Search Results - "Backman JD"

Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource.

Authors: Koch C Khalid S Khan MZ et al.

Corporate Authors: Koch C Khalid S Khan MZ et al.

Source: Nature [Nature] 2026 Jun 17. Date of Electronic Publication: 2026 Jun 17.

Publication Type: Journal Article

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

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.

Envisioning population‐scale immune multi‐omics atlas projects.

Authors: Zheng, Yuhui Yin, Jianhua Liu, Chuanyu

Source: Clinical & Translational Medicine. May2026, Vol. 16 Issue 5, p1-4. 4p.

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

Authors: Butler-Laporte, Guillaume Povysil, Gundula Kosmicki, Jack A. et al.

Source: PLoS Genetics. 11/3/2022, Vol. 18 Issue 11, p1-26. 26p.

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.

Genetic testing in individuals with extreme HDL-C levels: Diagnostic yield and clinical implications from the Tromsø Study.

Authors: Ølnes, Åsa Schawlann Teigen, Marianne Strøm, Thea Bismo et al.

Source: PLoS ONE. 4/20/2026, Vol. 21 Issue 4, p1-18. 18p.

Monogenic and SLE-like disorders in the pediatric population: insights from a Northern Israel cohort.

Authors: Spivak, Ilia Hershkovitz, Tova Weiss, Karin et al.

Source: Lupus. Mar2026, Vol. 35 Issue 3, p289-300. 12p.

Unsupervised feature extraction using deep learning empowers discovery of genetic determinants of the electrocardiogram.

Authors: Sieliwonczyk, Ewa Sau, Arunashis Patlatzoglou, Konstantinos et al.

Source: Genome Medicine. 10/9/2025, Vol. 17 Issue 1, p1-17. 17p.

Effect of healthy lifestyle on renal dysfunction risk: interactions with genetic risk.

Authors: Takase, Masato Nakaya, Naoki Kogure, Mana et al.

Source: Clinical Kidney Journal. Oct2025, Vol. 18 Issue 10, p1-11. 11p.

Meta-evolutionary exome analysis identifies novel type 2 diabetes mellitus genes in the UK Biobank and all of us.

Authors: Wilhelm, Kevin Asmussen, Jennifer Lee, Kwanghyuk et al.

Source: PLoS Genetics. 9/30/2025, Vol. 21 Issue 9, p1-28. 28p.

Exome sequencing identifies novel genetic variants associated with varicose veins.

Authors: Zhang, Dan-Dan He, Xiao-Yu Yang, Liu et al.

Source: PLoS Genetics. 7/9/2024, Vol. 20 Issue 7, p1-25. 25p.

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes.

Authors: Henry A Mo X Finan C et al.

Corporate Authors: Henry A Mo X Finan C et al.

Source: Nature genetics [Nat Genet] 2025 Apr; Vol. 57 (4), pp. 815-828. Date of Electronic Publication: 2025 Mar 04.

Publication Type: Journal Article; Meta-Analysis

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies.

Authors: Cavazos, Taylor B. Kachuri, Linda Graff, Rebecca E. et al.

Source: BMC Medicine. 10/6/2022, Vol. 20 Issue 1, p1-12. 12p.

Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy.

Authors: Zheng SL Henry A Cannie D et al.

Corporate Authors: Zheng SL Henry A Cannie D et al.

Source: Nature genetics [Nat Genet] 2024 Dec; Vol. 56 (12), pp. 2646-2658. Date of Electronic Publication: 2024 Nov 21.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

Exome‐wide molecular insights from blood and urine liquid biopsies in genitourinary cancers.

Authors: Jia, Eric Zheng, Tiantian Huang, Yong et al.

Source: UroPrecision. Dec2025, Vol. 3 Issue 4, p254-262. 9p.

Predicting clopidogrel resistance in acute ischemic stroke patients: key clinical insights and a novel diagnostic nomogram.

Authors: Tang, Mingzhu Li, Xiaoying Zhong, Gaoxian et al.

Source: BMC Neurology. 6/3/2025, Vol. 25 Issue 1, p1-11. 11p.

A Mendelian randomization study: causal relationship between immune cells and the risks of social phobia, specific phobia, and agoraphobia.

Authors: Wang, Jun-Neng Yu, Dong-Hu Li, Zhi-Yu et al.

Source: BMC Psychiatry. 4/8/2025, Vol. 25 Issue 1, p1-7. 7p.

Circulating transthyretin with atrial morpho-functional phenotypes and atrial fibrillation risk, and the modifying role of BMI.

Authors: Zhang, Nan Jia, Ziheng Zhao, Jinhua et al.

Source: BMC Medicine. 10/14/2025, Vol. 23 Issue 1, p1-15. 15p.

Genome‐wide association study and polygenic risk scores of eosinophilia in Taiwan.

Authors: Lu, Hsing‐Fang Boon‐Yong, Su Yang, Chi‐Ya et al.

Source: Clinical & Translational Immunology. 2025, Vol. 14 Issue 10, p1-10. 10p.

Trans-ancestry analysis in over 799,000 individuals yields new insights into the genetic etiology of colorectal cancer.

Authors: Yang, Changlong Chang, Zhenglin Dai, Youguo et al.

Source: PLoS ONE. 7/18/2024, Vol. 19 Issue 7, p1-15. 15p.