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PINHEIRO MB, MOROSOLI JJ, COLODRO-CONDE L, et al. Genetic and environmental influences to low back pain and symptoms of depression and anxiety: A population-based twin study. J Psychosom Res. 2018 Feb;105:92-98. doi: 10.1016/j.jpsychores.2017.12.007. Epub 2017 Dec 6
VIDAL-TABOADA JM, PUGLIESE M, SALVADÓ M, et al. KATP Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis. Mol Neurobiol. 2018 Feb 28. doi: 10.1007/s12035-018-0970-7
LÓPEZ-LÓPEZ A, GELPI E, LOPATEGUI DM, et al. Association of the CX3CR1-V249I Variant with Neurofibrillary Pathology Progression in Late-Onset Alzheimer's Disease. Mol Neurobiol. 2018 Mar;55(3):2340-2349. doi: 10.1007/s12035-017-0489-3. Epub 2017 Mar 25
SEGURA V, VALERO ML, CANTERO L, et al. In-Depth Proteomic Characterization of Classical and Non-Classical Monocyte Subsets. Proteomes. 2018 Feb 5;6(1). pii: E8. doi: 10.3390/proteomes6010008
UMBRIA M, RAMOS A, CANER J, e al. Involvement of mitochondrial haplogroups in myocardial infarction and stroke: A case-control study in Castile and Leon (Spain) population. Mitochondrion. 2017 Dec 16. pii: S1567-7249(17)30024-7. doi: 10.1016/j.mito.2017.12.004
CRIADO I, MUÑOZ-CRIADO S, RODRÍGUEZ-CABALLERO A, et al; Primary Health Care Group of Salamanca for the Study of MBL. Host virus and pneumococcus-specific immune responses in high-count monoclonal B-cell lymphocytosis and chronic lymphocytic leukemia: implications for disease progression. Haematologica. 2017 Jul;102(7):1238-1246. doi: 10.3324/haematol.2016.159012. Epub 2017 Apr 6
PINHEIRO MB, MOROSOLI JJ, FERREIRA ML, et al. Genetic and environmental contributions to sleep quality and low back pain: a population-based twin study. Psychosom Med. 2017 Dec 13. doi: 10.1097/PSY.0000000000000548
GÓMEZ-TORTOSA E, RUGGIERO M, SAINZ MJ, et al. SORL1 variants in familiar alzheimer´s disease. Journal of Alzheimer Disease. 2017
ORTIZ-FERNÁNDEZ L, MONTES-CANO MA, GARCÍA-LOZANO JR, et al. PTPN22 is not associated with Behçet's disease. Study spanning the complete gene region in the Spanish population and meta-analysis of the functional variant R620W. Clin Exp Rheumatol. 2016 Apr 1
BOSSINI-CASTILLO L, CAMPILLO-DAVÓ D, LÓPEZ-ISAC E, et al; Spanish Scleroderma Group. An MIF Promoter Polymorphism Is Associated with Susceptibility to Pulmonary Arterial Hypertension in Diffuse Cutaneous Systemic Sclerosis. J Rheumatol. 2017 Oct;44(10):1453-1457. doi: 10.3899/jrheum.161369. Epub 2017 Jul 1.
MÁRQUEZ A, CORDERO-COMA M, MARTÍN-VILLA JM, et al. New insights into the genetic component of non-infectious uveitis through an Immunochip strategy. J Med Genet. 2017 Jan;54(1):38-46. doi: 10.1136/jmedgenet-2016-104144
LOPEZ-ISAC E, BOSSINI-CASTILLO L, PALMA AB, et al. Analysis of ATP8B4 F436L Missense Variant in a Large Systemic Sclerosis Cohort. Arthritis Rheumatol. 2017 Jun;69(6):1337-1338. doi: 10.1002/art.40058. Epub 2017 May 9.
GÓMEZ-TORTOSA E, VAN DER ZEE J, RUGGIERO M, et al; EU EOD Consortium. Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation. J Neurol Neurosurg Psychiatry. 2017 Nov;88(11):996-997. doi: 10.1136/jnnp-2016-315250.
HISADO-OLIVA A, RUZAFA-MARTIN A, SENTCHORDI L, et al. Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature. Genet Med. 2017 Jun 29. doi: 10.1038/gim.2017.66
LÓPEZ-LÓPEZ A, GELPI E, LOPATEGUI DM, VIDAL-TABOADA JM. Association of the CX3CR1-V249I Variant with Neurofibrillary Pathology Progression in Late-Onset Alzheimer's Disease. Mol Neurobiol. 2017 Mar 25. doi: 10.1007/s12035-017-0489-3.
SERRA-JUHÉ C, MARTOS-MORENO GÁ, BOU DE PIERI F, et al. Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants. PLoS Genet. 2017 May 10;13(5):e1006657. doi: 10.1371/journal.pgen.1006657. eCollection 2017 May.
ORDOÑANA JR, SÁNCHEZ ROMERA JF, COLODRO-CONDE L, CARRILLO E, et al. The Murcia Twin Registry. A resource for research on health-related behaviour. Gac Sanit. 2017 Mar 8. pii: S0213-9111(16)30259-X. doi: 10.1016/j.gaceta.2016.10.008
FERNÁNDEZ-GUTIÉRREZ B, PERROTTI PP, GISBERT JP, et al;IMID Consortium. Cardiovascular disease in immune-mediated inflammatory diseases: A cross-sectional analysis of 6 cohorts. Medicine (Baltimore). 2017 Jun;96(26):e7308. doi: 10.1097/MD.0000000000007308
GAGO-DÍAZ M, BRION M, GALLEGO P, et al. The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study. J Mol Cell Cardiol. 2017 Jan;102:3-9. doi: 10.1016/j.yjmcc.2016.11.012. Epub 2016 Nov 25.
DÍEZ P, IBARROLA N, DÉGANO RM, LÉCREVISSE et al. A systematic approach for peptide characterization of B-cell receptor in chronic lymphocytic leukemia cells. Oncotarget. 2017 Jun 27;8(26):42836-42846. doi: 10.18632/oncotarget.17076.
CARRERAS-TORRES R, FERRAN A, ZANETTI D, et al. Population structure from NOS genes correlates with geographical differences in coronary incidence across Europe. Am J Phys Anthropol. 2016 Dec;161(4):634-645. doi: 10.1002/ajpa.23063. Epub 2016 Aug 8.
POTRONY M, PUIG-BUTILLE JA, AGUILERA P, el al. Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations. JAMA Dermatol. 2016 Apr;152(4):405-12. doi: 10.1001/jamadermatol.2015.4356
BARRETO-LUIS A, CORRALES A, ACOSTA-HERRERA M, et al. A pathway-based association study reveals variants from Wnt signalling genes contributing to asthma susceptibility.. Clin Exp Allergy. 2017 Jan 12. doi: 10.1111/cea.12883
BARRETO-LUIS A, PINO-YANES M, CORRALES A, et al. Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene. J Allergy Clin Immunol. 2016 Mar;137(3):964-6. doi: 10.1016/j.jaci.2015.09.051
POZNIK GD, XUE Y, MENDEZ FL, et al; 1000 GENOMES PROJECT CONSORTIUM. Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Tyler-Smith C. Nat Genet. 2016 Jun;48(6):593-9. doi: 10.1038/ng.3559.
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Universidad de Salamanca
Nucleus
PRB2
Red de biobancos
Instituto Carlos III
Junta de Castilla y León
Union Europea
Banco Nacional de ADN
Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
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