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elahe elahi
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Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays
S Shojaee, F Sina, SS Banihosseini, MH Kazemi, R Kalhor, GA Shahidi, ...
The American Journal of Human Genetics 82 (6), 1375-1384, 2008
3152008
Kavosh: a new algorithm for finding network motifs
ZRM Kashani, H Ahrabian, E Elahi, A Nowzari-Dalini, ES Ansari, S Asadi, ...
BMC bioinformatics 10, 1-12, 2009
2862009
Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations
C Paisán‐Ruiz, R Guevara, M Federoff, H Hanagasi, F Sina, E Elahi, ...
Movement Disorders 25 (12), 1791-1800, 2010
2852010
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
M Narooie-Nejad, SH Paylakhi, S Shojaee, Z Fazlali, M Rezaei Kanavi, ...
Human molecular genetics 18 (20), 3969-3977, 2009
1702009
Bioemulsifier production by a halothermophilic Bacillus strain with potential applications in microbially enhanced oil recovery
SMM Dastgheib, MA Amoozegar, E Elahi, S Asad, IM Banat
Biotechnology letters 30, 263-270, 2008
1682008
Multiplex pyrosequencing
N Pourmand, E Elahi, RW Davis, M Ronaghi
Nucleic acids research 30 (7), e31-e31, 2002
1312002
Pyrosequencing for microbial typing
M Ronaghi, E Elahi
Journal of Chromatography B 782 (1-2), 67-72, 2002
1292002
LTBP2 mutations cause Weill–Marchesani and Weill–Marchesani‐like syndrome and affect disruptions in the extracellular matrix
R Haji‐Seyed‐Javadi, S Jelodari‐Mamaghani, SH Paylakhi, S Yazdani, ...
Human mutation 33 (8), 1182-1187, 2012
1252012
Pyrosequencing: a tool for DNA sequencing analysis
E Elahi, M Ronaghi
Bacterial Artificial Chromosomes: Volume 1 Library Construction, Physical …, 2004
1142004
R632W mutation in PLA2G6 segregates with dystonia‐parkinsonism in a consanguineous Iranian family
F Sina, S Shojaee, E Elahi, C Paisan‐Ruiz
European journal of neurology 16 (1), 101-104, 2009
1082009
Neural differentiation of mouse embryonic stem cells on conductive nanofiber scaffolds
M Kabiri, M Soleimani, I Shabani, K Futrega, N Ghaemi, HH Ahvaz, ...
Biotechnology letters 34, 1357-1365, 2012
942012
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes
F Chitsazian, BK Tusi, E Elahi, HA Saroei, MH Sanati, S Yazdani, ...
The Journal of Molecular Diagnostics 9 (3), 382-393, 2007
902007
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
H Asgharian, HH Sahafi, AA Ardalan, S Shekarriz, E Elahi
Molecular Ecology Resources 11 (3), 461-472, 2011
752011
Contributions of MYOC and CYP1B1 mutations to JOAG
B Bayat, S Yazdani, A Alavi, M Chiani, F Chitsazian, BK Tusi, F Suri, ...
Molecular vision 14, 508, 2008
752008
Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype
E Elahi, R Kalhor, SS Banihosseini, N Torabi, H Pour-Jafari, ...
Journal of investigative dermatology 126 (7), 1506-1509, 2006
752006
Determination of hepatitis C virus genotype by Pyrosequencing
E Elahi, N Pourmand, R Chaung, A Rofoogaran, J Boisver, K Samimi-Rad, ...
Journal of virological methods 109 (2), 171-176, 2003
672003
Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma
F Suri, S Yazdani, M Narooie-Nejhad, SJ Zargar, SH Paylakhi, S Zeinali, ...
Ophthalmology 116 (11), 2101-2109, 2009
592009
Contribution of the latent transforming growth factor-beta binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome
S Jelodari-Mamaghani, R Haji-Seyed-Javadi, F Suri, N Nilforushan, ...
Molecular vision 19, 333, 2013
562013
FOXC1 in human trabecular meshwork cells is involved in regulatory pathway that includes miR-204, MEIS2, and ITGβ1
SH Paylakhi, H Moazzeni, S Yazdani, P Rassouli, E Arefian, E Jaberi, ...
Experimental Eye Research 111, 112-121, 2013
542013
Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain
E Jaberi, M Rohani, GA Shahidi, S Nafissi, E Arefian, M Soleimani, ...
Neurobiology of Aging 38, 216. e11-216. e18, 2016
532016
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