Complexo Hospitalario Universitario de Santiago
Centro de atención
David Geffen School of Medicine at UCLA
Los Ángeles, Estados UnidosPublicacións en colaboración con investigadores/as de David Geffen School of Medicine at UCLA (19)
2024
-
Agreement between local and central anti-synthetase antibodies detection: results from the Classification Criteria of Anti-Synthetase Syndrome project biobank
Clinical and experimental rheumatology, Vol. 42, Núm. 2, pp. 277-287
-
Severity-adjusted evaluation of liver transplantation on health outcomes in urea cycle disorders
Genetics in Medicine, Vol. 26, Núm. 4
-
The genomic evolutionary dynamics and global circulation patterns of respiratory syncytial virus
Nature communications, Vol. 15, Núm. 1, pp. 3083
2023
-
A second update on mapping the human genetic architecture of COVID-19
Nature
-
Lenvatinib plus pembrolizumab versus lenvatinib plus placebo for advanced hepatocellular carcinoma (LEAP-002): a randomised, double-blind, phase 3 trial
The Lancet Oncology, Vol. 24, Núm. 12, pp. 1399-1410
2022
-
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
PLoS genetics, Vol. 18, Núm. 11, pp. e1010367
-
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Nature, Vol. 604, Núm. 7906, pp. 502-508
2021
-
A 300 IR sublingual tablet is an effective, safe treatment for house dust mite–induced allergic rhinitis: An international, double-blind, placebo-controlled, randomized phase III clinical trial
Journal of Allergy and Clinical Immunology, Vol. 147, Núm. 3, pp. 1020-1030.e10
-
TIPICO XI: report of the first series and podcast on infectious diseases and vaccines (aTIPICO)
Human Vaccines and Immunotherapeutics, Vol. 17, Núm. 11, pp. 4299-4327
2020
-
Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36
Neuron, Vol. 107, Núm. 2, pp. 292-305.e6
-
Long-term effects of medical management on growth and weight in individuals with urea cycle disorders
Scientific Reports, Vol. 10, Núm. 1
2019
-
Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—A successful strategy for clinical research of rare diseases
Journal of Inherited Metabolic Disease, Vol. 42, Núm. 1, pp. 93-106
2016
-
LMNA missense mutations causing familial partial lipodystrophy do not lead to an accumulation of prelamin A
Nucleus, Vol. 7, Núm. 5, pp. 512-521
-
Specific premature epigenetic aging of cartilage in osteoarthritis
Aging, Vol. 8, Núm. 9, pp. 2222-2231
2015
-
Associated Links Among Smoking, Chronic Obstructive Pulmonary Disease, and Small Cell Lung Cancer: A Pooled Analysis in the International Lung Cancer Consortium
EBioMedicine, Vol. 2, Núm. 11, pp. 1677-1685
2013
-
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
Nature Genetics, Vol. 45, Núm. 9, pp. 1077-1082
2012
-
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration
Nature Genetics, Vol. 44, Núm. 6, pp. 704-708
2010
-
Meta-analysis of the performance of 18F-FDG PET in cutaneous melanoma
European Journal of Nuclear Medicine and Molecular Imaging, Vol. 37, Núm. 2, pp. 284-300
-
Reply to: The diagnostic accuracy of 18F-FDG PET in cutaneous malignant melanoma
European Journal of Nuclear Medicine and Molecular Imaging