Enrique Galán‐Gómez
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- Genomics and Rare Diseases 2
- Connective tissue disorders research 2
- Congenital Ear and Nasal Anomalies 1
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- Glycogen Storage Diseases and Myoclonus 2
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- Lysosomal Storage Disorders Research 2
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- Genomics and Rare Diseases 2
- Connective tissue disorders research 2
- Congenital Ear and Nasal Anomalies 1
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- Congenital gastrointestinal and neural anomalies 2
- Gastrointestinal disorders and treatments 1
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- RNA regulation and disease 1
- Co-authors
- Rebecca SutphenBoris G. KousseffMaría Luisa Martínez‐FríasJaime L. FríasGuillem Pintos‐MorellLuis González Gutiérrez-SolanaEncarna Guillén‐NavarroMaría L. Couce
- Cited by
- PharmacyGeneticsRheumatology
- Journals
- Orphanet Journal of Rare Diseases (1 paper)American Journal of Medical Genetics (2 papers)Clinical Genetics (1 paper)
- Partner nations
- SpainUnited States
In The Last Decade
Enrique Galán‐Gómez
12 papers receiving 214 citations
Peers
Comparison fields: 5 of 49
- Pharmacy 18
- Genetics 91
- Rheumatology 35
- Physiology 56
- Genetics 20
Countries citing papers authored by Enrique Galán‐Gómez
This map shows the geographic impact of Enrique Galán‐Gómez'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 Enrique Galán‐Gómez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Enrique Galán‐Gómez more than expected).
Fields of papers citing papers by Enrique Galán‐Gómez
This network shows the impact of papers produced by Enrique Galán‐Gómez. 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 Enrique Galán‐Gómez. The network helps show where Enrique Galán‐Gómez may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Enrique Galán‐Gómez, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 1 | |
| 2 | 2021 | 3 | |
| 3 | 2017 | 1 | |
| 4 | 2013 | 19 | |
| 5 | 2013 | 18 | |
| 6 | 2010 | 38 | |
| 7 | 2008 | 14 | |
| 8 | 2007 | 15 | |
| 9 | 2003 | 6 | |
| 10 | 1995 | 48 | |
| 11 | 1995 | 33 | |
| 12 | 1995 | 23 |
About Enrique Galán‐Gómez
Enrique Galán‐Gómez is a scholar working on Genetics, Pharmacy and Rheumatology, having authored 12 papers that have together received 219 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Connective tissue disorders research (2 papers), Lysosomal Storage Disorders Research (2 papers), Congenital gastrointestinal and neural anomalies (2 papers), Congenital Ear and Nasal Anomalies (1 paper), RNA regulation and disease (1 paper) and Gastrointestinal disorders and treatments (1 paper). The work is most often cited by research in Pharmacy (18 citations), Genetics (91 citations) and Rheumatology (35 citations). Enrique Galán‐Gómez has collaborated with scholars based in Spain and United States. Frequent co-authors include Rebecca Sutphen, Boris G. Kousseff, María Luisa Martínez‐Frías, Jaime L. Frías, Guillem Pintos‐Morell, Luis González Gutiérrez-Solana, Encarna Guillén‐Navarro, María L. Couce, Rosario Domingo‐Jiménez and Salud Borrego. Their work appears in journals such as Orphanet Journal of Rare Diseases, American Journal of Medical Genetics and Clinical 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.