DNA Patenting and Licensing

由 Henry, Michelle R., Cho, Mildred K., Weaver, Meredith A., Merz, Jon F.
出版 2002

A Pilot Survey on the Licensing of DNA Inventions

由 Henry, Michelle R., Cho, Mildred K., Weaver, Meredith A., Merz, Jon F.
出版 2003

Effects of Patents and Licenses on the Provision of Clinical Genetic Testing Services

由 Cho, Mildred K., Illangasekare, Samantha, Weaver, Meredith A., Leonard, Debra G. B., Merz, Jon F.
出版 2003

Providing access to genomic variant knowledge in a healthcare setting: A vision for the ClinGen electronic health records workgroup

由 Overby, Casey, Heale, Bret, Aronson, Samuel, Cherry, J. Michael, Dwight, Selina, Milosavljevic, Aleksandar, Nelson, Tristan, Niehaus, Annie, Weaver, Meredith A., Ramos, Erin M., Williams, Marc S.
發表在 Clin Pharmacol Ther (2015)

Somatic cancer variant curation and harmonization through consensus minimum variant level data

由 Ritter, Deborah I., Roychowdhury, Sameek, Roy, Angshumoy, Rao, Shruti, Landrum, Melissa J., Sonkin, Dmitriy, Shekar, Mamatha, Davis, Caleb F., Hart, Reece K., Micheel, Christine, Weaver, Meredith, Van Allen, Eliezer M., Parsons, Donald W., McLeod, Howard L., Watson, Michael S., Plon, Sharon E., Kulkarni, Shashikant, Madhavan, Subha
發表在 Genome Med (2016)

Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): Lessons Learned and Plans for the Future

由 Milko, Laura V., Funke, Birgit H., Hershberger, Ray E., Azzariti, Danielle R., Lee, Kristy, Riggs, Erin R., Rivera-Munoz, Edgar A., Weaver, Meredith A., Niehaus, Annie, Currey, Erin L., Craigen, William J., Mao, Rong, Offit, Kenneth, Steiner, Robert D., Martin, Christa L., Rehm, Heidi L., Watson, Michael S., Ramos, Erin M., Plon, Sharon E., Berg, Jonathan S.
發表在 Genet Med (2018)

Unique Aspects of Sequence Variant Interpretation for Inborn Errors of Metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene

由 Zastrow, Diane B., Baudet, Heather, Shen, Wei, Thomas, Amanda, Si, Yue, Weaver, Meredith A., Lager, Angela, Liu, Jixia, Mangels, Rachel, Dwight, Selina S., Wright, Matt W., Dobrowolski, Steven F., Eilbeck, Karen, Enns, Gregory M., Feigenbaum, Annette, Lichter-Konecki, Uta, Lyon, Elaine, Pasquali, Marzia, Watson, Michael, Blau, Nenad, Steiner, Robert D., Craigen, William J., Mao, Rong
發表在 Hum Mutat (2018)

ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation...

由 Rivera-Muñoz, Edgar A., Milko, Laura V., Harrison, Steven, Azarriti, Danielle, Kurtz, C. Lisa, Lee, Kristy, Mester, Jessica L., Weaver, Meredith A., Currey, Erin, Craigen, William, Eng, Charis, Funke, Birgit, Hegde, Madhuri, Hershberger, Ray E., Mao, Rong, Steiner, Robert D., Vincent, Lisa M., Martin, Christa L., Plon, Sharon E., Ramos, Erin, Rehm, Heidi, Watson, Michael, Berg, Jonathan S.
發表在 Hum Mutat (2018)

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

由 Hunter, Jessica Ezzell, Irving, Stephanie A., Biesecker, Leslie G., Buchanan, Adam, Jensen, Brian, Lee, Kristy, Martin, Christa Lese, Milko, Laura, Muessig, Kristin, Niehaus, Annie D., O'Daniel, Julianne, Piper, Margaret A., Ramos, Erin M., Schully, Sheri D., Scott, Alan F., Slavotinek, Anne, Sobreira, Nara, Strande, Natasha, Weaver, Meredith, Webber, Elizabeth M., Williams, Marc S., Berg, Jonathan S., Evans, James P., Goddard, Katrina A.B.
發表在 Genet Med (2016)

Evidence-Based Assessments of Clinical Actionability in the Context of Secondary Findings: Updates from ClinGen’s Actionability Working Group

由 Webber, Elizabeth M., Hunter, Jessica Ezzell, Biesecker, Leslie G., Buchanan, Adam H., Clarke, Elizabeth V., Currey, Erin, Dagan-Rosenfeld, Orit, Lee, Kristy, Lindor, Noralane M., Martin, Christa Lese, Milosavljevic, Aleksandar, Mittendorf, Kathleen F., Muessig, Kristin R, O’Daniel, Julianne M., Patel, Ronak Y., Ramos, Erin M., Rego, Shannon, Slavotinek, Anne M., Sobriera, Nara Lygia M., Weaver, Meredith A., Williams, Marc S., Evans, James P., Goddard, Katrina A.B.
發表在 Hum Mutat (2018)