Candidate SNPs for a universal individual identification panel Andrew J. PakstisWilliam C. SpeedKenneth K. Kidd Original Investigation 27 February 2007 Pages: 305 - 317
A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis Ghazanfar AliMuhammad Salman ChishtiWasim Ahmad Original Investigation 27 February 2007 Pages: 319 - 325
Common variation in KLKB1 and essential hypertension risk: tagging-SNP haplotype analysis in a case-control study Xiangfeng LuWeiyan ZhaoDongfeng Gu Original Investigation 23 February 2007 Pages: 327 - 335
AZFc somatic microdeletions and copy number polymorphism of the DAZ genes in human males exposed to natural background radiation Sanjay PremiJyoti SrivastavaSher Ali Original Investigation 17 February 2007 Pages: 337 - 346
Enrichment of longevity phenotype in mtDNA haplogroups D4b2b, D4a, and D5 in the Japanese population Gabriela AlexeNoriyuki FukuMasashi Tanaka Original Investigation 17 February 2007 Pages: 347 - 356
An entropy-based genome-wide transmission/disequilibrium test Jinying ZhaoEric BoerwinkleMomiao Xiong Original Investigation 13 February 2007 Pages: 357 - 367
Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome Dagmar WieczorekMichael LudwigBernhard Horsthemke Original Investigation 13 February 2007 Pages: 369 - 376
Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms Hiroyuki AkagawaAkira NaritaIturo Inoue Original Investigation 08 February 2007 Pages: 377 - 387
Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations Piotr KozlowskiPenelope RobertsDavid J. Kwiatkowski Original Investigation 08 February 2007 Pages: 389 - 400
Cholesteryl ester transfer protein gene haplotypes, plasma high-density lipoprotein levels and the risk of coronary heart disease Pamela A. McCaskieJohn P. BeilbyLyle J. Palmer Original Investigation 08 February 2007 Pages: 401 - 411
A novel locus for autosomal recessive spastic ataxia on chromosome 17p Naima BouslamAhmed BouhoucheGiovanni Stevanin Original Investigation 02 February 2007 Pages: 413 - 420
Quantitative effects of common genetic variations in the 3′UTR of the human LDL-receptor gene and their associations with plasma lipid levels in the Atherosclerosis Risk in Communities study Hind MuallemKari E. NorthNobuyo Maeda Original Investigation 02 February 2007 Pages: 421 - 431
Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for the visual phenotype in the original report of uniparental disomy 14 Wojciech WiszniewskiRichard Alan LewisJames R. Lupski Original Investigation 31 January 2007 Pages: 433 - 439
Epigenetic control of the critical region for premature ovarian failure on autosomal genes translocated to the X chromosome: a hypothesis Flavio RizzolioCinzia SalaDaniela Toniolo Original Investigation 31 January 2007 Pages: 441 - 450
Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia Justine A. EllisKatrina J. ScurrahStephen B. Harrap Original Investigation 26 January 2007 Pages: 451 - 457
The advantages of dense marker sets for linkage analysis with very large families Russell ThomsonStephen QuinnJim Stankovich Original Investigation 25 January 2007 Pages: 459 - 468
The physical phenotype of girls and women with Turner syndrome is not X-imprinted Carolyn A. BondyLea Ann MaturaVladimir K. Bakalov Original Investigation 23 January 2007 Pages: 469 - 474
Autosomal recessive juvenile onset cataract associated with mutation in BFSP1 Ramya Devi RamachandranVijayalakshmi PerumalsamyJ. Fielding Hejtmancik Original Investigation 16 January 2007 Pages: 475 - 482
Genetic variation in tumor necrosis factor and lymphotoxin-alpha (TNF–LTA) and breast cancer risk Mia M. GaudetKathleen M. EganMontserrat Garcia-Closas Original Investigation 11 January 2007 Pages: 483 - 490
CYP19A1 polymorphisms are associated with bone mineral density in Chinese men Xiumei HongYi-Hsiang HsuXiping Xu Original Investigation 11 January 2007 Pages: 491 - 500
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation Vera M. KalscheuerDavid FitzPatrickReinhard Ullmann Original Investigation 09 January 2007 Pages: 501 - 509
Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study Christine Yi-Chin ChenKatrina Jacqueline ScurrahPaul Nigel Baird Original Investigation 05 January 2007 Pages: 511 - 520
SP110 polymorphisms are not associated with pulmonary tuberculosis in a South African population C. BabbE. Hanekom KeetE. G. Hoal Short Report 08 February 2007 Pages: 521 - 522
M. K. Raizada, J. F. R. Paton, S. Kasparov, M. J. Katovich (eds): Cardiovascular genomics Siobhan LoughnaCatrin Rutland Book Review 16 January 2007 Pages: 523 - 524
Edwin K. Silverman, Steven D. Shapiro, David A. Lomas, Scott T. Weiss: Respiratory Genetics Ian P. Hall Book Review 11 January 2007 Pages: 525 - 525
