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Gene Set Enrichment Analysis of Interaction Networks Weighted by Node Centrality

Frontiers in genetics, 2021-02, Vol.12, p.577623-577623

2021

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Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: A collaborative study of 1027 patients

American journal of hematology, 2014-08, Vol.89 (8), p.E121-E124

2014

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Platelet count predicts driver mutations’ co-occurrence in low JAK2 mutated essential thrombocythemia and myelofibrosis

Leukemia, 2021-05, Vol.35 (5), p.1490-1493

2021

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Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches

Frontiers in genetics, 2022-03, Vol.13, p.798607-798607

2022

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WWP1 germline variants are associated with normocephalic autism spectrum disorder

Cell death & disease, 2020-07, Vol.11 (7), p.529-529, Article 529

2020

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Koolen-de Vries Syndrome: Preliminary Observations of Topiramate Efficacy

Child neurology open, 2021-01, Vol.8

2021

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It is time to change thrombosis risk assessment for PV and ET?

Best practice & research. Clinical haematology, 2014-06, Vol.27 (2), p.121-127

2014

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Isolation and Characterization of Multipotent Cells from Human Fetal Dermis

Cell transplantation, 2014-01, Vol.23 (10), p.1169-1185

2014

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Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate

Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1056-n/a

2020

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A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene

Clinical chemistry and laboratory medicine, 2019-02, Vol.57 (2), p.e30-e33

2019

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Culture of skeletal myoblasts from human donors aged over 40 years: dynamics of cell growth and expression of differentiation markers

Journal of translational medicine, 2005-05, Vol.3 (1), p.21-21, Article 21

2005

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The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss

International journal of pediatric otorhinolaryngology, 2019-12, Vol.127, p.109653-109653, Article 109653

2019

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Analysis of three screening methods for the detection of calreticulin gene mutations

International journal of laboratory hematology, 2020-04, Vol.42 (2), p.e76-e79

2020

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Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia

Molecular diagnosis & therapy, 2015-06, Vol.19 (3), p.139-140

2015

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Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations

Seizure (London, England), 2020-08, Vol.80, p.145-152

2020

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Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia

Molecular diagnosis & therapy, 2015-08, Vol.19 (4), p.253-254

2015

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Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study)

Prenatal diagnosis, 2022-12, Vol.42 (13), p.1575-1586

2022

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Positive Predictive Values and Outcomes for Uninformative Cell-Free DNA Tests: An Italian Multicentric Cytogenetic and Cytogenomic Audit of DiagnOstic Testing (ICARO Study)

Obstetrical & gynecological survey, 2023-06, Vol.78 (6), p.318-320

2023

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A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion

Leukemia & lymphoma, 2017-08, Vol.58 (8), p.1977-1980

2017

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Mutations and thrombosis in essential thrombocythemia: prognostic interaction with age and thrombosis history

European journal of haematology, 2015-01, Vol.94 (1), p.31-36

2015

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Platelet Count Predicts Co-occurrence of Driver Mutations in Essential Thrombocythemia and Myelofibrosis with a Low JAK2 Allele Burden

Clinical lymphoma, myeloma and leukemia, 2019-09, Vol.19, p.S352-S353

2019

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FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy

Clinical chemistry and laboratory medicine, 2015-09, Vol.53 (10), p.e275

2015

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gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML

Cell death & disease, 2018-03, Vol.9 (3), p.349-8, Article 349

2018

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Gene Set Enrichment Analysis of Interaction Networks Weighted by Node Centrality

Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: A collaborative study of 1027 patients

Platelet count predicts driver mutations’ co-occurrence in low JAK2 mutated essential thrombocythemia and myelofibrosis

Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches

Value of cytogenetic abnormalities in post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a study of the MYSEC project

WWP1 germline variants are associated with normocephalic autism spectrum disorder

Koolen-de Vries Syndrome: Preliminary Observations of Topiramate Efficacy

It is time to change thrombosis risk assessment for PV and ET?

Isolation and Characterization of Multipotent Cells from Human Fetal Dermis

Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate

A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene

Culture of skeletal myoblasts from human donors aged over 40 years: dynamics of cell growth and expression of differentiation markers

The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss

Analysis of three screening methods for the detection of calreticulin gene mutations

Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia

Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations

Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia

Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study)

Positive Predictive Values and Outcomes for Uninformative Cell-Free DNA Tests: An Italian Multicentric Cytogenetic and Cytogenomic Audit of DiagnOstic Testing (ICARO Study)

A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion

Mutations and thrombosis in essential thrombocythemia: prognostic interaction with age and thrombosis history

Optimizing the Molecular Diagnosis of GALNS: Novel Methods to Define and Characterize Morquio-A Syndrome-Associated Mutations

Platelet Count Predicts Co-occurrence of Driver Mutations in Essential Thrombocythemia and Myelofibrosis with a Low JAK2 Allele Burden

FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy

gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML

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