Works matching IS 03406717 AND DT 2024 AND VI 143 AND IP 9/10
Results: 16
A methodology for gene level omics-WAS integration identifies genes influencing traits associated with cardiovascular risks: the Long Life Family Study.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1241, doi. 10.1007/s00439-024-02701-1
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Genome-wide assessment of shared genetic landscape of idiopathic pulmonary fibrosis and its comorbidities.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1223, doi. 10.1007/s00439-024-02696-9
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- Article
Fine mapping of candidate effector genes for heart rate.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1207, doi. 10.1007/s00439-024-02684-z
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- Article
R2ROC: an efficient method of comparing two or more correlated AUC from out-of-sample prediction using polygenic scores.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1193, doi. 10.1007/s00439-024-02682-1
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- Article
Unraveling the significance of AGPAT4 for the pathogenesis of endometriosis via a multi-omics approach.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1163, doi. 10.1007/s00439-024-02681-2
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- Article
Advances in long-read single-cell transcriptomics.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1005, doi. 10.1007/s00439-024-02678-x
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Retrospective studies and quantitative proteomics reveal that abnormal expression of blood pressure, blood lipids, and coagulation related proteins is associated with hypospadias.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1175, doi. 10.1007/s00439-024-02676-z
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- Article
A novel network-based method identifies a cuproplasia-related pan-cancer gene signature to predict patient outcome.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1145, doi. 10.1007/s00439-024-02673-2
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- Article
Phenotypic and genetic effect of carotid intima-media thickness on the risk of stroke.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1131, doi. 10.1007/s00439-024-02666-1
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- Article
The crucial prognostic signaling pathways of pancreatic ductal adenocarcinoma were identified by single-cell and bulk RNA sequencing data.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1109, doi. 10.1007/s00439-024-02663-4
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- Article
Genetic evidence for T-wave area from 12-lead electrocardiograms to monitor cardiovascular diseases in patients taking diabetes medications.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1095, doi. 10.1007/s00439-024-02661-6
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- Article
Identification of TACSTD2 as novel therapeutic targets for cisplatin-induced acute kidney injury by multi-omics data integration.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1061, doi. 10.1007/s00439-024-02641-w
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- Article
Bayesian network-based Mendelian randomization for variant prioritization and phenotypic causal inference.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1081, doi. 10.1007/s00439-024-02640-x
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- Article
Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertility.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1049, doi. 10.1007/s00439-023-02633-2
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- Article
Protein-centric omics integration analysis identifies candidate plasma proteins for multiple autoimmune diseases.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1035, doi. 10.1007/s00439-023-02627-0
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- Article
Plasma-derived exosomal miRNA profiles reveal potential epigenetic pathogenesis of premature ovarian failure.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1021, doi. 10.1007/s00439-023-02618-1
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- Article