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There are 16173 results for: content related to: Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome

  1. Scoping the family history: Assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings—A primer for nurse practitioners

    Journal of the American Academy of Nurse Practitioners

    Volume 20, Issue 2, February 2008, Pages: 76–84, Ann Maradiegue, Kory Jasperson, Quannetta T. Edwards, Katrina Lowstuter and Jeffrey Weitzel

    Version of Record online : 7 FEB 2008, DOI: 10.1111/j.1745-7599.2007.00282.x

  2. Epigenetic mechanisms in the pathogenesis of Lynch syndrome

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 403–412, P. Peltomäki

    Version of Record online : 17 FEB 2014, DOI: 10.1111/cge.12349

  3. Pre- and postassessment of nurse practitioners' knowledge of hereditary colorectal cancer

    Journal of the American Academy of Nurse Practitioners

    Volume 23, Issue 7, July 2011, Pages: 361–369, Quannetta T. Edwards, Ann Maradiegue, Diane Seibert and Kory Jasperson

    Version of Record online : 9 JUN 2011, DOI: 10.1111/j.1745-7599.2011.00625.x

  4. Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 215–220, AM Burton-Chase, SR Hovick, SK Peterson, SK Marani, SW Vernon, CI Amos, ML Frazier, PM Lynch and ER Gritz

    Version of Record online : 18 FEB 2013, DOI: 10.1111/cge.12091

  5. You have full text access to this OnlineOpen article
    Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers


    Volume 121, Issue 18, September 15, 2015, Pages: 3281–3289, Jessica Ezzell Hunter, Jamilyn M. Zepp, Mari J. Gilmore, James V. Davis, Elizabeth J. Esterberg, Kristin R. Muessig, Susan K. Peterson, Sapna Syngal, Louise S. Acheson, Georgia L. Wiesner, Jacob A. Reiss and Katrina A.B. Goddard

    Version of Record online : 2 JUN 2015, DOI: 10.1002/cncr.29470

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    Evidence for the role of aberrant DNA methylation in the pathogenesis of Lynch syndrome adenomas

    International Journal of Cancer

    Volume 120, Issue 9, 1 May 2007, Pages: 1922–1929, Andrew Kaz, Young-Ho Kim, Slavomir Dzieciatkowski, Henry Lynch, Patrice Watson, Mary Kay Washington, Li Lin and William M. Grady

    Version of Record online : 2 FEB 2007, DOI: 10.1002/ijc.22544

  7. Colonoscopy screening compliance and outcomes in patients with Lynch syndrome

    Colorectal Disease

    Volume 17, Issue 1, January 2015, Pages: 38–46, K. Newton, K. Green, F. Lalloo, D. G. Evans and J. Hill

    Version of Record online : 23 DEC 2014, DOI: 10.1111/codi.12778

  8. Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of lynch syndrome

    Human Mutation

    Volume 33, Issue 7, July 2012, Pages: 1051–1055, Heleen M. van der Klift, Carli M. Tops, Frederik J. Hes, Peter Devilee and Juul T. Wijnen

    Version of Record online : 30 APR 2012, DOI: 10.1002/humu.22092

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    BRAF V600E-specific immunohistochemistry for the exclusion of Lynch syndrome in MSI-H colorectal cancer

    International Journal of Cancer

    Volume 133, Issue 7, 1 October 2013, Pages: 1624–1630, David Capper, Anita Voigt, Gergana Bozukova, Aysel Ahadova, Philipp Kickingereder, Andreas von Deimling, Magnus von Knebel Doeberitz and Matthias Kloor

    Version of Record online : 25 APR 2013, DOI: 10.1002/ijc.28183

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    Population-based screening for Lynch syndrome in Western Australia

    International Journal of Cancer

    Volume 135, Issue 5, 01 September 2014, Pages: 1085–1091, Lyn Schofield, Fabienne Grieu, Benhur Amanuel, Amerigo Carrello, Dominic Spagnolo, Cathy Kiraly, Nicholas Pachter, Jack Goldblatt, Cameron Platell, Michael Levitt, Colin Stewart, Paul Salama, Hooi Ee, Spiro Raftopoulous, Paul Katris, Tim Threlfall, Edward Edkins, Marina Wallace and Barry Iacopetta

    Version of Record online : 24 FEB 2014, DOI: 10.1002/ijc.28744

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    Initiation of universal tumor screening for Lynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice


    Volume 122, Issue 3, February 1, 2016, Pages: 393–401, Stacey A. Cohen, Mercy Laurino, Deborah J. Bowen, Melissa P. Upton, Colin Pritchard, Fuki Hisama, Gail Jarvik, Alessandro Fichera, Britta Sjoding, Robin L. Bennett, Lorraine Naylor, Angela Jacobson, Wylie Burke and William M. Grady

    Version of Record online : 19 OCT 2015, DOI: 10.1002/cncr.29758

  12. Easy-to-use online referral test detects most patients with a high familial risk of colorectal cancer

    Colorectal Disease

    Volume 16, Issue 1, January 2014, Pages: O26–O34, N. Dekker, R. P. M. G. Hermens, A. R. Mensenkamp, W. A. G. van Zelst-Stams and N. Hoogerbrugge

    Version of Record online : 16 DEC 2013, DOI: 10.1111/codi.12407

  13. Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility

    Human Mutation

    Volume 33, Issue 1, January 2012, Pages: 180–188, Michel Crépin, Marie-Claire Dieu, Sophie Lejeune, Fabienne Escande, Denis Boidin, Nicole Porchet, Gilles Morin, Sylvie Manouvrier, Michèle Mathieu and Marie-Pierre Buisine

    Version of Record online : 31 OCT 2011, DOI: 10.1002/humu.21617

  14. Hereditary gynaecological malignancies: advances in screening and treatment


    Volume 62, Issue 1, January 2013, Pages: 2–30, Ann K Folkins and Teri A Longacre

    Version of Record online : 13 DEC 2012, DOI: 10.1111/his.12028

  15. Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome

    The Journal of Pathology

    Volume 226, Issue 5, April 2012, Pages: 764–774, Margot GF van Lier, Celine HM Leenen, Anja Wagner, Dewkoemar Ramsoekh, Hendrikus J Dubbink, Ans MW van den Ouweland, Pieter J Westenend, Eelco JR de Graaf, Leonieke MM Wolters, Wietske W Vrijland, Ernst J Kuipers, Monique E van Leerdam, Ewout W Steyerberg, Winand NM Dinjens and on behalf of the LIMO Study Group

    Version of Record online : 17 JAN 2012, DOI: 10.1002/path.3963

  16. Loss of Mismatch Repair Protein Expression in Breast Carcinoma in Patients with Lynch Syndrome: Report of Two Cases

    The Breast Journal

    Volume 19, Issue 2, March/April 2013, Pages: 193–195, Andrew D Beggs, George Kousparos and Shirley V Hodgson

    Version of Record online : 7 JAN 2013, DOI: 10.1111/tbj.12077

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    Review article: the Lynch syndrome (hereditary nonpolyposis colorectal cancer)

    Alimentary Pharmacology & Therapeutics

    Volume 26, Issue s2, December 2007, Pages: 113–126, H. F. A. VASEN

    Version of Record online : 7 DEC 2007, DOI: 10.1111/j.1365-2036.2007.03479.x

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    American founder mutation for Lynch syndrome


    Volume 106, Issue 2, 15 January 2006, Pages: 448–452, Henry T. Lynch, Albert de la Chapelle, Heather Hampel, Anja Wagner, Riccardo Fodde, Jane F. Lynch, Ross Okimoto, Mary Beth Clark, Stephanie Coronel, Abdon Trowonou, Yun-Xin Fu, Gleb R. Haynatzki and Gordon Gong

    Version of Record online : 13 DEC 2005, DOI: 10.1002/cncr.21624

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    Oral Abstracts

    Asia-Pacific Journal of Clinical Oncology

    Volume 11, Issue S4, November 2015, Pages: 63–103,

    Version of Record online : 3 NOV 2015, DOI: 10.1111/ajco.12432

  20. You have full text access to this Open Access content
    Hereditary ovarian carcinoma: Heterogeneity, molecular genetics, pathology, and management

    Molecular Oncology

    Volume 3, Issue 2, April 2009, Pages: 97–137, Henry T. Lynch, Murray Joseph Casey, Carrie L. Snyder, Chhanda Bewtra, Jane F. Lynch, Matthew Butts, Andrew K. Godwin

    Version of Record online : 21 FEB 2009, DOI: 10.1016/j.molonc.2009.02.004