1
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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.
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Nature
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2007
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75.09
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2
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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
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Science
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2008
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20.68
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3
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High-resolution mapping and characterization of open chromatin across the genome.
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Cell
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2008
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15.93
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4
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NCBI GEO: archive for functional genomics data sets--update.
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Nucleic Acids Res
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2012
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15.84
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5
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BioMart and Bioconductor: a powerful link between biological databases and microarray data analysis.
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Bioinformatics
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2005
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9.84
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6
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Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
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Nat Genet
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2011
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7.31
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7
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DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarrays.
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Nat Methods
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2006
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6.25
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8
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Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS).
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Genome Res
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2005
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5.71
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9
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A single IGF1 allele is a major determinant of small size in dogs.
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Science
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2007
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4.68
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10
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Interferon-γ links ultraviolet radiation to melanomagenesis in mice.
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Nature
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2011
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3.56
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11
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Statistics for ChIP-chip and DNase hypersensitivity experiments on NimbleGen arrays.
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Methods Enzymol
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2006
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3.53
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12
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Gene expression profiling of human sarcomas: insights into sarcoma biology.
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Cancer Res
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2005
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2.64
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13
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Genome-wide analysis of menin binding provides insights into MEN1 tumorigenesis.
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PLoS Genet
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2006
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2.62
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14
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Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma.
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Nat Genet
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2009
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2.58
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15
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Database of mRNA gene expression profiles of multiple human organs.
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Genome Res
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2005
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2.11
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16
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Evidence for an unanticipated relationship between undifferentiated pleomorphic sarcoma and embryonal rhabdomyosarcoma.
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Cancer Cell
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2011
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1.96
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17
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RCircos: an R package for Circos 2D track plots.
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BMC Bioinformatics
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2013
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1.95
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18
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A molecular function map of Ewing's sarcoma.
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PLoS One
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2009
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1.69
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19
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GEOmetadb: powerful alternative search engine for the Gene Expression Omnibus.
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Bioinformatics
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2008
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1.68
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20
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Large-scale profiling of archival lymph nodes reveals pervasive remodeling of the follicular lymphoma methylome.
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Cancer Res
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2009
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1.58
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21
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Canine tumor cross-species genomics uncovers targets linked to osteosarcoma progression.
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BMC Genomics
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2009
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1.57
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22
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Identification of an inhibitor of the EWS-FLI1 oncogenic transcription factor by high-throughput screening.
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J Natl Cancer Inst
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2011
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1.55
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23
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Vorinostat inhibits brain metastatic colonization in a model of triple-negative breast cancer and induces DNA double-strand breaks.
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Clin Cancer Res
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2009
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1.40
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24
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Analyses of resected human brain metastases of breast cancer reveal the association between up-regulation of hexokinase 2 and poor prognosis.
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Mol Cancer Res
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2009
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1.36
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25
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Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma.
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Proc Natl Acad Sci U S A
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2013
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1.35
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26
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Suppressor role of activating transcription factor 2 (ATF2) in skin cancer.
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Proc Natl Acad Sci U S A
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2008
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1.26
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27
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Assessment of automated image analysis of breast cancer tissue microarrays for epidemiologic studies.
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Cancer Epidemiol Biomarkers Prev
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2010
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1.25
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28
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Oncogenic ETS fusions deregulate E2F3 target genes in Ewing sarcoma and prostate cancer.
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Genome Res
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2013
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1.11
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29
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Molecular grading of ductal carcinoma in situ of the breast.
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Clin Cancer Res
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2008
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1.09
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30
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Chromothripsis and focal copy number alterations determine poor outcome in malignant melanoma.
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Cancer Res
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2012
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1.05
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31
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Preferential localization of human origins of DNA replication at the 5'-ends of expressed genes and at evolutionarily conserved DNA sequences.
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PLoS One
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2011
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1.04
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32
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Chemical analysis of four capsules containing the controlled substance analogues 4-methylmethcathinone, 2-fluoromethamphetamine, alpha-phthalimidopropiophenone and N-ethylcathinone.
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Forensic Sci Int
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2010
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0.99
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33
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Constitutive Fms-like tyrosine kinase 3 activation results in specific changes in gene expression in myeloid leukaemic cells.
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Br J Haematol
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2007
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0.99
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34
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Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes.
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J Med Genet
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2006
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0.95
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35
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Genome-wide methylation patterns in papillary thyroid cancer are distinct based on histological subtype and tumor genotype.
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J Clin Endocrinol Metab
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2013
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0.90
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36
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Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma.
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BMC Genomics
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2012
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0.88
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37
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Archival fine-needle aspiration cytopathology (FNAC) samples: untapped resource for clinical molecular profiling.
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J Mol Diagn
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2010
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0.87
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38
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A methyl-deviator epigenotype of estrogen receptor-positive breast carcinoma is associated with malignant biology.
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Am J Pathol
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2011
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0.87
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39
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In vivo role of alternative splicing and serine phosphorylation of the microphthalmia-associated transcription factor.
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Genetics
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2012
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0.83
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40
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Advanced bone formation in mice with a dominant-negative mutation in the thyroid hormone receptor β gene due to activation of Wnt/β-catenin protein signaling.
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J Biol Chem
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2012
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0.82
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41
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Whole genome and transcriptome sequencing of a B3 thymoma.
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PLoS One
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2013
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0.81
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42
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Photodestructible vesicles.
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Langmuir
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2006
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0.81
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43
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Public data and open source tools for multi-assay genomic investigation of disease.
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Brief Bioinform
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2015
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0.80
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44
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Detection of novel amplicons in prostate cancer by comprehensive genomic profiling of prostate cancer cell lines using oligonucleotide-based arrayCGH.
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PLoS One
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2007
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0.79
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45
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Genome-wide methylation profiling in archival formalin-fixed paraffin-embedded tissue samples.
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Methods Mol Biol
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2012
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0.77
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46
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Exclusion of the 750-kb genetically unstable region at Xq27 as a candidate locus for prostate malignancy in HPCX1-linked families.
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Genes Chromosomes Cancer
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2012
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0.76
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47
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Prohibitin expression is associated with high grade breast cancer but is not a driver of amplification at 17q21.33.
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Pathology
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2013
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0.75
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48
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The therapeutic pyramid: a common factors synthesis of techniques, alliance, and way of being.
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J Marital Fam Ther
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2013
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0.75
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49
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Precipitation of inorganic salts inside hollow micrometer-sized polyelectrolyte shells.
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J Colloid Interface Sci
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2002
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0.75
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