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Connection

ALEKSANDAR MILOSAVLJEVIC to Genetic Variation

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This is a "connection" page, showing publications ALEKSANDAR MILOSAVLJEVIC has written about Genetic Variation.
ALEKSANDAR MILOSAVLJEVIC
Connection Strength
2.314
Genetic Variation
  1. ClinGen API platform for classification of human genetic variants. Cell Genom. 2026 Apr 08; 6(4):101211.
    View in: PubMed
    Score: 0.592
  2. Aggregation of gene regulatory information and knowledge on FAIR principles enables discovery of pathogenic gene regulatory variants. Bioinformatics. 2026 Feb 28; 42(3).
    View in: PubMed
    Score: 0.588
  3. Emerging patterns of epigenomic variation. Trends Genet. 2011 Jun; 27(6):242-50.
    View in: PubMed
    Score: 0.210
  4. Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing. BMC Bioinformatics. 2010 Nov 23; 11:572.
    View in: PubMed
    Score: 0.204
  5. Mapping MAVE data for use in human genomics applications. Genome Biol. 2025 Jun 25; 26(1):179.
    View in: PubMed
    Score: 0.140
  6. CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase. Nucleic Acids Res. 2023 01 06; 51(D1):D1230-D1241.
    View in: PubMed
    Score: 0.118
  7. ClinGen Allele Registry links information about genetic variants. Hum Mutat. 2018 11; 39(11):1690-1701.
    View in: PubMed
    Score: 0.088
  8. ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants. Genome Med. 2017 01 12; 9(1):3.
    View in: PubMed
    Score: 0.078
  9. 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: 0.074
  10. Characterization of single-nucleotide variation in Indian-origin rhesus macaques (Macaca mulatta). BMC Genomics. 2011 Jun 13; 12:311.
    View in: PubMed
    Score: 0.053
  11. Putting epigenome comparison into practice. Nat Biotechnol. 2010 Oct; 28(10):1053-6.
    View in: PubMed
    Score: 0.050
  12. A community approach to the cancer-variant-interpretation bottleneck. Nat Cancer. 2022 05; 3(5):522-525.
    View in: PubMed
    Score: 0.028
  13. ClinGen advancing genomic data-sharing standards as a GA4GH driver project. Hum Mutat. 2018 11; 39(11):1686-1689.
    View in: PubMed
    Score: 0.022
  14. 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: 0.022
  15. Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup. Clin Pharmacol Ther. 2016 Feb; 99(2):157-60.
    View in: PubMed
    Score: 0.018
  16. Integrative analysis of 111 reference human epigenomes. Nature. 2015 Feb 19; 518(7539):317-30.
    View in: PubMed
    Score: 0.017
  17. Evolutionary and biomedical insights from the rhesus macaque genome. Science. 2007 Apr 13; 316(5822):222-34.
    View in: PubMed
    Score: 0.010
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.