Items where Author is "Sadeghian, L."

Article

(2024) Comparing vitamin D receptor gene polymorphisms in rs11568820, rs7970314, rs4334089 between COVID-19 patients with mild and severe symptoms: a case control study. Scientific Reports. p. 7. ISSN 2045-2322

(2024) Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family. Egyptian Journal of Medical Human Genetics. p. 8. ISSN 1110-8630

(2023) Genetic variation in salt taste receptors impact salt intake and blood pressure. Scientific Reports. p. 8. ISSN 2045-2322

(2023) Isfahan Twin Cohort: A Ten-Year Longitudinal Prospective Study Based on A Twin Registry. Arya Atherosclerosis. pp. 117-124. ISSN 1735-3955

(2022) Association study of polymorphism in Thrombomodulin gene rs1042579 with cardiovascular disease. Acta Biomed. e2021282. ISSN 0392-4203 (Print) 0392-4203

(2022) Precision medicine and metabolic syndrome. ARYA Atherosclerosis. p. 10. ISSN 1735-3955

(2021) Apolipoprotein B gene mutation related to familial hypercholesterolemia in an Iranian population: With or without hypothyroidism. JOURNAL OF RESEARCH IN MEDICAL SCIENCES. ISSN 1735-1995 1735-7136 J9 - J RES MED SCI

(2021) Association study of polymorphism in Thrombomodulin gene (rs1042579) with cardiovascular disease. Acta Biomedica. ISSN 03924203 (ISSN)

(2021) Polymorphisms of LPA gene, rs1801693 and rs7765781, are not associated with premature myocardial infarction in the Iranian population. ARYA Atheroscler. pp. 1-8. ISSN 1735-3955 (Print) 1735-3955

(2019) Isfahan Twins Registry (ITR): An Invaluable Platform for Epidemiological and Epigenetic Studies: Design and Methodology of ITR. Twin Research and Human Genetics. pp. 579-582. ISSN 1832-4274

(2019) Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred. Int J Pediatr Otorhinolaryngol. pp. 99-105. ISSN 1872-8464 (Electronic) 0165-5876 (Linking)

(2018) Frequency of gjb2 mutations in families with autosomal recessive non-syndromic hearing loss in Khuzestan province. Genetika. pp. 837-846. ISSN 05340012 (ISSN)