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:
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family
Amaia Carrión-Castillo, Sara B. Estruch, Ben Maassen, et al.
Human Genetics (2021) Vol. 140, Iss. 8, pp. 1183-1200
Open Access | Times Cited: 7
Amaia Carrión-Castillo, Sara B. Estruch, Ben Maassen, et al.
Human Genetics (2021) Vol. 140, Iss. 8, pp. 1183-1200
Open Access | Times Cited: 7
Showing 7 citing articles:
Human‐specific insights into candidate genes and boosted discoveries of novel loci illuminate roles of neuroglia in reading disorders
Wenhua Wei, Shaowei Ma, Bo Fu, et al.
Genes Brain & Behavior (2024) Vol. 23, Iss. 3
Open Access | Times Cited: 2
Wenhua Wei, Shaowei Ma, Bo Fu, et al.
Genes Brain & Behavior (2024) Vol. 23, Iss. 3
Open Access | Times Cited: 2
Targeted analysis of dyslexia-associated regions on chromosomes 6, 12 and 15 in large multigenerational cohorts
Nicola H. Chapman, Patrick A. Navas, Michael O. Dorschner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Nicola H. Chapman, Patrick A. Navas, Michael O. Dorschner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Semaphorin class 3C, vascular permeability, and the swollen injured kidney
Christian Rosenberger
Kidney International (2022) Vol. 101, Iss. 4, pp. 670-673
Closed Access | Times Cited: 2
Christian Rosenberger
Kidney International (2022) Vol. 101, Iss. 4, pp. 670-673
Closed Access | Times Cited: 2
Hydrocephalus and Growth Retardation: A Fetal <b><i>RNU4ATAC</i></b>-opathy Missed by Whole-Exome Sequencing
Yong-Shan Chen, Jie-Fu He, Quan Tao, et al.
Molecular Syndromology (2022) Vol. 13, Iss. 6, pp. 522-526
Open Access | Times Cited: 1
Yong-Shan Chen, Jie-Fu He, Quan Tao, et al.
Molecular Syndromology (2022) Vol. 13, Iss. 6, pp. 522-526
Open Access | Times Cited: 1
Linkage and next generation sequencing (NGS) data in six large Danish families with dyslexia
Hans Eiberg, Lars Hestbjerg Hansen
Research Square (Research Square) (2023)
Open Access
Hans Eiberg, Lars Hestbjerg Hansen
Research Square (Research Square) (2023)
Open Access
Gelişimsel Dil Bozukluğu Olan Çocukların Disleksi Açısından Değerlendirilmesi
Selim Ünsal, Merve Yurttutar, Senanur Kahraman Beğen, et al.
Sağlık Akademisi Kastamonu (2023) Vol. 9, Iss. 2, pp. 332-344
Open Access
Selim Ünsal, Merve Yurttutar, Senanur Kahraman Beğen, et al.
Sağlık Akademisi Kastamonu (2023) Vol. 9, Iss. 2, pp. 332-344
Open Access
Linkage and Next Generation Sequencing (NGS) Data in Six Large Danish Families with Dyslexia
Open Access Journal of Applied Science and Technology (2023) Vol. 1, Iss. 2
Open Access
Open Access Journal of Applied Science and Technology (2023) Vol. 1, Iss. 2
Open Access
