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There are 6818 results for: content related to: Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families

  1. Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 507–516, G. Ponti, E. Castellsagué, C. Ruini, A. Percesepe and A. Tomasi

    Version of Record online : 9 DEC 2014, DOI: 10.1111/cge.12529

  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. The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families

    Clinical Genetics

    Volume 84, Issue 3, September 2013, Pages: 244–250, M Pinheiro, C Pinto, A Peixoto, I Veiga, B Mesquita, R Henrique, P Lopes, O Sousa, M Fragoso, LM Dias, M Baptista, C Marinho, E Mangold, C Vaccaro, DG Evans, S Farrington, MG Dunlop and MR MR Teixeira

    Version of Record online : 27 DEC 2012, DOI: 10.1111/cge.12062

  4. 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

    Version of Record online : 17 OCT 2012, DOI: 10.1111/cge.12025

  5. Long-term psychosocial and behavioral adjustment in individuals receiving genetic test results in Lynch syndrome

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 525–532, M.J. Esplen, J. Wong, M. Aronson, K. Butler, H. Rothenmund, K. Semotiuk, L. Madlensky, C. Way, E. Dicks, J. Green and S. Gallinger

    Version of Record online : 28 OCT 2014, DOI: 10.1111/cge.12509

  6. Improving the uptake of predictive testing and colorectal screening in Lynch syndrome: a regional primary care survey

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 517–524, P. Barrow, K. Green, T. Clancy, F. Lalloo, J. Hill and D.G. Evans

    Version of Record online : 4 FEB 2015, DOI: 10.1111/cge.12559

  7. You have full text access to this OnlineOpen article
    Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome

    Clinical Genetics

    Maren F. Hansen, Jostein Johansen, Anna E. Sylvander, Inga Bjørnevoll, Bente A. Talseth-Palmer, Liss A. S. Lavik, Alexandre Xavier, Lars F. Engebretsen, Rodney J. Scott, Finn Drabløs and Wenche Sjursen

    Version of Record online : 22 MAR 2017, DOI: 10.1111/cge.12994

  8. Screening adherence and cancer risk perceptions in colorectal cancer survivors with Lynch-like syndrome

    Clinical Genetics

    Volume 89, Issue 3, March 2016, Pages: 392–398, L.H. Katz, A.M. Burton-Chase, S. Advani, B. Fellman, K.M. Polivka, Y. Yuan, P.M. Lynch and S.K. Peterson

    Version of Record online : 14 SEP 2015, DOI: 10.1111/cge.12653

  9. Gynecologic cancer screening and communication with health care providers in women with Lynch syndrome

    Clinical Genetics

    Volume 86, Issue 2, August 2014, Pages: 185–189, A.M. Burton-Chase, S.R. Hovick, C.C. Sun, S. Boyd-Rogers, P.M. Lynch, K.H. Lu and S.K. Peterson

    Version of Record online : 27 AUG 2013, DOI: 10.1111/cge.12246

  10. You have full text access to this OnlineOpen article
    Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory

    Clinical Genetics

    Volume 86, Issue 6, December 2014, Pages: 510–520, D. Cragun, C. Radford, J.S. Dolinsky, M. Caldwell, E. Chao and T. Pal

    Version of Record online : 20 MAR 2014, DOI: 10.1111/cge.12359

  11. Recurrent and founder mutations in the PMS2 gene

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 238–243, J Tomsic, L Senter, S Liyanarachchi, M Clendenning, C P Vaughn, M A Jenkins, J L Hopper, J Young, W Samowitz and A de la Chapelle

    Version of Record online : 4 JUN 2012, DOI: 10.1111/j.1399-0004.2012.01898.x

  12. You have free access to this content
    Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review

    Clinical Genetics

    Volume 92, Issue 2, August 2017, Pages: 121–133, A.M. Willis, S.K. Smith, B. Meiser, M.L. Ballinger, D.M. Thomas and M.-A. Young

    Version of Record online : 23 OCT 2016, DOI: 10.1111/cge.12868

  13. 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

    Version of Record online : 1 APR 2014, DOI: 10.1111/cge.12369

  14. Identification of a founder EPCAM deletion in Spanish Lynch syndrome families

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 260–266, P. Mur, M. Pineda, A. Romero, J. del Valle, E. Borràs, A. Canal, M. Navarro, J. Brunet, D. Rueda, T. Ramón y Cajal, C. Lázaro, T. Caldés, I. Blanco, J.L. Soto and G. Capellá

    Version of Record online : 26 APR 2013, DOI: 10.1111/cge.12152

  15. Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 536–542, E. Castellsagué, J. Liu, A. Volenik, S. Giroux, R. Gagné, B. Maranda, A. Roussel-Jobin, J. Latreille, R. Laframboise, L. Palma, L. Kasprzak, V.A. Marcus, M. Breguet, S. Nolet, Z. El-Haffaf, K. Australie, A. Gologan, O. Aleynikova, K. Oros-Klein, C. Greenwood, A.M. Mes-Masson, D. Provencher, M. Tischkowitz, G. Chong, F. Rousseau and W.D. Foulkes

    Version of Record online : 22 NOV 2014, DOI: 10.1111/cge.12526

  16. High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families

    Clinical Genetics

    Volume 85, Issue 6, June 2014, Pages: 583–588, A.J. Brea-Fernández, J.M. Cameselle-Teijeiro, C. Alenda, C. Fernández-Rozadilla, J. Cubiella, J. Clofent, J.M. Reñé, U. Anido, M. Milá, F. Balaguer, A. Castells, S. Castellvi-Bel, R. Jover, A. Carracedo and C. Ruiz-Ponte

    Version of Record online : 28 JUL 2013, DOI: 10.1111/cge.12232

  17. Communication and technology in genetic counseling for familial cancer

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 213–222, H.T. Lynch, C. Snyder, M. Stacey, B. Olson, S.K. Peterson, S. Buxbaum, T. Shaw and P.M. Lynch

    Version of Record online : 20 DEC 2013, DOI: 10.1111/cge.12317

  18. You have full text access to this OnlineOpen article
    Evaluation of a population-based approach to familial colorectal cancer

    Clinical Genetics

    Volume 91, Issue 5, May 2017, Pages: 672–682, P.S. Parfrey, E. Dicks, O. Parfrey, P.J. McNicholas, H. Noseworthy, M.O. Woods, C. Negriin and J. Green

    Version of Record online : 8 MAR 2017, DOI: 10.1111/cge.12877

  19. The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer

    Clinical Genetics

    Volume 88, Issue 5, November 2015, Pages: 474–478, Z. Levi, R. Kariv, I. Barnes-Kedar, Y. Goldberg, E. Half, S. Morgentern, B. Eli, H.N. Baris, A. Vilkin, R.G. Belfer, Y. Niv, R. Elhasid, R. Dvir, N. Abu-Freha and S. Cohen

    Version of Record online : 10 NOV 2014, DOI: 10.1111/cge.12518

  20. A population-based study of hereditary non-polyposis colorectal cancer: evidence of pathologic and genetic heterogeneity

    Clinical Genetics

    Volume 84, Issue 6, December 2013, Pages: 522–530, G Warden, D Harnett, J Green, T Wish, MO Woods, R Green, E Dicks, P Rahman, G Zhai and P Parfrey

    Version of Record online : 7 FEB 2013, DOI: 10.1111/cge.12080