Concepts (107)
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?
|
|---|
| Radiosurgery | 3 | 1998 | 66 | 0.390 |
Why?
|
| Radiotherapy Dosage | 3 | 1998 | 125 | 0.310 |
Why?
|
| Psychometrics | 3 | 1999 | 514 | 0.280 |
Why?
|
| Auditory Perception | 2 | 1997 | 89 | 0.270 |
Why?
|
| Particle Accelerators | 2 | 1995 | 10 | 0.260 |
Why?
|
| Cochlea | 3 | 1997 | 169 | 0.260 |
Why?
|
| Computer Simulation | 3 | 1999 | 706 | 0.240 |
Why?
|
| Models, Biological | 4 | 1999 | 981 | 0.240 |
Why?
|
| Physical Stimulation | 1 | 1999 | 67 | 0.170 |
Why?
|
| Models, Theoretical | 3 | 1997 | 384 | 0.160 |
Why?
|
| Therapy, Computer-Assisted | 1 | 1998 | 57 | 0.150 |
Why?
|
| Phantoms, Imaging | 1 | 1998 | 189 | 0.140 |
Why?
|
| Proteins | 1 | 1999 | 474 | 0.130 |
Why?
|
| Acoustics | 1 | 1994 | 20 | 0.120 |
Why?
|
| Psychoacoustics | 1 | 1994 | 33 | 0.120 |
Why?
|
| Drug Therapy, Computer-Assisted | 1 | 1993 | 12 | 0.120 |
Why?
|
| Psychophysics | 3 | 1999 | 30 | 0.120 |
Why?
|
| Delayed-Action Preparations | 1 | 1993 | 120 | 0.110 |
Why?
|
| Biometry | 1 | 1992 | 72 | 0.100 |
Why?
|
| Speech Perception | 1 | 1995 | 261 | 0.100 |
Why?
|
| Neoplasms | 1 | 1998 | 1667 | 0.070 |
Why?
|
| Myocardial Contraction | 2 | 1997 | 383 | 0.060 |
Why?
|
| Binding Sites | 2 | 1999 | 631 | 0.060 |
Why?
|
| Signal Transduction | 1 | 1992 | 2689 | 0.050 |
Why?
|
| Algorithms | 2 | 1999 | 1196 | 0.050 |
Why?
|
| Mathematics | 3 | 1997 | 83 | 0.050 |
Why?
|
| Humans | 10 | 1999 | 68618 | 0.050 |
Why?
|
| Fourier Analysis | 1 | 1999 | 31 | 0.040 |
Why?
|
| Databases as Topic | 1 | 1999 | 49 | 0.040 |
Why?
|
| Crystallization | 1 | 1999 | 57 | 0.040 |
Why?
|
| Protein Structure, Secondary | 1 | 1999 | 136 | 0.040 |
Why?
|
| Complement C1 Inactivator Proteins | 1 | 1998 | 19 | 0.040 |
Why?
|
| Complement C1q | 1 | 1998 | 18 | 0.040 |
Why?
|
| Antibody Affinity | 1 | 1998 | 26 | 0.040 |
Why?
|
| Protein Structure, Tertiary | 1 | 1999 | 322 | 0.040 |
Why?
|
| Physical Phenomena | 1 | 1998 | 10 | 0.040 |
Why?
|
| Physics | 1 | 1998 | 9 | 0.040 |
Why?
|
| Ligands | 1 | 1999 | 317 | 0.040 |
Why?
|
| Automation | 1 | 1998 | 45 | 0.040 |
Why?
|
| Receptors, Cell Surface | 1 | 1999 | 248 | 0.040 |
Why?
|
| Magnetic Resonance Imaging | 2 | 1998 | 2223 | 0.040 |
Why?
|
| Cochlear Microphonic Potentials | 1 | 1997 | 15 | 0.040 |
Why?
|
| Complement Activation | 1 | 1998 | 145 | 0.040 |
Why?
|
| Models, Molecular | 1 | 1999 | 546 | 0.040 |
Why?
|
| Sodium-Potassium-Exchanging ATPase | 1 | 1997 | 72 | 0.040 |
Why?
|
| Tomography, X-Ray Computed | 2 | 1998 | 2324 | 0.040 |
Why?
|
| Auditory Threshold | 1 | 1997 | 206 | 0.040 |
Why?
|
| Protein Binding | 1 | 1999 | 1027 | 0.030 |
Why?
|
| Television | 1 | 1996 | 28 | 0.030 |
Why?
|
| Antibodies, Monoclonal | 1 | 1998 | 511 | 0.030 |
Why?
|
| Stereotaxic Techniques | 1 | 1995 | 35 | 0.030 |
Why?
|
| Audiometry, Pure-Tone | 1 | 1995 | 96 | 0.030 |
Why?
|
| Basilar Membrane | 1 | 1994 | 16 | 0.030 |
Why?
|
| Ear, Middle | 1 | 1994 | 32 | 0.030 |
Why?
|
| Models, Anatomic | 1 | 1994 | 51 | 0.030 |
Why?
|
| Physicians | 1 | 1998 | 324 | 0.030 |
Why?
|
| Hair Cells, Auditory | 1 | 1994 | 60 | 0.030 |
Why?
|
| Ventricular Function, Left | 1 | 1997 | 481 | 0.030 |
Why?
|
| Hearing Loss, Sensorineural | 1 | 1995 | 110 | 0.030 |
Why?
|
| Nonlinear Dynamics | 1 | 1993 | 55 | 0.030 |
Why?
|
| Reproducibility of Results | 1 | 1998 | 2077 | 0.030 |
Why?
|
| Time Factors | 2 | 1997 | 4655 | 0.030 |
Why?
|
| Heart | 1 | 1997 | 850 | 0.030 |
Why?
|
| Image Processing, Computer-Assisted | 1 | 1996 | 689 | 0.030 |
Why?
|
| Interleukin-2 | 1 | 1992 | 133 | 0.020 |
Why?
|
| Longitudinal Studies | 1 | 1995 | 1054 | 0.020 |
Why?
|
| Microscopy | 1 | 1991 | 64 | 0.020 |
Why?
|
| Blood Vessels | 1 | 1991 | 102 | 0.020 |
Why?
|
| Aging | 1 | 1997 | 911 | 0.020 |
Why?
|
| Regression Analysis | 3 | 1997 | 737 | 0.020 |
Why?
|
| Aged | 2 | 1997 | 14862 | 0.020 |
Why?
|
| Lymphocyte Activation | 1 | 1992 | 397 | 0.020 |
Why?
|
| Protein-Tyrosine Kinases | 1 | 1991 | 195 | 0.020 |
Why?
|
| Severity of Illness Index | 1 | 1995 | 1851 | 0.020 |
Why?
|
| Diabetes Mellitus, Experimental | 1 | 1991 | 195 | 0.020 |
Why?
|
| Middle Aged | 2 | 1997 | 21147 | 0.020 |
Why?
|
| T-Lymphocytes | 1 | 1992 | 597 | 0.020 |
Why?
|
| Heart Failure | 1 | 1997 | 1180 | 0.020 |
Why?
|
| Adult | 2 | 1997 | 21403 | 0.020 |
Why?
|
| Models, Cardiovascular | 2 | 1997 | 133 | 0.020 |
Why?
|
| Liver | 1 | 1991 | 1118 | 0.020 |
Why?
|
| Swine | 2 | 1997 | 672 | 0.020 |
Why?
|
| Kinetics | 2 | 1997 | 1047 | 0.010 |
Why?
|
| Animals | 5 | 1998 | 20881 | 0.010 |
Why?
|
| Male | 3 | 1997 | 37321 | 0.010 |
Why?
|
| Enzyme-Linked Immunosorbent Assay | 1 | 1998 | 507 | 0.010 |
Why?
|
| Gerbillinae | 1 | 1997 | 156 | 0.010 |
Why?
|
| Female | 2 | 1997 | 38074 | 0.010 |
Why?
|
| Blotting, Western | 1 | 1998 | 954 | 0.010 |
Why?
|
| Presbycusis | 1 | 1997 | 84 | 0.010 |
Why?
|
| Evaluation Studies as Topic | 1 | 1996 | 219 | 0.010 |
Why?
|
| Cell Separation | 1 | 1996 | 132 | 0.010 |
Why?
|
| Cardiomyopathy, Dilated | 1 | 1996 | 106 | 0.010 |
Why?
|
| Cells, Cultured | 1 | 1997 | 2673 | 0.010 |
Why?
|
| Refractometry | 1 | 1991 | 23 | 0.010 |
Why?
|
| Dithiothreitol | 1 | 1991 | 17 | 0.010 |
Why?
|
| Receptor, Insulin | 1 | 1991 | 71 | 0.010 |
Why?
|
| Rats, Inbred Strains | 1 | 1991 | 532 | 0.010 |
Why?
|
| Substrate Specificity | 1 | 1991 | 234 | 0.010 |
Why?
|
| Histones | 1 | 1991 | 111 | 0.010 |
Why?
|
| Myocardium | 1 | 1996 | 1204 | 0.010 |
Why?
|
| Reference Values | 1 | 1991 | 579 | 0.010 |
Why?
|
| Adenosine Triphosphate | 1 | 1991 | 314 | 0.010 |
Why?
|
| Phosphorylation | 1 | 1991 | 1200 | 0.000 |
Why?
|
| Insulin | 1 | 1991 | 619 | 0.000 |
Why?
|
| Mice | 1 | 1998 | 8474 | 0.000 |
Why?
|
| Rats | 1 | 1991 | 5300 | 0.000 |
Why?
|