Leila Youssefian (L Youssefian)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 17

Top Topics

Dna Methylation

Duchenne Muscular Dystrophy

Vascular Smooth Muscle Cells

Top Venues

Dermatologic therapy

Experimental dermatology

The Journal of experimental medicine

Journal of the European Academy of Dermatology and Venereology : JEADV

This page only lists publications with an associated author ORCID identifier.

Publications

Douglas Ralph, Yvonne Nitschke, Michael A Levine, Matthew Caffet, Tamara Wurst, Amir Hossein Saeidian, Leila Youssefian, Hassan Vahidnezhad, Sharon F Terry, Frank Rutsch, Jouni Uitto, Qiaoli Li
ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification. PLoS genetics 18 (4) (2022)
Masato Ogishi, Jean-Laurent Casanova, Rémy Rodriguez, Dominic P Golec, Emmanuel Martin, Quentin Philippot, Jonathan Bohlen, Simon J Pelham, Andrés Augusto Arias, Taushif Khan, Manar Mahmoud Ahmad Ata, Fatima Al Ali, Flore Rozenberg, Xiao-Fei Kong, Maya Chrabieh, Candice Lainé, Wei-Te Lei, Ji Eun Han, Yoann Seeleuthner, Zenia Kaul, Emmanuelle Jouanguy, Vivien Béziat, Leila Youssefian, Hassan Vahidnezhad, V Koneti Rao, Bénédicte Neven, Claire Fieschi, Davood Mansouri, Mohammad Shahrooei, Sevgi Pekcan, Gülsüm Alkan, Melike Emiroğlu, Hüseyin Tokgöz, Jouni Uitto, Fabian H Hauck, Jacinta Bustamante, Laurent Abel, Sevgi Keles, Nima Parvaneh, Nico Marr, Pamela L Schwartzberg, Sylvain Latour, Jean Laurent Casanova, Stéphanie Boisson-Dupuis
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis. The Journal of experimental medicine 220 (1) (2022)
Mohammad Reza Pourani, Hassan Vahidnezhad, Parvin Mansuri, Leila Youssefian, Azadeh Rakhshan, Behzad Hajimoradi, Fahimeh Abdollahimajd, Jouni Uitto
Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case series. Dermatologic therapy 35 (7) (2022)
Fatemeh Mohaghegh, Leila Youssefian, Hamid Galehdari, Narjes Tavakoli, Hassan Vahidnezhad, Jouni Uitto
Whole-transcriptome sequencing identifies postzygotic ATP2A2 mutations in a patient misdiagnosed with herpes zoster, confirming the diagnosis of very late-onset segmental Darier disease. Experimental dermatology 31 (6) (2022)
Hassan Vahidnezhad, Leila Youssefian, Nailah Harvey, Ali Reza Tavasoli, Amir Hossein Saeidian, Soheila Sotoudeh, Aida Varghaei, Hamidreza Mahmoudi, Parvin Mansouri, Nikoo Mozafari, Omid Zargari, Sirous Zeinali, Jouni Uitto
Mutation update: The spectra of PLEC sequence variants and related plectinopathies. Human mutation (2022)
Jason S Park, Amir Hossein Saeidian, Leila Youssefian, Sylvia Hsu, Hassan Vahidnezhad, Jouni Uitto
Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug-induced associations. Journal of the European Academy of Dermatology and Venereology : JEADV (2022)
Leila Youssefian, Mahtab Naji, Jason S Park, Fateme Rajabi, Fahimeh Abdollahimajd, Hamid Reza Mahmoudi, Kambiz Kamyab-Hesari, Fariba Ghalamkarpour, Masoud Zabihi, Mehrdad Teimoorian, Laya Youssefian, Sirous Zeinali, Hassan Vahidnezhad, Jouni Uitto
Ichthyosis follicularis syndromes in patients with mutations in GJB2. Clinical and experimental dermatology 47 (8) (2022)
Irene Navarro-Navarro, David Jimenez-Gallo, Raquel de la Varga-Martínez, I Villegas-Romero, F Mora-López, Mario Linares-Barrios, Leila Youssefian, Hassan Vahidnezhad, Jouni Uitto
Novel splice mutation in CDSN gene causing type b peeling skin syndrome. Journal of the European Academy of Dermatology and Venereology : JEADV 36 (6) (2022)
Mohammad Reza Pourani, Sayyed Mojtaba Nekooghadam, Leila Youssefian, Hassan Vahidnezhad, Fahimeh Abdollahimajd
CD147 inhibitors as a treatment for melanoma: Promising agents against SARS-CoV-2 infection. Dermatologic therapy 33 (6) (2020)
Tina Asgari, Mahtab Naji, Parvin Mansuri, Hamid Reza Mahmoudi, Masoud Zabihi, Leila Youssefian, Mohammadreza Mahdavi, Zahra Safaei Naraghi, Sirous Zeinali, Hassan Vahidnezhad, Jouni Uitto
Keratitis-ichthyosis-deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation. Dermatologic therapy 33 (6) (2020)
Leila Youssefian, Hassan Vahidnezhad
Management of symptomatic mucosal involvement in paediatric pachyonychia congenita. The British journal of dermatology 182 (3) (2020)
Amir Hossein Saeidian, Adam J Cohen-Nowak, Megan O'Donnell, Doaa Shalabi, Kathleen P McGuinn, Leila Youssefian, Hassan Vahidnezhad, Fatemeh Niaziorimi, Bahar Dasgeb, David A Kasper, Jason B Lee, Jouni Uitto, Neda Nikbakht
Linear basal cell nevus with a novel mosaic PTCH1 mutation. Experimental dermatology 29 (6) (2020)
D Li, E Ryu, A H Saeidian, Leila Youssefian, E Oliphant, S F Terry, P L Tong, Jouni Uitto, Nikolas K Haass, Qiaoli Li
GGCX mutations in a patient with overlapping pseudoxanthoma elasticum/cutis laxa-like phenotype. The British journal of dermatology 184 (6) (2020)
Elham Behrangi, Afsaneh Sadeghzadeh-Bazargan, Sepehr Khosravi, Mahsa Shemshadi, Leila Youssefian, Hassan Vahidnezhad, Azadeh Goodarzi, Jouni Uitto
Mycophenolate mofetil treatment of an H syndrome patient with a SLC29A3 mutation. Dermatologic therapy 33 (6) (2020)
Amir Hossein Saeidian, Hassan Vahidnezhad, Leila Youssefian, Soheila Sotudeh, Meisam Sargazi, Sirous Zeinali, Jouni Uitto
Hypotrichosis with juvenile macular dystrophy: Combination of whole-genome sequencing and genome-wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole-exome sequencing-A lesson from next-generation sequencing. Molecular genetics & genomic medicine 7 (11) (2019)
Tina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, Shadab Salehpour, Aria Setoodeh, Mohammad Reza Alaei, Leila Youssefian, Ashraf Samavat, Andrew Touati, Mohammad-Sadegh Fallah, Hassan Vahidnezhad, Morteza Karimipoor, Sarah Azadmehr, Marzieh Raeisi, Ameneh Bandehi Sarhadi, Fatemeh Zafarghandi Motlagh, Mojdeh Jamali, Zahra Zeinali, Maryam Abiri, Sirous Zeinali, null null
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population. Journal of inherited metabolic disease 41 (6) (2018)
Sarah Jill de Jong, Amandine Créquer, Irina Matos, David Hum, Vignesh Gunasekharan, Lazaro Lorenzo, Fabienne Jabot-Hanin, Elias Imahorn, Andrés Augusto Arias, Hassan Vahidnezhad, Leila Youssefian, Janet G Markle, Etienne Patin, Aurelia D'Amico, Claire Q F Wang, Florian Full, Ensser Armin, Tina M Leisner, Leslie V Parise, Matthieu Bouaziz, Nataly Portilla Maya, Xavier Rueda Cadena, Bayaki Saka, Amir Hossein Saeidian, Nessa Aghazadeh, Sirous Zeinali, Peter Itin, James G Krueger, Lou Laimins, Laurent Abel, Elaine Fuchs, Jouni Uitto, Jose Luis Franco, Bettina Burger, Gérard Orth, Emmanuelle Jouanguy, Jean Laurent Casanova
The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses. The Journal of experimental medicine 215 (9) (2018)