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OpenAlex Citation Counts

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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:

Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts
Marco Garieri, Georgios Stamoulis, Xavier Blanc, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 51, pp. 13015-13020
Open Access | Times Cited: 91

Showing 1-25 of 91 citing articles:

Sex disparities matter in cancer development and therapy
Sue Haupt, Franco Caramia, Sabra L. Klein, et al.
Nature reviews. Cancer (2021) Vol. 21, Iss. 6, pp. 393-407
Open Access | Times Cited: 224
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development
Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang, et al.
Neuron (2020) Vol. 106, Iss. 3, pp. 404-420.e8
Open Access | Times Cited: 178
The human inactive X chromosome modulates expression of the active X chromosome
Adrianna K. San Roman, Alexander K. Godfrey, Helen Skaletsky, et al.
Cell Genomics (2023) Vol. 3, Iss. 2, pp. 100259-100259
Open Access | Times Cited: 59
Aging activates escape of the silent X chromosome in the female mouse hippocampus
Margaret Gadek, Cayce K. Shaw, Samira Abdulai-Saiku, et al.
Science Advances (2025) Vol. 11, Iss. 10
Open Access | Times Cited: 8
X Inactivation and Escape: Epigenetic and Structural Features
He Fang, Christine M. Distèche, Joel B. Berletch
Frontiers in Cell and Developmental Biology (2019) Vol. 7
Open Access | Times Cited: 139
Escape From X-Chromosome Inactivation: An Evolutionary Perspective
Bronwyn J. Posynick, Carolyn J. Brown
Frontiers in Cell and Developmental Biology (2019) Vol. 7
Open Access | Times Cited: 90
XIST loss impairs mammary stem cell differentiation and increases tumorigenicity through Mediator hyperactivation
Laia Richart, Mary-Loup Picod-Chedotel, Michel Wassef, et al.
Cell (2022) Vol. 185, Iss. 12, pp. 2164-2183.e25
Open Access | Times Cited: 47
X chromosome agents of sexual differentiation
Arthur P. Arnold
Nature Reviews Endocrinology (2022) Vol. 18, Iss. 9, pp. 574-583
Open Access | Times Cited: 40
The human Y and inactive X chromosomes similarly modulate autosomal gene expression
Adrianna K. San Roman, Helen Skaletsky, Alexander K. Godfrey, et al.
Cell Genomics (2023) Vol. 4, Iss. 1, pp. 100462-100462
Open Access | Times Cited: 30
Role of the X Chromosome in Alzheimer Disease Genetics
Michaël E. Belloy, Yann Le Guen, Ilaria Stewart, et al.
JAMA Neurology (2024)
Closed Access | Times Cited: 11
Evolutionary and biomedical implications of sex differences in the primate brain transcriptome
Alex R. DeCasien, Kenneth L. Chiou, Camille Testard, et al.
Cell Genomics (2024) Vol. 4, Iss. 7, pp. 100589-100589
Open Access | Times Cited: 9
DDX3X Suppresses the Susceptibility of Hindbrain Lineages to Medulloblastoma
Deanna M. Patmore, Amir Jassim, Erica Nathan, et al.
Developmental Cell (2020) Vol. 54, Iss. 4, pp. 455-470.e5
Open Access | Times Cited: 65
Genes that escape from X‐chromosome inactivation: Potential contributors to Klinefelter syndrome
María José Navarro-Cobos, Bradley P. Balaton, Carolyn J. Brown
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2020) Vol. 184, Iss. 2, pp. 226-238
Open Access | Times Cited: 64
X chromosome escapee genes are involved in ischemic sexual dimorphism through epigenetic modification of inflammatory signals
Shaohua Qi, Abdullah Al Mamun, Conelius Ngwa, et al.
Journal of Neuroinflammation (2021) Vol. 18, Iss. 1
Open Access | Times Cited: 51
Prospective and detailed behavioral phenotyping in DDX3X syndrome
Lara Tang, Tess Levy, Sylvia Guillory, et al.
Molecular Autism (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 45
The variant landscape and function of DDX3X in cancer and neurodevelopmental disorders
Margaret Gadek, Elliott H. Sherr, Stephen N. Floor
Trends in Molecular Medicine (2023) Vol. 29, Iss. 9, pp. 726-739
Open Access | Times Cited: 21
Escape from X-inactivation in twins exhibits intra- and inter-individual variability across tissues and is heritable
Antonino Zito, Amy L. Roberts, Alessia Visconti, et al.
PLoS Genetics (2023) Vol. 19, Iss. 2, pp. e1010556-e1010556
Open Access | Times Cited: 19
Loss of epigenetic modifications on the inactive X chromosome and sex-biased gene expression profiles in B cells from NZB/W F1 mice with lupus-like disease
Camille M. Syrett, Isabel Sierra, Zachary T. Beethem, et al.
Journal of Autoimmunity (2019) Vol. 107, pp. 102357-102357
Open Access | Times Cited: 48
Integrated analysis of Xist upregulation and X-chromosome inactivation with single-cell and single-allele resolution
Guido Pacini, Ilona Dunkel, Norbert Mages, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 41
Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases
Renan Sauteraud, Jill M. Stahl, J. Chen James, et al.
Genome Research (2021) Vol. 31, Iss. 9, pp. 1629-1637
Open Access | Times Cited: 37
Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome
Andrea Boitnott, Marta Garcia‐Forn, Dévina C. Ung, et al.
Biological Psychiatry (2021) Vol. 90, Iss. 11, pp. 742-755
Open Access | Times Cited: 34
OFD1: One gene, several disorders
Nunziana Pezzella, Guglielmo Bove, Roberta Tammaro, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 1, pp. 57-71
Open Access | Times Cited: 27
Quantification of escape from X chromosome inactivation with single-cell omics data reveals heterogeneity across cell types and tissues
Yoshihiko Tomofuji, Ryuya Edahiro, Kyuto Sonehara, et al.
Cell Genomics (2024) Vol. 4, Iss. 8, pp. 100625-100625
Open Access | Times Cited: 6
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types
Laura V. Blanton, Adrianna K. San Roman, Geryl Wood, et al.
Cell Genomics (2024) Vol. 4, Iss. 9, pp. 100628-100628
Open Access | Times Cited: 6
Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance
Georgios Stamoulis, Marco Garieri, Periklis Makrythanasis, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 39
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