Gene polymorphisms, apoptotic capacity and cancer risk Evgeny N. Imyanitov Review Article 12 February 2009 Pages: 239 - 246
Analysis of the MTHFD1 promoter and risk of neural tube defects Nicola CarrollFaith PangilinanAnne Parle-McDermott Original Investigation 08 January 2009 Pages: 247 - 256
Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele Jennelle C. HodgeKaren T.CuencoCynthia C. Morton Original Investigation 09 January 2009 Pages: 257 - 263
New genetic evidence for involvement of the dopamine system in migraine with aura Unda TodtChristian NetzerChristian Kubisch Original Investigation 17 January 2009 Pages: 265 - 279
Association of Y chromosome haplogroup I with HIV progression, and HAART outcome Efe SezginJoanne M. LindMichael W. Smith Original Investigation 24 January 2009 Pages: 281 - 294
Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation Matthew R. L. EgyudZofia K. Z. GajdosJoel N. Hirschhorn Original Investigation 28 January 2009 Pages: 295 - 303
Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans Yohan BosséFrançois BacotMartin Desrosiers Original Investigation 29 January 2009 Pages: 305 - 318
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype J. M. CameronM. MajB. H. Robinson Original Investigation 30 January 2009 Pages: 319 - 326
Huntington F. Willard and Geoffrey S. Ginsburg (eds): Genomic and personalized medicine David N. Cooper Book Review 31 December 2008 Pages: 327 - 328
Dhavendra Kumar (ed): Genomics and clinical medicine Dian Donnai Book Review 11 January 2009 Pages: 329 - 330
Charles J. Epstein, Robert P. Erickson, Anthony Wynshaw-Boris (eds): Inborn errors of development John Tolmie Book Review 29 January 2009 Pages: 331 - 331
Novel human pathological mutations Dolores Martínez-RubioJosé M. MillánCarmen Espinós Erratum 05 March 2009 Pages: 353 - 353
