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:
Rare Modifier Variants Alter the Severity of Cardiovascular Disease in Pseudoxanthoma Elasticum: Identification of Novel Candidate Modifier Genes and Disease Pathways Through Mixture of Effects Analysis
Eva De Vilder, Ludovic Martin, Georges Lefthériotis, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 7
Eva De Vilder, Ludovic Martin, Georges Lefthériotis, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 7
Showing 7 citing articles:
ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification
Douglas Ralph, Yvonne Nitschke, Michael A. Levine, et al.
PLoS Genetics (2022) Vol. 18, Iss. 4, pp. e1010192-e1010192
Open Access | Times Cited: 23
Douglas Ralph, Yvonne Nitschke, Michael A. Levine, et al.
PLoS Genetics (2022) Vol. 18, Iss. 4, pp. e1010192-e1010192
Open Access | Times Cited: 23
Identification of modifier gene variants overrepresented in familial hypomagnesemia with hypercalciuria and nephrocalcinosis patients with a more aggressive renal phenotype
Mònica Vall‐Palomar, Joseph Torchia, Jordi Morata, et al.
PLoS Genetics (2025) Vol. 21, Iss. 4, pp. e1011568-e1011568
Open Access
Mònica Vall‐Palomar, Joseph Torchia, Jordi Morata, et al.
PLoS Genetics (2025) Vol. 21, Iss. 4, pp. e1011568-e1011568
Open Access
The Impact of Inflammatory Stimuli on Xylosyltransferase-I Regulation in Primary Human Dermal Fibroblasts
Thanh-Diep Ly, Christopher Lindenkamp, Eva Kara, et al.
Biomedicines (2022) Vol. 10, Iss. 6, pp. 1451-1451
Open Access | Times Cited: 7
Thanh-Diep Ly, Christopher Lindenkamp, Eva Kara, et al.
Biomedicines (2022) Vol. 10, Iss. 6, pp. 1451-1451
Open Access | Times Cited: 7
Matrix Metalloproteinases Contribute to the Calcification Phenotype in Pseudoxanthoma Elasticum
Ricarda Plümers, Christopher Lindenkamp, Michel Robin Osterhage, et al.
Biomolecules (2023) Vol. 13, Iss. 4, pp. 672-672
Open Access | Times Cited: 2
Ricarda Plümers, Christopher Lindenkamp, Michel Robin Osterhage, et al.
Biomolecules (2023) Vol. 13, Iss. 4, pp. 672-672
Open Access | Times Cited: 2
IDENTIFICATION OF MODIFIER GENE VARIANTS OVERREPRESENTED IN FAMILIAL HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS PATIENTS WITH A MORE AGGRESSIVE RENAL PHENOTYPE
Mònica Vall‐Palomar, Jordi Morata, M. Durán, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Mònica Vall‐Palomar, Jordi Morata, M. Durán, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Assessment of rare genetic variants to identify candidate modifier genes underlying neurological manifestations in neurofibromatosis 1 patients
Jie Tang, Niu Li, Guo Qiang Li, et al.
Research Square (Research Square) (2022)
Open Access
Jie Tang, Niu Li, Guo Qiang Li, et al.
Research Square (Research Square) (2022)
Open Access
Assessment of Rare Genetic Variants to Identify Candidate Modifier Genes Underlying Neurological Manifestations in Neurofibromatosis 1 Patients
Jie Tang, Niu Li, Guoqiang Li, et al.
Genes (2022) Vol. 13, Iss. 12, pp. 2218-2218
Open Access
Jie Tang, Niu Li, Guoqiang Li, et al.
Genes (2022) Vol. 13, Iss. 12, pp. 2218-2218
Open Access
