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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency
Hassan Abolhassani, Asghar Aghamohammadi, Mingyan Fang, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 1, pp. 243-251
Open Access | Times Cited: 97

Showing 26-50 of 97 citing articles:

Health Professionals’ Preferences for Next-Generation Sequencing in the Diagnosis of Suspected Genetic Disorders in the Paediatric Population
Mario Cesare Nurchis, Gerardo Altamura, Gian Marco Raspolini, et al.
Journal of Personalized Medicine (2025) Vol. 15, Iss. 1, pp. 25-25
Open Access
<span>APOBEC2&nbsp;</span>Deficiency Disrupts Hematopoietic Lineage Commitment, Leading to the Emergence of T/B Hybrid Lymphocytes in Mouse Models and Human Patients
Elias Amro, Christos Gkougkousis, Irem Tellioglu, et al.
(2025)
Closed Access
Exploring Monogenic, Polygenic, and Epigenetic Models of Common Variable Immunodeficiency
Tayebeh Ranjbarnejad, Hassan Abolhassani, Roya Sherkat, et al.
Human Mutation (2025) Vol. 2025, Iss. 1
Open Access
Epigenetic Deregulation in Human Primary Immunodeficiencies
Elena Campos-Sánchez, Jorge Martínez-Cano, Lucía del Pino Molina, et al.
Trends in Immunology (2018) Vol. 40, Iss. 1, pp. 49-65
Open Access | Times Cited: 29
Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency
Hassan Abolhassani, Yasser M. El‐Sherbiny, Gururaj Arumugakani, et al.
Journal of Clinical Immunology (2019) Vol. 40, Iss. 2, pp. 277-288
Open Access | Times Cited: 29
The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long‐term follow‐up and genetic analysis
Mahmood Tavassoli, Hassan Abolhassani, Reza Yazdani, et al.
Pediatric Allergy and Immunology (2019) Vol. 30, Iss. 4, pp. 469-478
Closed Access | Times Cited: 23
A 2020 update on the use of genetic testing for patients with primary immunodeficiency
Iván K. Chinn, Jordan S. Orange
Expert Review of Clinical Immunology (2020) Vol. 16, Iss. 9, pp. 897-909
Closed Access | Times Cited: 23
Screening for primary immunodeficiency diseases by next‐generation sequencing in early life
Jinqiao Sun, Lin Yang, Yulan Lu, et al.
Clinical & Translational Immunology (2020) Vol. 9, Iss. 5
Open Access | Times Cited: 21
All Patients With Common Variable Immunodeficiency Disorders (CVID) Should Be Routinely Offered Diagnostic Genetic Testing
Rohan Ameratunga, Klaus Lehnert, See‐Tarn Woon
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 22
The Heterogeneous Pathogenesis of Selective Immunoglobulin A Deficiency
Yasser Bagheri, Roozbeh Sanaei, Reza Yazdani, et al.
International Archives of Allergy and Immunology (2019) Vol. 179, Iss. 3, pp. 231-246
Open Access | Times Cited: 21
Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity
Mohammad Hossein Asgardoon, Gholamreza Azizi, Reza Yazdani, et al.
International Archives of Allergy and Immunology (2020) Vol. 181, Iss. 9, pp. 706-714
Closed Access | Times Cited: 20
VIPPID: a gene-specific single nucleotide variant pathogenicity prediction tool for primary immunodeficiency diseases
Mingyan Fang, Zheng Su, Hassan Abolhassani, et al.
Briefings in Bioinformatics (2022) Vol. 23, Iss. 5
Open Access | Times Cited: 12
Information and Communication Technology (ICT) and youth unemployment in Africa
Ahamuefula E. Ogbonna, Idris A. Adediran, Tirimisiyu F. Oloko, et al.
Quality & Quantity (2022) Vol. 57, Iss. 6, pp. 5055-5077
Open Access | Times Cited: 12
The Autoimmune Manifestations in Patients with Genetic Defects in the B Cell Development and Differentiation Stages
Gholamreza Azizi, Mina Fattah Hesari, Niusha Sharifinejad, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 4, pp. 819-834
Open Access | Times Cited: 7
Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients
Yasser Bagheri, Ahmad Vosoughi Motlagh, Gholamreza Azizi, et al.
Immunology Letters (2019) Vol. 210, pp. 55-62
Closed Access | Times Cited: 19
Epigenetic Priming in Immunodeficiencies
Jorge Martínez-Cano, Elena Campos-Sánchez, César Cobaleda
Frontiers in Cell and Developmental Biology (2019) Vol. 7
Open Access | Times Cited: 18
Comprehensive Assessment of Skin Disorders in Patients with Common Variable Immunodeficiency (CVID)
Ali Zarezadeh Mehrabadi, Nazanin Aghamohamadi, Hassan Abolhassani, et al.
Journal of Clinical Immunology (2022) Vol. 42, Iss. 3, pp. 653-664
Closed Access | Times Cited: 11
How do nuclear factor kappa B (NF-κB)1 and NF-κB2 defects lead to the incidence of clinical and immunological manifestations of inborn errors of immunity?
Nazanin Fathi, Hanieh Mojtahedi, Marzieh Nasiri, et al.
Expert Review of Clinical Immunology (2023) Vol. 19, Iss. 3, pp. 329-339
Closed Access | Times Cited: 6
Clinical heterogeneity in families with multiple cases of inborn errors of immunity
Samaneh Delavari, Seyed Erfan Rasouli, Saba Fekrvand, et al.
Clinical Immunology (2024) Vol. 259, pp. 109896-109896
Closed Access | Times Cited: 2
Limitations in the clinical utility of vaccine challenge responses in the evaluation of primary antibody deficiency including Common Variable Immunodeficiency Disorders
Rohan Ameratunga, Hilary Longhurst, Euphemia Leung, et al.
Clinical Immunology (2024) Vol. 266, pp. 110320-110320
Closed Access | Times Cited: 2
Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran
Zahra Shahbazi, Reza Yazdani, Sepideh Shahkarami, et al.
Immunology Letters (2019) Vol. 216, pp. 70-78
Closed Access | Times Cited: 17
Genetic health professionals’ experiences with initiating reanalysis of genomic sequence data
Danya F. Vears, Karine Sénécal, Pascal Borry
Familial Cancer (2020) Vol. 19, Iss. 3, pp. 273-280
Closed Access | Times Cited: 15
The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-δ (PI3Kδ) Syndrome (APDS)
Saba Fekrvand, Samaneh Delavari, Zahra Chavoshzadeh, et al.
Immunological Investigations (2021) Vol. 51, Iss. 3, pp. 644-659
Closed Access | Times Cited: 13
Evaluation of miR-210 expression in common variable immunodeficiency: patients with unsolved genetic defect
Fateme Babaha, Reza Yazdani, Sepideh Shahkarami, et al.
Allergologia et Immunopathologia (2021) Vol. 49, Iss. 2, pp. 84-93
Open Access | Times Cited: 13
Specific Immune Response and Cytokine Production in CD70 Deficiency
Hassan Abolhassani
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 13

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