Aurelia M Meloni-Ehrig

Summary

Affiliation: Quest Diagnostics
Country: USA

Publications

  1. ncbi request reprint Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia
    Aurelia M Meloni-Ehrig
    Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 161:82-5. 2005
  2. doi request reprint Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma
    Aurelia Meloni-Ehrig
    Department of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 191:43-5. 2009
  3. doi request reprint Cytogenetics and genetics of human cancer: methods and accomplishments
    Avery A Sandberg
    Cancer Genet Cytogenet 203:102-26. 2010
  4. ncbi request reprint Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion
    Carlos A Tirado
    Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 161:70-3. 2005
  5. ncbi request reprint Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies
    Carlos A Tirado
    Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 170:61-4. 2006
  6. doi request reprint Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia
    Joann C Kelly
    Cytogenetics Department, Quest Diagnostics Nichols Institute, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 192:36-9. 2009
  7. doi request reprint Exon scanning by reverse transcriptase-polymerase chain reaction for detection of known and novel EML4-ALK fusion variants in non-small cell lung cancer
    Heather R Sanders
    Department of Hematology and Oncology, Quest Diagnostics Nichols Institute, San Juan Capistrano, CA, USA
    Cancer Genet 204:45-52. 2011
  8. ncbi request reprint Commentary on ISCN 2005
    Aurelia M Meloni-Ehrig
    Cancer Genet Cytogenet 175:89-90. 2007

Detail Information

Publications8

  1. ncbi request reprint Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia
    Aurelia M Meloni-Ehrig
    Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 161:82-5. 2005
    ..Fluorescence in situ hybridization performed using the probes TEL/AML1 and immunoglobulin heavy chain (IGH) showed no fusion involving the TEL and AML1 genes and only a single IGH signal in 20% of the interphase cells analyzed...
  2. doi request reprint Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma
    Aurelia Meloni-Ehrig
    Department of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 191:43-5. 2009
    ..We postulate that the t(2;8)(q35;q13) is a specific abnormality in congenital ERMS, and that it involves the PAX3 gene at 2q35 and a non-yet identified gene at 8q13...
  3. doi request reprint Cytogenetics and genetics of human cancer: methods and accomplishments
    Avery A Sandberg
    Cancer Genet Cytogenet 203:102-26. 2010
    ..We also look at a few of the more recent genomic developments in cancer and offer an opinion as to what all these findings add up to...
  4. ncbi request reprint Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion
    Carlos A Tirado
    Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 161:70-3. 2005
    ....
  5. ncbi request reprint Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies
    Carlos A Tirado
    Laboratory of Cytogenetics, Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 170:61-4. 2006
    ..The key mechanism might be the loss of TP53 as well as other tumor suppressor genes in 20q that may have a critical role in tumor genesis...
  6. doi request reprint Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia
    Joann C Kelly
    Cytogenetics Department, Quest Diagnostics Nichols Institute, Chantilly, VA 20151, USA
    Cancer Genet Cytogenet 192:36-9. 2009
    ..CML patients with an ABL1/ETV6 fusion historically have demonstrated a variable and sometimes transient response to treatment with imatinib mesylate, which was also the case in the present patient...
  7. doi request reprint Exon scanning by reverse transcriptase-polymerase chain reaction for detection of known and novel EML4-ALK fusion variants in non-small cell lung cancer
    Heather R Sanders
    Department of Hematology and Oncology, Quest Diagnostics Nichols Institute, San Juan Capistrano, CA, USA
    Cancer Genet 204:45-52. 2011
    ..This RT-PCR-based exon scanning approach avoids the limitations of screening only for previously identified EML4-ALK fusions and provides a simple molecular assay for fusion detection in a clinical diagnostics setting...
  8. ncbi request reprint Commentary on ISCN 2005
    Aurelia M Meloni-Ehrig
    Cancer Genet Cytogenet 175:89-90. 2007