How Geisinger made the case for an institutional duty to return genomic results to biobank participants

由 Faucett, W. Andrew, Davis, F. Daniel
發表在 Appl Transl Genom (2016)

Genetic Testing: Consent and Result Disclosure for the Primary Care Provider

由 Faucett, W. Andrew, Peay, Holly, Coghlin II, Curtis R.
發表在 Med Clin North Am (2019)

An Assessment of Time Involved in Pre-test Case Review and Counseling for a Whole Genome Sequencing Clinical Research Program

由 Williams, Janet L., Faucett, W. Andrew, Smith-Packard, Bethanny, Wagner, Monisa, Williams, Marc S.
出版 2014

An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing

由 Bernhardt, Barbara A., Kellom, Katherine, Barbarese, Alexandra, Faucett, W. Andrew, Wapner, Ronald J.
出版 2014

The Laboratory-Clinician Team: A Professional Call to Action to Improve Communication and Collaboration for Optimal Patient Care in Chromosomal Microarray Testing

由 Wain, Karen E., Riggs, Erin, Hanson, Karen, Savage, Melissa, Riethmaier, Darlene, Muirhead, Andrea, Mitchell, Elyse, Packard, Bethanny Smith, Faucett, W. Andrew
出版 2012

GenomeConnect: matchmaking between patients, clinical laboratories and researchers to improve genomic knowledge

由 Kirkpatrick, Brianne E., Riggs, Erin Rooney, Azzariti, Danielle R., Miller, Vanessa Rangel, Ledbetter, David H., Miller, David T., Rehm, Heidi, Martin, Christa Lese, Faucett, W. Andrew
發表在 Hum Mutat (2015)

Towards a Universal Clinical Genomics Database: The 2012 International Standards for Cytogenomic Arrays (ISCA) Consortium Meeting

由 Riggs, Erin Rooney, Wain, Karen E., Riethmaier, Darlene, Savage, Melissa, Smith-Packard, Bethanny, Kaminsky, Erin B., Rehm, Heidi L., Martin, Christa Lese, Ledbetter, David H., Faucett, W. Andrew
出版 2013

Human Germline Genome Editing

由 Ormond, Kelly E., Mortlock, Douglas P., Scholes, Derek T., Bombard, Yvonne, Brody, Lawrence C., Faucett, W. Andrew, Garrison, Nanibaa’ A., Hercher, Laura, Isasi, Rosario, Middleton, Anna, Musunuru, Kiran, Shriner, Daniel, Virani, Alice, Young, Caroline E.
發表在 Am J Hum Genet (2017)

ClinGen’s GenomeConnect Registry Enables Patient-Centered Data Sharing

由 Savatt, Juliann M., Azzariti, Danielle R., Faucett, W. Andrew, Harrison, Steven, Hart, Jennifer, Kattman, Brandi, Landrum, Melissa J., Ledbetter, David H., Miller, Vanessa Rangel, Palen, Emily, Rehm, Heidi L., Rhode, Jud, Turner, Stefanie, Vidal, Jo Anne, Wain, Karen E., Riggs, Erin Rooney, Martin, Christa Lese
發表在 Hum Mutat (2018)

Application of a framework to guide genetic testing communication across clinical indications

由 Hallquist, Miranda L. G., Tricou, Eric P., Ormond, Kelly E., Savatt, Juliann M., Coughlin, Curtis R., Faucett, W. Andrew, Hercher, Laura, Levy, Howard P., O’Daniel, Julianne M., Peay, Holly L., Stosic, Melissa, Smith, Maureen, Uhlmann, Wendy R., Wand, Hannah, Wain, Karen E., Buchanan, Adam H.
發表在 Genome Med (2021)

Developing a Conceptual, Reproducible, Rubric-Based Approach to Consent and Result Disclosure for Genetic Testing by Clinicians with Minimal Genetics Background

由 Ormond, Kelly E., Hallquist, Miranda L.G., Buchanan, Adam H., Dondanville, Danielle, Cho, Mildred K., Smith, Maureen, Roche, Myra, Brothers, Kyle B., Coughlin, Curtis R., Hercher, Laura, Hudgins, Louanne, Jamal, Seema, Levy, Howard P., Raskin, Misha, Stosic, Melissa, Uhlmann, Wendy, Wain, Karen E., Currey, Erin, Faucett, W. Andrew
發表在 Genet Med (2018)

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort

由 Schwartz, Marci L.B., McCormick, Cara Zayac, Lazzeri, Amanda L., Lindbuchler, D’Andra M., Hallquist, Miranda L.G., Manickam, Kandamurugu, Buchanan, Adam H., Rahm, Alanna Kulchak, Giovanni, Monica A., Frisbie, Lauren, Flansburg, Carroll N., Davis, F. Daniel, Sturm, Amy C., Nicastro, Christine, Lebo, Matthew S., Mason-Suares, Heather, Mahanta, Lisa Marie, Carey, David J., Williams, Janet L., Williams, Marc S., Ledbetter, David H., Faucett, W. Andrew, Murray, Michael F.
發表在 Am J Hum Genet (2018)

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

由 Gottesman, Omri, Kuivaniemi, Helena, Tromp, Gerard, Faucett, W. Andrew, Li, Rongling, Manolio, Teri A., Sanderson, Saskia C., Kannry, Joseph, Zinberg, Randi, Basford, Melissa A., Brilliant, Murray, Carey, David J., Chisholm, Rex L., Chute, Christopher G., Connolly, John J., Crosslin, David, Denny, Joshua C., Gallego, Carlos J., Haines, Jonathan L., Hakonarson, Hakon, Harley, John, Jarvik, Gail P., Kohane, Isaac, Kullo, Iftikhar J., Larson, Eric B., McCarty, Catherine, Ritchie, Marylyn D., Roden, Dan M., Smith, Maureen E., Böttinger, Erwin P., Williams, Marc S.
出版 2013

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

由 Miller, David T., Adam, Margaret P., Aradhya, Swaroop, Biesecker, Leslie G., Brothman, Arthur R., Carter, Nigel P., Church, Deanna M., Crolla, John A., Eichler, Evan E., Epstein, Charles J., Faucett, W. Andrew, Feuk, Lars, Friedman, Jan M., Hamosh, Ada, Jackson, Laird, Kaminsky, Erin B., Kok, Klaas, Krantz, Ian D., Kuhn, Robert M., Lee, Charles, Ostell, James M., Rosenberg, Carla, Scherer, Stephen W., Spinner, Nancy B., Stavropoulos, Dimitri J., Tepperberg, James H., Thorland, Erik C., Vermeesch, Joris R., Waggoner, Darrel J., Watson, Michael S., Martin, Christa Lese, Ledbetter, David H.
出版 2010

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

由 Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen, Maillard, Anne M, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sébastien, Ledbetter, David H, Martin, Christa Lese, Männik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sébastien
出版 2012

Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

由 Buchanan, Adam H, Manickam, Kandamurugu, Meyer, Michelle N, Wagner, Jennifer K, Hallquist, Miranda L G, Williams, Janet L, Rahm, Alanna Kulchak, Williams, Marc S, Chen, Zong-Ming E, Shah, Chaitali K, Garg, Tullika K, Lazzeri, Amanda L, Schwartz, Marci L B, Lindbuchler, D'Andra M, Fan, Audrey L, Leeming, Rosemary, Servano, Pedro O, Smith, Ashlee L, Vogel, Victor G, Abul-Husn, Noura S, Dewey, Frederick E, Lebo, Matthew S, Mason-Suares, Heather M, Ritchie, Marylyn D, Davis, F Daniel, Carey, David J, Feinberg, David T, Faucett, W Andrew, Ledbetter, David H, Murray, Michael F
發表在 Genet Med (2017)

Toward clinical genomics in everyday medicine: perspectives and recommendations

由 Delaney, Susan K., Hultner, Michael L., Jacob, Howard J., Ledbetter, David H., McCarthy, Jeanette J., Ball, Michael, Beckman, Kenneth B., Belmont, John W., Bloss, Cinnamon S., Christman, Michael F., Cosgrove, Andy, Damiani, Stephen A., Danis, Timothy, Delledonne, Massimo, Dougherty, Michael J., Dudley, Joel T., Faucett, W. Andrew, Friedman, Jennifer R., Haase, David H., Hays, Tom S., Heilsberg, Stu, Huber, Jeff, Kaminsky, Leah, Ledbetter, Nikki, Lee, Warren H., Levin, Elissa, Libiger, Ondrej, Linderman, Michael, Love, Richard L., Magnus, David C., Martland, AnneMarie, McClure, Susan L., Megill, Scott E., Messier, Helen, Nussbaum, Robert L., Palaniappan, Latha, Patay, Bradley A., Popovich, Bradley W., Quackenbush, John, Savant, Mark J., Su, Michael M., Terry, Sharon F., Tucker, Steven, Wong, William T., Green, Robert C.
發表在 Expert Rev Mol Diagn (2016)

Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants

由 Manickam, Kandamurugu, Buchanan, Adam H., Schwartz, Marci L. B., Hallquist, Miranda L. G., Williams, Janet L., Rahm, Alanna Kulchak, Rocha, Heather, Savatt, Juliann M., Evans, Alyson E., Butry, Loren M., Lazzeri, Amanda L., Lindbuchler, D’Andra M., Flansburg, Carroll N., Leeming, Rosemary, Vogel, Victor G., Lebo, Matthew S., Mason-Suares, Heather M., Hoskinson, Derick C., Abul-Husn, Noura S., Dewey, Frederick E., Overton, John D., Reid, Jeffrey G., Baras, Aris, Willard, Huntington F., McCormick, Cara Z., Krishnamurthy, Sarath B., Hartzel, Dustin N., Kost, Korey A., Lavage, Daniel R., Sturm, Amy C., Frisbie, Lauren R., Person, T. Nate, Metpally, Raghu P., Giovanni, Monica A., Lowry, Lacy E., Leader, Joseph B., Ritchie, Marylyn D., Carey, David J., Justice, Anne E., Kirchner, H. Lester, Faucett, W. Andrew, Williams, Marc S., Ledbetter, David H., Murray, Michael F.
發表在 JAMA Netw Open (2018)

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

由 D’Angelo, Debra, Lebon, Sébastien, Chen, Qixuan, Martin-Brevet, Sandra, Snyder, LeeAnne Green, Hippolyte, Loyse, Hanson, Ellen, Maillard, Anne M., Faucett, W. Andrew, Macé, Aurélien, Pain, Aurélie, Bernier, Raphael, Chawner, Samuel J. R. A., David, Albert, Andrieux, Joris, Aylward, Elizabeth, Baujat, Genevieve, Caldeira, Ines, Conus, Philippe, Ferrari, Carrina, Forzano, Francesca, Gérard, Marion, Goin-Kochel, Robin P., Grant, Ellen, Hunter, Jill V., Isidor, Bertrand, Jacquette, Aurélia, Jønch, Aia E., Keren, Boris, Lacombe, Didier, Caignec, Cédric Le, Martin, Christa Lese, Männik, Katrin, Metspalu, Andres, Mignot, Cyril, Mukherjee, Pratik, Owen, Michael J., Passeggeri, Marzia, Rooryck-Thambo, Caroline, Rosenfeld, Jill A., Spence, Sarah J., Steinman, Kyle J., Tjernagel, Jennifer, Van Haelst, Mieke, Shen, Yiping, Draganski, Bogdan, Sherr, Elliott H., Ledbetter, David H., van den Bree, Marianne B. M., Beckmann, Jacques S., Spiro, John E., Reymond, Alexandre, Jacquemont, Sébastien, Chung, Wendy K.
發表在 JAMA Psychiatry (2016)