Associated Papers
A cell and transcriptome atlas of human arterial vasculature.
Zhao Q et al.
Biorxiv : the Preprint Server for Biology, 2025
The interaction of vitamin D supplementation with Omentin-1 gene polymorphism on metabolic biomarkers, omentin-1 levels and anthropometric measures in women with prediabetes: A double-blind randomized controlled trial.
Molani-Gol R et al.
Diabetes, Obesity & Metabolism, 2025
The role of visfatin and omentin-1 gene polymorphism in pancreatic ductal adenocarcinoma (PDAC).
Badr EA et al.
Molecular Biology Reports, 2025
The role of rs2236242 at SERPINA12 gene and vaspin level on papillary thyroid carcinoma.
Torki S et al.
Nucleosides, Nucleotides & Nucleic Acids, 2025
Role of genetic variants and DNA methylation of lipid metabolism-related genes in metabolic dysfunction-associated steatotic liver disease.
Wang JJ et al.
Frontiers in Physiology, 2025
Whole exome sequencing and machine learning germline analysis of individuals presenting with extreme phenotypes of high and low risk of developing tobacco-associated lung adenocarcinoma.
Patiño-García A et al.
Ebiomedicine, 2024
Association of single nucleotide polymorphisms in ITLN1 gene with ischemic stroke risk in Xi'an population, Shaanxi province.
Shi W et al.
Peerj, 2024
Association of Intelectin 1 Gene rs2274907 A > T Polymorphism with Obesity, Type 2 Diabetes, Serum Intelectin-1 Levels and Lipid Profiles in Turkish Adults.
Guclu-Geyik F et al.
Biochemical Genetics, 2023
Forkhead Box Class O3A Gene Polymorphism and Psoriasis.
Keebayoon A et al.
The Journal of Clinical and Aesthetic Dermatology, 2023
Genetics of Chronic Kidney Disease in Low-Resource Settings.
Ilori T et al.
Seminars in Nephrology, 2022
Val109Asp polymorphism in Intelectin 1 gene is associated with coronary artery disease severity in women.
Güçlü-Geyik F et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir, 2022
Characterization of an intelectin-1 (Itln1) knockout mouse model.
Nonnecke EB et al.
Frontiers in Immunology, 2022
Association between intelectin-1 variation and human kidney stone disease in northeastern Thai population.
Pungsrinont T et al.
Urolithiasis, 2021
Association of the Adipokines Chemerin, Apelin, Vaspin and Omentin and Their Functional Genetic Variants with Rheumatoid Arthritis.
Wahba AS et al.
Journal of Personalized Medicine, 2021
Human intelectin-1 (ITLN1) genetic variation and intestinal expression.
Nonnecke EB et al.
Scientific Reports, 2021
Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer.
Liu S et al.
Communications Biology, 2021
Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis.
Heng AHS et al.
Bmc Medical Genomics, 2021
Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.
Somineni HK et al.
American Journal of Human Genetics, 2021
Val109Asp Polymorphism of the Omentin-1 Gene and Incidence of Knee Osteoarthritis in a Chinese Han Population: A Correlation Analysis.
Chen R et al.
Drug Design, Development and Therapy, 2021
Are Omentin Rs2274907 and Vaspin Rs2236242 Gene Polymorphisms Related to Body Composition, Lipid Profile and Other Adipokines in Prepubertal Healthy Children?
Gajewska J et al.
Endocrine Research, 2020
Association between serum cell adhesion molecules with hs-CRP, uric acid and VEGF genetic polymorphisms in subjects with metabolic syndrome.
Ghazizadeh H et al.
Molecular Biology Reports, 2020
Circulatory Omentin-1 levels but not genetic variants influence the pathophysiology of Type 2 diabetes.
Rathwa N et al.
Cytokine, 2019
Association of Omentin rs2274907 and FTO rs9939609 gene polymorphisms with insulin resistance in Iranian individuals with newly diagnosed type 2 diabetes.
Khoshi A et al.
Lipids in Health and Disease, 2019
Evaluation of the Association of Omentin 1 rs2274907 A>T and rs2274908 G>A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case Control Study.
Jha CK et al.
Journal of Personalized Medicine, 2019
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Khan MJ et al.
Scientific Reports, 2018
Omentin Val/Val genotype increases predisposition to acne vulgaris without changing omentin serum level.
Soguktas H et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2018
The association of Val109Asp polymorphic marker of intelectin 1 gene with abdominal obesity in Kyrgyz population.
Isakova J et al.
Bmc Endocrine Disorders, 2018
Fine-mapping inflammatory bowel disease loci to single-variant resolution.
Huang H et al.
Nature, 2017
Omentin Val109Asp polymorphism and risk of coronary artery disease.
Jamshidi J et al.
Asian Cardiovascular & Thoracic Annals, 2017
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015
Omentin-1 plasma levels and omentin-1 expression are decreased in psoriatic lesions of psoriasis patients.
Zhang C et al.
Archives of Dermatological Research, 2015
Omentin Polymorphism and its Relations to Bone Mineral Density in Women.
Boron D et al.
Archives of Medical Research, 2015
Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.
Ilyas M et al.
Bmc Genomics, 2015
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
The common polymorphism Val109Asp in the omentin gene is associated with daily energy intake in the Central-European population.
Splichal Z et al.
Nutritional Neuroscience, 2015
IBD candidate genes and intestinal barrier regulation.
McCole DF
Inflammatory Bowel Diseases, 2014
Association of omentin Val109Asp polymorphism with coronary artery disease.
Yörük U et al.
Anadolu Kardiyoloji Dergisi : Akd = the Anatolian Journal of Cardiology, 2014
Omentin serum levels and omentin gene Val109Asp polymorphism in patients with psoriasis.
Turan H et al.
International Journal of Dermatology, 2014
Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population.
Tabassum R et al.
Journal of Human Genetics, 2012