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Publication

How to know when physicians are ready for genomic medicine

Sci Transl Med

Vassy, J. L., Korf, B. R., Green, R. C.

2015

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): KL2-TR001100, L30-DK089597, R01-HG005092, U01-HG006500, and U19-HD077671

Publication

Online education and e-Consent for GeneScreen, a preventive genomic screening study

Public Health Genomics

Cadigan, R. J., Butterfield, R., Rini, C., Waltz, M., Kuczynski, K. J., Muessig, K., Goddard, K. A. B., Henderson, G. E.

2017

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): 2P50HG004488, UL1 RR024140

Publication

How well do customers of direct-to-consumer personal genomic testing services comprehend genetic test results? Findings from the impact of personal genomics study

Public Health Genomics

Ostergren, J. E., Gornick, M. C., Carere, D. A., Kalia, S. S., Uhlmann, W. R., Ruffin, M. T., Mountain, J. L., Green, R. C., Roberts, J. S., PGen Study Group

2015

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): R01-HG005092, U01-HG006500, U19-HD077671, R01-HG002213

Publication

Preference for secondary findings in prenatal and pediatric exome sequencing

Prenat Diagn

Swanson, K., Sparks, T. N., Lianoglou, B. R., Chen, F., Downum, S., Patel, S., Rego, S., Yip, T., Van Ziffle, J., Koenig, B. A., Slavotinek, A. M., Norton, M. E.

2022

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01HG009599, 5K12HD001262-18

Publication

Examining the cascade of participant attrition in a genomic medicine research study: Barriers and facilitators to achieving diversity

Public Health Genomics

Moore, E. G., Roche, M., Rini, C., Corty, E. W., Girnary, Z., O'Daniel, J. M., Lin, F. C., Corbie-Smith, G., Evans, J. P., Henderson, G. E., Berg, J. S.

2017

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01 HG006487

Publication

Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis

Prenat Diagn

Swanson, K., Loeliger, K. B., Chetty, S. P., Sparks, T. N., Norton, M. E.

2022

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): 5K12HD001262-18

Publication

Expectation versus reality: The impact of utility on emotional outcomes after returning individualized genetic research results in pediatric rare disease research, a qualitative interview study

PLoS One

Cacioppo, C. N., Chandler, A. E., Towne, M. C., Beggs, A. H., Holm, I. A.

2016

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): R01HG006615, RCHG005491, U01HG006828, U19HD077671

Publication

Characterizing participants in the ClinSeq genome sequencing cohort as early adopters of a new health technology

PLoS One

Lewis, K. L., Han, P. K., Hooker, G. W., Klein, W. M., Biesecker, L. G., Biesecker, B. B.

2015

Clinical Sequencing Evidence-Generating Research (CSER) Consortium..

Publication

Closing the gap between knowledge and clinical application: Challenges for genomic translation

PLoS Genet

Burke, W., Korngiebel, D. M.

2015

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): P50 HG003374, U01HG006507

Publication

Assessment of willingness to pay for expanded carrier screening among women and couples undergoing preconception carrier screening

PLoS One

Clarke, E. V., Schneider, J. L., Lynch, F., Kauffman, T. L., Leo, M. C., Rosales, A. G., Dickerson, J. F., Shuster, E., Wilfond, B. S., Goddard, K. A. B.

2018

Clinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): UM1HG007292, U01HG007307

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How to know when physicians are ready for genomic medicine

Online education and e-Consent for GeneScreen, a preventive genomic screening study

How well do customers of direct-to-consumer personal genomic testing services comprehend genetic test results? Findings from the impact of personal genomics study

Preference for secondary findings in prenatal and pediatric exome sequencing

Examining the cascade of participant attrition in a genomic medicine research study: Barriers and facilitators to achieving diversity

Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis

Expectation versus reality: The impact of utility on emotional outcomes after returning individualized genetic research results in pediatric rare disease research, a qualitative interview study

Characterizing participants in the ClinSeq genome sequencing cohort as early adopters of a new health technology

Closing the gap between knowledge and clinical application: Challenges for genomic translation

Assessment of willingness to pay for expanded carrier screening among women and couples undergoing preconception carrier screening

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