G. Glóver

887 total citations
26 papers, 484 citations indexed

About

G. Glóver is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, G. Glóver has authored 26 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 12 papers in Molecular Biology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in G. Glóver's work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Chromosomal and Genetic Variations (4 papers). G. Glóver is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Chromosomal and Genetic Variations (4 papers). G. Glóver collaborates with scholars based in Spain, United States and Australia. G. Glóver's co-authors include Pablo Carbonell, Montserrat Milà, I. López, F Ballesta, Xavier Estivill, H. Kruyer, Ana Luisa Jiménez, Ági K. Gedeon, Danuta Z. Loesch and David Hay and has published in prestigious journals such as NeuroImage, BioMed Research International and Journal of Medical Genetics.

In The Last Decade

G. Glóver

25 papers receiving 468 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
G. Glóver Spain 12 364 257 126 86 47 26 484
Sheila Youings United Kingdom 15 831 2.3× 428 1.7× 221 1.8× 166 1.9× 162 3.4× 18 978
Grant Sutherland Australia 12 312 0.9× 287 1.1× 26 0.2× 55 0.6× 42 0.9× 26 535
Sophie Dahoun Switzerland 14 271 0.7× 371 1.4× 64 0.5× 98 1.1× 23 0.5× 26 629
Christalena Sofocleous Greece 14 261 0.7× 218 0.8× 67 0.5× 81 0.9× 16 0.3× 45 459
Patricia Robbins‐Furman United States 10 424 1.2× 214 0.8× 71 0.6× 153 1.8× 70 1.5× 17 604
Antonia Paula Marques‐de‐Faria Brazil 15 391 1.1× 383 1.5× 65 0.5× 75 0.9× 25 0.5× 51 617
Vikram Jaswaney United States 7 424 1.2× 245 1.0× 43 0.3× 154 1.8× 51 1.1× 12 489
S. L. Sherman United States 11 642 1.8× 424 1.6× 199 1.6× 392 4.6× 151 3.2× 18 1.0k
J Boué France 7 163 0.4× 141 0.5× 65 0.5× 98 1.1× 17 0.4× 23 358
Bella Davidov Israel 11 270 0.7× 112 0.4× 111 0.9× 141 1.6× 12 0.3× 17 422

Countries citing papers authored by G. Glóver

Since Specialization
Citations

This map shows the geographic impact of G. Glóver'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 G. Glóver with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G. Glóver more than expected).

Fields of papers citing papers by G. Glóver

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. Glóver. 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 G. Glóver. The network helps show where G. Glóver may publish in the future.

Co-authorship network of co-authors of G. Glóver

This figure shows the co-authorship network connecting the top 25 collaborators of G. Glóver. A scholar is included among the top collaborators of G. Glóver 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 G. Glóver. G. Glóver is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Barreda‐Sánchez, María, et al.. (2015). Acute intermittent porphyria in a paediatric population in the region of Murcia: Phenotype and prevalence. Anales de Pediatría (English Edition). 84(2). 114–115. 2 indexed citations
2.
Ballesta‐Martínez, María Juliana, et al.. (2010). Molecular characterization of a new patient with a non‐recurrent inv dup del 2q and review of the mechanisms for this rearrangement. American Journal of Medical Genetics Part A. 152A(10). 2670–2680. 10 indexed citations
3.
Moya‐Quiles, María Rosa, et al.. (2009). CFTR H609R mutation in Ecuadorian patients with cystic fibrosis. Journal of Cystic Fibrosis. 8(4). 280–281. 7 indexed citations
4.
Moya‐Quiles, María Rosa, et al.. (2009). A compound heterozygous mutation in the EDAR gene in a Spanish family with autosomal recessive hypohidrotic ectodermal dysplasia. Archives of Dermatological Research. 302(4). 307–310. 8 indexed citations
5.
Bustamante‐Aragonés, Ana, J. Gallego‐Merlo, María José Trujillo-Tiebas, et al.. (2008). New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma. Journal of Cystic Fibrosis. 7(6). 505–510. 39 indexed citations
6.
Carbonell, Pablo, et al.. (2006). Pancreatitis hereditaria causada por una nueva mutación en el gen del tripsinógeno. Presentación de una familia. Cirugía Española. 79(4). 252–254. 1 indexed citations
7.
8.
Guillén‐Navarro, Encarna, Pablo Carbonell, G. Glóver, Manuel Sánchez‐Solís, & A Fernández-Barreiro. (2004). Novel HMBS founder mutation and significant intronic polymorphism in Spanish patients with acute intermittent porphyria. Annals of Human Genetics. 68(5). 509–514. 16 indexed citations
9.
Rifé, M., Célia Bádenas, Josep Mallolas, et al.. (2003). Incidence of Fragile X in 5,000 Consecutive Newborn Males. Genetic Testing. 7(4). 339–343. 44 indexed citations
10.
Munítiz, Vicente, et al.. (2003). Diagnosis and treatment of oculopharyngeal dystrophy: a report of three cases from the same family. Diseases of the Esophagus. 16(2). 160–164. 7 indexed citations
11.
Glóver, G., et al.. (2001). [Diagnosis of fragile X syndrome].. PubMed. 33 Suppl 1. S6–9. 1 indexed citations
12.
Gómez, E., Antonio Ballesteros, G. Glóver, et al.. (2000). Screening for AZF Deletion in a Large Series of Severely Impaired Spermatogenesis Patients. Journal of Andrology. 21(5). 651–655. 53 indexed citations
13.
Carbonell, Pablo, et al.. (1996). FRAXE mutation analysis in three spanish families. American Journal of Medical Genetics. 64(2). 434–440. 20 indexed citations
14.
Kruyer, H., Montserrat Milà, G. Glóver, et al.. (1994). Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins.. PubMed. 54(3). 437–42. 79 indexed citations
15.
Kruyer, H., G. Glóver, Pablo Carbonell, et al.. (1994). Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families. Human Genetics. 94(4). 395–400. 21 indexed citations
16.
López, I., et al.. (1992). Fragile X screening program in a spanish region. American Journal of Medical Genetics. 43(1-2). 333–338. 8 indexed citations
17.
Glóver, G., et al.. (1988). Partial monosomy 6q(q15q21) by de novo interstitial deletion. Clinical Genetics. 33(4). 308–310. 15 indexed citations
18.
Glóver, G., et al.. (1988). Chromosomal imbalance in the offspring of translocation carriers involving 7p. Clinical Genetics. 33(3). 211–219. 14 indexed citations
19.
Glóver, G., et al.. (1987). De novo 10q(q21q22) interstitial deletion. Human Genetics. 76(2). 205–205. 8 indexed citations
20.

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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