INSTITUTO DE INVESTIGACIÓN BIOMÉDICA DE SALAMANCA
Institute
Cardiff University
Cardiff, Reino UnidoPublications in collaboration with researchers from Cardiff University (21)
2022
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Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
Human Brain Mapping, Vol. 43, Núm. 1, pp. 300-328
2021
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1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
Translational psychiatry, Vol. 11, Núm. 1, pp. 182
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Development and external validation of the Psychosis Metabolic Risk Calculator (PsyMetRiC): a cardiometabolic risk prediction algorithm for young people with psychosis
The Lancet Psychiatry, Vol. 8, Núm. 7, pp. 589-598
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Integrated metastate functional connectivity networks predict change in symptom severity in clinical high risk for psychosis
Human Brain Mapping, Vol. 42, Núm. 2, pp. 439-451
2020
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Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region with Cortical and Subcortical Morphology and Cognition
JAMA Psychiatry, Vol. 77, Núm. 4, pp. 420-430
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Correction: Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph+ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1 (Leukemia, (2019), 33, 8, (1910-1922), 10.1038/s41375-019-0413-0)
Leukemia
2019
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Barley-ß-glucans reduce systemic inflammation, renal injury and aortic calcification through ADAM17 and neutral-sphingomyelinase2 inhibition
Scientific Reports, Vol. 9, Núm. 1
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Disaggregating physiological components of cortisol output: A novel approach to cortisol analysis in a clinical sample – A proof-of-principle study
Neurobiology of Stress, Vol. 10
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Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph + ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1
Leukemia, Vol. 33, Núm. 8, pp. 1910-1922
2018
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Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease
Neurology, Vol. 91, Núm. 22, pp. e2078-e2088
2016
2015
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A global reference for human genetic variation
Nature, Vol. 526, Núm. 7571, pp. 68-74
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Designing a broad-spectrum integrative approach for cancer prevention and treatment
Seminars in Cancer Biology, Vol. 35, pp. S276-S304
2014
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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Nature Communications, Vol. 5
2012
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An integrated map of genetic variation from 1,092 human genomes
Nature, Vol. 491, Núm. 7422, pp. 56-65
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Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, Vol. 8, Núm. 4, pp. 445-544
2010
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Quality, quantity and harmony: The DataSHaPER approach to integrating data across bioclinical studies
International Journal of Epidemiology, Vol. 39, Núm. 5, pp. 1383-1393