Human Molecular Genetics

The pressure rises: update on the genetics of phaeochromocytoma
pp. 2347-2354(8)
Authors: E.R. Maher; C. Eng

Gene therapy of muscular dystrophy
pp. 2355-2362(8)
Author: J.S. Chamberlain

DiGeorge syndrome: the use of model organisms to dissect complex genetics
pp. 2363-2369(7)
Author: A. Baldini

The NF-B signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes
pp. 2371-2375(5)
Authors: Asma Smahi; Gilles Courtois; Smail Hadj Rabia; Rainer Döffinger; Christine Bodemer; Arnold Munnich; Jean-Laurent Casanova; Alain Israël

Molecular genetics of calcium sensing in bone cells
pp. 2377-2384(8)
Authors: J. Purroy; N.K. Spurr

Molecular genetics of too much bone
pp. 2385-2393(9)
Authors: K. Janssens; W. van Hul

Impaired dopamine storage resulting from -synuclein mutations may contribute to the pathogenesis of Parkinson's disease
pp. 2395-2407(13)
Authors: J. Lotharius; P. Brundin

Signals and their transduction pathways regulating alternative splicing: a new dimension of the human genome
pp. 2409-2416(8)
Author: S. Stamm

The allelic architecture of human disease genes: common disease–common variant… or not?
pp. 2417-2423(7)
Authors: J.K. Pritchard; N.J. Cox

Ion channels: structural bioinformatics and modelling
pp. 2425-2433(9)
Authors: C.E. Capener; H.J. Kim; Y. Arinaminpathy; M.S.P. Sansom

Ion channel diseases
pp. 2435-2445(11)
Authors: Christian A. Hübner; Thomas J. Jentsch

Protecting genomic integrity during DNA replication: correlation between Werner's and Bloom's syndrome gene products and the MRE11 complex
pp. 2447-2453(7)
Authors: A. Franchitto; P. Pichierri

The allelic structure of common disease
pp. 2455-2461(7)
Authors: D.J. Smith; A.J. Lusis

Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans
pp. 2463-2468(6)
Author: H.J. Cordell

Susceptibility to malaria as a complex trait: big pressure from a tiny creature
pp. 2469-2478(10)
Authors: A. Fortin; M.M. Stevenson; P. Gros

Cancer epigenomics
pp. 2479-2488(10)
Author: Christoph Plass

Understanding familial and non-familial renal cell cancer
pp. 2489-2498(10)
Authors: D. Bodmer; W. van den Hurk; J.J.M. van Groningen; M.J. Eleveld; G.J.M. Martens; M.A.J. Weterman; A. Geurts van Kessel

Phenotypic diversity in hypertrophic cardiomyopathy
pp. 2499-2506(8)
Authors: M. Arad; J.G. Seidman; C.E. Seidman

Gene finding in genetically isolated populations
pp. 2507-2515(9)
Authors: Peter Heutink; Ben A. Oostra

Pharmacogenomics in schizophrenia: the quest for individualized therapy
pp. 2517-2530(14)
Authors: V.S. Basile; M. Masellis; S.G. Potkin; J.L. Kennedy