 Wayne Wahls
Concepts (145)
Concept scores are derived automatically based on a person's publications. Keywords in the their attributed publications are matched to keywords from the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). The strength of a person's concept scores is based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the topic.Concepts cannot be directly edited. You can help ensure your concepts are accurate by making sure your attributed publications are correct and up-to-date. We recommend checking over your attributed publications list every three to four months.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Schizosaccharomyces | 19 | 2025 | 48 | 6.640 |
Why?
| | Schizosaccharomyces pombe Proteins | 14 | 2024 | 34 | 4.700 |
Why?
| | Meiosis | 16 | 2024 | 56 | 4.460 |
Why?
| | Recombination, Genetic | 13 | 2024 | 96 | 3.140 |
Why?
| | National Institutes of Health (U.S.) | 4 | 2019 | 46 | 2.020 |
Why?
| | Homologous Recombination | 5 | 2025 | 41 | 1.900 |
Why?
| | Research Support as Topic | 3 | 2019 | 46 | 1.870 |
Why?
| | Gene Targeting | 3 | 2025 | 30 | 1.590 |
Why?
| | Alleles | 4 | 2025 | 250 | 1.420 |
Why?
| | Phosphoproteins | 6 | 2014 | 108 | 1.380 |
Why?
| | Chromatin Assembly and Disassembly | 3 | 2019 | 25 | 1.370 |
Why?
| | Activating Transcription Factor 1 | 6 | 2014 | 18 | 1.280 |
Why?
| | Financing, Government | 2 | 2018 | 23 | 1.190 |
Why?
| | DNA | 6 | 2024 | 542 | 0.850 |
Why?
| | Mutation Rate | 2 | 2019 | 36 | 0.810 |
Why?
| | Base Pairing | 2 | 2019 | 27 | 0.790 |
Why?
| | Nucleotide Motifs | 2 | 2019 | 24 | 0.780 |
Why?
| | RNA, Fungal | 2 | 2013 | 21 | 0.750 |
Why?
| | Gene Expression Regulation, Fungal | 2 | 2013 | 52 | 0.670 |
Why?
| | MAP Kinase Signaling System | 2 | 2013 | 118 | 0.650 |
Why?
| | Biomedical Research | 2 | 2019 | 237 | 0.620 |
Why?
| | Research Personnel | 1 | 2018 | 65 | 0.580 |
Why?
| | Organizational Policy | 1 | 2017 | 39 | 0.570 |
Why?
| | Saccharomyces cerevisiae | 3 | 2024 | 189 | 0.540 |
Why?
| | Genetic Loci | 3 | 2025 | 48 | 0.530 |
Why?
| | Saccharomyces cerevisiae Proteins | 3 | 2024 | 154 | 0.530 |
Why?
| | Peptide Termination Factors | 1 | 2014 | 2 | 0.500 |
Why?
| | Histones | 5 | 2018 | 313 | 0.490 |
Why?
| | RNA, Transfer | 1 | 2014 | 16 | 0.490 |
Why?
| | Codon, Nonsense | 1 | 2014 | 26 | 0.490 |
Why?
| | DNA, Fungal | 4 | 2024 | 41 | 0.470 |
Why?
| | Evolution, Molecular | 2 | 2012 | 99 | 0.470 |
Why?
| | Base Sequence | 4 | 2022 | 644 | 0.450 |
Why?
| | RNA Stability | 1 | 2013 | 24 | 0.440 |
Why?
| | Protein Biosynthesis | 1 | 2014 | 254 | 0.420 |
Why?
| | DNA Helicases | 2 | 2024 | 144 | 0.410 |
Why?
| | Chromosomes, Fungal | 3 | 2008 | 12 | 0.400 |
Why?
| | Proteome | 3 | 2020 | 174 | 0.400 |
Why?
| | Mutation | 6 | 2024 | 1296 | 0.380 |
Why?
| | Histone Code | 1 | 2010 | 32 | 0.350 |
Why?
| | Chromosome Segregation | 2 | 2010 | 10 | 0.330 |
Why?
| | Activating Transcription Factors | 2 | 2008 | 5 | 0.330 |
Why?
| | Chromatin | 3 | 2014 | 152 | 0.320 |
Why?
| | Genome, Fungal | 2 | 2025 | 39 | 0.320 |
Why?
| | p38 Mitogen-Activated Protein Kinases | 1 | 2009 | 96 | 0.320 |
Why?
| | Gene Library | 1 | 2008 | 43 | 0.320 |
Why?
| | Mitogen-Activated Protein Kinases | 1 | 2009 | 155 | 0.320 |
Why?
| | Plasmids | 1 | 2008 | 163 | 0.300 |
Why?
| | Molecular Sequence Data | 5 | 2010 | 793 | 0.290 |
Why?
| | Transcription Factors | 3 | 2022 | 564 | 0.290 |
Why?
| | United States | 4 | 2019 | 4887 | 0.290 |
Why?
| | Binding Sites | 5 | 2024 | 375 | 0.270 |
Why?
| | Recombinases | 1 | 2005 | 9 | 0.260 |
Why?
| | Glycine | 1 | 2005 | 75 | 0.250 |
Why?
| | 3',5'-Cyclic-AMP Phosphodiesterases | 1 | 2004 | 6 | 0.240 |
Why?
| | Genetic Vectors | 2 | 2019 | 125 | 0.240 |
Why?
| | Mutagenesis, Insertional | 1 | 2004 | 24 | 0.240 |
Why?
| | DNA Mutational Analysis | 1 | 2025 | 176 | 0.240 |
Why?
| | Cyclic AMP-Dependent Protein Kinases | 1 | 2004 | 51 | 0.240 |
Why?
| | Amino Acid Sequence | 4 | 2010 | 587 | 0.220 |
Why?
| | Cell Nucleus | 1 | 2024 | 188 | 0.220 |
Why?
| | DNA, Mitochondrial | 1 | 2024 | 113 | 0.220 |
Why?
| | G-Quadruplexes | 1 | 2024 | 80 | 0.220 |
Why?
| | Models, Genetic | 3 | 2011 | 170 | 0.210 |
Why?
| | Mitochondria | 1 | 2024 | 404 | 0.180 |
Why?
| | Cultural Diversity | 1 | 2019 | 38 | 0.160 |
Why?
| | Protein Structure, Tertiary | 3 | 2014 | 253 | 0.160 |
Why?
| | Protein Binding | 3 | 2024 | 668 | 0.160 |
Why?
| | Genotype | 2 | 2013 | 533 | 0.160 |
Why?
| | Promoter Regions, Genetic | 2 | 2014 | 475 | 0.150 |
Why?
| | DNA-Binding Proteins | 3 | 2012 | 428 | 0.150 |
Why?
| | RNA, Messenger | 2 | 2013 | 1108 | 0.150 |
Why?
| | Fungal Proteins | 1 | 2018 | 123 | 0.150 |
Why?
| | Proteomics | 1 | 2020 | 327 | 0.140 |
Why?
| | Phenotype | 1 | 2019 | 732 | 0.140 |
Why?
| | Dimerization | 2 | 2008 | 50 | 0.140 |
Why?
| | Alcohol Drinking | 1 | 2018 | 225 | 0.140 |
Why?
| | Mitosis | 2 | 2008 | 93 | 0.130 |
Why?
| | Reproducibility of Results | 1 | 2019 | 1189 | 0.130 |
Why?
| | Ethanol | 1 | 2018 | 341 | 0.130 |
Why?
| | Codon, Terminator | 1 | 2014 | 8 | 0.120 |
Why?
| | Prions | 1 | 2014 | 7 | 0.120 |
Why?
| | Nucleosomes | 1 | 2014 | 13 | 0.120 |
Why?
| | DNA, Single-Stranded | 2 | 2024 | 88 | 0.110 |
Why?
| | Nucleic Acid Conformation | 1 | 2013 | 83 | 0.110 |
Why?
| | Transcription, Genetic | 1 | 2014 | 370 | 0.110 |
Why?
| | Genes, Fungal | 3 | 2014 | 29 | 0.100 |
Why?
| | Liver | 1 | 2018 | 1119 | 0.100 |
Why?
| | Selection, Genetic | 1 | 2011 | 23 | 0.100 |
Why?
| | Gene Conversion | 1 | 2010 | 2 | 0.090 |
Why?
| | DNA Topoisomerases, Type II | 1 | 2010 | 16 | 0.090 |
Why?
| | Archaeal Proteins | 1 | 2010 | 15 | 0.090 |
Why?
| | Mutagenesis, Site-Directed | 1 | 2010 | 99 | 0.090 |
Why?
| | DNA Breaks, Double-Stranded | 1 | 2010 | 72 | 0.090 |
Why?
| | Regulatory Sequences, Nucleic Acid | 1 | 2010 | 40 | 0.090 |
Why?
| | Humans | 4 | 2019 | 50251 | 0.080 |
Why?
| | Homeostasis | 1 | 2010 | 201 | 0.080 |
Why?
| | Genetic Code | 1 | 2008 | 4 | 0.080 |
Why?
| | Chromosome Breakage | 1 | 2008 | 16 | 0.080 |
Why?
| | Gene Dosage | 1 | 2008 | 78 | 0.080 |
Why?
| | Osmotic Pressure | 1 | 2008 | 11 | 0.080 |
Why?
| | Animals | 3 | 2018 | 13285 | 0.080 |
Why?
| | Amino Acid Motifs | 1 | 2008 | 58 | 0.080 |
Why?
| | Conserved Sequence | 1 | 2008 | 56 | 0.080 |
Why?
| | Stress, Physiological | 1 | 2009 | 174 | 0.080 |
Why?
| | Mutagenesis | 1 | 2008 | 60 | 0.080 |
Why?
| | Sequence Homology, Amino Acid | 1 | 2008 | 144 | 0.080 |
Why?
| | Phosphorylation | 1 | 2009 | 534 | 0.070 |
Why?
| | Polymerase Chain Reaction | 1 | 2008 | 455 | 0.070 |
Why?
| | DNA Damage | 1 | 2008 | 301 | 0.070 |
Why?
| | Mass Spectrometry | 2 | 2020 | 302 | 0.070 |
Why?
| | Models, Biological | 1 | 2009 | 726 | 0.070 |
Why?
| | Crossing Over, Genetic | 1 | 2005 | 8 | 0.060 |
Why?
| | Chromatography, Gel | 1 | 2004 | 38 | 0.060 |
Why?
| | Mutation, Missense | 1 | 2005 | 106 | 0.060 |
Why?
| | Tandem Repeat Sequences | 1 | 2004 | 7 | 0.060 |
Why?
| | Transformation, Genetic | 1 | 2004 | 16 | 0.060 |
Why?
| | Protein Folding | 1 | 2004 | 49 | 0.060 |
Why?
| | Spores, Fungal | 1 | 2004 | 17 | 0.060 |
Why?
| | Hydrolysis | 1 | 2024 | 62 | 0.060 |
Why?
| | Cell Separation | 1 | 2004 | 90 | 0.060 |
Why?
| | Cyclic AMP | 1 | 2004 | 92 | 0.060 |
Why?
| | Nitrogen | 1 | 2004 | 68 | 0.060 |
Why?
| | Transcriptional Activation | 1 | 2004 | 121 | 0.060 |
Why?
| | Crystallography, X-Ray | 1 | 2024 | 150 | 0.060 |
Why?
| | Genomic Instability | 1 | 2024 | 93 | 0.060 |
Why?
| | Escherichia coli | 1 | 2004 | 189 | 0.060 |
Why?
| | DNA Replication | 1 | 2024 | 152 | 0.050 |
Why?
| | Recombinant Proteins | 1 | 2004 | 489 | 0.050 |
Why?
| | Reverse Transcriptase Polymerase Chain Reaction | 1 | 2004 | 594 | 0.050 |
Why?
| | Adenosine Triphosphate | 1 | 2024 | 234 | 0.050 |
Why?
| | Models, Molecular | 1 | 2024 | 342 | 0.050 |
Why?
| | Acetylation | 2 | 2018 | 97 | 0.050 |
Why?
| | Flow Cytometry | 1 | 2004 | 478 | 0.050 |
Why?
| | Heat-Shock Response | 1 | 2020 | 28 | 0.040 |
Why?
| | Time Factors | 1 | 2005 | 2911 | 0.040 |
Why?
| | Chromatography, Liquid | 1 | 2020 | 224 | 0.040 |
Why?
| | Signal Transduction | 1 | 2004 | 1624 | 0.040 |
Why?
| | Protein Processing, Post-Translational | 1 | 2014 | 170 | 0.030 |
Why?
| | Mice, Inbred C57BL | 1 | 2018 | 1823 | 0.030 |
Why?
| | Mice | 1 | 2018 | 5770 | 0.020 |
Why?
| | Acetyltransferases | 1 | 2004 | 19 | 0.010 |
Why?
| | Sequence Alignment | 1 | 2004 | 121 | 0.010 |
Why?
| | Gene Deletion | 1 | 2004 | 270 | 0.010 |
Why?
| | Male | 1 | 2018 | 25483 | 0.010 |
Why?
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Concepts  Derived automatically based on a person's publications. Keywords from attributed publications are matched to keywords from the MeSH. _
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