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American Journal of Human Genetics|August 5, 2005
Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficitJoachim F Hallmayer, Luba Kalaydjieva, Johanna Badcock, et al.
American Journal of Human Genetics|August 5, 2005
The BTNL2 gene and sarcoidosis susceptibility in African Americans and WhitesBenjamin A Rybicki, Jose L Walewski, Mary J Maliarik, et al.
American Journal of Human Genetics|August 5, 2005
Genomewide significant linkage to migrainous headache on chromosome 5q21Dale R Nyholt, Katherine I Morley, Manuel A R Ferreira, et al.
American Journal of Human Genetics|September 22, 2005
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritisVictoria E H Carlton, Xiaolan Hu, Anand P Chokkalingam, et al.
American Journal of Human Genetics|September 22, 2005
A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitorsQing Ling Duan, Borzoo Nikpoor, Marie-Pierre Dube, et al.
American Journal of Human Genetics|September 22, 2005
Charting the ancestry of African AmericansAntonio Salas, Angel Carracedo, Martin Richards, et al.
American Journal of Human Genetics|April 28, 2006
Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping methodDmitri V Zaykin, Zhaoling Meng, Margaret G Ehm
American Journal of Human Genetics|April 28, 2006
Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12Patrick M Gaffney, Carl D Langefeld, Robert R Graham, et al.
American Journal of Human Genetics|August 16, 2006
The value of molecular haplotypes in a family-based linkage studyE M Gillanders, J V Pearson, A J M Sorant, et al.
American Journal of Human Genetics|August 16, 2006
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humansHuimin Wu, Jill A Cowing, Michel Michaelides, et al.
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