Publicaciones (56) Publicaciones de MARÍA LUISA CAÑADAS GARRE

2023

  1. Albuminuria-Related Genetic Biomarkers: Replication and Predictive Evaluation in Individuals with and without Diabetes from the UK Biobank

    International Journal of Molecular Sciences, Vol. 24, Núm. 13

  2. Correction to: The power of genetic diversity in genome-wide association studies of lipids (Nature, (2021), 600, 7890, (675-679), 10.1038/s41586-021-04064-3)

    Nature

  3. Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans

    Frontiers in Endocrinology, Vol. 14

2022

  1. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

    American Journal of Human Genetics, Vol. 109, Núm. 8, pp. 1366-1387

  2. A saturated map of common genetic variants associated with human height

    Nature, Vol. 610, Núm. 7933, pp. 704-712

  3. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

    Genome Biology, Vol. 23, Núm. 1

  4. Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia: a CRuCIAL study

    Blood Cancer Journal

2021

  1. Pharmacogenetic Predictors of Response to Interferon Beta Therapy in Multiple Sclerosis

    Molecular Neurobiology, Vol. 58, Núm. 9, pp. 4716-4726

  2. The power of genetic diversity in genome-wide association studies of lipids

    Nature, Vol. 600, Núm. 7890, pp. 675-679

2020

  1. Association of ABCB1 and VEGFA gene polymorphisms with breast cancer susceptibility and prognosis

    Pathology Research and Practice, Vol. 216, Núm. 4

  2. Effect of DPYD, MTHFR, ABCB1, XRCC1, ERCC1 and GSTP1 on chemotherapy related toxicity in colorectal carcinoma

    Surgical Oncology, Vol. 35, pp. 388-398

  3. Genetic Strategies to Understand Human Diabetic Nephropathy: In Silico Strategies for Molecular Data—Association Studies

    Methods in Molecular Biology (Humana Press Inc.), pp. 241-275

  4. Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease

    BMC Medical Genomics, Vol. 13, Núm. 1

2019

  1. Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals

    Clinical Pharmacology and Therapeutics, Vol. 105, Núm. 6, pp. 1477-1491

  2. Genetic associations between genes in the renin-angiotensin-aldosterone system and renal disease: A systematic review and meta-analysis

    BMJ Open, Vol. 9, Núm. 4

  3. Genetic susceptibility to chronic kidney disease - Some more pieces for the heritability puzzle

    Frontiers in Genetics, Vol. 10, Núm. MAY

  4. Impact of single nucleotide polymorphisms on the efficacy and toxicity of EGFR tyrosine kinase inhibitors in advanced non-small cell lung cancer patients

    Mutation Research - Reviews in Mutation Research, Vol. 781, pp. 63-70

  5. Information on Genetic Variants Does Not Increase Identification of Individuals at Risk of Esophageal Adenocarcinoma Compared to Clinical Risk Factors

    Gastroenterology, Vol. 156, Núm. 1, pp. 43-45

  6. Pharmacogenetics of platinum-based chemotherapy: impact of DNA repair and folate metabolism gene polymorphisms on prognosis of non-small cell lung cancer patients

    Pharmacogenomics Journal, Vol. 19, Núm. 2, pp. 164-177

  7. Proteomic and metabolomic approaches in the search for biomarkers in chronic kidney disease

    Journal of Proteomics, Vol. 193, pp. 93-122