Medicina
Departamento
Lund University
Lund, SueciaPublicaciones en colaboración con investigadores/as de Lund University (33)
2023
2022
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Dissecting platelet proteomics to understand the pathophysiology of immune thrombocytopenia: studies in mouse models
Blood Advances, Vol. 6, Núm. 11, pp. 3529-3534
2021
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Causal relationships between body mass index, smoking and lung cancer: Univariable and multivariable Mendelian randomization
International Journal of Cancer, Vol. 148, Núm. 5, pp. 1077-1086
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Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
Frontiers of Medicine, Vol. 15, Núm. 2, pp. 275-291
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Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers
PLoS Genetics, Vol. 17, Núm. 3
2020
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Association Analysis of Driver Gene-Related Genetic Variants Identified Novel Lung Cancer Susceptibility Loci with 20,871 Lung Cancer Cases and 15,971 Controls
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Vol. 29, Núm. 7, pp. 1423-1429
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C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts
Neurology, Vol. 95, Núm. 24, pp. E3288-E3302
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Genome-wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk
International Journal of Cancer, Vol. 146, Núm. 10, pp. 2855-2864
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Protein-altering germline mutations implicate novel genes related to lung cancer development
Nature Communications, Vol. 11, Núm. 1
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Transcriptome-wide association study reveals candidate causal genes for lung cancer
International Journal of Cancer, Vol. 146, Núm. 7, pp. 1862-1878
2019
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Elevated platelet count appears to be causally associated with increased risk of lung cancer: A mendelian randomization analysis
Cancer Epidemiology Biomarkers and Prevention, Vol. 28, Núm. 5, pp. 935-942
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Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development
Oncotarget, Vol. 10, Núm. 19, pp. 1760-1774
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Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region
Journal of Thoracic Oncology, Vol. 14, Núm. 8, pp. 1360-1369
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Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4)
Nature Communications
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Shared heritability and functional enrichment across six solid cancers
Nature Communications, Vol. 10, Núm. 1
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Systematic analyses of regulatory variants in DNase i hypersensitive sites identified two novel lung cancer susceptibility loci
Carcinogenesis, Vol. 40, Núm. 3, pp. 432-440
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Systemic manifestations of primary Sjögren's syndrome out of the ESSDAI classification: Prevalence and clinical relevance in a large international, multi-ethnic cohort of patients
Clinical and Experimental Rheumatology, Vol. 37, pp. S97-S106
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The Big Data Sjögren consortium: A project for a new data science era
Clinical and Experimental Rheumatology, Vol. 37, pp. S19-S23
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Treatment and long-Term outcome in primary distal renal tubular acidosis
Nephrology Dialysis Transplantation, Vol. 34, Núm. 6, pp. 981-991
2018
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Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners
International Archives of Occupational and Environmental Health, Vol. 91, Núm. 8, pp. 937-950