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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:

Random monoallelic expression of autosomal genes: stochastic transcription and allele-level regulation
Björn Reinius, Rickard Sandberg
Nature Reviews Genetics (2015) Vol. 16, Iss. 11, pp. 653-664
Closed Access | Times Cited: 181

Showing 1-25 of 181 citing articles:

Single-Cell RNA-Seq Reveals Lineage and X Chromosome Dynamics in Human Preimplantation Embryos
Sophie Petropoulos, Daniel Edsgärd, Björn Reinius, et al.
Cell (2016) Vol. 165, Iss. 4, pp. 1012-1026
Open Access | Times Cited: 996
Genomic encoding of transcriptional burst kinetics
Anton J. M. Larsson, Per Johnsson, Michael Hagemann-Jensen, et al.
Nature (2018) Vol. 565, Iss. 7738, pp. 251-254
Open Access | Times Cited: 499
Genetic diagnosis of Mendelian disorders via RNA sequencing
Laura S. Kremer, Daniel M. Bader, Christian Mertes, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 498
TLR7 escapes X chromosome inactivation in immune cells
Mélanie Souyris, Claire Cénac, Pascal Azar, et al.
Science Immunology (2018) Vol. 3, Iss. 19
Closed Access | Times Cited: 496
Single-cell RNA sequencing: Technical advancements and biological applications
Eva Hedlund, Qiaolin Deng
Molecular Aspects of Medicine (2017) Vol. 59, pp. 36-46
Closed Access | Times Cited: 327
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts
Laure Frésard, Craig Smail, Nicole M. Ferraro, et al.
Nature Medicine (2019) Vol. 25, Iss. 6, pp. 911-919
Open Access | Times Cited: 280
Somatic mutations and cell identity linked by Genotyping of Transcriptomes
Anna S. Nam, Kyu-Tae Kim, Ronan Chaligné, et al.
Nature (2019) Vol. 571, Iss. 7765, pp. 355-360
Open Access | Times Cited: 264
Applying high-dimensional single-cell technologies to the analysis of cancer immunotherapy
Satyen H. Gohil, J. Bryan Iorgulescu, David A. Braun, et al.
Nature Reviews Clinical Oncology (2020) Vol. 18, Iss. 4, pp. 244-256
Open Access | Times Cited: 213
scSLAM-seq reveals core features of transcription dynamics in single cells
Florian Erhard, Marisa A. P. Baptista, Tobias Krammer, et al.
Nature (2019) Vol. 571, Iss. 7765, pp. 419-423
Open Access | Times Cited: 198
Haplotype-aware analysis of somatic copy number variations from single-cell transcriptomes
Teng Gao, Ruslan Soldatov, Hirak Sarkar, et al.
Nature Biotechnology (2022) Vol. 41, Iss. 3, pp. 417-426
Closed Access | Times Cited: 91
Heritable transcriptional defects from aberrations of nuclear architecture
Stamatis Papathanasiou, Nikos A. Mynhier, Shiwei Liu, et al.
Nature (2023) Vol. 619, Iss. 7968, pp. 184-192
Open Access | Times Cited: 49
Monoallelic expression can govern penetrance of inborn errors of immunity
O’Jay Stewart, Conor Gruber, Haley E. Randolph, et al.
Nature (2025)
Closed Access | Times Cited: 9
Analysis of allelic expression patterns in clonal somatic cells by single-cell RNA–seq
Björn Reinius, Jeff E. Mold, Daniel Ramsköld, et al.
Nature Genetics (2016) Vol. 48, Iss. 11, pp. 1430-1435
Open Access | Times Cited: 155
Mapping the mouse Allelome reveals tissue-specific regulation of allelic expression
Daniel Andergassen, Christoph Dotter, D. Wénzel, et al.
eLife (2017) Vol. 6
Open Access | Times Cited: 151
Genomic structural variation-mediated allelic suppression causes hybrid male sterility in rice
Rongxin Shen, Lan Wang, Xupeng Liu, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 149
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
Single-cell analyses of X Chromosome inactivation dynamics and pluripotency during differentiation
Geng Chen, John P. Schell, Julio Aguila Benitez, et al.
Genome Research (2016) Vol. 26, Iss. 10, pp. 1342-1354
Open Access | Times Cited: 115
Human genes escaping X-inactivation revealed by single cell expression data
Kerem Wainer-Katsir, Michal Linial
BMC Genomics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 112
SCALE: modeling allele-specific gene expression by single-cell RNA sequencing
Yuchao Jiang, Nancy Zhang, Mingyao Li
Genome biology (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 103
NASC-seq monitors RNA synthesis in single cells
Gert‐Jan Hendriks, Lisa Anna Jung, Anton J. M. Larsson, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 98
Complex Autoinflammatory Syndrome Unveils Fundamental Principles of JAK1 Kinase Transcriptional and Biochemical Function
Conor Gruber, Jorg J. A. Calis, Sofija Buta, et al.
Immunity (2020) Vol. 53, Iss. 3, pp. 672-684.e11
Open Access | Times Cited: 95
Dynamic Enhancer DNA Methylation as Basis for Transcriptional and Cellular Heterogeneity of ESCs
Yuelin Song, Patrick R. van den Berg, Styliani Markoulaki, et al.
Molecular Cell (2019) Vol. 75, Iss. 5, pp. 905-920.e6
Open Access | Times Cited: 84
Incomplete penetrance in primary immunodeficiency: a skeleton in the closet
Conor Gruber, Dusan Bogunovic
Human Genetics (2020) Vol. 139, Iss. 6-7, pp. 745-757
Open Access | Times Cited: 78
Megabase-scale methylation phasing using nanopore long reads and NanoMethPhase
Vahid Akbari, Jean‐Michel Garant, Kieran O’Neill, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 57
Elastic dosage compensation by X-chromosome upregulation
Antonio Lentini, Huaitao Cheng, Joyce Noble, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 40
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