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Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer

Current genomics, 2008-09, Vol.9 (6), p.394-408

2008

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The Role of RUNX2 in Osteosarcoma Oncogenesis

Sarcoma, 2011, Vol.2011 (2011), p.81-93

2011

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Chromosome 6p amplification and cancer progression

Journal of Clinical Pathology, 2007-01, Vol.60 (1), p.1-7

2007

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Integrated Cytogenetic and High-Resolution Array CGH Analysis of Genomic Alterations Associated with MYCN Amplification

Cytogenetic and genome research, 2011-04, Vol.134 (1), p.27-39

2011

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Analysis of Segmental Duplications, Mouse Genome Synteny and Recurrent Cancer-Associated Amplicons in Human Chromosome 6p21–p12

Cytogenetic and genome research, 2010-06, Vol.128 (4), p.199-213

2010

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Genomic mechanisms and measurement of structural and numerical instability in cancer cells

Seminars in cancer biology, 2007-02, Vol.17 (1), p.5-18

2007

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Telomerase activity as a prognostic factor in neuroblastomas

Pediatric and developmental pathology, 2001-01, Vol.4 (1), p.62-67

2001

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Chronic encephalitis and epilepsy (Rasmussen's encephalitis): detection of cytomegalovirus and herpes simplex virus 1 by the polymerase chain reaction and in situ hybridization

Neurology, 1995-01, Vol.45 (1), p.108-117

1995

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The Role of Telomere Maintenance in the Spontaneous Growth Arrest of Pediatric Low-Grade Gliomas

Neoplasia (New York, N.Y.), 2006-02, Vol.8 (2), p.136-142

2006

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Use of chromogenic in situ hybridization to identify MYCN gene copy number in neuroblastoma using routine tissue sections

The American journal of surgical pathology, 2006-05, Vol.30 (5), p.635-642

2006

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Establishment of a Cytokine-Producing Anaplastic Large-Cell Lymphoma Cell Line Containing the t(2;5) Translocation: Potential Role of Cytokines in Clinical Manifestations

Leukemia & lymphoma, 2001-02, Vol.40 (5-6), p.599-611

2001

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Imatinib mesylate: An attractive alternative in young children with large, surgically challenging dermatofibrosarcoma protuberans

Pediatric blood & cancer, 2005-05, Vol.44 (5), p.511-515

2005

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Mutational specificity of alkylating agents and the influence of DNA repair

Environmental and molecular mutagenesis, 1990, Vol.15 (2), p.107-122

1990

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Anemia, blueberry-muffin rash, and hepatomegaly in a newborn infant

The Journal of pediatrics, 1996-04, Vol.128 (4), p.579-586

1996

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Association of the t(12;22)(q13;q12) EWS/ATF1 rearrangement with polyphenotypic round cell sarcoma of bone: a case report

The American journal of surgical pathology, 2005-12, Vol.29 (12), p.1673-1679

2005

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Topographical analysis of telomere length and correlation with genomic instability in whole mount prostatectomies

Journal of clinical oncology, 2009-05, Vol.27 (15_suppl), p.11107-11107

2009

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Stem cell enrichment approaches

Seminars in cancer biology, 2007-06, Vol.17 (3), p.257-264

2007

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An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma

Genes chromosomes & cancer, 2005-04, Vol.42 (4), p.392-403

2005

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Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

Oncogene, 2002-05, Vol.21 (19), p.3029-3037

2002

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Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

Oncogene, 2002-05, Vol.21 (19), p.3029-3037

2002

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Primary subcutaneous primitive neuroectodermal tumor with aggressive behavior and an unusual karyotype: case report

Pediatric and developmental pathology, 2004-09, Vol.7 (5), p.538-545

2004

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Application of Comparative Genomic Hybridization, Spectral Karyotyping, and Microarray Analysis in the Identification of Subtype-Specific Patterns of Genomic Changes in Rhabdomyosarcoma

Neoplasia (New York, N.Y.), 1999-08, Vol.1 (3), p.262-275

1999

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Detection of novel variant TMPRSS2 /ERG fusion transcripts suggests independent genomic alterations may underlie origin of multi-centric prostate cancer

Journal of clinical oncology, 2006-06, Vol.24 (18_suppl), p.10029-10029

2006

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Molecular Detection of the (2;5) Translocation of Non-Hodgkin's Lymphoma by Reverse Transcriptase-Polymerase Chain Reaction

Blood, 1995-06, Vol.85 (12), p.3416-3422

1995

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Clinical and molecular characteristics of pediatric gastrointestinal stromal tumors (GISTs)

Journal of clinical oncology, 2004-07, Vol.22 (14_suppl), p.8537-8537

2004

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Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer

The Role of RUNX2 in Osteosarcoma Oncogenesis

Chromosome 6p amplification and cancer progression

Integrated Cytogenetic and High-Resolution Array CGH Analysis of Genomic Alterations Associated with MYCN Amplification

Analysis of Segmental Duplications, Mouse Genome Synteny and Recurrent Cancer-Associated Amplicons in Human Chromosome 6p21–p12

Genomic mechanisms and measurement of structural and numerical instability in cancer cells

Telomerase activity as a prognostic factor in neuroblastomas

Chronic encephalitis and epilepsy (Rasmussen's encephalitis): detection of cytomegalovirus and herpes simplex virus 1 by the polymerase chain reaction and in situ hybridization

The Role of Telomere Maintenance in the Spontaneous Growth Arrest of Pediatric Low-Grade Gliomas

Use of chromogenic in situ hybridization to identify MYCN gene copy number in neuroblastoma using routine tissue sections

Establishment of a Cytokine-Producing Anaplastic Large-Cell Lymphoma Cell Line Containing the t(2;5) Translocation: Potential Role of Cytokines in Clinical Manifestations

Imatinib mesylate: An attractive alternative in young children with large, surgically challenging dermatofibrosarcoma protuberans

Mutational specificity of alkylating agents and the influence of DNA repair

Anemia, blueberry-muffin rash, and hepatomegaly in a newborn infant

Association of the t(12;22)(q13;q12) EWS/ATF1 rearrangement with polyphenotypic round cell sarcoma of bone: a case report

Topographical analysis of telomere length and correlation with genomic instability in whole mount prostatectomies

Stem cell enrichment approaches

An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma

Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between Rhabdomyosarcoma subtypes

Primary subcutaneous primitive neuroectodermal tumor with aggressive behavior and an unusual karyotype: case report

Application of Comparative Genomic Hybridization, Spectral Karyotyping, and Microarray Analysis in the Identification of Subtype-Specific Patterns of Genomic Changes in Rhabdomyosarcoma

Detection of novel variant TMPRSS2 /ERG fusion transcripts suggests independent genomic alterations may underlie origin of multi-centric prostate cancer

Molecular Detection of the (2;5) Translocation of Non-Hodgkin's Lymphoma by Reverse Transcriptase-Polymerase Chain Reaction

Clinical and molecular characteristics of pediatric gastrointestinal stromal tumors (GISTs)

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