Concepts (129)
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?
|
|---|
| Genetic Counseling | 8 | 2024 | 236 | 0.830 |
Why?
|
| Prenatal Diagnosis | 8 | 2024 | 646 | 0.680 |
Why?
|
| Telemedicine | 1 | 2024 | 511 | 0.520 |
Why?
|
| Otorhinolaryngologic Diseases | 1 | 2011 | 13 | 0.340 |
Why?
|
| Medical History Taking | 1 | 2011 | 109 | 0.330 |
Why?
|
| Nucleic Acid Hybridization | 2 | 2008 | 296 | 0.320 |
Why?
|
| Genetic Testing | 5 | 2018 | 1086 | 0.310 |
Why?
|
| Genomics | 3 | 2022 | 1619 | 0.250 |
Why?
|
| Late Onset Disorders | 1 | 2025 | 6 | 0.230 |
Why?
|
| Mutation | 6 | 2025 | 6129 | 0.230 |
Why?
|
| Ornithine Carbamoyltransferase | 1 | 2025 | 23 | 0.230 |
Why?
|
| Ornithine Carbamoyltransferase Deficiency Disease | 1 | 2025 | 42 | 0.230 |
Why?
|
| Exostoses, Multiple Hereditary | 1 | 2005 | 14 | 0.230 |
Why?
|
| Sickness Impact Profile | 1 | 2005 | 37 | 0.220 |
Why?
|
| CADASIL | 1 | 2024 | 7 | 0.220 |
Why?
|
| Oligonucleotide Array Sequence Analysis | 1 | 2008 | 1004 | 0.220 |
Why?
|
| Trisomy | 2 | 2022 | 112 | 0.210 |
Why?
|
| Aneuploidy | 3 | 2022 | 138 | 0.190 |
Why?
|
| Pain | 1 | 2005 | 428 | 0.180 |
Why?
|
| Genetics, Medical | 1 | 2022 | 120 | 0.180 |
Why?
|
| Pregnancy | 9 | 2024 | 7423 | 0.170 |
Why?
|
| Patient Satisfaction | 1 | 2024 | 451 | 0.160 |
Why?
|
| Down Syndrome | 1 | 2022 | 234 | 0.150 |
Why?
|
| Mitogen-Activated Protein Kinase Kinases | 1 | 2019 | 89 | 0.150 |
Why?
|
| DNA | 3 | 2017 | 1411 | 0.150 |
Why?
|
| Translocation, Genetic | 1 | 2021 | 348 | 0.150 |
Why?
|
| ras Proteins | 1 | 2019 | 146 | 0.150 |
Why?
|
| Heterozygote | 2 | 2019 | 721 | 0.130 |
Why?
|
| Pedigree | 3 | 2024 | 1683 | 0.130 |
Why?
|
| Congenital Abnormalities | 1 | 2021 | 323 | 0.130 |
Why?
|
| Connexins | 2 | 2008 | 64 | 0.130 |
Why?
|
| Heart Defects, Congenital | 2 | 2021 | 1878 | 0.130 |
Why?
|
| Homozygote | 1 | 2019 | 540 | 0.130 |
Why?
|
| Octamer Transcription Factors | 1 | 2016 | 9 | 0.120 |
Why?
|
| Nuclear Matrix-Associated Proteins | 1 | 2016 | 18 | 0.120 |
Why?
|
| Ryanodine Receptor Calcium Release Channel | 1 | 2019 | 241 | 0.120 |
Why?
|
| Attitude to Health | 1 | 2018 | 244 | 0.120 |
Why?
|
| Pregnancy, Twin | 1 | 2018 | 191 | 0.120 |
Why?
|
| Men | 1 | 2016 | 7 | 0.120 |
Why?
|
| Abortion, Habitual | 1 | 2016 | 15 | 0.120 |
Why?
|
| Autopsy | 1 | 2016 | 116 | 0.120 |
Why?
|
| Hearing Loss, Central | 1 | 2015 | 3 | 0.120 |
Why?
|
| Genetic Diseases, Inborn | 1 | 2019 | 470 | 0.110 |
Why?
|
| Prenatal Care | 1 | 2018 | 339 | 0.110 |
Why?
|
| Hearing | 1 | 2015 | 58 | 0.110 |
Why?
|
| Humans | 23 | 2025 | 130403 | 0.110 |
Why?
|
| Obstetrics | 1 | 2017 | 240 | 0.110 |
Why?
|
| Spermatozoa | 1 | 2016 | 254 | 0.100 |
Why?
|
| Female | 14 | 2025 | 70343 | 0.100 |
Why?
|
| Genetic Variation | 2 | 2019 | 1557 | 0.100 |
Why?
|
| Hearing Loss | 1 | 2015 | 203 | 0.100 |
Why?
|
| Infertility, Male | 1 | 2016 | 295 | 0.100 |
Why?
|
| Genotype | 3 | 2015 | 2607 | 0.100 |
Why?
|
| RNA-Binding Proteins | 1 | 2016 | 541 | 0.090 |
Why?
|
| Genetic Predisposition to Disease | 3 | 2019 | 3410 | 0.090 |
Why?
|
| Polymorphism, Genetic | 1 | 2015 | 775 | 0.090 |
Why?
|
| Chromosome Aberrations | 2 | 2022 | 575 | 0.090 |
Why?
|
| Heart Ventricles | 1 | 2016 | 757 | 0.090 |
Why?
|
| Adult | 9 | 2025 | 31125 | 0.090 |
Why?
|
| Heredity | 1 | 2011 | 15 | 0.090 |
Why?
|
| Preimplantation Diagnosis | 1 | 2010 | 25 | 0.080 |
Why?
|
| Practice Guidelines as Topic | 1 | 2017 | 1292 | 0.080 |
Why?
|
| In Situ Hybridization, Fluorescence | 2 | 2016 | 752 | 0.080 |
Why?
|
| Gene Dosage | 2 | 2009 | 439 | 0.080 |
Why?
|
| Microarray Analysis | 2 | 2009 | 224 | 0.080 |
Why?
|
| Neoplastic Syndromes, Hereditary | 1 | 2010 | 84 | 0.080 |
Why?
|
| Phenotype | 2 | 2019 | 4475 | 0.070 |
Why?
|
| Infant | 5 | 2024 | 13276 | 0.070 |
Why?
|
| Male | 11 | 2025 | 64486 | 0.070 |
Why?
|
| Comparative Genomic Hybridization | 1 | 2009 | 569 | 0.060 |
Why?
|
| Monosomy | 1 | 2006 | 25 | 0.060 |
Why?
|
| Karyotyping | 2 | 2021 | 312 | 0.060 |
Why?
|
| Blastocyst | 1 | 2006 | 72 | 0.060 |
Why?
|
| Hearing Loss, Sensorineural | 1 | 2006 | 155 | 0.060 |
Why?
|
| Receptor, Notch3 | 1 | 2024 | 12 | 0.050 |
Why?
|
| Genome, Human | 1 | 2011 | 1322 | 0.050 |
Why?
|
| Health Knowledge, Attitudes, Practice | 1 | 2010 | 906 | 0.050 |
Why?
|
| Physicians | 1 | 2010 | 634 | 0.050 |
Why?
|
| Base Sequence | 3 | 2015 | 2753 | 0.050 |
Why?
|
| Risk Assessment | 1 | 2011 | 3692 | 0.040 |
Why?
|
| Chromosomes, Human, Pair 16 | 1 | 2021 | 148 | 0.040 |
Why?
|
| Middle Aged | 4 | 2025 | 28395 | 0.040 |
Why?
|
| Biopsy | 2 | 2019 | 1239 | 0.040 |
Why?
|
| Child, Preschool | 3 | 2016 | 14982 | 0.040 |
Why?
|
| Child | 4 | 2021 | 26159 | 0.040 |
Why?
|
| Mosaicism | 1 | 2021 | 251 | 0.040 |
Why?
|
| Connexin 26 | 2 | 2008 | 13 | 0.030 |
Why?
|
| Germ-Line Mutation | 1 | 2019 | 372 | 0.030 |
Why?
|
| Lung Diseases | 1 | 2021 | 401 | 0.030 |
Why?
|
| Consent Forms | 1 | 2016 | 22 | 0.030 |
Why?
|
| Coroners and Medical Examiners | 1 | 2016 | 15 | 0.030 |
Why?
|
| Hypertension, Pulmonary | 1 | 2021 | 450 | 0.030 |
Why?
|
| Retrospective Studies | 3 | 2025 | 17633 | 0.030 |
Why?
|
| Gynecology | 1 | 2017 | 127 | 0.030 |
Why?
|
| Sequence Analysis, DNA | 2 | 2015 | 1723 | 0.030 |
Why?
|
| Confidentiality | 1 | 2016 | 105 | 0.030 |
Why?
|
| Disclosure | 1 | 2016 | 150 | 0.030 |
Why?
|
| Immunohistochemistry | 1 | 2019 | 1605 | 0.030 |
Why?
|
| Genetic Association Studies | 1 | 2019 | 823 | 0.030 |
Why?
|
| Ultrasonography | 1 | 2019 | 967 | 0.030 |
Why?
|
| Young Adult | 2 | 2019 | 9974 | 0.030 |
Why?
|
| Ethics, Medical | 1 | 2016 | 398 | 0.020 |
Why?
|
| Adolescent | 2 | 2018 | 20731 | 0.020 |
Why?
|
| Syndrome | 1 | 2015 | 1160 | 0.020 |
Why?
|
| Exome | 1 | 2016 | 1075 | 0.020 |
Why?
|
| Developmental Disabilities | 1 | 2016 | 773 | 0.020 |
Why?
|
| Case-Control Studies | 2 | 2008 | 3408 | 0.020 |
Why?
|
| Chorionic Villi Sampling | 1 | 2009 | 43 | 0.020 |
Why?
|
| Data Collection | 1 | 2010 | 366 | 0.020 |
Why?
|
| Amniocentesis | 1 | 2009 | 77 | 0.020 |
Why?
|
| DNA-Binding Proteins | 1 | 2016 | 1949 | 0.020 |
Why?
|
| Surveys and Questionnaires | 1 | 2018 | 4015 | 0.020 |
Why?
|
| Signal Transduction | 1 | 2019 | 4649 | 0.020 |
Why?
|
| DNA Primers | 1 | 2008 | 604 | 0.020 |
Why?
|
| Aged | 1 | 2025 | 20899 | 0.020 |
Why?
|
| United States | 1 | 2022 | 11826 | 0.020 |
Why?
|
| Chromosome Banding | 1 | 2006 | 135 | 0.020 |
Why?
|
| Chromosomes, Human, Pair 3 | 1 | 2006 | 91 | 0.020 |
Why?
|
| Embryo Transfer | 1 | 2006 | 43 | 0.010 |
Why?
|
| Maternal Age | 1 | 2006 | 133 | 0.010 |
Why?
|
| Gene Frequency | 1 | 2006 | 738 | 0.010 |
Why?
|
| DNA Mutational Analysis | 1 | 2006 | 788 | 0.010 |
Why?
|
| Infant, Newborn | 1 | 2016 | 8525 | 0.010 |
Why?
|
| Neoplasms | 1 | 2018 | 2946 | 0.010 |
Why?
|
| Amino Acid Sequence | 1 | 2006 | 2397 | 0.010 |
Why?
|
| Mutation, Missense | 1 | 2006 | 931 | 0.010 |
Why?
|
| Alleles | 1 | 2006 | 1672 | 0.010 |
Why?
|
| Decision Making | 1 | 2006 | 687 | 0.010 |
Why?
|
| Cohort Studies | 1 | 2006 | 5084 | 0.010 |
Why?
|