Discovery of Single Nucleotide Polymorphisms and Mutations by Pyrosequencing

Por Ronaghi, Mostafa, Elahi, Elahe
Publicado em 2002

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

Por Suri, Fatemeh, Yazdani, Shahin, Elahi, Elahe
Publicado no J Ophthalmic Vis Res (2015)

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

Por Chitsazian, Fereshteh, Sadeghi, Mehdi, Elahi, Elahe
Publicado no BMC Bioinformatics (2017)

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

Por Inanloo Rahatloo, Kolsoum, Davaran, Saeid, Elahi, Elahe
Publicado em 2013

Global haplotype partitioning for maximal associated SNP pairs

Por Katanforoush, Ali, Sadeghi, Mehdi, Pezeshk, Hamid, Elahi, Elahe
Publicado em 2009

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

Por Safari, Iman, Akbarian, Shadi, Yazdani, Shahin, Elahi, Elahe
Publicado no 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

Por Khani, Marzieh, Alavi, Afagh, Nafissi, Shahriar, Elahi, Elahe
Publicado no Iran J Neurol (2015)

Multiplex Pyrosequencing

Por Pourmand, Nader, Elahi, Elahe, Davis, Ronald W., Ronaghi, Mostafa
Publicado em 2002

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

Por Elahi, Elahe, Narooie-Nejhad, Mehrnaz, Suri, Fatemeh, yazdani, Shahin
Publicado em 2010

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

Por Alavi, Afagh, Khani, Marzieh, Nafissi, Shahriar, Shamshiri, Hosein, Elahi, Elahe
Publicado no Iran J Basic Med Sci (2014)

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

Por Ghorbanpour, Elham, Pasalar, Parvin, Yazdani, Shahin, Moazzeni, Hamidreza, Elahi, Elahe
Publicado no J Ophthalmic Vis Res (2017)

Screening for MIR184 Mutations in Iranian Patients with Keratoconus

Por Farzadfard, Azad, Nassiri, Nader, Moghadam, Tayebeh Nekuie, Paylakhi, Seyed Hassan, Elahi, Elahe
Publicado no J Ophthalmic Vis Res (2016)

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

Por Dezfouli, Mitra Ansari, Jaberi, Elham, Alavi, Afagh, Rezvani, Mohammad, Shahidi, Gholamali, Elahi, Elahe, Rohani, Mohammad
Publicado em 2012

Non-housekeeping genes expressed in human trabecular meshwork cell cultures

Por Paylakhi, Seyed Hassan, Yazdani, Shahin, April, Craig, Fan, Jian-Bing, Moazzeni, Hamidreza, Ronaghi, Mostafa, Elahi, Elahe
Publicado em 2012

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

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

Contribution of the latent transforming growth factor-beta binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome

Por Jelodari-Mamaghani, Sahar, Haji-Seyed-Javadi, Ramona, Suri, Fatemeh, Nilforushan, Naveed, Yazdani, Shahin, Kamyab, Kambiz, Elahi, Elahe
Publicado em 2013

MicroRNAs that target RGS5

Por Banaei-Esfahani, Amir, Moazzeni, Hamidreza, Nosar, Pooya Naseri, Amin, Sadaf, Arefian, Ehsan, Soleimani, Masoud, Yazdani, Shahin, Elahi, Elahe
Publicado no Iran J Basic Med Sci (2015)

Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist

Por Narooie-Nejad, Mehrnaz, Chitsazian, Fereshteh, Khoramian Tusi, Betsabeh, Mousavi, Faride, Houshmand, Massoud, Rohani, Mohammad R., Hosseinipour, Azam S., Rismanchian, Akram, Elahi, Elahe
Publicado em 2009

Effect of PITX2 knockdown on transcriptome of primary human trabecular meshwork cell cultures

Por Paylakhi, Seyed Hassan, Fan, Jian-Bing, Mehrabian, Mohadeseh, Sadeghizadeh, Majid, Yazdani, Shahin, Katanforoush, Ali, Kanavi, Mozhgan Rezaei, Ronaghi, Mostafa, Elahi, Elahe
Publicado em 2011

Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pedigree by 500 K SNP Arrays

Por Shojaee, Seyedmehdi, Sina, Farzad, Banihosseini, Setareh Sadat, Kazemi, Mohammad Hossein, Kalhor, Reza, Shahidi, Gholam-Ali, Fakhrai-Rad, Hossein, Ronaghi, Mostafa, Elahi, Elahe
Publicado em 2008