Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience
Williams, Marc S, Buchanan, Adam H, Davis, F Daniel, Faucett, W Andrew, Hallquist, Miranda L G, Leader, Joseph B, Martin, Christa L, McCormick, Cara Z, Meyer, Michelle N, Murray, Michael F, Rahm, Alanna K, Schwartz, Marci L B, Sturm, Amy C, Wagner, Jennifer K, Williams, Janet L, Willard, Huntington F, Ledbetter, David H
Published in Health Affairs (01.05.2018)
Published in Health Affairs (01.05.2018)
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Journal Article
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
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
Published in Genetics in medicine (01.05.2018)
Published in Genetics in medicine (01.05.2018)
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Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists
Hallquist, Miranda L G, Borensztein, Maia J, Coughlin, 2nd, Curtis R, Buchanan, Adam H, Andrew Faucett, W, Peay, Holly L, Smith, Maureen E, Tricou, Eric P, Uhlmann, Wendy R, Wain, Karen E, Ormond, Kelly E
Published in European journal of human genetics : EJHG (01.10.2023)
Published in European journal of human genetics : EJHG (01.10.2023)
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Journal Article
Application of a framework to guide genetic testing communication across clinical indications
Hallquist, Miranda L G, Tricou, Eric P, Ormond, Kelly E, Savatt, Juliann M, Coughlin, 2nd, 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
Published in Genome medicine (29.04.2021)
Published in Genome medicine (29.04.2021)
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Journal Article
Human Germline Genome Editing
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.
Published in American journal of human genetics (03.08.2017)
Published in American journal of human genetics (03.08.2017)
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Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
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.
Published in American journal of human genetics (14.05.2010)
Published in American journal of human genetics (14.05.2010)
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A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
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.
Published in American journal of human genetics (06.09.2018)
Published in American journal of human genetics (06.09.2018)
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Journal Article
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
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
Published in Journal of medical genetics (01.10.2012)
Published in Journal of medical genetics (01.10.2012)
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Journal Article
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions
Moreno-De-Luca, Andres, Evans, David W, Boomer, K B, Hanson, Ellen, Bernier, Raphael, Goin-Kochel, Robin P, Myers, Scott M, Challman, Thomas D, Moreno-De-Luca, Daniel, Slane, Mylissa M, Hare, Abby E, Chung, Wendy K, Spiro, John E, Faucett, W Andrew, Martin, Christa L, Ledbetter, David H
Published in JAMA psychiatry (Chicago, Ill.) (01.02.2015)
Published in JAMA psychiatry (Chicago, Ill.) (01.02.2015)
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Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background
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
Published in Genetics in medicine (01.03.2019)
Published in Genetics in medicine (01.03.2019)
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Journal Article
ClinGen's GenomeConnect registry enables patient‐centered data sharing
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
Published in Human mutation (01.11.2018)
Published in Human mutation (01.11.2018)
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Journal Article
Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants
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
Published in JAMA network open (07.09.2018)
Published in JAMA network open (07.09.2018)
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GenomeConnect: Matchmaking Between Patients, Clinical Laboratories, and Researchers to Improve Genomic Knowledge
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
Published in Human mutation (01.10.2015)
Published in Human mutation (01.10.2015)
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Journal Article
Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics-Based Communities
Rocha, Heather Mae, Savatt, Juliann M., Riggs, Erin Rooney, Wagner, Jennifer K., Faucett, W. Andrew, Martin, Christa Lese
Published in Journal of genetic counseling (01.04.2018)
Published in Journal of genetic counseling (01.04.2018)
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Journal Article
O22: Integrating genomic medicine into healthcare: Experience disclosing >5,000 clinically relevant results within the Geisinger MyCode Community Health Initiative
Kelly, Melissa, Savatt, Juliann, Sturm, Amy, McCormick, Cara, Williams, Marc, Strande, Natasha, Faucett, W. Andrew, Ledbetter, David, Buchanan, Adam, Martin, Christa
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Towards a Universal Clinical Genomics Database: The 2012 International Standards for Cytogenomic Arrays Consortium Meeting
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
Published in Human mutation (01.06.2013)
Published in Human mutation (01.06.2013)
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Conference Proceeding
An Assessment of Time Involved in Pre-test Case Review and Counseling for a Whole Genome Sequencing Clinical Research Program
Williams, Janet L., Faucett, W. Andrew, Smith-Packard, Bethanny, Wagner, Monisa, Williams, Marc S.
Published in Journal of genetic counseling (01.08.2014)
Published in Journal of genetic counseling (01.08.2014)
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