Concepts (145)
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?
|
|---|
| Reflex, Vestibulo-Ocular | 25 | 2008 | 55 | 2.530 |
Why?
|
| Vestibular Nuclei | 21 | 2009 | 28 | 2.180 |
Why?
|
| Saimiri | 35 | 2009 | 48 | 1.660 |
Why?
|
| Head Movements | 12 | 2008 | 41 | 1.520 |
Why?
|
| Movement | 12 | 2009 | 304 | 1.140 |
Why?
|
| Vestibular Nerve | 17 | 2003 | 33 | 1.100 |
Why?
|
| Neurons | 26 | 2008 | 1575 | 1.090 |
Why?
|
| Eye Movements | 20 | 2006 | 119 | 1.080 |
Why?
|
| Vestibule, Labyrinth | 10 | 2008 | 43 | 0.970 |
Why?
|
| Rotation | 14 | 2009 | 90 | 0.800 |
Why?
|
| Fixation, Ocular | 8 | 2004 | 50 | 0.710 |
Why?
|
| Saccades | 12 | 2004 | 75 | 0.700 |
Why?
|
| Cerebellum | 9 | 2006 | 248 | 0.680 |
Why?
|
| Head | 9 | 2004 | 131 | 0.650 |
Why?
|
| Thalamus | 4 | 2009 | 132 | 0.580 |
Why?
|
| Pursuit, Smooth | 8 | 2001 | 31 | 0.570 |
Why?
|
| Semicircular Canals | 6 | 2003 | 29 | 0.550 |
Why?
|
| Wakefulness | 2 | 2009 | 131 | 0.540 |
Why?
|
| Motion Perception | 4 | 2009 | 100 | 0.470 |
Why?
|
| Brain Stem | 12 | 1996 | 163 | 0.440 |
Why?
|
| Distance Perception | 3 | 1999 | 5 | 0.440 |
Why?
|
| Afferent Pathways | 11 | 2009 | 63 | 0.410 |
Why?
|
| Abducens Nerve | 12 | 2006 | 14 | 0.400 |
Why?
|
| Orientation | 3 | 2008 | 111 | 0.380 |
Why?
|
| Animals | 58 | 2009 | 28041 | 0.360 |
Why?
|
| Hypoglossal Nerve | 6 | 2006 | 26 | 0.340 |
Why?
|
| Proprioception | 2 | 2001 | 24 | 0.340 |
Why?
|
| Neck Muscles | 5 | 2000 | 19 | 0.340 |
Why?
|
| Medulla Oblongata | 5 | 2006 | 90 | 0.330 |
Why?
|
| Oculomotor Muscles | 4 | 2006 | 29 | 0.320 |
Why?
|
| Neural Inhibition | 8 | 2001 | 105 | 0.300 |
Why?
|
| Neurons, Afferent | 3 | 2000 | 72 | 0.300 |
Why?
|
| Signal Transduction | 5 | 2008 | 3498 | 0.300 |
Why?
|
| Electric Stimulation | 14 | 2009 | 344 | 0.300 |
Why?
|
| Posture | 5 | 2000 | 123 | 0.290 |
Why?
|
| Sensory Receptor Cells | 1 | 2009 | 37 | 0.280 |
Why?
|
| Purkinje Cells | 7 | 2004 | 86 | 0.280 |
Why?
|
| Midline Thalamic Nuclei | 1 | 2008 | 1 | 0.280 |
Why?
|
| Synaptic Transmission | 8 | 2001 | 223 | 0.270 |
Why?
|
| Cerebellar Cortex | 6 | 2004 | 14 | 0.260 |
Why?
|
| Spinal Cord | 5 | 2000 | 239 | 0.210 |
Why?
|
| Neural Pathways | 12 | 2006 | 324 | 0.210 |
Why?
|
| Cebidae | 3 | 1988 | 4 | 0.200 |
Why?
|
| Otolithic Membrane | 1 | 2003 | 13 | 0.200 |
Why?
|
| Reticular Formation | 7 | 1988 | 17 | 0.190 |
Why?
|
| Motor Neurons | 10 | 1990 | 176 | 0.190 |
Why?
|
| Functional Laterality | 5 | 2009 | 204 | 0.190 |
Why?
|
| Cervical Vertebrae | 2 | 2001 | 228 | 0.180 |
Why?
|
| Action Potentials | 4 | 2009 | 581 | 0.160 |
Why?
|
| Brain Mapping | 8 | 2009 | 570 | 0.150 |
Why?
|
| Pons | 4 | 1987 | 25 | 0.150 |
Why?
|
| Cats | 19 | 1987 | 285 | 0.150 |
Why?
|
| Microelectrodes | 3 | 2008 | 87 | 0.140 |
Why?
|
| Acceleration | 2 | 2009 | 20 | 0.140 |
Why?
|
| Space Perception | 1 | 2000 | 112 | 0.140 |
Why?
|
| Axons | 12 | 1990 | 178 | 0.140 |
Why?
|
| Vestibular Nucleus, Lateral | 1 | 1998 | 1 | 0.140 |
Why?
|
| Convergence, Ocular | 1 | 1998 | 2 | 0.140 |
Why?
|
| Horseradish Peroxidase | 10 | 1988 | 34 | 0.130 |
Why?
|
| Psychomotor Performance | 1 | 2000 | 497 | 0.130 |
Why?
|
| Behavior, Animal | 2 | 2000 | 390 | 0.130 |
Why?
|
| Reflex | 4 | 2000 | 80 | 0.130 |
Why?
|
| Muscimol | 3 | 2000 | 18 | 0.120 |
Why?
|
| Models, Neurological | 3 | 2009 | 408 | 0.120 |
Why?
|
| Photic Stimulation | 4 | 2000 | 509 | 0.120 |
Why?
|
| Physical Stimulation | 2 | 2008 | 54 | 0.100 |
Why?
|
| Electrophysiology | 6 | 2000 | 390 | 0.100 |
Why?
|
| Oculomotor Nerve | 6 | 1988 | 7 | 0.100 |
Why?
|
| Motion | 2 | 2004 | 94 | 0.100 |
Why?
|
| Evoked Potentials | 7 | 1999 | 194 | 0.090 |
Why?
|
| Cerebellar Nuclei | 4 | 1979 | 6 | 0.090 |
Why?
|
| Interneurons | 3 | 1996 | 106 | 0.080 |
Why?
|
| Electrooculography | 2 | 2000 | 21 | 0.080 |
Why?
|
| Sensory Thresholds | 2 | 2000 | 51 | 0.080 |
Why?
|
| Injections | 2 | 2000 | 124 | 0.080 |
Why?
|
| GABA Agonists | 2 | 2000 | 18 | 0.080 |
Why?
|
| Muscles | 2 | 1980 | 184 | 0.070 |
Why?
|
| Superior Colliculi | 2 | 2006 | 25 | 0.070 |
Why?
|
| Ego | 1 | 2008 | 4 | 0.070 |
Why?
|
| Time Factors | 4 | 2003 | 5406 | 0.070 |
Why?
|
| Electrodes, Implanted | 2 | 2000 | 198 | 0.070 |
Why?
|
| Darkness | 1 | 2008 | 47 | 0.070 |
Why?
|
| Restraint, Physical | 2 | 2000 | 31 | 0.060 |
Why?
|
| Ear, Inner | 2 | 1998 | 36 | 0.060 |
Why?
|
| Light | 1 | 2008 | 287 | 0.060 |
Why?
|
| Data Interpretation, Statistical | 1 | 2008 | 306 | 0.060 |
Why?
|
| Neurotransmitter Agents | 1 | 2006 | 102 | 0.060 |
Why?
|
| Reaction Time | 5 | 2000 | 317 | 0.060 |
Why?
|
| Primates | 1 | 2006 | 157 | 0.050 |
Why?
|
| Nitric Oxide | 1 | 2006 | 281 | 0.050 |
Why?
|
| Electromyography | 2 | 1993 | 198 | 0.050 |
Why?
|
| Dendrites | 5 | 1985 | 97 | 0.040 |
Why?
|
| Efferent Pathways | 3 | 1988 | 22 | 0.040 |
Why?
|
| Nystagmus, Physiologic | 2 | 2000 | 13 | 0.040 |
Why?
|
| Macaca mulatta | 1 | 2003 | 448 | 0.040 |
Why?
|
| Nystagmus, Pathologic | 1 | 2000 | 36 | 0.040 |
Why?
|
| Volition | 1 | 2000 | 17 | 0.040 |
Why?
|
| Eye | 1 | 1980 | 109 | 0.040 |
Why?
|
| Neck | 1 | 2000 | 98 | 0.040 |
Why?
|
| Auditory Pathways | 1 | 1999 | 35 | 0.040 |
Why?
|
| Visual Pathways | 2 | 1993 | 152 | 0.040 |
Why?
|
| Regression Analysis | 1 | 2000 | 580 | 0.040 |
Why?
|
| Adaptation, Physiological | 1 | 2001 | 329 | 0.040 |
Why?
|
| Calibration | 1 | 1998 | 107 | 0.030 |
Why?
|
| Olivary Nucleus | 4 | 1985 | 7 | 0.030 |
Why?
|
| Synapses | 4 | 1987 | 274 | 0.030 |
Why?
|
| Motor Activity | 1 | 1999 | 323 | 0.030 |
Why?
|
| Peroxidases | 1 | 1976 | 34 | 0.030 |
Why?
|
| Perception | 1 | 1996 | 179 | 0.030 |
Why?
|
| Evoked Potentials, Visual | 2 | 1993 | 90 | 0.030 |
Why?
|
| Kinesthesis | 1 | 1993 | 15 | 0.030 |
Why?
|
| Dominance, Cerebral | 1 | 1993 | 60 | 0.020 |
Why?
|
| Wheat Germ Agglutinins | 1 | 1988 | 15 | 0.020 |
Why?
|
| Autoradiography | 2 | 1985 | 50 | 0.020 |
Why?
|
| Raphe Nuclei | 1 | 1988 | 37 | 0.020 |
Why?
|
| Electronystagmography | 1 | 1986 | 6 | 0.010 |
Why?
|
| Microinjections | 1 | 1986 | 67 | 0.010 |
Why?
|
| Nissl Bodies | 1 | 1985 | 1 | 0.010 |
Why?
|
| Stereotaxic Techniques | 1 | 1986 | 83 | 0.010 |
Why?
|
| Mesencephalon | 1 | 1985 | 67 | 0.010 |
Why?
|
| Motor Cortex | 1 | 1985 | 209 | 0.010 |
Why?
|
| Rabbits | 1 | 1983 | 613 | 0.010 |
Why?
|
| Substantia Nigra | 1 | 1981 | 27 | 0.010 |
Why?
|
| Neuromuscular Junction | 1 | 1979 | 82 | 0.010 |
Why?
|
| Neural Conduction | 1 | 1978 | 71 | 0.010 |
Why?
|
| Thalamic Nuclei | 1 | 1978 | 32 | 0.010 |
Why?
|
| Humans | 1 | 2006 | 93615 | 0.010 |
Why?
|
| Linear Models | 1 | 1997 | 414 | 0.010 |
Why?
|
| Male | 3 | 1986 | 44578 | 0.010 |
Why?
|
| Septum Pellucidum | 1 | 1973 | 3 | 0.010 |
Why?
|
| Serotonin | 1 | 1973 | 209 | 0.010 |
Why?
|
| Hippocampus | 1 | 1973 | 452 | 0.000 |
Why?
|
| Axonal Transport | 1 | 1981 | 30 | 0.000 |
Why?
|
| Electric Conductivity | 1 | 1981 | 142 | 0.000 |
Why?
|
| Ophthalmic Nerve | 1 | 1980 | 1 | 0.000 |
Why?
|
| Corpus Striatum | 1 | 1981 | 83 | 0.000 |
Why?
|
| Maxillary Nerve | 1 | 1980 | 2 | 0.000 |
Why?
|
| Trigeminal Nerve | 1 | 1980 | 14 | 0.000 |
Why?
|
| Cornea | 1 | 1980 | 55 | 0.000 |
Why?
|
| Facial Nerve | 1 | 1980 | 33 | 0.000 |
Why?
|
| Iontophoresis | 1 | 1979 | 4 | 0.000 |
Why?
|
| Amino Acids | 1 | 1979 | 246 | 0.000 |
Why?
|
| Fenclonine | 1 | 1973 | 2 | 0.000 |
Why?
|
| Septal Nuclei | 1 | 1973 | 10 | 0.000 |
Why?
|
| Stimulation, Chemical | 1 | 1973 | 55 | 0.000 |
Why?
|