Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patients

Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results

(2019) Margret Matias et al.   Journal of Genetic Counseling

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census

(2019) Amy Nisselle et al.   Journal of Genetic Counseling

Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study

(2019) Jessica Park et al.   Journal of Genetic Counseling

Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era

(2019) Ellen F. Macnamara et al.   Journal of Genetic Counseling

Clinical providers’ experiences with returning results from genomic sequencing: an interview study

(2018) Julia Wynn et al.   BMC Medical Genomics

Meeting the challenges of implementing rapid genomic testing in acute pediatric care

(2018) Zornitza Stark et al.   GENETICS IN MEDICINE

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms

(2018) Danya F. Vears et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Distinguishing Variant Pathogenicity From Genetic Diagnosis

(2018) Leslie G. Biesecker et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Reporting practices for variants of uncertain significance from next generation sequencing technologies

(2017) Danya F. Vears et al.   European Journal of Medical Genetics

Reporting practices for unsolicited and secondary findings from next-generation sequencing technologies: Perspectives of laboratory personnel

(2017) Danya F Vears et al.   HUMAN MUTATION

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit

(2016) Hussein Daoud et al.   CANADIAN MEDICAL ASSOCIATION JOURNAL

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

(2016) Zornitza Stark et al.   GENETICS IN MEDICINE

Experiences with obtaining informed consent for genomic sequencing

(2015) Barbara A. Bernhardt et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

(2014) Yaping Yang et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

(2014) Hane Lee et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Diagnostic Clinical Genome and Exome Sequencing

(2014) Leslie G. Biesecker et al.   NEW ENGLAND JOURNAL OF MEDICINE

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

(2014) S. E. Soden et al.   Science Translational Medicine

Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process

(2013) Carmen Ayuso et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders

(2013) Yaping Yang et al.   NEW ENGLAND JOURNAL OF MEDICINE