P. Gallano
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 5%
- Muscle Physiology and Disorders
Papers in
- Genetics 29
- Genomics and Rare Diseases 22
- Neurogenetic and Muscular Disorders Research 4
- Genomic variations and chromosomal abnormalities 3
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- Muscle Physiology and Disorders 50
- Ion channel regulation and function 3
- Co-authors
- André Boué (6 shared papers)Montserrat Baiget (18 shared papers)Eduard Gallardo (15 shared papers)Isabel Illa (9 shared papers)Lidia González‐Quereda (33 shared papers)Adriana Lasa (9 shared papers)J. Palmer (2 shared papers)Carmen Serrano (1 shared paper)
- Journals
- Neuromuscular Disorders (17 papers)Clinical Genetics (4 papers)Human Genetics (4 papers)Journal of Medical Genetics (3 papers)Journal of Neurology (3 papers)
- Partner nations
- SpainUnited KingdomFrance
In The Last Decade
P. Gallano
86 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 75
- Genetics 595
- Molecular Biology 1.3k
- Genetics 138
- Pediatrics, Perinatology and Child Health 143
- Cell Biology 105
Countries citing papers authored by P. Gallano
This map shows the geographic impact of P. Gallano'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 P. Gallano with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. Gallano more than expected).
Fields of papers citing papers by P. Gallano
This network shows the impact of papers produced by P. Gallano. 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 P. Gallano. The network helps show where P. Gallano may publish in the future.
Co-authors
The 25 scholars most cited alongside P. Gallano, 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 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 229 | |
| 2 | 2001 | 222 | |
| 3 | 1999 | 165 | |
| 4 | 2015 | 119 | |
| 5 | 2017 | 66 | |
| 6 | 1986 | 64 | |
| 7 | 2006 | 61 | |
| 8 | 2008 | 59 | |
| 9 | 2020 | 57 | |
| 10 | 1983 | 56 | |
| 11 | 2005 | 56 | |
| 12 | 2000 | 51 | |
| 13 | 2007 | 48 | |
| 14 | 2015 | 44 | |
| 15 | 2018 | 42 | |
| 16 | Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP. | 1989 | 40 |
| 17 | 2013 | 40 | |
| 18 | 2020 | 39 | |
| 19 | 2012 | 38 | |
| 20 | 2016 | 37 |
About P. Gallano
P. Gallano is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Genetics and Cell Biology, having authored 92 papers that have together received 2.2k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (50 papers), Genomics and Rare Diseases (22 papers), Hereditary Neurological Disorders (7 papers), Neurogenetic and Muscular Disorders Research (4 papers), Myasthenia Gravis and Thymoma (4 papers), Genetic Neurodegenerative Diseases (3 papers), Ion channel regulation and function (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (595 citations), Molecular Biology (1.3k citations), Genetics (138 citations), Pediatrics, Perinatology and Child Health (143 citations) and Cell Biology (105 citations). P. Gallano has collaborated with scholars based in Spain, United Kingdom and France. Frequent co-authors include André Boué, Montserrat Baiget, Eduard Gallardo, Isabel Illa, Lidia González‐Quereda, Adriana Lasa, J. Palmer, Carmen Serrano, Noemí de Luna and Robert H. Brown. Their work appears in journals such as Neuromuscular Disorders, Clinical Genetics, Human Genetics, Journal of Medical Genetics and Journal of Neurology.
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.