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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:

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Yingjie Zhao, Alexander Diacou, H. Richard Johnston, et al.
The American Journal of Human Genetics (2019) Vol. 106, Iss. 1, pp. 26-40
Open Access | Times Cited: 57

Showing 1-25 of 57 citing articles:

Genomic frontiers in congenital heart disease
Sarah U. Morton, Daniel Quiat, Jonathan G. Seidman, et al.
Nature Reviews Cardiology (2021) Vol. 19, Iss. 1, pp. 26-42
Open Access | Times Cited: 159
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8317-8317
Open Access | Times Cited: 17
In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease
Francesco Nappi
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1734-1734
Open Access | Times Cited: 6
Clinical Manifestations of 22q11.2 Deletion Syndrome
Annapaola Cirillo, Michele Lioncino, Annachiara Maratea, et al.
Heart Failure Clinics (2021) Vol. 18, Iss. 1, pp. 155-164
Closed Access | Times Cited: 33
Craniofacial Phenotypes and Genetics of DiGeorge Syndrome
Noriko Funato
Journal of Developmental Biology (2022) Vol. 10, Iss. 2, pp. 18-18
Open Access | Times Cited: 24
Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome
Marwa Zafarullah, Kathleen Angkustsiri, Austin Quach, et al.
Metabolomics (2024) Vol. 20, Iss. 2
Open Access | Times Cited: 5
Hypoparathyroidism: Genetics and Diagnosis
Michael Mannstadt, Luisella Cianferotti, Rachel I. Gafni, et al.
Journal of Bone and Mineral Research (2020) Vol. 37, Iss. 12, pp. 2615-2629
Open Access | Times Cited: 31
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects
Carolina Putotto, Flaminia Pugnaloni, Marta Unolt, et al.
Children (2022) Vol. 9, Iss. 6, pp. 772-772
Open Access | Times Cited: 18
The Genetics of Neurodevelopment in Congenital Heart Disease
Eli Patt, Asmita Singhania, Amy E. Roberts, et al.
Canadian Journal of Cardiology (2022) Vol. 39, Iss. 2, pp. 97-114
Open Access | Times Cited: 17
Impacto del síndrome de deleción 22q11.2 en la mortalidad de los pacientes pediátricos con defectos conotruncales corregidos
Carlos Alcántara Noguez, Alejandra Contreras‐Ramos, Maria M. P. Melo, et al.
REC CardioClinics (2025)
Closed Access
22q11.21 Deletions: A Review on the Interval Mediated by Low-Copy Repeats C and D
Veronica Bertini, Francesca Cambi, Annalisa Legitimo, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 72-72
Open Access
When Should We Raise Clinical Suspicion of DiGeorge Syndrome: Two Case Reports from a Tertiary Hospital in Indonesia
Joni Indah Sari, Nydia Rena Benita Sihombing, Nani Maharani, et al.
OBM Genetics (2025) Vol. 09, Iss. 01, pp. 1-16
Open Access
Molecular Insights Into the Causes of Human Thymic Hypoplasia With Animal Models
Pratibha Bhalla, Christian Wysocki, Nicolai S. C. van Oers
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 23
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Cinical Approach
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
(2023)
Open Access | Times Cited: 7
Whole exome sequencing in patients with Williams–Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk
Phoebe C. R. Parrish, Delong Liu, Russell H. Knutsen, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 12, pp. 2035-2050
Open Access | Times Cited: 20
A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve
Weifeng Jiang, Ying‐Jia Xu, Cuimei Zhao, et al.
Genetics and Molecular Biology (2020) Vol. 43, Iss. 4
Open Access | Times Cited: 19
Genetics and etiology of congenital heart disease
Priyanka Narayan, Felix Richter, Sarah U. Morton
Current topics in developmental biology/Current Topics in Developmental Biology (2024), pp. 297-331
Closed Access | Times Cited: 2
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation
Elizabeth Goldmuntz, Anne S. Bassett, Erik Boot, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 6-7, pp. 804-814
Open Access | Times Cited: 2
Human Genetics of Truncus Arteriosus
Hiroyuki Yamagishi
Advances in experimental medicine and biology (2024), pp. 841-852
Closed Access | Times Cited: 2
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights
Giulio Calcagni, Flaminia Pugnaloni, M. Cristina Digilio, et al.
Genes (2021) Vol. 12, Iss. 7, pp. 1047-1047
Open Access | Times Cited: 15
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 680-680
Open Access | Times Cited: 6
Clinically Relevant Genetic Considerations for Patients With Tetralogy of Fallot
Anne S. Bassett, Miriam S. Reuter, Sarah Malecki, et al.
CJC Pediatric and Congenital Heart Disease (2023) Vol. 2, Iss. 6, pp. 426-439
Open Access | Times Cited: 5
The current state of prenatal detection of genetic conditions in congenital heart defects
Tina O. Findley, Hope Northrup
Translational Pediatrics (2021) Vol. 10, Iss. 8, pp. 2157-2170
Open Access | Times Cited: 12
Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation
Xuechao Jiang, Tingting Li, Sijie Liu, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 12
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation
Eva-Cristiana Gavril, Roxana Popescu, Irina Nucă, et al.
Genes (2022) Vol. 13, Iss. 11, pp. 2083-2083
Open Access | Times Cited: 9
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