Associated Papers
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
Genetic polymorphisms associated with obesity in the Arab world: a systematic review.
Younes S et al.
International Journal of Obesity (2005), 2021
Whole genome mapping and identification of single nucleotide polymorphisms of four Bangladeshi individuals and their functional significance.
Khan S et al.
Bmc Research Notes, 2021
Assessment of Genetic Aspects of Non-alcoholic Fatty Liver and Premature Cardiovascular Events.
Saki S et al.
Middle East Journal of Digestive Diseases, 2020
Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.
Yupanqui-Lozno H et al.
Genes, 2019
Melanocortin 4 Receptor Pathway Dysfunction in Obesity: Patient Stratification Aimed at MC4R Agonist Treatment.
Ayers KL et al.
The Journal of Clinical Endocrinology and Metabolism, 2018
Contribution of polymorphisms in the LEP, LEPR and RETN genes on serum leptin and resistin levels in young adults from Mexico.
López-Quintero A et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2017
The Association between Pediatric NAFLD and Common Genetic Variants.
Umano GR et al.
Children (basel, Switzerland), 2017
Associations of TNF-α and IL-6 polymorphisms with osteoporosis through joint effects and interactions with LEPR gene in Taiwan: Taichung Community Health Study for Elders (TCHS-E).
Lin CC et al.
Molecular Biology Reports, 2016
Correlations Between Leptin Gene Polymorphisms 223 A/G, 1019 G/A, 492 G/C, 976 C/A, and Anthropometrical and Biochemical Parameters in Children With Obesity: A Prospective Case-Control Study in a Romanian Population-The Nutrichild Study.
Mărginean CO et al.
Medicine, 2016
The Association of Polymorphisms in Leptin/Leptin Receptor Genes and Ghrelin/Ghrelin Receptor Genes With Overweight/Obesity and the Related Metabolic Disturbances: A Review.
Ghalandari H et al.
International Journal of Endocrinology and Metabolism, 2015
Seven novel deleterious LEPR mutations found in early-onset obesity: a ΔExon6-8 shared by subjects from Reunion Island, France, suggests a founder effect.
Huvenne H et al.
The Journal of Clinical Endocrinology and Metabolism, 2015
Genetic association studies of obesity in Africa: a systematic review.
Yako YY et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity, 2015
Association of adiponectin gene polymorphism with nonalcoholic fatty liver disease in Taiwanese patients with type 2 diabetes.
Hsieh CJ et al.
Plos One, 2015
Novel variants in the MC4R and LEPR genes among severely obese children from the Iberian population.
Albuquerque D et al.
Annals of Human Genetics, 2014
Leptin and leptin receptor genetic variants associate with habitual physical activity and the arm body composition response to resistance training.
Walsh S et al.
Gene, 2012
[Meta-analysis on the relationship between leptin receptor Gln223Arg and Pro1019Pro gene polymorphism and obesity in the Chinese population].
Yang GP et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi, 2011
The G3057A LEPR polymorphism is associated with obesity in Tunisian women.
Ben Ali S et al.
Nutrition, Metabolism, and Cardiovascular Diseases : Nmcd, 2011
Genetic polymorphisms in non-alcoholic fatty liver disease: clues to pathogenesis and disease progression.
Duvnjak M et al.
World Journal of Gastroenterology, 2009
Polymorphism of human leptin receptor gene is associated with type 2 diabetic patients complicated with non-alcoholic fatty liver disease in China.
Lu H et al.
Journal of Gastroenterology and Hepatology, 2009
Linkages and associations between the leptin receptor (LEPR) gene and human body composition in the Québec Family Study.
Chagnon YC et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity, 1999