Isabel Tapia‐Páez
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
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- Reading and Literacy Development
Papers in
- Genetics 15
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Kidney Cyst Diseases 6
- Estrogen and related hormone effects 3
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- Renal and related cancers 3
- Ubiquitin and proteasome pathways 2
- Congenital heart defects research 2
- Co-authors
- Juha Kere (18 shared papers)Kristiina Tammimies (8 shared papers)Satu Massinen (4 shared papers)Jan P. Dumanski (5 shared papers)Hans Matsson (8 shared papers)Elisabeth Blennow (3 shared papers)Eero Ċastrén (4 shared papers)Laura E. Parton (1 shared paper)
- Journals
- Human Genetics (3 papers)The FASEB Journal (2 papers)PLoS ONE (2 papers)Human Molecular Genetics (1 paper)Biochemical and Biophysical Research Communications (1 paper)
- Partner nations
- SwedenFinlandUnited States
In The Last Decade
Isabel Tapia‐Páez
29 papers receiving 858 citations
Peers
Comparison fields: 5 of 78
- Genetics 439
- Developmental and Educational Psychology 199
- Endocrinology, Diabetes and Metabolism 114
- Statistics and Probability 60
- Molecular Biology 350
Countries citing papers authored by Isabel Tapia‐Páez
This map shows the geographic impact of Isabel Tapia‐Páez'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 Isabel Tapia‐Páez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Isabel Tapia‐Páez more than expected).
Fields of papers citing papers by Isabel Tapia‐Páez
This network shows the impact of papers produced by Isabel Tapia‐Páez. 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 Isabel Tapia‐Páez. The network helps show where Isabel Tapia‐Páez may publish in the future.
Co-authors
The 25 scholars most cited alongside Isabel Tapia‐Páez, 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 | 2007 | 176 | |
| 2 | 2011 | 98 | |
| 3 | 2002 | 63 | |
| 4 | 2008 | 59 | |
| 5 | 2009 | 57 | |
| 6 | 2009 | 51 | |
| 7 | 2013 | 51 | |
| 8 | 2004 | 45 | |
| 9 | 2001 | 40 | |
| 10 | 2012 | 33 | |
| 11 | 2014 | 30 | |
| 12 | 2012 | 27 | |
| 13 | 2016 | 24 | |
| 14 | 2020 | 21 | |
| 15 | 2000 | 18 | |
| 16 | 2011 | 15 | |
| 17 | 2017 | 15 | |
| 18 | 2000 | 12 | |
| 19 | 2020 | 9 | |
| 20 | 2016 | 8 |
About Isabel Tapia‐Páez
Isabel Tapia‐Páez is a scholar working on Genetics, Molecular Biology, Dermatology, Cellular and Molecular Neuroscience and Endocrinology, Diabetes and Metabolism, having authored 29 papers that have together received 885 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genetic and Kidney Cyst Diseases (6 papers), Dermatology and Skin Diseases (4 papers), Renal and related cancers (3 papers), Estrogen and related hormone effects (3 papers), Allergic Rhinitis and Sensitization (2 papers), Ubiquitin and proteasome pathways (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (439 citations), Developmental and Educational Psychology (199 citations), Endocrinology, Diabetes and Metabolism (114 citations), Statistics and Probability (60 citations) and Molecular Biology (350 citations). Isabel Tapia‐Páez has collaborated with scholars based in Sweden, Finland and United States. Frequent co-authors include Juha Kere, Kristiina Tammimies, Satu Massinen, Jan P. Dumanski, Hans Matsson, Elisabeth Blennow, Eero Ċastrén, Laura E. Parton, Ilkka Sipilä and Roel Quintens. Their work appears in journals such as Human Genetics, The FASEB Journal, PLoS ONE, Human Molecular Genetics and Biochemical and Biophysical Research Communications.
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.