Works by Mojarrad, Majid


Results: 58
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    Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98677-3
    By:
    • Rehman, Atta Ur;
    • Sepahi, Neda;
    • Bedoni, Nicola;
    • Ravesh, Zeinab;
    • Salmaninejad, Arash;
    • Cancellieri, Francesca;
    • Peter, Virginie G.;
    • Quinodoz, Mathieu;
    • Mojarrad, Majid;
    • Pasdar, Alireza;
    • Asad, Ali Ghanbari;
    • Ghalamkari, Saman;
    • Piran, Mehran;
    • Piran, Mehrdad;
    • Superti-Furga, Andrea;
    • Rivolta, Carlo
    Publication type:
    Article
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    Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies.

    Published in:
    Brain Communications, 2023, v. 5, n. 5, p. 1, doi. 10.1093/braincomms/fcad222
    By:
    • Accogli, Andrea;
    • Zaki, Maha S.;
    • Al-Owain, Mohammed;
    • Otaif, Mansour Y.;
    • Jackson, Adam;
    • Argilli, Emanuela;
    • Chandler, Kate E.;
    • De Goede, Christian G. E. L.;
    • Cora, Tülün;
    • Alvi, Javeria Raza;
    • Eslahi, Atieh;
    • Mohajeri, Mahsa Sadat Asl;
    • Ashtiani, Setareh;
    • Au, P. Y. Billie;
    • Scocchia, Alicia;
    • Alakurtti, Kirsi;
    • Pagnamenta, Alistair T.;
    • Toosi, Mehran Beiraghi;
    • Karimiani, Ehsan Ghayoor;
    • Mojarrad, Majid
    Publication type:
    Article
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    Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis.

    Published in:
    Clinical Genetics, 2024, v. 106, n. 6, p. 693, doi. 10.1111/cge.14599
    By:
    • Alerasool, Masoome;
    • Eslahi, Atieh;
    • Vona, Barbara;
    • Kahaei, Mir Salar;
    • Mojaver, Nasrin Kaseb;
    • Rajati, Mohsen;
    • Pasdar, Alireza;
    • Ghasemi, Mohammad Mehdi;
    • Saburi, Ehsan;
    • Ardehaie, Reza Mousavi;
    • Aval, Majid Hadadi;
    • Tale, Mohammad Reza;
    • Nourizadeh, Navid;
    • Afzalzadeh, Mohammad Reza;
    • Niknezhad, Hamid Tayarani;
    • Mojarrad, Majid
    Publication type:
    Article
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    Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants.

    Published in:
    2020
    By:
    • Neuray, Caroline;
    • Maroofian, Reza;
    • Scala, Marcello;
    • Sultan, Tipu;
    • Pai, Gurpur S;
    • Mojarrad, Majid;
    • Khashab, Heba El;
    • deHoll, Leigh;
    • Yue, Wyatt;
    • Alsaif, Hessa S;
    • Zanetti, Maria N;
    • Bello, Oscar;
    • Person, Richard;
    • Eslahi, Atieh;
    • Khazaei, Zaynab;
    • Feizabadi, Masoumeh H;
    • Efthymiou, Stephanie;
    • Group, SYNaPS Study;
    • El-Bassyouni, Hala T;
    • Soliman, Doaa R
    Publication type:
    journal article
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    PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment.

    Published in:
    2017
    By:
    • Zollo, Massimo;
    • Ahmed, Mustafa;
    • Ferrucci, Veronica;
    • Salpietro, Vincenzo;
    • Asadzadeh, Fatemeh;
    • Carotenuto, Marianeve;
    • Maroofian, Reza;
    • Al-Amri, Ahmed;
    • Singh, Royana;
    • Scognamiglio, Iolanda;
    • Mojarrad, Majid;
    • Musella, Luca;
    • Duilio, Angela;
    • Di Somma, Angela;
    • Karaca, Ender;
    • Rajab, Anna;
    • Al-Khayat, Aisha;
    • Mohapatra, Tribhuvan Mohan;
    • Eslahi, Atieh;
    • Ashrafzadeh, Farah
    Publication type:
    journal article
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    Identification of Novel Hypoxia Response Genes in Human Glioma Cell Line A172.

    Published in:
    Iranian Journal of Basic Medical Sciences, 2013, v. 16, n. 5, p. 666
    By:
    • Baghbani, Fatemeh;
    • Raoofian, Reza;
    • Hasanzadeh Nazarabadi, Mohammad;
    • Hamzehloei, Tayebeh;
    • Soukhtanloo, Mohammad;
    • Heidari, Mansur;
    • Morteza Afsharzadeh, Seyed;
    • Shekouhi, Sahar;
    • Moradi, Fahimeh;
    • Sarli, Abdol-Azim;
    • Zavar-Reza, Javad;
    • Mojarrad, Majid
    Publication type:
    Article
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