Publicacions
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Antón-Galindo E, Dalla Vecchia E, Orlandi JG, Castro G, Gualda EJ, Young AMJ, Guasch-Piqueras M, Arenas C, Herrera-Úbeda C, Garcia-Fernàndez J, Aguado F, Loza-Alvarez P, Cormand B, Norton WHJ and Fernandez-Castillo N.
Deficiency of the ywhaz gene, involved in neurodevelopmental disorders, alters brain activity and behaviour in zebrafish.
MOLECULAR PSYCHIATRY . 27(9): 3739-3748. Nº de cites: 8
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Ovejero D, Garcia-Giralt N, Martinez-Gil N, Rabionet-Janssen R, Balcells S, Grinberg-Vaisman DR, Pérez-Jurado L, Nogués X and Foronda IE.
Clinical description and genetic analysis of a novel familial skeletal dysplasia characterized by high bone mass and lucent bone lesions.
Bone . 161: 116450-116450. Nº de cites: 2
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Martinez-Gil N, Mellibovsky L, Manzano-López González D, Patiño JD, Cozar M, Rabionet-Janssen R, Grinberg-Vaisman DR and Balcells S.
On the association between Chiari malformation type 1, bone mineral density and bone related genes.
Bone Reports . 16: 101181-101181. Nº de cites: 3
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Garcia-Blanco, A, Domingo-Rodriguez, L, Cabana-Domínguez J, Fernandez-Castillo N, Pineda L, Mayneris-Perxachs, J, Burokas, A, Espinosa-Carrasco, J, Arboleya, S, Latorre, J, Stanton, C, Cormand B, Fernandez-Real, JM, Martin-Garcia, E and Maldonado, R.
miRNA signatures associated with vulnerability to food addiction in mice and humans
JOURNAL OF CLINICAL INVESTIGATION . 132(10): . Nº de cites: 10
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Bullich G, Matalonga L, Pujadas M, Papakonstantinou A, Piscia D, Tonda R, Artuch-Iriberri R, Gallano P, Garrabou G, González JR, Grinberg-Vaisman DR, Guitart M, Laurie S, Lázaro C, Luengo C, Martí R, Milà M, Ovelleiro D, Parra G, Pujol A, Tizzano E, Macaya A, Palau F, Ribes A, Pérez-Jurado LA and Beltran S.
Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases.
JOURNAL OF MOLECULAR DIAGNOSTICS . 24(5): 529-542. Nº de cites: 6
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Luque J, Mendes I, Gómez B, Morte B, de Heredia ML, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch-Iriberri R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F, CIBERER Network and Lapunzina P.
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative
CLINICAL GENETICS . 101(5-6): 481-493. Nº de cites: 8
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López-Marquez A, Morín M, Fernández-Peñalver S, Badosa-Gallego MC, Hernández-Delgado A, Natera-de Benito D, Ortez-Gonzalez CI, Nascimento-Osorio A, Grinberg-Vaisman DR, Balcells S, Roldan-Molina M, Moreno-Pelayo MÁ and Jimenez-Mallebrera C.
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. Nº de cites: 8
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Martinez-Gil N, Ovejero, D, Garcia-Giralt, N, Bruque, CD, Mellibovsky, L, Nogues, X, Rabionet, R, Grinberg-Vaisman DR and Balcells S.
Genetic Analysis in a Familial Case With High Bone Mineral Density Suggests Additive Effects at Two Loci.
jbmr plus . 6(4): . Nº de cites: 1
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Pineda L, Cabana-Domínguez J, Lee, PH, Fernandez-Castillo N and Cormand B.
Identification of genetic variants influencing methylation in brain with pleiotropic effects on psychiatric disorders
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY . 113: 110454-110454. Nº de cites: 8
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Domènech L, Willis J, Alemany-Navarro M, Morell M, Real E, Escaramís G, Bertolín S, Sánchez Chinchilla D, Balcells S, Segalàs C, Estivill X, Menchón JM, Gabaldón T, Alonso P and Rabionet-Janssen R.
Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder
SCIENTIFIC REPORTS . 12(1): 1448-1448. Nº de cites: 18