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A framework to rank genomic alterations as targets for cancer precision medicine: the ESMO Scale for Clinical Actionability of molecular Targets (ESCAT)

Annals of oncology, 2018-09, Vol.29 (9), p.1895-1902

2018

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A DNA methylation map of human cancer at single base-pair resolution

Oncogene, 2017-10, Vol.36 (40), p.5648-5657

2017

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Improving data and knowledge management to better integrate health care and research

Journal of internal medicine, 2013-10, Vol.274 (4), p.321-328

2013

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The transcriptional repressor HDAC7 promotes apoptosis and c-Myc downregulation in particular types of leukemia and lymphoma

Cell death & disease, 2015-02, Vol.6 (2), p.e1635-e1635

2015

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Genome-wide identification of genes likely to be involved in human genetic disease

Nucleic acids research, 2004, Vol.32 (10), p.3108-3114

2004

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Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

Human molecular genetics, 2001-04, Vol.10 (9), p.947-952

2001

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p27Kip1 represses transcription by direct interaction with p130/E2F4 at the promoters of target genes

Oncogene, 2012-09, Vol.31 (38), p.4207-4220

2012

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455: The role of new cancer hallmarks in tumorigenesis

European journal of cancer (1990), 2014-07, Vol.50, p.S110-S110

2014

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Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

Nature genetics, 1999-09, Vol.23 (1), p.16-18

1999

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Biological reprogramming in acquired resistance to endocrine therapy of breast cancer

Oncogene, 2010-11, Vol.29 (45), p.6071-6083

2010

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46: Proffered Paper: Therapeutical landscape of cancer drivers

European journal of cancer (1990), 2014-07, Vol.50, p.S12-S12

2014

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BioMart Central Portal: an open database network for the biological community

Database : the journal of biological databases and curation, 2011-01, Vol.2011, p.bar041-bar041

2011

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The 1+Million Genomes Minimal Dataset for Cancer

Nature genetics, 2024-05, Vol.56 (5), p.733-736

2024

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CLL cells cumulate genetic aberrations prior to the first therapy even in outwardly inactive disease phase

Leukemia, 2019-02, Vol.33 (2), p.518-558

2019

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CoGenT++: an extensive and extensible data environment for computational genomics

Bioinformatics, 2005-10, Vol.21 (19), p.3806-3810

2005

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Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

Human genetics, 2000-01, Vol.106 (1), p.40-44

2000

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Identification of novel markers in rheumatoid arthritis through integrated analysis of DNA methylation and microRNA expression

Journal of autoimmunity, 2013-03, Vol.41, p.6-16

2013

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Are splicing mutations the most frequent cause of hereditary disease?

FEBS letters, 2005-03, Vol.579 (9), p.1900-1903

2005

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Expansion of the BioCyc collection of pathway/genome databases to 160 genomes

Nucleic acids research, 2005-01, Vol.33 (19), p.6083-6089

2005

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Mutational and Clonal Dynamics During Progression from MDS to SAML by Whole-Exome and Targeted-Deep Sequencing

Leukemia research, 2017-04, Vol.55, p.S55-S55

2017

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OA04.05 MESOMICS Project: Using Whole-Genome Sequencing Data to Fill the Gaps in Malignant Pleural Mesothelioma Molecular Studies

Journal of thoracic oncology, 2022-09, Vol.17 (9), p.S12-S13

2022

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Structural and functional properties of genes involved in human cancer

BMC genomics, 2006-01, Vol.7 (1), p.3-3, Article 3

2006

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P1.08-A Sherlock Lung Tracing Lung Cancer Mutational Processes in Never-smokers

Journal of thoracic oncology, 2019-11, Vol.14 (11), p.S1176-S1177

2019

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Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

Human mutation, 2001-12, Vol.18 (6), p.548-548

2001

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A framework to rank genomic alterations as targets for cancer precision medicine: the ESMO Scale for Clinical Actionability of molecular Targets (ESCAT)

A DNA methylation map of human cancer at single base-pair resolution

Improving data and knowledge management to better integrate health care and research

The transcriptional repressor HDAC7 promotes apoptosis and c-Myc downregulation in particular types of leukemia and lymphoma

Genome-wide identification of genes likely to be involved in human genetic disease

Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

p27Kip1 represses transcription by direct interaction with p130/E2F4 at the promoters of target genes

Integrating genomic alterations in diffuse large B-cell lymphoma identifies new relevant pathways and potential therapeutic targets

455: The role of new cancer hallmarks in tumorigenesis

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

Biological reprogramming in acquired resistance to endocrine therapy of breast cancer

46: Proffered Paper: Therapeutical landscape of cancer drivers

BioMart Central Portal: an open database network for the biological community

The 1+Million Genomes Minimal Dataset for Cancer

CLL cells cumulate genetic aberrations prior to the first therapy even in outwardly inactive disease phase

CoGenT++: an extensive and extensible data environment for computational genomics

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

Identification of novel markers in rheumatoid arthritis through integrated analysis of DNA methylation and microRNA expression

Are splicing mutations the most frequent cause of hereditary disease?

Expansion of the BioCyc collection of pathway/genome databases to 160 genomes

Mutational and Clonal Dynamics During Progression from MDS to SAML by Whole-Exome and Targeted-Deep Sequencing

OA04.05 MESOMICS Project: Using Whole-Genome Sequencing Data to Fill the Gaps in Malignant Pleural Mesothelioma Molecular Studies

Structural and functional properties of genes involved in human cancer

P1.08-A Sherlock Lung Tracing Lung Cancer Mutational Processes in Never-smokers

Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

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