Resultados de procura - David E. Goldgar

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  1. 1
    A Full-Likelihood Method for the Evaluation of Causality of Sequence Variants from Family Data

    A Full-Likelihood Method for the Evaluation of Causality of Sequence Variants from Family Data por Deborah J. Thompson, Douglas F. Easton, David E. Goldgar

    Publicado 2003
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  2. 2
    Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group

    Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group por Sean V. Tavtigian, Marc S. Greenblatt, David E. Goldgar, Paolo Boffetta

    Publicado 2008
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  3. 3
    Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications

    Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications por Sean V. Tavtigian, Graham Byrnes, David E. Goldgar, Alun Thomas

    Publicado 2008
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  4. 4
    Effect of Fish Oil Supplementation on the n-3 Fatty Acid Content of Red Blood Cell Membranes in Preterm Infants

    Effect of Fish Oil Supplementation on the n-3 Fatty Acid Content of Red Blood Cell Membranes in Preterm Infants por Susan E. Carlson, Philip G. Rhodes, Vatsala S Rao, David E. Goldgar

    Publicado 1987
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  5. 5
    Genetic evidence and integration of various data sources for classifying uncertain variants into a single model

    Genetic evidence and integration of various data sources for classifying uncertain variants into a single model por David E. Goldgar, Douglas F. Easton, Graham Byrnes, Amanda B. Spurdle, Edwin S. Iversen, Marc S. Greenblatt

    Publicado 2008
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  6. 6
    BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management

    BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management por Noralane M. Lindor, David E. Goldgar, Sean V. Tavtigian, Sharon E. Plon, Fergus J. Couch

    Publicado 2013
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  7. 7
    A Computational Method to Classify Variants of Uncertain Significance Using Functional Assay Data with Application to <i>BRCA1</i>

    A Computational Method to Classify Variants of Uncertain Significance Using Functional Assay Data with Application to <i>BRCA1</i> por Edwin S. Iversen, Fergus J. Couch, David E. Goldgar, Sean V. Tavtigian, Álvaro N.A. Monteiro

    Publicado 2011
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  8. 8
    Obesity in Early Adulthood as a Risk Factor for Psoriatic Arthritis

    Obesity in Early Adulthood as a Risk Factor for Psoriatic Arthritis por Razieh Soltani‐Arabshahi, Bob Wong, Bing Feng, David E. Goldgar, Kristina Callis Duffin, Gerald G. Krueger

    Publicado 2010
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  9. 9
    An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)

    An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMB... por Georgia Chenevix‐Trench, Roger L. Milne, Antonis C. Antoniou, Fergus J. Couch, Douglas F. Easton, David E. Goldgar

    Publicado 2007
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  10. 10
    Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2

    Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2 por David E. Goldgar, Douglas F. Easton, Amie M. Deffenbaugh, Álvaro N.A. Monteiro, Sean V. Tavtigian, Fergus J. Couch

    Publicado 2004
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  11. 11
    A weighted cohort approach for analysing factors modifying disease risks in carriers of high‐risk susceptibility genes

    A weighted cohort approach for analysing factors modifying disease risks in carriers of high‐risk susceptibility genes por Antonis C. Antoniou, David E. Goldgar, Nadine Andrieu, Jenny Chang‐Claude, Richard M. Brohet, Matti A. Rookus, Douglas F. Easton

    Publicado 2005
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  12. 12
    An Alu-Mediated 6-kb Duplication in the BRCA1 Gene: A New Founder Mutation?

    An Alu-Mediated 6-kb Duplication in the BRCA1 Gene: A New Founder Mutation? por Nadine Puget, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Carole Audoynaud, Sabine Pagès, Henry T. Lynch, David E. Goldgar, Gilbert Lenoir, Sylvie Mazoyer

    Publicado 1999
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  13. 13
    A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS)

    A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS) por Noralane M. Lindor, Lucia Guidugli, Xianshu Wang, Maxime Vallée, Álvaro N.A. Monteiro, Sean V. Tavtigian, David E. Goldgar, Fergus J. Couch

    Publicado 2011
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  14. 14
    Classification of missense substitutions in the BRCA genes: A database dedicated to Ex-UVs

    Classification of missense substitutions in the BRCA genes: A database dedicated to Ex-UVs por Maxime Vallée, Tiana C. Francy, Megan K. Judkins, Davit Babikyan, Fabienne Lesueur, Amanda Gammon, David E. Goldgar, Fergus J. Couch, Sean V. Tavtigian

    Publicado 2011
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  15. 15
    A Model Protocol for Evaluating the Behavioral and Psychosocial Effects of BRCA1 Testing

    A Model Protocol for Evaluating the Behavioral and Psychosocial Effects of BRCA1 Testing por Jeffery R. Botkin, Robert T. Croyle, Ken R. Smith, Bonnie J. Baty, Caryn Lerman, David E. Goldgar, John M. Ward, Bonnie J. Flick, Jamie Nash

    Publicado 1996
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  16. 16
    Association between IL13 Polymorphisms and Psoriatic Arthritis Is Modified by Smoking

    Association between IL13 Polymorphisms and Psoriatic Arthritis Is Modified by Smoking por Kristina Callis Duffin, Ingrid C Freeny, Steven J. Schrodi, Bob Wong, Bing Feng, Razieh Soltani‐Arabshahi, Tina Rakkhit, David E. Goldgar, Gerald G. Krueger

    Publicado 2009
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  17. 17
    Functional Evaluation and Cancer Risk Assessment of BRCA2 Unclassified Variants

    Functional Evaluation and Cancer Risk Assessment of BRCA2 Unclassified Variants por Kangjian Wu, Shannon R. Hinson, Akihiro Ohashi, Daniel J. Farrugia, Patricia Wendt, Sean V. Tavtigian, Amie M. Deffenbaugh, David E. Goldgar, Fergus J. Couch

    Publicado 2005
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  18. 18
    Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results

    Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results por Mary Pritzlaff, Pia Summerour, Rachel McFarland, Shuwei Li, Patrick Reineke, Jill S. Dolinsky, David E. Goldgar, Hermela Shimelis, Fergus J. Couch, Elizabeth Chao, Holly LaDuca

    Publicado 2016
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  19. 19
    Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls

    Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls por Jenna Lilyquist, Holly LaDuca, Eric C. Polley, Brigette Tippin Davis, Hermela Shimelis, Chunling Hu, Steven N. Hart, Jill S. Dolinsky, Fergus J. Couch, David E. Goldgar

    Publicado 2017
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  20. 20
    Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families

    Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families por Zhi L. Teo, Daniel J. Park, Elena Provenzano, Catherine Chatfield, Fabrice Odefrey, Tú Nguyen‐Dumont, James G. Dowty, John L. Hopper, Ingrid Winship, David E. Goldgar, Melissa C. Southey

    Publicado 2013
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