Rare Diseases (3 papers), Genomics and Chromatin Dynamics (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Developmental Biology (95 citations), Endocrinology, Diabetes and Metabolism (237 citations), Rheumatology (183 citations), Genetics (211 citations) and Orthopedics and Sports Medicine (64 citations). Mark E. Nuñes has collaborated with scholars based in United States, France and Germany. Frequent co-authors include Peter H. Byers, Anne-Sophie Lia-Baldini, Deborah Krakow, Melanie Pepin, Brigitte Simon‐Bouy, Frederick W. Luthardt, Isabelle Brun‐Heath, Jason P. Evans, A. Taillandier and Mary K. Kukolich. Their work appears in journals such as Genetics in Medicine, Human Genetics, Mammalian Genome, British Journal of Haematology and Human Molecular 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.