منو
الهه الهی

استاد

تاریخ به‌روزرسانی: 1403/09/14

الهه الهی

دانشکدگان علوم‌ / دانشکده زیست‌ شناسی‌

مقالات علمی چاپ شده در مجلات

  1. "Identification of a mutation in TNRC18 in a patient with clinical features of Fazio‐Londe disease"
    Marziyeh Khani, Hosein Shamshiri, شهریار نفیسی, Najmeh Salehi, Elahe Allahi
    Clinical Case Reports, Vol. 12, No 1, 2024
  2. "Identification of UBA1 as the causative gene of an X‐linked non‐Kennedy spinal–bulbar muscular atrophy"
    Marziyeh Khani, شهریار نفیسی, Hosein Shamshiri, [] [], Haniyeh Taheri, مهدی صادقی, Najmeh Salehi, فرشته چیت سازیان , Elahe Allahi
    EUROPEAN JOURNAL OF NEUROLOGY, Vol. 29, No 12, pp.3556-3563, 2022
  3. "Identification ofRNF13as cause of recessively inherited ALS in a multi-case pedigree"
    Marziyeh Khani, شهریار نفیسی, Hosein Shamshiri, [] [], Haniyeh Taheri, Elahe Allahi
    JOURNAL OF MEDICAL GENETICS, Vol. 60, No 3, pp.301-309, 2022
  4. "Genetic screening of TGFBI in Iranian patients with TGFBI-associated corneal dystrophies and a meta-analysis of global variation frequencies"
    Roxanne Jozaei, Mohammadali Javadi, Iman Safari, Afrouz Moghaddasi, Sepehr Feizi, مژگان رضایی کنوی, Sajad Najafi, Bahareh Safdari, ایمان سلحشوری, Elahe Allahi, Fatemeh Suri
    OPHTHALMIC GENETICS, Vol. 43, No 4, pp.496-499, 2022
  5. "Mutation Screening of Six Exons of ABCA4 in Iranian Stargardt Disease Patients"
    Ensieh Darbari, Hamid Ahmadieh, Narsis Daftarian, مژگان رضایی کنوی, Fatemeh Suri, Hamideh Sabbaghi, Elahe Allahi
    Journal of Ophthalmic & Vision Research, Vol. 1, No 17, 2022
  6. "A case of adult onset Sandhoff disease that mimics Brown-Vialetto-Van Laere syndrome"
    Marziyeh Khani, Hosein Shamshiri, [] [], Hanieh Taheri, Hamid Ahmadieh, Afagh Alavi, نیلوفر فربودی, Shahriar Nafissi, Elahe Allahi
    NEUROMUSCULAR DISORDERS, Vol. 31, No 6, pp.528-531, 2021
  7. "BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes"
    Marziyeh Khani, Hosein Shamshiri, Hanieh Taheri, john hardy, Tomas Bras, Susana Carmona, [] [], Afagh Alavi, Ali Heshmati, Peyman Taghizadeh, Yalda Nilipour, Tooba Ghazanfari, Majid Shahabi, Ali Asghar Okhovat, Mohammad Rohani, Giorgio Valle, Reza Boostani, Siamak Abdi, Shaghayegh Eshghi, Shahriar Nafissi, Elahe Allahi
    NEUROBIOLOGY OF AGING, Vol. 99, No 10958, 2021
  8. "A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family"
    Ensieh Darbari, Davood Zare-Abdollahi, Afagh Alavi, Mozhgan Rezaei Kanavi, Sepehr Feizi, Seyed Bagher Hosseini, Alireza Baradaran- Rafii, Hamid Ahmadieh, Shohreh Issazadeh-Navikas, Elahe Allahi
    MOLECULAR VISION, Vol. 26, 2020
  9. "SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma"
    Terri L. Young, Kristina N. Whisenhunt, Jing Jin, Sarah M. LaMartina, Sean M. Martin, Tomokazu Souma, Fatemeh Suri, Emmanuelle Souzeau, Vachiranee Limviphuvadh, Xue Zhang, Yongwook Dan, Evie Anagnos, Susana Carmona, Nicole M. Jody, Nickie Stangel, Emily C. Higuchi, Samuel J. Huang, Owen M. Siggs, Maria Jose Simoes, Brendan M. Lawson, Jacob S. Martin, Elahe Allahi, Mehrnaz Narooie-Nejad, Behzad Fallahi Motlagh, Susan E. Quaggin, Heather D. Potter, Eduardo D. Silva, Jamie E. Craig, Conceicao Egas, Reza Maroofian, Sebastian Maurer-Stroh, Yasmin S. Bradfield, Stuart W. Tompson
    iovs( Investigative Ophthalmology & Visual Science), Vol. 61, No 12, 2020
  10. "Formulation of nanoliposome-encapsulated bevacizumab (Avastin): Statistical optimization for enhanced drug encapsulation and properties evaluation"
    Maryam Malakouti Nejad, Hassan Bardania, Farhang Aliakbari, Alireza Baradaran- Rafii, Elahe Allahi, Daniela Monti, Dina Morshedi
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, Vol. 590, No 119895, 2020
  11. "Insights into the regulatory molecules involved in glaucoma pathogenesis"
    [] [], Marziyeh Khani, Elahe Allahi
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, Vol. 184, No 3, pp.782-827, 2020
  12. "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"
    Magdalena Kuzma-Kozakiewicz, Peter M. Andersen, Elahe Allahi, Afagh Alavi, Peter C. Sapp, Mitsuya Morita, Cezary zekanowski, Mariusz Berdynski
    Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 22, pp.80-85, 2020
  13. "CHST6 mutations identified in Iranian MCD patients and CHST6 mutations reported worldwide identify targets for gene editing approaches including the CRISPR/Cas system"
    Iman Safari, Alireza Baradaran- Rafii, Shohreh Issazadeh-Navikas, Elahe Allahi
    INTERNATIONAL OPHTHALMOLOGY, Vol. 40, No 9, pp.2223-2235, 2020
  14. "Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations"
    Elahe Allahi, Marziyeh Khani, Hosein Shamshiri, Mohammad Rohani, Bahram Haghi Ashtiani, Fahimeh Haghi Ashtiani, Afagh Alavi, [] [], Haniyeh Taheri, [] [], Leila Javanparast, Seyed Saleh Hashemi, Shahriar Nafissi
    MOLECULAR GENETICS AND GENOMIC medicine, Vol. 8, No 7, 2020
  15. "Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigree"
    Afagh Alavi, Faezeh Darki, Mohammad Masoud Rahimi Bidgoli, Davood Zare Abdollahi, Ashraf Moini, Mostafa Shahshahani, Judith Fischer, Elahe Allahi
    MOLECULAR GENETICS AND GENOMICS, Vol. -, 2020
  16. "Genetic Basis of Primary Angle Closure Glaucoma: The Role of Collagens and Extracellular Matrix"
    Elahe Allahi
    Journal of Ophthalmic & Vision Research, Vol. 15, No 1, pp.1-3, 2020
  17. "Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies"
    Hamidreza Moazzeni, Mehraban Mirrahimi, Abolfazl Moghadam, Amir Banaei-esfahani, Shahin Yazdani , Elahe Allahi
    HUMAN MOLECULAR GENETICS, Vol. 28, No 21, pp.3637-3663, 2019
  18. "Mutation screening of SLC52A3, C19orf12, and TARDBP in Iranian ALS patients"
    Marzieh Khani, Afagh Alavi, Hosein Shamshiri, بابک زمانی, Hossein Hassanpour, Mohammad-hossein Kazemi, Shahriar Nafissi, Elahe Allahi
    NEUROBIOLOGY OF AGING, Vol. 75, No 225, 2019
  19. "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"
    Hamidreza Moazzeni , Mohammad Ali Javadi, Danial Asgari, Marzieh Khani, Mohammad Emami, Abolfazl Moghadam, Mahmoud-Reza Panahi-Bazaz, Mehdi Hosseini, Farid Karimian, Seyed Bagher Hosseini, Tayebeh Nekuie, Hossein Hassanpour, Mohammad Taghi Akbari, Elahe Allahi
    BRITISH JOURNAL OF OPHTHALMOLOGY, Vol. -, 2019
  20. "CYP4V2 mutation screening in an Iranian Bietti crystalline dystrophy pedigree and evidence for clustering of CYP4V2 mutations"
    Faezeh Darki, Sahba Fekri, Shaghayegh Farhangmehr, Hamid Ahmadieh, Mohammad Hossein Dehghan, Elahe Allahi
    Journal of Current Ophthalmology, Vol. 31, 2019
  21. "LTBP2 knockdown and oxidative stress affect glaucoma features including TGFβ pathways, ECM genes expression and apoptosis in trabecular meshwork cells"
    Fatemeh Suri, شاهین یزدانی , Elahe Allahi
    GENE, Vol. 673, No 10, pp.70-81, 2018
  22. "COL18A1 is a candidate eye iridocorneal angle-closure gene in humans"
    [] [], شاهین یزدانی , Marjan Chapi, Iman Safari, Paniz Rassouli, Narsis Daftarian, Mohammad Reza Jafarinasab, Saghar Ghasemi Firouzabad, Elham Alehabib, Hossein Darvishi, Brandy Klotzle , Jian-Bing Fan, Casey Turk, Elahe Allahi
    HUMAN MOLECULAR GENETICS, Vol. 27, No 21, pp.3772-3786, 2018
  23. "P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran"
    Mansoureh Ghashghaei, Fatemeh Suri, مهدی یاسری, Elahe Allahi
    Journal of Ophthalmic & Vision Research, Vol. 13, No 4, pp.403-410, 2018
  24. "FMN2 with functions related to the cytoskeleton is partially regulated by PITX2"
    [] [], پروین پاسالار , Shahin Yasdani, Hamid Moazzeni, Elahe Allahi
    Journal of Ophthalmic & Vision Research, Vol. 12, No 4, pp.407-412, 2018
  25. "Mutations in C19ORF72 and intronic repeat expansions not observed in Iranian Parkinson's disease patients"
    Afagh Alavi, Maryam Malakouti Nejad, Gholam Ali Shahidi, Elahe Allahi
    NEUROBIOLOGY OF AGING, Vol. 00001111, No 1, pp.100-120, 2017
  26. "PTRHD1 and possibly ADORA1 mutations contributeto Parkinsonism with intellectual disability"
    Elahe Allahi
    MOVEMENT DISORDERS, Vol. 10, No 12, pp.111-111, 2017
  27. "Mutations in C19orf12 and intronic repeat expansions in C9orf72 not observed in Iranian Parkinson’s disease patients"
    Afagh Alavi, Maryam Malakouti Nejad, Gholam Ali Shahidi, Elahe Allahi
    NEUROBIOLOGY OF AGING, Vol. 54, No 14, pp.214-214, 2017
  28. "Confident gene activity prediction based on single histone modification H2BK5ac in human cell lines"
    Fereshteh Chitsazian, Mehdi Sadeghi, Elahe Allahi
    BMC BIOINFORMATICS, Vol. 18, 2017
  29. "Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations"
    lمرضیه خانی, Hosein Shamshiri, افاق علوی , Shahriar Nafissi, Elahe Allahi
    JOURNAL OF THE NEUROLOGICAL SCIENCES, Vol. 15, No 369, pp.318-23, 2016
  30. "Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2"
    Hamid Reza Moazzeni, Mohammad Tghi Akbari, Shahin Yasdani, Elahe Allahi
    GENE, Vol. 593, 2016
  31. "Identification of mutation in GTPBP2 in patients of a family with"
    Elahe Allahi, Elham Jaberi, Mohammad Rohani, Gholam Ali Shahidi
    NEUROBIOLOGY OF AGING, Vol. 38, 2016
  32. "Screening for MIR184 mutations in Iranian patients with keratoconus"
    Azad Farzadfard, Nader Nasiri, Tayebeh Nekuie, Seyed Hasan Paylakhy, Elahe Allahi
    Journal of Ophthalmic & Vision Research, Vol. 11, No 1, 2016
  33. "Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients"
    Shahin Yasdani, Arezo Miraftabi, محمد پاکروان, حسن قهری , Betsabeh Khoramian Tosi, Mohammad Sedigh Mortazavi, Mehdi Yaseri, Elahe Allahi
    JOURNAL OF GLAUCOMA, Vol. 25, No 1, pp.33-38, 2016
  34. "The p.Gly61Glu Mutation in CYP1B1 Affects the Extracellular Matrix in Glaucoma Patients"
    Iman Safari, Fatemeh Suri, Ramona Haji-seyed -javadi, Shahin Yasdani, Elahe Allahi
    OPHTHALMIC RESEARCH, Vol. 56, No 2, pp.98-103, 2016
  35. "HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry"
    Afagh Alavi, Hosein Shamshiri, Shahriar Nafissi, Marzieh Khani, Brandy Klotzle, J.b Fan, Elahe Allahi, Steemers Steemers
    NEUROBIOLOGY OF AGING, Vol. 36, No 3, pp.1-7, 2015
  36. "Glaucoma in Iran and contributions of studies in Iran to the understanding of the etiology of glaucoma"
    Fatemeh Suri, Shahin Yasdani, Elahe Allahi
    Journal of Ophthalmic & Vision Research, Vol. 10, No 1, 2015
  37. "A possible role for LTBP2 in the etiology of primary angle closure glaucoma"
    Elahe Allahi, Iman Safari, Shahin Yasdani, Shadi Akbarian
    Journal of Ophthalmic & Vision Research, Vol. 10, No 2, 2015
  38. "An Iranian FALS pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report."
    Afagh Alavi, Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Elahe Allahi
    Iranian Journal of Basic Medical Sciences, Vol. 17, No 17, pp.735-739, 2014
  39. "An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report"
    Afagh Alavi, Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Elahe Allahi
    Iranian Journal of Basic Medical Sciences, Vol. 17, No 10, pp.735-9, 2014
  40. "Diagnosis of cystathionine beta-synthase deficiency by genetic analysis"
    Fatemeh Suri, Mehrnaz Narooie-nejad, Iman Safari, Hamidreza Moazzeni, Mohammad Reza Rohani, Ali Khajeh, Brandy Klotzle , Jiang Bin Fan, Elahe Allahi
    JOURNAL OF THE NEUROLOGICAL SCIENCES, Vol. 347, No 347, pp.305-309, 2014
  41. "Identification of p.Gln858* in ATP13A2 in two EOPD patients and presentation of their clinical features"
    Maryam Malakouti Nejad, gholam-ali shahidi, Sayed Mehdi Shojaee, mohammad rohani, Mehrdad Hashemi, Brandy Klotzle, Jian-Bing Fan, Elahe Allahi
    NEUROSCIENCE LETTERS, Vol. 577, No 1, pp.106-111, 2014
  42. "mutation in ST6GALNA5 identified in family with coronary artery disease"
    کلثوم اینانلو, Amir Farhang Zand Parsa, Klaus Huse, Paniz Rassouli, Saeid Davaran, Matthias Platzer, Marcel Kramer, Jian -bing Fan, Casey Turk, ساسان امینی, Frank Steemers, Kevin Gunderson, مصطفی رونقی, Elahe Allahi
    Scientific Reports, Vol. 14, No 28, 2014
  43. "Mutation in CYP27A1 identified in family with coronary artery disease"
    Kolsoom Inanloo, Amir Farhang Zand Parsa, Klaus Huse, Paniz Rasooli, Saeid Davaran, Matthias Platzer, Jian-Bing Fan, Saeideh Amini, Frank Steemers, Elahe Allahi
    European Journal of Medical Genetics, Vol. 56, No 12, pp.655-60, 2013
  44. "The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine"
    Elham Jaberi, Fereshteh Chitsazian, Gholam Ali Shahidi, Mohammad Rohani, Farzad Sina, Iman Safari, Maryam Malakouti Nejad, Masoud Houshmand, Brandy Klotzle, Elahe Allahi
    JOURNAL OF HUMAN GENETICS, Vol. 58, No 8, pp.526-530, 2013
  45. "Identification of mutation in NPC2 by exome sequencing results in diagnosis of Niemann–Pick disease type C"
    Afagh Alavi, Shahriar Nafisi, Hosein Shamshiri, Maryam Malakouti Nejad, Elahe Allahi
    MOLECULAR GENETICS AND METABOLISM, Vol. 110, pp.139-144, 2013
  46. "FOXC1 in human trabecular meshwork cells is involved in regulatory pathway that includes miR-204, MEIS2, and ITGβ1"
    سید حسن پایلاخی, Hamidreza Moazzeni, شاهین یزدانی, Paniz Rassouli, Ehsan Arefian, Elham Jaberi, Emad Heidari Arash, Ahmad Sadighi Gilani, Jian Bing Fan, Graig April, Sadaf Amin, Fatemeh Musavi, Elahe Allahi
    EXPERIMENTAL EYE RESEARCH, Vol. 111, No 111, pp.112-121, 2013
  47. "Normalization of miRNA qPCR high-throughput data: a comparison of methods"
    Ali Mohammadian, Seyed Javad Molwa, Elahe Allahi, Mohammad Taghavi, Mohammad Reza Nourani, Yu Liang
    BIOTECHNOLOGY LETTERS, Vol. 35, No 6, pp.843-851, 2013
  48. "lack of association between the MEF2A gene and coronary artery disease in Iranian families"
    Elahe Allahi
    Iranian Journal of Basic Medical Sciences, Vol. 16, No 1, pp.950-954, 2013
  49. "Erratum to: The frequency of spinocerebellar ataxia type 23 in a UK population"
    Katrherine Fawcett, Mohadeseh Mehrabian, Yo- Tsen Liu, Sherifi Hamed, Elahe Allahi, Tamas Revesez, Georgios Koutsis, Jodhua Herscheson, Lucia Schottlaender, Mark Wardle, Patrick-j Morridon, Huw. R Morris, Paola Giunti, Nicholas Wood
    JOURNAL OF NEUROLOGY, Vol. 260, No 3, pp.860-860, 2013
  50. "contribution of the latent transforming growth factor-beta binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome"
    Elahe Allahi, Sahar Jelodari, Ramona Haji-seyed -javadi, Fatemeh Suri, Naveed Nilforushan, Shahin Yasdani, Kambiz Kamyab
    MOLECULAR VISION, Vol. -, No 19, pp.333-347, 2013
  51. "PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation"
    Elahe Allahi, Mitra Ansari Dezfouli, Afagh Alavi, Mohammad Rohani, Mohammad Rezvani, Tayebeh Nekuie, Brandy Klotzle, Seyed Hasan Tonekaboni, Gholam Ali Shahidi
    MOVEMENT DISORDERS, Vol. 2, No 28, pp.228-231, 2013
  52. "Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian Patients"
    Elahe Allahi
    NEUROBIOLOGY OF AGING, Vol. 35, No 1, pp.261-7, 2013
  53. "Mutations in CYP27A1 identified in family with coronary artery disease"
    Elahe Allahi
    European Journal of Medical Genetics, Vol. 56, No 1, pp.655-660, 2013
  54. "linkage of parkinson disease in two very early onset siblings to a locus on chromosome 1"
    Elahe Allahi, Maryam Malakouti Nejad, Mehrdad Hashemi, Gholam Reza Shahidi
    Progress in Biological Sciences, Vol. 2, No 2, pp.23-29, 2012
  55. "The frequency of spinocerebellar ataxia type 23 in a UK population"
    Katherine Fawcett, Mohadeseh Mehrabian, Yo-tsen Liu, Sherifa Hamed, Elahe Allahi, Tamas Revesz, Georgios Koutsis, Joshua Herscheson, Lucia Schottlaender, Mark Wardle, Patrick J. Morrison, Huw R. Morris, Paola Giunti, Nicholas Wood, Henry Houlden
    JOURNAL OF NEUROLOGY, Vol. 260, No 3, pp.856-859, 2012
  56. "Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients"
    Elahe Allahi, Afagh Alavi, Shahriar Nafisi, Mohammad Rohani, Babak Zamani, Behnaz Sedighi, Hosein Shamshiri, Jian Bing Fan, Mostafa Ronaghi
    NEUROBIOLOGY OF AGING, Vol. 34, No 5, 2012
  57. "Pantothenate kinase 2 mutation with eye-of-the-tiger sign on magnetic resonance imaging in three siblings"
    Mitra Ansari Dezfouli, Elham Jaberi, Afagh Alavi, محمد رضوانی, غلامعلی شهیدی, Elahe Allahi, محمد روحانی
    Iranian Journal of Neurology, Vol. 11, No 4, pp.1-4, 2012
  58. "prediction of the pho regulon in streptomyces clavuligerus DSM 738"
    Ensieh Salehghamari, Javad Hamedi, Elahe Allahi, Zargham Sepehrizadeh, Mehdi Sadeghi, Guenther Muth
    New Microbiologica, Vol. 35, No 1, pp.447-457, 2012
  59. "Neural differentiation of mouse embryonic stem cells on conductive nanofiber scaffolds article"
    Elahe Allahi, Mahboubeh Kabiri, Masoud Soleimani, Iman Shabani, Kathryn Futrega, Naser Ghaemi, Hana Hanaee Ahvaz, Michael R. Doran
    BIOTECHNOLOGY LETTERS, Vol. 7, No 34, pp.1357-1365, 2012
  60. "Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients"
    Elahe Allahi
    JOURNAL OF HUMAN GENETICS, Vol. 57, No 9, pp.613-617, 2012
  61. "Mutation Screening of TGFBI in Two Iranian Avellino Corneal Dystrophy Pedigres"
    A Alavi , Elahe Allahi, M Rahmati Kamel , F Karimian , M Rezaei Kanavi
    CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, Vol. 36, No 1, pp.26-30, 2007
  62. "Four mutations ( three novel, one founder ) in TACSTD2 among Iranian GDLD patients"
    Afagh Alavi , Elahe Allahi, Mehdi Hosseni Tehrani , Fa Amoli , Ma Javadi , N Rafati , M Chiani , Ss Banihosseini , B Bayat , R Kalhor , Ss Amini
    Investigative Ophthalmology and Visual Science, Vol. 48, No 10, pp.4490-4497, 2007
  63. "Exclusion of TACSTD2 in an Iranian GDLD Pedigree"
    Elahe Allahi, Mehdi Hossein Tehrani , Afshin Hamidian , Fahimie Asadi Amoli
    MOLECULAR VISION, Vol. 13, No 159, pp.1445-1441, 2007
  64. "Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutation"
    Elahe Allahi, Yosof Shafaghati , Sare Asadi , Farnaz Absalan , Hani Goodarzi , Mohamad Hasan Karimi Nejad , Nava Gharaii , Farhad Shahram , Ae Hughes
    JOURNAL OF BONE AND MINERAL METABOLISM, Vol. 25, No 3, pp.159-164, 2007
  65. "CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes"
    Chitsazian F , Tusi Bk , Elahe Allahi, Saroei Ha , Sanati Mh , Yazdani S , Pakravan M , Nilforooshan N , Eslami Y , Mehrjerdi Ma , Zareei R , Jabbarvand M , Abdolahi A , Lasheyee Ar , Etemadi A , Bayat B , Sadeghi M , Banoei Mm , Ghafarzadeh B , Rohani Mr , Rismanchian A , Yvonne Thorstenson , Sarfarazi M
    no name4, Vol. 9, No 3, 2007
  66. "Homozygous missense mutation in fibulin - 5 in an iranian autosomal recessive cutis laxa pedigree and associated haplotype"
    Elahe Allahi, R Kalhor , Ss Banihosseini , N Torabi , H Pour Jafari , M Houshmand , Ss Amini , A Ramezani , Bart Loeys
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, Vol. 126, No 7, pp.1506-9, 2006
  67. "A New DNA Implementation of Finite State Machines"
    Abbas Nouzari Dalini, Elahe Allahi, Hayedeh Ahrabiyan, Mohammad Ronaghi
    International Journal of Computer Science and Applications, Vol. 3, No 1, pp.51-60, 2006
  68. "A Haplotype Framework for Cystic Fibrosis Mutations in Iran"
    Elahe Allahi, Ahmad Khodadad , Ilya Kupershmidt , Fereshteh Ghasemi , Babak Alinasab , Ramin Naghizadeh , Robert G Eason , Mahshid Amini , Mehran Esmaili , Mohammad R Esmaeili Dooki , Mohammad H Sanati , Ronald W Davis , Mostafa Ronaghi , Yvonne R Thorstenson
    JOURNAL OF MOLECULAR DIAGNOSTICS, Vol. 8, No 1, pp.119-127, 2006
  69. "A New DNA Implementation of Finite State Machine"
    A Nowzari Dalini , Elahe Allahi, H Ahrabian , M Ronaghi , Afshin Ahmadian
    International Journal of Computer Science and Applications, Vol. 3, No 1, pp.51-6, 2006
  70. "Expression of four CD44 isoforms ( CD44s, V3 , V6, V7 ) in cancer of the esophagus"
    افشین احمدیان , E Felfeli , F Soleimani , عیسی جهانزاد , M Mahmoodi , M Hazrati , Elahe Allahi
    Journal of Science University of Tehran, Vol. 30, No 3, pp.461-470, 2005
  71. "Subtype classification based on Phylogenetic analysis of NSSB ,core and 5 NCR regions of viral genome"
    K Samimi-rad , افشین احمدیان , Elahe Allahi
    Ir J Infec & Trop Dis, Vol. 8, pp.30-26, 2004
  72. "Global Genetic Analysis"
    Mostafa Ronaghi , Kumm Jochen , Elahe Allahi
    JOURNAL OF BIOCHEMISTRY AND MOLECULAR BIOLOGY, Vol. 37, No 1, 2004
  73. "The Chromosome Number of the Persian Gulf Shrimp penaeus semisulcatus"
    Seid Javad Hosseini , Elahe Allahi, Reza Raei
    IRANIAN INTERNATIONAL JOURNAL OF SCIENCE, Vol. 5, No 1, pp.23-13, 2004
  74. "Lack of Association between EBV DNA and Squamous Cell Carcinoma of the Esophagus in Iranian Patients"
    Issah Jahanzad , Firoozeh Salehzadeh , Elahe Allahi, Firoozeh Salehzadeh , Issah Jahanzad
    IRANIAN INTERNATIONAL JOURNAL OF SCIENCE, Vol. 4, No 2, pp.137-149, 2003
  75. "Determination of hepatitis C virus genotype by Pyrosequencing"
    Elahe Allahi, Nader Pourmand , Ramsey Chaung , Ara Rofoogaran , Judie Boisver , Katayon Samimi Rad , Ronald W Davis , Mostafa Ronaghi
    Journal of Virological Methods, Vol. 109, No 2, pp.171-176, 2003
  76. "Effects of inflammation and h.pylori infection on expression of CD-44 variant exons in Gastric tissue"
    Elahe Allahi, Afshin Ahmadian , M Khanipour Roshan , M Eskandarpour , F Reihani , Sabet
    Journal of Sciences, Islamic Republic of Iran, Vol. 14, No 1, pp.11-16, 2003
  77. "Pyrosequening for microbial typing"
    M Ronahgi , Elahe Allahi
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, Vol. 782, pp.72-67, 2002
  78. "Multiplex Pyrosequencing"
    N Pourmand , Elahe Allahi, Rw Davis , M Ronaghi
    NUCLEIC ACIDS RESEARCH, Vol. 30, No 7, pp.31-31, 2002
  79. "Discovery of single nucleotide Polymorphisms and mutations by Pyrossequencing"
    Mostafa Ronaghi , Elahe Allahi
    COMPARATIVE AND FUNCTIONAL GENOMICS, Vol. 3, No 1, pp.51-56, 2002
  80. "EBV infection of cancerous esophageal tissue as determined by PCR"
    Y Sedaghat , افشین احمدیان , M Raie , Elahe Allahi
    Iranian Journal of Medical Sciences, Vol. 24, pp.53-62, 1999
  81. "Detection of HIV -1 infection in Iranians by nested - PCR"
    S Kiaii , افشین احمدیان , Ah Najhad-moghadam , Elahe Allahi
    Iranian J of Infec and Tropical, Vol. 2, pp.51-63, 1998
  82. "Determination of frequency of the delta F508 mutation in Iranian AIDS patients"
    R Naghizadeh , افشین احمدیان , Elahe Allahi
    Medical Journal of the Islamic Republic of Iran, Vol. 16, pp.278-286, 1998
  83. "Identification of HIV - 1 subtypes in two Iranian AIDS patients"
    S Kiaii , افشین احمدیان , Ah Nejhad-moghadam , Elahe Allahi
    Iranian J of Infec and Tropical, Vol. 3, pp.27-23, 1998
  84. "Synthesis of human placental CDNA and demonstration of the expression of M - CSF in that tissue"
    R Arvan , Elahe Allahi
    Journal of Science University of Tehran, Vol. 56, No 5, pp.9-18, 1998
  85. "مشاهده جهش c.260A > G در ژن سوپراکسیداز1 و تغییر پروتئینی p.Asn86Ser در بیماران آمیوتروفیک لاترال سکلروزیس ایرانی و فقدان ارتباط ژنوتیپ و فنوتیپ در آنها"
    مرضیه خانی، آفاق علوی، شهریار نفیسی، الهه الهی
    Iranian Journal of Neurology، نسخه 3، شماره 14، صفحات:1-6، 1394
  86. "بررسی تجلی چهار ایزوفرم CD44 (V7, V6, V3, CD44s) در سرطان مری"
    الهه فلفلی ، الهه الهی، صالح محقق حضرتی ، عیسی جهانزاد ، محمد محمودی ، فرشته سلیمانی
    مجله علوم دانشگاه تهران، نسخه 3، شماره 30، صفحات:470-461، 1383

مقالات علمی ارائه شده در همایش‌ها

  1. "Micro_RNAs that target genes potentially related to glaucoma"
    Mehraban Mirrahimi, Elahe Allahi, Fatemeh Suri, Ehsan Arefian
    The 8th annual meeting of the Iranian Research Association for Vision and Ophthalmology (IRAVO), 2018
  2. "Risk of angle closure glaucoma for carriers of Knobloch syndrome"
    Fatemeh Suri, Elahe Allahi, Hossein Darvishi, Shahin Yasdani, Narsis Dftarian
    The 8th annual meeting of the Iranian Research Association for Vision and Ophthalmology (IRAVO), 2018
  3. "Possibl bidirectional regulation of PITX2 and TFGB signaling in human trabecular meshwork cells"
    Elahe Allahi
    The 8th annual meeting of the Iranian Research Association for Vision and Ophthalmology (IRAVO), 2018
  4. "obObesity associated locus sought by linkage analysis and exome sequencing in an extended pedigree"
    Nilofar Yousefi, Afagh Alavi, Iman Safari, Elahe Allahi
    International Student Congress Of Biomedical Sciences 2016, 2016
  5. "Iranian patients affected with familial forms of"
    Elahe Allahi
    Hereditary motor and sensory neuropathy with proximal, 2016
  6. "Bidirectional regulation of PITX2 and TGF-β signaling in human trabecular meshwork cells"
    Hamid Moazzeni, Hamid Ahmadieh, Elahe Allahi, Mohammad Tghi Akbari, شاهین یزدانی , مژگان رضایی کنوی , Mehraban Mirrahimi, Seied Hassan Paylakhi
    ARVO 2016 Annual Meeting Abstracts, 2016
  7. "Co-delivery of NF-κB and Stat3 transcription factor decoy oligodeoxynucleotides by"
    Shayan Shahsavari, Shohreh Mashayekhan, Hamidreza Moazzemi, Mehran Kianirad, Mohamadreza Moradi, سارا صعودی, Elahe Allahi, Fatemeh Atyabi
    Proceedings of the 6th International Conference on Nanostructures (ICNS6), 2016
  8. "co-delivery of NF-KB and stst3 transcription factor decoy oligodeoxynucleotides by CD44-targeted nanopa"
    Shahin Shahsavari, Shohreh Mashayekhan, حمید موذنی , Marzieh Kiani, Mohammad Ali Moradi, Sara Soudi, Elahe Allahi, Fatemeh Atyabi
    proceedings of the 6th international conference on nanostructure (ICNS6), 2016
  9. "complex regulatory network in human trabecular meshwork"
    Hamidreza Moazzeni , Elahe Allahi, Mohammad Taghi Akbari, Shahin Yazdani, Marzieh Khani, Abolfazl Moghadam, Masoume Mirrahimi, Elham Ghorbanpour, Afrooz Moghadasi
    the 5th annual congress of the Iranian research association for vision and ophthalmology, 2015
  10. "role of LTBP2 in glaucoma pathogenesis"
    Fatemeh Suri, Elahe Allahi, Azad Farzadfard, Shahin Yasdani
    the 5th annual congress of the Iranian research association for vision and ophthalmology, 2015
  11. "whole exome sequencing combined with homozygousity mapping in a family with encephalomyopathy and elevated succinyl carnitine"
    Elham Jaberi, Fereshteh Chitsazian, غلامعلی شهیدی, mohammad rohani, Brandy Klotzle, Elahe Allahi
    8th neurogenetics conference, 2015
  12. "DNA barcoding of fish from Chabahar bay in the Persian Gulf reveals possible cryptic species"
    Marzieh Khani, Elahe Allahi, Mojtaba Nemati, Shohreh Ariaeenejad, Homayoun Hosseinzadeh Sahafi, Afagh Alavi, Hamidreza Moazzeni
    IMFE 2014, 2014
  13. "Whole exome sequencing analysis in a large Primary Angle Closure Glaucoma (PACG) pedigree"
    Fatemeh Suri, Elahe Allahi, Iman Safari, شاهین یزدانی
    ESHG 2014, 2014
  14. "Repeat expansion in C9ORF72 is not a common couse of parkinsons disease among Iranian patients"
    Maryam Malakouti Nejad, Elahe Allahi, Afagh Alavi, gholam-ali shahidi
    ESHG 2014, 2014
  15. "Screening of TARDBP in Iranian amyotrophic lateral sclerosis (ALS) patients"
    Marzieh Khani, Elahe Allahi, Afagh Alavi, Shahriar Nafissi, Maryam Malakoti Nejad
    ESHG2014, 2014
  16. "Homozygosity mapping in an Iranian pedigree affected with muscular dystrophy limb girdle (LGMD) revealed linkage to chromosome 2p12-14 and and a mutation in Dysferlin gene"
    Afagh Alavi, Elahe Allahi, Marzieh Khani, Maryam Malakouti Nezhad
    ESHG 2014, 2014
  17. "TARDBP mutations are not a common cause of amyotrophic lateral sclerosis in iranian patients"
    Marzieh Khani, Elahe Allahi, Afagh Alavi, Shahriar Nafissi, Hosein Shamshiri
    1 internationl & 13th iranian genetics congress, 2014
  18. "PITX2 regulates expression of PLEKHG5, NOMO2, AUH and LDLRAD2 in human trabecular meshwork cells"
    Hamidreza Moazzeni , Elahe Allahi, Mohammad Taghi Akbari, Amir Banaei-esfahani, Abolfazl Moghadam, Masoume Mirahimi
    1st internationl & 13th iranian genetics congress, 2014
  19. "Genetics of ALS in Iran"
    Elahe Allahi, Shahriar Nafissi , Mohammad Rohani , Afagh Alavi, Marzieh Khani, Hosein Shamshiri
    1st internationl & 13th iranian genetics congress, 2014
  20. "Amplification of alpha globin gene amplicons of two caspian sea sturgeons and derivation of gene and protein sequences"
    Shohreh Ariaeenejad , Ali Akbar Moosavi Movahhedi, Elahe Allahi, Kaveh Kavousi
    1st internationl & 13th iranian genetics congress, 2014
  21. "Homozygosity mapping used for identification of disease causing genes in heterogenic disorders"
    Fatemeh Suri, Afagh Alavi, Elahe Allahi, Hosein Shamshiri
    1st internationl & 13th iranian genetics congress, 2014
  22. "Screening for large C9ORF72 repeat expansionamong Iranian patients with Parkinson’s disea"
    Maryam Malakouti Nejad, Elahe Allahi, Afagh Alavi, Gholam Ali Shahidi
    1st internationl & 13th iranian genetics congress, 2014
  23. "a novel locus for autosomal recessive dystonia with mental retardation maps to chromosome 6"
    Elham Jaberi, محمد روحانی, محمد رضوانی, Elahe Allahi
    statistical genetics, 2014
  24. "Diagnosis of Homocystinuria in Anterior Segment Dysgenesis (ASD) Pedigree by Whole Genome Genetic Analysis"
    Fatemeh Suri, Elahe Allahi, Hamidreza Moazzeni, Mehrnaz Narooi Nejad, Mohammad Reza Rohani
    the 4th annual congress of Iranian research association for vision and ophthalmology, 2014
  25. "FOXC1 Regulates Expression of CLOCK, GNG5, CXCL6, ITGβ1, LDLRAD2, FMNL2, KHDRBS3, MEIS2, PLEKHG5, and WWC2 in Human Trabecular Meshwork Cells"
    Hamidreza Moazzeni, Elahe Allahi, Hassan Paylakhi, Fatemeh Suri, Marzieh Khani, Abolfazl Moghadam, Shahin Yasdani
    the 4th annual congress of Iranian research association for vision and ophthalmology, 2014
  26. "dexamethasone treatment reduces LTBP1 expression in human trabecular meshwork cultured cells"
    Arootin Gharibiyan, Elahe Allahi, Shahin Yasdani, Fatemeh Suri
    the 4th annual congress of Iranian research association for vision and ophthalmology, 2014
  27. "FOXC1 regulates expression of CLOCK, GNG5, CXCL6, ITGβ1, LDLRAD2, FMNL2, KHDRBS3, MEIS2, PLEKHG5, and WWC2 in human trabecular meshwork cells"
    Hamidreza Moazzeni , Elahe Allahi, Seyed Hassan Paylakhi, Fatemeh Suri, Marzieh Khani, Abolfazl Moghadam, Shahin Yazdani
    IRAVO 2014, 2014
  28. "Exome sequencing revealed a NPC2 mutation in an Iranian Niemann Pick C-type 2 disease family"
    Afagh Alavi, Elahe Allahi, شهریار نفیسی, Hosein Shamshiri, مسعود هوشمند, Maryam Malakouti Nezhad
    ESHG 2013, 2013
  29. "Whole exome sequencing combined with linkage analysis in an Iranian family with recessive dystonia-parkinsonism"
    Elham Jaberi, B. Farham, Paniz Rassouli, غلامعلی شهیدی, محمد روحانی, Elahe Allahi
    ESHG 2013, 2013
  30. "Early onset Parkinson‘s disease caused by a novel ATP13A2 truncating mutation"
    Maryam Malakouti Nejad, Elahe Allahi, Afagh Alavi, Gholam Ali Shahidi, Mehrdad Hashemi, G. Shahidi
    ESHG 2013, 2013
  31. "exome sequencing revealed a NPC2 mutation in an Iranian Niemann Pick C-type 2 disease family"
    Afagh Alavi, Elahe Allahi, شهریار نفیسی, Hosein Shamshiri, مسعود هوشمند, Maryam Malakouti Nezhad
    European Society of human genetic, 2013
  32. "Homozygosity mapping in a large Iranian pedigree affected with autosomal recessive congenital Ichthyosis (ARCI) reveals linkage to region encompassing NIPAL4/Ichthyn"
    Afagh Alavi, Mostafa Mirshams Shahshahani, Hamidreza Moazzeni, Jian Bing Fan, Elahe Allahi
    Molecular basis of Mendelian disorders, 2013
  33. "novel ATP13A2 mutation associated with early onset parkinson disease"
    Maryam Malakouti Nejad, Afagh Alavi, Mehrdad Hashemi, Gholam Ali Shahidi, Elahe Allahi
    basic and clinical neuroscience congress 2012, 2012
  34. "Whole exome sequencing combined with linkage analysis identifies novel variations in a large Coronary Artery Disease family"
    Kolsum Inanloo Rahatloo, Elahe Allahi, S Davaran, T Fan
    European Human Genetics Conference 2012, 2012
  35. "Homozygosity mapping in two large Iranian pedigrees affected with autosomal recessive congenital Ichthyosis (ARCI) reveals linkage to regions 5q33 and 17p13"
    Elahe Allahi, Afagh Alavi, Mostafa Mirshams Shahshahani, Iman Safari
    the 17th national & 5th international Iranian biology confrence, 2012
  36. "Mutation screening of MEF2A gene in Iranian affected with coronary artery disease"
    Kolsum Inanloo, Elahe Allahi, S Davaran, Afagh Alavi, Elham Jaberi
    1st student congress on cell & molecular medicine, 2011
  37. "Hybridization of multiplex PrASE products to oligonucleotide spotted microarrays"
    Hossein Nezari, Reza Kalhor, ستاره سادات بنی حسینی, Fatemeh Suri, Afagh Alavi, Seyed Jalal Zargar, افشین احمدیان, Elahe Allahi
    The 9th Iranian Congress of Biochemistry and The 2nd International Congress of Biochemistry and Molecular Biology, 2007
  38. "Using multi-sample slides spotted with universal probes to detect common CYP1B1 mutations in primary open angle glaucoma patients"
    Fatemeh Suri, Reza Kalhor, نوید نیلفروشان, شاهین یزدانی, Hossein Nezari, ستاره سادات بنی حسینی, Seyed Jalal Zargar, افشین احمدیان, Elahe Allahi
    The 9th Iranian Congress of Biochemistry and The 2nd International Congress of Biochemistry and Molecular Biology, 2007
  39. "Identification of halotolerant bioemulsifier producing bacteria from persian oil fields"
    Mohammad Amozegar, سیدمحمد مهدی دستغیب , Elahe Allahi, Sedigheh Asad, رضا کلهر
    FEMS congress of europian microbiologist, 2006
  40. "homozygosity mapping of a family with dystonia plus syndrom linked to chromosome 1 and 2"
    Elahe Allahi, Elham Jaberi, Mohammad Rohani, Gholam Ali Shahidi, Babak Zamani, Mohammad Reza Rezvani
    the 1st international & 5th annual congress of Iranian Neurogenetic society, 1390
  41. "روش دیگر برای شناسایی ژنهای مرتبط با بیماریهای پیچیده"
    الهه الهی
    سومین کنگره بین المللی ژنتیک، 1397
  42. "بررسی جهش در ژن سی اچ اس تی 6"
    الهه الهی، ایمان صفری، علیرضا برادران رفیعی
    هشتمین کنگره علوم بینایی، 1397
  43. "شناخت ژن عامل بیماریهای دستگاه عصبی"
    روح الله خانی، الهه الهی، شهریار نفیسی ، آفاق علوی، حسین شمشیری، حمید طاهری، مینا طلوع قانی، حمید موذنی
    کنگره ژنتیک، 1397
  44. "تخمین فراوانی جهش های شایع عامل گلوکوم مادرزدی"
    منصوره قشقائی، فاطمه سوری، مهدی یاسری، الهه الهی
    کنگره چشم، 1397
  45. "بررسی جهش در ای بی سی ای 4"
    انسیه درباری، نارسیس دفتریان، حمید احمدیه، الهه الهی
    هشتمین کنگره چشم، 1397
  46. "زن درمانی برای بیماری های شبکیه چشم"
    الهه الهی
    هشتمین کنگره چشم، 1397
  47. "مطالعات روی بیماریهای ژنتیک با تاکید بر بیماریهای دستگاه عصبی"
    الهه الهی
    افق های زیست شناسی، 1396
  48. "ژن نامزد جدید برای تحلیل دستگاه عصبی"
    الهام جابری، محمد روحانی، محمدضا کرمی، غلامعلی شهیدی، الهه الهی
    ناتوانی های نادر ذهنی، 1396
  49. "ناتوانی های نادر ذهنی"
    الهام جابری، محمد روحانی، الهه الهی
    معایب غیرمعمول شناختی، 1396
  50. "جهش GVal LY در TFG بیماران در دومین....."
    مرضیه خانی، الهه الهی، حسین شمشیری، آفاق علوی، شهریار نفیسی
    پنجمین کنگره نورو ساینس، 1395
  51. "پژوهش های دانشجویان و همکاران الهی در طی 10 سال اخیر در دانشگاه تهران"
    الهه الهی
    نوزدهمین کنگره ملی وهفتمین کنگره بین المللی زیست شناسی ایران، 1395
  52. "تاریخچه مطالعات ما در بیماریهای نوروجنریتیو"
    الهه الهی
    دومین کنگره بین المللی و چهارمین کنگره ملی ژنتیک ایران، 1395
  53. "ریز RNAهایی که هدفشان NODAL و PITX2 است"
    معصومه میررحیمی، احسان عارفیان، شاهین یزدانی، الهه الهی
    ششمین همایش سالانه تحقیقات چشم پزشکی و علوم بینایی، 1394
  54. "ارزیابی عملکرد فاکتورهای رونویسی و microRNA های دخیل در پاتوژنز بیماری گلوکوم"
    حمیدرضا معظمی گودرزی، الهه الهی، محمدتقی اکبری، شاهین یزدانی
    اولین همایش بین المللی ونهمین همایش سالانه نوروژنتیک ایران، 1394
  55. "غربالگری جهش در ژن C20orf54 در بیماران ایرانی مبتلا به سندرم Brown-Vialetto-Von Lear (BVVL)"
    الهه الهی، مرضیه خانی، شهریار نفیسی
    اولین همایش بین المللی و نهمین همایش ملی نوروژنتیک ایران، 1394
  56. "بررسی جهش در اگزون های ژن CYP4V2 در خانواده ایرانی مبتلا به Bietti Crystalline Dystrophy"
    شقایق فرهنگ مهر، فائزه درکی، صهبا فکری، محمد حسین دهقان فیروزآبادی، حمید احمدیه، الهه الهی
    پنجمین همایش سالیانه تحقیقات چشم پزشکی و علوم بینایی ایران، 1393
  57. "هشتمین همایش سالیانه انجمن نوروژنتیک"
    Afagh Alavi، الهه الهی، Maryam Malakouti Nejad، Gholam Ali Shahidi
    بررسی هوموزیگوسیتی در یک خانواده مبتلا به پارکینسون زودرس و پیوستگی به کروموزوم 6، 1393
  58. "ای ال اس خانوادگی"
    الهه الهی
    دوازدهمین سمینار و کارگاه پیشگیری، تشخیص و درمان بیماری های نادر، 1392
  59. "شناخت جهش بیماری زا در اس پی جی 11"
    مرضیه خانی، الهه الهی، مینا طلوع قانی، حانیه طاهری، آفاق علوی، حمید موذنی، شهریار نفیسی
    ششمین کنگره علوم عصبی، 1386