Works matching IS 09646906 AND DT 2020 AND VI 29 AND IP R1
Results: 15
Implicit bias of encoded variables: frameworks for addressing structured bias in EHR–GWAS data.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R33, doi. 10.1093/hmg/ddaa192
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- Article
The phenomenal epigenome in neurodevelopmental disorders.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R42, doi. 10.1093/hmg/ddaa175
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- Article
Genetic risk factors of ME/CFS: a critical review.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R117, doi. 10.1093/hmg/ddaa169
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- Article
Regulation, diversity and function of MECP2 exon and 3′UTR isoforms.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R89, doi. 10.1093/hmg/ddaa154
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- Article
Genetics of early growth traits.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R66, doi. 10.1093/hmg/ddaa149
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Fine-mapping genetic associations.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R81, doi. 10.1093/hmg/ddaa148
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- Article
Functional annotation of genomic variation: DNA methylation episignatures in neurodevelopmental Mendelian disorders.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R27, doi. 10.1093/hmg/ddaa144
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- Article
Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R107, doi. 10.1093/hmg/ddaa133
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- Article
Understanding human gut diseases at single-cell resolution.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R51, doi. 10.1093/hmg/ddaa130
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Genomics at cellular resolution: insights into cognitive disorders and their evolution.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R1, doi. 10.1093/hmg/ddaa117
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- Article
Reviewing the genetics of heterogeneity in depression: operationalizations, manifestations and etiologies.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R10, doi. 10.1093/hmg/ddaa115
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Dissecting genome-wide studies for microbiome-related metabolic diseases.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R73, doi. 10.1093/hmg/ddaa105
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- Article
Functional genomics in autoimmune diseases.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R59, doi. 10.1093/hmg/ddaa097
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- Article
Androgen receptor variants: RNA-based mechanisms and therapeutic targets.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R19, doi. 10.1093/hmg/ddaa089
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- Article
Genome editing strategies for fetal hemoglobin induction in beta-hemoglobinopathies.
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- Human Molecular Genetics, 2020, v. 29, n. R1, p. R100, doi. 10.1093/hmg/ddaa088
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- Article