Facultad de Medicina y Enfermería
Zentrum
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University of Tübingen
Tubinga, AlemaniaPublikationen in Zusammenarbeit mit Forschern von University of Tübingen (35)
2024
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Ancient genomes reveal insights into ritual life at Chichén Itzá
Nature, Vol. 630, Núm. 8018, pp. 912-919
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Conformation- and activation-based BRET sensors differentially report on GPCR-G protein coupling
Science signaling, Vol. 17, Núm. 841, pp. eadi4747
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MetSCORE: a molecular metric to evaluate the risk of metabolic syndrome based on serum NMR metabolomics
Cardiovascular Diabetology, Vol. 23, Núm. 1
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Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease
Brain : a journal of neurology, Vol. 147, Núm. 5, pp. 1887-1898
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Stratified analyses refine association between TLR7 rare variants and severe COVID-19
Human Genetics and Genomics Advances, Vol. 5, Núm. 4
2023
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Alternative forms of portal vein revascularization in liver transplant recipients with complex portal vein thrombosis
Journal of Hepatology, Vol. 78, Núm. 4, pp. 794-804
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Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Movement Disorders, Vol. 38, Núm. 2, pp. 286-303
2022
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Longitudinal clinical and biomarker characteristics of non-manifesting LRRK2 G2019S carriers in the PPMI cohort
npj Parkinson's Disease, Vol. 8, Núm. 1
2021
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Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-y)
Scientific Reports
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Ecological conditions during the Middle to Upper Palaeolithic transition (MIS 3) in Iberia: the cold-adapted faunal remains from Mainea, northern Iberian Peninsula
Boreas, Vol. 50, Núm. 3, pp. 686-708
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Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Nature Communications, Vol. 12, Núm. 1
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Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications
Scientific Reports, Vol. 11, Núm. 1
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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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Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage
Nature Communications, Vol. 12, Núm. 1
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Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease
Annals of Neurology, Vol. 90, Núm. 1, pp. 35-42
2020
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Merlin: A novel BRET-based proximity biosensor for studying mitochondria–ER contact sites
Life Science Alliance, Vol. 3, Núm. 1
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Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
Nature Communications, Vol. 11, Núm. 1
2019
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FAHN/SPG35: A narrow phenotypic spectrum across disease classifications
Brain, Vol. 142, Núm. 6, pp. 1561-1572
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Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI)
Parkinsonism and Related Disorders, Vol. 62, pp. 201-209
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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
The Lancet Neurology, Vol. 18, Núm. 12, pp. 1091-1102