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:
Co-occurrence of a maternally inherited DNMT3A duplication and a paternally inherited pathogenic variant in EZH2 in a child with growth retardation and severe short stature: atypical Weaver syndrome or evidence of a DNMT3A dosage effect?
Katarzyna Polonis, Patrick R. Blackburn, Raúl Urrutia, et al.
Molecular Case Studies (2018) Vol. 4, Iss. 4, pp. a002899-a002899
Open Access | Times Cited: 11
Katarzyna Polonis, Patrick R. Blackburn, Raúl Urrutia, et al.
Molecular Case Studies (2018) Vol. 4, Iss. 4, pp. a002899-a002899
Open Access | Times Cited: 11
Showing 11 citing articles:
PRC2 functions in development and congenital disorders
Orla Deevy, Adrian P. Bracken
Development (2019) Vol. 146, Iss. 19
Open Access | Times Cited: 105
Orla Deevy, Adrian P. Bracken
Development (2019) Vol. 146, Iss. 19
Open Access | Times Cited: 105
PRC2‐complex related dysfunction in overgrowth syndromes: A review of EZH2, EED, and SUZ12 and their syndromic phenotypes
Sharri Cyrus, Deepika Burkardt, David D. Weaver, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2019) Vol. 181, Iss. 4, pp. 519-531
Closed Access | Times Cited: 57
Sharri Cyrus, Deepika Burkardt, David D. Weaver, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2019) Vol. 181, Iss. 4, pp. 519-531
Closed Access | Times Cited: 57
Minimally Humanized Ezh2 Exon-18 Mouse Cell Lines Validate Preclinical CRISPR/Cas9 Approach to Treat Weaver Syndrome
William T. Gibson, Tess C. Lengyell, Andrea J. Korecki, et al.
Human Gene Therapy (2025)
Closed Access
William T. Gibson, Tess C. Lengyell, Andrea J. Korecki, et al.
Human Gene Therapy (2025)
Closed Access
Novel epigenetic molecular therapies for imprinting disorders
Sung Eun Wang, Yong‐hui Jiang
Molecular Psychiatry (2023) Vol. 28, Iss. 8, pp. 3182-3193
Open Access | Times Cited: 10
Sung Eun Wang, Yong‐hui Jiang
Molecular Psychiatry (2023) Vol. 28, Iss. 8, pp. 3182-3193
Open Access | Times Cited: 10
Jana Sachwitz, Robert Meyer, G. Fekete, et al.
Clinical Genetics (2016) Vol. 91, Iss. 1, pp. 73-78
Closed Access | Times Cited: 24
Sequenced-based GWAS for linear classification traits in Belgian Blue beef cattle reveals new coding variants in genes regulating body size in mammals
José Luis Gualdrón Duarte, Can Yuan, Ann-Stephan Gori, et al.
Genetics Selection Evolution (2023) Vol. 55, Iss. 1
Open Access | Times Cited: 7
José Luis Gualdrón Duarte, Can Yuan, Ann-Stephan Gori, et al.
Genetics Selection Evolution (2023) Vol. 55, Iss. 1
Open Access | Times Cited: 7
Dominant negative and directional dysregulation of Polycomb function inEZH2-mutant human growth disorders
Orla Deevy, Craig Monger, Francesca Matrà, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Orla Deevy, Craig Monger, Francesca Matrà, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
The Influence of Physical Activity and Epigenomics On Cognitive Function and Brain Health in Breast Cancer
Monica A. Wagner, Kirk I. Erickson, Catherine M. Bender, et al.
Frontiers in Aging Neuroscience (2020) Vol. 12
Open Access | Times Cited: 11
Monica A. Wagner, Kirk I. Erickson, Catherine M. Bender, et al.
Frontiers in Aging Neuroscience (2020) Vol. 12
Open Access | Times Cited: 11
Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders
Pamela Magini, Emanuela Scarano, Ilaria Donati, et al.
Gene (2019) Vol. 706, pp. 162-171
Closed Access | Times Cited: 10
Pamela Magini, Emanuela Scarano, Ilaria Donati, et al.
Gene (2019) Vol. 706, pp. 162-171
Closed Access | Times Cited: 10
First Korean Case of Weaver Syndrome Along with Neuroblastoma and Genetic Confirmation of EZH2 Variant
Inseong Oh, Boram Kim, Jee‐Soo Lee, et al.
Laboratory Medicine Online (2022) Vol. 13, Iss. 1, pp. 48-52
Open Access | Times Cited: 2
Inseong Oh, Boram Kim, Jee‐Soo Lee, et al.
Laboratory Medicine Online (2022) Vol. 13, Iss. 1, pp. 48-52
Open Access | Times Cited: 2
Sequenced-based GWAS for linear classification traits in Belgian Blue beef cattle reveals new coding variants in genes regulating body size in mammals
JL Gualdron Duarte, Yuan Cheng, AS Gori, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
JL Gualdron Duarte, Yuan Cheng, AS Gori, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
