An insertion deletion polymorphism in the signal peptide of the human apolipoprotein b geneVISVIKIS, S; CHAN, L; SIEST, G et al.HUMAN GENETICS. 1990, Vol 84, pp 373-375Article

A genome-wide screen of gene―gene interactions for rheumatoid arthritis susceptibilityCHUNYU LIU; ACKERMAN, H. Hoxie; CARULLI, John P et al.Human genetics. 2011, Vol 129, Num 5, pp 473-485, issn 0340-6717, 13 p.Article

A novel survival multifactor dimensionality reduction method for detecting gene-gene interactions with application to bladder cancer prognosisJIANG GUI; MOORE, Jason H; KELSEY, Karl T et al.Human genetics. 2011, Vol 129, Num 1, pp 101-110, issn 0340-6717, 10 p.Article

Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patientsLEI YU; LV, Ji-Cheng; ZHOU, Xu-Jie et al.Human genetics. 2011, Vol 129, Num 3, pp 335-344, issn 0340-6717, 10 p.Article

Characterization of the ZBTB42 gene in humans and miceDEVANEY, Stephanie A; MATE, Suzanne E; DEVANEY, Joseph M et al.Human genetics. 2011, Vol 129, Num 4, pp 433-441, issn 0340-6717, 9 p.Article

Distribution of the number of false discoveries in large-scale family-based association testing with application to the association between PTPN1 and hypertension and obesityWANG, Wen-Chang; HSIUNG, Chao A; WANG, Lan-Chao et al.Human genetics. 2011, Vol 129, Num 4, pp 425-432, issn 0340-6717, 8 p.Article

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African AmericansSIN LO, Ken; WILSON, James G; O'DONNELL, Christopher J et al.Human genetics. 2011, Vol 129, Num 3, pp 307-317, issn 0340-6717, 11 p.Article

Genetic contribution of the leukotriene pathway to coronary artery diseaseHARTIALA, Jaana; DALIN LI; HAZEN, Stanley L et al.Human genetics. 2011, Vol 129, Num 6, pp 617-627, issn 0340-6717, 11 p.Article

Genetic variants in the KIF6 region and coronary event reduction from statin therapyYONGHONG LI; SABATINE, Marc S; DEVLIN, James J et al.Human genetics. 2011, Vol 129, Num 1, pp 17-23, issn 0340-6717, 7 p.Article

Modifier locus of the skeletal muscle involvement in Emery―Dreifuss muscular dystrophyGRANGER, B; GUENEAU, L; DROUIN-GARRAUD, V et al.Human genetics. 2011, Vol 129, Num 2, pp 149-159, issn 0340-6717, 11 p.Article

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani familiesWASIF, Naveed; UL-HASSAN NAQVI, Syed Kamran; NADIR ALI, Sulman Basit et al.Human genetics. 2011, Vol 129, Num 4, pp 419-424, issn 0340-6717, 6 p.Article

Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibilitySEHRAWAT, Badan; SRIDHARAN, Malinee; GHOSH, Sunita et al.Human genetics. 2011, Vol 130, Num 4, pp 529-537, issn 0340-6717, 9 p.Article

RNAi: a potential new class of therapeutic for human genetic diseaseSEYHAN, Attila A.Human genetics. 2011, Vol 130, Num 5, pp 583-605, issn 0340-6717, 23 p.Article

Recent progress in the study of the genetics of heightLETTRE, Guillaume.Human genetics. 2011, Vol 129, Num 5, pp 465-472, issn 0340-6717, 8 p.Article

Sperm rates of 7q11.23, 15q11q13 and 22q11.2 deletions and duplications: a FISH approachMOLINA, Oscar; ANTON, Ester; VIDAL, Francesca et al.Human genetics. 2011, Vol 129, Num 1, pp 35-44, issn 0340-6717, 10 p.Article

Statistical approaches for the analysis of DNA methylation microarray dataSIEGMUND, Kimberly D.Human genetics. 2011, Vol 129, Num 6, pp 585-595, issn 0340-6717, 11 p.Article

Tissue-specific splicing of ISCU results in a skeletal muscle phenotype in myopathy with lactic acidosis, while complete loss of ISCU results in early embryonic death in miceNORDIN, Angelica; LARSSON, Elin; THORNELL, Lars-Eric et al.Human genetics. 2011, Vol 129, Num 4, pp 371-378, issn 0340-6717, 8 p.Article

Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin―Lowry syndromeMEHMOOD, Tahir; SCHNEIDER, Anne; SIBILLEC, Jérémie et al.Human genetics. 2011, Vol 129, Num 3, pp 255-269, issn 0340-6717, 15 p.Article

Transcriptomic analysis of cell-free fetal RNA suggests a specific molecular phenotype in trisomy 18KOIDE, Keiko; SLONIM, Donna K; JOHNSON, Kirby L et al.Human genetics. 2011, Vol 129, Num 3, pp 295-305, issn 0340-6717, 11 p.Article

Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependenceCULVERHOUSE, Robert C; SACCONE, Nancy L; STITZEL, Jerry A et al.Human genetics. 2011, Vol 129, Num 2, pp 177-188, issn 0340-6717, 12 p.Article

Alterations of ATM and CADM1 in chromosomal 11q22.3-23.2 region are associated with the development of invasive cervical carcinomaDIPANJANA MAZUMDER INDRA; MITRA, Sraboni; ROY, Anup et al.Human genetics. 2011, Vol 130, Num 6, pp 735-748, issn 0340-6717, 14 p.Article

Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCDROSS, Jessica; BADNER, Judith; SHAW MURRAY, Sarah et al.Human genetics. 2011, Vol 130, Num 6, pp 795-805, issn 0340-6717, 11 p.Article

Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19pREHMAN, Atteeq U; GUL, Khitab; KHAN, Shaheen N et al.Human genetics. 2011, Vol 130, Num 6, pp 759-765, issn 0340-6717, 7 p.Article

Special Issue on Personalized MedicineCHANOCK, Stephen J; BIANKIN, Andrew V.Human genetics. 2011, Vol 130, Num 1, issn 0340-6717, 167 p.Serial Issue

Special 50th Anniversary Issue on X-inactivationCOOPER, David N; HARPER, Peter S.Human genetics. 2011, Vol 130, Num 2, issn 0340-6717, 162 p.Serial Issue