Using familial information for variant filtering in high-throughput sequencing studies Melanie BahloRick TankardKatherine R. Smith Review Paper Open access 17 August 2014 Pages: 1331 - 1341
Practical aspects of genome-wide association interaction analysis Elena S. GusarevaKristel Van Steen Review Paper 28 August 2014 Pages: 1343 - 1358
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation Nathalie FieremansMarijke BautersGuy Froyen Original Investigation 19 July 2014 Pages: 1359 - 1367
Improving the power of genetic association tests with imperfect phenotype derived from electronic medical records Jennifer A. SinnottWei DaiTianxi Cai Original Investigation 26 July 2014 Pages: 1369 - 1382
Differentially co-expressed genes in postmortem prefrontal cortex of individuals with alcohol use disorders: influence on alcohol metabolism-related pathways Huiping ZhangFan WangJoel Gelernter Original Investigation 30 July 2014 Pages: 1383 - 1394
Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans Ken BataiAdam B. MurphyRick A. Kittles Original Investigation Open access 02 August 2014 Pages: 1395 - 1405
Genetic polymorphisms associated with rubella virus-specific cellular immunity following MMR vaccination Richard B. KennedyInna G. OvsyannikovaGregory A. Poland Original Investigation 07 August 2014 Pages: 1407 - 1417
Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder Iltaf AhmedKirti MittalJohn B. Vincent Original Investigation 07 August 2014 Pages: 1419 - 1429
Common genetic variation in and near the melanocortin 4 receptor gene (MC4R) is associated with body mass index in American Indian adults and children Yunhua L. MullerMarie S. ThearleLeslie J. Baier Original Investigation Open access 08 August 2014 Pages: 1431 - 1441
Nasal chondromesenchymal hamartomas arise secondary to germline and somatic mutations of DICER1 in the pleuropulmonary blastoma tumor predisposition disorder Douglas R. StewartYoav MessingerD. Ashley Hill Original Investigation 14 August 2014 Pages: 1443 - 1450
