Genetic linkage of systemic lupus erythematosus to 13q32 in African American families with affected male members Chao XingCourtney Gray-McGuireJane M. Olson Original Investigation 28 September 2005 Pages: 309 - 321
One step closer to fixing association studies: evidence for age- and gender-specific allele frequency variations and deviations from Hardy-Weinberg expectations in controls Haydeh PayamiMotao ZhuLina Moses Original Investigation 28 September 2005 Pages: 322 - 330
Extensive Sequencing of the CFTR gene: lessons learned from the first 157 patient samples Matthew J. McGinnissChristina ChenCharles M. Strom Original Investigation 28 September 2005 Pages: 331 - 338
Comprehensive genetic evaluation of common E-cadherin sequence variants and prostate cancer risk: strong confirmation of functional promoter SNP Sara LindströmFredrik WiklundHenrik Grönberg Original Investigation 28 September 2005 Pages: 339 - 347
Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1 Helmut GrasbergerMartine VaxillaireSamuel Refetoff Original Investigation 28 September 2005 Pages: 348 - 355
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3–p21.2 between D1S2896 and D1S457 but outside ABCA4 Qingjiong ZhangFareeha ZulfiqarJ. Fielding Hejtmancik Original Investigation 28 September 2005 Pages: 356 - 365
Geography is a better determinant of human genetic differentiation than ethnicity Andrea ManicaFranck PrugnolleFrançois Balloux Original Investigation 28 September 2005 Pages: 366 - 371
The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis Michele D. BishopSteven D. FreedmanPeter R. Durie Original Investigation 29 September 2005 Pages: 372 - 381
Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicine Nan YangHongzhe LiMichael F. Seldin Original Investigation 29 September 2005 Pages: 382 - 392
Acyl-CoA: cholesterol acyltransferase-2 gene polymorphisms and their association with plasma lipids and coronary artery disease risks Xuelian HeYongjian LuChew-Kiat Heng Original Investigation 30 September 2005 Pages: 393 - 403
An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3′ haplotypes could modify circulating levels of mannose-binding lectin Toralf BernigWillemijn BreunisStephen Chanock Original Investigation 06 October 2005 Pages: 404 - 415
The EPAS1 gene influences the aerobic–anaerobic contribution in elite endurance athletes Jennifer HendersonJason M. Withford-CaveBing Yu Original Investigation 06 October 2005 Pages: 416 - 423
Comparison of three methods to estimate genetic ancestry and control for stratification in genetic association studies among admixed populations Hui-Ju TsaiShweta ChoudhryElad Ziv Original Investigation 06 October 2005 Pages: 424 - 433
Systemic lupus erythematosus susceptibility loci defined by genome scan meta-analysis Young Ho LeeSwapan K. Nath Original Investigation 06 October 2005 Pages: 434 - 443
Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference Shurong HuangLishan ChenJunko Oshima Original Investigation 06 October 2005 Pages: 444 - 450
A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1 Jost SchönbergerLeif KühlerMichael Zimmer Original Investigation 14 October 2005 Pages: 451 - 457
A new mutation in exon 7 of NEMO gene: late skewed X-chromosome inactivation in an incontinentia pigmenti female patient with immunodeficiency Natalia Martinez-PomarIvan Munoz-SaaNuria Matamoros Original Investigation 14 October 2005 Pages: 458 - 465
Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR Cynthia HelmsNancy L. SacconeAnne M. Bowcock Original Investigation 19 October 2005 Pages: 466 - 476
Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation Hiroki KanoKenji KurosawaTatsushi Toda Original Investigation 19 October 2005 Pages: 477 - 483
Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association E. K. TanK. Y. PuongY. Zhao Original Investigation 22 October 2005 Pages: 484 - 488
Generation or birth cohort effect on cancer risk in Li–Fraumeni syndrome Barry W. BrownTracy J. CostelloLouise C. Strong Original Investigation 12 November 2005 Pages: 489 - 498
A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population Agnes L. NishimuraAmmar Al-ChalabiMayana Zatz Short Report 27 September 2005 Pages: 499 - 500
A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p Myrto PapaioannouChristina F. ChakarovaShomi S. Bhattacharya Short Report 28 September 2005 Pages: 501 - 503
Allelic imbalance analysis of oral tongue squamous cell carcinoma by high-density single nucleotide polymorphism arrays using whole-genome amplified DNA Xiaofeng ZhouStephane TemamDavid T. W. Wong Short Report 29 September 2005 Pages: 504 - 507
Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome Giles D.J. WattsSarju G. MehtaVirginia E. Kimonis Short Report 22 October 2005 Pages: 508 - 514
Linkage methods in human genetics before the computer A. W. F. Edwards Historical and Personal Perspectives 11 November 2005 Pages: 515 - 530
Molecular characterization of histidinemia: identification of four missense mutations in the histidase gene Yoko KawaiAkihiko MoriyamaMariko Suchi Erratum 30 September 2005 Pages: 531 - 532
