
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:
Human and mouse essentiality screens as a resource for disease gene discovery
Pilar Cacheiro, Violeta Muñoz‐Fuentes, Stephen A. Murray, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 90
Pilar Cacheiro, Violeta Muñoz‐Fuentes, Stephen A. Murray, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 90
Showing 1-25 of 90 citing articles:
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource
Elliot Sollis, Abayomi Mosaku, Ala Abid, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D977-D985
Open Access | Times Cited: 1026
Elliot Sollis, Abayomi Mosaku, Ala Abid, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D977-D985
Open Access | Times Cited: 1026
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: 274
Tudor Groza, Federico López, Hamed Mashhadi, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1038-D1045
Open Access | Times Cited: 274
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: 187
Hao Luo, Yan Lin, Tao Liu, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D677-D686
Open Access | Times Cited: 187
What are housekeeping genes?
Chintan Joshi, Wenfan Ke, Anna Drangowska-Way, et al.
PLoS Computational Biology (2022) Vol. 18, Iss. 7, pp. e1010295-e1010295
Open Access | Times Cited: 84
Chintan Joshi, Wenfan Ke, Anna Drangowska-Way, et al.
PLoS Computational Biology (2022) Vol. 18, Iss. 7, pp. e1010295-e1010295
Open Access | Times Cited: 84
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration
Annalisa Vetro, Cristiana Pelorosso, Simona Balestrini, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 8, pp. 1356-1376
Open Access | Times Cited: 24
Annalisa Vetro, Cristiana Pelorosso, Simona Balestrini, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 8, pp. 1356-1376
Open Access | Times Cited: 24
Quantifying constraint in the human mitochondrial genome
Nicole J. Lake, Kaiyue Ma, Wei Liu, et al.
Nature (2024) Vol. 635, Iss. 8038, pp. 390-397
Closed Access | Times Cited: 13
Nicole J. Lake, Kaiyue Ma, Wei Liu, et al.
Nature (2024) Vol. 635, Iss. 8038, pp. 390-397
Closed Access | Times Cited: 13
Integration of graph neural networks and genome-scale metabolic models for predicting gene essentiality
Ramin Hasibi, Tom Michoel, Diego A. Oyarzún
npj Systems Biology and Applications (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 12
Ramin Hasibi, Tom Michoel, Diego A. Oyarzún
npj Systems Biology and Applications (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 12
Recent advances in the characterization of essential genes and development of a database of essential genes
Ya‐Ting Liang, Hao Luo, Yan Lin, et al.
iMeta (2024) Vol. 3, Iss. 1
Open Access | Times Cited: 10
Ya‐Ting Liang, Hao Luo, Yan Lin, et al.
iMeta (2024) Vol. 3, Iss. 1
Open Access | Times Cited: 10
Engineering Base Changes and Epitope‐Tagged Alleles in Mice Using Cas9 RNA‐Guided Nuclease
Marina Gertsenstein, Lauri G. Lintott, Lauryl M. J. Nutter
Current Protocols (2025) Vol. 5, Iss. 2
Open Access | Times Cited: 1
Marina Gertsenstein, Lauri G. Lintott, Lauryl M. J. Nutter
Current Protocols (2025) Vol. 5, Iss. 2
Open Access | Times Cited: 1
Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology
Ferdinand Dhombres, Patricia Morgan, Bimal P. Chaudhari, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 231-242
Open Access | Times Cited: 37
Ferdinand Dhombres, Patricia Morgan, Bimal P. Chaudhari, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 231-242
Open Access | Times Cited: 37
Into the Wild: A novel wild-derived inbred strain resource expands the genomic and phenotypic diversity of laboratory mouse models
Beth L. Dumont, Daniel M. Gatti, Mallory A. Ballinger, et al.
PLoS Genetics (2024) Vol. 20, Iss. 4, pp. e1011228-e1011228
Open Access | Times Cited: 8
Beth L. Dumont, Daniel M. Gatti, Mallory A. Ballinger, et al.
PLoS Genetics (2024) Vol. 20, Iss. 4, pp. e1011228-e1011228
Open Access | Times Cited: 8
Advances in mouse genetics for the study of human disease
Steve D. M. Brown
Human Molecular Genetics (2021) Vol. 30, Iss. R2, pp. R274-R284
Open Access | Times Cited: 39
Steve D. M. Brown
Human Molecular Genetics (2021) Vol. 30, Iss. R2, pp. R274-R284
Open Access | Times Cited: 39
Copy number losses of oncogenes and gains of tumor suppressor genes generate common driver mutations
Elizaveta Besedina, Fran Supek
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Elizaveta Besedina, Fran Supek
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Improving prenatal diagnosis through standards and aggregation
Michael H. Duyzend, Pilar Cacheiro, Julius O.B. Jacobsen, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 4, pp. 454-464
Open Access | Times Cited: 5
Michael H. Duyzend, Pilar Cacheiro, Julius O.B. Jacobsen, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 4, pp. 454-464
Open Access | Times Cited: 5
Revisiting Cardiac Biology in the Era of Single Cell and Spatial Omics
Jack A. Palmer, Nadia Rosenthal, Sarah A. Teichmann, et al.
Circulation Research (2024) Vol. 134, Iss. 12, pp. 1681-1702
Open Access | Times Cited: 5
Jack A. Palmer, Nadia Rosenthal, Sarah A. Teichmann, et al.
Circulation Research (2024) Vol. 134, Iss. 12, pp. 1681-1702
Open Access | Times Cited: 5
Membrane structure-responsive lipid scrambling by TMEM63B to control plasma membrane lipid distribution
Yugo Miyata, Katsuya Takahashi, Yongchan Lee, et al.
Nature Structural & Molecular Biology (2024)
Open Access | Times Cited: 5
Yugo Miyata, Katsuya Takahashi, Yongchan Lee, et al.
Nature Structural & Molecular Biology (2024)
Open Access | Times Cited: 5
Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets
Pankhuri Singhal, Yogasudha Veturi, Scott Dudek, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 4, pp. 575-591
Open Access | Times Cited: 13
Pankhuri Singhal, Yogasudha Veturi, Scott Dudek, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 4, pp. 575-591
Open Access | Times Cited: 13
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia
Zhongbo Chen, Arianna Tucci, Valentina Cipriani, et al.
Brain (2023) Vol. 146, Iss. 7, pp. 2869-2884
Open Access | Times Cited: 12
Zhongbo Chen, Arianna Tucci, Valentina Cipriani, et al.
Brain (2023) Vol. 146, Iss. 7, pp. 2869-2884
Open Access | Times Cited: 12
Genetics of recurrent pregnancy loss: a review
Christina G. Tise, Heather M. Byers
Current Opinion in Obstetrics & Gynecology (2021) Vol. 33, Iss. 2, pp. 106-111
Closed Access | Times Cited: 24
Christina G. Tise, Heather M. Byers
Current Opinion in Obstetrics & Gynecology (2021) Vol. 33, Iss. 2, pp. 106-111
Closed Access | Times Cited: 24
Progress towards completing the mutant mouse null resource
Kevin A. Peterson, Stephen A. Murray
Mammalian Genome (2021) Vol. 33, Iss. 1, pp. 123-134
Open Access | Times Cited: 24
Kevin A. Peterson, Stephen A. Murray
Mammalian Genome (2021) Vol. 33, Iss. 1, pp. 123-134
Open Access | Times Cited: 24
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
Ásmundur Oddsson, Patrick Sulem, Garðar Sveinbjörnsson, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Ásmundur Oddsson, Patrick Sulem, Garðar Sveinbjörnsson, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Speos: an ensemble graph representation learning framework to predict core gene candidates for complex diseases
Florin Ratajczak, Mitchell Joblin, Marcel Hildebrandt, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Florin Ratajczak, Mitchell Joblin, Marcel Hildebrandt, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
IMPC impact on preclinical mouse models
Sabine M. Hölter, Pilar Cacheiro, Damian Smedley, et al.
Mammalian Genome (2025)
Open Access
Sabine M. Hölter, Pilar Cacheiro, Damian Smedley, et al.
Mammalian Genome (2025)
Open Access
DBeQ derivative targets VPS4 functions in cancer cells and suppresses tumor growth in mice
Kevin A. Fundora, Zhuang Yan, Kouta Hamamoto, et al.
Journal of Pharmacology and Experimental Therapeutics (2025), pp. 103524-103524
Open Access
Kevin A. Fundora, Zhuang Yan, Kouta Hamamoto, et al.
Journal of Pharmacology and Experimental Therapeutics (2025), pp. 103524-103524
Open Access
Towards a Conceptual Framework to Better Understand the Advantages and Limitations of Model Organisms
Markus Kunze, Federica Malfatti
European Journal of Neuroscience (2025) Vol. 61, Iss. 7
Open Access
Markus Kunze, Federica Malfatti
European Journal of Neuroscience (2025) Vol. 61, Iss. 7
Open Access