The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
The Genetic Landscape of a Cell
Open accessAbstract
Making Connections: Genetic interaction profiles highlight cross-connections between bioprocesses, providing a global view of cellular pleiotropy, and enable the prediction of genetic network hubs. Costanzo et al. (p. 425 ) performed a pairwise fitness screen covering approximately one-third of all potential genetic interactions in yeast, examining 5.4 million gene-gene pairs and generating quantitative profiles for ∼75% of the genome. Of the pairwise interactions tested, about 3% of the genes investigated interact under the conditions tested. On the basis of these data, a reference map for the yeast genetic network was created.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Synthetic genetic interaction screens in yeast123,124 have demonstrated that thousands of combinations of individually viable mutations can jointly be lethal, and similar examples have been documented in Drosophila melanogaster and Caenorhabditis elegans125,126.”
From Rare and common variants: twenty arguments (2012) · cites this paper as [124]
In the citing paper
“Genes belonging to similar biological processes tend to share common genetic interactions, and genes encoding proteins that function together within the same pathway or complex display similar genetic interaction profiles (fig. S4)(1).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Genetic interaction networks highlight mechanistic connections between genes and their corresponding pathways (1).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Synthetic genetic array (SGA) analysis automates the combinatorial construction of defined mutants and enables the quantitative analysis of genetic interactions (1, 5).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Negative and positive genetic interactions were quantified and false negative/positive rates and data reproducibility were determined at defined confidence thresholds (1) from analysis of biological replicates and comparison of interactions for a subset of gene pairs represented on both mutant arrays (fig. S2)(8).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Genes belonging to similar biological processes tend to share common genetic interactions, and genes encoding proteins that function together within the same pathway or complex display similar genetic interaction profiles (fig. S4)(1).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Thus, genetic interaction profiles provide a quantitative measurement of functional similarity, and similarity networks generated from the large-scale mapping correlated genetic interaction profiles organizes genes into clusters that highlight biological processes (1).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Thus, genetic interaction profiles provide a quantitative measurement of functional similarity, and similarity networks generated from the large-scale mapping correlated genetic interaction profiles organizes genes into clusters that highlight biological processes (1).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“As observed previously (1), fitness defects associated with both deletion alleles of nonessential genes and TS alleles of essential genes were highly correlated with the degree of genetic interaction (figs. S11–S12; Table S1; Data File S10).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Consistent with previous observations (1), positive genetic interactions between nonessential genes also overlapped with protein-protein interactions, albeit to a lesser extent (0.5%, 3.7-fold enrichment; Figs. 5C, S15).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“First, consistent with the results of our previous smaller scale surveys (1, 24), essential genes are major hubs and form the basic scaffold of the global genetic interaction network.”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“One interesting case involves duplicated genes with overlapping function, which often are buffered more extensively, such that more complex triple mutant analysis will be required to reveal their genetic interaction profiles (1, 40).”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
In the citing paper
“Consistent with previous findings (1, 5, 28, 29), we found that protein complexes exhibited highly organized patterns of genetic interactions.”
From A global genetic interaction network maps a wiring diagram of cellular function (2016) · cites this paper as [1]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Inhibition of Poly(ADP-Ribose) Polymerase in Tumors from BRCA Mutation Carriers
Fong, P. C., Boss, D. S., Yap, T. A., Tutt, A., Wu, P., Mergui-Roelvink, M., Mortimer, P., Swaisland, H., Lau, A., O'Connor, M. J., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0900212 · Cited by 3,634
Global landscape of protein complexes in the yeast Saccharomyces cerevisiae
Krogan, N. J., Cagney, G., Yu, H., Zhong, G., Guo, X., Ignatchenko, A., Li, J., Pu, S., Datta, N., Tikuisis, A., et al. (2006) · Nature · doi:10.1038/nature04670 · Cited by 2,964
Self-citationProteome survey reveals modularity of the yeast cell machinery
Gavin, A., Aloy, P., Grandi, P., Krause, R., Böesche, M., Marzioch, M., Rau, C., Jensen, L. J., Bastuck, S., Dümpelfeld, B., et al. (2006) · Nature · doi:10.1038/nature04532 · Cited by 2,570
Waddington, C. H. (2014) · doi:10.4324/9781315765471 · Cited by 2,153
Systematic Genetic Analysis with Ordered Arrays of Yeast Deletion Mutants
Tong, A. H. Y., Evangelista, M., Parsons, A. B., Xu, H., Bader, G. D., Pagé, N., Robinson, M., Raghibizadeh, S., Hogue, C. W. V., Bussey, H., et al. (2001) · Science · doi:10.1126/science.1065810 · Cited by 2,138
Self-citationGlobal Mapping of the Yeast Genetic Interaction Network
Tong, A. H. Y., Lesage, G., Bader, G. D., Ding, H., Xu, H., Xin, X., Young, J., Berriz, G. F., Brost, R. L., Chang, M., et al. (2004) · Science · doi:10.1126/science.1091317 · Cited by 2,089
Self-citationHigh-Quality Binary Protein Interaction Map of the Yeast Interactome Network
Yu, H., Braun, P., Yıldırım, M. A., Lemmens, I., Venkatesan, K., Sahalie, J., Hirozane-Kishikawa, T., Gebreab, F., Li, N., Simonis, N., et al. (2008) · Science · doi:10.1126/science.1158684 · Cited by 1,392
Self-citationThe Chemical Genomic Portrait of Yeast: Uncovering a Phenotype for All Genes
Hillenmeyer, M. E., Fung, E., Wildenhain, J., Pierce, S. E., Hoon, S. S., Lee, W., Proctor, M. J., St.Onge, R. P., Tyers, M., Koller, D., et al. (2008) · Science · doi:10.1126/science.1150021 · Cited by 978
Self-citationAn in Vivo Map of the Yeast Protein Interactome
Tarassov, K., Messier, V., Landry, C. R., Radinovic, S., Molina, M. M. S., Shames, I., Malitskaya, Y., Vogel, J., Bussey, H., & Michnick, S. W. (2008) · Science · doi:10.1126/science.1153878 · Cited by 779
Self-citationComprehensive Characterization of Genes Required for Protein Folding in the Endoplasmic Reticulum
Jonikas, M. C., Collins, S. R., Denic, V., Oh, E., Toyama, E. Q., Schmid, V., Weibezahn, J., Schwappach, B., Walter, P., Weissman, J. S., et al. (2009) · Science · doi:10.1126/science.1167983 · Cited by 723
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 1,004
Addinall, S. G., Holstein, E., Lawless, C., Yu, M., Chapman, K. E., Banks, A. P., Ngo, H.-P., Maringele, L., Taschuk, M. L., Young, A. E., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1001362 · Cited by 72
Woodruff, J. B., Drubin, D. G., & Barnes, G. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201006028 · Cited by 72
Mirón-García, M. C., Garrido-Godino, A. I., García-Molinero, V., Hernández‐Torres, F., Rodríguez‐Navarro, S., & Navarro, F. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003297 · Cited by 75
Chemical-genetic profile analysis of five inhibitory compounds in yeast
Alamgir, M. S., Erukova, V., Jessulat, M., Azizi, A., & Golshani, A. (2010) · BMC Chemical Biology · doi:10.1186/1472-6769-10-6 · Cited by 72
tRNA anticodon loop modifications ensure protein homeostasis and cell morphogenesis in yeast
Klassen, R., Ciftci, A., Funk, J., Bruch, A., Butter, F., & Schaffrath, R. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw705 · Cited by 72
Potential of the Synthetic Lethality Principle
Nijman, S. M. B., & Friend, S. H. (2013) · Science · doi:10.1126/science.1244669 · Cited by 72
Bhardwaj, N., Kim, P. M., & Gerstein, M. (2010) · Science Signaling · doi:10.1126/scisignal.2001014 · Cited by 74
Self-citationAllan, C. M., Awad, A. M., Johnson, J. S., Shirasaki, D., Wang, C., Blaby, C., Merchant, S., Loo, J. A., & Clarke, C. F. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.633131 · Cited by 71
Systematic genetic interaction screens uncover cell polarity regulators and functional redundancy
Fievet, B. T., Rodríguez, J., Naganathan, S. R., Lee, C., Zeiser, E., Ishidate, T., Shirayama, M., Grill, S. W., & Ahringer, J. (2012) · Nature Cell Biology · doi:10.1038/ncb2639 · Cited by 71
Putting genetic interactions in context through a global modular decompositionPreprint
Bellay, J., Atluri, G., Sing, T. L., Toufighi, K., Costanzo, M., Ribeiro, P. S. M., Pandey, G. S., Baller, J. A., VanderSluis, B., Michaut, M., et al. (2011) · Genome Research · doi:10.1101/gr.117176.110 · Cited by 72
Self-citationThe Cellular Robustness by Genetic Redundancy in Budding Yeast
Li, J., Yuan, Z., & Zhang, Z. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001187 · Cited by 70
Talkish, J., Zhang, J., Jakovljevic, J., Horsey, E., & Woolford, J. L. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks609 · Cited by 70
SEA you later alli-GATOR – a dynamic regulator of the TORC1 stress response pathway
Dokudovskaya, S., & Rout, M. P. (2015) · Journal of Cell Science · doi:10.1242/jcs.168922 · Cited by 74
A chemical–genetic interaction map of small molecules using high‐throughput imaging in cancer cells
Breinig, M., Klein, F. A., Huber, W. K., & Boutros, M. (2015) · Molecular Systems Biology · doi:10.15252/msb.20156400 · Cited by 70
Genetic variation in adaptability and pleiotropy in budding yeast
Jerison, E. R., Kryazhimskiy, S., Mitchell, J. K., Bloom, J. S., Kruglyak, L., & Desai, M. M. (2017) · eLife · doi:10.7554/elife.27167 · Cited by 75
Prioritizing network communities
Žitnik, M., Sosič, R., & Leskovec, J. (2018) · Nature Communications · doi:10.1038/s41467-018-04948-5 · Cited by 72
Functional wiring of the yeast kinome revealed by global analysis of genetic network motifsPreprint
Sharifpoor, S., van Dyk, D., Costanzo, M., Baryshnikova, A., Friesen, H., Douglas, A. C., Youn, J.-Y., VanderSluis, B., Myers, C. L., Papp, B., et al. (2012) · Genome Research · doi:10.1101/gr.129213.111 · Cited by 71
Self-citationDistilling Pathophysiology from Complex Disease Genetics
Chakravarti, A., Clark, A. G., & Mootha, V. K. (2013) · Cell · doi:10.1016/j.cell.2013.09.001 · Cited by 70
Broad metabolic sensitivity profiling of a prototrophic yeast deletion collection
VanderSluis, B., Hess, D. C., Pesyna, C., Krumholz, E. W., Syed, T., Szappanos, B., Nislow, C., Papp, B., Troyanskaya, O. G., Myers, C. L., et al. (2014) · Genome biology · doi:10.1186/gb-2014-15-4-r64 · Cited by 69
Self-citationGlobal analysis of SUMO chain function reveals multiple roles in chromatin regulation
Srikumar, T., Lewicki, M. C., Costanzo, M., Tkach, J. M., van Bakel, H., Tsui, K., Johnson, E. S., Brown, G. W., Andrews, B., Boone, C. M., et al. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201210019 · Cited by 69
Self-citationConserved rules govern genetic interaction degree across species
Koch, E. N., Costanzo, M., Bellay, J., Deshpande, R., Chatfield-Reed, K., Chua, G., D'Urso, G., Andrews, B. J., Boone, C., & Myers, C. L. (2012) · Genome Biology · doi:10.1186/gb-2012-13-7-r57 · Cited by 68
Self-citationA Functional Variomics Tool for Discovering Drug-Resistance Genes and Drug Targets
Huang, Z., Chen, K., Zhang, J., Li, Y., Wang, H., Cui, D., Tang, J., Liu, Y., Shi, X., Li, W., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.01.019 · Cited by 68
Molecular Characterization of Propolis-Induced Cell Death in Saccharomyces cerevisiae
de Castro, P. A., Savoldi, M., Bonatto, D., de Barros, M. H., Goldman, M. H. S., Berretta, A. A., & Goldman, G. H. (2010) · Eukaryotic Cell · doi:10.1128/ec.00256-10 · Cited by 68
Hill, S. M., Hao, X., Grönvall, J., Spikings-Nordby, S., Widlund, P. O., Amen, T., Jörhov, A., Josefson, R., Kaganovich, D., Liu, B., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.06.016 · Cited by 70
Fasolo, J., Sboner, A., Sun, M., Yu, H., Chen, R., Sharon, D., Kim, P. M., Gerstein, M., & Snyder, M. P. (2011) · Genes & Development · doi:10.1101/gad.1998811 · Cited by 68
Self-citationKeane, O. M., Toft, C., Carretero‐Paulet, L., Jones, G. W., & Fares, M. A. (2014) · Genome Research · doi:10.1101/gr.176792.114 · Cited by 69
Kim, A., & Cunningham, K. W. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-08-0581 · Cited by 67
Widespread genetic epistasis among cancer genes
Wang, X., Fu, A. Q., McNerney, M. E., & White, K. P. (2014) · Nature Communications · doi:10.1038/ncomms5828 · Cited by 67
Fendt, S., Oliveira, A. P., Christen, S., Picotti, P., Dechant, R. C., & Sauer, U. (2010) · Molecular Systems Biology · doi:10.1038/msb.2010.91 · Cited by 67
North, M. R., Steffen, J., Loguinov, A. V., Zimmerman, G. R., Vulpe, C. D., & Eide, D. J. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002699 · Cited by 72
Functional Toxicogenomics: Mechanism-Centered Toxicology
North, M. R., & Vulpe, C. D. (2010) · International Journal of Molecular Sciences · doi:10.3390/ijms11124796 · Cited by 67
Fang, H., Gomes, A. R., Klages, N., Pino, P., Maco, B., Walker, E. M., Ζήνωνος, Ζ., Angrisano, F., Baum, J., Doerig, C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06733-w · Cited by 67
Pathway-based discovery of genetic interactions in breast cancer
Wang, W., Xu, Z., Costanzo, M., Boone, C. M., Lange, C. A., & Myers, C. L. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006973 · Cited by 68
Self-citationNetwork News: Innovations in 21st Century Systems Biology
Arkin, A. P., & Schaffer, D. V. (2011) · Cell · doi:10.1016/j.cell.2011.03.008 · Cited by 66
Exploiting epigenetic vulnerabilities for cancer therapeutics
Mair, B., Kubicek, S., & Nijman, S. M. B. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.01.001 · Cited by 66
The vacuole/lysosome is required for cell-cycle progression
Jin, Y., & Weisman, L. S. (2015) · eLife · doi:10.7554/elife.08160 · Cited by 66
Microtubule-Stabilizing Drugs from Marine Sponges: Focus on Peloruside A and Zampanolide
Miller, J. H., Singh, A. J., & Northcote, P. T. (2010) · Marine Drugs · doi:10.3390/md8041059 · Cited by 67
Han, L., Kon, Y., & Phizicky, E. M. (2014) · RNA · doi:10.1261/rna.048173.114 · Cited by 66
Popa, C., Li, L., Gil, S., Tatjer, L., Hashii, K., Tabuchi, M., Coll, N. S., Ariño, J., & Valls, M. (2016) · Scientific Reports · doi:10.1038/srep27058 · Cited by 66
The evolution of hybrid fitness during speciation
Dagilis, A. J., Kirkpatrick, M., & Bolnick, D. I. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008125 · Cited by 67
Proteomic and Metabolomic Characteristics of Extremophilic Fungi Under Simulated Mars Conditions
Blachowicz, A., Chiang, A. J., Elsaesser, A., Kalkum, M., Ehrenfreund, P., Stajich, J., Torok, T., Wang, C. C. C., & Venkateswaran, K. J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01013 · Cited by 66
The diphthamide modification pathway from S accharomyces cerevisiae – revisited
Schaffrath, R., Abdel-Fattah, W. R., Klassen, R., & Stark, M. J. R. (2014) · Molecular Microbiology · doi:10.1111/mmi.12845 · Cited by 67
Comprehensive prediction of robust synthetic lethality between paralog pairs in cancer cell lines
Kegel, B. D., Quinn, N., Thompson, N., Adams, D. J., & Ryan, C. J. (2021) · Cell Systems · doi:10.1016/j.cels.2021.08.006 · Cited by 67
Ba, A. N. N., Lawrence, K. R., Rego‐Costa, A., Gopalakrishnan, S., Temko, D., Michor, F., & Desai, M. M. (2022) · eLife · doi:10.7554/elife.73983 · Cited by 68
Measuring growth rate in high-throughput growth phenotyping
Blomberg, A. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.10.013 · Cited by 65
In silico characterization and prediction of global protein–mRNA interactions in yeast
Pancaldi, V., & Bähler, J. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr160 · Cited by 67
Melamed, S., Elad, T., & Belkin, S. (2011) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2011.11.024 · Cited by 65
Au, W.-C., Dawson, A. R., Rawson, D. W., Taylor, S. B., Baker, R. E., & Basrai, M. A. (2013) · Genetics · doi:10.1534/genetics.113.149898 · Cited by 65
Reconstitution and Protein Composition Analysis of Endocytic Actin Patches
Michelot, A., Costanzo, M., Sarkeshik, A., Boone, C. M., Yates, J. R., & Drubin, D. G. (2010) · Current Biology · doi:10.1016/j.cub.2010.10.016 · Cited by 70
Self-citationA Comparative Genomic Approach for Identifying Synthetic Lethal Interactions in Human Cancer
Deshpande, R., Asiedu, M. K., Klebig, M., Sutor, S., Kuzmin, E., Nelson, J., Piotrowski, J., Ho Shin, S., Yoshida, M., Costanzo, M., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-3956 · Cited by 64
Self-citationHaßdenteufel, S., Sicking, M., Schorr, S., Aviram, N., Fecher‐Trost, C., Schuldiner, M., Jung, M., Zimmermann, R., & Lang, S. (2017) · FEBS Letters · doi:10.1002/1873-3468.12831 · Cited by 66
Cooperativity between different tRNA modifications and their modification pathways
Sokołowski, M., Klassen, R., Bruch, A., Schaffrath, R., & Glatt, S. (2017) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2017.12.003 · Cited by 64
Ukai, H., Araki, Y., Kira, S., Oikawa, Y., May, A. I., & Noda, T. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007334 · Cited by 66
Herrmann, J. M., & Riemer, J. (2020) · Biological Chemistry · doi:10.1515/hsz-2020-0254 · Cited by 67
The Prefoldin Complex Regulates Chromatin Dynamics during Transcription Elongation
Millán-Zambrano, G., Rodríguez‐Gil, A., Peñate, X., de Miguel-Jiménez, L., Morillo‐Huesca, M., Krogan, N. J., & Chávez, S. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003776 · Cited by 64
Burrage, J., Termanis, A., Geissner, A., Myant, K., Gordon, K., & Stancheva, I. (2012) · Journal of Cell Science · doi:10.1242/jcs.111252 · Cited by 70
Forte, A., Cipollaro, M., & Galderisi, U. (2013) · Clinical Science · doi:10.1042/cs20130099 · Cited by 63
Scope and limitations of yeast as a model organism for studying human tissue-specific pathways
Mohammadi, S., Saberidokht, B., Subramaniam, S., & Grama, A. Y. (2015) · BMC Systems Biology · doi:10.1186/s12918-015-0253-0 · Cited by 74
Distinct complexes of yeast Snx4 family SNX‐BARs mediate retrograde trafficking of Snc1 and Atg27
Ma, M., Burd, C. G., & Chi, R. J. (2016) · Traffic · doi:10.1111/tra.12462 · Cited by 63
A Practical Guide to Genome-Scale Metabolic Models and Their Analysis
dos Santos, F. B., Boele, J., & Teusink, B. (2011) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-385118-5.00024-4 · Cited by 64
Antibiotics as probes of biological complexity
Falconer, S. B., Czarny, T. L., & Brown, E. D. (2011) · Nature Chemical Biology · doi:10.1038/nchembio.590 · Cited by 67
Lewis, J. A., Broman, A. T., Will, J., & Gasch, A. P. (2014) · Genetics · doi:10.1534/genetics.114.167429 · Cited by 62
Features of the Chaperone Cellular Network Revealed through Systematic Interaction Mapping
Rizzolo, K., Huen, J., Kumar, A., Phanse, S., Vlasblom, J., Kakihara, Y., Zeineddine, H. A., Minić, Z., Snider, J. D., Wang, W., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.074 · Cited by 64
Self-citationParkinson disease related ATP13A2 evolved early in animal evolution
Sørensen, D. M., Holemans, T., van Veen, S., Martin, S., Arslan, T., Haagendahl, I. W., Holen, H. W., Hamouda, N. N., Eggermont, J., Palmgren, M. B., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193228 · Cited by 67
The impact of the genetic background on gene deletion phenotypes in Saccharomyces cerevisiae
Galardini, M., Busby, B. P., Viéitez, C., Dunham, A. S., Typas, A., & Beltrão, P. (2019) · Molecular Systems Biology · doi:10.15252/msb.20198831 · Cited by 68
Mechanisms of drug interactions between translation-inhibiting antibiotics
Kavčič, B., Tkačik, G., & Bollenbach, T. (2020) · Nature Communications · doi:10.1038/s41467-020-17734-z · Cited by 65
Important challenges to finding new leads for new antibiotics
Farha, M. A., Tu, M. M., & Brown, E. D. (2024) · Current Opinion in Microbiology · doi:10.1016/j.mib.2024.102562 · Cited by 64
Chartron, J. W., Gonzalez, G. M., & Clemons, W. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.277798 · Cited by 61
Balony:a software package for analysis of data generated by synthetic genetic array experiments
Young, B. P., & Loewen, C. J. R. (2013) · BMC Bioinformatics · doi:10.1186/1471-2105-14-354 · Cited by 61
Brochado, A. R., & Typas, A. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.01.008 · Cited by 61
Wood, C. S., Hung, C.-S., Huoh, Y., Mousley, C. J., Stefan, C. J., Bankaitis, V. A., Ferguson, K. M., & Burd, C. G. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-01-0077 · Cited by 61
Identifying key nodes in multilayer networks based on tensor decomposition
Wang, D., Wang, H., & Zou, X. (2017) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/1.4985185 · Cited by 61
Combining CRISPRi and metabolomics for functional annotation of compound libraries
Anglada-Girotto, M., Handschin, G., Ortmayr, K., Campos, A. I., Gillet, L., Manfredi, P., Mulholland, C. V., Berney, M., Jenal, U., Picotti, P., et al. (2022) · Nature Chemical Biology · doi:10.1038/s41589-022-00970-3 · Cited by 60
High‐throughput screens in mammalian cells using the CRISPR‐Cas9 system
Peng, J., Zhou, Y., Zhu, S., & Wei, W. (2015) · FEBS Journal · doi:10.1111/febs.13251 · Cited by 60
Turner, S., Berg, R. L., Linneman, J. G., Peissig, P. L., Crawford, D. C., Denny, J. C., Roden, D. M., McCarty, C. A., Ritchie, M. D., & Wilke, R. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019586 · Cited by 63
Gonçalves, E., Behan, F. M., Louzada, S., Arnol, D., Stronach, E. A., Yang, F., Yusa, K., Stegle, O., Iorio, F., & Garnett, M. J. (2019) · Genome biology · doi:10.1186/s13059-019-1637-z · Cited by 60
High-throughput functional characterization of protein phosphorylation sites in yeast
Viéitez, C., Busby, B. P., Ochoa, D., Mateus, A., Memon, D., Galardini, M., Yildiz, U., Trovato, M., Jawed, A., Geiger, A. G., et al. (2021) · Nature Biotechnology · doi:10.1038/s41587-021-01051-x · Cited by 60
Complex Portal 2022: new curation frontiers
Meldal, B., Perfetto, L., Combe, C., Lubiana, T., Cavalcante, J. V. F., Bye‐A‐Jee, H., Waagmeester, A., del‐Toro, N., Shrivastava, A., Barrera, E., et al. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab991 · Cited by 60
Exploring the Yeast Acetylome Using Functional Genomics
Duffy, S., Friesen, H., Baryshnikova, A., Lambert, J., Chong, Y. T., Figeys, D., & Andrews, B. (2012) · Cell · doi:10.1016/j.cell.2012.02.064 · Cited by 63
Self-citationHow the Nucleus Copes with Proteotoxic Stress
Shibata, Y., & Morimoto, R. I. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.033 · Cited by 63
A portrait of the GET pathway as a surprisingly complicated young man
Denic, V. (2012) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2012.07.004 · Cited by 60
Pathogenesis and Antifungal Drug Resistance of the Human Fungal Pathogen Candida glabrata
Tscherner, M., Schwarzmüller, T., & Kuchler, K. (2011) · Pharmaceuticals · doi:10.3390/ph4010169 · Cited by 60
Ignea, C., Trikka, F. A., Kourtzelis, I., Argiriou, A., Kanellis, A. K., Kampranis, S. C., & Makris, A. M. (2012) · Microbial Cell Factories · doi:10.1186/1475-2859-11-162 · Cited by 60
Integrated network analysis and effective tools in plant systems biology
Fukushima, A., Kanaya, S., & Nishida, K. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00598 · Cited by 61
Rass, U. (2013) · Chromosoma · doi:10.1007/s00412-013-0431-z · Cited by 60
Chartron, J. W., VanderVelde, D. G., & Clemons, W. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.10.010 · Cited by 59
Epistatic Interaction Maps Relative to Multiple Metabolic Phenotypes
Snitkin, E. S., & Segrè, D. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1001294 · Cited by 59
Blm10 facilitates nuclear import of proteasome core particles
Weberruss, M. H., Savulescu, A. F., Jando, J., Bissinger, T., Harel, A., Glickman, M. H., & Enenkel, C. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.192 · Cited by 59
Secretory pathway genes assessed by high-throughput microscopy and synthetic genetic array analysis
Bircham, P. W., Maass, D. R., Roberts, C. A., Kiew, P. Y., Low, Y. S., Yegambaram, M., Matthews, J., Jack, C., & Atkinson, P. H. (2011) · Molecular BioSystems · doi:10.1039/c1mb05175j · Cited by 59
A quantitative literature-curated gold standard for kinase-substrate pairs
Sharifpoor, S., Ba, A. N. N., Young, J.-Y., van Dyk, D., Friesen, H., Douglas, A. C., Kurat, C. F., Chong, Y. T., Founk, K., Moses, A. M., et al. (2011) · Genome biology · doi:10.1186/gb-2011-12-4-r39 · Cited by 59
Self-citationDiscovery of a Regulatory Subunit of the Yeast Fatty Acid Synthase
Singh, K., Graf, B., Linden, A., Sautner, V., Urlaub, H., Tittmann, K., Stark, H., & Chari, A. (2020) · Cell · doi:10.1016/j.cell.2020.02.034 · Cited by 59
SCS3 and YFT2 Link Transcription of Phospholipid Biosynthetic Genes to ER Stress and the UPR
Moir, R. D., Gross, D. A., Silver, D. L., & Willis, I. M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002890 · Cited by 59
Genotype to Phenotype Mapping and the Fitness Landscape of the E. coli lac Promoter
Otwinowski, J., & Nemenman, I. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061570 · Cited by 61
Niehaus, T. D., Nguyen, T. N. D., Gidda, S. K., Elbadawi-Sidhu, M., Lambrecht, J. A., McCarty, D. R., Downs, D. M., Cooper, A. J. L., Fiehn, O., Mullen, R. T., et al. (2014) · The Plant Cell · doi:10.1105/tpc.114.126854 · Cited by 58
The developmental genetics of biological robustness
Mestek, L., & Barkoulas, M. (2015) · Annals of Botany · doi:10.1093/aob/mcv128 · Cited by 61
Ferrari, E., Bruhn, C., Peretti, M., Cassani, C., Carotenuto, W., Elgendy, M., Shubassi, G., Lucca, C., Bermejo, R., Varasi, M., et al. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.05.027 · Cited by 58
High‐resolution mapping of cancer cell networks using co‐functional interactions
Boyle, E. A., Pritchard, J. K., & Greenleaf, W. J. (2018) · Molecular Systems Biology · doi:10.15252/msb.20188594 · Cited by 63
Protein Complexes are Central in the Yeast Genetic Landscape
Michaut, M., Baryshnikova, A., Costanzo, M., Myers, C. L., Andrews, B., Boone, C. M., & Bader, G. D. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1001092 · Cited by 57
Self-citationArmean, I. M., Lilley, K. S., & Trotter, M. W. B. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.r112.019554 · Cited by 58
Integration of New Genes into Cellular Networks, and Their Structural Maturation
Abrusán, G. (2013) · Genetics · doi:10.1534/genetics.113.152256 · Cited by 60
Metadata
- Authors
- Costanzo, M., Baryshnikova, A., Bellay, J., Kim, Y., Spear, E. D., Sevier, C. S., Ding, H., Koh, J. L. Y., Toufighi, K., Mostafavi, S., Prinz, J., St. Onge, R. P., VanderSluis, B., Makhnevych, T., Vizeacoumar, F. J., Alizadeh, S., Bahr, S., Brost, R. L., Chen, Y., Cokol, M., Deshpande, R., Li, Z., Lin, Z.-Y., Liang, W., Marback, M., Paw, J., San Luis, B.-J., Shuteriqi, E., Tong, A. H. Y., van Dyk, N., Wallace, I. M., Whitney, J. A., Weirauch, M. T., Zhong, G., Zhu, H., Houry, W. A., Brudno, M., Ragibizadeh, S., Papp, B., Pál, C., Roth, F. P., Giaever, G., Nislow, C., Troyanskaya, O. G., Bussey, H., Bader, G. D., Gingras, A.-C., Morris, Q. D., Kim, P. M., Kaiser, C. A., Myers, C. L., Andrews, B. J., & Boone, C.
- Affiliations
- University of Toronto (CA)
- University of Minnesota (US)
- Massachusetts Institute of Technology (US)
- Department of Biochemistry, Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.
- Banting and Best Department of Medical Research, Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada.
- Harvard University (US)
- Mount Sinai Hospital (CA)
- University of California, Santa Cruz (US)
- S&P Robotics, Inc., 1181 Finch Avenue West, North York, Ontario M3J 2V8, Canada.
- Institute of Biochemistry (HU)
- Princeton University (US)
- McGill University (CA)
- Corresponding author
- Costanzo, Michael
- Baryshnikova, Anastasia
- Myers, Chad L.
- Andrews, Brenda J.
- Boone, Charles
- ORCID
- Costanzo, Michael
- Baryshnikova, Anastasia
- Spear, Eric D.
- Sevier, Carolyn S.
- Mostafavi, Sara
- VanderSluis, Benjamin
- Vizeacoumar, Franco J.
- Chen, Yiqun
- Cokol, Murat
- Li, Zhijian
- Liang, Wendy
- Tong, Amy Hin Yan
- Wallace, Iain M.
- Weirauch, Matthew T.
- Zhu, Hongwei
- Houry, Walid A.
- Brudno, Michael
- Papp, Balázs
- Pál, Csaba
- Roth, Frederick P.
- Giaever, Guri
- Nislow, Corey
- Troyanskaya, Olga G.
- Bader, Gary D.
- Gingras, Anne-Claude
- Morris, Quaid D.
- Kim, Philip M.
- Myers, Chad L.
- Andrews, Brenda J.
- Boone, Charles
- Venue
- Science
- Published
- 2010-01-22
- Volume
- 327
- Issue
- 5964
- Pages
- 425-431
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC5600254
- OpenAlex
- W2133102806
- Cited by
- 2,162
- References
- 38
- Citations by year
- 2026: 36 · 2025: 48 · 2024: 57 · 2023: 70 · 2022: 75 · 2021: 83 · 2020: 93 · 2019: 98 · 2018: 115 · 2017: 159 · 2016: 161 · 2015: 183 · 2014: 203 · 2013: 212 · 2012: 212
- FWCI
- 101.56
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Wellcome Trust (084314)
- Canadian Institutes of Health Research (GSP-415-67)
- National Human Genome Research Institute (R01HG003224)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Keywords
- synthetic genetic interactions, gene-gene interaction, genetic interaction networks, Saccharomyces cerevisiae, gene function annotation, pleiotropy, chemical-genetic interactions, drug target identification
- MeSH terms
- Genes, Fungal, Mutation, Saccharomyces cerevisiae, Gene Expression Regulation, Fungal, Genome, Fungal, Computational Biology, Gene Duplication, Protein Interaction Mapping, Saccharomyces cerevisiae Proteins, Gene Regulatory Networks, Metabolic Networks and Pathways, Genetic Fitness
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review