Literature DB >> 27124785

Section E6.1-6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalities.

Fady M Mikhail1, Nyla A Heerema2, Kathleen W Rao3,4,5, Rachel D Burnside6, Athena M Cherry7, Linda D Cooley8.   

Abstract

DISCLAIMER: These American College of Medical Genetics and Genomics standards and guidelines are developed primarily as an educational resource for clinical laboratory geneticists to help them provide quality clinical laboratory genetic services. Adherence to these standards and guidelines is voluntary and does not necessarily ensure a successful medical outcome. These standards and guidelines should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, the clinical laboratory geneticist should apply his or her own professional judgment to the specific circumstances presented by the individual patient or specimen. Clinical laboratory geneticists are encouraged to document in the patient's record the rationale for the use of a particular procedure or test, whether or not it is in conformance with these standards and guidelines. They also are advised to take notice of the date any particular guideline was adopted, and to consider other relevant medical and scientific information that becomes available after that date. It also would be prudent to consider whether intellectual property interests may restrict the performance of certain tests and other procedures.Cytogenetic analyses of hematological neoplasms are performed to detect and characterize clonal chromosomal abnormalities that have important diagnostic, prognostic, and therapeutic implications. At the time of diagnosis, cytogenetic abnormalities assist in the diagnosis of such disorders and can provide important prognostic information. At the time of relapse, cytogenetic analysis can be used to confirm recurrence of the original neoplasm, detect clonal disease evolution, or uncover a new unrelated neoplastic process. This section deals specifically with the standards and guidelines applicable to chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalities. This updated Section E6.1-6.4 has been incorporated into and supersedes the previous Section E6 in Section E: Clinical Cytogenetics of the 2009 Edition (Revised 01/2010), American College of Medical Genetics and Genomics Standards and Guidelines for Clinical Genetics Laboratories.Genet Med 18 6, 635-642.

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Year:  2016        PMID: 27124785     DOI: 10.1038/gim.2016.50

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  32 in total

Review 1.  World health organization classification, evaluation, and genetics of the myeloproliferative neoplasm variants.

Authors:  James Vardiman; Elizabeth Hyjek
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2011

2.  Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance.

Authors:  A Thiel; M Beier; D Ingenhag; K Servan; M Hein; V Moeller; B Betz; B Hildebrandt; C Evers; U Germing; B Royer-Pokora
Journal:  Leukemia       Date:  2011-01-28       Impact factor: 11.528

3.  Comparison of array comparative genomic hybridization (aCGH) to FISH and cytogenetics in prognostic evaluation of chronic lymphocytic leukemia.

Authors:  D P O'Malley; C Giudice; A S Chang; D Chang; T S Barry; M K Hibbard; R Chen; S-T Chen
Journal:  Int J Lab Hematol       Date:  2010-12-09       Impact factor: 2.877

4.  Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia.

Authors:  Brian Parkin; Harry Erba; Peter Ouillette; Diane Roulston; Anjali Purkayastha; Judith Karp; Moshe Talpaz; Lisa Kujawski; Sajid Shakhan; Cheng Li; Kerby Shedden; Sami N Malek
Journal:  Blood       Date:  2010-08-20       Impact factor: 22.113

5.  Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?

Authors:  Athena M Cherry; Marilyn L Slovak; Lynda J Campbell; Kathy Chun; Virginie Eclache; Detlef Haase; Claudia Haferlach; Barbara Hildebrandt; Anwar M Iqbal; Suresh C Jhanwar; Kazuma Ohyashiki; Francesc Sole; Peter Vandenberghe; Daniel L VanDyke; Yanming Zhang; Gordon W Dewald
Journal:  Leuk Res       Date:  2012-04-25       Impact factor: 3.156

6.  Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia.

Authors:  Annet Simons; Marian Stevens-Kroef; Najat El Idrissi-Zaynoun; Sabine van Gessel; Daniel Olde Weghuis; Eva van den Berg; Esmé Waanders; Peter Hoogerbrugge; Roland Kuiper; Ad Geurts van Kessel
Journal:  Genes Chromosomes Cancer       Date:  2011-08-31       Impact factor: 5.006

7.  Consensus recommendations for standard investigative workup: report of the International Myeloma Workshop Consensus Panel 3.

Authors:  Meletios Dimopoulos; Robert Kyle; Jean-Paul Fermand; S Vincent Rajkumar; Jesus San Miguel; Asher Chanan-Khan; Heinz Ludwig; Douglas Joshua; Jayesh Mehta; Morie Gertz; Hervé Avet-Loiseau; Meral Beksaç; Kenneth C Anderson; Philippe Moreau; Seema Singhal; Hartmut Goldschmidt; Mario Boccadoro; Shaji Kumar; Sergio Giralt; Nikhil C Munshi; Sundar Jagannath
Journal:  Blood       Date:  2011-02-03       Impact factor: 22.113

8.  IL-4 improves the detection of cytogenetic abnormalities in multiple myeloma and increases the proportion of clonally abnormal metaphases.

Authors:  J M Hernández; N C Gutiérrez; J Almeida; J L García; M A Sánchez; G Mateo; A Ríos; J F San Miguel
Journal:  Br J Haematol       Date:  1998-10       Impact factor: 6.998

9.  High detection rate of clinically relevant genomic abnormalities in plasma cells enriched from patients with multiple myeloma.

Authors:  Marian Stevens-Kroef; Daniel Olde Weghuis; Sandra Croockewit; Leo Derksen; Jeroen Hooijer; Najat Elidrissi-Zaynoun; Angelique Siepman; Annet Simons; Ad Geurts van Kessel
Journal:  Genes Chromosomes Cancer       Date:  2012-07-25       Impact factor: 5.006

Review 10.  Diagnosis and risk stratification in multiple myeloma.

Authors:  Niels W C J van de Donk; Pieter Sonneveld
Journal:  Hematol Oncol Clin North Am       Date:  2014-07-22       Impact factor: 3.722

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  6 in total

1.  Metaphase cytogenetics and plasma cell proliferation index for risk stratification in newly diagnosed multiple myeloma.

Authors:  Patrick W Mellors; Moritz Binder; Rhett P Ketterling; Patricia T Greipp; Linda B Baughn; Jess F Peterson; Dragan Jevremovic; Kathryn E Pearce; Francis K Buadi; Martha Q Lacy; Morie A Gertz; Angela Dispenzieri; Suzanne R Hayman; Prashant Kapoor; Wilson I Gonsalves; Yi L Hwa; Amie Fonder; Miriam Hobbs; Taxiarchis Kourelis; Rahma Warsame; John A Lust; Nelson Leung; Ronald S Go; Robert A Kyle; S Vincent Rajkumar; Shaji K Kumar
Journal:  Blood Adv       Date:  2020-05-26

Review 2.  Diagnostic and Prognostic Utility of Fluorescence In situ Hybridization (FISH) Analysis in Acute Myeloid Leukemia.

Authors:  Patrick R Gonzales; Fady M Mikhail
Journal:  Curr Hematol Malig Rep       Date:  2017-12       Impact factor: 3.952

3.  Interoperable genetic lab test reports: mapping key data elements to HL7 FHIR specifications and professional reporting guidelines.

Authors:  Aly Khalifa; Clinton C Mason; Jennifer Hornung Garvin; Marc S Williams; Guilherme Del Fiol; Brian R Jackson; Steven B Bleyl; Gil Alterovitz; Stanley M Huff
Journal:  J Am Med Inform Assoc       Date:  2021-11-25       Impact factor: 7.942

4.  Clinical Impact of Genomic Information in Pediatric Leukemia.

Authors:  Emilie Lalonde; Gerald Wertheim; Marilyn M Li
Journal:  Front Pediatr       Date:  2017-12-14       Impact factor: 3.418

5.  Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping.

Authors:  Kornelia Neveling; Tuomo Mantere; Susan Vermeulen; Michiel Oorsprong; Ronald van Beek; Ellen Kater-Baats; Marc Pauper; Guillaume van der Zande; Dominique Smeets; Daniel Olde Weghuis; Marian J P L Stevens-Kroef; Alexander Hoischen
Journal:  Am J Hum Genet       Date:  2021-07-07       Impact factor: 11.025

Review 6.  Fluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research Applications.

Authors:  Chenghua Cui; Wei Shu; Peining Li
Journal:  Front Cell Dev Biol       Date:  2016-09-05
  6 in total

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