Publications by authors named "Roya Sherkat"

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Association Between Pathogenic Variants in NLRP12 and Autoinflammatory Disease: A Comprehensive Systematic Review.
Nasimeh Vatandoost, Sajjad Biglari, Tayebeh Ranjbarnejad, Hassan Vahidnezhad, Sima Jafarpour, Roya Sherkat

Int J Immunogenet· October 2025

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Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry.
Zahra Chavoshzadeh, Shahrzad Fallah, Vahide Zeinali, Samin Sharafian, Samaneh Delavari, Roya Sherkat

Front Genet· September 2025

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Unraveling a novel missense mutation (c.A248C) in Wiskott-Aldrich syndrome gene by whole exome sequencing: Insights from dynamic simulation, molecular docking and in-silico studies.
Fatemeh Mohammad-Rezaei, Javad Saffari-Chaleshtori, Kolsoum InanlooRahatloo, Roya Sherkat, Mansoor Salehi

Int Immunopharmacol· August 2025

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Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulation.
Sajjad Biglari, Mohammad Shahrooei, Fatemeh Vahidnezhad, Leila Youssefian, Vahid Ziaee, Roya Sherkat

J Med Genet· May 2025

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A Systematic Review of Mendelian Pyoderma Gangrenosum: Clinical and Genetic Characteristics in 120 Published Patients.
Leyla Norouzi-Barough, Sajjad Biglari, Roya Sherkat, Johann E Gudjonsson, Hakon Hakonarson

Exp Dermatol· May 2025

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Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients: a multicenter study by ESID and EBMT IEWP.
Julia Fekadu-Siebald, Emilia Salzmann-Manrique, Jan Robert Heusel, Andre Willasch, Fabian Hauck, Roya Sherkat

Blood Adv· April 2025

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A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review.
Leyla Norouzi-Barough, Nasrin Alipour Olyaei, Raphael Carapito, Anne Molitor, Sajjad Biglari, Roya Sherkat

Arch Dermatol Res· April 2025

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Exploring Monogenic, Polygenic, and Epigenetic Models of Common Variable Immunodeficiency.
Tayebeh Ranjbarnejad, Hassan Abolhassani, Roya Sherkat, Mansoor Salehi, Fatemeh Ranjbarnejad

Hum Mutat· April 2025

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DOCK2 Deficiency and GATA2 Haploinsufficiency Can Underlie Critical Coronavirus Disease 2019 (COVID-19) Pneumonia.
Sajjad Biglari, Leila Youssefian, Mohammad Amin Tabatabaiefar, Amir Hossein Saeidian, Bahareh Abtahi-Naeini, Roya Sherkat

J Clin Immunol· March 2025

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Guillain-Barré syndrome (GBS) after severe/critical COVID-19 or COVID-19 vaccination.
Samira Bahrami, Behnaz Ansari, Leyla Norouzi-Barough, Bahram Bagherpour, Farzin Khorvash, Roya Sherkat

Eur J Med Res· February 2025

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Decreased expression of hsa-miR-142-3p and hsa-miR-155-5p in common variable immunodeficiency and involvement of their target genes and biological pathways.
Tayebeh Ranjbarnejad, Alieh Gholaminejad, Hassan Abolhassani, Roya Sherkat, Mansoor Salehi

Allergol Immunopathol (Madr)· January 2025

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The sufficiency of genetic diagnosis in managing patients with inborn errors of immunity during prenatal care and childbearing.
Negin Salemi, Shima Bakhshesh, Amir Bahreini, Rasoul Salehi, Aryana Zamanifar, Roya Sherkat

Immunogenetics· December 2024

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Diversity in the Clinical Course and Outcome of COVID-19 in Patients with Different Inborn Errors of Immunity can be Associated with the Type of Error.
Negin Salemi, Behrokh Shojaie, Paria Bolourinejad, Roya Sherkat, Aryana Zamanifar

Adv Biomed Res· November 2024

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B-cells absence in patients diagnosed as inborn errors of immunity: a registry-based study.
Razieh Khoshnevisan, Shakiba Hassanzadeh, Christoph Klein, Meino Rohlfs, Bodo Grimbacher, Roya Sherkat

Immunogenetics· June 2024

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COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report.
John McDonnell, Kimberley Cousins, M Elizabeth M Younger, Adam Lane, Hassan Abolhassani, Roya Sherkat

J Clin Immunol· April 2024

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Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review.
Sajjad Biglari, Atefeh Sohanforooshan Moghaddam, Mohammad Amin Tabatabaiefar, Roya Sherkat, Leila Youssefian

Genet Med· February 2024

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Clinical heterogeneity in families with multiple cases of inborn errors of immunity.
Samaneh Delavari, Seyed Erfan Rasouli, Saba Fekrvand, Zahra Chavoshzade, Seyed Alireza Mahdaviani, Roya Sherkat

Clin Immunol· February 2024

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Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
Mohadese Sadat Mousavi Khorshidi, Yoann Seeleuthner, Zahra Chavoshzadeh, Maryam Behfar, Amir Ali Hamidieh, Roya Sherkat

J Clin Immunol· November 2023

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Contradictory Effect of Lymphocyte Therapy and Prednisolone Therapy on CD3CD8CD56 Natural Killer T Population in Women with Recurrent Spontaneous Abortion.
Fatemeh Rezayat, Nafiseh Esmaeil, Abbas Rezaei, Roya Sherkat

J Hum Reprod Sci· September 2023

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Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patients.
Mohammad Reza Fazlollahi, Amir Ali Hamidieh, Leila Moradi, Raheleh Shokouhi Shoormati, Nastaran Sabetkish, Roya Sherkat

Pediatr Allergy Immunol· July 2023

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Hematologically important mutations: Leukocyte adhesion deficiency (second update).
Dirk Roos, Karin van Leeuwen, Manisha Madkaikar, Priyanka M Kambli, Maya Gupta, Roya Sherkat

Blood Cells Mol Dis· March 2023

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Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.
Romain Lévy, Florian Gothe, Mana Momenilandi, Thomas Magg, Marie Materna, Roya Sherkat

J Exp Med· February 2023

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Cytomegalovirus Specific Cell-Mediated Immunity Status in Women with Preeclampsia: A Case-Control Study.
Roya Sherkat, Zahra Shahshahan, Maryam Kalatehjari, Majid Yaran, Maryam Nasirian

Adv Biomed Res· January 2023

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Diversity of malignancies in patients with different types of inborn errors of immunity.
Marzieh Tavakol, Samaneh Delavari, Fereshte Salami, Sarina Ansari, Seyed Erfan Rasouli, Roya Sherkat

Allergy Asthma Clin Immunol· December 2022

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Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency.
Masato Ogishi, Andrés Augusto Arias, Rui Yang, Ji Eun Han, Peng Zhang, Roya Sherkat

J Exp Med· October 2022

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