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:
Examining the role of common variants in rare neurodevelopmental conditions
Qin Qin Huang, Emilie M. Wigdor, Daniel Malawsky, et al.
Nature (2024)
Open Access | Times Cited: 10
Qin Qin Huang, Emilie M. Wigdor, Daniel Malawsky, et al.
Nature (2024)
Open Access | Times Cited: 10
Showing 10 citing articles:
Familial confounding in the associations between maternal health and autism
Vahe Khachadourian, Elias Arildskov, Jakob Grove, et al.
Nature Medicine (2025)
Open Access | Times Cited: 2
Vahe Khachadourian, Elias Arildskov, Jakob Grove, et al.
Nature Medicine (2025)
Open Access | Times Cited: 2
Unveiling genetic substrates of brain–heart comorbidities: Integration of both common and rare variants
Shouyu Wang, Meian He, X. Chen, et al.
The Innovation Life (2025), pp. 100118-100118
Closed Access
Shouyu Wang, Meian He, X. Chen, et al.
The Innovation Life (2025), pp. 100118-100118
Closed Access
Mapping the regulatory effects of common and rare non-coding variants across cellular and developmental contexts in the brain and heart
Andrew R. Marderstein, Soumya Kundu, Evin M. Padhi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Andrew R. Marderstein, Soumya Kundu, Evin M. Padhi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Common Genetic Variants Modify Disease Risk and Clinical Presentation in Monogenic Diabetes
James H. Leech, Robin N. Beaumont, Ankit M Arni, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
James H. Leech, Robin N. Beaumont, Ankit M Arni, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Rapidly evolved genomic regions shape individual language abilities in present-day humans
Lucas G. Casten, Tanner Koomar, Taylor R. Thomas, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Lucas G. Casten, Tanner Koomar, Taylor R. Thomas, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Intergenerational transmission of polygenic predisposition for neuropsychiatric traits on emotional and behavioural difficulties in childhood
Andrea G. Allegrini, Laurie J. Hannigan, Leonard Frach, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Andrea G. Allegrini, Laurie J. Hannigan, Leonard Frach, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Pharmacogenomic and Pharmacomicrobiomic Aspects of Drugs of Abuse
Alejandro Borrego-Ruiz, Juan J. Borrego
Genes (2025) Vol. 16, Iss. 4, pp. 403-403
Open Access
Alejandro Borrego-Ruiz, Juan J. Borrego
Genes (2025) Vol. 16, Iss. 4, pp. 403-403
Open Access
Genetically Transitional Disease and the Road to Personalized Medicine
Qingping Yao, Peter D. Gorevic, Greg Gibson
Genes (2025) Vol. 16, Iss. 4, pp. 401-401
Open Access
Qingping Yao, Peter D. Gorevic, Greg Gibson
Genes (2025) Vol. 16, Iss. 4, pp. 401-401
Open Access
Common genetic variants contribute more to rare diseases than previously thought
Gerome Breen
Nature (2024)
Closed Access
Gerome Breen
Nature (2024)
Closed Access
