Lista de obras - Giorgio Melloni - Dominio Público Uruguay

A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data

artículo científico publicado en 2017

A polygenic risk score predicts atrial fibrillation in cardiovascular disease

scientific article published in 2022

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups

artículo científico

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups.

artículo científico publicado en 2013

Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

artículo científico publicado en 2018

Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients with Cardiometabolic Disease

artículo científico publicado en 2020

Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

artículo científico publicado en 2018

DOTS-Finder: a comprehensive tool for assessing driver genes in cancer genomes.

artículo científico publicado en 2014

Detecting the mutational signature of homologous recombination deficiency in clinical samples

scientific article published on 15 April 2019

INSPEcT: a computational tool to infer mRNA synthesis, processing and degradation dynamics from RNA- and 4sU-seq time course experiments.

artículo científico publicado en 2015

In Vivo Genetic Screens of Patient-Derived Tumors Revealed Unexpected Frailty of the Transformed Phenotype.

artículo científico publicado en 2016

LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancer

artículo científico publicado en 2016

PATRI, a Genomics Data Integration Tool for Biomarker Discovery

artículo científico publicado en 2018

PML-RARA-associated cooperating mutations belong to a transcriptional network that is deregulated in myeloid leukemias.

artículo científico

Release of paused RNA polymerase II at specific loci favors DNA double-strand-break formation and promotes cancer translocations

artículo científico publicado en 2019

The Effect of PCSK9 Inhibition on the Risk of Venous Thromboembolism

artículo científico publicado en 2020

Lista de obras de Giorgio Melloni

A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data

A polygenic risk score predicts atrial fibrillation in cardiovascular disease

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups

Acute promyelocytic leukemias share cooperative mutations with other myeloid-leukemia subgroups.

Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients with Cardiometabolic Disease

Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

DOTS-Finder: a comprehensive tool for assessing driver genes in cancer genomes.

Detecting the mutational signature of homologous recombination deficiency in clinical samples

INSPEcT: a computational tool to infer mRNA synthesis, processing and degradation dynamics from RNA- and 4sU-seq time course experiments.

In Vivo Genetic Screens of Patient-Derived Tumors Revealed Unexpected Frailty of the Transformed Phenotype.

LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancer

PATRI, a Genomics Data Integration Tool for Biomarker Discovery

PML-RARA-associated cooperating mutations belong to a transcriptional network that is deregulated in myeloid leukemias.

Release of paused RNA polymerase II at specific loci favors DNA double-strand-break formation and promotes cancer translocations

The Effect of PCSK9 Inhibition on the Risk of Venous Thromboembolism

Very low depth whole genome sequencing in complex trait association studies