 Steven Reppert
Concepts (196)
Concepts are derived automatically from a person's publications.
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?
|
|---|
| Butterflies | 25 | 2015 | 27 | 10.740 |
Why?
| | Animal Migration | 20 | 2015 | 22 | 8.510 |
Why?
| | Circadian Rhythm | 19 | 2010 | 268 | 4.570 |
Why?
| | Orientation | 10 | 2015 | 29 | 3.660 |
Why?
| | Biological Clocks | 9 | 2010 | 65 | 2.810 |
Why?
| | Flight, Animal | 10 | 2015 | 14 | 2.560 |
Why?
| | Sunlight | 8 | 2015 | 23 | 2.290 |
Why?
| | Flavoproteins | 9 | 2009 | 28 | 2.140 |
Why?
| | Cryptochromes | 13 | 2012 | 34 | 1.950 |
Why?
| | Photoreceptor Cells, Invertebrate | 10 | 2013 | 47 | 1.910 |
Why?
| | Brain | 10 | 2015 | 865 | 1.800 |
Why?
| | Trans-Activators | 11 | 2009 | 282 | 1.680 |
Why?
| | Sensation | 3 | 2015 | 16 | 1.600 |
Why?
| | Light | 7 | 2011 | 194 | 1.470 |
Why?
| | Magnetics | 3 | 2011 | 34 | 1.400 |
Why?
| | Animals | 43 | 2015 | 14790 | 1.340 |
Why?
| | Genome, Insect | 3 | 2015 | 21 | 1.270 |
Why?
| | Insect Proteins | 5 | 2012 | 78 | 1.250 |
Why?
| | Basic Helix-Loop-Helix Transcription Factors | 8 | 2007 | 102 | 1.160 |
Why?
| | Cues | 3 | 2012 | 43 | 1.140 |
Why?
| | Solar System | 5 | 2013 | 5 | 0.930 |
Why?
| | Nuclear Proteins | 8 | 2009 | 690 | 0.860 |
Why?
| | Suprachiasmatic Nucleus | 4 | 2007 | 124 | 0.770 |
Why?
| | Ultraviolet Rays | 3 | 2014 | 108 | 0.760 |
Why?
| | Drosophila Proteins | 6 | 2010 | 628 | 0.760 |
Why?
| | Transcription, Genetic | 5 | 2007 | 786 | 0.760 |
Why?
| | Mutagenesis, Site-Directed | 4 | 2012 | 255 | 0.740 |
Why?
| | Eye Proteins | 4 | 2010 | 86 | 0.730 |
Why?
| | Insects | 3 | 2011 | 25 | 0.710 |
Why?
| | Neuropil | 2 | 2013 | 4 | 0.700 |
Why?
| | Seasons | 3 | 2014 | 94 | 0.690 |
Why?
| | CLOCK Proteins | 9 | 2009 | 37 | 0.680 |
Why?
| | Period Circadian Proteins | 9 | 2012 | 61 | 0.660 |
Why?
| | Drosophila melanogaster | 2 | 2010 | 399 | 0.660 |
Why?
| | Nerve Tissue Proteins | 2 | 2007 | 365 | 0.630 |
Why?
| | Phylogeny | 4 | 2011 | 236 | 0.620 |
Why?
| | Gene Expression Regulation | 6 | 2009 | 1234 | 0.610 |
Why?
| | Behavior, Animal | 3 | 2009 | 137 | 0.590 |
Why?
| | Drosophila | 6 | 2011 | 383 | 0.590 |
Why?
| | Cold Temperature | 1 | 2013 | 28 | 0.580 |
Why?
| | Databases, Genetic | 1 | 2012 | 46 | 0.560 |
Why?
| | Endonucleases | 1 | 2012 | 41 | 0.550 |
Why?
| | Zinc Fingers | 1 | 2012 | 91 | 0.540 |
Why?
| | Expressed Sequence Tags | 2 | 2008 | 18 | 0.500 |
Why?
| | Photochemical Processes | 1 | 2010 | 12 | 0.470 |
Why?
| | Neural Pathways | 2 | 2011 | 65 | 0.460 |
Why?
| | ARNTL Transcription Factors | 6 | 2006 | 23 | 0.430 |
Why?
| | Transcription Factors | 6 | 2009 | 1201 | 0.400 |
Why?
| | Immunohistochemistry | 4 | 2013 | 768 | 0.370 |
Why?
| | Animals, Genetically Modified | 3 | 2012 | 220 | 0.360 |
Why?
| | Liver | 6 | 2009 | 545 | 0.350 |
Why?
| | Receptors, Retinoic Acid | 1 | 2004 | 50 | 0.310 |
Why?
| | Histones | 2 | 2006 | 326 | 0.310 |
Why?
| | Mice | 11 | 2014 | 7428 | 0.300 |
Why?
| | Feedback, Physiological | 4 | 2006 | 53 | 0.300 |
Why?
| | Mice, Knockout | 6 | 2009 | 1615 | 0.290 |
Why?
| | RNA, Messenger | 4 | 2012 | 1252 | 0.290 |
Why?
| | Protein Kinases | 1 | 2004 | 139 | 0.280 |
Why?
| | Mammals | 1 | 2002 | 75 | 0.270 |
Why?
| | Microscopy, Confocal | 2 | 2013 | 196 | 0.270 |
Why?
| | Motor Activity | 3 | 2011 | 304 | 0.250 |
Why?
| | Molecular Sequence Data | 5 | 2011 | 2074 | 0.250 |
Why?
| | Receptors, G-Protein-Coupled | 3 | 2008 | 68 | 0.240 |
Why?
| | DNA-Binding Proteins | 1 | 2006 | 1005 | 0.230 |
Why?
| | Moths | 2 | 2011 | 21 | 0.210 |
Why?
| | Transgenes | 2 | 2010 | 118 | 0.210 |
Why?
| | Mice, Inbred BALB C | 3 | 2006 | 807 | 0.210 |
Why?
| | Retina | 2 | 2011 | 91 | 0.210 |
Why?
| | Cell Line | 3 | 2008 | 1761 | 0.190 |
Why?
| | Protein Structure, Tertiary | 3 | 2004 | 686 | 0.190 |
Why?
| | Promoter Regions, Genetic | 3 | 2006 | 577 | 0.190 |
Why?
| | Binding Sites | 2 | 2012 | 761 | 0.180 |
Why?
| | Models, Biological | 3 | 2007 | 965 | 0.180 |
Why?
| | Amino Acid Sequence | 3 | 2011 | 1515 | 0.170 |
Why?
| | Climate Change | 1 | 2015 | 3 | 0.170 |
Why?
| | Gene Expression | 2 | 2009 | 606 | 0.170 |
Why?
| | Pigmentation | 1 | 2014 | 16 | 0.160 |
Why?
| | Flavins | 2 | 2007 | 21 | 0.160 |
Why?
| | Cell Cycle Proteins | 4 | 2009 | 293 | 0.160 |
Why?
| | Luciferases | 2 | 2005 | 103 | 0.160 |
Why?
| | Environment | 1 | 2015 | 92 | 0.160 |
Why?
| | Base Sequence | 4 | 2009 | 1246 | 0.150 |
Why?
| | Gene Deletion | 2 | 2007 | 241 | 0.150 |
Why?
| | Cloning, Molecular | 3 | 2003 | 369 | 0.150 |
Why?
| | Neurons | 2 | 2013 | 627 | 0.150 |
Why?
| | Evolution, Molecular | 2 | 2007 | 215 | 0.150 |
Why?
| | Synapsins | 1 | 2013 | 5 | 0.150 |
Why?
| | Biotin | 1 | 2013 | 34 | 0.140 |
Why?
| | Receptors, Cytoplasmic and Nuclear | 2 | 2004 | 118 | 0.140 |
Why?
| | Germ-Line Mutation | 1 | 2012 | 32 | 0.140 |
Why?
| | Phosphorylation | 3 | 2004 | 668 | 0.140 |
Why?
| | Computer Simulation | 1 | 2014 | 300 | 0.140 |
Why?
| | Exons | 1 | 2012 | 154 | 0.130 |
Why?
| | Smell | 1 | 2011 | 13 | 0.130 |
Why?
| | Time Factors | 2 | 2010 | 2594 | 0.130 |
Why?
| | Neuropeptides | 1 | 2011 | 75 | 0.130 |
Why?
| | Mutation | 2 | 2008 | 1745 | 0.130 |
Why?
| | Genomics | 1 | 2012 | 151 | 0.130 |
Why?
| | Choice Behavior | 1 | 2011 | 56 | 0.130 |
Why?
| | Imaging, Three-Dimensional | 1 | 2012 | 155 | 0.120 |
Why?
| | Sequence Alignment | 1 | 2011 | 271 | 0.120 |
Why?
| | Databases, Factual | 1 | 2013 | 403 | 0.120 |
Why?
| | Feeding Behavior | 1 | 2013 | 248 | 0.120 |
Why?
| | Phenotype | 3 | 2014 | 788 | 0.120 |
Why?
| | Software | 1 | 2012 | 237 | 0.120 |
Why?
| | Action Potentials | 1 | 2011 | 88 | 0.120 |
Why?
| | Image Processing, Computer-Assisted | 1 | 2013 | 426 | 0.120 |
Why?
| | North America | 2 | 2014 | 79 | 0.120 |
Why?
| | Sense Organs | 1 | 2009 | 1 | 0.120 |
Why?
| | Casein Kinase Idelta | 1 | 2009 | 5 | 0.110 |
Why?
| | Methoprene | 1 | 2009 | 2 | 0.110 |
Why?
| | Juvenile Hormones | 1 | 2009 | 4 | 0.110 |
Why?
| | Protein Binding | 2 | 2004 | 1229 | 0.110 |
Why?
| | Protein Array Analysis | 1 | 2009 | 19 | 0.110 |
Why?
| | Internet | 1 | 2012 | 354 | 0.110 |
Why?
| | Sexual Behavior, Animal | 1 | 2009 | 86 | 0.110 |
Why?
| | DNA, Complementary | 2 | 2005 | 183 | 0.100 |
Why?
| | Microsatellite Repeats | 1 | 2008 | 34 | 0.100 |
Why?
| | Sodium-Potassium-Exchanging ATPase | 1 | 2008 | 24 | 0.100 |
Why?
| | Humans | 5 | 2015 | 33703 | 0.100 |
Why?
| | Male | 5 | 2014 | 17040 | 0.100 |
Why?
| | Anions | 1 | 2007 | 26 | 0.100 |
Why?
| | Bees | 1 | 2007 | 3 | 0.100 |
Why?
| | Beetles | 1 | 2007 | 2 | 0.100 |
Why?
| | Gene Duplication | 1 | 2007 | 30 | 0.100 |
Why?
| | Mice, Transgenic | 2 | 2009 | 952 | 0.090 |
Why?
| | Alleles | 1 | 2008 | 310 | 0.090 |
Why?
| | Female | 5 | 2014 | 18561 | 0.090 |
Why?
| | Genes, Reporter | 1 | 2007 | 191 | 0.090 |
Why?
| | Mice, Inbred C57BL | 3 | 2009 | 2304 | 0.090 |
Why?
| | NIH 3T3 Cells | 1 | 2006 | 87 | 0.090 |
Why?
| | Photic Stimulation | 1 | 2006 | 74 | 0.090 |
Why?
| | Lysine | 1 | 2006 | 64 | 0.090 |
Why?
| | Cells, Cultured | 2 | 2009 | 1808 | 0.090 |
Why?
| | Dimerization | 1 | 2006 | 154 | 0.090 |
Why?
| | Polymorphism, Single Nucleotide | 1 | 2008 | 297 | 0.090 |
Why?
| | Oxidation-Reduction | 2 | 2007 | 224 | 0.090 |
Why?
| | Sequence Homology, Amino Acid | 2 | 2003 | 353 | 0.090 |
Why?
| | Cyclic AMP Response Element-Binding Protein | 2 | 2003 | 40 | 0.090 |
Why?
| | Analysis of Variance | 1 | 2007 | 533 | 0.090 |
Why?
| | Rod Opsins | 1 | 2005 | 4 | 0.090 |
Why?
| | Gene Expression Profiling | 1 | 2008 | 474 | 0.080 |
Why?
| | Blotting, Western | 1 | 2007 | 548 | 0.080 |
Why?
| | Models, Animal | 1 | 2006 | 176 | 0.080 |
Why?
| | United States | 1 | 2014 | 3957 | 0.080 |
Why?
| | In Situ Hybridization | 1 | 2005 | 197 | 0.080 |
Why?
| | Nuclear Receptor Subfamily 1, Group F, Member 1 | 1 | 2004 | 3 | 0.080 |
Why?
| | Hela Cells | 1 | 2006 | 484 | 0.080 |
Why?
| | Transfection | 2 | 2003 | 640 | 0.080 |
Why?
| | Lung | 1 | 2007 | 450 | 0.080 |
Why?
| | Casein Kinases | 1 | 2004 | 2 | 0.080 |
Why?
| | Filtration | 1 | 2004 | 21 | 0.080 |
Why?
| | Polymerase Chain Reaction | 1 | 2005 | 440 | 0.080 |
Why?
| | Darkness | 1 | 2003 | 21 | 0.070 |
Why?
| | Nuclear Localization Signals | 1 | 2003 | 13 | 0.070 |
Why?
| | Microscopy, Electron | 1 | 2004 | 259 | 0.070 |
Why?
| | Immunoassay | 1 | 2003 | 46 | 0.070 |
Why?
| | Acetyltransferases | 1 | 2002 | 35 | 0.070 |
Why?
| | Visual Pathways | 1 | 2002 | 13 | 0.070 |
Why?
| | RNA Polymerase II | 1 | 2002 | 60 | 0.070 |
Why?
| | Plasmids | 1 | 2003 | 247 | 0.070 |
Why?
| | Acetylation | 1 | 2002 | 99 | 0.070 |
Why?
| | Optic Chiasm | 1 | 2002 | 3 | 0.070 |
Why?
| | Photoreceptor Cells, Vertebrate | 1 | 2002 | 20 | 0.070 |
Why?
| | Histone Acetyltransferases | 1 | 2002 | 61 | 0.070 |
Why?
| | Protein Processing, Post-Translational | 1 | 2004 | 175 | 0.070 |
Why?
| | Models, Genetic | 1 | 2003 | 225 | 0.070 |
Why?
| | Transcriptional Activation | 1 | 2003 | 202 | 0.070 |
Why?
| | Active Transport, Cell Nucleus | 1 | 2002 | 84 | 0.070 |
Why?
| | Chromosome Mapping | 1 | 2003 | 246 | 0.070 |
Why?
| | Receptors, Cell Surface | 1 | 2003 | 444 | 0.060 |
Why?
| | DNA | 1 | 2002 | 610 | 0.050 |
Why?
| | Chromatin | 1 | 2002 | 373 | 0.050 |
Why?
| | Saccharomyces cerevisiae Proteins | 1 | 2002 | 378 | 0.050 |
Why?
| | Collagen Type IV | 1 | 2014 | 3 | 0.040 |
Why?
| | Myosin Type V | 1 | 2014 | 11 | 0.040 |
Why?
| | Selection, Genetic | 1 | 2014 | 63 | 0.040 |
Why?
| | Muscles | 1 | 2014 | 142 | 0.040 |
Why?
| | Casein Kinase Iepsilon | 1 | 2009 | 5 | 0.030 |
Why?
| | Half-Life | 1 | 2009 | 55 | 0.030 |
Why?
| | DNA Primers | 1 | 2009 | 301 | 0.030 |
Why?
| | Fibroblasts | 1 | 2009 | 287 | 0.020 |
Why?
| | Photochemistry | 1 | 2007 | 22 | 0.020 |
Why?
| | Receptors, Melatonin | 1 | 2003 | 31 | 0.020 |
Why?
| | Melatonin | 1 | 2003 | 61 | 0.020 |
Why?
| | Mice, Inbred C3H | 1 | 2003 | 171 | 0.020 |
Why?
| | Choriocarcinoma | 1 | 2002 | 5 | 0.020 |
Why?
| | Gene Targeting | 1 | 2003 | 73 | 0.020 |
Why?
| | Uterine Neoplasms | 1 | 2002 | 19 | 0.020 |
Why?
| | Sequence Deletion | 1 | 2002 | 99 | 0.020 |
Why?
| | Rats, Wistar | 1 | 2002 | 155 | 0.020 |
Why?
| | Organ Specificity | 1 | 2002 | 151 | 0.020 |
Why?
| | Mutagenesis | 1 | 2002 | 117 | 0.020 |
Why?
| | Tumor Cells, Cultured | 1 | 2002 | 386 | 0.020 |
Why?
| | Rats | 1 | 2002 | 1778 | 0.010 |
Why?
| | Pregnancy | 1 | 2002 | 1145 | 0.010 |
Why?
|
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Reppert's Networks
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