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There are 39547 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

    Article first published 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

    Article first published online : 17 FEB 2014, DOI: 10.1111/cge.12349

  3. 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

    Article first published online : 18 FEB 2013, DOI: 10.1111/cge.12091

  4. 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

    Article first published online : 9 JUN 2011, DOI: 10.1111/j.1745-7599.2011.00625.x

  5. 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

    Article first published online : 24 FEB 2014, DOI: 10.1002/ijc.28744

  6. Performance characteristics of screening strategies for Lynch syndrome in unselected women with newly diagnosed endometrial cancer who have undergone universal germline mutation testing

    Cancer

    Volume 120, Issue 24, December 15, 2014, Pages: 3932–3939, Sarah E. Ferguson, Melyssa Aronson, Aaron Pollett, Lua R. Eiriksson, Amit M. Oza, Steven Gallinger, Jordan Lerner-Ellis, Zahra Alvandi, Marcus Q. Bernardini, Helen J. MacKay, Golnessa Mojtahedi, Alicia A. Tone, Christine Massey and Blaise A. Clarke

    Article first published online : 31 JUL 2014, DOI: 10.1002/cncr.28933

  7. Dawning of the epigenetic era in hereditary cancer

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 413–416, M.P. Hitchins and H.T. Lynch

    Article first published online : 1 APR 2014, DOI: 10.1111/cge.12369

  8. You have full text access to this Open Access content
    A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory

    Journal of Cellular and Molecular Medicine

    Volume 14, Issue 1-2, January-February 2010, Pages: 181–197, Margot G.F. Van Lier, Anja Wagner, Monique E. Van Leerdam, Katharina Biermann, Ernst J. Kuipers, Ewout W. Steyerberg, Hendrikus Jan Dubbink and Winand N.M. Dinjens

    Article first published online : 19 NOV 2009, DOI: 10.1111/j.1582-4934.2009.00977.x

  9. 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

    Article first published online : 30 APR 2012, DOI: 10.1002/humu.22092

  10. You have free access to this content
    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

    Article first published online : 25 APR 2013, DOI: 10.1002/ijc.28183

  11. Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

    Clinical Genetics

    Volume 76, Issue 1, July 2009, Pages: 1–18, HT Lynch, PM Lynch, SJ Lanspa, CL Snyder, JF Lynch and CR Boland

    Article first published online : 15 JUL 2009, DOI: 10.1111/j.1399-0004.2009.01230.x

  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

    Article first published online : 16 DEC 2013, DOI: 10.1111/codi.12407

  13. Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome

    Clinical Genetics

    Volume 79, Issue 6, June 2011, Pages: 512–522, L Raskin, F Schwenter, M Freytsis, M Tischkowitz, N Wong, G Chong, SA Narod, DA Levine, F Bogomolniy, M Aronson, SN Thibodeau, KS Hunt, G Rennert, S Gallinger, SB Gruber and WD Foulkes

    Article first published online : 14 DEC 2010, DOI: 10.1111/j.1399-0004.2010.01594.x

  14. Hereditary gynaecological malignancies: advances in screening and treatment

    Histopathology

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

    Article first published 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

    Article first published 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

    Article first published online : 7 JAN 2013, DOI: 10.1111/tbj.12077

  17. You have free access to this content
    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

    Article first published online : 7 DEC 2007, DOI: 10.1111/j.1365-2036.2007.03479.x

  18. POLE mutations as an alternative pathway for microsatellite instability in endometrial cancer: Implications for Lynch syndrome testing

    Cancer

    Volume 121, Issue 3, February 1, 2015, Pages: 331–334, Panagiotis A. Konstantinopoulos and Ursula A. Matulonis

    Article first published online : 15 SEP 2014, DOI: 10.1002/cncr.29057

  19. You have free access to this content
    American founder mutation for Lynch syndrome

    Cancer

    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

    Article first published online : 13 DEC 2005, DOI: 10.1002/cncr.21624

  20. First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 70–73, G Daina, L Ramos, A Obradors, M Rius, O Martinez-Pasarell, A Polo, J del Rey, J Obradors, J Benet and J Navarro

    Article first published online : 17 OCT 2012, DOI: 10.1111/cge.12025