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:
Eyes on CHARGE syndrome: Roles of CHD7 in ocular development
Laura A. Krueger, Ann C. Morris
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 6
Laura A. Krueger, Ann C. Morris
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 6
Showing 6 citing articles:
Retinitis pigmentosa with iris coloboma due to miR‐204 gene variant in a Chinese family
Lei Zhang, Zhu He‐Lin, Haiyan Wang, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 6
Open Access | Times Cited: 2
Lei Zhang, Zhu He‐Lin, Haiyan Wang, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 6
Open Access | Times Cited: 2
Clinical and genetic characteristics of 36 children with Joubert syndrome
Yan Dong, Ke Zhang, Yao He, et al.
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 4
Yan Dong, Ke Zhang, Yao He, et al.
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 4
A novel CHD7 variant in a chinese family with CHARGE syndrome
Yanhong Shan, LingFang Yao, Linli Li, et al.
Genes & Genomics (2023) Vol. 46, Iss. 3, pp. 379-387
Closed Access | Times Cited: 1
Yanhong Shan, LingFang Yao, Linli Li, et al.
Genes & Genomics (2023) Vol. 46, Iss. 3, pp. 379-387
Closed Access | Times Cited: 1
Analysis of the CHD7 gene mutations in patients of congenital heart disease with extracardiac malformations
Xianghui Huang, Han Gao, Wei-Cheng Chen, et al.
Translational Pediatrics (2023) Vol. 12, Iss. 6, pp. 1148-1160
Open Access
Xianghui Huang, Han Gao, Wei-Cheng Chen, et al.
Translational Pediatrics (2023) Vol. 12, Iss. 6, pp. 1148-1160
Open Access
Generation and characterization of Chd7‐iCreERT2‐tdTomato mice
Zi'ang Han, Ze Wang, Zhuxi Huang, et al.
genesis (2023) Vol. 62, Iss. 1
Closed Access
Zi'ang Han, Ze Wang, Zhuxi Huang, et al.
genesis (2023) Vol. 62, Iss. 1
Closed Access
Digenic CHD7 and SMCHD1 inheritance Unveils phenotypic variability in a family mainly presenting with hypogonadotropic hypogonadism
Tian Wang, Wu Ren, Fangfang Fu, et al.
Heliyon (2023) Vol. 10, Iss. 1, pp. e23272-e23272
Open Access
Tian Wang, Wu Ren, Fangfang Fu, et al.
Heliyon (2023) Vol. 10, Iss. 1, pp. e23272-e23272
Open Access
