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

Por Faucett, W. Andrew, Davis, F. Daniel
Publicado no Appl Transl Genom (2016)

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

Por Faucett, W. Andrew, Peay, Holly, Coghlin II, Curtis R.
Publicado no 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

Por Williams, Janet L., Faucett, W. Andrew, Smith-Packard, Bethanny, Wagner, Monisa, Williams, Marc S.
Publicado em 2014

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

Por Bernhardt, Barbara A., Kellom, Katherine, Barbarese, Alexandra, Faucett, W. Andrew, Wapner, Ronald J.
Publicado em 2014

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

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

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

Por 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
Publicado no Hum Mutat (2015)

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

Por 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
Publicado em 2013

Human Germline Genome Editing

Por 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.
Publicado no Am J Hum Genet (2017)

ClinGen’s GenomeConnect Registry Enables Patient-Centered Data Sharing

Por 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
Publicado no Hum Mutat (2018)

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

Por 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
Publicado no Genet Med (2018)

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

Por 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.
Publicado no Am J Hum Genet (2018)

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

Por 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.
Publicado em 2013

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

Por 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.
Publicado em 2010

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

Por 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
Publicado em 2012

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

Por 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
Publicado no Genet Med (2017)

Toward clinical genomics in everyday medicine: perspectives and recommendations

Por 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.
Publicado no Expert Rev Mol Diagn (2016)

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

Por 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.
Publicado no JAMA Netw Open (2018)

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

Por 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.
Publicado no JAMA Psychiatry (2016)