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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:

Mapping histamine H4receptor–ligand binding modes
Sabine Schultes, Saskia Nijmeijer, Harald Engelhardt, et al.
MedChemComm (2012) Vol. 4, Iss. 1, pp. 193-204
Closed Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

POVME 2.0: An Enhanced Tool for Determining Pocket Shape and Volume Characteristics
Jacob D. Durrant, Lane Votapka, Jesper Givskov Sørensen, et al.
Journal of Chemical Theory and Computation (2014) Vol. 10, Iss. 11, pp. 5047-5056
Open Access | Times Cited: 217
Modelling three-dimensional protein structures for applications in drug design
Tobias Schmidt, Andreas Bergner, Torsten Schwede
Drug Discovery Today (2013) Vol. 19, Iss. 7, pp. 890-897
Open Access | Times Cited: 169
GPCR crystal structures: Medicinal chemistry in the pocket
Jeremy Shonberg, Ralf C. Kling, Peter Gmeiner, et al.
Bioorganic & Medicinal Chemistry (2014) Vol. 23, Iss. 14, pp. 3880-3906
Closed Access | Times Cited: 104
A structural chemogenomics analysis of aminergic GPCRs: lessons for histamine receptor ligand design
Albert J. Kooistra, Sebastiaan Kuhne, Iwan J. P. de Esch, et al.
British Journal of Pharmacology (2013) Vol. 170, Iss. 1, pp. 101-126
Open Access | Times Cited: 80
Aminergic GPCR–Ligand Interactions: A Chemical and Structural Map of Receptor Mutation Data
Márton Vass, Sabina Podlewska, Iwan J. P. de Esch, et al.
Journal of Medicinal Chemistry (2018) Vol. 62, Iss. 8, pp. 3784-3839
Open Access | Times Cited: 66
PDEStrIAn: A Phosphodiesterase Structure and Ligand Interaction Annotated Database As a Tool for Structure-Based Drug Design
Chimed Jansen, Albert J. Kooistra, Georgi K. Kanev, et al.
Journal of Medicinal Chemistry (2016) Vol. 59, Iss. 15, pp. 7029-7065
Closed Access | Times Cited: 61
Structural insights into the agonists binding and receptor selectivity of human histamine H4 receptor
Dohyun Im, Jun-ichi Kishikawa, Yuki Shiimura, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 15
Aryl-1,3,5-triazine derivatives as histamine H4 receptor ligands
Dorota Łażewska, Małgorzata Więcek, Joanna Ner, et al.
European Journal of Medicinal Chemistry (2014) Vol. 83, pp. 534-546
Closed Access | Times Cited: 48
Detailed analysis of biased histamine H4 receptor signalling by JNJ 7777120 analogues
Saskia Nijmeijer, Henry F. Vischer, Francesco Sirci, et al.
British Journal of Pharmacology (2013) Vol. 170, Iss. 1, pp. 78-88
Open Access | Times Cited: 39
Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4receptor
Enade Perdana Istyastono, Albert J. Kooistra, Henry F. Vischer, et al.
MedChemComm (2015) Vol. 6, Iss. 6, pp. 1003-1017
Open Access | Times Cited: 34
The Extracellular Loop 2 (ECL2) of the Human Histamine H4 Receptor Substantially Contributes to Ligand Binding and Constitutive Activity
David Wifling, Günther Bernhardt, Stefan Dove, et al.
PLoS ONE (2015) Vol. 10, Iss. 1, pp. e0117185-e0117185
Open Access | Times Cited: 33
Design and pharmacological characterization of VUF14480, a covalent partial agonist that interacts with cysteine 983.36 of the human histamine H4 receptor
Saskia Nijmeijer, Harald Engelhardt, Sabine Schultes, et al.
British Journal of Pharmacology (2013) Vol. 170, Iss. 1, pp. 89-100
Open Access | Times Cited: 31
Small and colorful stones make beautiful mosaics: fragment-based chemogenomics
Chris de Graaf, Henry F. Vischer, Gerdien E. de Kloe, et al.
Drug Discovery Today (2012) Vol. 18, Iss. 7-8, pp. 323-330
Closed Access | Times Cited: 29
Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H2 Receptor Agonists
Steffen Pockes, David Wifling, Max Keller, et al.
ACS Omega (2018) Vol. 3, Iss. 3, pp. 2865-2882
Open Access | Times Cited: 26
Histamine H4 Receptor Ligands: Future Applications and State of Art
Michelle Fidelis Corrêa, João Paulo S. Fernandes
Chemical Biology & Drug Design (2014) Vol. 85, Iss. 4, pp. 461-480
Closed Access | Times Cited: 24
Hybrid approach to structure modeling of the histamine H3 receptor: Multi-level assessment as a tool for model verification
Jakub Jończyk, Barbara Malawska, Marek Bajda
PLoS ONE (2017) Vol. 12, Iss. 10, pp. e0186108-e0186108
Open Access | Times Cited: 21
Structure-based discovery and binding site analysis of histamine receptor ligands
Róbert Kiss, György M. Keserü
Expert Opinion on Drug Discovery (2016) Vol. 11, Iss. 12, pp. 1165-1185
Open Access | Times Cited: 14
Bispyrimidines as Potent Histamine H4 Receptor Ligands: Delineation of Structure–Activity Relationships and Detailed H4 Receptor Binding Mode
Harald Engelhardt, Sabine Schultes, Chris de Graaf, et al.
Journal of Medicinal Chemistry (2013) Vol. 56, Iss. 11, pp. 4264-4276
Closed Access | Times Cited: 11
Discovery of nanomolar ligands with novel scaffolds for the histamine H4 receptor by virtual screening
Nicolas Levoin, Olivier Labeeuw, Xavier Billot, et al.
European Journal of Medicinal Chemistry (2016) Vol. 125, pp. 565-572
Closed Access | Times Cited: 10
The Receptor Concept in 3D: From Hypothesis and Metaphor to GPCR–Ligand Structures
Albert J. Kooistra, Chris de Graaf, Henk Timmerman
Neurochemical Research (2014) Vol. 39, Iss. 10, pp. 1850-1861
Closed Access | Times Cited: 9
Novel potent (dihydro)benzofuranyl piperazines as human histamine receptor ligands – Functional characterization and modeling studies on H3 and H4 receptors
Michelle Fidelis Corrêa, André L. Balico-Silva, Dóra Kiss, et al.
Bioorganic & Medicinal Chemistry (2020) Vol. 30, pp. 115924-115924
Closed Access | Times Cited: 7
Molecular Modelling Approaches for the Analysis of Histamine Receptors and Their Interaction with Ligands
Andrea Straßer, Hans‐Joachim Wittmann
Handbook of experimental pharmacology (2017), pp. 31-61
Closed Access | Times Cited: 3
Design and synthesis of histamine H3/H4 receptor ligands with a cyclopropane scaffold
Mizuki Watanabe, Takaaki Kobayashi, Yoshihiko Ito, et al.
Bioorganic & Medicinal Chemistry Letters (2018) Vol. 28, Iss. 23-24, pp. 3630-3633
Closed Access | Times Cited: 3
The effect of pKa on pyrimidine/pyridine-derived histamine H4 ligands
Brad M. Savall, Steven P. Meduna, Jennifer D. Venable, et al.
Bioorganic & Medicinal Chemistry Letters (2014) Vol. 24, Iss. 23, pp. 5489-5492
Closed Access | Times Cited: 2
New Chemical Biology Tools for the Histamine Receptor Family
Yang Zheng, Gábor Wágner, Niels J. Hauwert, et al.
Current topics in behavioral neurosciences (2022), pp. 3-28
Closed Access | Times Cited: 2
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