标题
Array CGH in Human Leukemia: From Somatics to Genetics
作者
关键词
-
出版物
CYTOGENETIC AND GENOME RESEARCH
Volume 135, Issue 3-4, Pages 260-270
出版商
S. Karger AG
发表日期
2011-11-01
DOI
10.1159/000330629
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Integrated Transcript and Genome Analyses Reveal NKX2-1 and MEF2C as Potential Oncogenes in T Cell Acute Lymphoblastic Leukemia
- (2011) Irene Homminga et al. CANCER CELL
- An accumulation of cytogenetic and molecular genetic events characterizes the progression from MDS to secondary AML: an analysis of 38 paired samples analyzed by cytogenetics, molecular mutation analysis and SNP microarray profiling
- (2011) J Flach et al. LEUKEMIA
- Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance
- (2011) A Thiel et al. LEUKEMIA
- Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia
- (2011) Jun J Yang et al. NATURE GENETICS
- Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis
- (2011) Roger A Schultz et al. Molecular Cytogenetics
- Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
- (2011) Renu Bajaj et al. Molecular Cytogenetics
- Monosomy 21q22.11-q22.13 presenting as a Fanconi anemia phenotype
- (2010) Robert S. Byrd et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection
- (2010) Julien Thevenon et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients
- (2010) Eleni Katzaki et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies
- (2010) C. O'Keefe et al. BLOOD
- Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes
- (2010) Vincenza Barresi et al. GENES CHROMOSOMES & CANCER
- WT1 Synonymous Single Nucleotide Polymorphism rs16754 Correlates With Higher mRNA Expression and Predicts Significantly Improved Outcome in Favorable-Risk Pediatric Acute Myeloid Leukemia: A Report From the Children's Oncology Group
- (2010) Phoenix A. Ho et al. JOURNAL OF CLINICAL ONCOLOGY
- Array Comparative Genomic Hybridization Detects Chromosomal Abnormalities in Hematological Cancers That Are Not Detected by Conventional Cytogenetics
- (2010) Lina Shao et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Array-Based Karyotyping for Prognostic Assessment in Chronic Lymphocytic Leukemia
- (2010) Jill M. Hagenkord et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients
- (2010) M Bardini et al. LEUKEMIA
- Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes
- (2010) Daniel T. Starczynowski et al. LEUKEMIA RESEARCH
- Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
- (2010) Dalemari Crowther-Swanepoel et al. NATURE GENETICS
- Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes
- (2010) Marilyn L Slovak et al. Molecular Cytogenetics
- Detailed molecular and clinical characterization of three patients with 21q deletions
- (2009) A Lindstrand et al. CLINICAL GENETICS
- Linking somatic genetic alterations in cancer to therapeutics
- (2009) Darrin Stuart et al. CURRENT OPINION IN CELL BIOLOGY
- Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype
- (2009) T. Akagi et al. HAEMATOLOGICA
- New Lesions Detected by Single Nucleotide Polymorphism Array–Based Chromosomal Analysis Have Important Clinical Impact in Acute Myeloid Leukemia
- (2009) Ramon V. Tiu et al. JOURNAL OF CLINICAL ONCOLOGY
- Single Nucleotide Polymorphism in the Mutational Hotspot of WT1 Predicts a Favorable Outcome in Patients With Cytogenetically Normal Acute Myeloid Leukemia
- (2009) Frederik Damm et al. JOURNAL OF CLINICAL ONCOLOGY
- Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics
- (2009) S Heinrichs et al. LEUKEMIA
- Insights into Familial Platelet Disorder with Propensity to Myeloid Malignancy (FPD/AML)
- (2009) Carolyn Owen LEUKEMIA RESEARCH
- Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation
- (2009) Saskia van der Crabben et al. LEUKEMIA RESEARCH
- FISH and SNP-A karyotyping in myelodysplastic syndromes: Improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q)
- (2009) Hideki Makishima et al. LEUKEMIA RESEARCH
- Inherited susceptibility to pediatric acute lymphoblastic leukemia
- (2009) Ross L Levine NATURE GENETICS
- A germline JAK2 SNP is associated with predisposition to the development of JAK2V617F-positive myeloproliferative neoplasms
- (2009) Outi Kilpivaara et al. NATURE GENETICS
- Germline genomic variants associated with childhood acute lymphoblastic leukemia
- (2009) Lisa R Treviño et al. NATURE GENETICS
- Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
- (2009) Elli Papaemmanuil et al. NATURE GENETICS
- Genomic analysis reveals few genetic alterations in pediatric acute myeloid leukemia
- (2009) I. Radtke et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Acquired copy number alterations in adult acute myeloid leukemia genomes
- (2009) M. J. Walter et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q
- (2008) M. Shinawi et al. BLOOD
- Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy
- (2008) C. J. Owen et al. BLOOD
- A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups
- (2008) S. Sulong et al. BLOOD
- Genome-wide copy number profiling reveals molecular evolution from diagnosis to relapse in childhood acute lymphoblastic leukemia
- (2008) J. J. Yang et al. BLOOD
- High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival
- (2008) D. T. Starczynowski et al. BLOOD
- Molecular allelokaryotyping of early-stage, untreated chronic lymphocytic leukemia
- (2008) Sören Lehmann et al. CANCER
- 250K Single Nucleotide Polymorphism Array Karyotyping Identifies Acquired Uniparental Disomy and Homozygous Mutations, Including Novel Missense Substitutions of c-Cbl, in Myeloid Malignancies
- (2008) A. J. Dunbar et al. CANCER RESEARCH
- Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21
- (2008) Robert Lyle et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions
- (2008) Mylène Béri-Dexheimer et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia—A comparative study of four differently designed, high resolution microarray platforms
- (2008) Rebeqa Gunnarsson et al. GENES CHROMOSOMES & CANCER
- Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia
- (2008) Manu Gupta et al. GENES CHROMOSOMES & CANCER
- Copy number variation at the breakpoint region of isochromosome 17q
- (2008) C. M.B. Carvalho et al. GENOME RESEARCH
- Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays
- (2008) L. Wang et al. HAEMATOLOGICA
- Whole-Genome Scanning by Array Comparative Genomic Hybridization as a Clinical Tool for Risk Assessment in Chronic Lymphocytic Leukemia
- (2008) Shelly R. Gunn et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Customized Oligonucleotide Array-Based Comparative Genomic Hybridization as a Clinical Assay for Genomic Profiling of Chronic Lymphocytic Leukemia
- (2008) Rachel Sargent et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene
- (2008) Shelly R. Gunn et al. LEUKEMIA RESEARCH
- A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia
- (2008) Maria Chiara Di Bernardo et al. NATURE GENETICS
- Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia
- (2008) Karen R. Rabin et al. PEDIATRIC BLOOD & CANCER
- Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease
- (2008) K. Paulsson et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia
- (2007) Ankita Patel et al. AMERICAN JOURNAL OF HEMATOLOGY
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