Search Results - "Sanger, Warren G."
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1
Expression of ALK1 and p80 in Inflammatory Myofibroblastic Tumor and Its Mesenchymal Mimics: A Study of 135 Cases
Published in Modern pathology (01-09-2002)“…Abnormalities of chromosome 2p23 with expression of ALK1 and p80 occur in both inflammatory myofibroblastic tumor (IMT) and anaplastic large cell lymphoma…”
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2
Papillary tumor of the pineal region with synchronous suprasellar focus and novel cytogenetic features
Published in Human pathology (01-08-2015)“…Summary Papillary tumor of the pineal region (PTPR) is an uncommon neoplasm with variable biologic behavior. Cytogenetic and molecular diagnostic studies are…”
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3
Clonal Evolution in t(14;18)-Positive Follicular Lymphoma, Evidence for Multiple Common Pathways, and Frequent Parallel Clonal Evolution
Published in Clinical cancer research (15-11-2008)“…Purpose: Follicular lymphoma typically has acquired a t(14;18) translocation, but subsequent additional cytogenetic abnormalities contribute to disease…”
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4
A novel t(6;13)(q15;q34) translocation in a giant cell reparative granuloma (solid aneurysmal bone cyst)
Published in Human pathology (01-06-2012)“…Abstract Aneurysmal bone cyst is a rapidly growing and locally aggressive lesion that commonly affects children and young adults. Initially regarded as a…”
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5
Immunohistochemical and molecular cytogenetic evaluation of potential targets for tyrosine kinase inhibitors in Langerhans cell histiocytosis
Published in Human pathology (01-12-2012)“…Summary Langerhans cell histiocytosis is a rare disorder of Langerhans cells, a component of the dendritic cell system, with an unknown pathogenesis…”
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6
Primary follicular lymphoma of the testis in children and adolescents
Published in Journal of pediatric hematology/oncology (01-01-2012)“…This study reports 6 cases of primary follicular lymphoma of the testis (PFLT) in children and adolescents correlated with clinical presentation, pathologic…”
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7
Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations
Published in Genetics in medicine (01-04-2008)“…Cytogenetic investigations are useful for etiologic determinations of mental retardation, developmental delay, multiple congenital anomalies, and pregnancy…”
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8
Lymphoma Cytogenetics
Published in Clinics in laboratory medicine (01-12-2011)“…Lymphomas are a heterogeneous group of neoplasms with distinct morphologic, immunologic, and cytogenetic characteristics. Overlapping morphologic and…”
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9
Role of Cytogenetics and Molecular Cytogenetics in the Diagnosis of Genetic Imbalances
Published in Seminars in pediatric neurology (01-03-2007)“…Five decades ago, Tijo and Levan (1956) first recognized the correct chromosome number in man to be 46. Shortly thereafter, several chromosome aneuploid…”
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10
Pontine Tegmental Cap Dysplasia With a 2q13 Microdeletion Involving the NPHP1 Gene: Insights Into Malformations of the Mid-Hindbrain
Published in Seminars in pediatric neurology (01-03-2010)“…The case of a young man with multiple brain and somatic anomalies that presented diagnostic difficulties, is discussed in this report. A majority of his…”
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11
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
Published in Genetics in medicine (01-09-2011)“…Purpose: Copy number variants have emerged as a major cause of human disease such as autism and intellectual disabilities. Because copy number variants are…”
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12
Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
Published in American journal of human genetics (12-11-2010)“…Autism spectrum disorders (ASD) and schizophrenia are neurodevelopmental disorders for which recent evidence indicates an important etiologic role for rare…”
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13
Chronic myeloid leukemia as a secondary malignancy after ALK-positive anaplastic large cell lymphoma
Published in Human pathology (01-10-2007)“…Summary The development of Philadelphia chromosome–positive chronic myelogenous leukemia (CML) in the adolescent population is very rare. CML occurring as a…”
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14
Similar patterns of genomic alterations characterize primary mediastinal large-B-cell lymphoma and diffuse large-B-cell lymphoma
Published in Genes chromosomes & cancer (01-02-2002)“…To address the possible genetic relationship between primary mediastinal large‐B‐cell lymphoma (PMLBCL) and diffuse large‐B‐cell lymphoma (DLBCL), we compared…”
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15
Early onset, EBV− PTLD in pediatric liver-small bowel transplantation recipients: a spectrum of plasma cell neoplasms with favorable prognosis
Published in Blood (21-02-2013)“…EBV− posttransplantation lymphoproliferative disorders (PTLDs) are rare compared with EBV+ PTLDs, occur later after transplantation, and have a poor response…”
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16
Section E6.5–6.8 of the ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor–acquired chromosomal abnormalities
Published in Genetics in medicine (01-06-2016)“…Disclaimer: These ACMG standards and guidelines are developed primarily as an educational resource for clinical laboratory geneticists to help them provide…”
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17
Cyclin D1–negative mantle cell lymphoma: a clinicopathologic study based on gene expression profiling
Published in Blood (15-12-2005)“…Cyclin D1 overexpression is believed to be essential in the pathogenesis of mantle cell lymphoma (MCL). Hence, the existence of cyclin D1-negative MCL has been…”
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Genome wide copy number analysis of paediatric Burkitt lymphoma using formalin‐fixed tissues reveals a subset with gain of chromosome 13q and corresponding miRNA over expression
Published in British journal of haematology (01-11-2011)“…Summary The majority of paediatric Burkitt lymphoma (pBL) patients that relapse will die of disease, but markers for this high‐risk subset are unknown. MYC…”
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19
The proliferation gene expression signature is a quantitative integrator of oncogenic events that predicts survival in mantle cell lymphoma
Published in Cancer cell (01-02-2003)“…We used gene expression profiling to establish a molecular diagnosis of mantle cell lymphoma (MCL), to elucidate its pathogenesis, and to predict the length of…”
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20
An increased frequency of 13q deletions detected by fluorescence in situ hybridization and its impact on survival in children and adolescents with Burkitt lymphoma: results from the Children’s Oncology Group study CCG‐5961
Published in British journal of haematology (01-02-2010)“…Summary Burkitt lymphoma (BL), an aggressive B‐cell malignancy, is often curable with short intensive treatment regiments. Nearly all BLs contain…”
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