Published in Melanoma Res on April 01, 2015
DNA Methylation Levels of Melanoma Risk Genes Are Associated with Clinical Characteristics of Melanoma Patients. Biomed Res Int (2015) 0.77
Global methylation of blood leukocyte DNA and risk of melanoma. Int J Cancer (2017) 0.77
Genome-wide methylation sequencing of paired primary and metastatic cell lines identifies common DNA methylation changes and a role for EBF3 as a candidate epigenetic driver of melanoma metastasis. Oncotarget (2016) 0.75
Low Expression of Mir-137 Predicts Poor Prognosis in Cutaneous Melanoma Patients. Med Sci Monit (2016) 0.75
Eukaryotic cytosine methyltransferases. Annu Rev Biochem (2005) 15.45
Aging and environmental exposures alter tissue-specific DNA methylation dependent upon CpG island context. PLoS Genet (2009) 7.07
Accounting for cellular heterogeneity is critical in epigenome-wide association studies. Genome Biol (2014) 3.89
CDKN2A mutations in multiple primary melanomas. N Engl J Med (1998) 3.52
DNA methylation and cancer. Adv Genet (2010) 3.50
Methylation at global LINE-1 repeats in human blood are affected by gender but not by age or natural hormone cycles. PLoS One (2011) 1.96
Blood leukocyte DNA hypomethylation and gastric cancer risk in a high-risk Polish population. Int J Cancer (2010) 1.67
Is there a link between genome-wide hypomethylation in blood and cancer risk? Cancer Prev Res (Phila) (2012) 1.61
LINE-1 hypomethylation is associated with bladder cancer risk among nonsmoking Chinese. Int J Cancer (2011) 1.56
Global DNA hypomethylation in peripheral blood leukocytes as a biomarker for cancer risk: a meta-analysis. PLoS One (2012) 1.43
Genetic risk factors for melanoma. Hum Genet (2009) 1.21
Comparison of methods for quantification of global DNA methylation in human cells and tissues. PLoS One (2013) 1.14
LINE-1 methylation levels in leukocyte DNA and risk of renal cell cancer. PLoS One (2011) 1.11
Global DNA hypomethylation in peripheral blood mononuclear cells as a biomarker of cancer risk. Cancer Epidemiol Biomarkers Prev (2013) 1.01
Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer. Epigenetics (2013) 0.94
Association of hypomethylation of LINE-1 repetitive element in blood leukocyte DNA with an increased risk of hepatocellular carcinoma. J Zhejiang Univ Sci B (2011) 0.88
LINE-1 methylation in peripheral blood and the risk of melanoma in melanoma-prone families with and without CDKN2A mutations. Melanoma Res (2013) 0.84
An epi [c] genetic battle: LINE-1 retrotransposons and intragenomic conflict in humans. Mob Genet Elements (2011) 0.81
Epigenetic choreography of stem cells: the DNA demethylation episode of development. Cell Mol Life Sci (2013) 0.80
Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutations. Exp Mol Pathol (2014) 0.79
Epigenetic markers of prognosis in melanoma. Methods Mol Biol (2014) 0.78
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
Swine and poultry pathogens: the complete genome sequences of two strains of Mycoplasma hyopneumoniae and a strain of Mycoplasma synoviae. J Bacteriol (2005) 2.15
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
Analysis and functional annotation of an expressed sequence tag collection for tropical crop sugarcane. Genome Res (2003) 1.70
The genome sequence of the gram-positive sugarcane pathogen Leifsonia xyli subsp. xyli. Mol Plant Microbe Interact (2004) 1.65
Gene stage-specific expression in the microenvironment of pediatric myelodysplastic syndromes. Leuk Res (2006) 1.62
Evidence that molecular changes in cells occur before morphological alterations during the progression of breast ductal carcinoma. Breast Cancer Res (2008) 1.38
Expression of putative pathogenicity-related genes in Xylella fastidiosa grown at low and high cell density conditions in vitro. FEMS Microbiol Lett (2003) 1.31
Insights from genomic microarrays into structural chromosome rearrangements. Am J Med Genet A (2005) 1.29
EGene: a configurable pipeline generation system for automated sequence analysis. Bioinformatics (2005) 1.24
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
Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion. Eur J Hum Genet (2007) 1.18
Epigenetic silencing of CRABP2 and MX1 in head and neck tumors. Neoplasia (2009) 1.14
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
Generation of longer 3' cDNA fragments from massively parallel signature sequencing tags. Nucleic Acids Res (2004) 1.07
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
A genome survey of Moniliophthora perniciosa gives new insights into Witches' Broom Disease of cacao. BMC Genomics (2008) 1.03
Chromosomal instability in MYH- and APC-mutant adenomatous polyps. Cancer Res (2006) 1.02
Polybromo-1 (PBRM1), a SWI/SNF complex subunit is a prognostic marker in clear cell renal cell carcinoma. BJU Int (2013) 1.01
Deletion of the RMGA and CHD2 genes in a child with epilepsy and mental deficiency. Eur J Med Genet (2011) 1.01
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
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
TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia. Orphanet J Rare Dis (2013) 0.98
The mitochondrial genome of the phytopathogenic basidiomycete Moniliophthora perniciosa is 109 kb in size and contains a stable integrated plasmid. Mycol Res (2008) 0.97
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia (2010) 0.93
Differential gene expression between the biotrophic-like and saprotrophic mycelia of the witches' broom pathogen Moniliophthora perniciosa. Mol Plant Microbe Interact (2008) 0.91
Amyloid-β oligomers induce differential gene expression in adult human brain slices. J Biol Chem (2012) 0.91
International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation. Breast Cancer Res Treat (2010) 0.91
Genomic array and expression analysis of frequent high-level amplifications in adenocarcinomas of the gastro-esophageal junction. Cancer Genet Cytogenet (2006) 0.90
Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour. Eur J Cancer (2011) 0.89
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
Molecular profiling of isolated histological components of wilms tumor implicates a common role for the Wnt signaling pathway in kidney and tumor development. Oncology (2008) 0.86
Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma. Cancer Genet Cytogenet (2007) 0.86
5q12.1 deletion: delineation of a phenotype including mental retardation and ocular defects. Am J Med Genet A (2011) 0.86
Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: case report. BMC Med Genet (2011) 0.85
Evaluation of quantitative rt-PCR using nonamplified and amplified RNA. Diagn Mol Pathol (2010) 0.83
Mutation spectrum in South American Lynch syndrome families. Hered Cancer Clin Pract (2013) 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
Single-nucleotide polymorphism-array improves detection rate of genomic alterations in core-binding factor leukemia. Med Oncol (2013) 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
Primary cutaneous melanoma arising in agminated melanocytic nevi: CDKN2A and CDK4 mutation screening. Acta Derm Venereol (2012) 0.82
Alternative splicing enriched cDNA libraries identify breast cancer-associated transcripts. BMC Genomics (2010) 0.82
Transcriptional alterations related to neuropathology and clinical manifestation of Alzheimer's disease. PLoS One (2012) 0.82
Gene network analyses point to the importance of human tissue kallikreins in melanoma progression. BMC Med Genomics (2011) 0.81
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
Morphologic and clinical effects of subretinal injection of indocyanine green and infracyanine green in rabbits. J Ocul Pharmacol Ther (2008) 0.81
A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate. Eur J Med Genet (2013) 0.80
Ductal carcinoma in situ of the breast: morphological and molecular features implicated in progression. Biosci Rep (2013) 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
Gene expression of peripheral blood lymphocytes may discriminate patients with schizophrenia from controls. Psychiatry Res (2012) 0.80
Characterization of SCAR markers of Eimeria spp. of domestic fowl and construction of a public relational database (The Eimeria SCARdb). FEMS Microbiol Lett (2004) 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
Molecular and clinical delineation of the 17q22 microdeletion phenotype. Eur J Hum Genet (2013) 0.80
Number of rare germline CNVs and TP53 mutation types. Orphanet J Rare Dis (2012) 0.79
Early gene expression changes in skeletal muscle from SOD1(G93A) amyotrophic lateral sclerosis animal model. Cell Mol Neurobiol (2014) 0.79
No-match ORESTES explored as tumor markers. Nucleic Acids Res (2009) 0.79
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
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
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
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
Array-CGH as an adjuvant tool in cytogenetic diagnosis of pediatric MDS and JMML. Med Oncol (2013) 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
A microdeletion in Alzheimer's disease disrupts NAMPT gene. J Genet (2014) 0.76
Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas. Future Oncol (2014) 0.75
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state. Eur J Med Genet (2012) 0.75
Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast. Tumour Biol (2014) 0.75
Large germline copy number variations as predisposing factor in childhood neoplasms. Future Oncol (2014) 0.75
Identification and complete sequencing of novel human transcripts through the use of mouse orthologs and testis cDNA sequences. Genet Mol Res (2004) 0.75
Germline Mutations in MLH1 Leading to Isolated Loss of PMS2 Expression in Lynch Syndrome: Implications for Diagnostics in the Clinic. Am J Surg Pathol (2017) 0.75
Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family. Int J Audiol (2015) 0.75