Epidemiology

Evidence of an association between genetic variation of the coactivator PGC-1β and obesity
G Andersen, L Wegner, K Yanagisawa, C S Rose, J Lin, C Glümer, T Drivsholm, K Borch-Johnsen, T Jørgensen, T Hansen, B M Spiegelman, O Pedersen

Journal of Medical Genetics May 2005, 42 (5) 402-407; DOI: 10.1136/jmg.2004.026278
Methodology in longitudinal studies on psychological effects of predictive DNA testing: a review
R Timman, T Stijnen, A Tibben

Journal of Medical Genetics Jul 2004, 41 (7) e100; DOI: 10.1136/jmg.2003.017541
Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer
P Watson, S A Narod, R Fodde, A Wagner, J F Lynch, S T Tinley, C L Snyder, S A Coronel, B Riley, Y Kinarsky, H T Lynch

Journal of Medical Genetics Aug 2003, 40 (8) 591-596; DOI: 10.1136/jmg.40.8.591
Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions
J Körkkö, I Kaitila, L Lönnqvist, L Peltonen, L Ala-Kokko

Journal of Medical Genetics Jan 2002, 39 (1) 34-41; DOI: 10.1136/jmg.39.1.34
Why do women attend familial breast cancer clinics?
Kate Brain, Jonathon Gray, Paul Norman, Evelyn Parsons, Angus Clarke, Cerilan Rogers, Robert Mansel, Peter Harper

Journal of Medical Genetics Mar 2000, 37 (3) 197-202; DOI: 10.1136/jmg.37.3.197
Guidelines for a genetic risk based approach to advising women with a family history of breast cancer
D M Eccles, D G R Evans, J Mackay

Journal of Medical Genetics Mar 2000, 37 (3) 203-209; DOI: 10.1136/jmg.37.3.203
Mutational analysis using oligonucleotide microarrays
Joseph G Hacia, Francis S Collins

Journal of Medical Genetics Oct 1999, 36 (10) 730-736; DOI: 10.1136/jmg.36.10.730
Mutational analysis of the N-ras,p53,p16^INK4a ,CDK4, and MC1R genes in human congenital melanocytic naevi
Thilo Papp, Heidi Pemsel, Regina Zimmermann, Ralf Bastrop, Dieter G Weiss, Dietmar Schiffmann

Journal of Medical Genetics Aug 1999, 36 (8) 610-614; DOI: 10.1136/jmg.36.8.610
Mucopolysaccharidosis type IIIB (Sanfilippo B): identification of 18 novel α-N-acetylglucosaminidase gene mutations
Susanna Bunge, Astrid Knigge, Cordula Steglich, Wim J Kleijer, Otto P van Diggelen, Michael Beck, Andreas Gal

Journal of Medical Genetics Jan 1999, 36 (1) 28-32; DOI: 10.1136/jmg.36.1.28

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