Concepts (60)
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?
|
|---|
| Pharmacogenetics | 3 | 2022 | 184 | 0.510 |
Why?
|
| Genomics | 5 | 2025 | 1501 | 0.400 |
Why?
|
| Population Health | 2 | 2024 | 37 | 0.400 |
Why?
|
| Klebsiella pneumoniae | 1 | 2025 | 76 | 0.230 |
Why?
|
| Genome, Bacterial | 1 | 2025 | 186 | 0.220 |
Why?
|
| Genetic Loci | 1 | 2025 | 339 | 0.210 |
Why?
|
| Cytochrome P-450 CYP2D6 | 1 | 2022 | 31 | 0.190 |
Why?
|
| Whole Genome Sequencing | 2 | 2022 | 281 | 0.170 |
Why?
|
| Software | 2 | 2022 | 683 | 0.170 |
Why?
|
| Bacterial Proteins | 1 | 2025 | 888 | 0.160 |
Why?
|
| Clinical Protocols | 1 | 2020 | 239 | 0.150 |
Why?
|
| Genetic Variation | 1 | 2025 | 1501 | 0.150 |
Why?
|
| Chromosomes, Human, Pair 17 | 1 | 2019 | 369 | 0.130 |
Why?
|
| Duodenal Neoplasms | 1 | 2016 | 20 | 0.130 |
Why?
|
| Proto-Oncogene Proteins c-ets | 1 | 2016 | 58 | 0.120 |
Why?
|
| Sequence Analysis, DNA | 2 | 2019 | 1758 | 0.120 |
Why?
|
| Wnt Signaling Pathway | 1 | 2016 | 190 | 0.110 |
Why?
|
| Mutation | 2 | 2019 | 5846 | 0.110 |
Why?
|
| Genetic Predisposition to Disease | 1 | 2024 | 3156 | 0.100 |
Why?
|
| Base Sequence | 3 | 2022 | 3102 | 0.080 |
Why?
|
| Pancreatic Neoplasms | 1 | 2016 | 691 | 0.080 |
Why?
|
| Adenocarcinoma | 1 | 2016 | 1026 | 0.080 |
Why?
|
| DNA-Binding Proteins | 1 | 2016 | 2047 | 0.070 |
Why?
|
| Humans | 10 | 2025 | 125037 | 0.070 |
Why?
|
| Transcription Factors | 1 | 2016 | 2588 | 0.060 |
Why?
|
| Klebsiella Infections | 1 | 2025 | 54 | 0.060 |
Why?
|
| Virulence | 1 | 2025 | 263 | 0.060 |
Why?
|
| Virulence Factors | 1 | 2025 | 173 | 0.050 |
Why?
|
| Genome, Human | 2 | 2019 | 1274 | 0.050 |
Why?
|
| Vertebrates | 1 | 2021 | 41 | 0.040 |
Why?
|
| Genome, Viral | 1 | 2021 | 168 | 0.040 |
Why?
|
| Academic Medical Centers | 1 | 2022 | 308 | 0.040 |
Why?
|
| Chromosome Breakpoints | 1 | 2019 | 80 | 0.040 |
Why?
|
| INDEL Mutation | 1 | 2019 | 87 | 0.040 |
Why?
|
| Chromosome Duplication | 1 | 2019 | 147 | 0.040 |
Why?
|
| Smith-Magenis Syndrome | 1 | 2019 | 105 | 0.040 |
Why?
|
| Genomic Structural Variation | 1 | 2019 | 86 | 0.040 |
Why?
|
| United States | 2 | 2024 | 10909 | 0.040 |
Why?
|
| Recombination, Genetic | 1 | 2019 | 448 | 0.030 |
Why?
|
| Gene Rearrangement | 1 | 2019 | 320 | 0.030 |
Why?
|
| DNA Replication | 1 | 2019 | 352 | 0.030 |
Why?
|
| Chromosome Disorders | 1 | 2019 | 311 | 0.030 |
Why?
|
| Precision Medicine | 1 | 2020 | 319 | 0.030 |
Why?
|
| Ampulla of Vater | 1 | 2016 | 16 | 0.030 |
Why?
|
| Genotype | 1 | 2022 | 2561 | 0.030 |
Why?
|
| Models, Genetic | 1 | 2019 | 760 | 0.030 |
Why?
|
| DNA Repair | 1 | 2019 | 585 | 0.030 |
Why?
|
| Microsatellite Repeats | 1 | 2016 | 221 | 0.030 |
Why?
|
| Chromosome Mapping | 1 | 2017 | 1080 | 0.030 |
Why?
|
| Genomic Instability | 1 | 2016 | 229 | 0.030 |
Why?
|
| DNA Copy Number Variations | 1 | 2019 | 950 | 0.030 |
Why?
|
| Abnormalities, Multiple | 1 | 2019 | 959 | 0.030 |
Why?
|
| Exome | 1 | 2017 | 1033 | 0.030 |
Why?
|
| High-Throughput Nucleotide Sequencing | 1 | 2017 | 881 | 0.020 |
Why?
|
| Molecular Sequence Data | 1 | 2016 | 3892 | 0.020 |
Why?
|
| Cohort Studies | 1 | 2020 | 4812 | 0.020 |
Why?
|
| Polymorphism, Single Nucleotide | 1 | 2019 | 2633 | 0.020 |
Why?
|
| Animals | 1 | 2021 | 34206 | 0.010 |
Why?
|
| Male | 1 | 2020 | 61439 | 0.010 |
Why?
|
| Female | 1 | 2020 | 66721 | 0.010 |
Why?
|