 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 | 238 | 1.360 |
Why?
| | Loss of Function Mutation | 4 | 2020 | 43 | 1.140 |
Why?
| | Intellectual Disability | 4 | 2021 | 130 | 0.900 |
Why?
| | Retinoblastoma-Binding Protein 4 | 1 | 2022 | 4 | 0.830 |
Why?
| | Zebrafish | 3 | 2022 | 419 | 0.820 |
Why?
| | Haploinsufficiency | 2 | 2021 | 45 | 0.780 |
Why?
| | Fanconi Anemia | 1 | 2021 | 12 | 0.770 |
Why?
| | GTP-Binding Protein beta Subunits | 1 | 2020 | 12 | 0.750 |
Why?
| | Megalencephaly | 1 | 2020 | 16 | 0.750 |
Why?
| | Neural Stem Cells | 1 | 2022 | 115 | 0.740 |
Why?
| | Guanine Nucleotide Exchange Factors | 1 | 2020 | 58 | 0.730 |
Why?
| | Neurodevelopmental Disorders | 5 | 2022 | 115 | 0.720 |
Why?
| | Microcephaly | 1 | 2020 | 54 | 0.710 |
Why?
| | Mitochondrial Myopathies | 1 | 2019 | 5 | 0.710 |
Why?
| | Cytoskeletal Proteins | 1 | 2019 | 146 | 0.660 |
Why?
| | Autistic Disorder | 1 | 2020 | 163 | 0.630 |
Why?
| | Phenotype | 12 | 2021 | 2854 | 0.630 |
Why?
| | Tumor Suppressor Protein p53 | 1 | 2022 | 442 | 0.630 |
Why?
| | Seizures | 1 | 2020 | 344 | 0.590 |
Why?
| | Cell Cycle Proteins | 1 | 2019 | 559 | 0.530 |
Why?
| | Mutation | 9 | 2023 | 3371 | 0.460 |
Why?
| | Pedigree | 5 | 2020 | 470 | 0.450 |
Why?
| | Genetic Association Studies | 4 | 2021 | 349 | 0.380 |
Why?
| | Rare Diseases | 2 | 2019 | 88 | 0.330 |
Why?
| | Abnormalities, Multiple | 2 | 2021 | 176 | 0.330 |
Why?
| | Genetic Predisposition to Disease | 4 | 2021 | 2202 | 0.320 |
Why?
| | DNA Methylation | 3 | 2021 | 505 | 0.320 |
Why?
| | Exome | 3 | 2021 | 208 | 0.260 |
Why?
| | Child, Preschool | 8 | 2021 | 9124 | 0.250 |
Why?
| | Inheritance Patterns | 2 | 2020 | 47 | 0.230 |
Why?
| | Alleles | 3 | 2022 | 812 | 0.220 |
Why?
| | Epigenesis, Genetic | 3 | 2021 | 534 | 0.210 |
Why?
| | Retinitis Pigmentosa | 1 | 2022 | 17 | 0.210 |
Why?
| | Genetic Variation | 3 | 2021 | 888 | 0.200 |
Why?
| | Dystonic Disorders | 1 | 2021 | 17 | 0.200 |
Why?
| | Spectrin | 1 | 2021 | 15 | 0.200 |
Why?
| | CRISPR-Cas Systems | 1 | 2022 | 84 | 0.200 |
Why?
| | Drosophila Proteins | 1 | 2023 | 161 | 0.200 |
Why?
| | Genes, Dominant | 1 | 2021 | 93 | 0.200 |
Why?
| | Fanconi Anemia Complementation Group Proteins | 1 | 2021 | 9 | 0.200 |
Why?
| | Acetylation | 1 | 2022 | 212 | 0.200 |
Why?
| | Ubiquitin-Conjugating Enzymes | 1 | 2021 | 11 | 0.190 |
Why?
| | Epilepsy, Generalized | 1 | 2021 | 14 | 0.190 |
Why?
| | RNA-Binding Proteins | 2 | 2022 | 367 | 0.190 |
Why?
| | Frameshift Mutation | 1 | 2020 | 28 | 0.190 |
Why?
| | Chromosomes, Human, X | 1 | 2021 | 59 | 0.190 |
Why?
| | Heart Septal Defects, Ventricular | 1 | 2021 | 41 | 0.190 |
Why?
| | Chromosome Disorders | 1 | 2021 | 36 | 0.190 |
Why?
| | Craniofacial Abnormalities | 1 | 2021 | 59 | 0.190 |
Why?
| | Chromosomes, Human, Pair 1 | 1 | 2021 | 71 | 0.190 |
Why?
| | Growth Disorders | 1 | 2021 | 80 | 0.190 |
Why?
| | Autism Spectrum Disorder | 2 | 2022 | 320 | 0.180 |
Why?
| | Uridine Diphosphate Glucose Dehydrogenase | 1 | 2020 | 2 | 0.180 |
Why?
| | Adenosine Triphosphatases | 1 | 2021 | 156 | 0.180 |
Why?
| | Histone-Lysine N-Methyltransferase | 1 | 2021 | 98 | 0.180 |
Why?
| | Humans | 20 | 2023 | 115296 | 0.180 |
Why?
| | Nervous System Diseases | 1 | 2023 | 254 | 0.180 |
Why?
| | Interferon Regulatory Factors | 1 | 2020 | 31 | 0.180 |
Why?
| | Heterozygote | 4 | 2022 | 254 | 0.180 |
Why?
| | Mutant Chimeric Proteins | 1 | 2019 | 4 | 0.180 |
Why?
| | Pyrophosphatases | 1 | 2020 | 22 | 0.180 |
Why?
| | Ataxia | 1 | 2019 | 36 | 0.180 |
Why?
| | Genes, Recessive | 1 | 2020 | 73 | 0.170 |
Why?
| | Carotid Intima-Media Thickness | 1 | 2020 | 66 | 0.170 |
Why?
| | Cleft Palate | 1 | 2020 | 46 | 0.170 |
Why?
| | Genetic Diseases, Inborn | 1 | 2019 | 37 | 0.170 |
Why?
| | Oxidoreductases | 1 | 2020 | 89 | 0.170 |
Why?
| | Zebrafish Proteins | 1 | 2022 | 248 | 0.170 |
Why?
| | Cell Cycle | 1 | 2022 | 541 | 0.170 |
Why?
| | Mitochondrial Diseases | 1 | 2019 | 77 | 0.170 |
Why?
| | Muscular Diseases | 1 | 2019 | 104 | 0.170 |
Why?
| | Muscle, Smooth | 1 | 2020 | 155 | 0.170 |
Why?
| | RNA Splicing | 1 | 2020 | 244 | 0.170 |
Why?
| | Mutation, Missense | 1 | 2020 | 294 | 0.160 |
Why?
| | Myosin Heavy Chains | 1 | 2020 | 174 | 0.160 |
Why?
| | Receptors, AMPA | 1 | 2019 | 121 | 0.160 |
Why?
| | HEK293 Cells | 1 | 2020 | 610 | 0.160 |
Why?
| | Phosphoproteins | 1 | 2020 | 297 | 0.150 |
Why?
| | Male | 10 | 2021 | 55796 | 0.150 |
Why?
| | Adolescent | 8 | 2021 | 17767 | 0.140 |
Why?
| | Female | 13 | 2021 | 59772 | 0.140 |
Why?
| | Child | 8 | 2021 | 18435 | 0.130 |
Why?
| | Family | 1 | 2019 | 573 | 0.130 |
Why?
| | Epilepsy | 1 | 2020 | 290 | 0.130 |
Why?
| | Gene Expression | 1 | 2020 | 1451 | 0.130 |
Why?
| | Mitochondria | 1 | 2019 | 756 | 0.120 |
Why?
| | Transcription Factors | 1 | 2022 | 1531 | 0.120 |
Why?
| | DNA-Binding Proteins | 1 | 2021 | 1308 | 0.120 |
Why?
| | Adult | 8 | 2023 | 30576 | 0.110 |
Why?
| | Infant | 6 | 2021 | 7955 | 0.110 |
Why?
| | Apoptosis | 1 | 2022 | 2363 | 0.110 |
Why?
| | Animals | 6 | 2023 | 32090 | 0.100 |
Why?
| | Syndrome | 2 | 2020 | 337 | 0.080 |
Why?
| | Young Adult | 5 | 2021 | 10413 | 0.080 |
Why?
| | Genetic Testing | 2 | 2020 | 381 | 0.070 |
Why?
| | Signal Transduction | 1 | 2020 | 4537 | 0.070 |
Why?
| | Cohort Studies | 3 | 2021 | 4960 | 0.070 |
Why?
| | Drosophila | 1 | 2023 | 133 | 0.050 |
Why?
| | Integrases | 1 | 2022 | 119 | 0.050 |
Why?
| | Status Epilepticus | 1 | 2021 | 35 | 0.050 |
Why?
| | Chromosome Deletion | 1 | 2021 | 94 | 0.050 |
Why?
| | Epilepsies, Myoclonic | 1 | 2021 | 42 | 0.050 |
Why?
| | Infant, Newborn | 2 | 2021 | 5060 | 0.050 |
Why?
| | Gastroparesis | 1 | 2020 | 9 | 0.040 |
Why?
| | Comparative Genomic Hybridization | 1 | 2019 | 28 | 0.040 |
Why?
| | Middle Aged | 4 | 2021 | 26936 | 0.040 |
Why?
| | Intestinal Diseases | 1 | 2020 | 30 | 0.040 |
Why?
| | Esophageal Motility Disorders | 1 | 2020 | 24 | 0.040 |
Why?
| | Phosphoric Diester Hydrolases | 1 | 2020 | 45 | 0.040 |
Why?
| | Age of Onset | 1 | 2021 | 451 | 0.040 |
Why?
| | Organoids | 1 | 2020 | 75 | 0.040 |
Why?
| | DNA Mutational Analysis | 1 | 2020 | 372 | 0.040 |
Why?
| | Protein Domains | 1 | 2020 | 210 | 0.040 |
Why?
| | Endoscopy, Digestive System | 1 | 2020 | 110 | 0.040 |
Why?
| | Workflow | 1 | 2019 | 137 | 0.040 |
Why?
| | Genetic Markers | 1 | 2019 | 339 | 0.040 |
Why?
| | Electromyography | 1 | 2020 | 323 | 0.040 |
Why?
| | Radiography | 1 | 2020 | 825 | 0.040 |
Why?
| | Kinetics | 1 | 2020 | 1549 | 0.030 |
Why?
| | RNA, Messenger | 1 | 2023 | 2579 | 0.030 |
Why?
| | Mice | 2 | 2021 | 15075 | 0.030 |
Why?
| | Age Factors | 1 | 2021 | 2908 | 0.030 |
Why?
| | Case-Control Studies | 1 | 2021 | 3035 | 0.030 |
Why?
| | Mice, Knockout | 1 | 2020 | 2607 | 0.030 |
Why?
| | Genome-Wide Association Study | 1 | 2020 | 1301 | 0.030 |
Why?
| | Polymorphism, Single Nucleotide | 1 | 2020 | 2016 | 0.030 |
Why?
| | Mice, Inbred C57BL | 1 | 2020 | 4770 | 0.020 |
Why?
| | Magnetic Resonance Imaging | 1 | 2019 | 3070 | 0.020 |
Why?
| | Brain | 1 | 2019 | 2371 | 0.020 |
Why?
| | Aged | 1 | 2019 | 19253 | 0.010 |
Why?
|
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Schultz-Rogers's Networks
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