Keyphrases
Expanded Carrier Screening
100%
Carrier Screening
84%
Uptake Rate
70%
Prenatal Diagnosis
64%
Advanced Paternal Age
54%
Noninvasive Prenatal Screening
45%
Single Gene Disorders
44%
Fetus
43%
Genetic Counselors
43%
Reproductive Risk
41%
Genetic Disease
39%
Genetic Counseling
38%
Preimplantation Genetic Diagnosis
37%
Ultrasound Abnormalities
36%
Reproductive Genetics
34%
New Jersey
34%
Diagnostic Performance
34%
Amniocentesis
31%
Retrospective Chart Review
31%
Medicaid
31%
Disease Carriers
27%
Hereditary Hemorrhagic Telangiectasia
27%
Reimbursement
27%
Commercial Insurance
27%
Unexpected Findings
27%
Counselor Perspective
27%
Aneuploidy Testing
27%
Prenatal Ultrasonography
27%
Conservative Management
27%
Fetal Sonography
27%
Payers
27%
Neonatal Diagnosis
27%
Manifesting Carriers
27%
Bardet-Biedl Syndrome
27%
Smith-Lemli-Opitz Syndrome
27%
Second Trimester
27%
Invasive Testing
27%
Male Partner
27%
Prenatal Ultrasound
27%
Trisomy 18
27%
Partner Testing
27%
Syndrome Diagnosis
27%
Fetal Anomalies
27%
Serological Screening
27%
Ashkenazi Jews
27%
Jewish Population
27%
Consanguineous
27%
Pediatric Patients
27%
Exome Sequencing
27%
Androgen Insensitivity Syndrome
27%
Medicine and Dentistry
Fetus Echography
90%
Uptake Rates
82%
Prenatal Diagnosis
64%
Genetic Counseling
61%
Exome Sequencing
54%
Genetic Screening
54%
Prenatal Screening
54%
Paternal Age
54%
Aneuploidy
49%
Counseling
46%
Genetic Disorder
45%
Diagnosis
45%
Single Gene Disorder
45%
Amniocentesis
38%
Diagnostic Testing
35%
Autosomal Recessive Inheritance
34%
Reproductive Genetics
34%
Diseases
34%
Prenatal Diagnostics
32%
Screening Test
27%
Fetus Malformation
27%
Gene Mutation
27%
Outpatient
27%
Conservative Treatment
27%
Bardet-Biedl Syndrome
27%
Hereditary Hemorrhagic Telangiectasia
27%
Pediatrics Patient
27%
Second Trimester Pregnancy
27%
Pathogenicity
27%
Allele
27%
Chromosome Aberration
27%
Androgen Insensitivity Syndrome
27%
Smith-Lemli-Opitz Syndrome
27%
Trisomy 18
27%
Disease Carrier
27%
Odds Ratio
27%
Recurrent Pregnancy Loss
27%
Maternal Age
21%
Pediatrics
19%
Preimplantation Genetic Diagnosis
18%
Observational Study
18%
Disease
17%
Cross Sectional Study
17%
Medicaid Managed Care
16%
Medicare
16%
Carrier Testing
16%
Occupation (Patient Social Context)
13%
Genetic Evaluation
13%
Obstetric Procedure
13%
Heterozygote
13%
