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significantly three » significant three (Expand Search), significantly worse (Expand Search), significantly altered (Expand Search)
significant source » significant burden (Expand Search), significant cause (Expand Search)
three variants » three variables (Expand Search), rare variants (Expand Search), three patients (Expand Search)
Showing 1 - 20 results of 14,120 for search '(( significant source decrease ) OR ( significantly three variants ))', query time: 0.64s Refine Results
  1. 1
    Variants of uncertain significance.

    Variants of uncertain significance. by Ghada Al-Kafaji (12054792)

    Published 2023
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  2. 2
    Numbers of stage 1 significant variants.

    Numbers of stage 1 significant variants. by Michael Francis (287202)

    Published 2021
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  3. 3
    Three genome-wide significant variants associated with T2D in G&H.

    Three genome-wide significant variants associated with T2D in G&H. by Sam Hodgson (8848157)

    Published 2022
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  4. 4
    Genetic variants significantly associated with the frailty index.

    Genetic variants significantly associated with the frailty index. by Liugang Xu (18605111)

    Published 2024
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  5. 5
    Regional association plots around the three most significant SNPs.

    Regional association plots around the three most significant SNPs. by Pei-Ying Kao (14642467)

    Published 2023
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  6. 6
    Variants of unknown significance present in fam 8.

    Variants of unknown significance present in fam 8. by Houda Afyouni (13020768)

    Published 2022
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  7. 7
    Variants with an unknown significance or conflicting interpretation of clinical significance.

    Variants with an unknown significance or conflicting interpretation of clinical significance. by J. Tyson McDonald (3687694)

    Published 2022
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  8. 8
    BLyS<sup>-/-</sup> significantly decreased IgM and IgG secreting cells.

    BLyS<sup>-/-</sup> significantly decreased IgM and IgG secreting cells. by Natalie M. Bath (6316517)

    Published 2022
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  9. 9
    Interpreting per trait associations from omnibus significant variants.

    Interpreting per trait associations from omnibus significant variants. by Kodi Taraszka (11339970)

    Published 2022
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  10. 10
    Sampling point (Source:

    Sampling point (Source: by Yonggang Huang (223155)

    Published 2025
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  11. 11
    Detected variants of genes classified according to potential clinically significance (Tier 2).

    Detected variants of genes classified according to potential clinically significance (Tier 2). by Weronika Przybyła (4217611)

    Published 2022
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  12. 12
    Significantly enriched Gene Ontology (GO) terms among the genes showing significant results in the ancestry-specific TWAS.

    Significantly enriched Gene Ontology (GO) terms among the genes showing significant results in the ancestry-specific TWAS. by Jenna C. Carlson (3950024)

    Published 2025
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  13. 13
    APRIL<sup>-/-</sup> and BLyS<sup>-/-</sup> lymphocyte proliferation significantly decreased when challenged with alloantigen.

    APRIL<sup>-/-</sup> and BLyS<sup>-/-</sup> lymphocyte proliferation significantly decreased when challenged with alloantigen. by Natalie M. Bath (6316517)

    Published 2022
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  14. 14
    Source data for Fig 3.

    Source data for Fig 3. by Qi Xu (134661)

    Published 2025
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  15. 15
    Non-replicated genome-wide significant Stage 1 variants.

    Non-replicated genome-wide significant Stage 1 variants. by Michael Francis (287202)

    Published 2021
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  16. 16
    Correlations of the significance ranks of SKCM drugs by three statistical tests.

    Correlations of the significance ranks of SKCM drugs by three statistical tests. by Zeyuan Wang (6956759)

    Published 2024
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  17. 17
    Correlations of the significance ranks of NSCLC drugs by three statistical tests.

    Correlations of the significance ranks of NSCLC drugs by three statistical tests. by Zeyuan Wang (6956759)

    Published 2024
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  18. 18
    Candidate causative pathogenic / likely pathogenic variants and variants of unknown significance compatible with patient phenotype and type of inheritance.

    Candidate causative pathogenic / likely pathogenic variants and variants of unknown significance compatible with patient phenotype and type of inheritance. by Magdaléna Neřoldová (16624956)

    Published 2023
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  19. 19
    Haplotype analysis revealed three polymorphic sites that constituted four haplotypes significantly associated with MI errors.

    Haplotype analysis revealed three polymorphic sites that constituted four haplotypes significantly associated with MI errors. by Upamanyu Pal (10345008)

    Published 2021
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  20. 20
    Supplementary Material for: Identification of Influential Variants in Significant Aggregate Rare Variant Tests

    Supplementary Material for: Identification of Influential Variants in Significant Aggregate Rare Variant Tests by Blumhagen R.Z. (10123769)

    Published 2021
    “…We present a novel method for prioritization of rare variants after a significant aggregate test by quantifying the influence of the variant on the aggregate test of association. …”
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