Results 251 to 260 of about 441,146 (309)

Multi‐Cohort Analysis Reveals Genetic Predispositions to Clonal Hematopoiesis as Mutation‐Specific Risk Factors for Stroke

Advanced Genetics, Volume 6, Issue 1, March 2025.
This study comprehensively evaluated the differential effect of clonal hematopoiesis (CH) mutations on the risk of various stroke subtypes and functional recovery. It shows that TET2 is associated with small vessel stroke possibly via a pro‐inflammatory pathway. Abstract Recent observational studies have found an association between Clonal Hematopoesis
Shuyang Lin, Yang E. Li, Yan Wang
wiley   +1 more source

Population structure and speciation history of two closely related wild tomato species [PDF]

, 2007
Arunyawat, Uraiwan
core  

The relationship of genetic signature for cardiometabolic risk with biomarkers of inflammatory and oxidative stress in diabetic patients. [PDF]

BMC Endocr Disord
Abaj F, Aali Y, Najafi F, Koohdani F.
europepmc   +1 more source

Mendelian randomization study reveals the causal effect of sex hormone binding globulin on osteoporosis. [PDF]

BMC Musculoskelet Disord
Zuo GS, Huang Y, Wang Z, Wang H, Wu F.
europepmc   +1 more source

Dissecting the Genetic Correlations and Causal Effects of Gut Microbiota on Pan-Cancer Phenotype: Driven by Common Dietary Preferences. [PDF]

Food Sci Nutr
Zhou Y, Feng Y, Wang Y, Wang Y, Liu X, Sun T, Xu J.   +6 more
europepmc   +1 more source

Gene polymorphisms of miR-323b and miR-1343 that regulate kininogen L are associated with schizophrenia susceptibility: A preliminary population‑based study. [PDF]

Biomol Biomed
Liu X, Jin M, Yang M, Yan L, Zhao W, Liu L, Wang H, Ding Y, Sun Y, Zhang Y, Yu Q.   +10 more
europepmc   +1 more source

The Impact of Selected <i>COL1A1</i> and <i>COL1A2</i> Gene Polymorphisms on Bone Mineral Density and the Risk of Metabolic Diseases in Postmenopausal Women. [PDF]

Int J Mol Sci
Cichocka E, Górczyńska-Kosiorz SB, Niemiec P, Trautsolt W, Gumprecht J.   +4 more
europepmc   +1 more source

Thyroid Hormone Dynamics and DIO2 Variants in Schizophrenia: Exploring Genetic Links to Neuroendocrine Imbalance. [PDF]

J Cell Mol Med
Akan G, Adolf IC, Colak A, Acar S, Oncu F, Yesilbursa D, Turkcan S, Atalar F, Gazioglu SB.   +8 more
europepmc   +1 more source

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Hypertension and single nucleotide polymorphisms

Current Hypertension Reports, 2000
Hypertension is a common, complex disease phenotype that has been intensively studied to identify susceptibility loci in humans. Candidate genes continue to be uncovered via genetic analysis in model organisms through linkage analysis with families and/or sib-pairs and through association studies using sequence variants in genes that play a role in key
Deborah A. Nickerson, Mark J. Rieder
openaire   +3 more sources

Classifying single nucleotide polymorphisms in humans

Molecular Genetics and Genomics, 2021
Single nucleotide polymorphisms (SNPs) are the most common form of genetic variation amongst the human population and are key to personalized medicine. New tests are presented to distinguish pathogenic/malign (i.e., likely to contribute to or cause a disease) from nonpathogenic/benign SNPs, regardless of whether they occur in coding (exon) or noncoding
Shima Azizzadeh-Roodpish, Max H Garzon, Sambriddhi Mainali   +2 more
openaire   +3 more sources