Published in Int J Oncol on October 01, 2006
Tumor heterogeneity: causes and consequences. Biochim Biophys Acta (2009) 5.90
Concordance between CYP2D6 genotypes obtained from tumor-derived and germline DNA. J Natl Cancer Inst (2013) 3.35
Tracing the tumor lineage. Mol Oncol (2010) 1.56
Identification of intrinsic imaging phenotypes for breast cancer tumors: preliminary associations with gene expression profiles. Radiology (2014) 1.12
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression. Eur J Hum Genet (2010) 0.92
Metabolism and transport of tamoxifen in relation to its effectiveness: new perspectives on an ongoing controversy. Future Oncol (2014) 0.85
Molecular profiles of pre- and postoperative breast cancer tumours reveal differentially expressed genes. ISRN Oncol (2012) 0.81
Cell-lineage heterogeneity and driver mutation recurrence in pre-invasive breast neoplasia. Genome Med (2015) 0.79
Genomic and phenotypic profiles of two Brazilian breast cancer cell lines derived from primary human tumors. Oncol Rep (2013) 0.79
Selection of a breast cancer subpopulation-specific antibody using phage display on tissue sections. Immunol Res (2015) 0.79
SULT1E1 and ID2 genes as candidates for inherited predisposition to breast and ovarian cancer in Jewish women. Fam Cancer (2008) 0.76
Clinical and genetic characterization of basal cell carcinoma and breast cancer in a single patient. Springerplus (2014) 0.75
Intratumor and Intertumor Heterogeneity in Melanoma. Transl Oncol (2017) 0.75
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles. Am J Hum Genet (2008) 5.53
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nat Med (2004) 3.00
Molecular recognition by LARGE is essential for expression of functional dystroglycan. Cell (2004) 2.33
Somatic mosaicism for copy number variation in differentiated human tissues. Hum Mutat (2008) 2.30
Age-related somatic structural changes in the nuclear genome of human blood cells. Am J Hum Genet (2012) 2.15
Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome. Am J Hum Genet (2005) 1.78
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications. Hum Mol Genet (2002) 1.69
The signal transducers Stat1 and Stat3 and their novel target Jmjd3 drive the expression of inflammatory genes in microglia. J Mol Med (Berl) (2013) 1.64
Genomic microarrays in the spotlight. Trends Genet (2004) 1.55
Interactions between effects of environmental chemicals and natural stressors: a review. Sci Total Environ (2009) 1.54
Neoadjuvant treatment for unresectable rectal cancer: an interim analysis of a multicentre randomized study. Radiother Oncol (2013) 1.50
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array. Hum Mutat (2008) 1.45
High-resolution DNA copy number profiling of malignant peripheral nerve sheath tumors using targeted microarray-based comparative genomic hybridization. Clin Cancer Res (2008) 1.34
Microbial community structure and functioning along metal pollution gradients. Environ Toxicol Chem (2013) 1.20
Trends in detoxification enzymes and heavy metal accumulation in ground beetles (Coleoptera: Carabidae) inhabiting a gradient of pollution. Comp Biochem Physiol C Toxicol Pharmacol (2002) 1.13
Metals affect soil bacterial and fungal functional diversity differently. Environ Toxicol Chem (2008) 1.13
A segmental maximum a posteriori approach to genome-wide copy number profiling. Bioinformatics (2008) 1.09
DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets. Int J Mol Med (2004) 1.07
Decreased energetic reserves, morphological changes and accumulation of metals in carabid beetles (Poecilus cupreus L.) exposed to zinc- or cadmium-contaminated food. Ecotoxicology (2002) 1.06
The mechanism of cystic fibrosis transmembrane conductance regulator transcriptional repression during the unfolded protein response. J Biol Chem (2008) 1.06
Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection. J Mol Med (Berl) (2003) 1.05
Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer. Genes Chromosomes Cancer (2006) 1.05
Susceptibility of a carabid beetle, Pterostichus oblongopunctatus fab., from a gradient of heavy metal pollution to additional stressors. Bull Environ Contam Toxicol (2007) 1.03
Common pathogenetic mechanism involving human chromosome 18 in familial and sporadic ileal carcinoid tumors. Genes Chromosomes Cancer (2011) 1.03
Structural genetic variation in the context of somatic mosaicism. Methods Mol Biol (2012) 1.02
A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene. Am J Med Genet A (2007) 1.02
Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array. Neuro Oncol (2009) 1.02
Evidence for between-generation effects in carabids exposed to heavy metals pollution. Ecotoxicology (2007) 1.01
Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma. Int J Cancer (2010) 0.99
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH. Genomics (2006) 0.98
Biodiversity and structure of spider communities along a metal pollution gradient. Ecotoxicology (2012) 0.97
The transcriptional map of the common eliminated region 1 (C3CER1) in 3p21.3. Eur J Hum Genet (2002) 0.96
Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation. Am J Med Genet A (2010) 0.95
Evaluation of the effects of mammography screening program on cancer progression and implemented treatment in patients with breast cancer. Pol Przegl Chir (2013) 0.95
Body mass and caloric value of the ground beetle (Pterostichus oblongopunctatus) (Coleoptera, Carabidae) along a gradient of heavy metal pollution. Environ Toxicol Chem (2006) 0.95
Two-phase uptake of nickel in the ground beetle Pterostichus oblongopunctatus (Coleoptera: Carabidae): implications for invertebrate metal kinetics. Arch Environ Contam Toxicol (2010) 0.94
Integrative epigenomic and genomic analysis of malignant pheochromocytoma. Exp Mol Med (2010) 0.93
Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus. BMC Genomics (2007) 0.93
Genetic population structure of the ground beetle, Pterostichus oblongopunctatus, inhabiting a fragmented and polluted landscape: evidence for sex-biased dispersal. J Insect Sci (2010) 0.93
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2. Hum Mutat (2005) 0.92
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression. Eur J Hum Genet (2010) 0.92
Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci. Cancer Res (2005) 0.91
High-resolution gene copy number and expression profiling of human chromosome 22 in ovarian carcinomas. Genes Chromosomes Cancer (2005) 0.91
The toxicokinetics cell demography model to explain metal kinetics in terrestrial invertebrates. Ecotoxicology (2012) 0.91
Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis. Endocr Relat Cancer (2010) 0.89
Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme. Genes Chromosomes Cancer (2005) 0.89
Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array. Genes Chromosomes Cancer (2009) 0.88
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas. Hum Genet (2005) 0.88
Comparative human/murine sequence analysis of the common eliminated region 1 from human 3p21.3. Mamm Genome (2002) 0.87
Distal 22q11.2 microduplication encompassing the BCR gene. Am J Med Genet A (2008) 0.86
Evaluation of FLT-PET/CT usefulness in diagnosis and qualification for surgical treatment of gastric cancer. Contemp Oncol (Pozn) (2013) 0.86
Collaborating with the enemy: function of macrophages in the development of neoplastic disease. Mediators Inflamm (2013) 0.84
Copy-number polymorphisms: mining the tip of an iceberg. Trends Genet (2005) 0.83
Environmental conditions enhance toxicant effects in larvae of the ground beetle Pterostichus oblongopunctatus (Coleoptera: Carabidae). Environ Pollut (2009) 0.83
Coincidence of synteny breakpoints with malignancy-related deletions on human chromosome 3. Proc Natl Acad Sci U S A (2003) 0.83
Effects of nickel and temperature on the ground beetle Pterostichus oblongopunctatus (Coleoptera: Carabidae). Ecotoxicology (2007) 0.82
Effect of interaction between density dependence and toxicant exposure on population growth rate of the potworm Enchytraeus doerjesi. Environ Toxicol Chem (2005) 0.81
Does chromosome 22 have anything to do with sex determination: further studies on a 46,XX,22q11.2 del male. Am J Med Genet A (2003) 0.81
A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland. Hered Cancer Clin Pract (2014) 0.81
High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH. Int J Oncol (2003) 0.80
Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene. Hum Mutat (2014) 0.80
Regeneration of comparative genomic hybridization oligonucleotide microarrays with dimethylurea. Anal Biochem (2012) 0.80
A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients. Am J Med Genet A (2007) 0.80
Polish consensus statement on the protective stoma. Pol Przegl Chir (2014) 0.79
Model-based experimental design for assessing effects of mixtures of chemicals. Environ Pollut (2009) 0.79
Autoantibodies to glutathione S-transferase theta 1 in patients with primary sclerosing cholangitis and other autoimmune diseases. J Autoimmun (2008) 0.78
Prevalence of the BRCA1 c.68_69delAG (BIC: 185delAG) mutation in women with breast cancer from north-central Poland and a review of the literature on other regions of the country. Contemp Oncol (Pozn) (2013) 0.78
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH. Int J Cancer (2006) 0.78
Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray. Genes Chromosomes Cancer (2005) 0.78
More ecological ERA: incorporating natural environmental factors and animal behavior. Integr Environ Assess Manag (2013) 0.77
NF2 tumor suppressor gene: a comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGH. Neuromolecular Med (2003) 0.77
Procoagulant activity in patients with sickle cell trait. Blood Coagul Fibrinolysis (2012) 0.77
Benign mesocolon schwannoma in PET/CT and immunohistochemistry assessment: a case report. Contemp Oncol (Pozn) (2012) 0.77