Payer decision making for next-generation sequencing–based genetic tests: insights from cell-free DNA prenatal screening

SMFM Statement: clarification of recommendations regarding cell-free DNA aneuploidy screening

(2015)   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

Generating and evaluating evidence of the clinical utility of molecular diagnostic tests in oncology

(2015) Patricia Deverka et al.   GENETICS IN MEDICINE

Too much, too soon?: Commercial provision of noninvasive prenatal screening for subchromosomal abnormalities and beyond

(2015) Megan Allyse et al.   GENETICS IN MEDICINE

Copy-Number Variation and False Positive Prenatal Aneuploidy Screening Results

(2015) Matthew W. Snyder et al.   NEW ENGLAND JOURNAL OF MEDICINE

Cell-free DNA Analysis for Noninvasive Examination of Trisomy

(2015) Mary E. Norton et al.   NEW ENGLAND JOURNAL OF MEDICINE

Committee Opinion No. 640

(2015)   OBSTETRICS AND GYNECOLOGY

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

(2015) Peter Benn et al.   PRENATAL DIAGNOSIS

Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146 958 pregnancies

(2015) H. Zhang et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis

(2015) M. M. Gil et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Utilization and Outcomes ofBRCAGenetic Testing and Counseling in a National Commercially Insured Population

(2015) Joanne Armstrong et al.   JAMA Oncology

Noninvasive Prenatal Screening by Next-Generation Sequencing

(2014) Anthony R. Gregg et al.   Annual Review of Genomics and Human Genetics

Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results

(2014) Francesca R. Grati et al.   GENETICS IN MEDICINE

Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases

(2014) Jia-Chi Wang et al.   GENETICS IN MEDICINE

Clinical Integration of Next Generation Sequencing: Coverage and Reimbursement Challenges

(2014) Patricia A. Deverka et al.   JOURNAL OF LAW MEDICINE & ETHICS

DNA Sequencing versus Standard Prenatal Aneuploidy Screening

(2014) Diana W. Bianchi et al.   NEW ENGLAND JOURNAL OF MEDICINE

ACMG statement on noninvasive prenatal screening for fetal aneuploidy

(2013)   GENETICS IN MEDICINE

Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors

(2013) Patricia L. Devers et al.   Journal of Genetic Counseling

“It just becomes much more complicated”: Genetic counselors' views on genetics and prenatal testing

(2013) Susan Markens   NEW GENETICS AND SOCIETY

Noninvasive Prenatal Testing for Fetal Aneuploidy

(2013) Mary E. Norton et al.   OBSTETRICS AND GYNECOLOGY

Genetic testing insurance coverage trends: a review of publicly available policies from the largest US payers

(2013) Michael D Graf et al.   Personalized Medicine

Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y

(2013) K. H. Nicolaides et al.   PRENATAL DIAGNOSIS

The role of noninvasive prenatal testing as a diagnostic versus a screening tool - a cost-effectiveness analysis

(2013) Mika Ohno et al.   PRENATAL DIAGNOSIS

Clinical implementation of noninvasive prenatal testing among maternal fetal medicine specialists

(2013) Lori Haymon et al.   PRENATAL DIAGNOSIS

A historical and practical review of first trimester aneuploidy screening

(2013) Melissa L. Russo et al.   Seminars in Fetal & Neonatal Medicine

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18

(2012) Mary E. Norton et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study

(2012) Glenn E. Palomaki et al.   GENETICS IN MEDICINE

Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing

(2012) Diana W. Bianchi et al.   OBSTETRICS AND GYNECOLOGY

Noninvasive Whole-Genome Sequencing of a Human Fetus

(2012) J. O. Kitzman et al.   Science Translational Medicine

DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study

(2011) Glenn E. Palomaki et al.   GENETICS IN MEDICINE

Evidence-based classification of recommendations on use of genomic tests in clinical practice: Dealing with insufficient evidence

(2010) Muin J Khoury et al.   GENETICS IN MEDICINE

Coverage Policy Development for Personalized Medicine: Private Payer Perspectives on Developing Policy for the 21-Gene Assay

(2010) Julia R. Trosman et al.   Journal of Oncology Practice

Pharmacogenomics, Evidence, and the Role of Payers

(2009) P.A. Deverka   Public Health Genomics