A Baldellou

656 total citations
23 papers, 392 citations indexed

About

A Baldellou is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, A Baldellou has authored 23 papers receiving a total of 392 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 6 papers in Rheumatology. Recurrent topics in A Baldellou's work include Metabolism and Genetic Disorders (10 papers), Biochemical and Molecular Research (5 papers) and Lysosomal Storage Disorders Research (5 papers). A Baldellou is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Biochemical and Molecular Research (5 papers) and Lysosomal Storage Disorders Research (5 papers). A Baldellou collaborates with scholars based in Spain, United States and Portugal. A Baldellou's co-authors include Joel Charrow, Paige Kaplan, Generoso Andria, Gregory A. Grabowski, Chris Harris, Eugen Mengel, Ian J. Cohen, Pauline Campbell, Ashok Vellodi and Miguel Pocovı́ and has published in prestigious journals such as Pediatric Research, Human Mutation and Acta Paediatrica.

In The Last Decade

A Baldellou

22 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A Baldellou Spain 10 194 163 160 80 77 23 392
Chuan‐Hong Kao Taiwan 7 204 1.1× 141 0.9× 158 1.0× 102 1.3× 103 1.3× 10 411
Alain Fouilhoux France 12 314 1.6× 134 0.8× 149 0.9× 98 1.2× 178 2.3× 22 533
Toju Tanaka Japan 10 274 1.4× 135 0.8× 101 0.6× 106 1.3× 121 1.6× 16 417
Juan Francisco Cabello Chile 11 126 0.6× 107 0.7× 86 0.5× 50 0.6× 51 0.7× 32 287
İlyas Okur Türkiye 12 136 0.7× 78 0.5× 124 0.8× 86 1.1× 43 0.6× 62 372
Roberta Taurisano Italy 14 257 1.3× 58 0.4× 174 1.1× 107 1.3× 72 0.9× 28 501
Rebecca Mardach United States 11 100 0.5× 164 1.0× 193 1.2× 53 0.7× 31 0.4× 17 351
P. J. Lee United Kingdom 13 186 1.0× 170 1.0× 109 0.7× 156 1.9× 29 0.4× 20 366
Cate Walsh Vockley United States 6 274 1.4× 71 0.4× 85 0.5× 48 0.6× 50 0.6× 8 368
David F. Kronn United States 7 114 0.6× 76 0.5× 156 1.0× 62 0.8× 52 0.7× 9 310

Countries citing papers authored by A Baldellou

Since Specialization
Citations

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

Fields of papers citing papers by A Baldellou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Baldellou

This figure shows the co-authorship network connecting the top 25 collaborators of A Baldellou. A scholar is included among the top collaborators of A Baldellou 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 A Baldellou. A Baldellou 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.
Remor, Eduardo & A Baldellou. (2018). Health-related quality of life in children and adolescents living with Gaucher disease and their parents. Health Psychology and Behavioral Medicine. 6(1). 79–92. 8 indexed citations
2.
Baldellou, A, Josep Dalmau, & Pablo Sanjurjo. (2016). Recomendaciones para el diagnóstico y el tratamiento de la enfermedad de Gaucher durante la infancia. Acta pediátrica española. 74(1). 4–15. 1 indexed citations
3.
Baldellou, A, M.T. García‐Silva, Àngels García‐Cazorla, et al.. (2011). Estudio epidemiológico de las enfermedades metabólicas con homocistinuria en España. Anales de Pediatría. 76(3). 133–139. 2 indexed citations
4.
Urreizti, Roser, Almudena Pino‐Ángeles, Mónica Cozar, et al.. (2010). Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency. Clinical Genetics. 78(5). 441–448. 15 indexed citations
5.
García‐Villoria, Judit, Aleix Navarro‐Sastre, Celia Pérez‐Cerdá, et al.. (2008). Study of patients and carriers with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: Difficulties in the diagnosis. Clinical Biochemistry. 42(1-2). 27–33. 30 indexed citations
6.
Baldellou, A, Generoso Andria, Pauline Campbell, et al.. (2004). Paediatric non-neuronopathic Gaucher disease: recommendations for treatment and monitoring. European Journal of Pediatrics. 163(2). 67–75. 48 indexed citations
7.
Grabowski, Gregory A., Generoso Andria, A Baldellou, et al.. (2004). Pediatric non-neuronopathic Gaucher disease: presentation, diagnosis and assessment. Consensus statements. European Journal of Pediatrics. 163(2). 58–66. 81 indexed citations
8.
Urreizti, Roser, Susana Balcells, Laura Vilarinho, et al.. (2003). Spectrum of CBS mutations in 16 homocystinuric patients from the Iberian Peninsula: High prevalence of T191M and absence of I278T or G307S. Human Mutation. 22(1). 103–103. 23 indexed citations
9.
Fukao, Toshiyuki, Haruki Nakamura, Kozue Nakamura, et al.. (2002). Characterization of Six Mutations in Five Spanish Patients with Mitochondrial Acetoacetyl-CoA Thiolase Deficiency: Effects of Amino Acid Substitutions on Tertiary Structure. Molecular Genetics and Metabolism. 75(3). 235–243. 23 indexed citations
10.
Gracia, Segundo Rite, A Baldellou, Pilar Giraldo, et al.. (2002). Insulin-Like Growth Factors in Childhood-Onset Gaucher Disease. Pediatric Research. 52(1). 109–112. 11 indexed citations
11.
Desviat, Lourdes R., Belén Pérez, Alejandra Gámez, et al.. (1999). Genetic and phenotypic aspects of phenylalanine hydroxylase deficiency in Spain: molecular survey by regions. European Journal of Human Genetics. 7(3). 386–392. 50 indexed citations
12.
Martı́nez, G, Antònia Ribes, P. Briones, et al.. (1998). Medium‐chain acyl‐CoA dehydrogenase deficiency in Spain. Journal of Inherited Metabolic Disease. 21(6). 693–694.
13.
Martínez, Gemma, José-Raúl Garcı́a-Lozano, Antònia Ribes, et al.. (1998). High Risk of Medium Chain Acyl-Coenzyme A Dehydrogenase Deficiency among Gypsies. Pediatric Research. 44(1). 83–84. 9 indexed citations
14.
Desviat, Lourdes R., Belén Pérez, Mercedes Martínez‐Pardo, et al.. (1998). Relationship between mutation genotype and biochemical phenotype in a heterogeneous Spanish phenylketonuria population.. PubMed. 5(4). 196–202. 19 indexed citations
15.
Pisón, Javier López, et al.. (1997). [Demand for neuropediatric services in a general referral hospital. III. Diagnosis].. PubMed. 25(148). 1896–905. 6 indexed citations
16.
Pons, Roser, Manuel G. Roig, E. Riudor, et al.. (1996). The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Pediatric Neurology. 14(3). 236–243. 42 indexed citations
17.
Bone, J. M., et al.. (1994). Cord blood IGE versus family history as atopic predictors in the newborn. Acta Paediatrica. 83(12). 1308–1309. 6 indexed citations
18.
Baldellou, A, et al.. (1991). On the occurrence of BBB syndrome and hereditary sensory motor neuropathy in the same family.. PubMed. 2(4). 255–7. 2 indexed citations
19.
Baldellou, A, et al.. (1991). Congenital hypoparathyroidism, ocular colobomata, unilateral renal agenesis and dysmorphic features.. PubMed. 2(4). 245–7. 4 indexed citations
20.
Baldellou, A, et al.. (1988). [Infantile cortical hyperostosis. Apropos of 8 cases].. PubMed. 28(2). 149–51. 2 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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