Hassan Vahidnezhad (H Vahidnezhad)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 22

Top Venues

Dermatologic therapy

Experimental dermatology

American journal of medical genetics. Part A

The Journal of experimental medicine

Thomas Jefferson University Hospitals

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

Affiliation History

Thomas Jefferson University Hospitals Aug 01 2019

United States

Faculty member :: Dermatology

Thomas Jefferson University Mar 05 2014 - Jul 31 2019

United States

Research associate :: Dermatology and Cutaneous Biology

Publications

Zahra Saffarian, Raana Samiei, Alireza Ghanadan, Hassan Vahidnezhad
De novo severe pemphigus vulgaris following SARS-CoV-2 vaccination with BBIBP-CorV. Dermatologic therapy 35 (6) (2022)
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)
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)
Zahra Saffarian, Raana Samiei, Alireza Hadizadeh, Alireza Ghanadan, Hassan Vahidnezhad
Purpuric dermatosis and lymphocytic vasculopathy following SARS-CoV-2 vaccination: Report of two patients. Dermatologic therapy 35 (11) (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)
Forough Shams, Azam Rahimpour, Hassan Vahidnezhad, Simzar Hosseinzadeh, Hamideh Moravvej Farshi, Bahram Kazemi, Masoumeh Rajabibazl, Fahimeh Abdollahimajd, Jouni Uitto
The utility of dermal fibroblasts in treatment of skin disorders: A paradigm of recessive dystrophic epidermolysis bullosa. Dermatologic therapy 34 (4) (2021)
Emily Mira Warshauer, Adam Brown, Ignacia Fuentes, Jonathan Shortt, Chris Gignoux, Francesco Montinaro, Mait Metspalu, Leila Youssefian, Hassan Vahidnezhad, Joanna Jacków, Angela M Christiano, Jouni Uitto, Óscar R Fajardo-Ramírez, Julio C Salas-Alanis, John A McGrath, Liliana Consuegra, Carolina Rivera, Paul A Maier, Goran Runfeldt, Doron M Behar, Karl Skorecki, Eli Sprecher, Francis Palisson, David A Norris, Anna L Bruckner, Igor Kogut, Ganna Bilousova, Dennis R Roop
Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry. American journal of medical genetics. Part A 185 (11) (2021)
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)
Jouni Uitto, Hassan Vahidnezhad
Losartan for treatment of epidermolysis bullosa: A new perspective. Dermatologic therapy 34 (1) (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)
Arash B Hamidi, Nastaran Namazi, Mahsa Mohammad Amoli, Maliheh Amani, Morteza Gholami, Leila Youssefian, Hassan Vahidnezhad, Fahimeh Abdollahimajd, Jouni Uitto
Association of MTHFR C677T polymorphism with elevated homocysteine level and disease development in vitiligo. International journal of immunogenetics 47 (4) (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)
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)
Ariana Kariminejad, Hassan Vahidnezhad, Siavash Ghaderi-Sohi, Ali R Ghannadan, Leila Youssefian, Elham Parsimehr, Mehrshid Faraji Zonooz, Mohammad H Kariminejad, Jouni Uitto, Hossein Najmabadi, Raoul C M Hennekam
Widespread aplasia cutis congenita in sibs with PLEC1 and ITGB4 variants. American journal of medical genetics. Part A 179 (8) (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)

Hassan Vahidnezhad.css-eqlu8i{font-size:small;padding-left:4px;} (H Vahidnezhad)

Publication Activity (10 Years)

Top Topics

Top Venues

Hassan Vahidnezhad (H Vahidnezhad)