Published in Breast Cancer Res on February 07, 2012
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Germline copy number variations in BRCA1-associated ovarian cancer patients. Genes Chromosomes Cancer (2010) 1.01
The contribution of germline rearrangements to the spectrum of BRCA2 mutations. J Med Genet (2006) 1.00
Genome-wide scan identifies a copy number variable region at 3q26 that regulates PPM1L in APC mutation-negative familial colorectal cancer patients. Genes Chromosomes Cancer (2010) 1.00
Copy-number variants in patients with a strong family history of pancreatic cancer. Cancer Biol Ther (2007) 0.99
Germline mutations and polymorphisms in the origins of cancers in women. J Oncol (2010) 0.96
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia (2010) 0.93
A gender-specific association of CNV at 6p21.3 with NPC susceptibility. Hum Mol Genet (2011) 0.92
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Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Hum Mutat (2007) 3.52
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Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching. Hum Mol Genet (2009) 2.50
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Identification of a new copper metabolism gene by positional cloning in a purebred dog population. Hum Mol Genet (2002) 2.24
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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
A major non-HLA locus in celiac disease maps to chromosome 19. Gastroenterology (2003) 1.69
The genome sequence of the gram-positive sugarcane pathogen Leifsonia xyli subsp. xyli. Mol Plant Microbe Interact (2004) 1.65
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VEGF-A and Tenascin-C produced by S100A4+ stromal cells are important for metastatic colonization. Proc Natl Acad Sci U S A (2011) 1.60
Stress-inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection. EMBO J (2002) 1.58
Interaction of cellular prion and stress-inducible protein 1 promotes neuritogenesis and neuroprotection by distinct signaling pathways. J Neurosci (2005) 1.54
Cellular prion protein transduces neuroprotective signals. EMBO J (2002) 1.47
Gene expression profile associated with response to doxorubicin-based therapy in breast cancer. Clin Cancer Res (2005) 1.46
Relationship of beta2-adrenergic receptor polymorphism with obesity in type 2 diabetes. Diabetes Care (2003) 1.39
Evidence that molecular changes in cells occur before morphological alterations during the progression of breast ductal carcinoma. Breast Cancer Res (2008) 1.38
Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect. Hum Mutat (2010) 1.32
Using credibility intervals instead of hypothesis tests in SAGE analysis. Bioinformatics (2003) 1.31
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
Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome. Am J Med Genet A (2007) 1.31
Insights from genomic microarrays into structural chromosome rearrangements. Am J Med Genet A (2005) 1.29
Identification of enolase as a laminin-binding protein on the surface of Staphylococcus aureus. Microbes Infect (2004) 1.21
Structural variation in the human genome: the impact of copy number variants on clinical diagnosis. Genet Med (2007) 1.21
Structural study of binding of flagellin by Toll-like receptor 5. J Bacteriol (2003) 1.19
Reciprocal changes in gene expression profiles of cocultured breast epithelial cells and primary fibroblasts. Int J Cancer (2009) 1.19
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Altered oxygen metabolism associated to neurogenesis of induced pluripotent stem cells derived from a schizophrenic patient. Cell Transplant (2012) 1.17
Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein. J Biol Chem (2002) 1.16
High sibling correlation on methylphenidate response but no association with DAT1-10R homozygosity in Dutch sibpairs with ADHD. J Child Psychol Psychiatry (2005) 1.14
UBE2A, which encodes a ubiquitin-conjugating enzyme, is mutated in a novel X-linked mental retardation syndrome. Am J Hum Genet (2006) 1.14
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
Cellular prion protein expression in astrocytes modulates neuronal survival and differentiation. J Neurochem (2007) 1.09
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
An unrecognized extracellular function for an intracellular adapter protein released from the cytoplasm into the tumor microenvironment. Proc Natl Acad Sci U S A (2009) 1.07
Germline copy number variations and cancer predisposition. Future Oncol (2012) 1.07
Mutations in the intellectual disability gene Ube2a cause neuronal dysfunction and impair parkin-dependent mitophagy. Mol Cell (2013) 1.06
Transcriptome signature of the adult mouse choroid plexus. Fluids Barriers CNS (2011) 1.05
Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH. Nucleic Acids Res (2004) 1.05
Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative trait loci influencing variation in human menopausal age. Am J Hum Genet (2004) 1.04
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
Short-term memory formation and long-term memory consolidation are enhanced by cellular prion association to stress-inducible protein 1. Neurobiol Dis (2007) 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
Gene expression arrays in cancer research: methods and applications. Crit Rev Oncol Hematol (2005) 1.01
Hippocampal synaptic plasticity in mice devoid of cellular prion protein. Brain Res Mol Brain Res (2004) 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
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
Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver-Russell syndrome. Am J Med Genet A (2011) 1.00
Current smoking at menopause rather than duration determines the onset of natural menopause. Epidemiology (2004) 1.00
Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil. PLoS One (2013) 0.99
Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9. Am J Med Genet A (2003) 0.99
Cellular prion protein: on the road for functions. FEBS Lett (2002) 0.98
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
SATR-1 hypomethylation is a common and early event in breast cancer. Cancer Genet Cytogenet (2006) 0.96
ORESTES are enriched in rare exon usage variants affecting the encoded proteins. C R Biol (2004) 0.95
Towards cellular receptors for prions. Rev Med Virol (2003) 0.94
Decreased AIRE expression and global thymic hypofunction in Down syndrome. J Immunol (2011) 0.94
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia (2010) 0.93
Accurate determination of microsatellite allele frequencies in pooled DNA samples. Eur J Hum Genet (2004) 0.92
Simcluster: clustering enumeration gene expression data on the simplex space. BMC Bioinformatics (2007) 0.92
Expression profile of malignant and nonmalignant lesions of esophagus and stomach: differential activity of functional modules related to inflammation and lipid metabolism. Cancer Res (2005) 0.91
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
High risk cohort study for psychiatric disorders in childhood: rationale, design, methods and preliminary results. Int J Methods Psychiatr Res (2014) 0.90
Cellular prion protein ablation impairs behavior as a function of age. Neuroreport (2003) 0.90
Expression of human papillomavirus type 16 E7 oncoprotein alters keratinocytes expression profile in response to tumor necrosis factor-alpha. Carcinogenesis (2009) 0.90
Genomic array and expression analysis of frequent high-level amplifications in adenocarcinomas of the gastro-esophageal junction. Cancer Genet Cytogenet (2006) 0.90
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry (2014) 0.90
A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes. Am J Hum Genet (2010) 0.90
Mutations, clinical findings and survival estimates in South American patients with X-linked adrenoleukodystrophy. PLoS One (2012) 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
Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour. Eur J Cancer (2011) 0.89
Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell lines. Cancer Genet Cytogenet (2006) 0.89
CTLA4 +49 A/G and CT60 polymorphisms in Dutch coeliac disease patients. Eur J Hum Genet (2004) 0.88
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes. Am J Med Genet A (2007) 0.88
The interaction between prion protein and laminin modulates memory consolidation. Eur J Neurosci (2006) 0.88