Genetic Testing, Interpretation, and Communication: Exploration Across Disciplines

Ashutosh Kumar Dubey, Umesh Gupta, Sonal Jain, None, Breast Cancer Statistics and Prediction Methodology: A Systematic Review and Analysis Asian Pacific Journal of Cancer Prevention. ,vol. 16, pp. 4237- 4245 ,(2015) , 10.7314/APJCP.2015.16.10.4237

Angela R. Bradbury, Linda Patrick-Miller, Brian L. Egleston, Olufunmilayo I. Olopade, Mary B. Daly, Cynthia W. Moore, Colleen B. Sands, Helen Schmidheiser, Preethi K. Kondamudi, Maia Feigon, Comfort N. Ibe, Christopher K. Daugherty, When parents disclose BRCA1/2 test results: Their communication and perceptions of offspring response Cancer. ,vol. 118, pp. 3417- 3425 ,(2012) , 10.1002/CNCR.26471

Allyn McConkie-Rosell, Gail A. Spiridigliozzi, Elizabeth Melvin, Deborah V. Dawson, Ave M. Lachiewicz, Living with genetic risk: Effect on adolescent self-concept American Journal of Medical Genetics Part C: Seminars in Medical Genetics. ,vol. 148C, pp. 56- 69 ,(2008) , 10.1002/AJMG.C.30161

Alison Metcalfe, Gill Plumridge, Jane Coad, Andrew Shanks, Paramjit Gill, Parents’ and children's communication about genetic risk: a qualitative study, learning from families’ experiences European Journal of Human Genetics. ,vol. 19, pp. 640- 646 ,(2011) , 10.1038/EJHG.2010.258

O. W J Quarrell, A. S Rigby, L Barron, Y Crow, A Dalton, N Dennis, A E Fryer, F Heydon, E Kinning, A Lashwood, M Losekoot, L Margerison, S McDonnell, P J Morrison, A Norman, M Peterson, F L Raymond, S Simpson, E Thompson, J Warner, Reduced penetrance alleles for Huntington’s disease: a multi-centre direct observational study Journal of Medical Genetics. ,vol. 44, ,(2006) , 10.1136/JMG.2006.045120

Gillian Forrest, Caroline Plumb, Sue Ziebland, Alan Stein, Breast cancer in young families: a qualitative interview study of fathers and their role and communication with their children following the diagnosis of maternal breast cancer. Psycho-oncology. ,vol. 18, pp. 96- 103 ,(2009) , 10.1002/PON.1387

Judy E. Garber, Kenneth Offit, Hereditary Cancer Predisposition Syndromes Journal of Clinical Oncology. ,vol. 23, pp. 276- 292 ,(2005) , 10.1200/JCO.2005.10.042

Deborah Ford, DF Easton, M Stratton, S Narod, D Goldgar, P Devilee, DT Bishop, B Weber, G Lenoir, J Chang-Claude, H Sobol, M Dawn Teare, J Struewing, A Arason, S Scherneck, J Peto, TR Rebbeck, P Tonin, S Neuhausen, R Barkardottir, J Eyfjord, H Lynch, BAJ Ponder, SA Gayther, JM Birch, A Lindblom, D Stoppa-Lyonnet, Y Bignon, A Borg, U Hamann, N Haites, RJ Scott, CM, and Maugard, H Vasen, S Seitz, LA Cannon-Albright, A Schofield, M Zelada-Hedman, Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families American Journal of Human Genetics. ,vol. 62, pp. 676- 689 ,(1998) , 10.1086/301749

Katja I. Aktan-Collan, Helena A. Kääriäinen, Eeva M. Kolttola, Kirsi Pylvänäinen, Heikki J. Järvinen, Ari H. Haukkala, Jukka-Pekka Mecklin, Sharing genetic risk with next generation: mutation-positive parents’ communication with their offspring in Lynch Syndrome Familial Cancer. ,vol. 10, pp. 43- 50 ,(2011) , 10.1007/S10689-010-9386-X

Karolina Budych, Thomas M. Helms, Carsten Schultz, How do patients with rare diseases experience the medical encounter? Exploring role behavior and its impact on patient–physician interaction Health Policy. ,vol. 105, pp. 154- 164 ,(2012) , 10.1016/J.HEALTHPOL.2012.02.018