Mitochondrial DNA and inflammatory diseases Germaine EscamesLuis Carlos LópezDarío Acuña-Castroviejo Review Paper 07 July 2011 Pages: 161 - 173
Preimplantation genetic diagnosis: State of the ART 2011 Joyce C. HarperSioban B. SenGupta Review Paper 12 July 2011 Pages: 175 - 186
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain Sarah L. WilliamsonLaura GiudiciJohn Christodoulou Original Investigation 12 July 2011 Pages: 187 - 200
Mitochondrial Haplogroup X is associated with successful aging in the Amish Monique D. CourtenayJohn R. GilbertWilliam K. Scott Original Investigation 13 July 2011 Pages: 201 - 208
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group Guntram BorckNaseebullah KakarChristian Kubisch Original Investigation 15 July 2011 Pages: 209 - 216
Meta-analysis of new genome-wide association studies of colorectal cancer risk Ulrike PetersCarolyn M. HutterGraham Casey Original Investigation 15 July 2011 Pages: 217 - 234
The cell adhesion gene PVRL3 is associated with congenital ocular defects Salil A. LachkeAnne W. HigginsRichard L. Maas Original Investigation 17 July 2011 Pages: 235 - 250
The impact of Converso Jews on the genomes of modern Latin Americans C. VelezP. F. PalamaraH. Ostrer Original Investigation 26 July 2011 Pages: 251 - 263
Successful COG8 and PDF overlap is mediated by alterations in splicing and polyadenylation signals Isabel Pereira-CastroRita QuentalLuisa Azevedo Original Investigation 30 July 2011 Pages: 265 - 274
Analysis of family- and population-based samples in cohort genome-wide association studies Ani ManichaikulWei-Min ChenJosyf C. Mychaleckyj Original Investigation 30 July 2011 Pages: 275 - 287
Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan children Collins OumaGregory C. DavenportDouglas J. Perkins Original Investigation 05 August 2011 Pages: 289 - 299
Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH Daniel E. Pineda-AlvarezErich RoesslerMaximilian Muenke Original Investigation 13 August 2011 Pages: 301 - 310
Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q Muhammad Hashim RazaRana AmjadDennis Drayna Short Report 29 December 2011 Pages: 311 - 313
Michelle Webb (ed): Cancer Susceptibility: Methods and Protocols Abeer AlsaeghDiana M. Eccles Book Review 10 September 2011 Pages: 315 - 316