Connection

Astrid Manuel to Polymorphism, Single Nucleotide

This is a "connection" page, showing publications Astrid Manuel has written about Polymorphism, Single Nucleotide.
  1. An integrative study of genetic variants with brain tissue expression identifies viral etiology and potential drug targets of multiple sclerosis. Mol Cell Neurosci. 2021 09; 115:103656.
    View in: PubMed
    Score: 0.086
  2. Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data. Am J Hum Genet. 2020 06 04; 106(6):805-817.
    View in: PubMed
    Score: 0.079
  3. Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nat Commun. 2023 05 30; 14(1):3111.
    View in: PubMed
    Score: 0.024
  4. Prioritization of risk genes in multiple sclerosis by a refined Bayesian framework followed by tissue-specificity and cell type feature assessment. BMC Genomics. 2022 May 11; 23(Suppl 4):362.
    View in: PubMed
    Score: 0.023
  5. Predicting regulatory variants using a dense epigenomic mapped CNN model elucidated the molecular basis of trait-tissue associations. Nucleic Acids Res. 2021 01 11; 49(1):53-66.
    View in: PubMed
    Score: 0.021
Connection Strength

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