Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Variability of cross-tissue X-chromosome inactivation characterizes timing of human embryonic lineage specification events
Jonathan M. Werner, Sara Ballouz, John Hover, et al.
Developmental Cell (2022) Vol. 57, Iss. 16, pp. 1995-2008.e5
Open Access | Times Cited: 24

Showing 24 citing articles:

The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models
Joel Rozowsky, Jiahao Gao, Beatrice Borsari, et al.
Cell (2023) Vol. 186, Iss. 7, pp. 1493-1511.e40
Open Access | Times Cited: 53
The human and non-human primate developmental GTEx projects
Tim H. H. Coorens, Amy Guillaumet-Adkins, Rothem Kovner, et al.
Nature (2025) Vol. 637, Iss. 8046, pp. 557-564
Closed Access | Times Cited: 3
Measuring X inactivation skew for X-linked diseases with adaptive nanopore sequencing
Sena A. Gocuk, James Lancaster, Shian Su, et al.
Genome Research (2024) Vol. 34, Iss. 11, pp. 1954-1965
Closed Access | Times Cited: 6
The transcriptional legacy of developmental stochasticity
Sara Ballouz, Risa Karakida Kawaguchi, Maria T. Peña, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 12
Unfavorable switching of skewed X chromosome inactivation leads to Menkes disease in a female infant
Ayumi Matsumoto, Shintaro Kano, Natsumi Kobayashi, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Variable expression of MECP2, CDKL5, and FMR1 in the human brain: Implications for gene restorative therapies
Antonino Zito, Jeannie T. Lee
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 9
Open Access | Times Cited: 4
Escape of Kdm6a from X Chromosome Is Detrimental to Ischemic Brains via IRF5 Signaling
Conelius Ngwa, Afzal Misrani, Kanaka Valli Manyam, et al.
Translational Stroke Research (2025)
Open Access
Stochasticity in genetics and gene regulation
Veronica van Heyningen
Philosophical Transactions of the Royal Society B Biological Sciences (2024) Vol. 379, Iss. 1900
Open Access | Times Cited: 3
F5 6665A>G Polymorphism Is Associated with Increased Risk of Venous Thromboembolism in Females
Sladjana Teofilov, Olivera Miljanović, Jelena Vučković-Filipović, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 6, pp. 2403-2403
Open Access
Gene reactivation upon erosion of X chromosome inactivation in female hiPSCs is predictable yet variable and persists through differentiation
Ana Cláudia Raposo, Paulo Caldas, Joana Jeremias, et al.
Stem Cell Reports (2025), pp. 102472-102472
Open Access
X-linked competition — implications for human development and disease
Philip M. Boone, Teresa Buenaventura, James W. D. King, et al.
Nature Reviews Genetics (2025)
Closed Access
Out of the Silence: Insights into How Genes Escape X-Chromosome Inactivation
Samantha B. Peeters, Bronwyn J. Posynick, Carolyn J. Brown
Epigenomes (2023) Vol. 7, Iss. 4, pp. 29-29
Open Access | Times Cited: 8
Population variability in X-chromosome inactivation across 10 mammalian species
Jonathan M. Werner, John Hover, Jesse Gillis
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Research progress and potential application of microRNA and other non-coding RNAs in forensic medicine
Binghui Song, Jie Qian, Junjiang Fu
International Journal of Legal Medicine (2023) Vol. 138, Iss. 2, pp. 329-350
Closed Access | Times Cited: 5
Régulation du chromosome X et spécificités fonctionnelles des cellules femelles
Julie Chaumeil, Céline Morey
médecine/sciences (2024) Vol. 40, Iss. 12, pp. 935-946
Open Access | Times Cited: 1
EpiTyping: analysis of epigenetic aberrations in parental imprinting and X-chromosome inactivation using RNA-seq
Roni Sarel-Gallily, Gal Keshet, Shay Kinreich, et al.
Nature Protocols (2023) Vol. 18, Iss. 12, pp. 3881-3917
Closed Access | Times Cited: 3
Escape from X-chromosome inactivation and sex differences in Alzheimer’s disease
Qinghua Song, Ke-Xuan Zhao, Shuai Huang, et al.
Reviews in the Neurosciences (2023) Vol. 35, Iss. 3, pp. 341-354
Closed Access | Times Cited: 2
Case Report: De novo DDX3X mutation caused intellectual disability in a female with skewed X-chromosome inactivation on the mutant allele
Yixi Sun, Yangwen Qian, Hai‐Xi Sun, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 3
Erosion of X-Chromosome Inactivation in female hiPSCs is heterogeneous and persists during differentiation
Ana Cláudia Raposo, Paulo Caldas, Maria Arez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Competition shapes the landscape of X-chromosome-linked genetic diversity
Teresa Buenaventura, Hakan Bagci, Ilinca Patrascan, et al.
Nature Genetics (2024) Vol. 56, Iss. 8, pp. 1678-1688
Open Access
Escape of Kdm6a from X chromosome is detrimental to ischemic brains via IRF5 signaling
Conelius Ngwa, Afzal Misrani, Kanaka Valli Manyam, et al.
Research Square (Research Square) (2024)
Closed Access
Genomic Landscape of Chromosome X Factor VIII: From Hemophilia A in Males to Risk Variants in Females
Olivia Morris, Michèle Morris, Shawn M. Jobe, et al.
Genes (2024) Vol. 15, Iss. 12, pp. 1522-1522
Open Access
A repository of Ogden syndrome (NAA10) and NAA15 patient derived iPSC lines and isogenic pairs by X-chromosome screening and genome-editing.
Josephine Wesely, Tom Rusielewicz, Yu-Ren Chen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Human X-chromosome inactivation: Complexity and clinical implications
María José Navarro-Cobos, Karanveer Bhangu, Carolyn J. Brown
Elsevier eBooks (2023), pp. 355-385
Closed Access
Population variability in X-chromosome inactivation across 9 mammalian species
Jonathan M. Werner, John Hover, Jesse Gillis
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Page 1

Scroll to top