Changing trends in carrier screening for genetic disease in the United States

Expanded Carrier Screening in Reproductive Medicine—Points to Consider

(2015) Janice G. Edwards et al.   OBSTETRICS AND GYNECOLOGY

Validation for Clinical Use of, and Initial Clinical Experience with, a Novel Approach to Population-Based Carrier Screening using High-Throughput, Next-Generation DNA Sequencing

(2014) Stephanie Hallam et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Trends in Office-Based Care for Reproductive-Aged Women According to Physician Specialty: A Ten-Year Study

(2014) Stephen M. Petterson et al.   JOURNAL OF WOMENS HEALTH

Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels

(2014) Gabriel A. Lazarin et al.   PLoS One

Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing

(2013) Peter Benn et al.   PRENATAL DIAGNOSIS

Next-generation DNA sequencing ofHEXA: a step in the right direction for carrier screening

(2013) Jodi D. Hoffman et al.   Molecular Genetics & Genomic Medicine

An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals

(2012) Gabriel A. Lazarin et al.   GENETICS IN MEDICINE

A re-examination of the use of ethnicity in prenatal carrier testing

(2011) Lainie Friedman Ross   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Cystic Fibrosis Carrier Screening in Obstetric Clinical Practice: Knowledge, Practices, and Barriers, a Decade After Publication of Screening Guidelines

(2011) Diana Darcy et al.   Genetic Testing and Molecular Biomarkers

Secretary's Advisory Committee on Heritable Disorders in Newborns and Children response to the President's Council on Bioethics report: The changing moral focus of newborn screening

(2011) Tracy L Trotter et al.   GENETICS IN MEDICINE

Technical standards and guidelines for spinal muscular atrophy testing

(2011) Thomas W Prior et al.   GENETICS IN MEDICINE

Looking ahead, looking behind

(2011) James P Evans   GENETICS IN MEDICINE

Committee Opinion No. 483: Primary and Preventive Care: Periodic Assessments

(2011)   OBSTETRICS AND GYNECOLOGY

Committee Opinion No. 486: Update on Carrier Screening for Cystic Fibrosis

(2011)   OBSTETRICS AND GYNECOLOGY

Committee Opinion No. 478: Family History as a Risk Assessment Tool

(2011)   OBSTETRICS AND GYNECOLOGY

Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing

(2011) C. J. Bell et al.   Science Translational Medicine

Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases

(2010) Stuart A. Scott et al.   HUMAN MUTATION

Can We Make Assumptions About the Psychosocial Impact of Living as a Carrier, Based on Studies Assessing the Effects of Carrier Testing?

(2010) Celine Lewis et al.   Journal of Genetic Counseling

Challenges in the clinical application of whole-genome sequencing

(2010) Kelly E Ormond et al.   LANCET

Committee Opinion No. 469: Carrier Screening for Fragile X Syndrome

(2010)   OBSTETRICS AND GYNECOLOGY

Improving Accuracy of Tay Sachs Carrier Screening of the Non-Jewish Population: Analysis of 34 Carriers and Six Late-Onset Patients With HEXA Enzyme and DNA Sequence Analysis

(2010) Noh Jin Park et al.   PEDIATRIC RESEARCH

A universal carrier test for the long tail of Mendelian disease

(2010) Balaji S. Srinivasan et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Disclosure ofAPOEGenotype for Risk of Alzheimer's Disease

(2009) Robert C. Green et al.   NEW ENGLAND JOURNAL OF MEDICINE

ACOG Committee Opinion No. 442: Preconception and Prenatal Carrier Screening for Genetic Diseases in Individuals of Eastern European Jewish Descent

(2009)   OBSTETRICS AND GYNECOLOGY

Carrier screening in individuals of Ashkenazi Jewish descent

(2008) Susan J Gross et al.   GENETICS IN MEDICINE