1. Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population

   • Kim W. Carter
   • Joseph Hung
   • Lyle J. Palmer

   Original Investigation 21 August 2008 Pages: 199 - 206

2. Genome-wide distribution of ancestry in Mexican Americans

   • Analabha Basu
   • Hua Tang
   • Neil Risch

   Original Investigation 28 August 2008 Pages: 207 - 214

   

3. Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome

   • Zubair M. Ahmed
   • Saima Riazuddin
   • Thomas B. Friedman

   Original Investigations 22 August 2008 Pages: 215 - 223

   

4. Network-based model weighting to detect multiple loci influencing complex diseases

   • Wei Pan

   Original Investigations 22 August 2008 Pages: 225 - 234

   

5. Gender influences monoallelic expression of ATP10A in human brain

   • Amber Hogart
   • Katherine A. Patzel
   • Janine M. LaSalle

   Original Investigation 23 August 2008 Pages: 235 - 242

   

6. Genetic regulation of amniotic fluid TNF-alpha and soluble TNF receptor concentrations affected by race and preterm birth

   • Ramkumar Menon
   • Digna R. Velez
   • Scott M. Williams

   Original Investigation 21 September 2008 Pages: 243 - 253

   

7. Sequence variants in the PLEKHH2 region are associated with diabetic nephropathy in the GoKinD study population

   • Christopher N. Greene
   • Lisa M. Keong
   • Patricia W. Mueller

   Original Investigation 28 August 2008 Pages: 255 - 262

   

8. Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease

   • Brenda L. Powell
   • Steven Wiltshire
   • John P. Beilby

   Original Investigations 30 August 2008 Pages: 263 - 270

9. Germline BRCA1 mutations predispose to pancreatic adenocarcinoma

   • Wigdan Al-Sukhni
   • Heidi Rothenmund
   • Steven Gallinger

   Original Investigation 02 September 2008 Pages: 271 - 278

   

10. A germline mutation of the KIF1Bβ gene on 1p36 in a family with neural and nonneural tumors

    • I-Tien Yeh
    • Romina E. Lenci
    • Patricia L. M. Dahia

    Original Investigations 26 August 2008 Pages: 279 - 285

    

11. LRRK2 R1628P increases risk of Parkinson’s disease: replication evidence

    • E. K. Tan
    • Louis C. Tan
    • Yi Zhao

    Short Report 10 September 2008 Pages: 287 - 288

12. Merlin G. Butler, Philip D. K. Lee, Barbara Y. Whitman: Management of Prader-Willi syndrome

    • Ruth Newbury-Ecob

    Book Review 10 September 2008 Pages: 289 - 290

13. Jan A. Witkowski and John R. Inglis (eds): Davenport’s dream. Twenty-first century reflections on heredity and eugenics

    • Ian D. Young

    Book Review 25 August 2008 Pages: 291 - 292

14. Novel human pathological mutations

    Human Gene Mutations 12 September 2008 Pages: 293 - 324