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:
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants
Jente Verbesselt, Cynthia Solot, Ellen Van Den Heuvel, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 679-679
Open Access | Times Cited: 8
Jente Verbesselt, Cynthia Solot, Ellen Van Den Heuvel, et al.
Genes (2023) Vol. 14, Iss. 3, pp. 679-679
Open Access | Times Cited: 8
Showing 8 citing articles:
Phonemic–Phonological Profile of People with 22q11.2 Deletion Syndrome: A Pilot Study
Esther Moraleda Sepúlveda, María Rubio-Lorca, Noelia Pulido-García, et al.
Brain Sciences (2025) Vol. 15, Iss. 3, pp. 298-298
Open Access
Esther Moraleda Sepúlveda, María Rubio-Lorca, Noelia Pulido-García, et al.
Brain Sciences (2025) Vol. 15, Iss. 3, pp. 298-298
Open Access
Verbal narrative ability and episodic autobiographical memory in adolescents and young adults with 22q11.2 deletion syndrome
Claire Dubois, Julie Husmann, Selma Benaghmouch, et al.
Journal of Neurodevelopmental Disorders (2025) Vol. 17, Iss. 1
Open Access
Claire Dubois, Julie Husmann, Selma Benaghmouch, et al.
Journal of Neurodevelopmental Disorders (2025) Vol. 17, Iss. 1
Open Access
Distinct neurocognitive profiles and clinical phenotypes associated with copy number variation at the 22q11.2 locus
Kathleen O’Hora, Leila Kushan, Charles Schleifer, et al.
Autism Research (2023) Vol. 16, Iss. 12, pp. 2247-2262
Open Access | Times Cited: 7
Kathleen O’Hora, Leila Kushan, Charles Schleifer, et al.
Autism Research (2023) Vol. 16, Iss. 12, pp. 2247-2262
Open Access | Times Cited: 7
Exploring Education for Children with 22q11.2 Deletion Syndrome: A Qualitative Study of Mothers Perspectives
Laura Roche, Traci Flynn, Linda Campbell
OBM Genetics (2024) Vol. 08, Iss. 01, pp. 1-36
Open Access | Times Cited: 1
Laura Roche, Traci Flynn, Linda Campbell
OBM Genetics (2024) Vol. 08, Iss. 01, pp. 1-36
Open Access | Times Cited: 1
Association of behavioural and social–communicative profiles in children with 16p11.2 copy number variants: a multi‐site study
Jente Verbesselt, Louisa Walsh, Marissa W Mitchel, et al.
Journal of Intellectual Disability Research (2024) Vol. 68, Iss. 8, pp. 969-984
Closed Access | Times Cited: 1
Jente Verbesselt, Louisa Walsh, Marissa W Mitchel, et al.
Journal of Intellectual Disability Research (2024) Vol. 68, Iss. 8, pp. 969-984
Closed Access | Times Cited: 1
Language Profiles of School-Age Children With 16p11.2 Copy Number Variants in a Clinically Ascertained Cohort
Jente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
Journal of Speech Language and Hearing Research (2024) Vol. 67, Iss. 11, pp. 4487-4503
Closed Access | Times Cited: 1
Jente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
Journal of Speech Language and Hearing Research (2024) Vol. 67, Iss. 11, pp. 4487-4503
Closed Access | Times Cited: 1
Distinct Neurocognitive Profiles and Clinical Phenotypes Associated with Copy Number Variation at the 22q11.2 Locus
Kathleen O’Hora, Leila Kushan, Gil D. Hoftman, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Kathleen O’Hora, Leila Kushan, Gil D. Hoftman, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Genetic etiology analysis of 244 fetal ventricular septal defect in the prenatal setting
Wei Bo, W. F. Mader, Xinyou Yu, et al.
Research Square (Research Square) (2024)
Open Access
Wei Bo, W. F. Mader, Xinyou Yu, et al.
Research Square (Research Square) (2024)
Open Access
