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S Mohsen Hosseini

Explore the profile of S Mohsen Hosseini including associated specialties, affiliations and a list of published articles. Areas
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Articles 32
Citations 1780
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Recent Articles
11.
Reuter M, Jobling R, Chaturvedi R, Manshaei R, Costain G, Heung T, et al.
Genet Med . 2018 Sep; 21(4):1001-1007. PMID: 30232381
Purpose: To determine disease-associated single-gene variants in conotruncal defects, particularly tetralogy of Fallot (TOF). Methods: We analyzed for rare loss-of-function and deleterious variants in FLT4 (VEGFR3) and other genes in...
12.
Hosseini S, Kim R, Udupa S, Costain G, Jobling R, Liston E, et al.
Circulation . 2018 Jul; 138(12):1195-1205. PMID: 29959160
Background: Implicit in the genetic evaluation of patients with suspected genetic diseases is the assumption that the genes evaluated are causative for the disease based on robust scientific and statistical...
13.
Tedja M, Wojciechowski R, Hysi P, Eriksson N, Furlotte N, Verhoeven V, et al.
Nat Genet . 2018 May; 50(6):834-848. PMID: 29808027
Refractive errors, including myopia, are the most frequent eye disorders worldwide and an increasingly common cause of blindness. This genome-wide association meta-analysis in 160,420 participants and replication in 95,505 participants...
14.
Reuter M, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, et al.
CMAJ . 2018 Feb; 190(5):E126-E136. PMID: 29431110
Background: The Personal Genome Project Canada is a comprehensive public data resource that integrates whole genome sequencing data and health information. We describe genomic variation identified in the initial recruitment...
15.
Lionel A, Costain G, Monfared N, Walker S, Reuter M, Hosseini S, et al.
Genet Med . 2017 Aug; 20(4):435-443. PMID: 28771251
PurposeGenetic testing is an integral diagnostic component of pediatric medicine. Standard of care is often a time-consuming stepwise approach involving chromosomal microarray analysis and targeted gene sequencing panels, which can...
16.
Khoshhali M, Kazemi I, Hosseini S, Seirafian S
Kidney Res Clin Pract . 2017 Jul; 36(2):182-191. PMID: 28680826
Background: In peritoneal dialysis, technique failure is an important metric to be considered. This study was performed in order to identify the relationship between trajectories of serum albumin levels and...
17.
Roshandel D, Klein R, Klein B, Wolffenbuttel B, van der Klauw M, van Vliet-Ostaptchouk J, et al.
Diabetes . 2016 May; 65(7):2060-71. PMID: 27207532
Skin fluorescence (SF) noninvasively measures advanced glycation end products (AGEs) in the skin and is a risk indicator for diabetes complications. N-acetyltransferase 2 (NAT2) is the only known locus influencing...
18.
Fan Q, Guo X, Tideman J, Williams K, Yazar S, Hosseini S, et al.
Sci Rep . 2016 May; 6:25853. PMID: 27174397
Myopia, currently at epidemic levels in East Asia, is a leading cause of untreatable visual impairment. Genome-wide association studies (GWAS) in adults have identified 39 loci associated with refractive error...
19.
Fan Q, Verhoeven V, Wojciechowski R, Barathi V, Hysi P, Guggenheim J, et al.
Nat Commun . 2016 Mar; 7:11008. PMID: 27020472
Myopia is the most common human eye disorder and it results from complex genetic and environmental causes. The rapidly increasing prevalence of myopia poses a major public health challenge. Here,...
20.
Porta M, Toppila I, Sandholm N, Hosseini S, Forsblom C, Hietala K, et al.
Diabetes . 2016 Jan; 65(4):1022-30. PMID: 26718501
The risk of long-term diabetes complications is not fully explained by diabetes duration or long-term glycemic exposure, suggesting the involvement of genetic factors. Because thiamine regulates intracellular glucose metabolism and...