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 801–900 of 1,004
Global Regulation of a Differentiation MAPK Pathway in Yeast
Chavel, C. A., Caccamise, L. M., Li, B., & Cullen, P. J. (2014) · Genetics · doi:10.1534/genetics.114.168252 · Cited by 30
Mayerle, M., & Guthrie, C. (2016) · RNA · doi:10.1261/rna.055459.115 · Cited by 30
Septins are involved at the early stages of macroautophagy in S. cerevisiae
Barve, G., Sridhar, S., Aher, A., Sahani, M. H., Chinchwadkar, S., Singh, S., K. N., L., McMurray, M. A., & Manjithaya, R. (2018) · Journal of Cell Science · doi:10.1242/jcs.209098 · Cited by 32
Candida glabrata : new tools and technologies—expanding the toolkit
Ho, H.-L., & Haynes, K. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov066 · Cited by 29
Phenotypic landscape of a fungal meningitis pathogen reveals its unique biology
Boucher, M. J., Banerjee, S., Joshi, M. B., Wei, A. L., Nalley, M. J., Huang, M. Y., Lei, S., Ciranni, M., Condon, A., Langen, A., et al. (2024) · Cell · doi:10.1016/j.cell.2025.05.017 · Cited by 30
Predicting functional gene interactions with the hierarchical interaction score
Snijder, B., Liberali, P., Fréchin, M., Stoeger, T., & Pelkmans, L. (2013) · Nature Methods · doi:10.1038/nmeth.2655 · Cited by 29
Reconstructing regulatory network transitions
Petricka, J. J., & Benfey, P. N. (2011) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.05.001 · Cited by 31
Mirón-García, M. C., Garrido-Godino, A. I., Martinez-Fernandez, V., Fernández-Pévida, A., Cuevas-Bermúdez, A., Martín‐Expósito, M., Chávez, S., de la Cruz, J., & Navarro, F. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku685 · Cited by 29
Splicing and Chromatin Factors Jointly Regulate Epidermal Differentiation
Tanis, S. E. J., Jansen, P. W. T. C., Zhou, H., van Heeringen, S. J., Vermeulen, M., Kretz, M., & Mulder, K. W. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.017 · Cited by 29
Balarezo-Cisneros, L. N., Parker, S., Fraczek, M. G., Timouma, S., Wang, P., O’Keefe, R. T., Millar, C. B., & Delneri, D. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1008761 · Cited by 30
Lenoir, W. F., Morgado, M. C., DeWeirdt, P. C., McLaughlin, M. E., Griffith, A. L., Sangree, A. K., Feeley, M. N., Anvar, N. E., Kim, E., Bertolet, L. L., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26867-8 · Cited by 31
Ubiquitin Ligase Ufd2 Is Required for Efficient Degradation of Mps1 Kinase
Liu, C., van Dyk, D., Choe, V., Yan, J. Y., Majumder, S., Costanzo, M., Bao, X., Boone, C. M., Huo, K., Winey, M., et al. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.286229 · Cited by 29
Self-citation38 Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome
Finch, A. J., Hilcenko, C., Basse, N., Drynan, L. F., Goyenechea, B., Menne, T., Fernández, Á. G., Simpson, P. J., D’Santos, C. S., Arends, M. J., et al. (2011) · Leukemia Research · doi:10.1016/s0145-2126(11)70040-6 · Cited by 29
Self-citationCSNK1E/CTNNB1 Are Synthetic Lethal To TP53 in Colorectal Cancer and Are Markers for Prognosis
Tiong, K.-L., Chang, K.-C., Yeh, K., Liu, T., Wu, J.-H., Hsieh, P.-H., Lin, S., Lai, W., Hsu, Y.-C., Chen, J.-Y., et al. (2014) · Neoplasia · doi:10.1016/j.neo.2014.04.007 · Cited by 29
Assembly, molecular organization, and membrane-binding properties of development-specific septins
García, G., Finnigan, G. C., Heasley, L. R., Sterling, S. M., Aggarwal, A., Pearson, C. G., Nogales, E., McMurray, M. A., & Thorner, J. W. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201511029 · Cited by 31
Evolution of protein-protein interaction networks in yeast
Schoenrock, A., Burnside, D. J., Moteshareie, H., Pitre, S., Hooshyar, M., Green, J. R., Golshani, A., Dehne, F., & Wong, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171920 · Cited by 30
Analysis of the Proteome of Saccharomyces cerevisiae for Methylarginine
Low, J. K. K., Hart‐Smith, G., Erce, M. A., & Wilkins, M. R. (2013) · Journal of Proteome Research · doi:10.1021/pr400556c · Cited by 28
Gautam, A., Grainger, R. J. R., Vilardell, J., Barrass, J. D., & Beggs, J. D. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv159 · Cited by 28
Gene-nutrient interaction markedly influences yeast chronological lifespan
Smith, D. L., Maharrey, C. H., Carey, C. R., White, R. A., & Hartman, J. L. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.04.012 · Cited by 28
Ist2 recruits the lipid transporters Osh6/7 to ER–PM contacts to maintain phospholipid metabolism
Wong, A. K. O., Young, B. P., & Loewen, C. J. R. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.201910161 · Cited by 28
From systems to structure — using genetic data to model protein structures
Braberg, H., Echeverria, I., Kaake, R. M., Šali, A., & Krogan, N. J. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-021-00441-w · Cited by 30
Community Detection in Multiplex Networks Based on Orthogonal Nonnegative Matrix Tri-Factorization
Ortiz-Bouza, M., & Aviyente, S. (2024) · IEEE Access · doi:10.1109/access.2024.3351709 · Cited by 29
Jaeger, P. A., McElfresh, C., Wong, L. R., & Ideker, T. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.01327-15 · Cited by 28
Opportunities in systems biology to discover mechanisms and repurpose drugs for CNS diseases
Mei, H., Xia, T., Feng, G., Zhu, J., Lin, S. M., & Qiu, Y. (2012) · Drug Discovery Today · doi:10.1016/j.drudis.2012.06.015 · Cited by 29
Determining the mode of action of bioactive compounds
Azad, M. A., & Wright, G. D. (2012) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2011.10.088 · Cited by 29
Norlin, S., Parekh, V. S., Naredi, P. L. J., & Edlund, H. (2015) · Diabetes · doi:10.2337/db15-0699 · Cited by 28
Fung, S., Sofiyev, V., Schneiderman, J., Hirschfeld, A. F., Victor, R. E., Woods, K., Piotrowski, J. S., Deshpande, R., Li, S. C., de Voogd, N. J., et al. (2013) · ACS Chemical Biology · doi:10.1021/cb400740c · Cited by 28
Self-citationCiftci-Yilmaz, S., Au, W.-C., Mishra, P. K., Eisenstatt, J. R., Chang, J. W., Dawson, A. R., Zhu, I., Rahman, M., Bilke, S., Costanzo, M., et al. (2018) · Genetics · doi:10.1534/genetics.118.301305 · Cited by 29
Self-citationHawer, H., Ütkür, K., Arend, M., Mayer, K., Adrian, L., Brinkmann, U., & Schaffrath, R. (2018) · PLoS ONE · doi:10.1371/journal.pone.0205870 · Cited by 28
Interaction of CK1δ with γTuSC ensures proper microtubule assembly and spindle positioning
Peng, Y., Moritz, M., Han, X., Giddings, T. H., Lyon, A. S., Kollman, J. M., Winey, M., Yates, J. R., Agard, D. A., Drubin, D. G., et al. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-12-1627 · Cited by 30
Cheng, C., Andrews, E. H., Yan, K., Ung, M. H., Wang, D., & Gerstein, M. (2015) · Genome biology · doi:10.1186/s13059-015-0624-2 · Cited by 27
Network-based functional modeling of genomics, transcriptomics and metabolism in bacteria
Cloots, L., & Marchal, K. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.09.003 · Cited by 27
Kyriakou, D., Stavrou, E., Demosthenous, P., Angelidou, G., Luis, B.-J. S., Boone, C. M., Promponas, V. J., & Kirmizis, A. (2016) · BMC Biology · doi:10.1186/s12915-016-0325-7 · Cited by 28
Self-citationGhavasieh, A., Bontorin, S., Artime, O., Verstraete, N., & Domenico, M. D. (2021) · Communications Physics · doi:10.1038/s42005-021-00582-8 · Cited by 28
Predicting protein function and other biomedical characteristics with heterogeneous ensembles
Whalen, S., Pandey, O. P., & Pandey, G. S. (2015) · Methods · doi:10.1016/j.ymeth.2015.08.016 · Cited by 29
Empirically determining the sample size for large-scale gene network inference algorithms
Altay, G. (2012) · IET Systems Biology · doi:10.1049/iet-syb.2010.0091 · Cited by 27
Dinér, P., Vilg, J. V., Kjellén, J., Migdal, I., Andersson, T., Gebbia, M., Giaever, G. N., Nislow, C., Hohmann, S., Wysocki, R., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020012 · Cited by 27
Self-citationFrancis, B. R., & Thorsness, P. E. (2011) · Mitochondrion · doi:10.1016/j.mito.2011.03.008 · Cited by 27
Genome-scale genetic manipulation methods for exploring bacterial molecular biology
Gagarinova, A. G., & Emili, A. (2012) · Molecular BioSystems · doi:10.1039/c2mb25040c · Cited by 27
Ricarte, F. R., Menjivar, R. E., Chhun, S., Soreta, T., Oliveira, L., Hsueh, T., Serranilla, M., & Gharakhanian, E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023696 · Cited by 27
Engineering Yeast Hexokinase 2 for Improved Tolerance Toward Xylose-Induced Inactivation
Bergdahl, B. M., Sandström, A. G., Borgström, C., Boonyawan, T., van Niel, E. W. J., & Gorwa‐Grauslund, M. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075055 · Cited by 27
Synthetic sickness or lethality points at candidate combination therapy targets in glioblastoma
Szczurek, E., Misra, N., & Vingron, M. (2013) · International Journal of Cancer · doi:10.1002/ijc.28235 · Cited by 27
Structure–function analysis and genetic interactions of the yeast branchpoint binding protein Msl5
Chang, J., Schwer, B., & Shuman, S. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks049 · Cited by 27
Current technologies to identify protein kinase substrates in high throughput
Xue, L., & Tao, W. A. (2013) · Frontiers in Biology · doi:10.1007/s11515-013-1257-z · Cited by 27
How Good Are Statistical Models at Approximating Complex Fitness Landscapes?
du Plessis, L., Leventhal, G. E., & Bonhoeffer, S. (2016) · Molecular Biology and Evolution · doi:10.1093/molbev/msw097 · Cited by 27
Budding Yeast Rif1 Controls Genome Integrity by Inhibiting rDNA Replication
Shyian, M., Mattarocci, S., Albert, B., Hafner, L., Lezaja, A., Costanzo, M., Boone, C., & Shore, D. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006414 · Cited by 27
Self-citationGlobal study of holistic morphological effectors in the budding yeast Saccharomyces cerevisiae
Suzuki, G., Wang, Y., Kubo, K., Hirata, E., Ohnuki, S., & Ohya, Y. (2018) · BMC Genomics · doi:10.1186/s12864-018-4526-z · Cited by 28
Spatial Analysis of Functional Enrichment (SAFE) in Large Biological Networks
Baryshnikova, A. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8618-7_12 · Cited by 28
Self-citationPhosphorylation by the stress-activated MAPK Slt2 down-regulates the yeast TOR complex 2Preprint
Leskoske, K. L., Roelants, F. M., Emmerstorfer‐Augustin, A., Augustin, C. M., Si, E. P., Hill, J. M., & Thorner, J. (2018) · Genes & Development · doi:10.1101/gad.318709.118 · Cited by 27
Crosstalk of promoter and terminator during RNA polymerase II transcription cycle
Al-Husini, N., Medler, S., & Ansari, A. (2020) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2020.194657 · Cited by 28
From beer to breadboards: yeast as a force for biological innovation
Gaikani, H. K., Stolar, M., Kriti, D., Nislow, C., & Giaever, G. N. (2024) · Genome biology · doi:10.1186/s13059-023-03156-9 · Cited by 29
Self-citationMa, C.-H., Cui, H., Hajra, S., Rowley, P. A., Fekete, C. A., Sarkeshik, A., Ghosh, S., Yates, J. R., & Jayaram, M. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1338 · Cited by 26
Dynamic epistasis for different alleles of the same gene
Xu, L., Barker, B., & Gu, Z. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121507109 · Cited by 29
A Scalable Approach for Discovering Conserved Active Subnetworks across Species
Deshpande, R., Sharma, S., Verfaillie, C. M., Hu, W.-S., & Myers, C. L. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1001028 · Cited by 26
Self-citationNguyen, H. D., Becker, J. R., Thu, Y. M., Costanzo, M., Koch, E. N., Smith, S. N., Myung, K., Myers, C. L., Boone, C. M., & Bielinsky, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066379 · Cited by 26
Self-citationDeterminants of Nam8-dependent splicing of meiotic pre-mRNAs
Qiu, Z. R., Schwer, B., & Shuman, S. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkq1328 · Cited by 26
McMurray, M. A., Stefan, C. J., Wemmer, M., Odorizzi, G., Emr, S. D., & Thorner, J. W. (2011) · Biological Chemistry · doi:10.1515/bc.2011.091 · Cited by 27
Serhan, G., Stack, C. M., Perrone, G. G., & Morton, C. O. (2014) · Annals of Clinical Microbiology and Antimicrobials · doi:10.1186/1476-0711-13-18 · Cited by 26
Identification of epistatic effects using a protein-protein interaction database
Sun, Y. V., & Kardia, S. L. R. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq356 · Cited by 26
Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1
Chauhan, N., Han, G., Somashekarappa, N., Gable, K. S., Dunn, T. M., & Kohlwein, S. D. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.693200 · Cited by 26
A genetic interaction map of cell cycle regulators
Billmann, M., Horn, T. L., Fischer, B., Sandmann, T., Huber, W. K., & Boutros, M. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-07-0467 · Cited by 26
Parsimonious Discovery of Synergistic Drug Combinations
Severyn, B. S., Liehr, R. A., Wolicki, A., Nguyen, K. H., Hudak, E. M., Ferrer, M., Caldwell, J. S., Hermes, J. D., Li, J., & Tudor, M. (2011) · ACS Chemical Biology · doi:10.1021/cb2003225 · Cited by 26
de Oliveira, E. A., de Lima, D. S., Cardozo, L. E., de Souza, G. F., de Souza, N., Alves-Fernandes, D. K., Faião‐Flores, F., Quincoces, J., Barros, S. B. D. M., Nakaya, H. I., et al. (2017) · Pharmacological Research · doi:10.1016/j.phrs.2017.08.018 · Cited by 26
Edskes, H. K., Mukhamedova, M., Edskes, B. K., & Wickner, R. B. (2018) · Genetics · doi:10.1534/genetics.118.300981 · Cited by 26
Using BEAN-counter to quantify genetic interactions from multiplexed barcode sequencing experiments
Simpkins, S. W., Deshpande, R., Nelson, J., Li, S. C., Piotrowski, J. S., Ward, H. N., Yashiroda, Y., Osada, H., Yoshida, M., Boone, C. M., et al. (2019) · Nature Protocols · doi:10.1038/s41596-018-0099-1 · Cited by 28
Self-citationAntifungal Drugs: The Current Armamentarium and Development of New Agents
Robbins, N., Wright, G. D., & Cowen, L. E. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch44 · Cited by 26
On the (un-)predictability of a large intragenic fitness landscapePreprint
Bank, C., Matuszewski, S., Hietpas, R. T., & Jensen, J. D. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/048769 · Cited by 26
Time-resolved mapping of genetic interactions to model rewiring of signaling pathways
Heigwer, F., Scheeder, C., Miersch, T., Schmitt, B. A., Blass, C., Pour-Jamnani, M. V., & Boutros, M. (2018) · eLife · doi:10.7554/elife.40174 · Cited by 25
A role for Mog1 in H2Bub1 and H3K4me3 regulation affecting RNAPII transcription and mRNA export
Oliete‐Calvo, P., Serrano‐Quílez, J., Nuño‐Cabanes, C., Pérez-Martínez, M. E., Soares, L. M. M., Dichtl, B., Buratowski, S., Pérez-Ortín, J. E., & Rodríguez‐Navarro, S. (2018) · EMBO Reports · doi:10.15252/embr.201845992 · Cited by 25
Córcoles-Sáez, I., Dong, K., & Rita, S. (2019) · Current Genetics · doi:10.1007/s00294-018-0920-y · Cited by 25
Wang, P., Xu, H., Li, H., Chen, H., Zhou, S., Tian, F., Li, B., Bo, X., Wu, Y., & Yuan, Y. (2020) · ACS Synthetic Biology · doi:10.1021/acssynbio.0c00059 · Cited by 25
Genetic profiling of protein burden and nuclear export overload
Kintaka, R., Makanae, K., Namba, S., Kato, H., Kito, K., Ohnuki, S., Ohya, Y., Andrews, B., Boone, C. M., & Moriya, H. (2020) · eLife · doi:10.7554/elife.54080 · Cited by 27
Self-citationNovel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafish
Musso, G. A., Tasan, M., Mosimann, C., Beaver, J. E., Plovie, E. R., Carr, L. A., Chua, H. N., Dunham, J., Zuberi, K., Rodriguez, H., et al. (2013) · Development · doi:10.1242/dev.099796 · Cited by 25
Self-citationMa, X., Chen, T., & Sun, F. (2013) · Briefings in Bioinformatics · doi:10.1093/bib/bbt041 · Cited by 26
Hang, M., & Smith, M. M. (2011) · Genetics · doi:10.1534/genetics.110.125419 · Cited by 25
Novel Interactions between Actin and the Proteasome Revealed by Complex Haploinsufficiency
Haarer, B. K., Aggeli, D., Viggiano, S. C., Burke, D. J., & Amberg, D. C. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002288 · Cited by 25
Epistasis from functional dependence of fitness on underlying traits
Chiu, H.-C., Marx, C. J., & Segrè, D. (2012) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2012.1449 · Cited by 25
A future of the model organism model
Rine, J. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-10-0768 · Cited by 26
Single-cell phenomics in budding yeast
Ohya, Y., Kimori, Y., Okada, H., & Ohnuki, S. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-07-0466 · Cited by 25
Community Detection in Protein-Protein Interaction Networks Using Spectral and Graph Approaches
Mahmoud, H., Masulli, F., Rovetta, S., & Russo, G. M. (2014) · Lecture notes in computer science · doi:10.1007/978-3-319-09042-9_5 · Cited by 25
iSeq: A New Double-Barcode Method for Detecting Dynamic Genetic Interactions in Yeast
Jaffe, M., Sherlock, G., & Levy, S. F. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.034207 · Cited by 26
Differential paralog divergence modulates genome evolution across yeast species
Sanchez, M. R., Miller, A. W., Liachko, I., Sunshine, A. B., Lynch, B., Huang, M., Alcantara, E., DeSevo, C. G., Pai, D. A., Tucker, C. M., et al. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006585 · Cited by 26
Layers of Cryptic Genetic Variation Underlie a Yeast Complex Trait
Lee, J. T., Coradini, A. L. V., Shen, A., & Ehrenreich, I. M. (2019) · Genetics · doi:10.1534/genetics.119.301907 · Cited by 25
GET pathway mediates transfer of mislocalized tail-anchored proteins from mitochondria to the ER
Matsumoto, S., Ono, S., Shinoda, S., Kakuta, C., Okada, S., Ito, T., Numata, T., & Endo, T. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202104076 · Cited by 25
Usher, J., Balderas‐Hernández, V. E., Quon, P., Gold, N. D., Martin, V. J. J., Mahadevan, R., & Baetz, K. (2011) · G3 Genes Genomes Genetics · doi:10.1534/g3.111.000695 · Cited by 25
Ste24p Mediates Proteolysis of Both Isoprenylated and Non-prenylated Oligopeptides
Hildebrandt, E. R., Arachea, B. T., Wiener, M. C., & Schmidt, W. K. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.718197 · Cited by 25
Krüger, A. V., Jelier, R., Dzyubachyk, O., Zimmerman, T., Meijering, E. H. W., & Lehner, B. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.10.014 · Cited by 24
Chiang, A. W. T., Liu, W., Charusanti, P., & Hwang, M. (2014) · BMC Systems Biology · doi:10.1186/1752-0509-8-4 · Cited by 28
Buchberger, E., Bilen, A., Ayaz, S., Salamanca-Díaz, D. A., Heras, C. M. D. L., Niksic, A., Almudí, I., Torres-Oliva, M., Casares, F., & Posnien, N. (2020) · Molecular Biology and Evolution · doi:10.1093/molbev/msaa335 · Cited by 25
Variance Heterogeneity in Saccharomyces cerevisiae Expression Data: Trans-Regulation and Epistasis
Nelson, R. M., Pettersson, M. E., Li, X., & Carlborg, Ö. (2013) · PLoS ONE · doi:10.1371/journal.pone.0079507 · Cited by 24
Mangiola, S., Young, N. D., Korhonen, P. K., Mondal, A., Scheerlinck, J. Y., Sternberg, P. W., Cantacessi, C., Hall, R. S., Jex, A. R., & Gasser, R. B. (2012) · Biotechnology Advances · doi:10.1016/j.biotechadv.2012.12.004 · Cited by 24
Ueno, K., Saito, M., Nagashima, M., Kojima, A., Nishinoaki, S., Toshima, J. Y., & Toshima, J. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.12.008 · Cited by 24
Turning gold into ‘junk’: transposable elements utilize central proteins of cellular networks
Abrusán, G., Szilágyi, A., Zhang, Y., & Papp, B. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt011 · Cited by 24
Self-citationAntagonistic Gcn5-Hda1 interactions revealed by mutations to the Anaphase Promoting Complex in yeast
Islam, A., Turner, E. L., Menzel, J. E., Malo, M. E., & Harkness, T. A. A. (2011) · Cell Division · doi:10.1186/1747-1028-6-13 · Cited by 24
Requirement of Phosphoinositides Containing Stearic Acid To Control Cell Polarity
Doignon, F., Laquel, P., Testet, E., Tuphile, K., Fouillen, L., & Bessoule, J. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00843-15 · Cited by 24
Simoneau, A., Ricard, É., Weber, S., Hammond-Martel, I., Wong, L. H., Sellam, A., Giaever, G. N., Nislow, C., Raymond, M., & Würtele, H. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1537 · Cited by 24
Self-citationThe chromatin remodeler Chd1 regulates cohesin in budding yeast and humans
Boginya, A., Detroja, R., Matityahu, A., Frenkel‐Morgenstern, M., & Onn, I. (2019) · Scientific Reports · doi:10.1038/s41598-019-45263-3 · Cited by 26
Sun, S., Baryshnikova, A., Brandt, N., & Gresham, D. (2020) · Molecular Systems Biology · doi:10.15252/msb.20199167 · Cited by 25
Self-citationThe ER protein Ema19 facilitates the degradation of nonimported mitochondrial precursor proteins
Laborenz, J., Bykov, Y. S., Knöringer, K., Räschle, M., Filker, S., Prescianotto‐Baschong, C., Spang, A., Tatsuta, T., Langer, T., Štorchová, Z., et al. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-11-0748 · Cited by 24
Molecular network analysis enhances understanding of the biology of mental disorders
Grennan, K. S., Chen, C., Gershon, E. S., & Liu, C. (2014) · BioEssays · doi:10.1002/bies.201300147 · Cited by 24
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