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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:

Chlamydia trachomatis CT229 Subverts Rab GTPase-Dependent CCV Trafficking Pathways to Promote Chlamydial Infection
Robert Faris, Marlena R. Merling, Shelby E. Andersen, et al.
Cell Reports (2019) Vol. 26, Iss. 12, pp. 3380-3390.e5
Open Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Chlamydial Infection From Outside to Inside
Arlieke Gitsels, Niek N. Sanders, Daisy Vanrompay
Frontiers in Microbiology (2019) Vol. 10
Open Access | Times Cited: 70
The multiple functions of the numerous Chlamydia trachomatis secreted proteins: the tip of the iceberg
Joana N. Bugalhão, Luı́s Jaime Mota
Microbial Cell (2019) Vol. 6, Iss. 9, pp. 414-449
Open Access | Times Cited: 59
Iron robbery by intracellular pathogen via bacterial effector–induced ferritinophagy
Qi Yan, Wenqing Zhang, Mingqun Lin, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 23
Open Access | Times Cited: 44
Sigma 54-Regulated Transcription Is Associated with Membrane Reorganization and Type III Secretion Effectors during Conversion to Infectious Forms of Chlamydia trachomatis
Katelyn R. Soules, Scott D. LaBrie, Benjamin May, et al.
mBio (2020) Vol. 11, Iss. 5
Open Access | Times Cited: 41
An endometrial organoid model of interactions between Chlamydia and epithelial and immune cells
Lee Dolat, Raphael H. Valdivia
Journal of Cell Science (2021) Vol. 134, Iss. 5
Open Access | Times Cited: 36
Persistence Alters the Interaction between Chlamydia trachomatis and Its Host Cell
Mary R. Brockett, George W. Liechti
Infection and Immunity (2021) Vol. 89, Iss. 8
Open Access | Times Cited: 35
The Chlamydia effector CpoS modulates the inclusion microenvironment and restricts the interferon response by acting on Rab35
Karsten Meier, Lana H. Jachmann, Gözde Türköz, et al.
mBio (2023)
Open Access | Times Cited: 15
The Chlamydia trachomatis type III-secreted effector protein CteG induces centrosome amplification through interactions with centrin-2
Brianna Steiert, Carolina M. Icardi, Robert Faris, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 20
Open Access | Times Cited: 14
The Chlamydia trachomatis IncM Protein Interferes with Host Cell Cytokinesis, Centrosome Positioning, and Golgi Distribution and Contributes to the Stability of the Pathogen-Containing Vacuole
Maria Pequito Luís, Inês Serrano Pereira, Joana N. Bugalhão, et al.
Infection and Immunity (2023) Vol. 91, Iss. 4
Open Access | Times Cited: 13
Pathogen-induced rerouting of host membrane trafficking
Patrick J. Woida, Rebecca L. Lamason
Current Opinion in Cell Biology (2025) Vol. 94, pp. 102520-102520
Closed Access
Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease
Kate L. Jordan, David J. Koss, Tiago F. Outeiro, et al.
Biomedicines (2022) Vol. 10, Iss. 5, pp. 1141-1141
Open Access | Times Cited: 15
Methylene Blue-Loaded NanoMOFs: Accumulation in Chlamydia trachomatis Inclusions and Light/Dark Antibacterial Effects
Xiaoli Qi, Ekaterina Grafskaia, Zhihao Yu, et al.
ACS Infectious Diseases (2023) Vol. 9, Iss. 8, pp. 1558-1569
Open Access | Times Cited: 9
Identification and Preliminary Characterization of Novel Type III Secreted Effector Proteins in Chlamydia trachomatis
Paige N. McCaslin, Shelby E. Andersen, Carolina M. Icardi, et al.
Infection and Immunity (2023) Vol. 91, Iss. 7
Open Access | Times Cited: 8
Plasmid-mediated virulence in Chlamydia
Breanna J. Turman, Toni Darville, Catherine M. O’Connell
Frontiers in Cellular and Infection Microbiology (2023) Vol. 13
Open Access | Times Cited: 8
Got mutants? How advances in chlamydial genetics have furthered the study of effector proteins
Shelby E. Andersen, Lanci M Bulman, Brianna Steiert, et al.
Pathogens and Disease (2020) Vol. 79, Iss. 2
Open Access | Times Cited: 22
Targeting Endosomal Recycling Pathways by Bacterial and Viral Pathogens
Yong Xin, Lejiao Mao, Xiaofei Shen, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 20
The emerging complexity of Chlamydia trachomatis interactions with host cells as revealed by molecular genetic approaches
Robert J. Bastidas, Raphael H. Valdivia
Current Opinion in Microbiology (2023) Vol. 74, pp. 102330-102330
Open Access | Times Cited: 7
Eukaryotic SNARE VAMP3 Dynamically Interacts with Multiple Chlamydial Inclusion Membrane Proteins
Duc‐Cuong Bui, Lisa M. Jorgenson, Scot P. Ouellette, et al.
Infection and Immunity (2020) Vol. 89, Iss. 2
Open Access | Times Cited: 19
Host cell death during infection withChlamydia: a double-edged sword
Barbara S. Sixt
FEMS Microbiology Reviews (2020) Vol. 45, Iss. 1
Open Access | Times Cited: 18
Establishing the intracellular niche of obligate intracellular vacuolar pathogens
Tatiana M. Clemente, Rajendra Kumar Angara, Stacey D. Gilk
Frontiers in Cellular and Infection Microbiology (2023) Vol. 13
Open Access | Times Cited: 6
The Chlamydia protein CpoS modulates the inclusion microenvironment and restricts the interferon response by acting on Rab35
Karsten Meier, Lana H. Jachmann, Lucía Peña‐Pérez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 9
The iron-dependent repressor YtgR is a tryptophan-dependent attenuator of the trpRBA operon in Chlamydia trachomatis
Nick D. Pokorzynski, Nathan D. Hatch, Scot P. Ouellette, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 13
In Search of a Mechanistic Link between Chlamydia trachomatis-Induced Cellular Pathophysiology and Oncogenesis
Brianna Steiert, Robert Faris, Mary M. Weber
Infection and Immunity (2023) Vol. 91, Iss. 2
Open Access | Times Cited: 4
Role of Rab GTPases in Bacteria Escaping from Vesicle Trafficking of Host Cells
Huiling Xu, Shengnan Wang, Xiaozhou Wang, et al.
The Journal of Microbiology (2024) Vol. 62, Iss. 8, pp. 581-590
Closed Access | Times Cited: 1
Coxiella burnetii-containing vacuoles interact with host recycling endosomal proteins Rab11a and Rab35 for vacuolar expansion and bacterial growth
B. Hall, Kristen E. Senior, Nicolle T. Ocampo, et al.
Frontiers in Cellular and Infection Microbiology (2024) Vol. 14
Open Access | Times Cited: 1
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