The genetics of kidney transplantation Nicolas PalletEric Thervet Review Paper 16 September 2011 Pages: 317 - 323
Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? Mark RichardsFrédérique CoppéeMeena Upadhyaya Review Paper 09 October 2011 Pages: 325 - 340
Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population Xin LiuGuoying WangXiaobin Wang Original Investigation 17 August 2011 Pages: 341 - 351
Sex differences in disease risk from reported genome-wide association study findings Linda Y. LiuMarc A. SchaubAtul J. Butte Original Investigation 20 August 2011 Pages: 353 - 364
The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations Myung-Ju AhnHong-Hee WonKeunchil Park Original Investigation 25 August 2011 Pages: 365 - 372
Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing Kathleen AsklandCynthia ReadJason H. Moore Original Investigation 25 August 2011 Pages: 373 - 391
Expression signature of epidermolysis bullosa simplex Mbarka BchetniaMarie-Lou TremblayCatherine Laprise Original Investigation 30 August 2011 Pages: 393 - 406
Novel Alu retrotransposon insertion leading to Alström syndrome Mustafa TaşkesenGayle B. CollinJürgen K. Naggert Original Investigation 30 August 2011 Pages: 407 - 413
Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genes Umm-e-KalsoomSulman BasitWasim Ahmad Original Investigation 30 August 2011 Pages: 415 - 422
High altitude adaptation in Daghestani populations from the Caucasus Luca PaganiQasim AyubChris Tyler-Smith Original Investigation Open access 09 September 2011 Pages: 423 - 433
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia Jose Felix Marti-MassoJavier Ruiz-MartínezCoro Paisán-Ruiz Original Investigation 13 September 2011 Pages: 435 - 442
Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population Kazuo YamadaYoshimi IwayamaTakeo Yoshikawa Original Investigation Open access 17 September 2011 Pages: 443 - 451
SLC39A2 and FSIP1 polymorphisms as potential modifiers of arsenic-related bladder cancer Margaret R. KaragasAngeline S. AndrewKarl T. Kelsey Original Investigation 25 September 2011 Pages: 453 - 461
Genome-wide association study identifies HMGN3 locus for spine bone size variation in Chinese Shu-Feng LeiHui ShenHong-Wen Deng Original Investigation 25 September 2011 Pages: 463 - 469
Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height Jae-Jung KimYoung-Mi ParkJong-Keuk Lee Original Investigation 29 September 2011 Pages: 471 - 478
Fine mapping of 14q24.1 breast cancer susceptibility locus Phoebe LeeYi-Ping FuStephen J. Chanock Original Investigation 30 September 2011 Pages: 479 - 490
Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II Hua ZhangHongsheng ChenYong Feng Original Investigation 01 October 2011 Pages: 491 - 503
Associations between common variants in GC and DHCR7/NADSYN1 and vitamin D concentration in Chinese Hans Ling LuHongguang ShengXu Lin Original Investigation 05 October 2011 Pages: 505 - 512
Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis Lluís ArmengolJulián NevadoLuis Alberto Pérez-Jurado Original Investigation Open access 06 October 2011 Pages: 513 - 523
Review of Aaron Gillette, Eugenics and the nature–nurture debate in the twentieth century 2007, paperback edition, 2011, New York: Palgrave Macmillan John Dupré Book Review 29 September 2011 Pages: 525 - 526
