AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data
Quinodoz, Mathieu, Peter, Virginie G, Bedoni, Nicola, Royer Bertrand, Béryl, Cisarova, Katarina, Salmaninejad, Arash, Sepahi, Neda, Rodrigues, Raquel, Piran, Mehran, Mojarrad, Majid, Pasdar, Alireza, Ghanbari Asad, Ali, Sousa, Ana Berta, Coutinho Santos, Luisa, Superti-Furga, Andrea, Rivolta, Carlo
Published in Nature communications (22.01.2021)
Published in Nature communications (22.01.2021)
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Non coding RNAs as the critical factors in chemo resistance of bladder tumor cells
Zangouei, Amir Sadra, Rahimi, Hamid Reza, Mojarrad, Majid, Moghbeli, Meysam
Published in Diagnostic pathology (12.11.2020)
Published in Diagnostic pathology (12.11.2020)
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Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies
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
Published in Scientific reports (29.09.2021)
Published in Scientific reports (29.09.2021)
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Journal Article
Role of tyrosine kinases in bladder cancer progression: an overview
Zangouei, Amir Sadra, Barjasteh, Amir Hossein, Rahimi, Hamid Reza, Mojarrad, Majid, Moghbeli, Meysam
Published in Cell communication and signaling (14.08.2020)
Published in Cell communication and signaling (14.08.2020)
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Journal Article
Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies
Salmaninejad, Arash, Bedoni, Nicola, Ravesh, Zeinab, Quinodoz, Mathieu, Shoeibi, Nasser, Mojarrad, Majid, Pasdar, Alireza, Rivolta, Carlo
Published in Scientific reports (10.11.2020)
Published in Scientific reports (10.11.2020)
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Journal Article
Common therapeutic advances for Duchenne muscular dystrophy (DMD)
Salmaninejad, Arash, Jafari Abarghan, Yousef, Bozorg Qomi, Saeed, Bayat, Hadi, Yousefi, Meysam, Azhdari, Sara, Talebi, Samaneh, Mojarrad, Majid
Published in International journal of neuroscience (03.04.2021)
Published in International journal of neuroscience (03.04.2021)
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Journal Article
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents
Yan, Denise, Tekin, Demet, Bademci, Guney, Foster, Joseph, Cengiz, F. Basak, Kannan-Sundhari, Abhiraami, Guo, Shengru, Mittal, Rahul, Zou, Bing, Grati, Mhamed, Kabahuma, Rosemary I., Kameswaran, Mohan, Lasisi, Taye J., Adedeji, Waheed A., Lasisi, Akeem O., Menendez, Ibis, Herrera, Marianna, Carranza, Claudia, Maroofian, Reza, Crosby, Andrew H., Bensaid, Mariem, Masmoudi, Saber, Behnam, Mahdiyeh, Mojarrad, Majid, Feng, Yong, Duman, Duygu, Mawla, Alex M., Nord, Alex S., Blanton, Susan H., Liu, Xue Z., Tekin, Mustafa
Published in Human genetics (01.08.2016)
Published in Human genetics (01.08.2016)
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Journal Article
Role of extra cellular proteins in gastric cancer progression and metastasis : an update
Abbaszadegan, Mohammad Reza, Mojarrad, Majid, Moghbeli, Meysam
Published in Genes and Environment (15.05.2020)
Published in Genes and Environment (15.05.2020)
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Journal Article
CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family
Ghouchanatigh, Mahdieh, Khan, Ranjha, Mojarrad, Majid, Hameed, Uzma, Zubair, Muhammad, Waqas, Ahmed, Jalali, Mohsen, Kalantari, Mahmoudreza, Shamsa, Ali, Zhang, Huan, Shi, Qing-Hua
Published in Asian journal of andrology (01.07.2022)
Published in Asian journal of andrology (01.07.2022)
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Journal Article
A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome
Ghosh, Shereen G, Scala, Marcello, Beetz, Christian, Helman, Guy, Stanley, Valentina, Yang, Xiaoxu, Breuss, Martin W, Mazaheri, Neda, Selim, Laila, Hadipour, Fatemeh, Pais, Lynn, Stutterd, Chloe A, Karageorgou, Vasiliki, Begtrup, Amber, Crunk, Amy, Juusola, Jane, Willaert, Rebecca, Flore, Leigh A, Kennelly, Kelly, Spencer, Christopher, Brown, Martha, Trapane, Pamela, Hurst, Anna C E, Lane Rutledge, S, Goodloe, Dana H, McDonald, Marie T, Shashi, Vandana, Schoch, Kelly, Tomoum, Hoda, Zaitoun, Raghda, Hadipour, Zahra, Galehdari, Hamid, Pagnamenta, Alistair T, Mojarrad, Majid, Sedaghat, Alireza, Dias, Patrícia, Quintas, Sofia, Eslahi, Atiyeh, Shariati, Gholamreza, Bauer, Peter, Simons, Cas, Houlden, Henry, Issa, Mahmoud Y, Zaki, Maha S, Maroofian, Reza, Gleeson, Joseph G
Published in European journal of human genetics : EJHG (01.02.2021)
Published in European journal of human genetics : EJHG (01.02.2021)
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Journal Article
Genetics of blood malignancies among Iranian population: an overview
Ghayour-Mobarhan, Majid, Zangouei, Amir Sadra, Hosseinirad, Seyed Mohammad, Mojarrad, Majid, Moghbeli, Meysam
Published in Diagnostic pathology (06.05.2020)
Published in Diagnostic pathology (06.05.2020)
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Journal Article
TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia
Mohajeri, Mahsa Sadat Asl, Eslahi, Atieh, Khazaii, Zeinab, Moradi, Mohammad Reza, Pazhoomand, Reza, Farrokhi, Shima, Feizabadi, Masoumeh Heidari, Alizadeh, Farzaneh, Mojarrad, Majid
Published in Human genomics (08.07.2021)
Published in Human genomics (08.07.2021)
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Journal Article
Genetic and molecular biology of systemic lupus erythematosus among Iranian patients: an overview
Gachpazan, Meisam, Akhlaghipour, Iman, Rahimi, Hamid Reza, Saburi, Ehsan, Mojarrad, Majid, Abbaszadegan, Mohammad Reza, Moghbeli, Meysam
Published in Autoimmunity highlights (30.01.2021)
Published in Autoimmunity highlights (30.01.2021)
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