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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:

Interpreting Neonatal Lethal Phenotypes in Mouse Mutants: Insights Into Gene Function and Human Diseases
Benjamin Turgeon, Sylvain Meloche
Physiological Reviews (2009) Vol. 89, Iss. 1, pp. 1-26
Closed Access | Times Cited: 144

Showing 1-25 of 144 citing articles:

Piezo2 senses airway stretch and mediates lung inflation-induced apnoea
Keiko Nonomura, Seung-Hyun Woo, Rui B. Chang, et al.
Nature (2016) Vol. 541, Iss. 7636, pp. 176-181
Open Access | Times Cited: 370
Loss of ceramide synthase 3 causes lethal skin barrier disruption
Richard Jennemann, Mariona Rabionet, Karin Gorgas, et al.
Human Molecular Genetics (2011) Vol. 21, Iss. 3, pp. 586-608
Open Access | Times Cited: 261
Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss
Jelena Scekic‐Zahirovic, Oliver Sendscheid, Hajer El Oussini, et al.
The EMBO Journal (2016) Vol. 35, Iss. 10, pp. 1077-1097
Open Access | Times Cited: 214
Reversible protein inactivation by optogenetic trapping in cells
Sangkyu Lee, Hye-Rim Park, Taeyoon Kyung, et al.
Nature Methods (2014) Vol. 11, Iss. 6, pp. 633-636
Closed Access | Times Cited: 204
Wnt signaling: Essential roles in osteoblast differentiation, bone metabolism and therapeutic implications for bone and skeletal disorders
Rexhina Vlashi, Xingen Zhang, Mengrui Wu, et al.
Genes & Diseases (2022) Vol. 10, Iss. 4, pp. 1291-1317
Open Access | Times Cited: 84
A Novel 4EHP-GIGYF2 Translational Repressor Complex Is Essential for Mammalian Development
Masahiro Morita, Lian Wee Ler, Marc R. Fabian, et al.
Molecular and Cellular Biology (2012) Vol. 32, Iss. 17, pp. 3585-3593
Open Access | Times Cited: 185
Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
D.N. Cooper, Jian‐Min Chen, Edward V. Ball, et al.
Human Mutation (2010) Vol. 31, Iss. 6, pp. 631-655
Open Access | Times Cited: 172
Bioenergetics, mitochondria, and cardiac myocyte differentiation
George A. Porter, Jennifer Hom, David L. Hoffman, et al.
Progress in Pediatric Cardiology (2011) Vol. 31, Iss. 2, pp. 75-81
Open Access | Times Cited: 141
Loss of motoneuron-specific microRNA-218 causes systemic neuromuscular failure
Neal D. Amin, Ge Bai, Jason R. Klug, et al.
Science (2015) Vol. 350, Iss. 6267, pp. 1525-1529
Open Access | Times Cited: 136
Conditional Knock-out Reveals a Requirement for O-Linked N-Acetylglucosaminase (O-GlcNAcase) in Metabolic Homeostasis
Chithra Keembiyehetty, Dona C. Love, Katryn R. Harwood, et al.
Journal of Biological Chemistry (2015) Vol. 290, Iss. 11, pp. 7097-7113
Open Access | Times Cited: 134
Mapping the epigenomic and transcriptomic interplay during memory formation and recall in the hippocampal engram ensemble
Asaf Marco, Hiruy S. Meharena, Vishnu Dileep, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 12, pp. 1606-1617
Open Access | Times Cited: 127
The miR‐379/miR‐410 cluster at the imprinted Dlk1‐Dio3 domain controls neonatal metabolic adaptation
Stéphane Labialle, Virginie Marty, Marie‐Line Bortolin‐Cavaillé, et al.
The EMBO Journal (2014) Vol. 33, Iss. 19, pp. 2216-2230
Open Access | Times Cited: 126
The Histone Demethylase Jarid1b Ensures Faithful Mouse Development by Protecting Developmental Genes from Aberrant H3K4me3
Mareike Albert, Sandra U. Schmitz, Susanne M. Kooistra, et al.
PLoS Genetics (2013) Vol. 9, Iss. 4, pp. e1003461-e1003461
Open Access | Times Cited: 125
Rescue of Peripheral and CNS Axon Defects in Mice Lacking NMNAT2
Jonathan Gilley, Róbert Adalbert, Gang Yu, et al.
Journal of Neuroscience (2013) Vol. 33, Iss. 33, pp. 13410-13424
Open Access | Times Cited: 116
Recognition of H3K9 methylation by GLP is required for efficient establishment of H3K9 methylation, rapid target gene repression, and mouse viability
Nan Liu, Zhuqiang Zhang, Hui Wu, et al.
Genes & Development (2015) Vol. 29, Iss. 4, pp. 379-393
Open Access | Times Cited: 109
Contribution of the Two Genes Encoding Histone Variant H3.3 to Viability and Fertility in Mice
Michelle C. W. Tang, Shelley Jacobs, Deidre M Mattiske, et al.
PLoS Genetics (2015) Vol. 11, Iss. 2, pp. e1004964-e1004964
Open Access | Times Cited: 103
Autophagy linked FYVE (Alfy/WDFY3) is required for establishing neuronal connectivity in the mammalian brain
Joanna M. Dragich, Takaaki Kuwajima, Megumi Hirose‐Ikeda, et al.
eLife (2016) Vol. 5
Open Access | Times Cited: 100
High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes
Robert Brommage, Jeff Liu, Gwenn M. Hansen, et al.
Bone Research (2014) Vol. 2, Iss. 1
Open Access | Times Cited: 95
AAV Gene Therapy Prevents and Reverses Heart Failure in a Murine Knockout Model of Barth Syndrome
Suya Wang, Yifei Li, Yang Xu, et al.
Circulation Research (2020) Vol. 126, Iss. 8, pp. 1024-1039
Open Access | Times Cited: 86
Tamoxifen-independent recombination of reporter genes limits lineage tracing and mosaic analysis using CreERT2 lines
Alberto Álvarez-Aznar, Inés Martínez‐Corral, Nina Daubel, et al.
Transgenic Research (2019) Vol. 29, Iss. 1, pp. 53-68
Open Access | Times Cited: 81
RBPMS is an RNA-binding protein that mediates cardiomyocyte binucleation and cardiovascular development
Peiheng Gan, Zhaoning Wang, María Gabriela Morales, et al.
Developmental Cell (2022) Vol. 57, Iss. 8, pp. 959-973.e7
Open Access | Times Cited: 53
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice
Anne‐Cécile Durieux, Alban Vignaud, Bernard Prudhon, et al.
Human Molecular Genetics (2010) Vol. 19, Iss. 24, pp. 4820-4836
Open Access | Times Cited: 120
CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs
Désirée Schatton, David Pla‐Martín, Marie‐Charlotte Marx, et al.
The Journal of Cell Biology (2017) Vol. 216, Iss. 3, pp. 675-693
Open Access | Times Cited: 86
Maternally provided LSD1/KDM1A enables the maternal-to-zygotic transition and prevents defects that manifest postnatally
Jadiel A. Wasson, Ashley Simon, Dexter A. Myrick, et al.
eLife (2016) Vol. 5
Open Access | Times Cited: 79
Neural blastocyst complementation enables mouse forebrain organogenesis
Amelia Chang, Zhuoyi Liang, Hai-Qiang Dai, et al.
Nature (2018) Vol. 563, Iss. 7729, pp. 126-130
Open Access | Times Cited: 60
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