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Clinical Utility of Microarray-Based Gene Expression Profiling in the Diagnosis and Subclassification of Leukemia: Report From the International Microarray Innovations in Leukemia Study Group

Journal of clinical oncology, 2010-05, Vol.28 (15), p.2529-2537

2010

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Clinical significance and mechanisms associated with segmental UPD

Molecular cytogenetics, 2021-07, Vol.14 (1), p.1-38, Article 38

2021

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B-lymphoblastic leukemia/lymphoma with MYC and BCL2 gene rearrangements shows evidence for clonal evolution and mitotic recombination

Journal of hematopathology, 2023-06, Vol.16 (2), p.111-117

2023

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Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy

Prenatal diagnosis, 2018-11, Vol.38 (12), p.920-923

2018

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FOXO1-FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma

Modern pathology, 2011-10, Vol.24 (10), p.1327-1335

2011

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Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes

Prenatal diagnosis, 2024-05, Vol.44 (5), p.586-594

2024

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Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency

Molecular genetics and metabolism, 2013-09, Vol.110 (1-2), p.191-194

2013

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Increased genomic instability may contribute to the development of kinase domain mutations in chronic myeloid leukemia

International journal of hematology, 2014-12, Vol.100 (6), p.567-574

2014

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Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic Neoplasms

Annals of clinical and laboratory science, 2018-05, Vol.48 (3), p.264-272

2018

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Four-Copy Number Intervals in SNP Microarray Analysis: Unique Patterns and Positions

Cytogenetic and genome research, 2014-01, Vol.144 (2), p.92-103

2014

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Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres

Chromosoma, 2011-12, Vol.120 (6), p.621-632

2011

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Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy

Orphanet journal of rare diseases, 2007-02, Vol.2 (1), p.9-9, Article 9

2007

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Unusual concurrence of T-cell large granular lymphocytic leukemia with Franklin disease (gamma heavy chain disease) manifested with massive splenomegaly

Leukemia & lymphoma, 2013-01, Vol.54 (1), p.205-208

2013

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Intraventricular twin fetuses in fetu

Journal of neurosurgery. Pediatrics, 2012-01, Vol.9 (1), p.17

2012

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Oncogene amplification in transforming myelodysplasia

Experimental and molecular pathology, 2005-10, Vol.79 (2), p.168-175

2005

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49. Cryptic Triple Hit Lymphoma: What's hiding in those chromosomes? A chromosome, FISH and microarray story

Cancer genetics, 2021-04, Vol.252-253, p.S17-S17

2021

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4. ETV6-ABL1 variant rearrangement described in a childhood ALL patient

Cancer genetics, 2021-04, Vol.252-253, p.S2-S2

2021

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Cytogenetic, Morphologic and Oncogene Analysis of a Cell Line Derived from a Heterologous Mixed Mullerian Tumor of the Ovary

In vitro cellular & developmental biology. Animal, 1997-05, Vol.33 (5), p.325-331

1997

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Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult

American journal of medical genetics, 1995-11, Vol.59 (3), p.271-275

1995

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Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation

Journal of medical genetics, 1996-11, Vol.33 (11), p.906-911

1996

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XX sex reversal: molecular analysis of the SRY/ZFY regions

The Journal of urology, 1997-09, Vol.158 (3 Pt 2), p.1305

1997

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Cytogenetic and Molecular Evaluation in Myelodysplastic Syndrome and in Acute and Chronic Leukemia: The advent of molecular cytogenetic techniques has provided a new tool for which quantitation of residual disease or transplant monitoring may be the major advantage

Cancer control, 1997-09, Vol.4 (5), p.389-398

1997

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Clinical Utility of Microarray-Based Gene Expression Profiling in the Diagnosis and Subclassification of Leukemia: Report From the International Microarray Innovations in Leukemia Study Group

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

Clinical significance and mechanisms associated with segmental UPD

B-lymphoblastic leukemia/lymphoma with MYC and BCL2 gene rearrangements shows evidence for clonal evolution and mitotic recombination

Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy

FOXO1-FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma

Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes

Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency

Increased genomic instability may contribute to the development of kinase domain mutations in chronic myeloid leukemia

An international standardization programme towards the application of gene expression profiling in routine leukaemia diagnostics: the Microarray Innovations in LEukemia study prephase

Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic Neoplasms

Four-Copy Number Intervals in SNP Microarray Analysis: Unique Patterns and Positions

Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres

Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy

Unusual concurrence of T-cell large granular lymphocytic leukemia with Franklin disease (gamma heavy chain disease) manifested with massive splenomegaly

Intraventricular twin fetuses in fetu

Oncogene amplification in transforming myelodysplasia

49. Cryptic Triple Hit Lymphoma: What's hiding in those chromosomes? A chromosome, FISH and microarray story

4. ETV6-ABL1 variant rearrangement described in a childhood ALL patient

Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database

Cytogenetic, Morphologic and Oncogene Analysis of a Cell Line Derived from a Heterologous Mixed Mullerian Tumor of the Ovary

Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult

Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation

XX sex reversal: molecular analysis of the SRY/ZFY regions

Cytogenetic and Molecular Evaluation in Myelodysplastic Syndrome and in Acute and Chronic Leukemia: The advent of molecular cytogenetic techniques has provided a new tool for which quantitation of residual disease or transplant monitoring may be the major advantage

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