Unidad de investigación
Servicio
Harvard Medical School
Boston, Estados UnidosPublicaciones en colaboración con investigadores/as de Harvard Medical School (20)
2024
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Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes
Nature Communications, Vol. 15, Núm. 1
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Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches
Journal of Extracellular Vesicles, Vol. 13, Núm. 2
2023
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Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (Nature Genetics, (2023), 55, 1, (89-99), 10.1038/s41588-022-01222-9)
Nature Genetics
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Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature Genetics, Vol. 55, Núm. 1, pp. 89-99
2021
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Characterization and miRNA Profiling of Extracellular Vesicles from Human Osteoarthritic Subchondral Bone Multipotential Stromal Cells (MSCs)
Stem Cells International, Vol. 2021
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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
2019
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Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data
Genome Medicine, Vol. 11, Núm. 1
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Hypothalamic miR-30 regulates puberty onset via repression of the puberty-suppressing factor, Mkrn3
PLoS Biology, Vol. 17, Núm. 11
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Nicotinamide mononucleotide (NMN) supplementation rescues cerebromicrovascular endothelial function and neurovascular coupling responses and improves cognitive function in aged mice
Redox Biology, Vol. 24
2018
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Erratum to: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition (Nature Genetics, (2018), 50, 4, (572-580), 10.1038/s41588-018-0088-x)
Nature Genetics
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Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
PLoS Genetics, Vol. 14, Núm. 12
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Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition
Nature Genetics, Vol. 50, Núm. 4, pp. 572-580
2015
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A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data
BMC Genomics, Vol. 16, Núm. 1
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Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
PLoS Genetics, Vol. 11, Núm. 7
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Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain
Heart, Vol. 101, Núm. 13, pp. 1047-1053
2014
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Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic
Israel Medical Association Journal, Vol. 16, Núm. 11, pp. 707
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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Núm. 36, pp. 13127-13132
2010
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Novel missense mutations in exon 15 of desmoglein-2: Role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?
Heart Rhythm, Vol. 7, Núm. 10, pp. 1446-1453
2009
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Planning the human variome project: The Spain report
Human Mutation, Vol. 30, Núm. 4, pp. 496-510
2005
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Gene mutations in apical hypertrophic cardiomyopathy
Circulation, Vol. 112, Núm. 18, pp. 2805-2811