نتائج البحث - Maren T. Scheuner

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  1. 1
    Population prevalence of familial cancer and common hereditary cancer syndromes. The 2005 California Health Interview Survey

    Population prevalence of familial cancer and common hereditary cancer syndromes. The 2005 California Health Interview Survey حسب Maren T. Scheuner, Timothy S. McNeel, Andrew N. Freedman

    منشور في 2010
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    Artigo
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  2. 2
    Research priorities for evaluating family history in the prevention of common chronic diseases

    Research priorities for evaluating family history in the prevention of common chronic diseases حسب Paula W. Yoon, Maren T. Scheuner, Muin J. Khoury

    منشور في 2003
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  3. 3
    Factors influencing organizational adoption and implementation of clinical genetic services

    Factors influencing organizational adoption and implementation of clinical genetic services حسب Alison Brown, Sabine Oishi, Elizabeth M. Yano, Cynthia E. Gammage, Nell Marshall, Maren T. Scheuner

    منشور في 2013
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  4. 4
    Are electronic health records ready for genomic medicine?

    Are electronic health records ready for genomic medicine? حسب Maren T. Scheuner, Han de Vries, Benjamin Kim, Robin Meili, Sarah H. Olmstead, Stephanie S. Teleki

    منشور في 2009
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  5. 5
    Family history of type 2 diabetes: A population-based screening tool for prevention?

    Family history of type 2 diabetes: A population-based screening tool for prevention? حسب Susan Hariri, Paula W. Yoon, Nadeem Qureshi, Rodolfo Valdéz, Maren T. Scheuner, Muin J. Khoury

    منشور في 2006
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  6. 6
    Can family history be used as a tool for public health and preventive medicine?

    Can family history be used as a tool for public health and preventive medicine? حسب Paula W. Yoon, Maren T. Scheuner, Kris L. Peterson-Oehlke, Marta Gwinn, Andrew Faucett, Muin J. Khoury

    منشور في 2002
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  7. 7
    Basic vs More Complex Definitions of Family History in the Prediction of Coronary Heart Disease: The Multi-Ethnic Study of Atherosclerosis

    Basic vs More Complex Definitions of Family History in the Prediction of Coronary Heart Disease: The Multi-Ethnic Study of Atherosclerosis حسب Jaideep Patel, Mahmoud Al Rifai, Maren T. Scheuner, Steven Shea, Roger S. Blumenthal, Khurram Nasir, Michael J. Blaha, John W. McEvoy

    منشور في 2018
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  8. 8
    Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG)

    Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG) حسب Marilyn M. Li, Elizabeth Chao, Edward D. Esplin, David T. Miller, Katherine L. Nathanson, Sharon E. Plon, Maren T. Scheuner, Douglas R. Stewart

    منشور في 2020
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  9. 9
    Multilevel Research and the Challenges of Implementing Genomic Medicine

    Multilevel Research and the Challenges of Implementing Genomic Medicine حسب Muin J. Khoury, Ralph J. Coates, Mary L. Fennell, Russell E. Glasgow, Maren T. Scheuner, Sheri D. Schully, Marc S. Williams, Steven B. Clauser

    منشور في 2012
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  10. 10
    Family History of Premature Coronary Heart Disease and Coronary Artery Calcification

    Family History of Premature Coronary Heart Disease and Coronary Artery Calcification حسب Khurram Nasir, Matthew J. Budoff, Nathan D. Wong, Maren T. Scheuner, David M. Herrington, Donna K. Arnett, Moysés Szklo, Philip Greenland, Roger S. Blumenthal

    منشور في 2007
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  11. 11
    Reporting genomic secondary findings: ACMG members weigh in

    Reporting genomic secondary findings: ACMG members weigh in حسب Maren T. Scheuner, Jane Peredo, Judith Benkendorf, Bruce Bowdish, Gerald L. Feldman, Lynn D. Fleisher, John J. Mulvihill, Michael S. Watson, Gail E. Herman, James P. Evans

    منشور في 2014
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  12. 12
    Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

    Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability حسب Jennifer Malinowski, David T. Miller, Laurie Demmer, Jennifer Gannon, Elaine M. Pereira, Molly C. Schroeder, Maren T. Scheuner, Anne Chun‐Hui Tsai, Scott E. Hickey, Jun Shen

    منشور في 2020
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    Revisão
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  13. 13
    DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG)

    DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG... حسب Michael F. Murray, Monica A. Giovanni, Debra Lochner Doyle, Steven M. Harrison, Elaine Lyon, Kandamurugu Manickam, Kristin G. Monaghan, Sonja A. Rasmussen, Maren T. Scheuner, Glenn E. Palomaki, Michael S. Watson

    منشور في 2021
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  14. 14
    Coronary Artery Calcium Improves Risk Assessment in Adults With a Family History of Premature Coronary Heart Disease

    Coronary Artery Calcium Improves Risk Assessment in Adults With a Family History of Premature Coronary Heart Disease حسب Jaideep Patel, Mahmoud Al Rifai, Michael J. Blaha, Matthew J. Budoff, Wendy S. Post, Joseph F. Polak, David A. Bluemke, Maren T. Scheuner, Richard A. Kronmal, Roger S. Blumenthal, Khurram Nasir, John W. McEvoy

    منشور في 2015
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  15. 15
    Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40

    Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40 حسب Frank Tiecke, Stefanie Katzke, Patrick Booms, Peter N. Robinson, Luitgard M. Neumann, Maurice Godfrey, Kurt R. Mathews, Maren T. Scheuner, Georg Klaus Hinkel, Rolf E. Brenner, Hedwig H. Hövels-Gürich, Christian Hagemeier, Josefine Fuchs, Flemming Skovby, Thomas Rosenberg

    منشور في 2001
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  16. 16
    Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting

    Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting حسب Cecelia Bellcross, Sara Bedrosian, Elvan Daniels, Debra Duquette, Heather Hampel, Kory Jasperson, Djenaba Joseph, Celia I. Kaye, Ira M. Lubin, Laurence J. Meyer, Michele Reyes, Maren T. Scheuner, Sheri D. Schully, Leigha Senter, Sherri L. Stewart, Jeanette St. Pierre, Judith A. Westman, Paul E. Wise, Vincent W. Yang, Muin J. Khoury

    منشور في 2012
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