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Connection

ALEKSANDAR MILOSAVLJEVIC to Genome, Human

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This is a "connection" page, showing publications ALEKSANDAR MILOSAVLJEVIC has written about Genome, Human.
ALEKSANDAR MILOSAVLJEVIC
Connection Strength
3.025
Genome, Human
  1. ClinGen API platform for classification of human genetic variants. Cell Genom. 2026 Apr 08; 6(4):101211.
    View in: PubMed
    Score: 0.583
  2. Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci. Science. 2018 09 28; 361(6409).
    View in: PubMed
    Score: 0.344
  3. Analysis of interactions between the epigenome and structural mutability of the genome using Genboree Workbench tools. BMC Bioinformatics. 2014; 15 Suppl 7:S2.
    View in: PubMed
    Score: 0.256
  4. Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines. Cancer Genet. 2011 Aug; 204(8):447-57.
    View in: PubMed
    Score: 0.211
  5. A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome. Genome Res. 2009 Feb; 19(2):167-77.
    View in: PubMed
    Score: 0.175
  6. Human-specific changes of genome structure detected by genomic triangulation. Science. 2007 Apr 13; 316(5822):235-7.
    View in: PubMed
    Score: 0.156
  7. Mapping MAVE data for use in human genomics applications. Genome Biol. 2025 Jun 25; 26(1):179.
    View in: PubMed
    Score: 0.138
  8. Pash: efficient genome-scale sequence anchoring by Positional Hashing. Genome Res. 2004 Apr; 14(4):672-8.
    View in: PubMed
    Score: 0.127
  9. ClinGen advancing genomic data-sharing standards as a GA4GH driver project. Hum Mutat. 2018 11; 39(11):1686-1689.
    View in: PubMed
    Score: 0.087
  10. Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group. Hum Mutat. 2018 11; 39(11):1677-1685.
    View in: PubMed
    Score: 0.087
  11. ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants. Genome Med. 2017 01 12; 9(1):3.
    View in: PubMed
    Score: 0.077
  12. Discovering distinct genes represented in 29,570 clones from infant brain cDNA libraries by applying sequencing by hybridization methodology. Genome Res. 1996 Feb; 6(2):132-41.
    View in: PubMed
    Score: 0.072
  13. Integrative analysis of 111 reference human epigenomes. Nature. 2015 Feb 19; 518(7539):317-30.
    View in: PubMed
    Score: 0.067
  14. Intermediate DNA methylation is a conserved signature of genome regulation. Nat Commun. 2015 Feb 18; 6:6363.
    View in: PubMed
    Score: 0.067
  15. Confounding by repetitive elements and CpG islands does not explain the association between hypomethylation and genomic instability. PLoS Genet. 2013; 9(2):e1003333.
    View in: PubMed
    Score: 0.059
  16. Atlas2 Cloud: a framework for personal genome analysis in the cloud. BMC Genomics. 2012; 13 Suppl 6:S19.
    View in: PubMed
    Score: 0.057
  17. Prototypic sequences for human repetitive DNA. J Mol Evol. 1992 Oct; 35(4):286-91.
    View in: PubMed
    Score: 0.057
  18. Spark: a navigational paradigm for genomic data exploration. Genome Res. 2012 Nov; 22(11):2262-9.
    View in: PubMed
    Score: 0.057
  19. Genomic hypomethylation in the human germline associates with selective structural mutability in the human genome. PLoS Genet. 2012; 8(5):e1002692.
    View in: PubMed
    Score: 0.056
  20. An integrative variant analysis suite for whole exome next-generation sequencing data. BMC Bioinformatics. 2012 Jan 12; 13:8.
    View in: PubMed
    Score: 0.054
  21. Discovering functional modules by identifying recurrent and mutually exclusive mutational patterns in tumors. BMC Med Genomics. 2011 Apr 14; 4:34.
    View in: PubMed
    Score: 0.052
  22. Pash 2.0: scaleable sequence anchoring for next-generation sequencing technologies. Pac Symp Biocomput. 2008; 102-13.
    View in: PubMed
    Score: 0.041
  23. A high-resolution map of synteny disruptions in gibbon and human genomes. PLoS Genet. 2006 Dec 29; 2(12):e223.
    View in: PubMed
    Score: 0.038
  24. Pooled genomic indexing of rhesus macaque. Genome Res. 2005 Feb; 15(2):292-301.
    View in: PubMed
    Score: 0.034
  25. Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium. Am J Hum Genet. 2016 06 02; 98(6):1067-1076.
    View in: PubMed
    Score: 0.018
  26. NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits. Genome Res. 2013 Sep; 23(9):1395-409.
    View in: PubMed
    Score: 0.015
  27. Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood. Genome Biol. 2012 Jun 15; 13(6):R43.
    View in: PubMed
    Score: 0.014
  28. The NIH Roadmap Epigenomics Mapping Consortium. Nat Biotechnol. 2010 Oct; 28(10):1045-8.
    View in: PubMed
    Score: 0.012
  29. Evolutionary breakpoints in the gibbon suggest association between cytosine methylation and karyotype evolution. PLoS Genet. 2009 Jun; 5(6):e1000538.
    View in: PubMed
    Score: 0.011
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.