Elahi E - Search Results

1

Evolution of SARS-CoV-2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations.

Safari I, InanlooRahatloo K, Elahi E. Safari I, et al. Among authors: elahi e. J Med Virol. 2021 Apr;93(4):2010-2020. doi: 10.1002/jmv.26553. Epub 2020 Nov 1. J Med Virol. 2021. PMID: 32975856 Free PMC article.

2

The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine.

Jaberi E, Chitsazian F, Ali Shahidi G, Rohani M, Sina F, Safari I, Malakouti Nejad M, Houshmand M, Klotzle B, Elahi E. Jaberi E, et al. Among authors: elahi e. J Hum Genet. 2013 Aug;58(8):526-30. doi: 10.1038/jhg.2013.45. Epub 2013 Jun 13. J Hum Genet. 2013. PMID: 23759946

3

Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients.

Alavi A, Nafissi S, Rohani M, Shahidi G, Zamani B, Shamshiri H, Safari I, Elahi E. Alavi A, et al. Among authors: elahi e. Neurobiol Aging. 2014 Jan;35(1):267.e1-7. doi: 10.1016/j.neurobiolaging.2013.07.016. Epub 2013 Aug 17. Neurobiol Aging. 2014. PMID: 23962495

4

Mutation in CYP27A1 identified in family with coronary artery disease.

Inanloorahatloo K, Zand Parsa AF, Huse K, Rasooli P, Davaran S, Platzer M, Fan JB, Amini S, Steemers F, Elahi E. Inanloorahatloo K, et al. Among authors: elahi e. Eur J Med Genet. 2013 Dec;56(12):655-60. doi: 10.1016/j.ejmg.2013.09.008. Epub 2013 Sep 28. Eur J Med Genet. 2013. PMID: 24080357

5

Lack of Association between the MEF2A Gene and Coronary Artery Disease in Iranian Families.

Inanloo Rahatloo K, Davaran S, Elahi E. Inanloo Rahatloo K, et al. Among authors: elahi e. Iran J Basic Med Sci. 2013 Aug;16(8):950-4. Iran J Basic Med Sci. 2013. PMID: 24106602 Free PMC article.

6

Mutation in ST6GALNAC5 identified in family with coronary artery disease.

InanlooRahatloo K, Parsa AF, Huse K, Rasooli P, Davaran S, Platzer M, Kramer M, Fan JB, Turk C, Amini S, Steemers F, Gunderson K, Ronaghi M, Elahi E. InanlooRahatloo K, et al. Among authors: elahi e. Sci Rep. 2014 Jan 8;4:3595. doi: 10.1038/srep03595. Sci Rep. 2014. PMID: 24399302 Free PMC article.

7

Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.

Suri F, Narooie-Nejad M, Safari I, Moazzeni H, Rohani MR, Khajeh A, Klotzle B, Fan JB, Elahi E. Suri F, et al. Among authors: elahi e. J Neurol Sci. 2014 Dec 15;347(1-2):305-9. doi: 10.1016/j.jns.2014.10.031. Epub 2014 Oct 22. J Neurol Sci. 2014. PMID: 25455305

8

A Possible Role for LTBP2 in the Etiology of Primary Angle Closure Glaucoma.

Safari I, Akbarian S, Yazdani S, Elahi E. Safari I, et al. Among authors: elahi e. J Ophthalmic Vis Res. 2015 Apr-Jun;10(2):123-9. doi: 10.4103/2008-322X.163783. J Ophthalmic Vis Res. 2015. PMID: 26425313 Free PMC article.

9

The p.Gly61Glu Mutation in CYP1B1 Affects the Extracellular Matrix in Glaucoma Patients.

Safari I, Suri F, Haji-Seyed-Javadi R, Yazdani S, Elahi E. Safari I, et al. Among authors: elahi e. Ophthalmic Res. 2016 Jul;56(2):98-103. doi: 10.1159/000443508. Epub 2016 Mar 17. Ophthalmic Res. 2016. PMID: 26982174

10

COL18A1 is a candidate eye iridocorneal angle-closure gene in humans.

Suri F, Yazdani S, Chapi M, Safari I, Rasooli P, Daftarian N, Jafarinasab MR, Ghasemi Firouzabadi S, Alehabib E, Darvish H, Klotzle B, Fan JB, Turk C, Elahi E. Suri F, et al. Among authors: elahi e. Hum Mol Genet. 2018 Nov 1;27(21):3772-3786. doi: 10.1093/hmg/ddy256. Hum Mol Genet. 2018. PMID: 30007336

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