Mark E. Nuñes
Impact in
- Developmental Biology top 1%
- Congenital limb and hand anomalies
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- Alkaline Phosphatase Research Studies
Papers in
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- Congenital limb and hand anomalies 6
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- Alkaline Phosphatase Research Studies 7
- Co-authors
- Peter H. Byers (2 shared papers)Melanie G. Pepin (1 shared paper)Deborah Krakow (1 shared paper)Anne-Sophie Lia-Baldini (3 shared papers)Brigitte Simon‐Bouy (2 shared papers)Roberta A Pagon (2 shared papers)Bryce A. Kerlin (1 shared paper)Étienne Mornet (2 shared papers)
- Journals
- Osteoporosis International (3 papers)Human Molecular Genetics (2 papers)Human Genetics (2 papers)Genetics in Medicine (2 papers)Journal of Women s Health (1 paper)
- Partner nations
- United StatesFranceCanada
In The Last Decade
Mark E. Nuñes
29 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 66
- Developmental Biology 237
- Endocrinology, Diabetes and Metabolism 326
- Genetics 320
- Pediatrics, Perinatology and Child Health 46
- Psychiatry and Mental health 60
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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 105 | |
| 2 | 1994 | 104 | |
| 3 | 2001 | 97 | |
| 4 | Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1. | 1994 | 94 |
| 5 | 2017 | 89 | |
| 6 | 2006 | 70 | |
| 7 | 1995 | 66 | |
| 8 | 2012 | 62 | |
| 9 | 1998 | 60 | |
| 10 | 1996 | 49 | |
| 11 | 2016 | 49 | |
| 12 | 2023 | 47 | |
| 13 | 2008 | 41 | |
| 14 | 2008 | 41 | |
| 15 | 2007 | 34 | |
| 16 | 2023 | 22 | |
| 17 | 1997 | 21 | |
| 18 | 2023 | 21 | |
| 19 | 1994 | 12 | |
| 20 | 2005 | 9 |
About Mark E. Nuñes
Mark E. Nuñes is a scholar working on Developmental Biology, Endocrinology, Diabetes and Metabolism, Genetics, Pediatrics, Perinatology and Child Health and Sensory Systems, having authored 29 papers that have together received 1.1k indexed citations. Recurring topics across this work include Alkaline Phosphatase Research Studies (7 papers), Congenital limb and hand anomalies (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Prenatal Screening and Diagnostics (2 papers), BRCA gene mutations in cancer (2 papers), Sexual Differentiation and Disorders (2 papers), Connective tissue disorders research (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Developmental Biology (237 citations), Endocrinology, Diabetes and Metabolism (326 citations), Genetics (320 citations), Pediatrics, Perinatology and Child Health (46 citations) and Psychiatry and Mental health (60 citations). Mark E. Nuñes has collaborated with scholars based in United States, France and Canada. Frequent co-authors include Peter H. Byers, Melanie G. Pepin, Deborah Krakow, Anne-Sophie Lia-Baldini, Brigitte Simon‐Bouy, Roberta A Pagon, Bryce A. Kerlin, Étienne Mornet, Isabelle Brun Heath and Agnes Taillandier. Their work appears in journals such as Osteoporosis International, Human Molecular Genetics, Human Genetics, Genetics in Medicine and Journal of Women s Health.
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.