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Replication timing influences DNA copy number determination by array-CGH

BioTechniques, 2013-11, Vol.55 (5), p.231-232

2013

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Induced G1 phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH

BioTechniques, 2012-10, Vol.53 (4), p.245-248

2012

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Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency

Haematologica (Roma), 2011-12, Vol.96 (12), p.1892-1894

2011

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Assessment of Differentiation and Progression of Hepatic Tumors Using Array-Based Comparative Genomic Hybridization

Clinical gastroenterology and hepatology, 2006-10, Vol.4 (10), p.1283-1291

2006

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Clonal heterogeneity in childhood myelodysplastic syndromes-Challenge for the detection of chromosomal imbalances by array-CGH

Genes chromosomes & cancer, 2010-10, Vol.49 (10), p.885-900

2010

Volltextzugriff (PDF)

Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?

Haematologica (Roma), 2010-09, Vol.95 (9), p.1616-1616

2010

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Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle cell lymphomas

Haematologica (Roma), 2007-04, Vol.92 (4), p.460-468

2007

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The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants

International journal of cancer, 2019-06, Vol.144 (11), p.2683-2694

2019

Volltextzugriff (PDF)

Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP‐BFM acute lymphoblastic leukemia protocol

Genes chromosomes & cancer, 2020-11, Vol.59 (11), p.667-671

2020

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Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotype

Genes chromosomes & cancer, 2021-06, Vol.60 (6), p.452-457

2021

Volltextzugriff (PDF)

Frequency and prognostic impact of PAX5 p. P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP‐BFM acute lymphoblastic leukemia protocol

Genes chromosomes & cancer, 2020-11, Vol.59 (11), p.667-671

2020

Volltextzugriff (PDF)

BCR-ABL1 positive AML or CML in blast crisis? A pediatric case report with inv(3) and t(9;22) in the initial clone

Cancer genetics, 2021-06, Vol.254-255, p.70-74

2021

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Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase

Scientific reports, 2016-12, Vol.6 (1), p.38198, Article 38198

2016

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GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families

Genes & cancer, 2017-01, Vol.8 (1-2), p.472-483

2017

Volltextzugriff (PDF)

No evidence for ITSN1 loss in a patient with mental retardation and complex chromosomal rearrangements of 21q21–21q22

Leukemia research, 2013-06, Vol.37 (6), p.721-723

2013

Volltextzugriff (PDF)

Induced Gl phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH

BioTechniques, 2012, Vol.53 (4), p.245-248

2012

Volltextzugriff (PDF)

Gene-expression profiles and their association with drug resistance in adult acute myeloid leukemia

Haematologica (Roma), 2005-11, Vol.90 (11), p.1484-1492

2005

Volltextzugriff (PDF)

Array-CGH in childhood MDS

Methods in molecular biology (Clifton, N.J.), 2013, Vol.973, p.267

2013

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Gain of the Centromeric Region of Chromosome 8, a New Germline Alteration In Juvenile Myelomonocytic Leukemia

Blood, 2010-11, Vol.116 (21), p.4830-4830

2010

Volltextzugriff (PDF)

Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease

Genes chromosomes & cancer, 2008-06, Vol.47 (6), p.471-480

2008

Volltextzugriff (PDF)

Significance of Copy Number Alterations for Molecular Treatment Response in Childhood Acute Lymphoblastic Leukemia

Blood, 2007-11, Vol.110 (11), p.1434-1434

2007

Volltextzugriff (PDF)

Gain of Chromosome 21 Is Associated with Early Treatment Sensitivity in Childhood Acute Lymphoblastic Leukemia

Blood, 2005-11, Vol.106 (11), p.1440-1440

2005

Volltextzugriff (PDF)

Analysis of Array-CGH Data Using the R and Bioconductor Software Suite

Comparative and functional genomics, 2009-01, Vol.2009, p.201325-8

2009

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Drug-Response Signature Predicts Outcome in Adult Acute Myeloid Leukemia and Associates Poor Response with Molecular Characteristics of Hematopoietic Stem Cells

Blood, 2004-11, Vol.104 (11), p.2024-2024

2004

Volltextzugriff (PDF)

Characterization of Secondary Alterations in Mantle Cell Lymphomas Using Matrix-/Array CGH

Blood, 2004-11, Vol.104 (11), p.4349-4349

2004

Volltextzugriff (PDF)

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Replication timing influences DNA copy number determination by array-CGH

Induced G1 phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH

Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency

Assessment of Differentiation and Progression of Hepatic Tumors Using Array-Based Comparative Genomic Hybridization

Clonal heterogeneity in childhood myelodysplastic syndromes-Challenge for the detection of chromosomal imbalances by array-CGH

Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?

Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle cell lymphomas

The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants

Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP‐BFM acute lymphoblastic leukemia protocol

Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotype

Frequency and prognostic impact of PAX5 p. P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP‐BFM acute lymphoblastic leukemia protocol

BCR-ABL1 positive AML or CML in blast crisis? A pediatric case report with inv(3) and t(9;22) in the initial clone

Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase

GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families

No evidence for ITSN1 loss in a patient with mental retardation and complex chromosomal rearrangements of 21q21–21q22

Induced Gl phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH

Gene-expression profiles and their association with drug resistance in adult acute myeloid leukemia

Array-CGH in childhood MDS

Gain of the Centromeric Region of Chromosome 8, a New Germline Alteration In Juvenile Myelomonocytic Leukemia

Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease

Significance of Copy Number Alterations for Molecular Treatment Response in Childhood Acute Lymphoblastic Leukemia

Gain of Chromosome 21 Is Associated with Early Treatment Sensitivity in Childhood Acute Lymphoblastic Leukemia

Analysis of Array-CGH Data Using the R and Bioconductor Software Suite

Drug-Response Signature Predicts Outcome in Adult Acute Myeloid Leukemia and Associates Poor Response with Molecular Characteristics of Hematopoietic Stem Cells

Characterization of Secondary Alterations in Mantle Cell Lymphomas Using Matrix-/Array CGH

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