Insight into the biochemical characteristics of a novel glucokinase gene mutation Yunfeng ShenMengyin CaiJianping Weng Original Investigation 23 November 2010 Pages: 231 - 238
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population Cong LiFan WangQing K. Wang Original Investigation 25 November 2010 Pages: 239 - 246
Genetic variants in telomere-maintaining genes and skin cancer risk Hongmei NanAbrar A. QureshiJiali Han Original Investigation 30 November 2010 Pages: 247 - 253
Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome Tahir MehmoodAnne SchneiderAndré Hanauer Original Investigation 30 November 2010 Pages: 255 - 269
Erratum to: Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome Tahir MehmoodAnne SchneiderAndré Hanauer Erratum 17 December 2010 Pages: 271 - 271
Investigation of 15 of the top candidate genes for late-onset Alzheimer’s disease Olivia BelbinMinerva M. CarrasquilloSteven G. Younkin Original Investigation Open access 04 December 2010 Pages: 273 - 282
Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes Maciej GeremekMarcel BruinenbergCisca Wijmenga Original Investigation 07 December 2010 Pages: 283 - 293
Transcriptomic analysis of cell-free fetal RNA suggests a specific molecular phenotype in trisomy 18 Keiko KoideDonna K. SlonimDiana W. Bianchi Original Investigation 09 December 2010 Pages: 295 - 305
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans Ken Sin LoJames G. WilsonGuillaume Lettre Original Investigation 12 December 2010 Pages: 307 - 317
Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis Wojciech WiszniewskiRichard Alan LewisJames R. Lupski Original Investigation 14 December 2010 Pages: 319 - 327
A novel locus for disseminated superficial actinic porokeratosis maps to chromosome 16q24.1-24.3 Jing LuanZhenmin NiuZhizhong Zheng Original Investigation 14 December 2010 Pages: 329 - 334
Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients Lei YuJi-Cheng LvHong Zhang Original Investigation 17 December 2010 Pages: 335 - 344
Germline PKHD1 mutations are protective against colorectal cancer Christopher J. WardYanhong WuLisa A. Boardman Short Report 28 January 2011 Pages: 345 - 349