Elahe Elahi

Elahe Elahi

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Elahe Elahi

Publications by authors named "Elahe Elahi"

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

Am J Med Genet A 2019 Aug 20;179(8):1507-1515. Epub 2019 May 20.

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1002/ajmg.a.61184DOI Listing
August 2019

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

J Curr Ophthalmol 2019 Jun 2;31(2):172-179. Epub 2019 Mar 2.

School of Biology, University College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1016/j.joco.2019.01.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611930PMC
June 2019

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

Neurobiol Aging 2019 03 16;75:225.e9-225.e14. Epub 2018 Nov 16.

School of Biology, College of Science, University of Tehran, Tehran, Iran; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2018.11.003DOI Listing
March 2019

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

J Ophthalmic Vis Res 2018 Oct-Dec;13(4):403-410

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.4103/jovr.jovr_147_17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210879PMC
November 2018

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

Gene 2018 Oct 14;673:70-81. Epub 2018 Jun 14.

School of Biology, University College of Science, University of Tehran, Tehran, Iran; Department of Biotechnology, University College of Science, University of Tehran, Tehran, Iran. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03781119183068
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http://dx.doi.org/10.1016/j.gene.2018.06.038DOI Listing
October 2018

PTRHD1 and possibly ADORA1 mutations contribute to Parkinsonism with intellectual disability.

Authors:
Elahe Elahi

Mov Disord 2018 01 16;33(1):174. Epub 2017 Nov 16.

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1002/mds.27126DOI Listing
January 2018

Action Myoclonus and Seizure in Kufor-Rakeb Syndrome.

Mov Disord Clin Pract 2018 Mar-Apr;5(2):195-199. Epub 2017 Dec 28.

Genetics research center University of Social Welfare and Rehabilitation Sciences Tehran Iran.

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http://dx.doi.org/10.1002/mdc3.12570DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407049PMC
December 2017

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

J Ophthalmic Vis Res 2017 Oct-Dec;12(4):407-412

Department of Cell and Molecular Biology, School of Biology, University College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.4103/jovr.jovr_8_17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644408PMC
November 2017

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

Neurobiol Aging 2017 06 18;54:214.e11-214.e12. Epub 2017 Mar 18.

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran; Department of Cellular and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2017.03.020DOI Listing
June 2017

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

BMC Bioinformatics 2017 Jan 25;18(1):67. Epub 2017 Jan 25.

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1186/s12859-016-1418-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264486PMC
January 2017

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

Gene 2016 Nov 9;593(1):76-83. Epub 2016 Aug 9.

School of Biology, College of Science, University of Tehran, Tehran, Iran; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2016.08.019DOI Listing
November 2016

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

J Neurol Sci 2016 Oct 17;369:318-323. Epub 2016 Aug 17.

School of Biology, College of Science, University of Tehran, Tehran, Iran; Dept. of Biotechnology, College of Science, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2016.08.035DOI Listing
October 2016

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

Ophthalmic Res 2016 Jul 17;56(2):98-103. Epub 2016 Mar 17.

School of Biology, University College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1159/000443508DOI Listing
July 2016

Screening for MIR184 Mutations in Iranian Patients with Keratoconus.

J Ophthalmic Vis Res 2016 Jan-Mar;11(1):3-7

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.4103/2008-322X.180715DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4860983PMC
May 2016

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

Neurobiol Aging 2016 Feb 6;38:216.e11-216.e18. Epub 2015 Nov 6.

School of Biology, College of Sciences, University of Tehran, Tehran, Iran; Department of Biotechnology, College of Sciences, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2015.10.034DOI Listing
February 2016

Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients.

J Glaucoma 2016 Jan;25(1):33-8

*Ophthalmic Research Center, Labbafinejad Medical Center, Shahid Beheshti University of Medical Sciences †Eye Research Center, Iran University of Medical Sciences ‡School of Biology, University College of Science ∥Department of Biotechnology ¶Center of Excellence in Biomathematics, School of Mathematics, Statistics and Computer Science §Department of Biostatistics and Epidemiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.1097/IJG.0000000000000206DOI Listing
January 2016

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

Zootaxa 2013 ;3670:440-8

School of Biology and Center of Excellence in Phylogeny of Living Organisms, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.11646/zootaxa.3670.4.2DOI Listing
October 2015

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

J Ophthalmic Vis Res 2015 Apr-Jun;10(2):123-9

School of Biology, College of Science, University of Tehran, Tehran, Iran ; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.4103/2008-322X.163783DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568608PMC
October 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.

Iran J Neurol 2015 Jul;14(3):152-7

Department of Biology AND Department of Biotechnology, School of Science, University of Tehran, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4662688PMC
July 2015

Glaucoma in iran and contributions of studies in iran to the understanding of the etiology of glaucoma.

J Ophthalmic Vis Res 2015 Jan-Mar;10(1):68-76

Department of Cell and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran ; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.4103/2008-322X.156120DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424722PMC
May 2015

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

Neurobiol Aging 2015 Mar 16;36(3):1606.e1-7. Epub 2014 Dec 16.

School of Biology, College of Science, University of Tehran, Tehran, Iran; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2014.11.021DOI Listing
March 2015

MicroRNAs that target RGS5.

Iran J Basic Med Sci 2015 Feb;18(2):108-14

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran ; School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366720PMC
February 2015

Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.

J Neurol Sci 2014 Dec 22;347(1-2):305-9. Epub 2014 Oct 22.

School of Biology, College of Science, University of Tehran, Tehran, Iran; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2014.10.031DOI Listing
December 2014

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

Iran J Basic Med Sci 2014 Oct;17(10):735-9

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340979PMC
October 2014

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

Neurosci Lett 2014 Aug 17;577:106-11. Epub 2014 Jun 17.

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran; School of Biology, College of Science, University of Tehran, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.neulet.2014.06.023DOI Listing
August 2014

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

Mol Genet Metab 2013 Sep-Oct;110(1-2):139-44. Epub 2013 Jun 6.

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1016/j.ymgme.2013.05.019DOI Listing
March 2014

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

Neurobiol Aging 2014 Jan 17;35(1):267.e1-7. Epub 2013 Aug 17.

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.07.016DOI Listing
January 2014

Mutation in ST6GALNAC5 identified in family with coronary artery disease.

Sci Rep 2014 Jan 8;4:3595. Epub 2014 Jan 8.

1] School of Biology, College of Science, University of Tehran, Tehran, Iran [2] Dept. of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1038/srep03595DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884232PMC
January 2014

Mutation in CYP27A1 identified in family with coronary artery disease.

Eur J Med Genet 2013 Dec 28;56(12):655-60. Epub 2013 Sep 28.

School of Biology, College of Science, University of Tehran, Tehran, Iran; Genome Analysis, Leibniz Institute for Age Research - Fritz Lipmann Institute, Jena, Germany.

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http://dx.doi.org/10.1016/j.ejmg.2013.09.008DOI Listing
December 2013

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

Iran J Basic Med Sci 2013 Aug;16(8):950-4

School of Biology, University College of Science, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786110PMC
August 2013

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

Biotechnol Lett 2013 Jun 2;35(6):843-51. Epub 2013 Mar 2.

Department of Biotechnology, College of Sciences, University of Tehran, P.O. Box 1417614411, Tehran, Iran.

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http://dx.doi.org/10.1007/s10529-013-1150-5DOI Listing
June 2013

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

Neurobiol Aging 2013 May 9;34(5):1516.e1-8. Epub 2012 Oct 9.

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.09.006DOI Listing
May 2013

The frequency of spinocerebellar ataxia type 23 in a UK population.

J Neurol 2013 Mar 30;260(3):856-9. Epub 2012 Oct 30.

Department of Molecular Neuroscience, Institute of Neurology and The National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK.

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http://dx.doi.org/10.1007/s00415-012-6721-1DOI Listing
March 2013

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

Mov Disord 2013 Feb 19;28(2):228-32. Epub 2012 Nov 19.

School of Biology, University College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1002/mds.25271DOI Listing
February 2013

Prediction of the pho regulon in Streptomyces clavuligerus DSM 738.

New Microbiol 2012 Oct 1;35(4):447-57. Epub 2012 Oct 1.

Department of Microbiology, College of Science, University of Tehran, Tehran, Iran.

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October 2012

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

J Hum Genet 2012 Sep 21;57(9):613-7. Epub 2012 Jun 21.

School of Biology, University College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1038/jhg.2012.70DOI Listing
September 2012

Neural differentiation of mouse embryonic stem cells on conductive nanofiber scaffolds.

Biotechnol Lett 2012 Jul 3;34(7):1357-65. Epub 2012 Apr 3.

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1007/s10529-012-0889-4DOI Listing
July 2012

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

Mol Vis 2011 5;17:1209-21. Epub 2011 May 5.

Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102028PMC
September 2011

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.

Mol Ecol Resour 2011 May 10;11(3):461-72. Epub 2011 Feb 10.

Department Biotechnology, College of Science, University of Tehran, No 13, Shafiie Alley, Qods St., Enghelab St., 14155-6455, Tehran, Iran.

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http://dx.doi.org/10.1111/j.1755-0998.2011.02989.xDOI Listing
May 2011

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

J Neurol Sci 2010 Jul;294(1-2):92-4

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1016/j.jns.2010.03.024DOI Listing
July 2010

Discovery of single nucleotide polymorphisms and mutations by pyrosequencing.

Comp Funct Genomics 2002 ;3(1):51-6

Stanford Genome Technology Center ,855 California Avenue, Palo Alto, CA 94304, USA.

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http://dx.doi.org/10.1002/cfg.132DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447241PMC
June 2010

Myocilin mutations are not a major cause of primary congenital glaucoma in Iranian patients.

J Ophthalmic Vis Res 2010 Apr;5(2):101-4

School of Biology, College of Science, University of Tehran, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380681PMC
April 2010

Kavosh: a new algorithm for finding network motifs.

BMC Bioinformatics 2009 Oct 4;10:318. Epub 2009 Oct 4.

Laboratory of Systems Biology and Bioinformatics, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1186/1471-2105-10-318DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765973PMC
October 2009

Global haplotype partitioning for maximal associated SNP pairs.

BMC Bioinformatics 2009 Aug 27;10:269. Epub 2009 Aug 27.

Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.

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http://dx.doi.org/10.1186/1471-2105-10-269DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2749056PMC
August 2009

Mutation screening of TGFBI in two Iranian Avellino corneal dystrophy pedigrees.

Clin Exp Ophthalmol 2008 Jan-Feb;36(1):26-30

National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.

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http://dx.doi.org/10.1111/j.1442-9071.2007.01649.xDOI Listing
March 2008

Contributions of MYOC and CYP1B1 mutations to JOAG.

Mol Vis 2008 Mar 13;14:508-17. Epub 2008 Mar 13.

National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2268862PMC
March 2008

Exclusion of TACSTD2 in an Iranian GDLD pedigree.

Mol Vis 2007 Aug 17;13:1441-5. Epub 2007 Aug 17.

National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.

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August 2007

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

J Bone Miner Metab 2007 20;25(3):159-64. Epub 2007 Apr 20.

National Institute for Genetic Engineering and Biotechnology, Tehran-Karaj Expressway, Km 17 Pajouhesh Boulevard, Tehran, Iran.

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http://link.springer.com/10.1007/s00774-007-0748-x
Publisher Site
http://dx.doi.org/10.1007/s00774-007-0748-xDOI Listing
May 2007

Pyrosequencing: a tool for DNA sequencing analysis.

Methods Mol Biol 2004 ;255:211-9

Stanford Genome Technology Center, Stanford University, Palo Alto, CA, USA.

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http://dx.doi.org/10.1385/1-59259-752-1:211DOI Listing
May 2004

Global genetic analysis.

J Biochem Mol Biol 2004 Jan;37(1):11-27

Faculty of Science, Tehran University, Tehran, Iran.

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January 2004

Determination of hepatitis C virus genotype by Pyrosequencing.

J Virol Methods 2003 May;109(2):171-6

Stanford Genome Technology Center, Stanford University, 855 California Avenue, Palo Alto, CA 94304, USA.

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http://dx.doi.org/10.1016/s0166-0934(03)00068-5DOI Listing
May 2003

Pyrosequencing for microbial typing.

J Chromatogr B Analyt Technol Biomed Life Sci 2002 Dec;782(1-2):67-72

Stanford Genome Technology Center, Stanford University, 855 California Avenue, Palo Alto 94304, USA.

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http://dx.doi.org/10.1016/s1570-0232(02)00693-1DOI Listing
December 2002

Multiplex Pyrosequencing.

Nucleic Acids Res 2002 Apr;30(7):e31

Stanford Genome Technology Center, Stanford University, 855 California Avenue, Palo Alto, CA 94304, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC101855PMC
http://dx.doi.org/10.1093/nar/30.7.e31DOI Listing
April 2002