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:
CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis
Mu Yang, Shujin Li, Li Huang, et al.
JCI Insight (2022) Vol. 7, Iss. 14
Open Access | Times Cited: 29
Mu Yang, Shujin Li, Li Huang, et al.
JCI Insight (2022) Vol. 7, Iss. 14
Open Access | Times Cited: 29
Showing 1-25 of 29 citing articles:
Assessment of Inner Blood–Retinal Barrier: Animal Models and Methods
Kiran Bora, Neetu Kushwah, Meenakshi Maurya, et al.
Cells (2023) Vol. 12, Iss. 20, pp. 2443-2443
Open Access | Times Cited: 24
Kiran Bora, Neetu Kushwah, Meenakshi Maurya, et al.
Cells (2023) Vol. 12, Iss. 20, pp. 2443-2443
Open Access | Times Cited: 24
Familial Exudative Vitreoretinopathy With and Without Pathogenic Variants of Norrin/β-Catenin Signaling Genes
Hiroyuki Kondo, Tomoko Tsukahara‐Kawamura, Itsuka Matsushita, et al.
Ophthalmology Science (2024) Vol. 4, Iss. 5, pp. 100514-100514
Open Access | Times Cited: 6
Hiroyuki Kondo, Tomoko Tsukahara‐Kawamura, Itsuka Matsushita, et al.
Ophthalmology Science (2024) Vol. 4, Iss. 5, pp. 100514-100514
Open Access | Times Cited: 6
Gene Variant Spectrum in Probands With Familial Exudative Vitreoretinopathy Using an Expanded Panel
Sarah van der Ende, Karen Bedard, Karin Wallace, et al.
Investigative Ophthalmology & Visual Science (2025) Vol. 66, Iss. 2, pp. 23-23
Open Access
Sarah van der Ende, Karen Bedard, Karin Wallace, et al.
Investigative Ophthalmology & Visual Science (2025) Vol. 66, Iss. 2, pp. 23-23
Open Access
New Genitourinary Findings in CTNND1 Blepharocheilodontic Syndrome
Lily Loughman, Naeem Samnakay, Geoffrey C. Lam, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Lily Loughman, Naeem Samnakay, Geoffrey C. Lam, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Mechanisms Underlying Rare Inherited Pediatric Retinal Vascular Diseases: FEVR, Norrie Disease, Persistent Fetal Vascular Syndrome
Vincent Le, Gabrielle Abdelmessih, Wendy A Dailey, et al.
Cells (2023) Vol. 12, Iss. 21, pp. 2579-2579
Open Access | Times Cited: 9
Vincent Le, Gabrielle Abdelmessih, Wendy A Dailey, et al.
Cells (2023) Vol. 12, Iss. 21, pp. 2579-2579
Open Access | Times Cited: 9
Selective Activation of the Wnt-Signaling Pathway as a Novel Therapy for the Treatment of Diabetic Retinopathy and Other Retinal Vascular Diseases
Huy Nguyen, Sung‐Jin Lee, Yang Li
Pharmaceutics (2022) Vol. 14, Iss. 11, pp. 2476-2476
Open Access | Times Cited: 14
Huy Nguyen, Sung‐Jin Lee, Yang Li
Pharmaceutics (2022) Vol. 14, Iss. 11, pp. 2476-2476
Open Access | Times Cited: 14
Frameshift variants in the C-terminal of CTNNB1 cause familial exudative vitreoretinopathy by AXIN1-mediated ubiquitin-proteasome degradation condensation
Yining Liu, Mu Yang, Fan Lin, et al.
International Journal of Biological Macromolecules (2023) Vol. 258, pp. 128570-128570
Closed Access | Times Cited: 8
Yining Liu, Mu Yang, Fan Lin, et al.
International Journal of Biological Macromolecules (2023) Vol. 258, pp. 128570-128570
Closed Access | Times Cited: 8
Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy
Shujin Li, Mu Yang, Rulian Zhao, et al.
Genes & Diseases (2022) Vol. 10, Iss. 6, pp. 2572-2585
Open Access | Times Cited: 12
Shujin Li, Mu Yang, Rulian Zhao, et al.
Genes & Diseases (2022) Vol. 10, Iss. 6, pp. 2572-2585
Open Access | Times Cited: 12
Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy
Jianbo Mao, Yijing Chen, Yuyan Fang, et al.
Annals of Medicine (2022) Vol. 54, Iss. 1, pp. 3285-3297
Open Access | Times Cited: 11
Jianbo Mao, Yijing Chen, Yuyan Fang, et al.
Annals of Medicine (2022) Vol. 54, Iss. 1, pp. 3285-3297
Open Access | Times Cited: 11
Familial Exudative Vitreoretinopathy and Systemic Abnormalities in Patients With CTNNB1 Mutations
Li Huang, Jinglin Lu, You Wang, et al.
Investigative Ophthalmology & Visual Science (2023) Vol. 64, Iss. 2, pp. 18-18
Open Access | Times Cited: 4
Li Huang, Jinglin Lu, You Wang, et al.
Investigative Ophthalmology & Visual Science (2023) Vol. 64, Iss. 2, pp. 18-18
Open Access | Times Cited: 4
Deciphering a crucial dimeric interface governing Norrin dimerization and the pathogenesis of familial exudative vitreoretinopathy
Rulian Zhao, Min Liu, Erkuan Dai, et al.
The FASEB Journal (2024) Vol. 38, Iss. 4
Closed Access | Times Cited: 1
Rulian Zhao, Min Liu, Erkuan Dai, et al.
The FASEB Journal (2024) Vol. 38, Iss. 4
Closed Access | Times Cited: 1
Investigating the Impact of Dimer Interface Mutations on Norrin's Secretion and Norrin/β-Catenin Pathway Activation
Min Liu, Erkuan Dai, Mu Yang, et al.
Investigative Ophthalmology & Visual Science (2024) Vol. 65, Iss. 3, pp. 31-31
Open Access | Times Cited: 1
Min Liu, Erkuan Dai, Mu Yang, et al.
Investigative Ophthalmology & Visual Science (2024) Vol. 65, Iss. 3, pp. 31-31
Open Access | Times Cited: 1
Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
Wenjing Liu, Shujin Li, Mu Yang, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Wenjing Liu, Shujin Li, Mu Yang, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
CTNND1 is involved in germline predisposition to early-onset gastric cancer by affecting cell-to-cell interactions
Cristina Herrera‐Pariente, Laia Bonjoch, Jenifer Muñoz, et al.
Gastric Cancer (2024) Vol. 27, Iss. 4, pp. 747-759
Open Access | Times Cited: 1
Cristina Herrera‐Pariente, Laia Bonjoch, Jenifer Muñoz, et al.
Gastric Cancer (2024) Vol. 27, Iss. 4, pp. 747-759
Open Access | Times Cited: 1
Progress in the development of modulators targeting Frizzleds
Junlan Chuan, Wěi Li, Shengliu Pan, et al.
Pharmacological Research (2024) Vol. 206, pp. 107286-107286
Open Access | Times Cited: 1
Junlan Chuan, Wěi Li, Shengliu Pan, et al.
Pharmacological Research (2024) Vol. 206, pp. 107286-107286
Open Access | Times Cited: 1
Modulation of recovery from neonatal hyperoxic lung injury by sex as a biological variable
Abiud Cantu, Manuel Cantu Gutierrez, Xiaoyu Dong, et al.
Redox Biology (2023) Vol. 68, pp. 102933-102933
Open Access | Times Cited: 2
Abiud Cantu, Manuel Cantu Gutierrez, Xiaoyu Dong, et al.
Redox Biology (2023) Vol. 68, pp. 102933-102933
Open Access | Times Cited: 2
A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy
Rulian Zhao, Erkuan Dai, Shiyuan Wang, et al.
Clinical Genetics (2022) Vol. 103, Iss. 3, pp. 320-329
Closed Access | Times Cited: 4
Rulian Zhao, Erkuan Dai, Shiyuan Wang, et al.
Clinical Genetics (2022) Vol. 103, Iss. 3, pp. 320-329
Closed Access | Times Cited: 4
Influence of TMX2-CTNND1 polymorphism on cortical thickness in schizophrenia and their unaffected sibling: an exploratory study based on target region sequencing
Wenjian Tan, Yixin Cheng, Danqing Huang, et al.
Brazilian Journal of Psychiatry (2024)
Open Access
Wenjian Tan, Yixin Cheng, Danqing Huang, et al.
Brazilian Journal of Psychiatry (2024)
Open Access
Early onset high myopia and severe anisometropia associated with familial exudative vitreoretinopathy of irregular dominant inheritance in 12 Chinese families：analysis of refraction features and pathogenic variations
Wanyu Cheng, Weining Rong, Huiping Li, et al.
Research Square (Research Square) (2024)
Open Access
Wanyu Cheng, Weining Rong, Huiping Li, et al.
Research Square (Research Square) (2024)
Open Access
Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients
Mu Yang, Peng Li, Liting Lv, et al.
Molecular Genetics and Genomics (2024) Vol. 299, Iss. 1
Closed Access
Mu Yang, Peng Li, Liting Lv, et al.
Molecular Genetics and Genomics (2024) Vol. 299, Iss. 1
Closed Access
Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations
Erkuan Dai, Min Liu, Shujin Li, et al.
Investigative Ophthalmology & Visual Science (2024) Vol. 65, Iss. 4, pp. 1-1
Open Access
Erkuan Dai, Min Liu, Shujin Li, et al.
Investigative Ophthalmology & Visual Science (2024) Vol. 65, Iss. 4, pp. 1-1
Open Access
Multimodal imaging of white preretinal lesions in atypical familial exudative vitreoretinopathy: Case report and literature review
Liam Redden, Douglas S.M. Iaboni, Sarah van der Ende, et al.
American Journal of Ophthalmology Case Reports (2024) Vol. 34, pp. 102051-102051
Open Access
Liam Redden, Douglas S.M. Iaboni, Sarah van der Ende, et al.
American Journal of Ophthalmology Case Reports (2024) Vol. 34, pp. 102051-102051
Open Access
Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
Wenjing Liu, Shujin Li, Mu Yang, et al.
eLife (2024) Vol. 13
Open Access
Wenjing Liu, Shujin Li, Mu Yang, et al.
eLife (2024) Vol. 13
Open Access
Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
Wenjing Liu, Shujin Li, Mu Yang, et al.
eLife (2024) Vol. 13
Open Access
Wenjing Liu, Shujin Li, Mu Yang, et al.
eLife (2024) Vol. 13
Open Access
CTNND1‐Related Disorder: New Insight on Prenatal Phenotype
Bárbara Conti, Claudia Di Napoli, Sara Hafdaoui, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
Bárbara Conti, Claudia Di Napoli, Sara Hafdaoui, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
