Published in Med Oncol on May 01, 2013
Identifying the similarities and differences between single nucleotide polymorphism array (SNPa) analysis and karyotyping in acute myeloid leukemia and myelodysplastic syndromes. Rev Bras Hematol Hemoter (2014) 0.80
CMTM4 is frequently downregulated and functions as a tumour suppressor in clear cell renal cell carcinoma. J Exp Clin Cancer Res (2015) 0.78
Double inv(3)(q21q26.2) in acute myeloid leukemia is resulted from an acquired copy neutral loss of heterozygosity of chromosome 3q and associated with disease progression. Mol Cytogenet (2015) 0.75
Use of single nucleotide polymorphism array technology to improve the identification of chromosomal lesions in leukemia. Curr Cancer Drug Targets (2013) 0.75
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet (2010) 13.70
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nat Genet (2006) 5.59
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Hum Mutat (2007) 3.52
Spinal Implants Can Be Inserted in Patients With Deep Spine Infection: Results From a Large Cohort Study. Spine (Phila Pa 1976) (2017) 2.02
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. Genome Res (2008) 1.81
A novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B gene. Cancer Genet Cytogenet (2004) 1.77
Insights from genomic microarrays into structural chromosome rearrangements. Am J Med Genet A (2005) 1.29
Germline DNA copy number variation in familial and early-onset breast cancer. Breast Cancer Res (2012) 1.24
Structural variation in the human genome: the impact of copy number variants on clinical diagnosis. Genet Med (2007) 1.21
Psychosocial adaptation and quality of life among Brazilian patients with different hematological malignancies. J Psychosom Res (2006) 1.21
Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion. Eur J Hum Genet (2007) 1.18
Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and prognostic parameters in primary cutaneous large B-cell lymphoma. J Clin Oncol (2005) 1.12
Array comparative genomic hybridization with cyanin cis-platinum-labeled DNAs. Biotechniques (2004) 1.09
Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH. Am J Med Genet A (2007) 1.08
Germline copy number variations and cancer predisposition. Future Oncol (2012) 1.07
Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH. Nucleic Acids Res (2004) 1.05
Chromosomal instability in MYH- and APC-mutant adenomatous polyps. Cancer Res (2006) 1.02
Deletion of the RMGA and CHD2 genes in a child with epilepsy and mental deficiency. Eur J Med Genet (2011) 1.01
Report of a del22q11 in a patient with Mayer-Rokitansky-Küster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women. Am J Med Genet A (2006) 1.00
Primary synovial sarcoma of the heart: a cytogenetic and molecular genetic analysis combining RT-PCR and COBRA-FISH of a case with a complex karyotype. Mod Pathol (2004) 1.00
TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia. Orphanet J Rare Dis (2013) 0.98
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia (2010) 0.93
Genomic array and expression analysis of frequent high-level amplifications in adenocarcinomas of the gastro-esophageal junction. Cancer Genet Cytogenet (2006) 0.90
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome. Am J Med Genet A (2005) 0.89
Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell lines. Cancer Genet Cytogenet (2006) 0.89
A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation. Am J Med Genet A (2010) 0.87
Isochromosome 17q in MDS: a marker of a distinct entity. Cancer Genet Cytogenet (2006) 0.87
SAGE analysis highlights the importance of p53csv, ddx5, mapkapk2 and ranbp2 to multiple myeloma tumorigenesis. Cancer Lett (2009) 0.87
Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma. Cancer Genet Cytogenet (2007) 0.86
Altered immunophenotypic features of peripheral blood platelets in myelodysplastic syndromes. Haematologica (2012) 0.86
5q12.1 deletion: delineation of a phenotype including mental retardation and ocular defects. Am J Med Genet A (2011) 0.86
Chronic myeloid leukemia in an XX male. Cancer Genet Cytogenet (2007) 0.83
A monoclonal antibody-based immunoassay for measuring the potency of 2009 pandemic influenza H1N1 vaccines. Influenza Other Respir Viruses (2014) 0.83
Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum. Am J Med Genet A (2013) 0.83
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization. Am J Med Genet A (2011) 0.82
Down-regulation of ANAPC13 and CLTCL1: Early Events in the Progression of Preinvasive Ductal Carcinoma of the Breast. Transl Oncol (2012) 0.82
FLT3 internal tandem duplication during myelodysplastic syndrome follow-up: a marker of transformation to acute myeloid leukemia. Cancer Genet Cytogenet (2008) 0.82
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome. Am J Med Genet A (2007) 0.81
Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion. BMC Cancer (2012) 0.81
The 5q- syndrome and autoimmune phenomena: report of three cases. Leuk Res (2005) 0.80
Molecular and clinical delineation of the 17q22 microdeletion phenotype. Eur J Hum Genet (2013) 0.80
LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis. Melanoma Res (2015) 0.80
A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate. Eur J Med Genet (2013) 0.80
Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8. Cancer Genet Cytogenet (2004) 0.80
A complex rearrangement on chromosome 22 affecting both homologues; haplo-insufficiency of the Cat eye syndrome region may have no clinical relevance. Hum Genet (2006) 0.80
Combined flow cytometric assessment of CD45, HLA-DR, CD34, and CD117 expression is a useful approach for reliable quantification of blast cells in myelodysplastic syndromes. Cytometry B Clin Cytom (2013) 0.79
Number of rare germline CNVs and TP53 mutation types. Orphanet J Rare Dis (2012) 0.79
Application of multicolor fluorescence in situ hybridization analysis for detection of cross-contamination and in vitro progression in commonly used murine tumor cell lines. Cancer Genet Cytogenet (2002) 0.78
Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. Am J Med Genet A (2012) 0.78
The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations. Orphanet J Rare Dis (2014) 0.78
A prediction tool for nosocomial multi-drug Resistant Gram-Negative Bacilli infections in critically ill patients - prospective observational study. BMC Infect Dis (2014) 0.78
Multiple supernumerary ring chromosomes of different origin in a patient: a clinical report and review of the literature. Am J Med Genet A (2003) 0.77
Chronic myeloid leukemia following kidney transplantation. Leuk Res (2005) 0.77
Germline BAX deletion in a patient with melanoma and gastrointestinal stromal tumor. Am J Gastroenterol (2013) 0.77
Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation. Am J Med Genet A (2010) 0.77
Adding FISH to karyotype in Myelodysplastic syndrome investigation diagnosis: are all questions answered? Leuk Res (2009) 0.77
Array-CGH as an adjuvant tool in cytogenetic diagnosis of pediatric MDS and JMML. Med Oncol (2013) 0.77
A microdeletion in Alzheimer's disease disrupts NAMPT gene. J Genet (2014) 0.76
Expression of eight genes of nuclear factor-kappa B pathway in multiple myeloma using bone marrow aspirates obtained at diagnosis. Histol Histopathol (2009) 0.76
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state. Eur J Med Genet (2012) 0.75
Association of myelodysplastic syndrome with CD5+, CD23+ monoclonal B-cell lymphocytosis. Clinics (Sao Paulo) (2012) 0.75
Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas. Future Oncol (2014) 0.75
Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast. Tumour Biol (2014) 0.75
Iron staining in gammopathy-related crystal-storing histiocytosis: a misleading feature to the differential diagnosis with Gaucher's disease. Mol Genet Metab (2013) 0.75
Amphotericin B-induced severe hypertension in a young patient: case report and review of the literature. Ren Fail (2006) 0.75
Aggressive systemic mastocytosis: is there a role for trisomy 8? Leuk Res (2004) 0.75
Response to the Letter: Spinal Implants Can be Inserted in Patients With Deep Spine Infection-Results from a Large Cohort Study. Spine (Phila Pa 1976) (2017) 0.75
A rare case of acute myeloid leukemia evolving from a myelodysplastic syndrome with der(19)t(1;19). Cancer Genet Cytogenet (2006) 0.75
Trisomies 14 and 22 in acute myelocytic leukemia with multilineage dysplasia. Cancer Genet Cytogenet (2004) 0.75
Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family. Int J Audiol (2015) 0.75
Large germline copy number variations as predisposing factor in childhood neoplasms. Future Oncol (2014) 0.75
FLT3 mutation and AML/ETO in a case of Myelodysplastic syndrome in transformation corroborates the two hit model of leukemogenesis. Leuk Res (2006) 0.75
TO THE EDITOR. Spine (Phila Pa 1976) (2017) 0.75