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Sequencing, de novo annotation and analysis of the first Anguilla anguilla transcriptome: EeelBase opens new perspectives for the study of the critically endangered European eel

BMC genomics, 2010-11, Vol.11 (1), p.635-635, Article 635

2010

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Small RNA Sequencing Uncovers New miRNAs and moRNAs Differentially Expressed in Normal and Primary Myelofibrosis CD34+ Cells

PloS one, 2015-10, Vol.10 (10), p.e0140445-e0140445

2015

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Transcriptome sequencing and microarray development for the Manila clam, Ruditapes philippinarum: genomic tools for environmental monitoring

BMC genomics, 2011-05, Vol.12 (1), p.234-234, Article 234

2011

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Novel definition files for human GeneChips based on GeneAnnot

BMC bioinformatics, 2007-11, Vol.8 (1), p.446-446, Article 446

2007

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A high definition picture of somatic mutations in chronic lymphoproliferative disorder of natural killer cells

Blood cancer journal (New York), 2020-04, Vol.10 (4), p.42-42, Article 42

2020

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Multiomic analysis of HER2-enriched and AR-positive breast carcinoma with apocrine differentiation and an oligometastatic course: a case report

Frontiers in oncology, 2023-07, Vol.13

2023

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A high definition picture of key genes and pathways mutated in pediatric follicular lymphoma

Haematologica (Roma), 2019-09, Vol.104 (9), p.e406-e409

2019

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Lack of Viral Load Within Chronic Lymphoproliferative Disorder of Natural Killer Cells: What Is Outside the Leukemic Clone?

Frontiers in oncology, 2021-01, Vol.10, p.613570-613570

2021

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Surviving in a toxic world: transcriptomics and gene expression profiling in response to environmental pollution in the critically endangered European eel

BMC genomics, 2012-09, Vol.13 (1), p.507-507

2012

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Impact of host genes and strand selection on miRNA and miRNA expression

PloS one, 2011-08, Vol.6 (8), p.e23854-e23854

2011

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Sequencing and characterization of striped venus transcriptome expand resources for clam fishery genetics

PloS one, 2012-09, Vol.7 (9), p.e44185-e44185

2012

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REEF: searching REgionally Enriched Features in genomes

BMC bioinformatics, 2006-10, Vol.7 (1), p.453-453, Article 453

2006

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A-MADMAN: annotation-based microarray data meta-analysis tool

BMC bioinformatics, 2009-06, Vol.10 (1), p.201-201, Article 201

2009

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TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources

BMC genomics, 2011-02, Vol.12 (1), p.121-121, Article 121

2011

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Genomic expression during human myelopoiesis

BMC genomics, 2007-08, Vol.8 (1), p.264-264

2007

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iWhale: a computational pipeline based on Docker and SCons for detection and annotation of somatic variants in cancer WES data

Briefings in bioinformatics, 2021-05, Vol.22 (3)

2021

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Transcriptome sequencing and de novo annotation of the critically endangered Adriatic sturgeon

BMC genomics, 2013-06, Vol.14 (1), p.407-407

2013

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Clinical effect of driver mutations of JAK2, CALR, or MPL in primary myelofibrosis

Blood, 2014-08, Vol.124 (7), p.1062-1069

2014

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Somatic mutations in specific and connected subpathways are associated with short neuroblastoma patients’ survival and indicate proteins targetable at onset of disease

International journal of cancer, 2018-11, Vol.143 (10), p.2525-2536

2018

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MAGIA, a web-based tool for miRNA and Genes Integrated Analysis

Nucleic acids research, 2010-07, Vol.38 (Web Server issue), p.W352-W359

2010

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A multistep bioinformatic approach detects putative regulatory elements in gene promoters

BMC bioinformatics, 2005-05, Vol.6 (1), p.121-121, Article 121

2005

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A guilt-by-association mutation network in LGL leukemia

Oncotarget, 2017-11, Vol.8 (55), p.93299-93300

2017

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Whole Exome Sequencing Analysis in Chronic Lymphoproliferative Disorder of NK Cells (CLPD-NK) Patients Fails to Detect Significant Viral Load

Blood, 2019-11, Vol.134 (Supplement_1), p.5214-5214

2019

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A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T‐cell acute lymphoblastic leukemia

American journal of hematology, 2020-12, Vol.95 (12), p.E335-E338

2020

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Sequencing, de novo annotation and analysis of the first Anguilla anguilla transcriptome: EeelBase opens new perspectives for the study of the critically endangered European eel

Small RNA Sequencing Uncovers New miRNAs and moRNAs Differentially Expressed in Normal and Primary Myelofibrosis CD34+ Cells

Transcriptome sequencing and microarray development for the Manila clam, Ruditapes philippinarum: genomic tools for environmental monitoring

Novel definition files for human GeneChips based on GeneAnnot

A high definition picture of somatic mutations in chronic lymphoproliferative disorder of natural killer cells

Multiomic analysis of HER2-enriched and AR-positive breast carcinoma with apocrine differentiation and an oligometastatic course: a case report

A high definition picture of key genes and pathways mutated in pediatric follicular lymphoma

Lack of Viral Load Within Chronic Lymphoproliferative Disorder of Natural Killer Cells: What Is Outside the Leukemic Clone?

Surviving in a toxic world: transcriptomics and gene expression profiling in response to environmental pollution in the critically endangered European eel

Impact of host genes and strand selection on miRNA and miRNA expression

Sequencing and characterization of striped venus transcriptome expand resources for clam fishery genetics

REEF: searching REgionally Enriched Features in genomes

A-MADMAN: annotation-based microarray data meta-analysis tool

TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources

Genomic expression during human myelopoiesis

iWhale: a computational pipeline based on Docker and SCons for detection and annotation of somatic variants in cancer WES data

Transcriptome sequencing and de novo annotation of the critically endangered Adriatic sturgeon

Clinical effect of driver mutations of JAK2, CALR, or MPL in primary myelofibrosis

Somatic mutations in specific and connected subpathways are associated with short neuroblastoma patients’ survival and indicate proteins targetable at onset of disease

MAGIA, a web-based tool for miRNA and Genes Integrated Analysis

High incidence of activating STAT5B mutations in CD4-positive T-cell large granular lymphocyte leukemia

A multistep bioinformatic approach detects putative regulatory elements in gene promoters

A guilt-by-association mutation network in LGL leukemia

Whole Exome Sequencing Analysis in Chronic Lymphoproliferative Disorder of NK Cells (CLPD-NK) Patients Fails to Detect Significant Viral Load

A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T‐cell acute lymphoblastic leukemia

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