Daniel Grinberg

5.6k citations

180 papers · 3.3k indexed · h-index 33

Impact in

Physiology top 1%
- Lysosomal Storage Disorders Research
Cell Biology top 2%
- Cellular transport and secretion

Papers in ⓘ

Physiology 64
- Lysosomal Storage Disorders Research 61
Cell Biology 33
- Cellular transport and secretion 33

Co-authors: Lluı̈sa Vilageliu (74 shared papers)Susana Balcells (97 shared papers)Amparo Chabás (39 shared papers)Xavier Nogués (41 shared papers)Natalia García‐Giralt (42 shared papers)Adolfo Díez‐Pérez (35 shared papers)Bru Cormand (23 shared papers)Leonardo Mellibovsky (31 shared papers)
Journals: Human Mutation (19 papers)Clinical Genetics (9 papers)Human Genetics (8 papers)Scientific Reports (7 papers)Blood Cells Molecules and Diseases (7 papers)
Partner nations: Spain United States Greece

In The Last Decade

Daniel Grinberg

174 papers receiving 3.3k citations

Peers

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-authors

The 25 scholars most cited alongside Daniel Grinberg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Daniel Grinberg Line = papers co-authored together Daniel Grinberg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 180 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course Movement Disorders ·Núria Setó‐Salvia, Javier Pagonabarraga, Henry Houlden, Berta Pascual‐Sedano, Oriol Dols‐Icardo, Arianna Tucci, Coro Paisán‐Ruíz, Antònia Campolongo, Sofía Antón‐Aguirre, I Rodríguez Martín, Laia Muñoz, Enric Bufill, Lluı̈sa Vilageliu, Daniel Grinberg, Mónica Cozar, Rafael Blesa, Alberto Lleó, John Hardy, Jaime Kulisevsky, Jordi Clarimón	2011	113
2	Cholesterol regulates Syntaxin 6 trafficking at the TGN-endosomal boundaries Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona) ·Meritxell Reverter, Carles Rentero, Ana García-Melero, Monira Hoque, Sandra Vilà de Muga, Anna Álvarez-Guaita, James R. W. Conway, Peta Wood, Rose Cairns, Lilia Lykopoulou, Daniel Grinberg, Lluı̈sa Vilageliu, Marta Bosch, Jöerg Heeren, Juan Blasi, Paul Timpson, Albert Pol, Francesc Tebar, Rachael Z. Murray, Thomas Grewal	2014	95
3	Unusual expression of Gaucher's disease: cardiovascular calcifications in three sibs homozygous for the D409H mutation. Journal of Medical Genetics ·Amparo Chabás, Bru Cormand, Daniel Grinberg, José M. Burguera, Susana Balcells, José Luís Merino, I Maté, José A. Sobrino, Roser Gonzàlez‐Duarte, Lluı̈sa Vilageliu	1995	91
4	Two New Single-Nucleotide Polymorphisms in the COL1A1 Upstream Regulatory Region and Their Relationship to Bone Mineral Density Journal of Bone and Mineral Research ·Natalia García‐Giralt, Xavier Nogués, Anna Enjuanes, Jordi Puig, Leonardo Mellibovsky, Anne‐Christine Bay‐Jensen, Ramón Carreras, Susana Balcells, Adolfo Díez‐Pérez, Daniel Grinberg	2002	84
5	MiRNA profiling of whole trabecular bone: identification of osteoporosis-related changes in MiRNAs in human hip bones BMC Medical Genomics ·Laura De‐Ugarte, Guy Yoskovitz, Susana Balcells, Robert Güerri‐Fernández, Santos Martínez‐Díaz, Leonardo Mellibovsky, Roser Urreizti, Xavier Nogués, Daniel Grinberg, Natalia García‐Giralt, Adolfo Díez‐Pérez	2015	76
6	Simvastatin and atorvastatin enhance gene expression of collagen type 1 and osteocalcin in primary human osteoblasts and MG‐63 cultures Journal of Cellular Biochemistry ·Sílvia Ruiz-Gaspà, Xavier Nogués, Anna Enjuanes, Joan Carles Monllau, Josep Blanch, Ramón Carreras, Leonardo Mellibovsky, Daniel Grinberg, Susana Balcells, Adolfo Díez‐Pérez, Juan Pedro‐Botet	2007	75
7	Functional analysis of 13GBAmutant alleles identified in Gaucher disease patients: Pathogenic changes and “modifier” polymorphisms Human Mutation ·Magda Montfort, Amparo Chabás, Lluı̈sa Vilageliu, Daniel Grinberg	2004	73
8	Homozygous tandem duplication within the gene encoding the β-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa Human Mutation ·Mónica Bayés, Mara Giordano, Susana Balcells, Daniel Grinberg, Llusïsa Vilageliu, I. Martinez, Carmen Ayuso, Javier Benı́tez, María A. Ramos-Arroyo, Pilar Chivelet, Teresa Torrent Solans, Diana Valverde, Serge Amselem, Michel Goossens, Montserrat Baiget, Roser Gonzàlez‐Duarte, Claude Besmond	1995	58
9	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 ·Raül Santamaría, Amparo Chabás, María Josep Coll, Clara Sá-Miranda, Lluı̈sa Vilageliu, Daniel Grinberg	2006	52
10	Regulation of CYP19 gene expression in primary human osteoblasts: effects of vitamin D and other treatments European Journal of Endocrinology ·Anna Enjuanes, Natalia García‐Giralt, August Supervía, Xavier Nogués, Leonardo Mellibovsky, J. Carbonell, Daniel Grinberg, Susana Balcells, Adolfo Díez‐Pérez	2003	49
11	Molecular analysis and clinical findings in the Spanish Gaucher disease population: Putative haplotype of the N370S ancestral chromosome Human Mutation ·Bru Cormand, Daniel Grinberg, Laura Gort, Amparo Chabás, Lluı̈sa Vilageliu	1998	49
12	COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal women Osteoporosis International ·Mariona Bustamante, Xavier Nogués, Anna Enjuanes, Roberto Elosúa, Natalia García‐Giralt, L Pérez-Edo, E. Cáceres, Ramón Carreras, Leonardo Mellibovsky, Susana Balcells, Adolfo Díez‐Pérez, Daniel Grinberg	2006	49
13	Haplotypes Defined by Promoter and Intron 1 Polymorphisms of the COLIA1 Gene Regulate Bone Mineral Density in Women The Journal of Clinical Endocrinology & Metabolism ·Tracy L. Stewart, Huilin Jin, Fiona E. McGuigan, Omar Albagha, Natalia García‐Giralt, Amelia Bassiti, Daniel Grinberg, Susana Balcells, David M. Reid, Stuart H. Ralston	2006	47
14	Mapping the genetic and clinical characteristics of Gaucher disease in the Iberian Peninsula Orphanet Journal of Rare Diseases ·Pilar Giraldo, Pilar Alfonso, Pilar Irún, Laura Gort, Amparo Chabás, Lluı̈sa Vilageliu, Daniel Grinberg, Clara Sá-Miranda, Miguel Pocovı́	2012	43
15	Therapeutic strategies based on modified U1 snRNAs and chaperones for Sanfilippo C splicing mutations Orphanet Journal of Rare Diseases ·Liliana Matos, Isaac Canals, Larbi Dridi, Yoo Choi, Maria João Prata, Peter Jordan, Lourdes R. Desviat, Belén Pérez, Alexey V. Pshezhetsky, Daniel Grinberg, Sandra Alves, Lluı̈sa Vilageliu	2014	42
16	Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas Scientific Reports ·Patricia Sarrión, Anna Sangorrin, Roser Urreizti, María Andrea Delgado, Rafael Artuch, Loreto Martorell, Judith Armstrong, Jordi Antón, Ferrán Torner, Marina Vilaseca, Julián Nevado, Pablo Lapunzina, Carla Asteggiano, Susana Balcells, Daniel Grinberg	2013	41
17	Antisense oligonucleotide treatment for a pseudoexon-generating mutation in theNPC1gene causing Niemann-Pick type C disease Human Mutation ·Laura Rodríguez‐Pascau, María Josep Coll, Lluı̈sa Vilageliu, Daniel Grinberg	2009	40
18	Polymorphisms in the interleukin-6 receptor gene are associated with bone mineral density and body mass index in Spanish postmenopausal women European Journal of Endocrinology ·Mariona Bustamante, Xavier Nogués, Leonardo Mellibovsky, Lídia Águeda, Susana Jurado, E. Cáceres, Josep Blanch, Ramón Carreras, Adolfo Díez‐Pérez, Daniel Grinberg, Susana Balcells	2007	40
19	β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease Molecular Genetics and Metabolism ·Marina Moraitou, Georgios M. Hadjigeorgiou, Ioannis Monopolis, Efthimios Dardiotis, Maria Bozi, Demetrios K. Vassilatis, Lluı̈sa Vilageliu, Daniel Grinberg, Georgia Xiromerisiou, Leonidas Stefanis, Helen Michelakakis	2011	38
20	Gaucher disease in Spanish patients: Analysis of eight mutations Human Mutation ·Bru Cormand, Lluı̈sa Vilageliu, José M. Burguera, Susana Balcells, Roser Gonzàlez‐Duarte, Daniel Grinberg, Amparo Chabás	1995	38

About Daniel Grinberg

Daniel Grinberg is a scholar working on Physiology, Cell Biology, Orthopedics and Sports Medicine, Rheumatology and Molecular Biology, having authored 180 papers that have together received 3.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (61 papers), Cellular transport and secretion (33 papers), Carbohydrate Chemistry and Synthesis (24 papers), Bone health and treatments (20 papers), Bone Metabolism and Diseases (20 papers), Glycosylation and Glycoproteins Research (19 papers), Trypanosoma species research and implications (19 papers) and Bone health and osteoporosis research (14 papers). The work is most often cited by research in Physiology (1.3k citations), Cell Biology (745 citations), Orthopedics and Sports Medicine (353 citations), Rheumatology (410 citations) and Physiology (110 citations). Daniel Grinberg has collaborated with scholars based in Spain, United States and Greece. Frequent 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. Their work appears in journals such as Human Mutation, Clinical Genetics, Human Genetics, Scientific Reports and Blood Cells Molecules and Diseases.

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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