Genetic Basis of Primary Angle Closure Glaucoma: The Role of Collagens and Extracellular Matrix

per Elahi, Elahe
Publicat a J Ophthalmic Vis Res (2020)

Discovery of Single Nucleotide Polymorphisms and Mutations by Pyrosequencing

per Ronaghi, Mostafa, Elahi, Elahe
Publicat 2002

Glaucoma in Iran and Contributions of Studies in Iran to the Understanding of the Etiology of Glaucoma

per Suri, Fatemeh, Yazdani, Shahin, Elahi, Elahe
Publicat a J Ophthalmic Vis Res (2015)

Confident gene activity prediction based on single histone modification H2BK5ac in human cell lines

per Chitsazian, Fereshteh, Sadeghi, Mehdi, Elahi, Elahe
Publicat a BMC Bioinformatics (2017)

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

per Inanloo Rahatloo, Kolsoum, Davaran, Saeid, Elahi, Elahe
Publicat 2013

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

per Safari, Iman, InanlooRahatloo, Kolsoum, Elahi, Elahe
Publicat a J Med Virol (2020)

Global haplotype partitioning for maximal associated SNP pairs

per Katanforoush, Ali, Sadeghi, Mehdi, Pezeshk, Hamid, Elahi, Elahe
Publicat 2009

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

per Safari, Iman, Akbarian, Shadi, Yazdani, Shahin, Elahi, Elahe
Publicat a J Ophthalmic Vis Res (2015)

Observation of c.260A > G mutation in superoxide dismutase 1 that causes p.Asn86Ser in Iranian amyotrophic lateral sclerosis patient and absence of genotype/phenotype correlation

per Khani, Marzieh, Alavi, Afagh, Nafissi, Shahriar, Elahi, Elahe
Publicat a Iran J Neurol (2015)

P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran

per Qashqai, Mansoure, Suri, Fatemeh, Yaseri, Mehdi, Elahi, Elahe
Publicat a J Ophthalmic Vis Res (2018)

Multiplex Pyrosequencing

per Pourmand, Nader, Elahi, Elahe, Davis, Ronald W., Ronaghi, Mostafa
Publicat 2002

Myocilin Mutations Are Not a Major Cause of Primary Congenital Glaucoma in Iranian Patients

per Elahi, Elahe, Narooie-Nejhad, Mehrnaz, Suri, Fatemeh, yazdani, Shahin
Publicat 2010

Impact of hfq and sigE on the tolerance of Zymomonas mobilis ZM4 to furfural and acetic acid stresses

per Nouri, Hoda, Moghimi, Hamid, Marashi, Sayed-Amir, Elahi, Elahe
Publicat a PLoS One (2020)

An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report

per Alavi, Afagh, Khani, Marzieh, Nafissi, Shahriar, Shamshiri, Hosein, Elahi, Elahe
Publicat a Iran J Basic Med Sci (2014)

FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6

per Ghorbanpour, Elham, Pasalar, Parvin, Yazdani, Shahin, Moazzeni, Hamidreza, Elahi, Elahe
Publicat a J Ophthalmic Vis Res (2017)

Screening for MIR184 Mutations in Iranian Patients with Keratoconus

per Farzadfard, Azad, Nassiri, Nader, Moghadam, Tayebeh Nekuie, Paylakhi, Seyed Hassan, Elahi, Elahe
Publicat a J Ophthalmic Vis Res (2016)

CYP4V2 mutation screening in an Iranian Bietti crystalline dystrophy pedigree and evidence for clustering of CYP4V2 mutations

per Darki, Faezeh, Fekri, Sahba, Farhangmehr, Shaghayegh, Ahmadieh, Hamid, Dehghan, Mohammad Hossein, Elahi, Elahe
Publicat a J Curr Ophthalmol (2019)

Pantothenate kinase 2 mutation with eye-of-the-tiger sign on magnetic resonance imaging in three siblings

per Dezfouli, Mitra Ansari, Jaberi, Elham, Alavi, Afagh, Rezvani, Mohammad, Shahidi, Gholamali, Elahi, Elahe, Rohani, Mohammad
Publicat 2012

Non-housekeeping genes expressed in human trabecular meshwork cell cultures

per Paylakhi, Seyed Hassan, Yazdani, Shahin, April, Craig, Fan, Jian-Bing, Moazzeni, Hamidreza, Ronaghi, Mostafa, Elahi, Elahe
Publicat 2012

Sex Bias in Primary Congenital Glaucoma Patients with and without CYP1B1 Mutations

per Suri, Fatemeh, Chitsazian, Fereshteh, Khoramian-Tusi, Betsabeh, Amini, Heidar, Yazdani, Shahin, Nilforooshan, Naveed, Zargar, S. Jalal, Elahi, Elahe
Publicat 2009