 Laura Schultz-Rogers
Concepts (130)
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?
|
|---|
| Developmental Disabilities | 3 | 2021 | 244 | 1.380 |
Why?
| | Loss of Function Mutation | 4 | 2020 | 43 | 1.160 |
Why?
| | Intellectual Disability | 4 | 2021 | 133 | 0.920 |
Why?
| | Retinoblastoma-Binding Protein 4 | 1 | 2022 | 4 | 0.850 |
Why?
| | Zebrafish | 3 | 2022 | 419 | 0.830 |
Why?
| | Haploinsufficiency | 2 | 2021 | 46 | 0.790 |
Why?
| | Fanconi Anemia | 1 | 2021 | 12 | 0.790 |
Why?
| | GTP-Binding Protein beta Subunits | 1 | 2020 | 13 | 0.760 |
Why?
| | Megalencephaly | 1 | 2020 | 16 | 0.760 |
Why?
| | Neural Stem Cells | 1 | 2022 | 119 | 0.750 |
Why?
| | Guanine Nucleotide Exchange Factors | 1 | 2020 | 59 | 0.740 |
Why?
| | Neurodevelopmental Disorders | 5 | 2022 | 116 | 0.730 |
Why?
| | Microcephaly | 1 | 2020 | 54 | 0.720 |
Why?
| | Mitochondrial Myopathies | 1 | 2019 | 5 | 0.720 |
Why?
| | Cytoskeletal Proteins | 1 | 2019 | 146 | 0.670 |
Why?
| | Autistic Disorder | 1 | 2020 | 165 | 0.640 |
Why?
| | Phenotype | 12 | 2021 | 2916 | 0.640 |
Why?
| | Tumor Suppressor Protein p53 | 1 | 2022 | 442 | 0.630 |
Why?
| | Seizures | 1 | 2020 | 350 | 0.600 |
Why?
| | Cell Cycle Proteins | 1 | 2019 | 563 | 0.540 |
Why?
| | Mutation | 9 | 2023 | 3426 | 0.460 |
Why?
| | Pedigree | 5 | 2020 | 479 | 0.460 |
Why?
| | Genetic Association Studies | 4 | 2021 | 351 | 0.390 |
Why?
| | Rare Diseases | 2 | 2019 | 92 | 0.340 |
Why?
| | Abnormalities, Multiple | 2 | 2021 | 182 | 0.330 |
Why?
| | DNA Methylation | 3 | 2021 | 501 | 0.330 |
Why?
| | Genetic Predisposition to Disease | 4 | 2021 | 2238 | 0.330 |
Why?
| | Exome | 3 | 2021 | 210 | 0.260 |
Why?
| | Child, Preschool | 8 | 2021 | 9442 | 0.250 |
Why?
| | Inheritance Patterns | 2 | 2020 | 47 | 0.230 |
Why?
| | Alleles | 3 | 2022 | 825 | 0.220 |
Why?
| | Epigenesis, Genetic | 3 | 2021 | 537 | 0.220 |
Why?
| | Retinitis Pigmentosa | 1 | 2022 | 18 | 0.210 |
Why?
| | Genetic Variation | 3 | 2021 | 907 | 0.210 |
Why?
| | Dystonic Disorders | 1 | 2021 | 17 | 0.200 |
Why?
| | Spectrin | 1 | 2021 | 15 | 0.200 |
Why?
| | CRISPR-Cas Systems | 1 | 2022 | 86 | 0.200 |
Why?
| | Fanconi Anemia Complementation Group Proteins | 1 | 2021 | 9 | 0.200 |
Why?
| | Genes, Dominant | 1 | 2021 | 96 | 0.200 |
Why?
| | Ubiquitin-Conjugating Enzymes | 1 | 2021 | 11 | 0.200 |
Why?
| | Drosophila Proteins | 1 | 2023 | 171 | 0.200 |
Why?
| | Acetylation | 1 | 2022 | 216 | 0.200 |
Why?
| | Epilepsy, Generalized | 1 | 2021 | 14 | 0.200 |
Why?
| | RNA-Binding Proteins | 2 | 2022 | 369 | 0.190 |
Why?
| | Frameshift Mutation | 1 | 2020 | 28 | 0.190 |
Why?
| | Chromosomes, Human, X | 1 | 2021 | 58 | 0.190 |
Why?
| | Chromosome Disorders | 1 | 2021 | 38 | 0.190 |
Why?
| | Heart Septal Defects, Ventricular | 1 | 2021 | 43 | 0.190 |
Why?
| | Craniofacial Abnormalities | 1 | 2021 | 59 | 0.190 |
Why?
| | Chromosomes, Human, Pair 1 | 1 | 2021 | 72 | 0.190 |
Why?
| | Growth Disorders | 1 | 2021 | 77 | 0.190 |
Why?
| | Autism Spectrum Disorder | 2 | 2022 | 322 | 0.190 |
Why?
| | Uridine Diphosphate Glucose Dehydrogenase | 1 | 2020 | 2 | 0.180 |
Why?
| | Adenosine Triphosphatases | 1 | 2021 | 158 | 0.180 |
Why?
| | Histone-Lysine N-Methyltransferase | 1 | 2021 | 99 | 0.180 |
Why?
| | Interferon Regulatory Factors | 1 | 2020 | 30 | 0.180 |
Why?
| | Humans | 20 | 2023 | 118066 | 0.180 |
Why?
| | Nervous System Diseases | 1 | 2023 | 262 | 0.180 |
Why?
| | Mutant Chimeric Proteins | 1 | 2019 | 4 | 0.180 |
Why?
| | Pyrophosphatases | 1 | 2020 | 22 | 0.180 |
Why?
| | Heterozygote | 4 | 2022 | 258 | 0.180 |
Why?
| | Genes, Recessive | 1 | 2020 | 73 | 0.180 |
Why?
| | Ataxia | 1 | 2019 | 38 | 0.180 |
Why?
| | Carotid Intima-Media Thickness | 1 | 2020 | 68 | 0.180 |
Why?
| | Cleft Palate | 1 | 2020 | 48 | 0.180 |
Why?
| | Genetic Diseases, Inborn | 1 | 2019 | 37 | 0.170 |
Why?
| | Zebrafish Proteins | 1 | 2022 | 249 | 0.170 |
Why?
| | Oxidoreductases | 1 | 2020 | 98 | 0.170 |
Why?
| | Muscle, Smooth | 1 | 2020 | 158 | 0.170 |
Why?
| | Cell Cycle | 1 | 2022 | 546 | 0.170 |
Why?
| | Mitochondrial Diseases | 1 | 2019 | 79 | 0.170 |
Why?
| | Muscular Diseases | 1 | 2019 | 107 | 0.170 |
Why?
| | RNA Splicing | 1 | 2020 | 242 | 0.170 |
Why?
| | Mutation, Missense | 1 | 2020 | 300 | 0.160 |
Why?
| | Myosin Heavy Chains | 1 | 2020 | 192 | 0.160 |
Why?
| | Receptors, AMPA | 1 | 2019 | 125 | 0.160 |
Why?
| | HEK293 Cells | 1 | 2020 | 626 | 0.160 |
Why?
| | Phosphoproteins | 1 | 2020 | 303 | 0.160 |
Why?
| | Male | 11 | 2021 | 57376 | 0.150 |
Why?
| | Adolescent | 8 | 2021 | 18342 | 0.140 |
Why?
| | Female | 13 | 2021 | 61147 | 0.140 |
Why?
| | Family | 1 | 2019 | 569 | 0.140 |
Why?
| | Epilepsy | 1 | 2020 | 293 | 0.130 |
Why?
| | Child | 8 | 2021 | 19029 | 0.130 |
Why?
| | Gene Expression | 1 | 2020 | 1480 | 0.130 |
Why?
| | Transcription Factors | 1 | 2022 | 1567 | 0.120 |
Why?
| | Mitochondria | 1 | 2019 | 785 | 0.120 |
Why?
| | DNA-Binding Proteins | 1 | 2021 | 1343 | 0.120 |
Why?
| | Adult | 8 | 2023 | 31230 | 0.110 |
Why?
| | Infant | 6 | 2021 | 8256 | 0.110 |
Why?
| | Apoptosis | 1 | 2022 | 2453 | 0.110 |
Why?
| | Animals | 6 | 2023 | 33107 | 0.100 |
Why?
| | Syndrome | 2 | 2020 | 343 | 0.080 |
Why?
| | Young Adult | 5 | 2021 | 10707 | 0.080 |
Why?
| | Genetic Testing | 2 | 2020 | 388 | 0.080 |
Why?
| | Signal Transduction | 1 | 2020 | 4677 | 0.070 |
Why?
| | Cohort Studies | 3 | 2021 | 5072 | 0.070 |
Why?
| | Drosophila | 1 | 2023 | 140 | 0.050 |
Why?
| | Integrases | 1 | 2022 | 122 | 0.050 |
Why?
| | Status Epilepticus | 1 | 2021 | 36 | 0.050 |
Why?
| | Chromosome Deletion | 1 | 2021 | 94 | 0.050 |
Why?
| | Epilepsies, Myoclonic | 1 | 2021 | 42 | 0.050 |
Why?
| | Infant, Newborn | 2 | 2021 | 5227 | 0.050 |
Why?
| | Gastroparesis | 1 | 2020 | 10 | 0.050 |
Why?
| | Comparative Genomic Hybridization | 1 | 2019 | 28 | 0.050 |
Why?
| | Intestinal Diseases | 1 | 2020 | 30 | 0.040 |
Why?
| | Esophageal Motility Disorders | 1 | 2020 | 24 | 0.040 |
Why?
| | Middle Aged | 4 | 2021 | 27434 | 0.040 |
Why?
| | Phosphoric Diester Hydrolases | 1 | 2020 | 45 | 0.040 |
Why?
| | Age of Onset | 1 | 2021 | 463 | 0.040 |
Why?
| | Organoids | 1 | 2020 | 75 | 0.040 |
Why?
| | DNA Mutational Analysis | 1 | 2020 | 375 | 0.040 |
Why?
| | Protein Domains | 1 | 2020 | 212 | 0.040 |
Why?
| | Endoscopy, Digestive System | 1 | 2020 | 111 | 0.040 |
Why?
| | Genetic Markers | 1 | 2019 | 338 | 0.040 |
Why?
| | Workflow | 1 | 2019 | 143 | 0.040 |
Why?
| | Electromyography | 1 | 2020 | 326 | 0.040 |
Why?
| | Radiography | 1 | 2020 | 860 | 0.040 |
Why?
| | Kinetics | 1 | 2020 | 1620 | 0.030 |
Why?
| | RNA, Messenger | 1 | 2023 | 2656 | 0.030 |
Why?
| | Mice | 2 | 2021 | 15425 | 0.030 |
Why?
| | Age Factors | 1 | 2021 | 2991 | 0.030 |
Why?
| | Case-Control Studies | 1 | 2021 | 3142 | 0.030 |
Why?
| | Mice, Knockout | 1 | 2020 | 2665 | 0.030 |
Why?
| | Genome-Wide Association Study | 1 | 2020 | 1308 | 0.030 |
Why?
| | Polymorphism, Single Nucleotide | 1 | 2020 | 2046 | 0.030 |
Why?
| | Mice, Inbred C57BL | 1 | 2020 | 4886 | 0.020 |
Why?
| | Magnetic Resonance Imaging | 1 | 2019 | 3160 | 0.020 |
Why?
| | Brain | 1 | 2019 | 2461 | 0.020 |
Why?
| | Aged | 1 | 2019 | 19557 | 0.010 |
Why?
|
|
Schultz-Rogers's Networks
Click the "See All" links for more information and interactive visualizations!
Concepts  Derived automatically from this person's publications. _
Co-Authors People in Profiles who have published with this person. _
Similar People People who share similar concepts with this person. _
Same Department
People who are also in this person's primary department.
|