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Justo Lorenzo Bermejo

Researcher at Heidelberg University

Publications -  235
Citations -  7151

Justo Lorenzo Bermejo is an academic researcher from Heidelberg University. The author has contributed to research in topics: Cancer & Population. The author has an hindex of 45, co-authored 227 publications receiving 6211 citations. Previous affiliations of Justo Lorenzo Bermejo include Karolinska Institutet & German Cancer Research Center.

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Atlas of the clinical genetics of human dilated cardiomyopathy

TL;DR: This is to the authors' knowledge, the first study that comprehensively investigated the genetics of DCM in a large-scale cohort and across a broad gene panel of the known DCM genes and underline the high analytical quality and feasibility of Next-Generation Sequencing in clinical genetic diagnostics.
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Systems-wide proteomic analysis in mammalian cells reveals conserved, functional protein turnover.

TL;DR: High-resolution mass spectrometry was employed to quantify protein dynamics in nondividing mammalian cells and observed statistically significant trends for the turnover of phosphoproteins and gene ontology categories that showed extensive covariation between mouse and human.
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The balance between heritable and environmental aetiology of human disease.

TL;DR: Using cancer as an example of complex disease, the scientific evidence for the hypothesis that human diseases result from interactions between genetic variants and the environment is examined.
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Methylome analysis and integrative profiling of human HCCs identify novel protumorigenic factors.

TL;DR: It is illustrated that vertical integration of methylation data with high‐resolution genomic and transcriptomic data facilitates the identification of new tumor‐suppressor gene candidates in human HCC.
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A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy

TL;DR: The present study reveals a novel genetic susceptibility locus that clearly underlines the role of genetically driven, inflammatory processes in the pathogenesis of idiopathic DCM.