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:
CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases
Lottie D. Morison, Olivia van Reyk, Elana Forbes, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 7, pp. 793-804
Open Access | Times Cited: 9
Lottie D. Morison, Olivia van Reyk, Elana Forbes, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 7, pp. 793-804
Open Access | Times Cited: 9
Showing 9 citing articles:
Genetic architecture of childhood speech disorder: a review
Angela Morgan, David J. Amor, Miya St John, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 5, pp. 1281-1292
Open Access | Times Cited: 10
Angela Morgan, David J. Amor, Miya St John, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 5, pp. 1281-1292
Open Access | Times Cited: 10
Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders
Emma K. Baker, Miya St John, Ruth Braden, et al.
Developmental Medicine & Child Neurology (2025)
Open Access
Emma K. Baker, Miya St John, Ruth Braden, et al.
Developmental Medicine & Child Neurology (2025)
Open Access
CDK13‐Related Disorder: Novel Insights From A Series of 27 Cases and Recommendations for Clinical Management
Gianluca Contrò, Maria Chiara Baroni, Stefano Giuseppe Caraffi, et al.
Clinical Genetics (2025)
Open Access
Gianluca Contrò, Maria Chiara Baroni, Stefano Giuseppe Caraffi, et al.
Clinical Genetics (2025)
Open Access
Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention
Elana Forbes, Lottie D. Morison, Fatma Lelik, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2024) Vol. 195, Iss. 6
Open Access | Times Cited: 2
Elana Forbes, Lottie D. Morison, Fatma Lelik, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2024) Vol. 195, Iss. 6
Open Access | Times Cited: 2
Speech and language classification in the human phenotype ontology
Angela Morgan, Ben Coleman, Adam P. Vogel, et al.
European Journal of Human Genetics (2024)
Open Access
Angela Morgan, Ben Coleman, Adam P. Vogel, et al.
European Journal of Human Genetics (2024)
Open Access
A pathogenic missense variant, c.2149G>A (p.Gly717Arg), in CDK13 in a female patient with CDK13-related disorder: A case report and literature review of 112 cases
Naoki Morooka, Jun Kido, Hiroe Ueno, et al.
Brain and Development Case Reports (2024) Vol. 2, Iss. 3, pp. 100023-100023
Open Access
Naoki Morooka, Jun Kido, Hiroe Ueno, et al.
Brain and Development Case Reports (2024) Vol. 2, Iss. 3, pp. 100023-100023
Open Access
Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development
Qazi Waheed‐Ullah, Anna Wilsdon, Aseel Abbad, et al.
Journal of Anatomy (2024)
Open Access
Qazi Waheed‐Ullah, Anna Wilsdon, Aseel Abbad, et al.
Journal of Anatomy (2024)
Open Access
Spotted around the web: CDK13; hippocampal plasticity; science Twitter
Jill Adams, Peter Hess
The Transmitter (2023)
Open Access
Jill Adams, Peter Hess
The Transmitter (2023)
Open Access
Unusual genomic variants require unusual analyses
Alisdair McNeill
European Journal of Human Genetics (2023) Vol. 31, Iss. 7, pp. 721-722
Open Access
Alisdair McNeill
European Journal of Human Genetics (2023) Vol. 31, Iss. 7, pp. 721-722
Open Access
