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Publication
The ACMG/AMP reputable source criteria for the interpretation of sequence variants
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. -
Publication
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s):U01HG006485, U01HG006487, U01HG006492, U01HG006500, U01HG006507, U01HG006546, U01HG007307, UM1HG007301, UM1HG006508… -
Publication
"Possibly positive or certainly uncertain?": Participants' responses to uncertain diagnostic results from exome sequencing
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01 HG006487-01, 2P50HG004488 -
Publication
Secondary findings in exome slices, virtual panels, and anticipatory sequencing
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): HG200387 04 -
Publication
Genomic sequencing identifies secondary findings in a cohort of parent study participants
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): UM1HG007301 -
Publication
Returning negative results to individuals in a genomic screening program: Lessons learned
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): 2P50HG004488, UL1 RR024140 -
Publication
Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): HG200387 04 -
Publication
The evolving landscape of expanded carrier screening: Challenges and opportunities
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): UM1HG007292, U01HG007307 -
Publication
Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01 HG006487–01 -
Publication
Secondary findings from clinical genomic sequencing: Prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01HG007307, U01HG006507, U01HG006485, U01HG006500, UM1HG007292, U01HG006546, U01HG007301, U01 HG006492,…