Concepts (125)
Concepts are derived automatically from a person's publications.
In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
- Abortion, Habitual
- Adolescent
- Adult
- Alleles
- Amino Acid Sequence
- Amniocentesis
- Aneuploidy
- Attitude to Health
- Autopsy
- Base Sequence
- Biopsy
- Blastocyst
- CADASIL
- Case-Control Studies
- Child
- Child, Preschool
- Chorionic Villi Sampling
- Chromosome Aberrations
- Chromosome Banding
- Chromosomes, Human, Pair 16
- Chromosomes, Human, Pair 3
- Cohort Studies
- Comparative Genomic Hybridization
- Confidentiality
- Congenital Abnormalities
- Connexin 26
- Connexins
- Consent Forms
- Coroners and Medical Examiners
- Data Collection
- Decision Making
- Developmental Disabilities
- Disclosure
- DNA
- DNA Mutational Analysis
- DNA Primers
- DNA-Binding Proteins
- Down Syndrome
- Embryo Transfer
- Ethics, Medical
- Exome
- Exostoses, Multiple Hereditary
- Female
- Gene Dosage
- Gene Frequency
- Genetic Association Studies
- Genetic Counseling
- Genetic Diseases, Inborn
- Genetic Predisposition to Disease
- Genetic Testing
- Genetic Variation
- Genetics, Medical
- Genome, Human
- Genomics
- Genotype
- Germ-Line Mutation
- Gynecology
- Health Knowledge, Attitudes, Practice
- Hearing
- Hearing Loss
- Hearing Loss, Central
- Hearing Loss, Sensorineural
- Heart Defects, Congenital
| - Heart Ventricles
- Heredity
- Heterozygote
- Homozygote
- Humans
- Hypertension, Pulmonary
- Immunohistochemistry
- In Situ Hybridization, Fluorescence
- Infant
- Infant, Newborn
- Infertility, Male
- Karyotyping
- Lung Diseases
- Male
- Maternal Age
- Medical History Taking
- Men
- Microarray Analysis
- Middle Aged
- Mitogen-Activated Protein Kinase Kinases
- Monosomy
- Mosaicism
- Mutation
- Mutation, Missense
- Neoplasms
- Neoplastic Syndromes, Hereditary
- Nuclear Matrix-Associated Proteins
- Nucleic Acid Hybridization
- Obstetrics
- Octamer Transcription Factors
- Oligonucleotide Array Sequence Analysis
- Otorhinolaryngologic Diseases
- Pain
- Patient Satisfaction
- Pedigree
- Phenotype
- Physicians
- Polymorphism, Genetic
- Practice Guidelines as Topic
- Pregnancy
- Pregnancy, Twin
- Preimplantation Diagnosis
- Prenatal Care
- Prenatal Diagnosis
- ras Proteins
- Receptor, Notch3
- Retrospective Studies
- Risk Assessment
- RNA-Binding Proteins
- Ryanodine Receptor Calcium Release Channel
- Sequence Analysis, DNA
- Sickness Impact Profile
- Signal Transduction
- Spermatozoa
- Surveys and Questionnaires
- Syndrome
- Telemedicine
- Translocation, Genetic
- Trisomy
- Ultrasonography
- United States
- Young Adult
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Concepts
(125)
Derived automatically from this person's publications.
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Co-Authors
(37)
People in Profiles who have published with this person.
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Similar People
(60)
People who share similar concepts with this person.
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Same Department
People who are also in this person's primary department.
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Physical Neighbors
People whose addresses are nearby this person.
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