Are Dyskeratosis Congenita patients at higher risk of symptomatic COVID-19?

por Dorgaleleh, Saeed, Naghipoor, Karim, Hozhabrpour, Amir, Vahidnezhad, Hassan
Publicado 2022

Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis

por UITTO, Jouni, YOUSSEFIAN, Leila, SAEIDIAN, Amir Hossein, VAHIDNEZHAD, Hassan
Publicado 2020

Skin Manifestations in COVID-19 Patients: Are They Indicators for Disease Severity? A Systematic Review

por Jamshidi, Parnian, Hajikhani, Bahareh, Mirsaeidi, Mehdi, Vahidnezhad, Hassan, Dadashi, Masoud, Nasiri, Mohammad Javad
Publicado 2021

The quality of life in epidermolysis bullosa (EB-QoL) questionnaire: Translation, cultural adaptation, and validation into the Farsi language

por Yazdanshenas, Atoosa, Naderi, Ezatollah, Moravvej, Hamideh, Heidari, Kazem, Faghankhani, Masoomeh, Vahidnezhad, Hassan, Mozafari, Nikoo
Publicado 2020

Advance trends in targeting homology-directed repair for accurate gene editing: An inclusive review of small molecules and modified CRISPR-Cas9 systems

por Shams, Forough, Bayat, Hadi, Mohammadian, Omid, Mahboudi, Somayeh, Vahidnezhad, Hassan, Soosanabadi, Mohsen, Rahimpour, Azam
Publicado 2022

A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome

por Youssefian, Leila, Touati, Andrew, Saeidian, Amir Hossein, Zargari, Omid, Zeinali, Sirous, Vahidnezhad, Hassan, Uitto, Jouni
Publicado 2017

Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected...

por Saeidian, Amir Hossein, Vahidnezhad, Hassan, Youssefian, Leila, Sotudeh, Soheila, Sargazi, Meisam, Zeinali, Sirous, Uitto, Jouni
Publicado 2019

Elevated Serum Levels of Interleukin-15 in Pemphigus Vulgaris Patients: a Potential Therapeutic Target

por Kheirodin, Maedeh, Tehranchinia, Zohreh, Ketabi, Yasaman, Tavakolpour, Soheil, Dadkhahfar, Sahar, Faghankhani, Masoomeh, Vahidnezhad, Hassan, Mozafari, Nikoo
Publicado 2022

The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series

por Youssefian, Leila, Vahidnezhad, Hassan, Touati, Andrew, Ziaee, Vahid, Saeidian, Amir Hossein, Pajouhanfar, Sara, Zeinali, Sirous, Uitto, Jouni
Publicado 2018

Genetic Predisposition to Numerous Large Ulcerating Basal Cell Carcinomas and Response to Immune Therapy

por Dasgeb, Bahar, Leila, Youssefian, Saeidian, Amir Hossein, Kang, Jun, Shi, Wenyin, Shoenberg, Elizabeth, Ertel, Adam, Fortina, Paolo, Vahidnezhad, Hassan, Uitto, Jouni
Publicado 2021

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification

por Ralph, Douglas, Nitschke, Yvonne, Levine, Michael A., Caffet, Matthew, Wurst, Tamara, Saeidian, Amir Hossein, Youssefian, Leila, Vahidnezhad, Hassan, Terry, Sharon F., Rutsch, Frank, Uitto, Jouni, Li, Qiaoli
Publicado 2022

Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

por Guerrero-Aspizua, Sara, Conti, Claudio J., Escamez, Maria Jose, Castiglia, Daniele, Zambruno, Giovanna, Youssefian, Leila, Vahidnezhad, Hassan, Requena, Luis, Itin, Peter, Tadini, Gianluca, Yordanova, Ivelina, Martin, Ludovic, Uitto, Jouni, Has, Cristina, Del Rio, Marcela
Publicado 2019

Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

por 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
Publicado 2023

Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

por 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
Publicado 2023

Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility

por Vahidnezhad, Hassan, Youssefian, Leila, Faghankhani, Masoomeh, Mozafari, Nikoo, Saeidian, Amir Hossein, Niaziorimi, Fatemeh, Abdollahimajd, Fahimeh, Sotoudeh, Soheila, Rajabi, Fateme, Mirsafaei, Liaosadat, Sani, Zahra Alizadeh, Liu, Lu, Guy, Alyson, Zeinali, Sirous, Kariminejad, Ariana, Ho, Reginald T., McGrath, John A., Uitto, Jouni
Publicado 2020

Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections

por Saeidian, Amir Hossein, Youssefian, Leila, Naji, Mahtab, Mahmoudi, Hamidreza, Barnada, Samantha M., Huang, Charles, Naghipoor, Karim, Hozhabrpour, Amir, Park, Jason S., Manzo Margiotta, Flavia, Vahidnezhad, Fatemeh, Saffarian, Zahra, Kamyab-Hesari, Kambiz, Tolouei, Mohammad, Faraji, Niloofar, Azimi, Seyyede Zeinab, Namdari, Ghazal, Mansouri, Parvin, Casanova, Jean-Laurent, Béziat, Vivien, Jouanguy, Emmanuelle, Uitto, Jouni, Vahidnezhad, Hassan
Publicado 2023

Whole-transcriptome sequencing–based concomitant detection of viral and human genetic determinants of cutaneous lesions

por Saeidian, Amir Hossein, Youssefian, Leila, Huang, Charles Y., Palizban, Fahimeh, Naji, Mahtab, Saffarian, Zahra, Mahmoudi, Hamidreza, Goodarzi, Azadeh, Sotoudeh, Soheila, Vahidnezhad, Fatemeh, Amani, Maliheh, Tavakoli, Narjes, Ajami, Ali, Mozafarpoor, Samaneh, Teimoorian, Mehrdad, Dorgaleleh, Saeed, Shokri, Sima, Shenagari, Mohammad, Abedi, Nima, Zeinali, Sirous, Fortina, Paolo, Béziat, Vivien, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, Uitto, Jouni, Vahidnezhad, Hassan
Publicado 2022

The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses

por de Jong, Sarah Jill, Créquer, Amandine, Matos, Irina, Hum, David, Gunasekharan, Vignesh, Lorenzo, Lazaro, Jabot-Hanin, Fabienne, Imahorn, Elias, Arias, Andres A., Vahidnezhad, Hassan, Youssefian, Leila, Markle, Janet G., Patin, Etienne, D’Amico, Aurelia, Wang, Claire Q.F., Full, Florian, Ensser, Armin, Leisner, Tina M., Parise, Leslie V., Bouaziz, Matthieu, Maya, Nataly Portilla, Cadena, Xavier Rueda, Saka, Bayaki, Saeidian, Amir Hossein, Aghazadeh, Nessa, Zeinali, Sirous, Itin, Peter, Krueger, James G., Laimins, Lou, Abel, Laurent, Fuchs, Elaine, Uitto, Jouni, Franco, Jose Luis, Burger, Bettina, Orth, Gérard, Jouanguy, Emmanuelle, Casanova, Jean-Laurent
Publicado 2018

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

por Ogishi, Masato, Yang, Rui, Rodriguez, Rémy, Golec, Dominic P., Martin, Emmanuel, Philippot, Quentin, Bohlen, Jonathan, Pelham, Simon J., Arias, Andrés 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, Béziat, Vivien, Youssefian, Leila, Vahidnezhad, Hassan, Rao, V. Koneti, Neven, Bénédicte, Fieschi, Claire, Mansouri, Davood, Shahrooei, Mohammad, Pekcan, Sevgi, Alkan, Gulsum, Emiroğlu, Melike, Tokgöz, Hüseyin, Uitto, Jouni, Hauck, Fabian, Bustamante, Jacinta, Abel, Laurent, Keles, Sevgi, Parvaneh, Nima, Marr, Nico, Schwartzberg, Pamela L., Latour, Sylvain, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie
Publicado 2022