الهه الهی(بازنشسته)

1. Identification of a mutation in TNRC18 in a patient with clinical features of Fazio‐Londe disease

Khani Marziyeh، Shamshiri Hosein، نفیسی شهریار، Salehi Najmeh، Allahi Elahe (2024)., Clinical Case Reports, 12(1).

2. Adding the Molecular Diversity Information of the Common Fouling Barnacle Amphibalanus amphitrite (Darwin, 1854) (Crustacea: Cirripedia) from the Persian Gulf and Gulf of Oman to the Global Diversity Pattern

Moeinaldini Asma، Sari Alireza، عدنان شهدادی، Katouzian Ahmad-Reza، علیمراد سرافرازی، Allahi Elahe (2023)., ZOOLOGICAL STUDIES, 62(16), 1-17.

1. Identification ofRNF13as cause of recessively inherited ALS in a multi-case pedigree

Khani Marziyeh، نفیسی شهریار، Shamshiri Hosein، [] []، Taheri Haniyeh، Allahi Elahe (2022)., JOURNAL OF MEDICAL GENETICS, 60(3), 301-309.

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

Jozaei Roxanne، Javadi Mohammadali، Safari Iman، Moghaddasi Afrouz، Feizi Sepehr، رضایی کنوی مژگان، Najafi Sajad، Safdari Bahareh، سلحشوری ایمان، Allahi Elahe، Suri Fatemeh (2022)., OPHTHALMIC GENETICS, 43(4), 496-499.

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

Darbari Ensieh، Ahmadieh Hamid، Daftarian Narsis، رضایی کنوی مژگان، Suri Fatemeh، Sabbaghi Hamideh، Allahi Elahe (2022)., Journal of Ophthalmic & Vision Research, 1(17).

1. A survey on genetic affinities and diversity of the common barnacle Amphibalanus amphitrite (Crustacea: Cirripedia) from the Persian Gulf and Gulf of Oman

Moeinaldini Asma، Sari Alireza، عدنان شهدادی، Katouzian Ahmad Reza، سرافرازی علیمراد، Allahi Elahe (2021)., First International Conference of Ecology and Conservation Biodiversity, 15-16 December, Damghan, Iran.

2. 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

Taghizadeh Peyman، Salehi Sadegh، Safari Iman، Houshmand Masoud، Inanloorahatloo Kolsoum، Mahjobi Frozandeh، محمدحسین صنعتی، Alavi Afagh، Heshmati Ali، Amel Jamehdar Saeid، Galehdari Hamid، Haghshenas Mohammad Reza، Hashemian Amir Masoud، Heidarzadeh Abtin، Jahanzad Issa، Kheyrani Elham، Piroozmand Ahmad، Mojtahedi Ali، Razavi Nikoo Hadi، Rahimi Bidgoli Mohammad Masoud، Rezvani Nayebali، Sepehrnejad Mehdi، Shakibzadeh Arash، Shariati Gholamreza، Seyyedi Noorossadat، Zahraei Seyed MohammadSaleh، Yari Hadi، Dabiri Soroosh، Allahi Elahe (2021)., VIROLOGY, 562(562), 63-73.

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

Khani Marziyeh، Shamshiri Hosein، [] []، Taheri Hanieh، Ahmadieh Hamid، Alavi Afagh، فربودی نیلوفر، Nafissi Shahriar، Allahi Elahe (2021)., NEUROMUSCULAR DISORDERS, 31(6), 528-531.

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

Khani Marziyeh، Shamshiri Hosein، Taheri Hanieh، hardy john، Bras Tomas، Carmona Susana، [] []، Alavi Afagh، Heshmati Ali، Taghizadeh Peyman، Nilipour Yalda، Ghazanfari Tooba، Shahabi Majid، Okhovat Ali Asghar، Rohani Mohammad، Valle Giorgio، Boostani Reza، Abdi Siamak، Eshghi Shaghayegh، Nafissi Shahriar، Allahi Elahe (2021)., NEUROBIOLOGY OF AGING, 99(10958), 102.e1-102.e10.

2. World‐wide tracking of major SARS‐CoV‐2 genome haplotypes in sequences of June 1 to November 15, 2020 and discovery of rapid expansion of a new haplotype

Safari Iman، Inanloorahatloo Kolsoum، Allahi Elahe (2021)., JOURNAL OF MEDICAL VIROLOGY, 1(1).

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

Darbari Ensieh، Zare-Abdollahi Davood، Alavi Afagh، Rezaei Kanavi Mozhgan، Feizi Sepehr، Hosseini Seyed Bagher، Baradaran- Rafii Alireza، Ahmadieh Hamid، Issazadeh-Navikas Shohreh، Allahi Elahe (2020)., MOLECULAR VISION, 26(ecollection 2020).

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

Safari Iman، Inanloorahatloo Kolsoum، Allahi Elahe (2020)., JOURNAL OF MEDICAL VIROLOGY, -(-).

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

Nouri Hoda، Moghimi Hamid، Marashi Sayed Amir، Allahi Elahe (2020)., PLoS One, 15(10), e0240330.

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

L. Young Terri، N. Whisenhunt Kristina، Jin Jing، M. LaMartina Sarah، M. Martin Sean، Souma Tomokazu، Suri Fatemeh، Souzeau Emmanuelle، Limviphuvadh Vachiranee، Zhang Xue، Dan Yongwook، Anagnos Evie، Carmona Susana، M. Jody Nicole، Stangel Nickie، C. Higuchi Emily، J. Huang Samuel، M. Siggs Owen، Jose Simoes Maria، M. Lawson Brendan، S. Martin Jacob، Allahi Elahe، Narooie-Nejad Mehrnaz، Fallahi Motlagh Behzad، E. Quaggin Susan، D. Potter Heather، D. Silva Eduardo، E. Craig Jamie، Egas Conceicao، Maroofian Reza، Maurer-Stroh Sebastian، S. Bradfield Yasmin، W. Tompson Stuart (2020)., iovs( Investigative Ophthalmology & Visual Science), 61(12), 6.

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

Malakouti Nejad Maryam، Bardania Hassan، Aliakbari Farhang، Baradaran- Rafii Alireza، Allahi Elahe، Monti Daniela، Morshedi Dina (2020)., INTERNATIONAL JOURNAL OF PHARMACEUTICS, 590(119895), 119895.

8. 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

Khani Marziyeh، Taheri Haniyeh، Shamshiri Hosein، [] []، hardy john، Bras Tomas، Inanloorahatloo Kolsoum، Alavi Afagh، Nafissi Shahriar، Allahi Elahe (2020)., JOURNAL OF NEUROLOGY, -(-).

9. Insights into the regulatory molecules involved in glaucoma pathogenesis

[] []، Khani Marziyeh، Allahi Elahe (2020)., AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 184(3), 782-827.

10. 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

Kuzma-Kozakiewicz Magdalena، M. Andersen Peter، Allahi Elahe، Alavi Afagh، C. Sapp Peter، Morita Mitsuya، zekanowski Cezary، Berdynski Mariusz (2020)., Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22(1-2), 80-85.

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

Safari Iman، Baradaran- Rafii Alireza، Issazadeh-Navikas Shohreh، Allahi Elahe (2020)., INTERNATIONAL OPHTHALMOLOGY, 40(9), 2223-2235.

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

Alavi Afagh، Darki Faezeh، Rahimi Bidgoli Mohammad Masoud، Zare Abdollahi Davood، Moini Ashraf، Shahshahani Mostafa، Fischer Judith، Allahi Elahe (2020)., MOLECULAR GENETICS AND GENOMICS, -(-).

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

Allahi Elahe (2020)., Journal of Ophthalmic & Vision Research, 15(1), 1-3.

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

Moazzeni Hamidreza، Mirrahimi Mehraban، Moghadam Abolfazl، Banaei-esfahani Amir، Shahin Yazdani، Allahi Elahe (2019)., HUMAN MOLECULAR GENETICS, 28(21), 3637-3663.

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

Khani Marzieh، Alavi Afagh، Shamshiri Hosein، زمانی بابک، Hassanpour Hossein، Kazemi Mohammad-hossein، Nafissi Shahriar، Allahi Elahe (2019)., NEUROBIOLOGY OF AGING, 75(225), 225.

4. 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، Javadi Mohammad Ali، Asgari Danial، Khani Marzieh، Emami Mohammad، Moghadam Abolfazl، Panahi-Bazaz Mahmoud-Reza، Hosseini Mehdi، Karimian Farid، Hosseini Seyed Bagher، Nekuie Tayebeh، Hassanpour Hossein، Akbari Mohammad Taghi، Allahi Elahe (2019)., BRITISH JOURNAL OF OPHTHALMOLOGY, -(-).

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

Darki Faezeh، Fekri Sahba، Farhangmehr Shaghayegh، Ahmadieh Hamid، Dehghan Mohammad Hossein، Allahi Elahe (2019)., Journal of Current Ophthalmology, 31(-).