Edibe Nehir Kurtas, 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?
|
|---|
| Translocation, Genetic | 3 | 2018 | 1393 | 0.600 |
Why?
|
| Trisomy | 1 | 2018 | 260 | 0.560 |
Why?
|
| Chromosomes | 1 | 2018 | 578 | 0.500 |
Why?
|
| Chromosome Disorders | 1 | 2018 | 498 | 0.480 |
Why?
|
| Chromosome Aberrations | 1 | 2018 | 1775 | 0.390 |
Why?
|
| Fibroblast Growth Factors | 1 | 2024 | 871 | 0.300 |
Why?
|
| Alleles | 2 | 2024 | 6891 | 0.280 |
Why?
|
| Comparative Genomic Hybridization | 2 | 2018 | 474 | 0.270 |
Why?
|
| Haplotypes | 2 | 2024 | 2726 | 0.170 |
Why?
|
| Arnold-Chiari Malformation | 1 | 2020 | 159 | 0.160 |
Why?
|
| Ring Chromosomes | 1 | 2018 | 26 | 0.150 |
Why?
|
| Genitalia, Female | 1 | 2018 | 146 | 0.140 |
Why?
|
| Chromosomes, Human, Pair 22 | 1 | 2018 | 348 | 0.140 |
Why?
|
| Meiosis | 1 | 2018 | 326 | 0.130 |
Why?
|
| Chromatin Assembly and Disassembly | 1 | 2020 | 632 | 0.130 |
Why?
|
| SOXB1 Transcription Factors | 1 | 2018 | 283 | 0.130 |
Why?
|
| Haploinsufficiency | 1 | 2018 | 334 | 0.130 |
Why?
|
| Maternal Age | 1 | 2018 | 804 | 0.120 |
Why?
|
| Eye Abnormalities | 1 | 2018 | 242 | 0.120 |
Why?
|
| Mosaicism | 1 | 2018 | 481 | 0.120 |
Why?
|
| Genome | 1 | 2022 | 1753 | 0.110 |
Why?
|
| Chromosome Deletion | 1 | 2018 | 1384 | 0.100 |
Why?
|
| In Situ Hybridization, Fluorescence | 1 | 2018 | 2510 | 0.100 |
Why?
|
| Prenatal Diagnosis | 1 | 2018 | 1271 | 0.090 |
Why?
|
| Mutation, Missense | 1 | 2020 | 2589 | 0.090 |
Why?
|
| Chromatin | 1 | 2022 | 2979 | 0.090 |
Why?
|
| Infant | 4 | 2020 | 36426 | 0.080 |
Why?
|
| Cesarean Section | 1 | 2018 | 1418 | 0.080 |
Why?
|
| Nerve Tissue Proteins | 1 | 2018 | 4394 | 0.060 |
Why?
|
| Genetic Loci | 1 | 2024 | 2630 | 0.060 |
Why?
|
| Chromosome Mapping | 2 | 2023 | 4617 | 0.060 |
Why?
|
| Genomics | 1 | 2018 | 5925 | 0.050 |
Why?
|
| Child, Preschool | 3 | 2020 | 42510 | 0.050 |
Why?
|
| Membrane Proteins | 1 | 2018 | 7847 | 0.050 |
Why?
|
| Phenotype | 1 | 2018 | 16714 | 0.040 |
Why?
|
| Pregnancy | 2 | 2023 | 30230 | 0.040 |
Why?
|
| Female | 7 | 2023 | 396141 | 0.040 |
Why?
|
| Genetic Variation | 1 | 2024 | 6612 | 0.040 |
Why?
|
| Pregnancy Trimester, First | 1 | 2023 | 917 | 0.040 |
Why?
|
| Germ Cells | 1 | 2022 | 646 | 0.040 |
Why?
|
| Paraparesis, Spastic | 1 | 2018 | 8 | 0.040 |
Why?
|
| Transcription Factors | 1 | 2018 | 12129 | 0.040 |
Why?
|
| Humans | 9 | 2024 | 765926 | 0.040 |
Why?
|
| Microcephaly | 1 | 2020 | 427 | 0.030 |
Why?
|
| Child | 3 | 2020 | 80568 | 0.030 |
Why?
|
| Adolescent | 3 | 2020 | 88811 | 0.030 |
Why?
|
| Karyotyping | 1 | 2018 | 1175 | 0.030 |
Why?
|
| Ultrasonography, Prenatal | 1 | 2023 | 1772 | 0.030 |
Why?
|
| MAP Kinase Signaling System | 1 | 2020 | 1489 | 0.030 |
Why?
|
| Mutation | 1 | 2018 | 30192 | 0.030 |
Why?
|
| Corpus Callosum | 1 | 2018 | 751 | 0.030 |
Why?
|
| Base Sequence | 1 | 2022 | 12405 | 0.020 |
Why?
|
| Male | 3 | 2020 | 363815 | 0.020 |
Why?
|
| Young Adult | 2 | 2020 | 59857 | 0.010 |
Why?
|
| Infant, Newborn | 1 | 2018 | 26380 | 0.010 |
Why?
|
| Magnetic Resonance Imaging | 1 | 2020 | 36547 | 0.010 |
Why?
|
| Adult | 1 | 2018 | 223088 | 0.000 |
Why?
|