Fallah MS - Search Results

1

Heritability of the metabolic syndrome and its components in the Tehran Lipid and Glucose Study (TLGS).

Zarkesh M, Daneshpour MS, Faam B, Fallah MS, Hosseinzadeh N, Guity K, Hosseinpanah F, Momenan AA, Azizi F. Zarkesh M, et al. Among authors: fallah ms. Genet Res (Camb). 2012 Dec;94(6):331-7. doi: 10.1017/S001667231200050X. Genet Res (Camb). 2012. PMID: 23374242

2

The Relation between Metabolic Syndrome Risk Factors and Genetic Variations of Apolipoprotein V in Relation with Serum Triglyceride and HDL-C Level.

Fallah MS, Sedaghatikhayat B, Guity K, Akbari F, Azizi F, Daneshpour MS. Fallah MS, et al. Arch Iran Med. 2016 Jan;19(1):46-50. Arch Iran Med. 2016. PMID: 26702748

3

Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS).

Daneshpour MS, Fallah MS, Sedaghati-Khayat B, Guity K, Khalili D, Hedayati M, Ebrahimi A, Hajsheikholeslami F, Mirmiran P, Ramezani Tehrani F, Momenan AA, Ghanbarian A, Amouzegar A, Amiri P, Azizi F. Daneshpour MS, et al. Among authors: fallah ms. JMIR Res Protoc. 2017 Feb 23;6(2):e28. doi: 10.2196/resprot.6050. JMIR Res Protoc. 2017. PMID: 28232301 Free PMC article.

4

Lack of association between FTO gene variations and metabolic healthy obese (MHO) phenotype: Tehran Cardio-metabolic Genetic Study (TCGS).

Sedaghati-Khayat B, Barzin M, Akbarzadeh M, Guity K, Fallah MS, Pourhassan H, Azizi F, Daneshpour MS. Sedaghati-Khayat B, et al. Among authors: fallah ms. Eat Weight Disord. 2020 Feb;25(1):25-35. doi: 10.1007/s40519-018-0493-2. Epub 2018 Mar 10. Eat Weight Disord. 2020. PMID: 29525920

5

Increased Risk of CHD in the Presence of rs7865618 (A allele): Tehran Lipid and Glucose Study.

Matoo S, Fallah MS, Daneshpour MS, Mousavi R, Sedaghati Khayat B, Hasanzad M, Azizi F. Matoo S, et al. Among authors: fallah ms. Arch Iran Med. 2017 Mar;20(3):153-157. Arch Iran Med. 2017. PMID: 28287809

6

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.

Steinthorsdottir V, Thorleifsson G, Sulem P, Helgason H, Grarup N, Sigurdsson A, Helgadottir HT, Johannsdottir H, Magnusson OT, Gudjonsson SA, Justesen JM, Harder MN, Jørgensen ME, Christensen C, Brandslund I, Sandbæk A, Lauritzen T, Vestergaard H, Linneberg A, Jørgensen T, Hansen T, Daneshpour MS, Fallah MS, Hreidarsson AB, Sigurdsson G, Azizi F, Benediktsson R, Masson G, Helgason A, Kong A, Gudbjartsson DF, Pedersen O, Thorsteinsdottir U, Stefansson K. Steinthorsdottir V, et al. Among authors: fallah ms. Nat Genet. 2014 Mar;46(3):294-8. doi: 10.1038/ng.2882. Epub 2014 Jan 26. Nat Genet. 2014. PMID: 24464100

7

Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS).

Najd Hassan Bonab L, Moazzam-Jazi M, Miri Moosavi RS, Fallah MS, Lanjanian H, Masjoudi S, Daneshpour MS. Najd Hassan Bonab L, et al. Among authors: fallah ms. Gene. 2021 Apr 30;778:145485. doi: 10.1016/j.gene.2021.145485. Epub 2021 Feb 11. Gene. 2021. PMID: 33581269

8

Reporting the presence of three different diseases causing GJB2 mutations in a consanguineous deaf family.

Davoudi-Dehaghani E, Fallah MS, Shirzad T, Tavakkoly-Bazzaz J, Bagherian H, Zeinali S. Davoudi-Dehaghani E, et al. Among authors: fallah ms. Int J Audiol. 2014 Feb;53(2):128-31. doi: 10.3109/14992027.2013.850748. Epub 2013 Nov 13. Int J Audiol. 2014. PMID: 24224790

9

Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing.

Davoudi-Dehaghani E, Fallah MS, Tavakkoly-Bazzaz J, Bagherian H, Zeinali S. Davoudi-Dehaghani E, et al. Among authors: fallah ms. Acta Otolaryngol. 2015 Feb;135(2):125-9. doi: 10.3109/00016489.2014.969383. Epub 2014 Nov 25. Acta Otolaryngol. 2015. PMID: 25423259

10

Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran.

Sharifi Z, Taheri M, Fallah MS, Abiri M, Golnabi F, Bagherian H, Zeinali R, Farahzadi H, Alborji M, Tehrani PG, Amini M, Asnavandi S, Hashemi M, Forouzesh F, Zeinali S. Sharifi Z, et al. Among authors: fallah ms. J Mol Neurosci. 2021 Nov;71(11):2281-2298. doi: 10.1007/s12031-020-01789-0. Epub 2021 Jan 22. J Mol Neurosci. 2021. PMID: 33481221

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