Search Results - "Burren OS"

Author Correction: Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Authors: Zou XZ Hu F Lou H et al.

Corporate Authors: Zou XZ Hu F Lou H et al.

Source: Nature [Nature] 2026 Apr; Vol. 652 (8110), pp. E7.

Publication Type: Published Erratum

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium: Internet ISSN: 1476-4687 (Electronic) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE; In Process

La benchmarking large language models for extracting biobank-derived insights into health and disease.

Authors: Corpas, Manuel Iacoangeli, Alfredo

Source: PLoS Computational Biology. 4/20/2026, Vol. 22 Issue 4, p1-18. 18p.

Rare heterozygous missense variants in VSX2 are associated with retinal detachment.

Authors: Brock, Daniel C. Dhindsa, Justin S. Chen, Yifan et al.

Source: PLoS Genetics. 2/3/2026, Vol. 22 Issue 2, p1-25. 25p.

Author Correction: Approaches and advances in the genetic causes of autoimmune disease and their implications.

Authors: Inshaw JRJ Cutler AJ Burren OS et al.

Source: Nature immunology [Nat Immunol] 2020 Jun; Vol. 21 (6), pp. 695.

Publication Type: Journal Article; Published Erratum

Journal Info: Publisher: Nature America Inc Country of Publication: United States NLM ID: 100941354 Publication Model: Print Cited Medium: Internet ISSN: 1529-2916 (Electronic) Linking ISSN: 15292908 NLM ISO Abbreviation: Nat Immunol Subsets: MEDLINE; PubMed not MEDLINE

A plasma-based protein signature association with all-cause mortality.

Authors: Koziar, Natalia Whetton, Anthony D. Geifman, Nophar

Source: PLoS ONE. 11/21/2025, Vol. 20 Issue 11, p1-15. 15p.

Enhancing infectious intestinal disease diagnosis through metagenomic and metatranscriptomic sequencing of 1000 human diarrhoeal samples.

Authors: Cunningham-Oakes, Edward Perez-Sepulveda, Blanca M. Li, Yan et al.

Source: Genome Medicine. 5/20/2025, Vol. 17 Issue 1, p1-16. 16p.

Simplifying causal gene identification in GWAS loci.

Authors: Schipper, Marijn Ulirsch, Jacob Posthuma, Danielle et al.

Source: PLoS Genetics. 3/17/2026, Vol. 22 Issue 3, p1-17. 17p.

Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Authors: Zou XZ Hu F Lou H et al.

Corporate Authors: Zou XZ Hu F Lou H et al.

Source: Nature [Nature] 2026 Apr; Vol. 652 (8110), pp. 675-685. Date of Electronic Publication: 2026 Feb 04.

Publication Type: Journal Article; Research Support, N.I.H., Extramural

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-4687 (Electronic) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE

Population-scale sequencing resolves determinants of persistent EBV DNA.

Authors: Nyeo SS Cumming EM Burren OS et al.

Source: Nature [Nature] 2026 Feb; Vol. 650 (8102), pp. 664-672. Date of Electronic Publication: 2026 Jan 28.

Publication Type: Journal Article; Research Support, N.I.H., Extramural

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-4687 (Electronic) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Authors: Mitchell J Camacho N Shea P et al.

Source: Nature communications [Nat Commun] 2025 Feb 19; Vol. 16 (1), pp. 1779. Date of Electronic Publication: 2025 Feb 19.

Publication Type: Journal Article; Meta-Analysis

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Human CD33 deficiency is associated with mild alteration of circulating white blood cell counts.

Authors: Dominy, John Bai, Jirong Koch, Christopher et al.

Source: PLoS Genetics. 3/5/2025, Vol. 21 Issue 3, p1-21. 21p.

Bayesian clustering with uncertain data.

Authors: Nicholls, Kath Kirk, Paul D. W. Wallace, Chris

Source: PLoS Computational Biology. 9/3/2024, Vol. 20 Issue 9, p1-17. 17p.

GWAS and 3D chromatin mapping identifies multicancer risk genes associated with hormone-dependent cancers.

Authors: Rivera, Isela Sarahi French, Juliet D. Bitar, Mainá et al.

Source: PLoS Genetics. 11/25/2024, Vol. 20 Issue 11, p1-14. 14p.

Linkage: an interactive web application for linking of DNA regulatory peaks to genes.

Authors: Xu, Siwen Luo, Yuyan Liu, Zenghui et al.

Source: BMC Genomics. 10/7/2025, Vol. 26 Issue 1, p1-9. 9p.

Differences in Endocrine Manifestations in HIV-Infected Subjects on Anti-Retroviral Therapy (ART) Versus not on ART.

Authors: Manna, Satyaki Das, Tapas C. Pandit, Kaushik et al.

Source: Indian Journal of Endocrinology & Metabolism. Jan/Feb2026, Vol. 30 Issue 1, p96-101. 6p.

Machine learning-guided deconvolution of plasma protein levels.

Authors: Pietzner, Maik Beuchel, Carl Demircan, Kamil et al.

Source: Molecular Systems Biology. Dec2025, Vol. 21 Issue 12, p1822-1844. 23p.

Severity of acute SARS-CoV-2 infection and risk of new-onset autoimmune disease: A RECOVER initiative study in nationwide U.S. cohorts.

Authors: Wuller, Shannon Singer, Nora G. Lewis, Colby et al.

Source: PLoS ONE. 6/4/2025, Vol. 20 Issue 6, p1-26. 26p.

Functional investigation suggests CNTNAP5 involvement in glaucomatous neurodegeneration obtained from a GWAS in primary angle closure glaucoma.

Authors: Chakraborty, Sudipta Sarma, Jyotishman Roy, Shantanu Saha et al.

Source: PLoS Genetics. 12/5/2024, Vol. 20 Issue 12, p1-24. 24p.

Population-scale sequencing resolves correlates and determinants of latent Epstein-Barr Virus infection.

Authors: Nyeo SS Cumming EM Burren OS et al.

Source: BioRxiv : the preprint server for biology [bioRxiv] 2025 Jul 18. Date of Electronic Publication: 2025 Jul 18.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101680187 Publication Model: Electronic Cited Medium: Internet ISSN: 2692-8205 (Electronic) Linking ISSN: 26928205 NLM ISO Abbreviation: bioRxiv Subsets: PubMed not MEDLINE

An introduction to polygenic scores – methodological basics and recent advances.

Authors: Klinkhammer, Hannah Mayr, Andreas Maj, Carlo

Source: Medizinische Genetik. Jul2026, Vol. 38 Issue 3, p157-168. 12p.