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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:

High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson, Ann M. Flenniken, Xiao Ji, et al.
Nature (2016) Vol. 537, Iss. 7621, pp. 508-514
Open Access | Times Cited: 1149

Showing 1-25 of 1149 citing articles:

The single-cell transcriptional landscape of mammalian organogenesis
Junyue Cao, Malte Spielmann, Xiaojie Qiu, et al.
Nature (2019) Vol. 566, Iss. 7745, pp. 496-502
Open Access | Times Cited: 3319
Genetic compensation: A phenomenon in search of mechanisms
Mohamed A. El-Brolosy, Didier Y. R. Stainier
PLoS Genetics (2017) Vol. 13, Iss. 7, pp. e1006780-e1006780
Open Access | Times Cited: 757
Gene expression across mammalian organ development
Margarida Cardoso-Moreira, Jean Halbert, Delphine Valloton, et al.
Nature (2019) Vol. 571, Iss. 7766, pp. 505-509
Open Access | Times Cited: 690
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases
Yiheng Chen, Tianyuan Lu, U. Pettersson, et al.
Nature Genetics (2023) Vol. 55, Iss. 1, pp. 44-53
Open Access | Times Cited: 467
Calcium at the Center of Cell Signaling: Interplay between Endoplasmic Reticulum, Mitochondria, and Lysosomes
Anna Raffaello, Cristina Mammucari, Gaia Gherardi, et al.
Trends in Biochemical Sciences (2016) Vol. 41, Iss. 12, pp. 1035-1049
Open Access | Times Cited: 454
Thalidomide promotes degradation of SALL4, a transcription factor implicated in Duane Radial Ray syndrome
Katherine A. Donovan, An Jian, Radosław P. Nowak, et al.
eLife (2018) Vol. 7
Open Access | Times Cited: 429
Variant interpretation using population databases: Lessons from gnomAD
Sanna Gudmundsson, Moriel Singer‐Berk, Nicholas A. Watts, et al.
Human Mutation (2021) Vol. 43, Iss. 8, pp. 1012-1030
Open Access | Times Cited: 391
Mechanisms of early placental development in mouse and humans
Myriam Hemberger, Courtney W. Hanna, Wendy Dean
Nature Reviews Genetics (2019) Vol. 21, Iss. 1, pp. 27-43
Closed Access | Times Cited: 379
Placentation defects are highly prevalent in embryonic lethal mouse mutants
Vicente Pérez-García, Elena Fineberg, Robert Wilson, et al.
Nature (2018) Vol. 555, Iss. 7697, pp. 463-468
Open Access | Times Cited: 339
Unexplored therapeutic opportunities in the human genome
Tudor I. Oprea, Cristian Bologa, Søren Brunak, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 5, pp. 317-332
Open Access | Times Cited: 339
Rab family of small GTPases: an updated view on their regulation and functions
Yuta Homma, Shu Hiragi, Mitsunori Fukuda
FEBS Journal (2020) Vol. 288, Iss. 1, pp. 36-55
Open Access | Times Cited: 338
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
Carolina Medina‐Gómez, John P. Kemp, Katerina Trajanoska, et al.
The American Journal of Human Genetics (2018) Vol. 102, Iss. 1, pp. 88-102
Open Access | Times Cited: 304
Unexplored therapeutic opportunities in the human genome.
Tudor I. Oprea, Cristian Bologa, Søren Brunak, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 5, pp. 377-377
Open Access | Times Cited: 303
The roles of Polycomb repressive complexes in mammalian development and cancer
Andrea Piunti, Ali Shilatifard
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 5, pp. 326-345
Closed Access | Times Cited: 295
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease
Tudor Groza, Federico López, Hamed Mashhadi, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1038-D1045
Open Access | Times Cited: 270
Emerging and evolving concepts in gene essentiality
Giulia Rancati, Jason Moffat, Athanasios Typas, et al.
Nature Reviews Genetics (2017) Vol. 19, Iss. 1, pp. 34-49
Closed Access | Times Cited: 256
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium
Terrence F. Meehan, Nathalie Conte, David B. West, et al.
Nature Genetics (2017) Vol. 49, Iss. 8, pp. 1231-1238
Open Access | Times Cited: 241
Human gene essentiality
István Bartha, Julia di Iulio, J. Craig Venter, et al.
Nature Reviews Genetics (2017) Vol. 19, Iss. 1, pp. 51-62
Closed Access | Times Cited: 238
A genomics approach reveals insights into the importance of gene losses for mammalian adaptations
Virag Sharma, Nikolai Hecker, Juliana G. Roscito, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 226
Sixteen diverse laboratory mouse reference genomes define strain-specific haplotypes and novel functional loci
Jingtao Lilue, Anthony Doran, Ian T. Fiddes, et al.
Nature Genetics (2018) Vol. 50, Iss. 11, pp. 1574-1583
Open Access | Times Cited: 220
Sour Sensing from the Tongue to the Brain
Jin Zhang, Hao Jin, Wenyi Zhang, et al.
Cell (2019) Vol. 179, Iss. 2, pp. 392-402.e15
Open Access | Times Cited: 208
Glioma tumor suppressor candidate region gene 1 (GLTSCR1) and its paralog GLTSCR1-like form SWI/SNF chromatin remodeling subcomplexes
Aktan Alpsoy, Emily C. Dykhuizen
Journal of Biological Chemistry (2018) Vol. 293, Iss. 11, pp. 3892-3903
Open Access | Times Cited: 207
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
Miguel Verbitsky, Rik Westland, Alejandra Perez, et al.
Nature Genetics (2018) Vol. 51, Iss. 1, pp. 117-127
Open Access | Times Cited: 185
DEG 15, an update of the Database of Essential Genes that includes built-in analysis tools
Hao Luo, Yan Lin, Tao Liu, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D677-D686
Open Access | Times Cited: 182
Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis
Leslie O. Goodwin, Erik Splinter, Tiffany L. Davis, et al.
Genome Research (2019) Vol. 29, Iss. 3, pp. 494-505
Open Access | Times Cited: 175
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