Search Results - "Dron JS"

Exome-wide association study of blood lipids in 1,158,017 individuals from diverse populations.

Authors: Koyama S Yu Z Choi SH et al.

Corporate Authors: Koyama S Yu Z Choi SH et al.

Source: Nature genetics [Nat Genet] 2026 Jun; Vol. 58 (6), pp. 1268-1279. Date of Electronic Publication: 2026 May 25.

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

Human plasma proteomic profile of clonal hematopoiesis.

Authors: Yu Z Vromman A Nguyen NQH et al.

Corporate Authors: Yu Z Vromman A Nguyen NQH et al.

Source: Nature communications [Nat Commun] 2025 Nov 27; Vol. 16 (1), pp. 11688. Date of Electronic Publication: 2025 Nov 27.

Publication Type: Journal Article

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

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.

Analysis of targeted and whole genome sequencing of PacBio HiFi reads for a comprehensive genotyping of gene-proximal and phenotype-associated Variable Number Tandem Repeats.

Authors: Javadzadeh, Sara Adamson, Aaron Park, Jonghun et al.

Source: PLoS Computational Biology. 4/7/2025, Vol. 21 Issue 4, p1-21. 21p.

Evaluating the impact of a new educational tool on understanding of polygenic risk scores for alcohol use disorder.

Authors: Driver MN Kuo SI Petronio L et al.

Source: Frontiers in psychiatry [Front Psychiatry] 2022 Nov 23; Vol. 13, pp. 1025483. Date of Electronic Publication: 2022 Nov 23 (Print Publication: 2022).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101545006 Publication Model: eCollection Cited Medium: Print ISSN: 1664-0640 (Print) Linking ISSN: 16640640 NLM ISO Abbreviation: Front Psychiatry Subsets: PubMed not MEDLINE

Transient islet-antigen 2 positivity at diagnosis of diabetes during COVID-19 infection in an adolescent with a NEUROD1 variant: a case report.

Authors: Yee, Jennifer K. Anand, Seerat Sanabria, Juan C. et al.

Source: Journal of Medical Case Reports. 6/5/2025, Vol. 19 Issue 1, p1-5. 5p.

Evaluation of glycemic status and subclinical atherosclerosis in familial hypercholesterolemia subjects with or without LDL receptor mutation.

Authors: Di Giacomo Barbagallo, Francesco Bosco, Giosiana Di Marco, Maurizio et al.

Source: Cardiovascular Diabetology. 3/20/2025, Vol. 24 Issue 1, p1-10. 10p.

A multidisciplinary management model for severe gestational hypertriglyceridemia: using plasmapheresis to prevent pancreatitis in pregnancy.

Authors: Zheng, Xixi Xia, Peng Yue, Cai et al.

Source: BMC Pregnancy & Childbirth. 10/14/2025, Vol. 25 Issue 1, p1-11. 11p.

Gain of function variants in PCSK9 gene in high risk patients after myocardial infarction with increased lipoprotein (a) values and treated with statins.

Authors: Ugovšek, Sabina Likozar, Andreja Rehberger Levstek, Tina et al.

Source: Scientific Reports. 7/23/2025, Vol. 15 Issue 1, p1-11. 11p.

Lipoprotein lipase deficiency: heterozygotes match homozygotes in severity.

Authors: Szczęśniak, Dominika Bednarska-Makaruk, Małgorzata Drgas, Olga et al.

Source: Archives of Medical Science. 2025, Vol. 21 Issue 3, p750-756. 7p.

Early‐onset familial hypercholesterolemia: A case of extensive xanthomas and premature coronary artery disease.

Authors: Kalsi, Harsimran Singla, Ankur Kaur, Sukhjot et al.

Source: Clinical Case Reports. Oct2024, Vol. 12 Issue 10, p1-6. 6p.

Association between dyslipidemia and the risk of incident chronic kidney disease affected by genetic susceptibility: Polygenic risk score analysis.

Authors: Weon, Boram Jang, Yunjeong Jo, Jinyeon et al.

Source: PLoS ONE. 4/16/2024, Vol. 19 Issue 4, p1-14. 14p.

Significant but partial lipoprotein lipase functional loss caused by a novel occurrence of rare LPL biallelic variants.

Authors: Hu, Yuepeng Chen, Jian-Min Zuo, Han et al.

Source: Lipids in Health & Disease. 4/1/2024, Vol. 23 Issue 1, p1-10. 10p.

Genetic Architecture and Clinical Outcomes of Combined Lipid Disturbances.

Authors: Gilliland T Dron JS Selvaraj MS et al.

Source: Circulation research [Circ Res] 2024 Jul 05; Vol. 135 (2), pp. 265-276. Date of Electronic Publication: 2024 Jun 03.

Publication Type: Journal Article

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0047103 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1524-4571 (Electronic) Linking ISSN: 00097330 NLM ISO Abbreviation: Circ Res Subsets: MEDLINE

BIOCHEMICAL CHARACTERISATION OF FAMILIAL HYPERCHOLESTEROLEMIA: ASSOCIATIONS BETWEEN GENETIC AND LIPID PROFILES.

Alternate Title: BIOHEMIJSKA KARAKTERIZACIJA FAMILIJARNE HIPERHOLESTEROLEMIJE: POVEZANOST GENETIČKIH I LIPIDNIH PARAMETARA.

Authors: Lukač, Sandra Singh Gašić, Vladimir Komazec, Jovana et al.

Source: Journal of Medical Biochemistry. Dec2025, Vol. 44 Issue 9, p2026-2034. 9p.

Identification of a novel heterozygous GPD1 missense variant in a Chinese adult patient with recurrent HTG-AP consuming a high-fat diet and heavy smoking.

Authors: Li, Xiao-Yao Zhang, Bei-Yuan Liang, Xin-Ran et al.

Source: BMC Medical Genomics. 1/23/2025, Vol. 18 Issue 1, p1-14. 14p.

Mistranslating tRNA variants have anticodon- and sex-specific impacts on Drosophila melanogaster.

Authors: Isaacson, Joshua R Berg, Matthew D Jagiello, Jessica et al.

Source: G3: Genes | Genomes | Genetics. Dec2024, Vol. 14 Issue 12, p1-13. 13p.

Polygenic Risk Score Predicts Sudden Death in Patients With Coronary Disease and Preserved Systolic Function.

Authors: Sandhu RK Dron JS Liu Y et al.

Source: Journal of the American College of Cardiology [J Am Coll Cardiol] 2022 Aug 30; Vol. 80 (9), pp. 873-883.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Biomedical Country of Publication: United States NLM ID: 8301365 Publication Model: Print Cited Medium: Internet ISSN: 1558-3597 (Electronic) Linking ISSN: 07351097 NLM ISO Abbreviation: J Am Coll Cardiol Subsets: MEDLINE

Clinical characteristics of heart failure with reduced ejection fraction patients with rare pathogenic variants in dilated cardiomyopathy‐associated genes: A subgroup analysis of the PARADIGM‐HF trial.

Authors: Barat, Ana Chen, Chien‐Wei Patel‐Murray, Natasha et al.

Source: European Journal of Heart Failure. Aug2023, Vol. 25 Issue 8, p1256-1266. 11p. 2 Diagrams, 3 Charts, 2 Graphs.

Tachol1 QTL on mouse chromosome 1 is responsible for hypercholesterolemia and diet-induced obesity.

Authors: Kim, Jung Han Simpkins, Marvin A. Williams, Nicholas T. et al.

Source: Mammalian Genome. Sep2024, Vol. 35 Issue 3, p324-333. 10p.