1. Editorial

   • David N. Cooper
   • Thomas J. Hudson

   Editorial 10 August 2007 Pages: 217 - 217

2. Progress in defining the molecular biology of age related macular degeneration

   • Andrew Lotery
   • Dorothy Trump

   Review 21 July 2007 Pages: 219 - 236

   

3. Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations

   • Rita Y. Y. Yong
   • Linda S. H. Gan
   • Eric P. H. Yap

   Original Investigation 23 June 2007 Pages: 237 - 249

   

4. Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin

   • Prodipto Pal
   • Huifeng Xi
   • Ranjan Deka

   Original Investigation 26 June 2007 Pages: 251 - 259

   

5. A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3

   • Sylvain Hanein
   • Alexandra Dürr
   • Giovanni Stevanin

   Original Investigation 28 June 2007 Pages: 261 - 273

   

6. 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. Asselbergs
   • Scott M. Williams
   • Jason H. Moore

   Original Investigation 26 June 2007 Pages: 275 - 281

   

7. Refinement of the genetic cause of ATR-16

   • Cornelis L. Harteveld
   • Marjolein Kriek
   • Piero C. Giordano

   Original Investigation 28 June 2007 Pages: 283 - 292

   

8. Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene

   • Qingjiong Zhang
   • Fareeha Zulfiqar
   • J. Fielding Hejtmancik

   Original Investigation 29 June 2007 Pages: 293 - 299

   

9. Variation in estimated recombination rates across human populations

   • Jan Graffelman
   • David J. Balding
   • Jaume Bertranpetit

   Original Investigation 03 July 2007 Pages: 301 - 310

   

10. Multilocus OCA2 genotypes specify human iris colors

    • Tony Frudakis
    • Timothy Terravainen
    • Matthew Thomas

    Original Investigation 07 July 2007 Pages: 311 - 326

    

11. Genetic variation in prehistoric Sardinia

    • David Caramelli
    • Cristiano Vernesi
    • Guido Barbujani

    Original Investigation 13 July 2007 Pages: 327 - 336

    

12. Evidence for a large double-cruciform DNA structure on the X chromosome of human and chimpanzee

    • Florian O. Losch
    • Anne Bredenbeck
    • Paul Wrede

    Original Investigation 19 July 2007 Pages: 337 - 343

    

13. Germ-line DNA copy number variation frequencies in a large North American population

    • George Zogopoulos
    • Kevin C. H. Ha
    • Steven Gallinger

    Original Investigation 19 July 2007 Pages: 345 - 353

    

14. Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts

    • Mervi Alanne
    • Kati Kristiansson
    • Markus Perola

    Original Investigation 20 July 2007 Pages: 355 - 365

    

15. Synergistic contribution of CD14 and HLA loci in the susceptibility to Buerger disease

    • Zhiyong Chen
    • Megumi Takahashi
    • Akinori Kimura

    Original Investigation 25 July 2007 Pages: 367 - 372

16. In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndrome

    • Annie Rebibo-Sabbah
    • Igor Nudelman
    • Tamar Ben-Yosef

    Original Investigation 25 July 2007 Pages: 373 - 381

    

17. Y chromosomes of prehistoric people along the Yangtze River

    • Hui Li
    • Ying Huang
    • Li Jin

    Original Investigation 27 July 2007 Pages: 383 - 388

    

18. Novel Robinow syndrome causing mutations in the proximal region of the frizzled-like domain of ROR2 are retained in the endoplasmic reticulum

    • Bassam R. Ali
    • Steve Jeffery
    • Ali R. Afzal

    Original Investigation 31 July 2007 Pages: 389 - 395

    

19. Polymorphisms in the 3′ UTR in the neurocalcin δ gene affect mRNA stability, and confer susceptibility to diabetic nephropathy

    • Masumi Kamiyama
    • Masaaki Kobayashi
    • Shiro Maeda

    Original Investigation 02 August 2007 Pages: 397 - 407

    

20. 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

21. Novel human pathological mutations

    Human Gene Mutations 24 August 2007 Pages: 413 - 420

22. 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 Muallem
    • Kari E. North
    • Nobuyo Maeda

    Erratum 24 August 2007 Pages: 421 - 422