Progress in defining the molecular biology of age related macular degeneration Andrew LoteryDorothy Trump Review 21 July 2007 Pages: 219 - 236
Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations Rita Y. Y. YongLinda S. H. GanEric P. H. Yap Original Investigation 23 June 2007 Pages: 237 - 249
Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin Prodipto PalHuifeng XiRanjan Deka Original Investigation 26 June 2007 Pages: 251 - 259
A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3 Sylvain HaneinAlexandra DürrGiovanni Stevanin Original Investigation 28 June 2007 Pages: 261 - 273
The effects of polymorphisms in genes from the renin–angiotensin, bradykinin, and fibrinolytic systems on plasma t-PA and PAI-1 levels are dependent on environmental context Folkert W. AsselbergsScott M. WilliamsJason H. Moore Original Investigation 26 June 2007 Pages: 275 - 281
Refinement of the genetic cause of ATR-16 Cornelis L. HarteveldMarjolein KriekPiero C. Giordano Original Investigation 28 June 2007 Pages: 283 - 292
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene Qingjiong ZhangFareeha ZulfiqarJ. Fielding Hejtmancik Original Investigation 29 June 2007 Pages: 293 - 299
Variation in estimated recombination rates across human populations Jan GraffelmanDavid J. BaldingJaume Bertranpetit Original Investigation 03 July 2007 Pages: 301 - 310
Multilocus OCA2 genotypes specify human iris colors Tony FrudakisTimothy TerravainenMatthew Thomas Original Investigation 07 July 2007 Pages: 311 - 326
Genetic variation in prehistoric Sardinia David CaramelliCristiano VernesiGuido Barbujani Original Investigation 13 July 2007 Pages: 327 - 336
Evidence for a large double-cruciform DNA structure on the X chromosome of human and chimpanzee Florian O. LoschAnne BredenbeckPaul Wrede Original Investigation 19 July 2007 Pages: 337 - 343
Germ-line DNA copy number variation frequencies in a large North American population George ZogopoulosKevin C. H. HaSteven Gallinger Original Investigation 19 July 2007 Pages: 345 - 353
Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts Mervi AlanneKati KristianssonMarkus Perola Original Investigation 20 July 2007 Pages: 355 - 365
Synergistic contribution of CD14 and HLA loci in the susceptibility to Buerger disease Zhiyong ChenMegumi TakahashiAkinori Kimura Original Investigation 25 July 2007 Pages: 367 - 372
In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndrome Annie Rebibo-SabbahIgor NudelmanTamar Ben-Yosef Original Investigation 25 July 2007 Pages: 373 - 381
Y chromosomes of prehistoric people along the Yangtze River Hui Li Ying HuangLi Jin Original Investigation 27 July 2007 Pages: 383 - 388
Novel Robinow syndrome causing mutations in the proximal region of the frizzled-like domain of ROR2 are retained in the endoplasmic reticulum Bassam R. AliSteve JefferyAli R. Afzal Original Investigation 31 July 2007 Pages: 389 - 395
Polymorphisms in the 3′ UTR in the neurocalcin δ gene affect mRNA stability, and confer susceptibility to diabetic nephropathy Masumi KamiyamaMasaaki KobayashiShiro Maeda Original Investigation 02 August 2007 Pages: 397 - 407
Comments on the paper by D. Li and L. He: Meta-analysis shows association between the tryptophan hydroxylase (TPH) gene and schizophrenia P. G. Sand Letter to the Editors 25 July 2007 Pages: 409 - 411
Quantitative effects of common genetic variations in the 3′UTR of the human LDL-receptor gene and their associations with plasma lipid levels in the Atherosclerosis Risk in Communities study Hind MuallemKari E. NorthNobuyo Maeda Erratum 24 August 2007 Pages: 421 - 422