OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel disease
Luca Bosa, Vritika Batura, Davide Colavito, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 15

Showing 15 citing articles:

Evolution and long‐term outcomes of combined immunodeficiency due to CARMIL2 deficiency
Burcu Kolukısa, Dilek Başer, Bengü Akçam, et al.
Allergy (2021) Vol. 77, Iss. 3, pp. 1004-1019
Open Access | Times Cited: 35

Atopy as Immune Dysregulation: Offender Genes and Targets
Maryam Vaseghi‐Shanjani, Andrew L. Snow, David J. Margolis, et al.
The Journal of Allergy and Clinical Immunology In Practice (2022) Vol. 10, Iss. 7, pp. 1737-1756
Closed Access | Times Cited: 23

Genetic/Environmental Contributions and Immune Dysregulation in Children with Atopic Dermatitis
Albert C. Chong, Kittipos Visitsunthorn, Peck Y. Ong
Journal of Asthma and Allergy (2022) Vol. Volume 15, pp. 1681-1700
Open Access | Times Cited: 21

Epstein–Barr Virus in Inborn Immunodeficiency—More Than Infection
Ciro N. R. Lino, Sujal Ghosh
Cancers (2021) Vol. 13, Iss. 19, pp. 4752-4752
Open Access | Times Cited: 20

Inborn errors of immunity underlying a susceptibility to pyogenic infections: from innate immune system deficiency to complex phenotypes
Francesca Conti, Antonio Marzollo, Mattia Moratti, et al.
Clinical Microbiology and Infection (2022) Vol. 28, Iss. 11, pp. 1422-1428
Open Access | Times Cited: 8

Case Report: Intestinal Nodular Lymphoid Hyperplasia as First Manifestation of Activated PI3Kδ Syndrome Due to a Novel PIK3CD Variant
Antonio Marzollo, Silvia Bresolin, Davide Colavito, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 9

CARMIL2 Immunodeficiency with Epstein Barr Virus Associated Smooth Muscle Tumor (EBV-SMT). Report of a Case with Comprehensive Review of Literature
Mukul Vij, Meena Sivasankaran, Dhaarani Jayaraman, et al.
Fetal and Pediatric Pathology (2021) Vol. 41, Iss. 6, pp. 1023-1034
Closed Access | Times Cited: 9

Monogenic inflammatory bowel disease-genetic variants, functional mechanisms and personalised medicine in clinical practice
Aline Azabdaftari, Kelsey Jones, Jochen Kammermeier, et al.
Human Genetics (2022) Vol. 142, Iss. 5, pp. 599-611
Closed Access | Times Cited: 6

Secondary Membranous Nephropathy and Immunodeficiency due to a Novel Biallelic Variant in CARMIL2
Lakshmi Priya Rao, Vishaka Kothiwale, Periyasamy Radhakrishnan, et al.
Indian Journal of Nephrology (2024) Vol. 34, pp. 667-669
Open Access

Functional analysis of HECA variants identified in congenital heart disease in the Chinese population
Ting Li, Yao Wu, Wei‐Cheng Chen, et al.
Journal of Clinical Laboratory Analysis (2022) Vol. 36, Iss. 9
Open Access | Times Cited: 2

An insight into genetic landscape of inflammatory bowel disease
Zunaira Ali Baig, Asifa Majeed
Journal of the Pakistan Medical Association (2023) Vol. 73, Iss. 12, pp. 2415-2422
Open Access

Page 1

Scroll to top