Concepts (64)
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?
|
|---|
| DNA Methylation | 3 | 2019 | 1148 | 1.150 |
Why?
|
| Severe Acute Malnutrition | 1 | 2019 | 21 | 0.640 |
Why?
|
| Uniparental Disomy | 1 | 2019 | 51 | 0.600 |
Why?
|
| Arginine | 1 | 2020 | 351 | 0.560 |
Why?
|
| Fetal Diseases | 1 | 2019 | 462 | 0.460 |
Why?
|
| Autism Spectrum Disorder | 1 | 2020 | 429 | 0.450 |
Why?
|
| Polymorphism, Single Nucleotide | 2 | 2019 | 2949 | 0.400 |
Why?
|
| Sequence Analysis, DNA | 1 | 2019 | 1835 | 0.400 |
Why?
|
| Diabetes Mellitus | 1 | 2019 | 937 | 0.340 |
Why?
|
| CpG Islands | 2 | 2019 | 347 | 0.290 |
Why?
|
| Mouth Mucosa | 2 | 2021 | 53 | 0.210 |
Why?
|
| Megalencephaly | 1 | 2021 | 60 | 0.170 |
Why?
|
| Rare Diseases | 1 | 2022 | 209 | 0.170 |
Why?
|
| Jamaica | 1 | 2019 | 28 | 0.160 |
Why?
|
| Mosaicism | 1 | 2021 | 248 | 0.160 |
Why?
|
| Bias | 1 | 2020 | 147 | 0.160 |
Why?
|
| Epigenomics | 1 | 2019 | 196 | 0.150 |
Why?
|
| Chromosomes, Human, Pair 16 | 1 | 2019 | 150 | 0.150 |
Why?
|
| Malawi | 1 | 2019 | 426 | 0.150 |
Why?
|
| Genomic Imprinting | 1 | 2019 | 130 | 0.140 |
Why?
|
| Microcephaly | 1 | 2021 | 354 | 0.140 |
Why?
|
| Diabetes Complications | 1 | 2019 | 206 | 0.140 |
Why?
|
| Quantitative Trait Loci | 1 | 2019 | 317 | 0.140 |
Why?
|
| Survivors | 1 | 2019 | 358 | 0.130 |
Why?
|
| Exome | 1 | 2021 | 1087 | 0.130 |
Why?
|
| Skin | 1 | 2019 | 545 | 0.120 |
Why?
|
| Infant | 3 | 2021 | 13256 | 0.120 |
Why?
|
| Abnormalities, Multiple | 1 | 2021 | 979 | 0.110 |
Why?
|
| Fibroblasts | 1 | 2019 | 918 | 0.110 |
Why?
|
| Escherichia coli | 1 | 2020 | 1030 | 0.110 |
Why?
|
| Genomics | 1 | 2022 | 1678 | 0.110 |
Why?
|
| Alleles | 1 | 2019 | 1724 | 0.110 |
Why?
|
| Intellectual Disability | 1 | 2021 | 1091 | 0.100 |
Why?
|
| Cells, Cultured | 1 | 2019 | 3180 | 0.100 |
Why?
|
| Gene Expression Profiling | 1 | 2019 | 1922 | 0.100 |
Why?
|
| Case-Control Studies | 1 | 2019 | 3677 | 0.100 |
Why?
|
| Genome-Wide Association Study | 1 | 2019 | 1880 | 0.090 |
Why?
|
| Humans | 7 | 2022 | 134145 | 0.080 |
Why?
|
| Female | 4 | 2021 | 72004 | 0.080 |
Why?
|
| Biomarkers | 1 | 2019 | 3431 | 0.080 |
Why?
|
| Heart Defects, Congenital | 1 | 2021 | 1885 | 0.080 |
Why?
|
| Young Adult | 2 | 2021 | 9960 | 0.070 |
Why?
|
| Prospective Studies | 1 | 2019 | 6610 | 0.070 |
Why?
|
| Child, Preschool | 2 | 2021 | 14895 | 0.070 |
Why?
|
| Pregnancy | 1 | 2019 | 7600 | 0.060 |
Why?
|
| Infant, Newborn | 1 | 2019 | 8636 | 0.060 |
Why?
|
| Retrospective Studies | 2 | 2022 | 17565 | 0.060 |
Why?
|
| Male | 3 | 2021 | 66171 | 0.060 |
Why?
|
| Adolescent | 2 | 2021 | 20643 | 0.060 |
Why?
|
| Homologous Recombination | 1 | 2022 | 100 | 0.050 |
Why?
|
| Adult | 2 | 2021 | 31944 | 0.050 |
Why?
|
| Failure to Thrive | 1 | 2021 | 93 | 0.040 |
Why?
|
| Chromosomes, Human, Pair 1 | 1 | 2021 | 152 | 0.040 |
Why?
|
| Genetic Counseling | 1 | 2021 | 246 | 0.040 |
Why?
|
| Base Sequence | 1 | 2022 | 3180 | 0.040 |
Why?
|
| Chromosome Deletion | 1 | 2021 | 666 | 0.030 |
Why?
|
| Pedigree | 1 | 2021 | 1732 | 0.030 |
Why?
|
| High-Throughput Nucleotide Sequencing | 1 | 2021 | 963 | 0.030 |
Why?
|
| Developmental Disabilities | 1 | 2021 | 742 | 0.030 |
Why?
|
| Seizures | 1 | 2021 | 892 | 0.030 |
Why?
|
| DNA Copy Number Variations | 1 | 2021 | 1036 | 0.030 |
Why?
|
| Parents | 1 | 2021 | 1072 | 0.030 |
Why?
|
| Genetic Testing | 1 | 2021 | 1105 | 0.030 |
Why?
|
| Child | 1 | 2021 | 25911 | 0.010 |
Why?
|