Mark E. Nuñes
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
-
- Alkaline Phosphatase Research Studies
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 3
- Connective tissue disorders research 3
- Genomics and Rare Diseases 3
- BRCA gene mutations in cancer 2
- Co-authors
- Peter H. Byers (2 shared papers)Melanie Pepin (1 shared paper)Deborah Krakow (1 shared paper)Anne-Sophie Lia-Baldini (3 shared papers)Roberta A Pagon (2 shared papers)Brigitte Simon‐Bouy (2 shared papers)A. Taillandier (2 shared papers)Raj P. Kapur (1 shared paper)
- Journals
- Human Genetics (2 papers)Mammalian Genome (2 papers)Genetics in Medicine (2 papers)European Journal of Medical Genetics (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United StatesFranceGermany
In The Last Decade
Mark E. Nuñes
25 papers receiving 720 citations
Peers
Comparison fields: 5 of 70
- Developmental Biology 144
- Endocrinology, Diabetes and Metabolism 241
- Rheumatology 153
- Genetics 247
- Pediatrics, Perinatology and Child Health 99
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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 98 | |
| 2 | 2001 | 89 | |
| 3 | Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1. | 1994 | 84 |
| 4 | 2012 | 61 | |
| 5 | 1995 | 60 | |
| 6 | 2006 | 58 | |
| 7 | 1996 | 46 | |
| 8 | 2008 | 39 | |
| 9 | 2016 | 35 | |
| 10 | 2008 | 31 | |
| 11 | 2007 | 30 | |
| 12 | 1997 | 21 | |
| 13 | 1994 | 13 | |
| 14 | 1996 | 10 | |
| 15 | 2005 | 9 | |
| 16 | 2017 | 9 | |
| 17 | 1994 | 9 | |
| 18 | 2002 | 7 | |
| 19 | c-myc expression in the thyroid. I: Normal, adenomatous, and cancerous thyroid tissue. | 1987 | 7 |
| 20 | 1997 | 7 |
About Mark E. Nuñes
Mark E. Nuñes is a scholar working on Genetics, Molecular Biology, Developmental Biology, Pediatrics, Perinatology and Child Health and Endocrinology, Diabetes and Metabolism, having authored 25 papers that have together received 736 indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (6 papers), Prenatal Screening and Diagnostics (4 papers), Alkaline Phosphatase Research Studies (4 papers), Heterotopic Ossification and Related Conditions (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Connective tissue disorders research (3 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Developmental Biology (144 citations), Endocrinology, Diabetes and Metabolism (241 citations), Rheumatology (153 citations), Genetics (247 citations) and Pediatrics, Perinatology and Child Health (99 citations). Mark E. Nuñes has collaborated with scholars based in United States, France and Germany. Frequent co-authors include Peter H. Byers, Melanie Pepin, Deborah Krakow, Anne-Sophie Lia-Baldini, Roberta A Pagon, Brigitte Simon‐Bouy, A. Taillandier, Raj P. Kapur, Étienne Mornet and Isabelle Brun‐Heath. Their work appears in journals such as Human Genetics, Mammalian Genome, Genetics in Medicine, European Journal of Medical Genetics 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.