E. Elahi

发表

M. Ronaghi, E. Elahi, 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

LTBP2 mutations cause Weill–Marchesani and Weill–Marchesani‐like syndrome and affect disruptions in the extracellular matrix

Seyed Hassan Paylakhi, M. Ronaghi, Jian-Bing Fan, 2012, Human mutation.

Pyrosequencing: a tool for DNA sequencing analysis.

Mostafa Ronaghi, Elahe Elahi, M. Ronaghi, 2004, Methods in molecular biology.

Mutation in ST6GALNAC5 identified in family with coronary artery disease

K. Huse, Sasan Amini, M. Ronaghi, 2014, Scientific Reports.

Study on SARS-CoV-2 strains in Iran reveals potential contribution of co-infection with and recombination between different strains to the emergence of new strains

A. Heidarzadeh, A. Heshmati, H. Galehdari, 2021, Virology.

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

E. Elahi, M. Houshmand, M. Rohani, 2009, Molecular vision.

Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2.

E. Elahi, S. Yazdani, H. Moazzeni, 2016, Gene.

FOXC1 in human trabecular meshwork cells is involved in regulatory pathway that includes miR-204, MEIS2, and ITGβ1.

Seyed Hassan Paylakhi, Jian-Bing Fan, Craig S. April, 2013, Experimental eye research.

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

Seyed Hassan Paylakhi, M. Ronaghi, Jian-Bing Fan, 2011, Molecular vision.

Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma.

Seyed Hassan Paylakhi, E. Elahi, S. J. Zargar, 2009, Ophthalmology.

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

E. Elahi, M. Rezvani, M. Rohani, 2012, Iranian journal of neurology.

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

E. Elahi, Iman Safari, Kolsoum Inanloorahatloo, 2020, Journal of medical virology.

Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patients

Homayoun Sadeghi, M. Ronaghi, E. Elahi, 2009, Neuroscience Letters.

Action Myoclonus and Seizure in Kufor‐Rakeb Syndrome

J. Hardy, A. Lang, A. Fasano, 2018, Movement disorders clinical practice.

Identification of p.Gln858* in ATP13A2 in two EOPD patients and presentation of their clinical features

Jian-Bing Fan, Brandy Klotzle, E. Elahi, 2014, Neuroscience Letters.

R632W mutation in PLA2G6 segregates with dystonia‐parkinsonism in a consanguineous Iranian family

E. Elahi, C. Paisán-Ruiz, S. Shojaee, 2009, European journal of neurology.

Mutation Screening of Six Exons of ABCA4 in Iranian Stargardt Disease Patients

H. Ahmadieh, E. Elahi, N. Daftarian, 2022, Journal of ophthalmic & vision research.

Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation

J. Hardy, J. Bras, E. Elahi, 2020, Journal of Neurology.

Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype.

Reza Kalhor, E. Elahi, M. Houshmand, 2006, The Journal of investigative dermatology.

Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigree

E. Elahi, S. Nafissi, H. Moazzeni, 2022, Journal of Medical Genetics.

Iranian Journal of Basic Medical Sciences an Iranian Familial Amyotrophic Lateral Sclerosis Pedigree with P.val48phe Causing Mutation in Sod1: a Genetic and Clinical Report

E. Elahi, S. Nafissi, Hosein Shamshiri, 2022 .

Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with cytochrome p4501B1 mutations

E. Elahi, S. Yazdani, M. Hajizadeh, 2021, European journal of ophthalmology.

SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma

S. Maurer-Stroh, R. Maroofian, E. Souzeau, 2020, Investigative ophthalmology & visual science.

Manifestation of diffuse yellowish keratoderma on the palms and soles in autosomal recessive congenital ichthyosis patients may be indicative of mutations in NIPAL4

M. Ronaghi, Jian-Bing Fan, Brandy Klotzle, 2012, The Journal of dermatology.

Neural differentiation of mouse embryonic stem cells on conductive nanofiber scaffolds

M. Soleimani, E. Elahi, I. Shabani, 2012, Biotechnology Letters.

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

E. Elahi, S. Yazdani, Ramona Haji-Seyed-Javadi, 2016, Ophthalmic Research.

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

E. Elahi, S. Yazdani, Fatemeh Suri, 2010, Journal of ophthalmic & vision research.

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

E. Elahi, S. J. Zargar, S. Yazdani, 2009, Journal of ophthalmic & vision research.

Sturgeons: An Evolutionary Insight to The α-globin Protein Speciation and Diversification

E. Elahi, A. Moosavi-Movahedi, K. Kavousi, 2022, bioRxiv.

HADHA identified as a CMT2 causative gene and a GDAP1 intronic mutation identified as a 1 CMT2 causative mutation 2

E. Elahi, J. Hardy, S. Nafissi, 2020 .

Screening for MIR184 Mutations in Iranian Patients with Keratoconus

Seyed Hassan Paylakhi, E. Elahi, N. Nassiri, 2016, Journal of ophthalmic & vision research.

Multi-stage analysis of FOXM1, PYROXD1, hTERT, PPARA, PIM3, BMI1 and MCTP1 expression patterns in colorectal cancer

E. Elahi, A. Talebi, F. Mahjoubi, 2022, Gastroenterology and hepatology from bed to bench.

Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.

M. Ronaghi, Reza Kalhor, E. Elahi, 2008, American journal of human genetics.

Mesobuthus eupeus (Scorpiones: Buthidae) from Iran: A polytypic species complex

E. Elahi, O. Mirshamsi, S. Hosseini, 2011 .

Phylogenetic relationships of Mesobuthus eupeus (C.L. Koch, 1839) inferred from COI sequences (Scorpiones: Buthidae)

E. Elahi, O. Mirshamsi, A. Sari, 2010 .

Discovery of Single Nucleotide Polymorphisms and Mutations by Pyrosequencing

M. Ronaghi, E. Elahi, 2002, Comparative and functional genomics.

Formulation of nanoliposome-encapsulated bevacizumab (Avastin): Statistical optimization for enhanced drug encapsulation and properties evaluation.

E. Elahi, D. Monti, D. Morshedi, 2020, International journal of pharmaceutics.

Prediction of the pho regulon in Streptomyces clavuligerus DSM 738.

M. Sadeghi, E. Elahi, Z. Sepehrizadeh, 2012, The new microbiologica.

CHST6 mutations identified in Iranian MCD patients and CHST6 mutations reported worldwide identify targets for gene editing approaches including the CRISPR/Cas system

E. Elahi, S. Issazadeh-Navikas, Iman Safari, 2020, International Ophthalmology.

Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family

M. Emami, E. Elahi, M. Javadi, 2019, British Journal of Ophthalmology.

Genetic screening of TGFBI in Iranian patients with TGFBI-associated corneal dystrophies and a meta-analysis of global variation frequencies

E. Elahi, I. Salahshourifar, M. Kanavi, 2022, Ophthalmic genetics.

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

E. Elahi, H. Moghimi, H. Nouri, 2020, PloS one.

Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

A. Singleton, J. Hardy, S. Schneider, 2010, Movement disorders : official journal of the Movement Disorder Society.

Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran

H. Ahmadieh, M. Yaseri, A. Heshmati, 2021, Journal of ophthalmic & vision research.

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

M. Yaseri, E. Elahi, Fatemeh Suri, 2018, Journal of ophthalmic & vision research.

Global genetic analysis.

Mostafa Ronaghi, Elahe Elahi, Jochen Kumm, 2004, Journal of biochemistry and molecular biology.

A New DNA Implementation of Finite State Machines

M. Ronaghi, A. Nowzari-Dalini, E. Elahi, 2006, Int. J. Comput. Sci. Appl..

PRKN, DJ‐1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ‐1 mutations

Homayoun Sadeghi, M. Ronaghi, E. Elahi, 2011, Movement disorders : official journal of the Movement Disorder Society.

Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients

E. Elahi, S. Nafissi, S. Yadegari, 2012, Journal of Human Genetics.

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

E. Elahi, M. Rohani, G. Shahidi, 2014, Neurobiology of Aging.

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

Brandy Klotzle, E. Elahi, M. Houshmand, 2013, Journal of Human Genetics.

A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family

H. Ahmadieh, E. Elahi, S. Feizi, 2020, Molecular vision.

Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients

M. Yaseri, E. Elahi, S. Yazdani, 2016, Journal of glaucoma.

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

E. Elahi, S. Yazdani, Fatemeh Suri, 2015, Journal of ophthalmic & vision research.

COL18A1 is a candidate eye iridocorneal angle‐closure gene in humans

Jian-Bing Fan, Brandy Klotzle, E. Elahi, 2018, Human molecular genetics.

Mutation in CYP27A1 identified in family with coronary artery disease.

K. Huse, Sasan Amini, F. Steemers, 2013, European journal of medical genetics.

Cytochrome c oxidase subunit 1 barcode data of fish of the Nayband National Park in the Persian Gulf and analysis using meta‐data flag several cryptic species

E. Elahi, Hossein Asgharian, S. Shekarriz, 2011, Molecular ecology resources.

SEQUENCE DATA ON FOUR GENES SUGGEST NOMINAL GERRES FILAMENTOSUS SPECIMENS FROM NAYBAND NATIONAL PARK IN THE PERSIAN GULF REPRESENT TWO DISTINCT SPECIES

E. Elahi, Hossein Asgharian, A. Kalirad, 2010 .

Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigree

E. Elahi, A. Moini, J. Fischer, 2020, Molecular Genetics and Genomics.

Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations

E. Elahi, F. Fatehi, M. Rohani, 2020, Molecular genetics & genomic medicine.

Determination of hepatitis C virus genotype by Pyrosequencing.

Ronald W. Davis, M. Ronaghi, N. Pourmand, 2003, Journal of Virological Methods.

Kavosh: a new algorithm for finding network motifs

Sahar Asadi, Ali Masoudi-Nejad, Falk Schreiber, 2009, BMC Bioinformatics.

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

B. Tusi, M. Sadeghi, E. Elahi, 2007, The Journal of molecular diagnostics : JMD.

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma.

Seyed Hassan Paylakhi, M. Ronaghi, E. Elahi, 2009, Human molecular genetics.

Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol

Seyed Hassan Paylakhi, Reza Kalhor, A. Ahmadian, 2008, Molecular vision.

Contributions of MYOC and CYP1B1 mutations to JOAG

B. Tusi, E. Elahi, M. Sanati, 2008, Molecular vision.

Evolution of the SARS-CoV-2 genome and emergence of variants of concern

E. Elahi, I. Safari, 2021, Archives of Virology.

Insights into the regulatory molecules involved in glaucoma pathogenesis

E. Elahi, H. Moazzeni, Marzieh Khani, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Exclusion of TACSTD2 in an Iranian GDLD pedigree.

E. Elahi, F. Amoli, A. Alavi, 2007, Molecular vision.

A haplotype framework for cystic fibrosis mutations in Iran.

M. Ronaghi, E. Elahi, Y. Thorstenson, 2006, The Journal of molecular diagnostics : JMD.

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

E. Elahi, S. Yazdani, K. Kamyab, 2013, Molecular vision.

LTBP2 knockdown and oxidative stress affect glaucoma features including TGFβ pathways, ECM genes expression and apoptosis in trabecular meshwork cells.

E. Elahi, S. Yazdani, Fatemeh Suri, 2018, Gene.

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

E. Elahi, S. Yazdani, Shadi Akbarian, 2015, Journal of ophthalmic & vision research.

Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies.

E. Elahi, Amir Banaei-Esfahani, S. Yazdani, 2019, Human molecular genetics.

Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain

F. Steemers, Jian-Bing Fan, H. Ahmadieh, 2016, Neurobiology of Aging.

Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutation

E. Elahi, F. Shahram, H. Goodarzi, 2007, Journal of Bone and Mineral Metabolism.

Identification of UBA1 as the causative gene of an X‐linked non‐Kennedy spinal–bulbar muscular atrophy

M. Sadeghi, E. Elahi, N. Salehi, 2022, European journal of neurology.

Mutation in ADORA1 identified as likely cause of early‐onset parkinsonism and cognitive dysfunction

F. Steemers, Jian-Bing Fan, M. Soleimani, 2016, Movement disorders : official journal of the Movement Disorder Society.

A case of adult onset Sandhoff disease that mimics Brown-Vialetto-Van Laere syndrome

H. Ahmadieh, E. Elahi, S. Nafissi, 2021, Neuromuscular Disorders.

PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation

Brandy Klotzle, E. Elahi, M. Rohani, 2013, Movement disorders : official journal of the Movement Disorder Society.

Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot–Marie–Tooth patients with TFG mutation

S. Efthymiou, H. Houlden, E. Elahi, 2019, American journal of medical genetics. Part A.

Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations

E. Elahi, S. Nafissi, Hosein Shamshiri, 2016, Journal of Neurological Sciences.

HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry

F. Steemers, Jian-Bing Fan, Brandy Klotzle, 2015, Neurobiology of Aging.

Diagnosis of cystathionine beta-synthase deficiency by genetic analysis

Jian-Bing Fan, Brandy Klotzle, E. Elahi, 2014, Journal of the Neurological Sciences.

MicroRNAs that target RGS5

M. Soleimani, E. Elahi, Amir Banaei-Esfahani, 2015, Iranian journal of basic medical sciences.

Mutations in C19orf12 and intronic repeat expansions in C9orf72 not observed in Iranian Parkinson's disease patients

E. Elahi, G. Shahidi, A. Alavi, 2017, Neurobiology of Aging.

BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes

J. Hardy, G. Valle, R. Boostani, 2020, Neurobiology of Aging.

Identification of mutation in NPC2 by exome sequencing results in diagnosis of Niemann-Pick disease type C.

E. Elahi, S. Nafissi, Hosein Shamshiri, 2013, Molecular genetics and metabolism.

Mutation screening of TGFBI in two Iranian Avellino corneal dystrophy pedigrees

E. Elahi, M. Rahmati-Kamel, F. Karimian, 2008, Clinical & experimental ophthalmology.

Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients.

Reza Kalhor, E. Elahi, M. Javadi, 2007, Investigative ophthalmology & visual science.

Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients

M. Ronaghi, Jian-Bing Fan, E. Elahi, 2013, Neurobiology of Aging.

LACK OF ASSOCIATION BETWEEN EBV DNA AND SQUAMOUS CELL CARCINOMA OF THE ESOPHAGUS IN IRANIAN PATIENTS

E. Elahi, I. Jahanzad, F. Zadeh, 2003 .

BVVL / FL : Features caused by SLC 52 A 3 mutations ; WDFY 4 and TNFSF 13 B may be 1 novel causative genes 2

A. Heshmati, J. Bras, E. Elahi, 2021 .

Review of the earthworm fauna of Iran with emphasis on Kohgiluyeh & Boyer-Ahmad Province.

E. Elahi, M. Malek, Z. Farhadi, 2013, Zootaxa.

Putative founder effect in the Polish, Iranian and United States populations for the L144S SOD1 mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis

P. Andersen, M. Morita, E. Elahi, 2020, Amyotrophic lateral sclerosis & frontotemporal degeneration.

The Chromosome Number of the Persian Gulf Shrimp Penaeus semisulcatus

E. Elahi, S. Hosseini, Razieh M. Raie, 2004 .

Mutation screening of SLC52A3, C19orf12, and TARDBP in Iranian ALS patients

E. Elahi, S. Nafissi, B. Zamani, 2019, Neurobiology of Aging.

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

E. Elahi, S. Nafissi, A. Alavi, 2015, Iranian journal of neurology.

Neural differentiation of mouse embryonic stem cells on conductive nanofiber scaffolds

M. Soleimani, E. Elahi, I. Shabani, 2012, Biotechnology Letters.

A clinic‐based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients

Homayoun Sadeghi, M. Ronaghi, E. Elahi, 2009, Movement disorders : official journal of the Movement Disorder Society.

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

E. Elahi, 2020, Journal of ophthalmic & vision research.

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

E. Elahi, S. Davaran, Kolsoum Inanloo Rahatloo, 2013, Iranian journal of basic medical sciences.

The frequency of spinocerebellar ataxia type 23 in a UK population

T. Révész, H. Morris, H. Houlden, 2013, Journal of Neurology.

Concentrations of nitric oxide metabolites in the serum of Iranian multiple sclerosis patients

Ali Naji Esfahani, M. Etemadifar, E. Elahi, 2010, Journal of the Neurological Sciences.

EFFECTS OF INFLAMMATION AND H. PYLORI INFECTION ON EXPRESSION OF CD44 VARIANT EXONS IN GASTRIC TISSUE

E. Elahi, M. Eskandarpour, M. Mahmoudi, 2003 .

PTRHD1 and possibly ADORA1 mutations contribute to Parkinsonism with intellectual disability

E. Elahi, 2018, Movement disorders : official journal of the Movement Disorder Society.

Multiplex Pyrosequencing.

Ronald W Davis, Nader Pourmand, Ronald W. Davis, 2002, Nucleic acids research.

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

H. Ahmadieh, E. Elahi, M. Dehghan, 2019, Journal of current ophthalmology.

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

M. Sadeghi, E. Elahi, F. Chitsazian, 2017, BMC Bioinformatics.

Discovery of Single Nucleotide Polymorphisms and Mutations by Pyrosequencing

M. Ronaghi, E. Elahi, 2002, Comparative and functional genomics.

LINKAGE OF PARKINSON’S DISEASE IN TWO VERY EARLY ONSET SIBLINGS TO A LOCUS ON CHROMOSOME 1

E. Elahi, M. Hashemi, G. Shahidi, 2013 .

Global haplotype partitioning for maximal associated SNP pairs

Hamid Pezeshk, Mehdi Sadeghi, Ali Katanforoush, 2009, BMC Bioinformatics.

Normalization of miRNA qPCR high-throughput data: a comparison of methods

E. Elahi, M. Tavallaei, S. Mowla, 2013, Biotechnology Letters.

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

Mehdi Sadeghi, Elahe Elahi, Fereshteh Chitsazian, 2017, BMC Bioinformatics.

Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.

M. Ronaghi, Reza Kalhor, E. Elahi, 2008, American journal of human genetics.

Non-housekeeping genes expressed in human trabecular meshwork cell cultures

Seyed Hassan Paylakhi, M. Ronaghi, Jian-Bing Fan, 2012, Molecular vision.

Preliminary data suggest possible association between IL-32 expression level and time of MS attack

M. Sahraian, M. Etemadifar, E. Elahi, 2011 .

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

E. Elahi, P. Pasalar, S. Yazdani, 2017, Journal of ophthalmic & vision research.

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

E. Elahi, S. Nafissi, Hosein Shamshiri, 2014, Iranian journal of basic medical sciences.

Cytochrome c oxidase subunit 1 barcode data of fish of the Nayband National Park in the Persian Gulf and analysis using meta‐data flag several cryptic species

E. Elahi, Hossein Asgharian, S. Shekarriz, 2011, Molecular ecology resources.