Daniel Grinberg

5.6k total citations
180 papers, 3.3k citations indexed

About

Daniel Grinberg is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, Daniel Grinberg has authored 180 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 64 papers in Physiology and 33 papers in Cell Biology. Recurrent topics in Daniel Grinberg's work include Lysosomal Storage Disorders Research (61 papers), Cellular transport and secretion (33 papers) and Carbohydrate Chemistry and Synthesis (24 papers). Daniel Grinberg is often cited by papers focused on Lysosomal Storage Disorders Research (61 papers), Cellular transport and secretion (33 papers) and Carbohydrate Chemistry and Synthesis (24 papers). Daniel Grinberg collaborates with scholars based in Spain, United States and Greece. Daniel Grinberg's co-authors include Lluı̈sa Vilageliu, Susana Balcells, Amparo Chabás, Xavier Nogués, Natalia García‐Giralt, Adolfo Díez‐Pérez, Bru Cormand, Leonardo Mellibovsky, Roser Urreizti and Laura Gort and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Daniel Grinberg

174 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Grinberg Spain 33 1.6k 1.3k 745 512 440 180 3.3k
Maja Di Rocco Italy 34 1.5k 1.0× 1.2k 0.9× 498 0.7× 860 1.7× 350 0.8× 147 3.6k
Sung‐Chul Jung South Korea 34 1.1k 0.7× 600 0.4× 333 0.4× 360 0.7× 86 0.2× 102 2.7k
Marianne Rohrbach Switzerland 26 631 0.4× 897 0.7× 253 0.3× 1.0k 2.0× 238 0.5× 81 2.4k
Robert Steinfeld Germany 29 1.6k 1.0× 820 0.6× 655 0.9× 279 0.5× 84 0.2× 56 2.8k
Susana Balcells Spain 26 1.2k 0.8× 290 0.2× 228 0.3× 467 0.9× 72 0.2× 105 2.0k
Vishwas Paralkar United States 30 1.4k 0.9× 339 0.3× 158 0.2× 395 0.8× 63 0.1× 50 3.0k
Philippe M. Campeau Canada 33 1.8k 1.2× 369 0.3× 298 0.4× 1.0k 2.0× 51 0.1× 123 3.3k
Ronald D. Cohn United States 24 3.4k 2.2× 888 0.7× 671 0.9× 523 1.0× 29 0.1× 38 4.4k
Christina N. Bennett United States 15 3.6k 2.3× 895 0.7× 367 0.5× 645 1.3× 17 0.0× 17 5.0k
Beth L. Thurberg United States 34 1.1k 0.7× 2.6k 1.9× 461 0.6× 320 0.6× 667 1.5× 77 3.6k

Countries citing papers authored by Daniel Grinberg

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Grinberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Grinberg

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Grinberg. A scholar is included among the top collaborators of Daniel Grinberg 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 Daniel Grinberg. Daniel Grinberg 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.
Grinberg, Daniel, et al.. (2024). Subcellular localisation of truncated MAGEL2 proteins: insight into the molecular pathology of Schaaf-Yang syndrome. Journal of Medical Genetics. 61(8). 780–782. 2 indexed citations
2.
López‐Márquez, Arístides, Matías Morin, Daniel Natera‐de Benito, et al.. (2022). CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant COL6A1 Pathogenic Variant Improves Collagen VI Network in Patient Fibroblasts. International Journal of Molecular Sciences. 23(8). 4410–4410. 15 indexed citations
3.
García‐Giralt, Natalia, Josep F. Abril, Diana Ovejero, et al.. (2022). Gene Network of Susceptibility to Atypical Femoral Fractures Related to Bisphosphonate Treatment. Genes. 13(1). 146–146. 7 indexed citations
4.
Serrano, Mercedes, Juan A. G. Ranea, Pedro Seoane, et al.. (2022). Advancing in Schaaf-Yang syndrome pathophysiology: from bedside to subcellular analyses of truncated MAGEL2. Journal of Medical Genetics. 60(4). 406–415. 5 indexed citations
5.
Giugliani, Roberto, Catarina Pereira, Claudia Cozma, et al.. (2022). Fifteen years of enzyme replacement therapy for mucopolysaccharidosis type VI (Maroteaux–Lamy syndrome): a case report. Journal of Medical Case Reports. 16(1). 46–46. 3 indexed citations
6.
Grinberg, Daniel, et al.. (2021). Búsqueda de variantes del gen LRP4 en mujeres con alta masa ósea y en pacientes con malformación de Chiari tipo I. SHILAP Revista de lepidopterología. 13(1). 17–20. 1 indexed citations
7.
Cozar, Mónica, Antònia Ribes, Henrik Ahlenius, et al.. (2020). Neuronal and Astrocytic Differentiation from Sanfilippo C Syndrome iPSCs for Disease Modeling and Drug Development. Journal of Clinical Medicine. 9(3). 644–644. 8 indexed citations
8.
Vilageliu, Lluı̈sa, et al.. (2020). Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches. International Journal of Molecular Sciences. 21(21). 7819–7819. 28 indexed citations
9.
Castellanos, Elisabeth, Bernat Gel, Andreu Alibés, et al.. (2019). Mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Clinical Genetics. 97(2). 264–275. 12 indexed citations
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Urreizti, Roser, Semra Gürsoy, Raquel Rabionet, et al.. (2018). The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring‐Opitz Syndrome. Clinical Case Reports. 6(8). 1452–1456. 5 indexed citations
13.
Herrera, Sabina, Xavier Nogués, Robert Güerri‐Fernández, et al.. (2017). Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann disease. Osteoporosis International. 28(12). 3489–3493. 5 indexed citations
14.
Cammarata‐Scalisi, Francisco, et al.. (2015). Alelo doble mutante en el gen EXT1 no informado previamente en una adolescente con exostosis múltiple hereditaria. Archivos Argentinos de Pediatria. 113(2). e109–12. 2 indexed citations
15.
Reverter, Meritxell, Carles Rentero, Ana García-Melero, et al.. (2014). Cholesterol regulates Syntaxin 6 trafficking at the TGN-endosomal boundaries. Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona). 95 indexed citations
16.
García‐Giralt, Natalia, Guy Yoskovitz, Roser Urreizti, et al.. (2013). Gene-wide association study of RANK and RANKL genes in the bone context: functional study of BMD-associated SNPs. Bone Abstracts. 1 indexed citations
17.
Águeda, Lídia, Roser Urreizti, Mariona Bustamante, et al.. (2010). Analysis of Three Functional Polymorphisms in Relation to Osteoporosis Phenotypes: Replication in a Spanish Cohort. Calcified Tissue International. 87(1). 14–24. 25 indexed citations
18.
Grinberg, Daniel. (2008). Formes de la militance juive radicale en Pologne. Cairn.info. 159–171.
19.
Urreizti, Roser, Carla Asteggiano, María Antònia Vilaseca, et al.. (2007). A CBS haplotype and a polymorphism at the MSR gene are associated with cardiovascular disease in a Spanish case–control study. Clinical Biochemistry. 40(12). 864–868. 8 indexed citations
20.
Santamaría, Raül, Amparo Chabás, María Josep Coll, et al.. (2006). Twenty-one novel mutations in the GLB1 gene identified in a large group of GM1-gangliosidosis and Morquio B patients: possible common origin for the prevalent p.R59H mutation among gypsies. Human Mutation. 27(10). 1060–1060. 52 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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