INSTITUTO DE INVESTIGACIÓN BIOMÉDICA DE SALAMANCA
Instituto
Broad Institute
Cambridge, Estados UnidosPublicaciones en colaboración con investigadores/as de Broad Institute (23)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Generation of mouse models carrying B cell restricted single or multiplexed loss-of-function mutations through CRISPR-Cas9 gene editing
STAR Protocols, Vol. 4, Núm. 4
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IGLV3-21R110 mutation has prognostic value in patients with treatment-naive chronic lymphocytic leukemia
Blood Advances
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In Vivo Modeling of CLL Transformation to Richter Syndrome Reveals Convergent Evolutionary Paths and Therapeutic Vulnerabilities
Blood cancer discovery, Vol. 4, Núm. 2, pp. 150-169
2022
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Immune biomarkers of response to immunotherapy in patients with high-risk smoldering myeloma
Cancer Cell, Vol. 40, Núm. 11, pp. 1358-1373.e8
2021
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1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
Translational psychiatry, Vol. 11, Núm. 1, pp. 182
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Biological significance of monoallelic and biallelic BIRC3 loss in del(11q) chronic lymphocytic leukemia progression
Blood Cancer Journal, Vol. 11, Núm. 7
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Counterpoint. Early intervention for psychosis risk syndromes: Minimizing risk and maximizing benefit
Schizophrenia Research, Vol. 227, pp. 10-17
2020
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Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region with Cortical and Subcortical Morphology and Cognition
JAMA Psychiatry, Vol. 77, Núm. 4, pp. 420-430
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CRISPR/Cas9-generated models uncover therapeutic vulnerabilities of del(11q) CLL cells to dual BCR and PARP inhibition
Leukemia, Vol. 34, Núm. 6, pp. 1599-1612
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High throughput single-cell detection of multiplex CRISPR-edited gene modifications
Genome Biology, Vol. 21, Núm. 1
2019
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Mitochondrial Reprogramming Underlies Resistance to BCL-2 Inhibition in Lymphoid Malignancies
Cancer Cell, Vol. 36, Núm. 4, pp. 369-384.e13
2018
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A community approach to mortality prediction in sepsis via gene expression analysis
Nature Communications, Vol. 9, Núm. 1
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Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
Annals of the rheumatic diseases, Vol. 77, Núm. 3, pp. 378-385
2016
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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
Autophagy
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy, Vol. 12, Núm. 1, pp. 1-222
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The T300A Crohn's disease risk polymorphism impairs function of the WD40 domain of ATG16L1
Nature Communications, Vol. 7
2015
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A global reference for human genetic variation
Nature, Vol. 526, Núm. 7571, pp. 68-74
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Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy
EBioMedicine, Vol. 2, Núm. 9, pp. 1063-1070
2014
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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Nature Communications, Vol. 5