Enrique Galán‐Gómez

495 total citations
12 papers, 219 citations indexed

About

Enrique Galán‐Gómez is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Enrique Galán‐Gómez has authored 12 papers receiving a total of 219 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in Enrique Galán‐Gómez's work include Genomics and Rare Diseases (2 papers), Glycogen Storage Diseases and Myoclonus (2 papers) and Connective tissue disorders research (2 papers). Enrique Galán‐Gómez is often cited by papers focused on Genomics and Rare Diseases (2 papers), Glycogen Storage Diseases and Myoclonus (2 papers) and Connective tissue disorders research (2 papers). Enrique Galán‐Gómez collaborates with scholars based in Spain and United States. Enrique Galán‐Gómez's co-authors include Boris G. Kousseff, Rebecca Sutphen, Jaime L. Frías, María Luisa Martínez‐Frías, Guillem Pintos‐Morell, Luis González Gutiérrez-Solana, María L. Couce, Encarna Guillén‐Navarro, Rosario Domingo‐Jiménez and Salud Borrego and has published in prestigious journals such as Orphanet Journal of Rare Diseases, American Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

Enrique Galán‐Gómez

12 papers receiving 214 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Enrique Galán‐Gómez 91 56 54 39 39 12 219
Elena Piozzi 33 0.4× 26 0.5× 28 0.5× 81 2.1× 47 1.2× 26 373
Monica J. Basehore 61 0.7× 119 2.1× 18 0.3× 84 2.2× 27 0.7× 15 264
Lavinia Caba 119 1.3× 22 0.4× 40 0.7× 140 3.6× 21 0.5× 37 283
Barbara Sibbles 70 0.8× 19 0.3× 70 1.3× 121 3.1× 43 1.1× 12 283
Wenbing Xu 48 0.5× 107 1.9× 53 1.0× 118 3.0× 22 0.6× 25 351
Márta Czakó 141 1.5× 18 0.3× 20 0.4× 112 2.9× 16 0.4× 40 245
Rogelio Simón 41 0.5× 10 0.2× 31 0.6× 41 1.1× 30 0.8× 19 192
Sun-Wha Im 29 0.3× 15 0.3× 27 0.5× 38 1.0× 20 0.5× 18 174
Nina B. Gold 220 2.4× 24 0.4× 34 0.6× 186 4.8× 22 0.6× 37 457
Heather B. Radtke 40 0.4× 11 0.2× 24 0.4× 42 1.1× 55 1.4× 13 219

Countries citing papers authored by Enrique Galán‐Gómez

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Enrique Galán‐Gómez

This figure shows the co-authorship network connecting the top 25 collaborators of Enrique Galán‐Gómez. A scholar is included among the top collaborators of Enrique Galán‐Gómez based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Enrique Galán‐Gómez. Enrique Galán‐Gómez is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Galán‐Gómez, Enrique, et al.. (2024). Consenso de expertos para el manejo de pacientes con acondroplasia en tratamiento con vosoritida. Anales de Pediatría. 101(6). 401–410. 1 indexed citations
2.
Modamio‐Høybjør, Silvia, et al.. (2021). Early clinical and radiological improvement in a young boy with metaphyseal anadysplasia type 2. European Journal of Medical Genetics. 64(10). 104307–104307. 3 indexed citations
3.
Fernandez, Raquel, et al.. (2017). A Scoring System to Predict the Severity of Hirschsprung Disease at Diagnosis and Its Correlation With Molecular Genetics. Pediatric and Developmental Pathology. 20(1). 28–37. 1 indexed citations
4.
Fernández, Raquel M., et al.. (2013). Waardenburg syndrome type 4: Report of two new cases caused by SOX10 mutations in Spain. American Journal of Medical Genetics Part A. 164(2). 542–547. 18 indexed citations
5.
Guillén‐Navarro, Encarna, et al.. (2013). Clinical manifestations in female carriers of mucopolysaccharidosis type II: a spanish cross-sectional study. Orphanet Journal of Rare Diseases. 8(1). 92–92. 19 indexed citations
6.
Gutiérrez-Solana, Luis González, et al.. (2010). First experience of enzyme replacement therapy with idursulfase in Spanish patients with Hunter syndrome under 5 years of age: Case observations from the Hunter Outcome Survey (HOS). European Journal of Medical Genetics. 53(6). 371–377. 38 indexed citations
7.
Fernández, Luís, Pablo Lapunzina, I. López Pajares, et al.. (2008). Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion. American Journal of Medical Genetics Part A. 146A(9). 1134–1141. 14 indexed citations
8.
Galán‐Gómez, Enrique, et al.. (2007). Intrauterine growth retardation, duodenal and extrahepatic biliary atresia, hypoplastic pancreas and other intestinal anomalies: Further evidence of the Martínez-Frías syndrome. European Journal of Medical Genetics. 50(2). 144–148. 15 indexed citations
9.
Galán‐Gómez, Enrique, et al.. (2003). A diagnostic conundrum: Two siblings with features overlapping the Kabuki and Malpuech syndromes. A new MCA syndrome?. American Journal of Medical Genetics Part A. 125A(3). 306–309. 6 indexed citations
10.
Galán‐Gómez, Enrique, et al.. (1995). Kabuki make‐up (Niikawa‐Kuroki) syndrome in five Spanish children. American Journal of Medical Genetics. 59(3). 276–282. 48 indexed citations
11.
Sutphen, Rebecca, et al.. (1995). Tracheoesophageal anomalies in oculoauriculovertebral (Goldenhar) spectrum. Clinical Genetics. 48(2). 66–71. 23 indexed citations
12.
Sutphen, Rebecca, Enrique Galán‐Gómez, & Boris G. Kousseff. (1995). Clitoromegaly in neurofibromatosis. American Journal of Medical Genetics. 55(3). 325–330. 33 indexed citations

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.

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