Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consort
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Vanessa L. Horner | J. Biegel | G. Raca | F. Mikhail | Lina Shao | A. Dubuc | B. Hirsch | L. Cooley | D. Wolff | S. Newman
[1] Trevor J Pugh,et al. Assessing genome-wide copy number aberrations and copy-neutral loss-of-heterozygosity as best practice: An evidence-based review from the Cancer Genomics Consortium working group for plasma cell disorders. , 2018, Cancer genetics.
[2] S. Kantarci,et al. Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia. , 2018, Cancer genetics.
[3] M. Slovak,et al. Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group. , 2018, Cancer genetics.
[4] M. Slovak,et al. Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative n , 2018, Cancer genetics.
[5] S. Jhanwar,et al. Gain of chromosome 1q portends worse prognosis in multiple myeloma despite novel agent-based induction regimens and autologous transplantation , 2017, Leukemia & lymphoma.
[6] W. Chung,et al. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics , 2016, Genetics in Medicine.
[7] Lina Shao,et al. Genome-Wide Single-Nucleotide Polymorphism Array Analysis Improves Prognostication of Acute Lymphoblastic Leukemia/Lymphoma. , 2016, The Journal of molecular diagnostics : JMD.
[8] Mario Cazzola,et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. , 2016, Blood.
[9] S. Rajkumar,et al. Updated Diagnostic Criteria and Staging System for Multiple Myeloma. , 2016, American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting.
[10] C. Harrison,et al. Blood Spotlight on iAMP21 acute lymphoblastic leukemia (ALL), a high-risk pediatric disease. , 2015, Blood.
[11] Heather L. Mulder,et al. Targetable kinase-activating lesions in Ph-like acute lymphoblastic leukemia. , 2014, The New England journal of medicine.
[12] J. Biegel,et al. Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors. , 2014, Cancer genetics.
[13] Y. Miyazaki,et al. [Revised international prognostic scoring system (IPSS-R) for myelodysplastic syndromes]. , 2013, [Rinsho ketsueki] The Japanese journal of clinical hematology.
[14] Matthew S. Lebo,et al. American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders , 2013, Genetics in Medicine.
[15] J. Korbel,et al. Criteria for Inference of Chromothripsis in Cancer Genomes , 2013, Cell.
[16] Sean Davis,et al. Chromothripsis and focal copy number alterations determine poor outcome in malignant melanoma. , 2013, Cancer research.
[17] A. Kemper,et al. An approach to family-centered coordinated co-management for individuals with conditions identified through newborn screening , 2013, Genetics in Medicine.
[18] Luca Malcovati,et al. Revised international prognostic scoring system for myelodysplastic syndromes. , 2012, Blood.
[19] E. Thorland,et al. Towards an evidence‐based process for the clinical interpretation of copy number variation , 2012, Clinical genetics.
[20] David T. W. Jones,et al. Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations , 2012, Cell.
[21] R. Hills,et al. Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials. , 2010, Blood.
[22] H. Barnard,et al. The Children's Hospital, Los Angeles , 1915 .
[23] Marilyn M. Li,et al. Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists. , 2017, The Journal of molecular diagnostics : JMD.
[24] S. South,et al. Integration of cytogenomic data for furthering the characterization of pediatric B-cell acute lymphoblastic leukemia: a multi-institution, multi-platform microarray study. , 2015, Cancer genetics.
[25] H. Hakonarson,et al. Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors. , 2012, Cancer genetics.
[26] R. Hills,et al. Refinement of cytogenetic classification in acute myeloid leukaemia: Determination of prognostic significance of rarer recurring chromosomal abnormalities amongst 5,876 younger adult patients treated in the UK Medical Research Council trials , 2010 .
[27] C. Pratt,et al. St. Jude Children's Research Hospital. , 1997, Pediatric hematology and oncology.
[28] Iscn. An international system for human cytogenetic nomenclature , 1978 .