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Novel Frameshift Deletion Pathogenic Variant Characterization in Tuberous Sclerosis-2 Using Exome Sequencing and Molecular Dynamics Simulation Fadaie, Mahmood; Biglari, Sajjad; Vahidnezhad, Hassan; Tabatabaiefar, Mohammad Amin; Moghaddam, Atefeh Sohanforooshan; Khalafiyan, Anis; Onagh, Latifeh; Sarli, Abdolazim; Khorshid, Hamid Reza Khorram; Esmaeilzadeh, Emran Share Save
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Mitochondrial DNA Copy Number as a Hidden Player in the Progression of Multiple Sclerosis: A Bidirectional Two-Sample Mendelian Randomization Study Sabaie, Hani; Taghavi Rad, Ali; Shabestari, Motahareh; Habibi, Danial; Saadattalab, Toktam; Seddiq, Sahar; Saeidian, Amir Hossein; Zahedi, Asiyeh Sadat; Sanoie, Maryam; Vahidnezhad, Hassan; Zarkesh, Maryam; Foroutani, Laleh; Azizi, Fereidoun; Hedayati, Mehdi; Daneshpour, Maryam Sadat; Akbarzadeh, Mahdi Share Save
Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis Oliva, Meritxell; Sarkar, Mrinal K.; March, Michael E.; Saeidian, Amir Hossein; Mentch, Frank D.; Hsieh, Chen-Lin; Tang, Fanying; Uppala, Ranjitha; Patrick, Matthew T.; Li, Qinmengge; Bogle, Rachael; Kahlenberg, J. Michelle; Watson, Deborah; Glessner, Joseph T.; Youssefian, Leila; Vahidnezhad, Hassan; Tsoi, Lam C.; Gudjonsson, Johann E.; Smith, Kathleen M.; Riley-Gillis, Bridget Share Save
Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulation Biglari, Sajjad; Shahrooei, Mohammad; Vahidnezhad, Fatemeh; Youssefian, Leila; Ziaee, Vahid; Rezaei, Nima; Moghaddam, Atefeh Sohanforooshan; Sedighzadeh, Sahar; Moravej, Hossein; Safari Foroushani, Parisa; Keivanfar, Majid; Ilkhanipoor, Homa; Hozhabrpour, Amir; Seyedhosseini-Ghaheh, Hooria; Mohammadzadeh, Iraj; Naderi, Majid; Sheikhi Ghayur, Elham; Mansour Samaei, Nader; Dorgaleleh, Saeed; Esmaeilzadeh, Emran; Sherkat, Roya; Khorram Khorshid, Hamid Reza; Tabatabaiefar, Mohammad Amin; Hakonarson, Hakon; Vahidnezhad, Hassan Share Save
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The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes Roudbar, Mahmoud Amiri; Vahedi, Seyed Milad; Jin, Jin; Jahangiri, Mina; Lanjanian, Hossein; Habibi, Danial; Masjoudi, Sajedeh; Riahi, Parisa; Fateh, Sahand Tehrani; Neshati, Farideh; Zahedi, Asiyeh Sadat; Moazzam-Jazi, Maryam; Najd-Hassan-Bonab, Leila; Mousavi, Seyedeh Fatemeh; Asgarian, Sara; Zarkesh, Maryam; Moghaddas, Mohammad Reza; Tenesa, Albert; Kazemnejad, Anoshirvan; Vahidnezhad, Hassan; Hakonarson, Hakon; Azizi, Fereidoun; Hedayati, Mehdi; Daneshpour, Maryam Sadat; Akbarzadeh, Mahdi Share Save
DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity Hozhabrpour, Amir; Mojbafan, Marzieh; Palizban, Fahimeh; Vahidnezhad, Fatemeh; Talebi, Saeed; Amani, Maliheh; Garshasbi, Masoud; Naghavi, Anoosh; Khalesi, Raziyeh; Mansouri, Parvin; Sotoudeh, Soheila; Mahmoudi, Hamidreza; Varghaei, Aida; Daneshpazhooh, Maryam; Karimi, Fatemeh; Zeinali, Sirous; Kalamati, Elnaz; Uitto, Jouni; Youssefian, Leila; Vahidnezhad, Hassan Share Save
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review Biglari, Sajjad; Moghaddam, Atefeh Sohanforooshan; Tabatabaiefar, Mohammad Amin; Sherkat, Roya; Saeidian, Amir Hossein; Vahidnezhad, Fatemeh; Tsoi, Lam C.; Gudjonsson, Johann E.; Hakonarson, Hakon; Casanova, Jean -Laurent; Beziat, Vivien; Jouanguy, Emmanuelle; Vahidnezhad, Hassan Share Save
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Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients (vol 18, 177, 2023) Dehnavi, Ali Zare; Bemanalizadeh, Maryam; Kahani, Seyyed Mohammad; Ashrafi, Mahmoud Reza; Rohani, Mohammad; Toosi, Mehran Beiraghi; Heidari, Morteza; Hosseinpour, Sareh; Amini, Behnam; Zokaei, Shaghayegh; Rezaei, Zahra; Aryan, Hajar; Amanat, Man; Vahidnezhad, Hassan; Mohammadi, Pouria; Garshasbi, Masoud; Tavasoli, Ali Reza Share Save
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients Dehnavi, Ali Zare; Bemanalizadeh, Maryam; Kahani, Seyyed Mohammad; Ashrafi, Mahmoud Reza; Rohani, Mohammad; Toosi, Mehran Beiraghi; Heidari, Morteza; Hosseinpour, Sareh; Amini, Behnam; Zokaei, Shaghayegh; Rezaei, Zahra; Aryan, Hajar; Amanat, Man; Vahidnezhad, Hassan; Mohammadi, Pouria; Garshasbi, Masoud; Tavasoli, Ali Reza Share Save
Whole transcriptome-based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections Saeidian, Amir Hossein; Youssefian, Leila; Naji, Mahtab; Mahmoudi, Hamidreza; Barnada, Samantha M.; Huang, Charles; Naghipoor, Karim; Hozhabrpour, Amir; Park, Jason S.; Margiotta, Flavia Manzo; Vahidnezhad, Fatemeh; Saffarian, Zahra; Kamyab-Hesari, Kambiz; Tolouei, Mohammad; Faraji, Niloofar; Azimi, Seyyede Zeinab; Namdari, Ghazal; Mansouri, Parvin; Casanova, Jean-Laurent; Beziat, Vivien; Jouanguy, Emmanuelle; Uitto, Jouni; Vahidnezhad, Hassan Share Save
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis Ogishi, Masato; Yang, Rui; Rodriguez, Remy; Golec, Dominic P.; Martin, Emmanuel; Philippot, Quentin; Bohlen, Jonathan; Pelham, Simon J.; Arias, Andres Augusto; Khan, Taushif; Ata, Manar; Al Ali, Fatima; Rozenberg, Flore; Kong, Xiao-Fei; Chrabieh, Maya; Laine, Candice; Lei, Wei-Te; Han, Ji Eun; Seeleuthner, Yoann; Kaul, Zenia; Jouanguy, Emmanuelle; Beziat, Vivien; Youssefian, Leila; Vahidnezhad, Hassan; Rao, V. Koneti; Neven, Benedicte; Fieschi, Claire; Mansouri, Davood; Shahrooei, Mohammad; Pekcan, Sevgi; Alkan, Gulsum; Emiroglu, Melike; Tokgoez, Hueseyin; Uitto, Jouni; Hauck, Fabian; Bustamante, Jacinta; Abel, Laurent; Keles, Sevgi; Parvaneh, Nima; Marr, Nico; Schwartzberg, Pamela L.; Latour, Sylvain; Casanova, Jean-Laurent; Boisson-Dupuis, Stephanie Share Save
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