Search Results - "Taliun SAG"

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.

Authors: Cade, Brian E. Lee, Jiwon Sofer, Tamar et al.

Source: Genome Medicine. 8/26/2021, Vol. 13 Issue 1, p1-17. 17p.

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.

Authors: Georgakis, Marios K. Malik, Rainer Bounkari, Omar El et al.

Source: Genome Medicine. 3/21/2025, Vol. 17 Issue 1, p1-14. 14p.

Insights into pharmacogenetics, drug-gene interactions, and drug-drug-gene interactions.

Authors: Russell, Laura E. Claw, Katrina G. Aagaard, Kaja M. et al.

Source: Drug Metabolism Reviews. Aug2025, Vol. 57 Issue 3, p272-290. 19p.

Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis.

Authors: Kawai, Yosuke Watanabe, Yusuke Omae, Yosuke et al.

Source: PLoS Genetics. 12/7/2023, Vol. 19 Issue 12, p1-23. 23p.

Deep single-cell decoding of human pancreatic islets reveals T2D β-cell gene expression defects.

Authors: Bandesh K Motakis E Nargund S et al.

Source: The EMBO journal [EMBO J] 2026 Jun; Vol. 45 (11), pp. 3978-4005. Date of Electronic Publication: 2026 Apr 15.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 8208664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2075 (Electronic) Linking ISSN: 02614189 NLM ISO Abbreviation: EMBO J Subsets: MEDLINE

A comprehensive whole genome database of ethnic minority populations.

Authors: He, Yan Lei, Changgui Wan, Chanjuan et al.

Source: Scientific Reports. 6/17/2024, Vol. 14 Issue 1, p1-9. 9p.

The role of the hippocampus and SLC39A8 in chronic musculoskeletal pain-induced dementia: a Mendelian randomization study.

Authors: Du, Kai Zuo, Yong-Li Zhang, Zi-Meng et al.

Source: Scientific Reports. 4/16/2025, Vol. 15 Issue 1, p1-16. 16p.

A genomic strategy for precision medicine in rare diseases: integrating customized algorithms into clinical practice.

Authors: Méndez-Vidal, Cristina Bravo-Gil, Nereida Pérez-Florido, Javier et al.

Source: Journal of Translational Medicine. 1/20/2025, Vol. 23 Issue 1, p1-15. 15p.

Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings.

Authors: Dapas, Matthew Thompson, Emma E. Wentworth-Sheilds, William et al.

Source: PLoS Genetics. 1/13/2023, Vol. 18 Issue 1, p1-32. 32p.

This result is not displayed to guests.
Login for full access.

Transcriptomic changes in oligodendrocytes and precursor cells associate with clinical outcomes of Parkinson's disease.

Authors: Dehestani, Mohammad Kozareva, Velina Blauwendraat, Cornelis et al.

Source: Molecular Brain. 8/13/2024, Vol. 17 Issue 1, p1-10. 10p.

This result is not displayed to guests.
Login for full access.

Expanding our understanding of synucleinopathies: proteinopathy, proteinopenia, and lipidopathy.

Authors: Flores‐León, Manuel Outeiro, Tiago F.

Source: FEBS Journal. 9/15/2025, Vol. 292 Issue 18, p4774-4788. 15p.

Single-nucleus transcriptomics reveals a distinct microglial state and increased MSR1-mediated phagocytosis as common features across dementia subtypes.

Authors: Chia, Sook-Yoong Li, Mengwei Li, Zhihong et al.

Source: Genome Medicine. 8/18/2025, Vol. 17 Issue 1, p1-22. 22p.

Bioinformatic insights into five Chinese population substructures inferred from the East Asian-specific AISNP panel.

Authors: Chen, Jing Huang, Yuguo Zhong, Jie et al.

Source: BMC Genomics. 8/18/2025, Vol. 26 Issue 1, p1-14. 14p.

Exploring the role of HLA variants in neuroblastoma susceptibility through whole exome sequencing.

Authors: Bonfiglio, Ferdinando Lasorsa, Vito Alessandro Aievola, Vincenzo et al.

Source: HLA: Immune Response Genetics. May2024, Vol. 103 Issue 5, p1-12. 12p.

Delineating the Genetic Basis of RNF213-related vasculopathies: The association of PKHD1 variants with bilateral cerebral vasculopathy.

Authors: Ishigami D Namba S Miyawaki S et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 Jun; Vol. 34 (6), pp. 788-795. Date of Electronic Publication: 2026 Feb 12.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Tracing the genetic legacy of Altaic-speaking populations suggested long-distance migration and multi-source admixture shape the genomic diversity of Xibe and Daur.

Authors: Wang Y Zhang L Jiang Y et al.

Source: Human genetics [Hum Genet] 2026 May 19; Vol. 145 (1). Date of Electronic Publication: 2026 May 19.

Publication Type: Journal Article

Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

Aggregating single nucleotide polymorphisms improves filtering for false-positive associations postimputation.

Authors: Stahl, Katharina Papiol, Sergi Budde, Monika et al.

Source: G3: Genes | Genomes | Genetics. May2025, Vol. 15 Issue 5, p1-14. 14p.

Genome-wide association study provides insights into the genetic basis of Lewy body dementia.

Authors: Zhu P Jin Z Wu S et al.

Source: Molecular psychiatry [Mol Psychiatry] 2025 Dec; Vol. 30 (12), pp. 5813-5827. Date of Electronic Publication: 2025 Oct 09.

Publication Type: Journal Article; Meta-Analysis

Journal Info: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE