Sarah Louise Stenton, M.B.,Ch.B., Ph.D.
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?
|
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Mitochondrial Diseases | 11 | 2024 | 343 | 3.100 |
Why?
|
Leigh Disease | 5 | 2024 | 89 | 3.060 |
Why?
|
Optic Atrophy, Hereditary, Leber | 3 | 2024 | 50 | 1.730 |
Why?
|
Molecular Diagnostic Techniques | 2 | 2020 | 611 | 0.930 |
Why?
|
Rare Diseases | 3 | 2024 | 621 | 0.820 |
Why?
|
HSP40 Heat-Shock Proteins | 1 | 2021 | 82 | 0.730 |
Why?
|
Electron Transport Complex I | 2 | 2024 | 153 | 0.730 |
Why?
|
Optic Atrophy | 1 | 2021 | 79 | 0.700 |
Why?
|
Genome, Mitochondrial | 1 | 2018 | 66 | 0.600 |
Why?
|
Metabolism, Inborn Errors | 1 | 2019 | 286 | 0.560 |
Why?
|
Genome, Human | 4 | 2024 | 4425 | 0.510 |
Why?
|
Neurodegenerative Diseases | 2 | 2022 | 1087 | 0.510 |
Why?
|
Systems Biology | 1 | 2019 | 481 | 0.500 |
Why?
|
Computational Biology | 2 | 2024 | 3517 | 0.500 |
Why?
|
Mutation, Missense | 1 | 2024 | 2571 | 0.490 |
Why?
|
Mutation | 11 | 2024 | 30045 | 0.430 |
Why?
|
Genetic Association Studies | 2 | 2022 | 2734 | 0.390 |
Why?
|
DNA, Mitochondrial | 3 | 2024 | 865 | 0.300 |
Why?
|
Nephrotic Syndrome | 2 | 2022 | 391 | 0.300 |
Why?
|
Muscular Diseases | 2 | 2024 | 553 | 0.290 |
Why?
|
RNA, Small Nuclear | 1 | 2024 | 75 | 0.230 |
Why?
|
Ubiquinone | 2 | 2022 | 183 | 0.230 |
Why?
|
Optic Atrophies, Hereditary | 1 | 2022 | 27 | 0.210 |
Why?
|
Genes, Recessive | 2 | 2021 | 628 | 0.190 |
Why?
|
Phenotype | 4 | 2024 | 16606 | 0.190 |
Why?
|
Dystonia | 1 | 2024 | 370 | 0.180 |
Why?
|
High-Throughput Nucleotide Sequencing | 2 | 2023 | 3639 | 0.170 |
Why?
|
Penetrance | 1 | 2021 | 388 | 0.160 |
Why?
|
Genetic Variation | 2 | 2024 | 6581 | 0.160 |
Why?
|
Gene Knockout Techniques | 1 | 2021 | 802 | 0.150 |
Why?
|
Protein Subunits | 1 | 2021 | 943 | 0.140 |
Why?
|
Gene Frequency | 1 | 2024 | 3647 | 0.140 |
Why?
|
Membrane Transport Proteins | 1 | 2022 | 1035 | 0.130 |
Why?
|
Pedigree | 2 | 2021 | 4589 | 0.130 |
Why?
|
Homozygote | 1 | 2021 | 1796 | 0.130 |
Why?
|
Spasms, Infantile | 1 | 2019 | 298 | 0.130 |
Why?
|
Humans | 26 | 2024 | 761423 | 0.130 |
Why?
|
NAD | 1 | 2020 | 614 | 0.130 |
Why?
|
Early Diagnosis | 1 | 2020 | 1186 | 0.120 |
Why?
|
Child | 8 | 2024 | 80162 | 0.120 |
Why?
|
Sequence Analysis, RNA | 2 | 2022 | 2020 | 0.120 |
Why?
|
Epigenomics | 1 | 2019 | 942 | 0.110 |
Why?
|
Metabolomics | 2 | 2021 | 1657 | 0.110 |
Why?
|
Reactive Oxygen Species | 1 | 2021 | 2141 | 0.110 |
Why?
|
Zebrafish | 1 | 2024 | 3007 | 0.100 |
Why?
|
RNA | 1 | 2022 | 2723 | 0.100 |
Why?
|
Autophagy | 1 | 2019 | 1326 | 0.100 |
Why?
|
Mitochondria | 2 | 2022 | 3623 | 0.090 |
Why?
|
Genetic Predisposition to Disease | 2 | 2024 | 17912 | 0.090 |
Why?
|
Software | 1 | 2024 | 4434 | 0.090 |
Why?
|
Ataxia | 2 | 2022 | 306 | 0.090 |
Why?
|
Child, Preschool | 5 | 2024 | 42254 | 0.080 |
Why?
|
Proteomics | 2 | 2021 | 3845 | 0.080 |
Why?
|
Adaptor Proteins, Signal Transducing | 1 | 2019 | 2898 | 0.080 |
Why?
|
Muscle Weakness | 2 | 2022 | 412 | 0.080 |
Why?
|
Hospitals | 1 | 2022 | 3882 | 0.080 |
Why?
|
Steroids | 2 | 2022 | 929 | 0.070 |
Why?
|
Genomics | 2 | 2021 | 5820 | 0.070 |
Why?
|
Cell Line | 1 | 2021 | 15605 | 0.070 |
Why?
|
Nerve Tissue Proteins | 1 | 2019 | 4414 | 0.070 |
Why?
|
Genome-Wide Association Study | 1 | 2024 | 12688 | 0.060 |
Why?
|
NADH Dehydrogenase | 1 | 2024 | 47 | 0.060 |
Why?
|
Adolescent | 5 | 2024 | 88313 | 0.060 |
Why?
|
Young Adult | 4 | 2024 | 59207 | 0.060 |
Why?
|
Spliceosomes | 1 | 2024 | 130 | 0.060 |
Why?
|
Male | 9 | 2024 | 360736 | 0.050 |
Why?
|
Gene Expression Profiling | 1 | 2019 | 9418 | 0.050 |
Why?
|
RNA Splice Sites | 1 | 2024 | 211 | 0.050 |
Why?
|
Electron Transport Complex IV | 1 | 2022 | 190 | 0.050 |
Why?
|
Adult | 5 | 2024 | 221148 | 0.050 |
Why?
|
Alleles | 2 | 2024 | 6922 | 0.050 |
Why?
|
Female | 8 | 2024 | 392581 | 0.050 |
Why?
|
Genetic Testing | 2 | 2024 | 3538 | 0.050 |
Why?
|
Acyl-CoA Dehydrogenase | 1 | 2020 | 57 | 0.040 |
Why?
|
Movement Disorders | 1 | 2024 | 459 | 0.040 |
Why?
|
Hydro-Lyases | 1 | 2020 | 94 | 0.040 |
Why?
|
Genetic Diseases, Inborn | 1 | 2024 | 605 | 0.040 |
Why?
|
Proteinuria | 1 | 2022 | 607 | 0.040 |
Why?
|
Metalloendopeptidases | 1 | 2020 | 393 | 0.040 |
Why?
|
Syndrome | 1 | 2024 | 3268 | 0.040 |
Why?
|
Heterozygote | 1 | 2024 | 2803 | 0.040 |
Why?
|
Brain | 2 | 2024 | 27107 | 0.030 |
Why?
|
DNA Copy Number Variations | 1 | 2024 | 2020 | 0.030 |
Why?
|
Lysosomes | 1 | 2019 | 923 | 0.030 |
Why?
|
Sequence Analysis, DNA | 1 | 2024 | 4741 | 0.030 |
Why?
|
Databases, Genetic | 1 | 2020 | 1742 | 0.030 |
Why?
|
Gene Expression Regulation, Developmental | 1 | 2024 | 3612 | 0.030 |
Why?
|
Cohort Studies | 2 | 2024 | 41446 | 0.020 |
Why?
|
Middle Aged | 2 | 2024 | 220826 | 0.020 |
Why?
|
Infant | 2 | 2024 | 36205 | 0.020 |
Why?
|
Dietary Supplements | 1 | 2022 | 3414 | 0.020 |
Why?
|
Genotype | 1 | 2023 | 13009 | 0.020 |
Why?
|
Muscle, Skeletal | 1 | 2024 | 4946 | 0.020 |
Why?
|
Kidney | 1 | 2022 | 7049 | 0.020 |
Why?
|
Polymorphism, Single Nucleotide | 1 | 2024 | 15941 | 0.010 |
Why?
|
Electroencephalography | 1 | 2019 | 6224 | 0.010 |
Why?
|
Disease Progression | 1 | 2019 | 13502 | 0.010 |
Why?
|
Animals | 2 | 2024 | 168441 | 0.010 |
Why?
|
Magnetic Resonance Imaging | 1 | 2019 | 36423 | 0.010 |
Why?
|