9 Matching Annotations
  1. Jul 2024
  2. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Association of ESR1 Germline Variants with TP53 Somatic Variants in Breast Tumors in a Genome-wide Study
    1
    1. scibot 02 Jul 2024
      SCR_006796

      DOI: 10.1158/2767-9764.CRC-24-0026

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @scibot

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796
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    ncbi.nlm.nih.gov/pmc/articles/PMC11210444/
  3. Aug 2023
  4. www.mdpi.com www.mdpi.com
    Identification of Novel Intronic SNPs in Transporter Genes Associated with Metformin Side Effects
    1
    1. scibot 17 Aug 2023
      RRID:SCR_006796

      DOI: 10.3390/genes14081609

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @scibot

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796
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    mdpi.com/2073-4425/14/8/1609
  5. Mar 2023
  6. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Association study between polymorphisms in DNA methylation-related genes and testicular germ cell tumor risk
    1
    1. scibot 05 Mar 2023
      RRID:SCR_006796

      DOI: 10.1158/1055-9965.EPI-22-0123

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @scibot

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796
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    ncbi.nlm.nih.gov/pmc/articles/PMC9444936/
  7. Jul 2022
  8. 52.53.155.43 52.53.155.43
    epi-22-0123-html.html
    1
    1. scibot 29 Jul 2022
      RRID:SCR_006796

      DOI: 10.1158/1055-9965.epi-22-0123

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @scibot

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796
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    52.53.155.43/3de3cb90d6c0869d24f8e6633a22fe84eaf377d7/epi-22-0123-html.html
  9. Feb 2022
  10. link.springer.com link.springer.com
    BDNF Levels According to Variations in the CACNA1C Gene: Sex-Based Disparity
    1
    1. scibot 08 Feb 2022
      RRID:SCR_006796

      DOI: 10.1007/s10571-022-01189-5

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @scibot

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796
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    link.springer.com/article/10.1007/s10571-022-01189-5
  11. Aug 2021
  12. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Untitled document
    1
    1. scibot 11 Aug 2021
      RRID:SCR_006796

      DOI: 10.1002/brb3.1144

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @scibot

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796
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    ncbi.nlm.nih.gov/pmc/articles/PMC6305932/
  13. Jul 2021
  14. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Untitled document
    1
    1. scibot 30 Jul 2021
      RRID:SCR_006796

      DOI: 10.1002/brb3.1144

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @scibot

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796
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    onlinelibrary.wiley.com/doi/full/10.1002/brb3.1144
  15. Sep 2020
  16. www.dovepress.com www.dovepress.com
    <p>Intronic Variants in OCT1 are Associated with All-Cause and Cardiovascular Mortality in Metformin Users with Type 2 Diabetes</p>
    1
    1. scibot 26 Sep 2020
      RRID:SCR_006796

      DOI: 10.2147/DMSO.S235663

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @evieth

      SciCrunch record: RRID:SCR_006796

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      RRIDCUR:Validated RRID:SCR_006796
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    dovepress.com/intronic-variants-in-oct1-are-associated-with-all-cause-and-cardiovasc-peer-reviewed-fulltext-article-DMSO
  17. www.frontiersin.org www.frontiersin.org
    Functional Genetic Polymorphisms in the IL1RL1–IL18R1 Region Confer Risk for Ocular Behçet’s Disease in a Chinese Han Population
    1
    1. scibot 23 Sep 2020
      RRID:SCR_006796

      DOI: 10.3389/fgene.2020.00645

      Resource: HaploReg (RRID:SCR_006796)

      Curator: @evieth

      SciCrunch record: RRID:SCR_006796

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      RRID:SCR_006796 RRIDCUR:Validated
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    frontiersin.org/article/10.3389/fgene.2020.00645/full