Screening (oncology)

A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations
J R F Wilson, A C Bateman, H Hanson, Q An, G Evans, N Rahman, J L Jones, D M Eccles

Journal of Medical Genetics Nov 2010, 47 (11) 771-774; DOI: 10.1136/jmg.2010.078113
Pre-test prediction models of BRCA1 or BRCA2 mutation in breast/ovarian families attending familial cancer clinics
M de la Hoya, O Díez, P Pérez-Segura, J Godino, J M Fernández, J Sanz, C Alonso, M Baiget, E Díaz-Rubio, T Caldés

Journal of Medical Genetics Jul 2003, 40 (7) 503-510; DOI: 10.1136/jmg.40.7.503
Apoptosis and cancer: mutations within caspase genes
S Ghavami, M Hashemi, S R Ande, B Yeganeh, W Xiao, M Eshraghi, C J Bus, K Kadkhoda, E Wiechec, A J Halayko, M Los

Journal of Medical Genetics Aug 2009, 46 (8) 497-510; DOI: 10.1136/jmg.2009.066944
Screening families with endometrial and colorectal cancers for germline mutations
Tao Liu, Jindong Chen, Sima Salahshor, Shannon Kuismanen, Eva Holmberg, Henrik Grönberg, Päivi Peltomäki, Annika Lindblom

Journal of Medical Genetics Sep 2001, 38 (9) e29; DOI: 10.1136/jmg.38.9.e29
MDM2 SNP309 accelerates colorectal tumour formation in women
Gareth L Bond, Chiara Menin, Roberta Bertorelle, Pia Alhopuro, Lauri A Aaltonen, Arnold J Levine

Journal of Medical Genetics Dec 2006, 43 (12) 950-952; DOI: 10.1136/jmg.2006.043539
An interstitial deletion within 9p21.3 and extending beyond CDKN2A predisposes to melanoma, neural system tumours and possible haematological malignancies
Maria J Baker, Alisa M Goldstein, Patricia L Gordon, Kimberly S Harbaugh, Heath B Mackley, Michael J Glantz, Joseph J Drabick

Journal of Medical Genetics Nov 2016, 53 (11) 721-727; DOI: 10.1136/jmedgenet-2015-103446
Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas
Femme Harinck, Irma Kluijt, Nienke van der Stoep, Rogier A Oldenburg, Anja Wagner, Cora M Aalfs, Rolf H Sijmons, Jan-Werner Poley, Ernst J Kuipers, Paul Fockens, Theo A M van Os, Marco J Bruno

Journal of Medical Genetics Jun 2012, 49 (6) 362-365; DOI: 10.1136/jmedgenet-2011-100563
Effect of TNF and LTA polymorphisms on biological markers of response to oxidative stimuli in coal miners: a model of gene-environment interaction
R Nadif, A Jedlicka, M Mintz, J-P Bertrand, S Kleeberger, F Kauffmann

Journal of Medical Genetics Feb 2003, 40 (2) 96-103; DOI: 10.1136/jmg.40.2.96
Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research
Rebecca C Fitzgerald, Richard Hardwick, David Huntsman, Fatima Carneiro, Parry Guilford, Vanessa Blair, Daniel C Chung, Jeff Norton, Krishnadath Ragunath, J Han Van Krieken, Sarah Dwerryhouse, Carlos Caldas

Journal of Medical Genetics Jul 2010, 47 (7) 436-444; DOI: 10.1136/jmg.2009.074237
BHD mutations, clinical and molecular genetic investigations of Birt–Hogg–Dubé syndrome: a new series of 50 families and a review of published reports
J R Toro, M-H Wei, G M Glenn, M Weinreich, O Toure, C Vocke, M Turner, P Choyke, M J Merino, P A Pinto, S M Steinberg, L S Schmidt, W M Linehan

Journal of Medical Genetics Jun 2008, 45 (6) 321-331; DOI: 10.1136/jmg.2007.054304

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