Personal information

Activities

Employment (1)

University of Barcelona: Barcelona, Catalonia, ES

2008 to present | Full Professor (Genetics, Microbiology and Statistic)
Employment
Source: Self-asserted source
Daniel Grinberg

Works (50 of 148)

Items per page:
Page 1 of 3

Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches

International Journal of Molecular Sciences
2020-10-22 | Journal article
Contributors: Noelia Benetó; Lluïsa Vilageliu; Daniel Grinberg; Isaac Canals
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Effect of the Tumor Suppressor miR-320a on Viability and Functionality of Human Osteosarcoma Cell Lines Compared to Primary Osteoblasts

Applied Sciences
2020-04-20 | Journal article
Contributors: Laura De-Ugarte; Susanna Balcells; Robert Guerri-Fernandez; Daniel Grinberg; Adolfo Diez-Perez; Xavier Nogues; Natalia Garcia-Giralt
Source: check_circle
Crossref

Neuronal and Astrocytic Differentiation from Sanfilippo C Syndrome iPSCs for Disease Modeling and Drug Development

Journal of Clinical Medicine
2020-02-28 | Journal article
Contributors: Noelia Benetó; Monica Cozar; Laura Castilla-Vallmanya; Oskar G. Zetterdahl; Madalina Sacultanu; Eulalia Segur-Bailach; María García-Morant; Antonia Ribes; Henrik Ahlenius; Daniel Grinberg et al.
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum.

Orphanet journal of rare diseases
2020-02-10 | Journal article
Source: Self-asserted source
Daniel Grinberg

Bone development and remodeling in metabolic disorders

Journal of Inherited Metabolic Disease
2020-01 | Journal article
Contributors: Jenny Serra‐Vinardell; Neus Roca‐Ayats; Laura De‐Ugarte; Lluïsa Vilageliu; Susanna Balcells; Daniel Grinberg
Source: check_circle
Crossref

Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients

European Journal of Human Genetics
2020-01-12 | Journal article
Contributors: Roser Urreizti; Klaus Mayer; Gilad D. Evrony; Edith Said; Laura Castilla-Vallmanya; Neal A. L. Cody; Guillem Plasencia; Bruce D. Gelb; Daniel Grinberg; Ulrich Brinkmann et al.
Source: check_circle
Crossref

DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients

European Journal of Human Genetics
2020-01-01 | Journal article
Contributors: Roser Urreizti; Klaus Mayer; Gilad D. Evrony; Edith Said; Laura Castilla-Vallmanya; Neal A. L. Cody; Guillem Plasencia; Bruce D. Gelb; Daniel Grinberg; Ulrich Brinkmann et al.
Source: check_circle
Crossref

Case report of a child bearing a novel deleterious splicing variant in PIGT.

Medicine
2019-02 | Journal article
Contributors: Mason S; Castilla-Vallmanya L; James C; Andrews PI; Balcells S; Grinberg D; Kirk EP; Urreizti R
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Pro-osteoporotic miR-320a impairs osteoblast function and induces oxidative stress.

PloS one
2018-11 | Journal article
Contributors: De-Ugarte L; Balcells S; Nogues X; Grinberg D; Diez-Perez A; Garcia-Giralt N
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Functional Characterization of a GGPPS Variant Identified in Atypical Femoral Fracture Patients and Delineation of the Role of GGPPS in Bone-Relevant Cell Types.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
2018-09 | Journal article
Contributors: Roca-Ayats N; Ng PY; Garcia-Giralt N; Falcó-Mascaró M; Cozar M; Abril JF; Quesada Gómez JM; Prieto-Alhambra D; Nogués X; Dunford JE et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.

BMJ (Clinical research ed.)
2018-08 | Journal article
Contributors: Trajanoska K; Morris JA; Oei L; Zheng HF; Evans DM; Kiel DP; Ohlsson C; Richards JB; Rivadeneira F; GEFOS/GENOMOS consortium and the 23andMe research team
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density.

Scientific reports
2018-07 | Journal article
Contributors: Martínez-Gil N; Roca-Ayats N; Monistrol-Mula A; García-Giralt N; Díez-Pérez A; Nogués X; Mellibovsky L; Grinberg D; Balcells S
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

The ASXL1 mutation p.Gly646Trpfs*12 found in a Turkish boy with Bohring-Opitz Syndrome.

Clinical case reports
2018-06 | Journal article
Contributors: Urreizti R; Gürsoy S; Castilla-Vallmanya L; Cunill G; Rabionet R; Erçal D; Grinberg D; Balcells S
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

[Clinical and molecular study in a family with multiple osteochondromatosis].

Acta ortopedica mexicana
2018-03 | Journal article
Contributors: Cammarata-Scalisi F; Stock F; Avendaño A; Cozar M; Balcells S; Grinberg D
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome.

Scientific reports
2018-01 | Journal article
Contributors: Urreizti R; Damanti S; Esteve C; Franco-Valls H; Castilla-Vallmanya L; Tonda R; Cormand B; Vilageliu L; Opitz JM; Neri G et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Stereodivergent synthesis of right- and left-handed iminoxylitol heterodimers and monomers. Study of their impact on β-glucocerebrosidase activity

Organic & Biomolecular Chemistry
2017 | Journal article
Contributors: Fabien Stauffert; Jenny Serra-Vinardell; Marta Gómez-Grau; Helen Michelakakis; Irene Mavridou; Daniel Grinberg; Lluïsa Vilageliu; Josefina Casas; Anne Bodlenner; Antonio Delgado et al.
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

The Spectrum of Niemann-Pick Type C Disease in Greece.

JIMD reports
2017 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Discrepancy between bone density and bone material strength index in three siblings with Camurati-Engelmann disease.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
2017-12 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Correction: Stereodivergent synthesis of right- and left-handed iminoxylitol heterodimers and monomers. Study of their impact on β-glucocerebrosidase activity.

Organic & biomolecular chemistry
2017-09 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Expression profiling of microRNAs in human bone tissue from postmenopausal women.

Human cell
2017-09 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Erratum to: MiRNA profiling of whole trabecular bone: identification of osteoporosis-related changes in MiRNAs in human hip bones.

BMC medical genomics
2017-05 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

GGPS1 Mutation and Atypical Femoral Fractures with Bisphosphonates.

The New England journal of medicine
2017-05 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes.

Scientific reports
2017-03 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

New murine Niemann-Pick type C models bearing a pseudoexon-generating mutation recapitulate the main neurobehavioural and molecular features of the disease.

Scientific Reports
2017-02 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

The Spectrum of Krabbe Disease in Greece: Biochemical and Molecular Findings.

2016 | Journal article
Contributors: Dimitriou E; Cozar M; Mavridou I; Grinberg D; Vilageliu L; Michelakakis H
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Involvement of Gaucher Disease Mutations in Parkinson Disease.

2016-03 | Journal article
Contributors: Vilageliu L; Grinberg D
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes.

2016-01 | Journal article
Contributors: Urreizti R; Roca-Ayats N; Trepat J; Garcia-Garcia F; Aleman A; Orteschi D; Marangi G; Neri G; Opitz JM; Dopazo J et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage Diseases.

PLoS ONE
2015 | Journal article
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

EXTL2 and EXTL3 inhibition with siRNAs as a promising substrate reduction therapy for Sanfilippo C syndrome.

2015 | Journal article
Contributors: Canals I; Benetó N; Cozar M; Vilageliu L; Grinberg D
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

MiRNA profiling of whole trabecular bone: identification of osteoporosis-related changes in MiRNAs in human hip bones.

2015 | Journal article
Contributors: De-Ugarte L; Yoskovitz G; Balcells S; Güerri-Fernández R; Martinez-Diaz S; Mellibovsky L; Urreizti R; Nogués X; Grinberg D; García-Giralt N et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Activity and High-Order Effective Connectivity Alterations in Sanfilippo C Patient-Specific Neuronal Networks.

2015-10 | Journal article
Contributors: Canals I; Soriano J; Orlandi JG; Torrent R; Richaud-Patin Y; Jiménez-Delgado S; Merlin S; Follenzi A; Consiglio A; Vilageliu L et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.

2015-10 | Journal article
Contributors: Zheng HF; Forgetta V; Hsu YH; Estrada K; Rosello-Diez A; Leo PJ; Dahia CL; Park-Min KH; Tobias JH; Kooperberg C et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

CYP11A1 expression in bone is associated with aromatase inhibitor-related bone loss.

2015-08 | Journal article
Contributors: Rodríguez-Sanz M; García-Giralt N; Prieto-Alhambra D; Servitja S; Balcells S; Pecorelli R; Díez-Pérez A; Grinberg D; Tusquets I; Nogués X
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses].

2015-04 | Journal article
Contributors: Cammarata-Scalisi F; Cozar M; Grinberg D; Balcells S; Asteggiano CG; Martínez-Domenech G; Bracho A; Sánchez Y; Stock F; Delgado-Luengo W et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG.

2014 | Journal article
DOI:

10.1038/srep06407

PMID:

25230886

Contributors: Delgado MA; Martinez-Domenech G; Sarrión P; Urreizti R; Zecchini L; Robledo HH; Segura F; de Kremer RD; Balcells S; Grinberg D et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Genetic analysis of high bone mass cases from the BARCOS cohort of spanish postmenopausal women.

2014 | Journal article
DOI:

10.1371/journal.pone.0094607

PMID:

24736728

PMC:

PMC3988071

Contributors: Sarrión P; Mellibovsky L; Urreizti R; Civit S; Cols N; García-Giralt N; Yoskovitz G; Aranguren A; Malouf J; Di Gregorio S et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Therapeutic strategies based on modified U1 snRNAs and chaperones for Sanfilippo C splicing mutations.

2014 | Journal article
Contributors: Matos L; Canals I; Dridi L; Choi Y; Prata MJ; Jordan P; Desviat LR; Pérez B; Pshezhetsky AV; Grinberg D et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

[Cardiofaciocutaneous syndrome, a Noonan syndrome related disorder: Clinical and molecular findings in 11 patients.]

2014-09 | Journal article
DOI:

10.1016/j.medcli.2014.06.009

PMID:

25194980

Contributors: Carcavilla A; García-Miñaúr S; Pérez-Aytés A; Vendrell T; Pinto I; Guillén-Navarro E; González-Meneses A; Aoki Y; Grinberg D; Ezquieta B
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Selective chaperone effect of aminocyclitol derivatives on G202R and other mutant glucocerebrosidases causing Gaucher disease.

2014-09 | Journal article
DOI:

10.1016/j.biocel.2014.07.017

PMID:

25084554

Contributors: Serra-Vinardell J; Díaz L; Guitiérrez-de Terán H; Sánchez-Ollé G; Bujons J; Michelakakis H; Mavridou I; Aerts JM; Delgado A; Grinberg D et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Glucocerebrosidase enhancers for selected Gaucher disease genotypes by modification of α-1-C-substituted imino-D-xylitols (DIXs) by click chemistry.

2014-08 | Journal article
DOI:

10.1002/cmdc.201402023

PMID:

24976039

Contributors: Serra-Vinardell J; Díaz L; Casas J; Grinberg D; Vilageliu L; Michelakakis H; Mavridou I; Aerts JM; Decroocq C; Compain P et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Description of extreme longevity in the Balearic Islands: Exploring a potential Blue Zone in Menorca, Spain.

2014-07 | Journal article
DOI:

10.1111/ggi.12148

PMID:

24112374

Contributors: Soriano JB; Fernández Vázquez S; Carretero S; Puga González MD; Soriano C; Romaguera D; Alonso-Fernández A; Busquets X; Balcells S; Grinberg D et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Niemann-Pick type C disease: a novel NPC1 mutation segregating in a Greek island.

2014-06 | Journal article
DOI:

10.1111/cge.12200

PMID:

23701245

Contributors: Mavridou I; Cozar M; Douzgou S; Xaidara A; Lianou D; Vanier MT; Dimitriou E; Grinberg D; Vilageliu L; Michelakakis H
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Cholesterol regulates Syntaxin 6 trafficking at trans-Golgi network endosomal boundaries.

2014-05 | Journal article
DOI:

10.1016/j.celrep.2014.03.043

PMID:

24746815

Contributors: Reverter M; Rentero C; Garcia-Melero A; Hoque M; Vilà de Muga S; Alvarez-Guaita A; Conway JR; Wood P; Cairns R; Lykopoulou L et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Antisense mediated splicing modulation for inherited metabolic diseases: challenges for delivery.

2014-02 | Journal article
DOI:

10.1089/nat.2013.0453

PMID:

24506780

Contributors: Pérez B; Vilageliu L; Grinberg D; Desviat LR
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Mucopolysaccharidosis type VI phenotypes-genotypes and antibody response to galsulfase.

2013 | Journal article
DOI:

10.1186/1750-1172-8-51

PMID:

23557332

PMC:

PMC3637222

Contributors: Brands MM; Hoogeveen-Westerveld M; Kroos MA; Nobel W; Ruijter GJ; Özkan L; Plug I; Grinberg D; Vilageliu L; Halley DJ et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas.

2013 | Journal article
DOI:

10.1038/srep01346

PMID:

23439489

PMC:

PMC3581825

Contributors: Sarrión P; Sangorrin A; Urreizti R; Delgado A; Artuch R; Martorell L; Armstrong J; Anton J; Torner F; Vilaseca MA et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Screening of cacna1a and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studies.

2013 | Journal article
PMC:

PMC3620192

Contributors: Sintas C; Carreño O; Corominas R; Serra S; Vila M; Fernández-Castillo N; Toma C; Pons R; Llaneza M; Sobrido M et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Analyses of RANK and RANKL in the post-GWAS context: functional evidence of vitamin D stimulation through a RANKL distal region.

2013-12 | Journal article
DOI:

10.1002/jbmr.2001

PMID:

23744843

Contributors: Yoskovitz G; Garcia-Giralt N; Rodriguez-Sanz M; Urreizti R; Guerri R; Ariño-Ballester S; Prieto-Alhambra D; Mellibovsky L; Grinberg D; Nogues X et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.

2013-11 | Journal article
DOI:

10.1002/mgg3.24

PMID:

24498617

PMC:

PMC3865589

Contributors: Carreño O; Corominas R; Serra SA; Sintas C; Fernández-Castillo N; Vila-Pueyo M; Toma C; Gené GG; Pons R; Llaneza M et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central

Genetic determinants of aromatase inhibitor-related arthralgia: the B-ABLE cohort study.

2013-07 | Journal article
DOI:

10.1007/s10549-013-2638-3

PMID:

23868189

Contributors: Garcia-Giralt N; Rodríguez-Sanz M; Prieto-Alhambra D; Servitja S; Torres-Del Pliego E; Balcells S; Albanell J; Grinberg D; Diez-Perez A; Tusquets I et al.
Source: Self-asserted source
Daniel Grinberg via Europe PubMed Central
Items per page:
Page 1 of 3