Leila Youssefian

2.4k citations

79 papers · 1.1k indexed · h-index 19

Co-authors: Hassan Vahidnezhad Jouni Uitto Amir Hossein Saeidian Sirous Zeinali Soheila Sotoudeh Paolo Fortina Hamidreza Mahmoudi Andrew Touati
Topics: Skin and Cellular Biology Research (41 papers)Wnt/β-catenin signaling in development and cancer (14 papers)Autoimmune Bullous Skin Diseases (12 papers)
Cited by: Cell Biology Immunology and Allergy Pathology and Forensic Medicine
Journals: SHILAP Revista de lepidopterologíaClinical Infectious Diseases Scientific Reports
Partner nations: United States Iran Italy

In The Last Decade

Leila Youssefian

75 papers receiving 1.1k citations

Peers

Countries citing papers authored by Leila Youssefian

Since Specialization

Citations

This map shows the geographic impact of Leila Youssefian's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Leila Youssefian with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Leila Youssefian more than expected).

Fields of papers citing papers by Leila Youssefian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leila Youssefian. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Leila Youssefian. The network helps show where Leila Youssefian may publish in the future.

Co-authorship network of co-authors of Leila Youssefian

This figure shows the co-authorship network connecting the top 25 collaborators of Leila Youssefian. A scholar is included among the top collaborators of Leila Youssefian based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Leila Youssefian. Leila Youssefian is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Successful and Sustained Treatment of Cutaneous Tumoral Lesions in Brooke–Spiegler Syndrome ( BSS ) Using Ablative CO ₂ Laser: A Case Series and Literature Review 2025 ·Clinical Case Reports ·Nikoo Mozafari,(unknown),(unknown),Hassan Vahidnezhad,Leila Youssefian,(unknown),Farnoosh Seirafianpour,Arash Pour Mohammad,Alireza Jafarzadeh,Azadeh Goodarzi	0
2	Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review 2023 ·Genetics in Medicine ·Sajjad Biglari,(unknown),Mohammad Amin Tabatabaiefar,Roya Sherkat,Leila Youssefian,Amir Hossein Saeidian,(unknown),Lam C. Tsoi,Jóhann E. Guðjónsson,Håkon Håkonarson,Jean‐Laurent Casanova,Vivien Béziat,Emmanuelle Jouanguy,Hassan Vahidnezhad	1
3	Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case series 2022 ·Dermatologic Therapy ·(unknown),Hassan Vahidnezhad,Parvin Mansouri,Leila Youssefian,Azadeh Rakhshan,(unknown),Fahimeh Abdollahimajd,Jouni Uitto	16
4	Mutation update: The spectra of PLEC sequence variants and related plectinopathies 2022 ·Human Mutation ·Hassan Vahidnezhad,Leila Youssefian,(unknown),Ali Reza Tavasoli,Amir Hossein Saeidian,Soheila Sotoudeh,(unknown),Hamidreza Mahmoudi,Parvin Mansouri,Nikoo Mozafari,Omid Zargari,Sirous Zeinali,Jouni Uitto	8
5	Pathomechanisms of epidermolysis bullosa: Beyond structural proteins 2022 ·Matrix Biology ·(unknown),Leila Youssefian,Amir Hossein Saeidian,Hassan Vahidnezhad,Jouni Uitto	7
6	Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency 2022 ·Journal of Investigative Dermatology ·Leila Youssefian,Amir Hossein Saeidian,Ali Reza Tavasoli,(unknown),(unknown),(unknown),Mehrnaz Mesdaghi,(unknown),Hamidreza Mahmoudi,Mohammad Nabavi,Sima Shokri,Sirous Zeinali,Vivien Béziat,Jean‐Laurent Casanova,Emmanuelle Jouanguy,Jouni Uitto,Hassan Vahidnezhad	4
7	Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP 2021 ·Journal of the European Academy of Dermatology and Venereology ·Leila Youssefian,Sadegh Khodavaisy,(unknown),(unknown),Amir Hossein Saeidian,Hamidreza Mahmoudi,(unknown),Z Safaei Naraghi,Kambiz Kamyab‐Hesari,Sirous Zeinali,Hassan Vahidnezhad,Jouni Uitto	2
8	Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous Human Papillomavirus Infections at the Intersection of Genetic Variability of Viral and Human Genomes 2021 ·Journal of Investigative Dermatology ·Jouni Uitto,Amir Hossein Saeidian,Leila Youssefian,(unknown),Jean‐Laurent Casanova,Vivien Béziat,Emmanuelle Jouanguy,Hassan Vahidnezhad	9
9	Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation 2021 ·Matrix Biology ·Hassan Vahidnezhad,Leila Youssefian,Amir Hossein Saeidian,Lynn M. Boyden,Andrew Touati,(unknown),(unknown),(unknown),(unknown),Soheila Sotoudeh,Lu Liu,Alyson Guy,Ariana Kariminejad,Sirous Zeinali,Keith A. Choate,John A. McGrath,Jouni Uitto	5
10	Very-Early-Onset Inflammatory Bowel Disease in a Patient With Junctional Epidermolysis Bullosa With a Homozygous Mutation in the α6 Integrin Gene (ITGA6) 2021 ·Inflammatory Bowel Diseases ·Hassan Vahidnezhad,Leila Youssefian,Mohammad Hossein Anbardar,Sirous Zeinali,(unknown),Jouni Uitto	1
11	Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica 2020 ·Human Mutation ·Hassan Vahidnezhad,Leila Youssefian,Soheila Sotoudeh,Lu Liu,Alyson Guy,Patricia A. Lovell,Ariana Kariminejad,Sirous Zeinali,John A. McGrath,Jouni Uitto	12
12	Mycophenolate mofetil treatment of an H syndrome patient with a SLC29A3 mutation 2020 ·Dermatologic Therapy ·Elham Behrangi,Afsaneh Sadeghzadeh‐Bazargan,Sepehr Khosravi,(unknown),Leila Youssefian,Hassan Vahidnezhad,Azadeh Goodarzi,Jouni Uitto	10
13	Research Techniques Made Simple: Whole-Transcriptome Sequencing by RNA-Seq for Diagnosis of Monogenic Disorders 2020 ·Journal of Investigative Dermatology ·Amir Hossein Saeidian,Leila Youssefian,Hassan Vahidnezhad,Jouni Uitto	60
14	Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis 2020 ·Acta Dermato Venereologica ·Jouni Uitto,Leila Youssefian,Amir Hossein Saeidian,Hassan Vahidnezhad	21
15	Pachyonychia congenita: a case report of a successful treatment with rosuvastatin in a patient with a KRT6A mutation 2018 ·British Journal of Dermatology ·Fahimeh Abdollahimajd,Fateme Rajabi,Mohammad Shahidi‐Dadras,(unknown),Leila Youssefian,Hassan Vahidnezhad,Jouni Uitto	15
16	Research Techniques Made Simple: Genome-Wide Homozygosity/Autozygosity Mapping Is a Powerful Tool for Identifying Candidate Genes in Autosomal Recessive Genetic Diseases 2018 ·Journal of Investigative Dermatology ·Hassan Vahidnezhad,Leila Youssefian,Ali Jazayeri,Jouni Uitto	29
17	Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosa 2018 ·Human Mutation ·Hassan Vahidnezhad,Leila Youssefian,Amir Hossein Saeidian,Andrew Touati,Soheila Sotoudeh,Ali Jazayeri,Alyson Guy,Patricia A. Lovell,Lu Liu,Ariana Kariminejad,John A. McGrath,Sirous Zeinali,Jouni Uitto	24
18	Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families 2018 ·Human Mutation ·Leila Youssefian,Hassan Vahidnezhad,Amir Hossein Saeidian,Andrew Touati,Soheila Sotoudeh,Hamidreza Mahmoudi,Parvin Mansouri,Maryam Daneshpazhooh,Nessa Aghazadeh,Kambiz Kamyab Hesari,(unknown),Eric Londin,Gaurav Kumar,Sirous Zeinali,Paolo Fortina,Jouni Uitto	39
19	Seven novel COL7A1 mutations identified in patients with recessive dystrophic epidermolysis bullosa from Mexico 2018 ·Clinical and Experimental Dermatology ·Amir Hossein Saeidian,Leila Youssefian,María G. Moreno‐Treviño,Giulio Fortuna,Hassan Vahidnezhad,Velina S. Atanasova,Jouni Uitto,(unknown),Andrew P. South	7
20	A novel autosomal recessiveGJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma 2018 ·Human Mutation ·Leila Youssefian,Hassan Vahidnezhad,Amir Hossein Saeidian,Hamidreza Mahmoudi,Razieh Karamzadeh,Ariana Kariminejad,Jianhe Huang,Leping Li,(unknown),Paolo Fortina,Sirous Zeinali,Thomas W. White,Jouni Uitto	12

About Leila Youssefian

Leila Youssefian is a scholar working on Cell Biology, Immunology and Allergy and Pathology and Forensic Medicine, having authored 79 papers that have together received 1.1k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (41 papers), Wnt/β-catenin signaling in development and cancer (14 papers) and Autoimmune Bullous Skin Diseases (12 papers). The work is most often cited by research in Cell Biology (504 citations), Immunology and Allergy (79 citations) and Pathology and Forensic Medicine (205 citations). Leila Youssefian has collaborated with scholars based in United States, Iran and Italy. Frequent co-authors include Hassan Vahidnezhad, Jouni Uitto, Amir Hossein Saeidian, Sirous Zeinali, Soheila Sotoudeh, Paolo Fortina, Hamidreza Mahmoudi, Andrew Touati, Maryam Abiri and Ali Jazayeri. Their work appears in journals such as SHILAP Revista de lepidopterología, Clinical Infectious Diseases and Scientific Reports.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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