 Wayne Wahls
Concepts (204)
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 | 28 | 2025 | 60 | 7.310 |
Why?
| | Schizosaccharomyces pombe Proteins | 20 | 2024 | 42 | 5.290 |
Why?
| | Meiosis | 24 | 2024 | 64 | 5.050 |
Why?
| | Recombination, Genetic | 25 | 2024 | 102 | 4.160 |
Why?
| | National Institutes of Health (U.S.) | 4 | 2019 | 44 | 1.930 |
Why?
| | Phosphoproteins | 11 | 2014 | 116 | 1.870 |
Why?
| | Homologous Recombination | 5 | 2025 | 41 | 1.810 |
Why?
| | Research Support as Topic | 3 | 2019 | 45 | 1.790 |
Why?
| | Gene Targeting | 4 | 2025 | 29 | 1.680 |
Why?
| | Activating Transcription Factor 1 | 10 | 2014 | 22 | 1.520 |
Why?
| | Alleles | 5 | 2025 | 252 | 1.380 |
Why?
| | Chromatin Assembly and Disassembly | 3 | 2019 | 23 | 1.310 |
Why?
| | Financing, Government | 2 | 2018 | 23 | 1.140 |
Why?
| | DNA | 10 | 2024 | 534 | 1.080 |
Why?
| | Mutation Rate | 2 | 2019 | 35 | 0.780 |
Why?
| | Base Pairing | 2 | 2019 | 27 | 0.750 |
Why?
| | Nucleotide Motifs | 2 | 2019 | 21 | 0.750 |
Why?
| | RNA, Fungal | 2 | 2013 | 19 | 0.720 |
Why?
| | Gene Expression Regulation, Fungal | 4 | 2013 | 51 | 0.680 |
Why?
| | Chromosome Segregation | 4 | 2010 | 12 | 0.640 |
Why?
| | Genes, Fungal | 9 | 2014 | 31 | 0.640 |
Why?
| | Saccharomyces cerevisiae Proteins | 4 | 2024 | 142 | 0.640 |
Why?
| | MAP Kinase Signaling System | 2 | 2013 | 117 | 0.620 |
Why?
| | Activating Transcription Factors | 6 | 2008 | 8 | 0.610 |
Why?
| | DNA-Binding Proteins | 9 | 2012 | 410 | 0.610 |
Why?
| | Base Sequence | 12 | 2022 | 622 | 0.610 |
Why?
| | DNA, Fungal | 6 | 2024 | 44 | 0.600 |
Why?
| | Biomedical Research | 2 | 2019 | 243 | 0.590 |
Why?
| | Chromosomes, Fungal | 5 | 2008 | 12 | 0.580 |
Why?
| | Research Personnel | 1 | 2018 | 65 | 0.560 |
Why?
| | Saccharomyces cerevisiae | 4 | 2024 | 173 | 0.550 |
Why?
| | Organizational Policy | 1 | 2017 | 39 | 0.550 |
Why?
| | Transcription Factors | 5 | 2022 | 561 | 0.510 |
Why?
| | Genetic Loci | 3 | 2025 | 45 | 0.510 |
Why?
| | Histones | 5 | 2018 | 294 | 0.480 |
Why?
| | Peptide Termination Factors | 1 | 2014 | 2 | 0.470 |
Why?
| | RNA, Transfer | 1 | 2014 | 13 | 0.470 |
Why?
| | Codon, Nonsense | 1 | 2014 | 26 | 0.470 |
Why?
| | Evolution, Molecular | 2 | 2012 | 86 | 0.460 |
Why?
| | Mitogen-Activated Protein Kinases | 2 | 2009 | 154 | 0.450 |
Why?
| | Molecular Sequence Data | 12 | 2010 | 760 | 0.430 |
Why?
| | Mutation | 8 | 2024 | 1275 | 0.420 |
Why?
| | RNA Stability | 1 | 2013 | 22 | 0.420 |
Why?
| | Protein Biosynthesis | 1 | 2014 | 231 | 0.410 |
Why?
| | DNA Helicases | 2 | 2024 | 147 | 0.390 |
Why?
| | Proteome | 3 | 2020 | 161 | 0.380 |
Why?
| | Polymerase Chain Reaction | 5 | 2008 | 447 | 0.340 |
Why?
| | Histone Code | 1 | 2010 | 30 | 0.340 |
Why?
| | Binding Sites | 7 | 2024 | 362 | 0.320 |
Why?
| | DNA, Satellite | 3 | 1998 | 14 | 0.320 |
Why?
| | Plasmids | 3 | 2008 | 159 | 0.320 |
Why?
| | Chromatin | 3 | 2014 | 133 | 0.310 |
Why?
| | Gene Library | 2 | 2008 | 39 | 0.310 |
Why?
| | Genome, Fungal | 2 | 2025 | 28 | 0.310 |
Why?
| | p38 Mitogen-Activated Protein Kinases | 1 | 2009 | 90 | 0.310 |
Why?
| | Models, Genetic | 7 | 2011 | 166 | 0.300 |
Why?
| | Fungal Proteins | 5 | 2018 | 119 | 0.280 |
Why?
| | United States | 4 | 2019 | 5005 | 0.280 |
Why?
| | Genome | 2 | 1998 | 57 | 0.280 |
Why?
| | Genetic Vectors | 3 | 2019 | 128 | 0.250 |
Why?
| | Recombinases | 1 | 2005 | 8 | 0.250 |
Why?
| | Glycine | 1 | 2005 | 78 | 0.240 |
Why?
| | 3',5'-Cyclic-AMP Phosphodiesterases | 1 | 2004 | 5 | 0.230 |
Why?
| | Mutagenesis, Insertional | 1 | 2004 | 21 | 0.230 |
Why?
| | DNA Mutational Analysis | 1 | 2025 | 175 | 0.230 |
Why?
| | Cyclic AMP-Dependent Protein Kinases | 1 | 2004 | 53 | 0.220 |
Why?
| | Amino Acid Sequence | 4 | 2010 | 575 | 0.210 |
Why?
| | Cell Nucleus | 1 | 2024 | 183 | 0.210 |
Why?
| | DNA, Single-Stranded | 3 | 2024 | 88 | 0.210 |
Why?
| | DNA, Mitochondrial | 1 | 2024 | 110 | 0.210 |
Why?
| | G-Quadruplexes | 1 | 2024 | 75 | 0.210 |
Why?
| | Centromere | 2 | 1999 | 13 | 0.200 |
Why?
| | Aneuploidy | 2 | 1999 | 18 | 0.200 |
Why?
| | Regulatory Sequences, Nucleic Acid | 2 | 2010 | 39 | 0.200 |
Why?
| | Genotype | 3 | 2013 | 525 | 0.190 |
Why?
| | Protein Binding | 4 | 2024 | 648 | 0.180 |
Why?
| | Mitochondria | 1 | 2024 | 400 | 0.180 |
Why?
| | Gene Conversion | 2 | 2010 | 3 | 0.170 |
Why?
| | Cloning, Molecular | 4 | 1997 | 190 | 0.170 |
Why?
| | RNA, Messenger | 3 | 2013 | 1085 | 0.170 |
Why?
| | Dimerization | 3 | 2008 | 50 | 0.170 |
Why?
| | Polydeoxyribonucleotides | 2 | 1990 | 5 | 0.170 |
Why?
| | Spores, Fungal | 4 | 2004 | 21 | 0.170 |
Why?
| | Phenotype | 2 | 2019 | 736 | 0.170 |
Why?
| | Mitosis | 3 | 2008 | 87 | 0.160 |
Why?
| | Cultural Diversity | 1 | 2019 | 37 | 0.160 |
Why?
| | Protein Structure, Tertiary | 3 | 2014 | 241 | 0.160 |
Why?
| | Calcium-Calmodulin-Dependent Protein Kinases | 1 | 1998 | 34 | 0.150 |
Why?
| | Minisatellite Repeats | 1 | 1998 | 5 | 0.150 |
Why?
| | Promoter Regions, Genetic | 2 | 2014 | 455 | 0.150 |
Why?
| | Antigens, Viral, Tumor | 1 | 1998 | 6 | 0.150 |
Why?
| | Immunoglobulin Variable Region | 1 | 1998 | 15 | 0.140 |
Why?
| | Nucleic Acid Conformation | 3 | 2013 | 71 | 0.140 |
Why?
| | Transcription, Genetic | 3 | 2014 | 354 | 0.140 |
Why?
| | Vesicular Transport Proteins | 1 | 1997 | 41 | 0.140 |
Why?
| | Proteomics | 1 | 2020 | 313 | 0.140 |
Why?
| | Alcohol Drinking | 1 | 2018 | 228 | 0.130 |
Why?
| | DNA Replication | 2 | 2024 | 155 | 0.130 |
Why?
| | Nuclear Proteins | 1 | 1997 | 235 | 0.130 |
Why?
| | Reproducibility of Results | 1 | 2019 | 1181 | 0.130 |
Why?
| | Ethanol | 1 | 2018 | 336 | 0.120 |
Why?
| | Animals | 8 | 2018 | 13063 | 0.120 |
Why?
| | Simian virus 40 | 2 | 1998 | 14 | 0.120 |
Why?
| | Prions | 1 | 2014 | 3 | 0.120 |
Why?
| | Codon, Terminator | 1 | 2014 | 5 | 0.120 |
Why?
| | Nucleosomes | 1 | 2014 | 11 | 0.120 |
Why?
| | Formate-Tetrahydrofolate Ligase | 1 | 1993 | 1 | 0.110 |
Why?
| | Methylenetetrahydrofolate Dehydrogenase (NADP) | 1 | 1993 | 3 | 0.110 |
Why?
| | Aminohydrolases | 1 | 1993 | 4 | 0.110 |
Why?
| | Multienzyme Complexes | 1 | 1993 | 36 | 0.110 |
Why?
| | RNA | 1 | 1994 | 164 | 0.100 |
Why?
| | Humans | 9 | 2019 | 50419 | 0.100 |
Why?
| | Liver | 1 | 2018 | 1126 | 0.100 |
Why?
| | Escherichia coli | 3 | 2004 | 176 | 0.100 |
Why?
| | DNA Damage | 2 | 2008 | 299 | 0.100 |
Why?
| | Selection, Genetic | 1 | 2011 | 22 | 0.090 |
Why?
| | DNA Topoisomerases, Type II | 1 | 2010 | 15 | 0.090 |
Why?
| | Mutagenesis, Site-Directed | 1 | 2010 | 96 | 0.090 |
Why?
| | Chromosome Mapping | 3 | 1999 | 143 | 0.090 |
Why?
| | Chromatography, Gel | 2 | 2004 | 39 | 0.090 |
Why?
| | Archaeal Proteins | 1 | 2010 | 15 | 0.090 |
Why?
| | DNA Breaks, Double-Stranded | 1 | 2010 | 65 | 0.090 |
Why?
| | Antigens, Polyomavirus Transforming | 1 | 1990 | 9 | 0.080 |
Why?
| | Sequence Homology, Amino Acid | 2 | 2008 | 141 | 0.080 |
Why?
| | Homeostasis | 1 | 2010 | 203 | 0.080 |
Why?
| | Genetic Variation | 1 | 1990 | 197 | 0.080 |
Why?
| | Genetic Code | 1 | 2008 | 3 | 0.080 |
Why?
| | Chromosome Breakage | 1 | 2008 | 14 | 0.080 |
Why?
| | Gene Dosage | 1 | 2008 | 73 | 0.070 |
Why?
| | Osmotic Pressure | 1 | 2008 | 11 | 0.070 |
Why?
| | Amino Acid Motifs | 1 | 2008 | 55 | 0.070 |
Why?
| | Conserved Sequence | 1 | 2008 | 52 | 0.070 |
Why?
| | Stress, Physiological | 1 | 2009 | 171 | 0.070 |
Why?
| | Mutagenesis | 1 | 2008 | 58 | 0.070 |
Why?
| | Phosphorylation | 1 | 2009 | 520 | 0.070 |
Why?
| | Transformation, Genetic | 2 | 2004 | 18 | 0.070 |
Why?
| | Mass Spectrometry | 2 | 2020 | 285 | 0.060 |
Why?
| | Models, Biological | 1 | 2009 | 717 | 0.060 |
Why?
| | Crossing Over, Genetic | 1 | 2005 | 7 | 0.060 |
Why?
| | Transfection | 3 | 1990 | 353 | 0.060 |
Why?
| | Mutation, Missense | 1 | 2005 | 103 | 0.060 |
Why?
| | Tandem Repeat Sequences | 1 | 2004 | 7 | 0.060 |
Why?
| | Protein Folding | 1 | 2004 | 45 | 0.060 |
Why?
| | Hydrolysis | 1 | 2024 | 64 | 0.060 |
Why?
| | Cell Separation | 1 | 2004 | 92 | 0.060 |
Why?
| | Cyclic AMP | 1 | 2004 | 90 | 0.060 |
Why?
| | Nitrogen | 1 | 2004 | 69 | 0.060 |
Why?
| | Transcriptional Activation | 1 | 2004 | 120 | 0.060 |
Why?
| | Crystallography, X-Ray | 1 | 2024 | 145 | 0.060 |
Why?
| | Genomic Instability | 1 | 2024 | 90 | 0.050 |
Why?
| | Reverse Transcriptase Polymerase Chain Reaction | 1 | 2004 | 568 | 0.050 |
Why?
| | Recombinant Proteins | 1 | 2004 | 477 | 0.050 |
Why?
| | Chromatography, Ion Exchange | 2 | 1994 | 15 | 0.050 |
Why?
| | Adenosine Triphosphate | 1 | 2024 | 230 | 0.050 |
Why?
| | Models, Molecular | 1 | 2024 | 333 | 0.050 |
Why?
| | Chromatography, Affinity | 2 | 1994 | 39 | 0.050 |
Why?
| | Cell Line | 3 | 1990 | 997 | 0.050 |
Why?
| | Acetylation | 2 | 2018 | 94 | 0.050 |
Why?
| | Kinetics | 2 | 1994 | 634 | 0.050 |
Why?
| | Oligodeoxyribonucleotides | 2 | 1994 | 33 | 0.050 |
Why?
| | Flow Cytometry | 1 | 2004 | 472 | 0.050 |
Why?
| | Heat-Shock Response | 1 | 2020 | 25 | 0.040 |
Why?
| | Nondisjunction, Genetic | 1 | 1999 | 1 | 0.040 |
Why?
| | Genes, Essential | 1 | 1999 | 10 | 0.040 |
Why?
| | Sequence Homology, Nucleic Acid | 1 | 1999 | 43 | 0.040 |
Why?
| | Epistasis, Genetic | 1 | 1999 | 29 | 0.040 |
Why?
| | Heterozygote | 1 | 1999 | 83 | 0.040 |
Why?
| | Genetic Markers | 1 | 1999 | 104 | 0.040 |
Why?
| | Osmosis | 1 | 1998 | 5 | 0.040 |
Why?
| | Time Factors | 1 | 2005 | 2933 | 0.040 |
Why?
| | DNA Footprinting | 1 | 1998 | 9 | 0.040 |
Why?
| | Chromatography, Liquid | 1 | 2020 | 231 | 0.040 |
Why?
| | Urinary Bladder Neoplasms | 2 | 1990 | 158 | 0.040 |
Why?
| | COS Cells | 1 | 1998 | 73 | 0.040 |
Why?
| | Mice | 2 | 2018 | 5659 | 0.040 |
Why?
| | Signal Transduction | 1 | 2004 | 1608 | 0.040 |
Why?
| | Endopeptidases | 1 | 1997 | 64 | 0.040 |
Why?
| | RNA-Binding Proteins | 1 | 1997 | 116 | 0.030 |
Why?
| | Clostridium | 1 | 1993 | 17 | 0.030 |
Why?
| | Binding, Competitive | 1 | 1993 | 93 | 0.030 |
Why?
| | Carbon | 1 | 1993 | 54 | 0.030 |
Why?
| | Species Specificity | 1 | 1993 | 182 | 0.030 |
Why?
| | Protein Processing, Post-Translational | 1 | 2014 | 155 | 0.030 |
Why?
| | Mice, Inbred C57BL | 1 | 2018 | 1796 | 0.030 |
Why?
| | Nucleic Acid Hybridization | 1 | 1991 | 56 | 0.020 |
Why?
| | Electrophoresis, Polyacrylamide Gel | 1 | 1991 | 98 | 0.020 |
Why?
| | HeLa Cells | 1 | 1991 | 257 | 0.020 |
Why?
| | Viral Structural Proteins | 1 | 1990 | 4 | 0.020 |
Why?
| | Restriction Mapping | 1 | 1990 | 33 | 0.020 |
Why?
| | Cell Fusion | 1 | 1990 | 18 | 0.020 |
Why?
| | Genes, Viral | 1 | 1990 | 38 | 0.020 |
Why?
| | Repetitive Sequences, Nucleic Acid | 1 | 1990 | 89 | 0.020 |
Why?
| | Chromosome Deletion | 1 | 1990 | 134 | 0.020 |
Why?
| | Acetyltransferases | 1 | 2004 | 19 | 0.010 |
Why?
| | Sequence Alignment | 1 | 2004 | 115 | 0.010 |
Why?
| | Gene Deletion | 1 | 2004 | 260 | 0.010 |
Why?
| | Male | 1 | 2018 | 25866 | 0.010 |
Why?
| | Electrophoresis, Agar Gel | 1 | 1997 | 11 | 0.010 |
Why?
| | Blotting, Southern | 1 | 1997 | 41 | 0.010 |
Why?
| | Genetic Complementation Test | 1 | 1997 | 47 | 0.010 |
Why?
| | Blotting, Northern | 1 | 1997 | 109 | 0.010 |
Why?
| | Introns | 1 | 1997 | 49 | 0.010 |
Why?
| | Sequence Deletion | 1 | 1997 | 66 | 0.010 |
Why?
| | Sequence Analysis, DNA | 1 | 1997 | 194 | 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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Same Department
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