Lista de obras - Rosario M. Piro - Dominio Público Uruguay

Author Correction: The landscape of genomic alterations across childhood cancers

artículo científico publicado en 2018

BCAT1 promotes cell proliferation through amino acid catabolism in gliomas carrying wild-type IDH1.

artículo científico publicado en 2013

Candidate gene prioritization based on spatially mapped gene expression: an application to XLMR

artículo científico publicado en 2010

Computational approaches to disease-gene prediction: rationale, classification and successes.

artículo científico

Disease-gene discovery by integration of 3D gene expression and transcription factor binding affinities

artículo científico publicado en 2012

Epigenomic alterations define lethal CIMP-positive ependymomas of infancy

artículo científico publicado en 2014

Evaluation of candidate genes from orphan FEB and GEFS+ loci by analysis of human brain gene expression atlases

artículo científico publicado en 2011

Functional annotation and identification of candidate disease genes by computational analysis of normal tissue gene expression data.

artículo científico publicado en 2008

Generation of functional hepatocytes from mouse germ line cell-derived pluripotent stem cells in vitro.

artículo científico

Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition

artículo científico publicado en 2014

Meningeal hemangiopericytoma and solitary fibrous tumors carry the NAB2-STAT6 fusion and can be diagnosed by nuclear expression of STAT6 protein

artículo científico publicado en 2013

Molecular Transition of an Adult Low-Grade Brain Tumor to an Atypical Teratoid/Rhabdoid Tumor Over a Time-Course of 14 Years

artículo científico

Network medicine: linking disorders.

artículo científico publicado en 2012

Network topology-based detection of differential gene regulation and regulatory switches in cell metabolism and signaling

artículo científico publicado en 2014

Network-Based Methods and Other Approaches for Predicting lncRNA Functions and Disease Associations

scientific article published on 01 January 2019

No correlation between NF1 mutation position and risk of optic pathway glioma in 77 unrelated NF1 patients

artículo científico publicado en 2016

Prediction of human disease genes by human-mouse conserved coexpression analysis

artículo científico publicado en 2008

SPLICE-q: a Python tool for genome-wide quantification of splicing efficiency

artículo científico publicado en 2021

Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations

artículo científico publicado en 2013

Stem cell characteristics in glioblastoma are maintained by the ecto-nucleotidase E-NPP1.

artículo científico publicado en 2014

The landscape of genomic alterations across childhood cancers

artículo científico publicado en 2018

Tracing Resource Usage over Heterogeneous Grid Platforms: A Prototype RUS Interface for DGAS

Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants

article published in 2014

decompTumor2Sig: identification of mutational signatures active in individual tumors

artículo científico publicado en 2019

Lista de obras de Rosario M. Piro

Author Correction: The landscape of genomic alterations across childhood cancers

BCAT1 promotes cell proliferation through amino acid catabolism in gliomas carrying wild-type IDH1.

Candidate gene prioritization based on spatially mapped gene expression: an application to XLMR

Computational approaches to disease-gene prediction: rationale, classification and successes.

Disease-gene discovery by integration of 3D gene expression and transcription factor binding affinities

Epigenomic alterations define lethal CIMP-positive ependymomas of infancy

Evaluation of candidate genes from orphan FEB and GEFS+ loci by analysis of human brain gene expression atlases

Functional annotation and identification of candidate disease genes by computational analysis of normal tissue gene expression data.

Generation of functional hepatocytes from mouse germ line cell-derived pluripotent stem cells in vitro.

Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition

Meningeal hemangiopericytoma and solitary fibrous tumors carry the NAB2-STAT6 fusion and can be diagnosed by nuclear expression of STAT6 protein

Molecular Transition of an Adult Low-Grade Brain Tumor to an Atypical Teratoid/Rhabdoid Tumor Over a Time-Course of 14 Years

Network medicine: linking disorders.

Network topology-based detection of differential gene regulation and regulatory switches in cell metabolism and signaling

Network-Based Methods and Other Approaches for Predicting lncRNA Functions and Disease Associations

No correlation between NF1 mutation position and risk of optic pathway glioma in 77 unrelated NF1 patients

Prediction of human disease genes by human-mouse conserved coexpression analysis

SPLICE-q: a Python tool for genome-wide quantification of splicing efficiency

Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations

Stem cell characteristics in glioblastoma are maintained by the ecto-nucleotidase E-NPP1.

The landscape of genomic alterations across childhood cancers

Tracing Resource Usage over Heterogeneous Grid Platforms: A Prototype RUS Interface for DGAS

Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants

decompTumor2Sig: identification of mutational signatures active in individual tumors