G. Ribeiro

925 total citations
23 papers, 673 citations indexed

About

G. Ribeiro is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, G. Ribeiro has authored 23 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Physiology, 9 papers in Molecular Biology and 9 papers in Cell Biology. Recurrent topics in G. Ribeiro's work include Lysosomal Storage Disorders Research (19 papers), Cellular transport and secretion (9 papers) and Trypanosoma species research and implications (7 papers). G. Ribeiro is often cited by papers focused on Lysosomal Storage Disorders Research (19 papers), Cellular transport and secretion (9 papers) and Trypanosoma species research and implications (7 papers). G. Ribeiro collaborates with scholars based in Portugal, United States and Canada. G. Ribeiro's co-authors include Clara Sá-Miranda, Rui Pinto, Lúcia Lacerda, Lurdes Lopes, Helena Ribeiro, Isaura Ribeiro, Carlos Bessa, Eugénia Pinto, Olga Amaral and Manuela Nascimento de Lemos and has published in prestigious journals such as Clinical Microbiology and Infection, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Journal of Medical Genetics.

In The Last Decade

G. Ribeiro

23 papers receiving 653 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. Ribeiro Portugal 14 516 215 207 199 115 23 673
Stefanos A. Kalamidas Greece 14 119 0.2× 317 1.5× 192 0.9× 81 0.4× 108 0.9× 21 592
Marie‐Anne Skomorowski Canada 14 330 0.6× 94 0.4× 197 1.0× 77 0.4× 56 0.5× 23 476
Raul Chertkoff Israel 16 421 0.8× 193 0.9× 293 1.4× 166 0.8× 32 0.3× 54 655
A. M. Boer Netherlands 7 264 0.5× 114 0.5× 182 0.9× 53 0.3× 46 0.4× 9 401
Brett A. Tortelli United States 6 182 0.4× 97 0.5× 122 0.6× 34 0.2× 36 0.3× 8 327
Kyrieckos A. Aleck United States 10 85 0.2× 72 0.3× 300 1.4× 35 0.2× 34 0.3× 17 532
Ainu Prakash‐Cheng United States 7 314 0.6× 165 0.8× 151 0.7× 129 0.6× 28 0.2× 9 409
Piyali Saha India 11 126 0.2× 56 0.3× 163 0.8× 70 0.4× 9 0.1× 20 387
Hisao Fukushima Japan 9 207 0.4× 65 0.3× 177 0.9× 71 0.4× 2 0.0× 13 432
Ole Kristian Tollersrud Norway 12 290 0.6× 68 0.3× 247 1.2× 101 0.5× 24 0.2× 21 469

Countries citing papers authored by G. Ribeiro

Since Specialization
Citations

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

Fields of papers citing papers by G. Ribeiro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of G. Ribeiro. A scholar is included among the top collaborators of G. Ribeiro 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. Ribeiro. G. Ribeiro 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.
Silva, Cláudia, et al.. (2017). Dieta mediterrânica e genómica nutricional: potencialidades e desafios. Acta Portuguesa de Nutrição. 11. 36–41. 3 indexed citations
2.
Ribeiro, Isaura, et al.. (2013). Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene. Molecular Genetics and Metabolism. 109(3). 276–281. 18 indexed citations
3.
Sabanay, Helena, Judith Storch, Thierry Levade, et al.. (2013). Accumulation of Ordered Ceramide-Cholesterol Domains in Farber Disease Fibroblasts. JIMD Reports. 12. 71–77. 13 indexed citations
4.
Novais, Ângela, Carla Rodrigues, Patrı́cia Antunes, et al.. (2012). Spread of an OmpK36-modified ST15 Klebsiella pneumoniae variant during an outbreak involving multiple carbapenem-resistant Enterobacteriaceae species and clones. European Journal of Clinical Microbiology & Infectious Diseases. 31(11). 3057–3063. 40 indexed citations
5.
Bessa, Carlos, et al.. (2010). The neuronal ceroid lipofuscinosis protein CLN5: new insights into cellular maturation, transport, and consequences of mutations. Human Mutation. 31(3). 356–365. 39 indexed citations
6.
Nogueira, Célia, Maria João Prata, Lúcia Lacerda, et al.. (2008). Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian Peninsula. Clinical Genetics. 73(3). 251–256. 15 indexed citations
7.
Bessa, Carlos, Carla Andreia Teixeira, Ana Cristi Basile Dias, et al.. (2007). CLN2/TPP1 deficiency: The novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype. Molecular Genetics and Metabolism. 93(1). 66–73. 27 indexed citations
8.
Teixeira, Carla Andreia, Simon Lin, Carlos Bessa, et al.. (2006). Gene expression profiling in vLINCL CLN6-deficient fibroblasts: Insights into pathobiology. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1762(7). 637–646. 11 indexed citations
9.
Bessa, Carlos, Carla Andreia Teixeira, Ana Cristi Basile Dias, et al.. (2006). Two novel CLN5 mutations in a Portuguese patient with vLINCL: Insights into molecular mechanisms of CLN5 deficiency. Molecular Genetics and Metabolism. 89(3). 245–253. 28 indexed citations
10.
Alves, Sandra, Maria João Prata, G. Ribeiro, et al.. (2006). Molecular characterization of Portuguese patients with mucopolysaccharidosis type II shows evidence that the IDS gene is prone to splicing mutations. Journal of Inherited Metabolic Disease. 29(6). 743–754. 31 indexed citations
11.
Teixeira, Carla Andreia, Janice A. Espinola, Liang Huo, et al.. (2003). Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis. Human Mutation. 21(5). 502–508. 32 indexed citations
12.
Teixeira, Carla Andreia, Carlos Bessa, Lurdes Lopes, et al.. (2003). Clinicopathological and molecular characterization of neuronal ceroid lipofuscinosis in the Portuguese population. Journal of Neurology. 250(6). 661–667. 33 indexed citations
13.
Pinto, Rui, Manuela Nascimento de Lemos, Lurdes Lopes, et al.. (2003). Prevalence of lysosomal storage diseases in Portugal. European Journal of Human Genetics. 12(2). 87–92. 243 indexed citations
14.
15.
Ribeiro, G., Rui Pinto, Kunihiko Suzuki, & Clara Sá-Miranda. (1997). Two novel (1334delC and 1363G to A, G455R) mutations in exon 12 of the β-hexosaminidase α-chain gene in two Portuguese patients. Human Mutation. 10(5). 359–360. 2 indexed citations
16.
Ribeiro, G., Rui Pinto, Aparecida Maria Fontes, et al.. (1996). Clinical, enzymatic, and molecular characterisation of a Portuguese family with a chronic form of GM2-gangliosidosis B1 variant.. Journal of Medical Genetics. 33(4). 341–343. 13 indexed citations
17.
Ribeiro, G., Rui Pinto, Clara Sá-Miranda, & Kunihiko Suzuki. (1995). Tay-Sachs disease: Intron 7 splice junction mutation in two Portuguese patients. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1270(1). 44–51. 11 indexed citations
18.
Pinto, Rui, et al.. (1995). Prenatal diagnosis of GM2‐gangliosidosis B1 variant. Prenatal Diagnosis. 15(6). 585–588. 2 indexed citations
19.
Ribeiro, G., et al.. (1990). Biochemical characterization of β‐hexosaminidase in different biological specimens from eleven patients with GM2‐gangliosidosis B1 variant. Journal of Inherited Metabolic Disease. 14(5). 715–720. 7 indexed citations
20.
Ribeiro, G., et al.. (1990). Juvenile GM2Gangliosidosis Variant B1: Clinical and Biochemical Study in Seven Patients. Neuropediatrics. 21(1). 18–23. 15 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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