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American Journal of Human Genetics|August 16, 2006
Schizophrenia and oxidative stress: glutamate cysteine ligase modifier as a susceptibility geneMirjana Tosic, Jurg Ott, Sandra Barral, et al.American Journal of Human Genetics|September 9, 2006
Reduction of sample heterogeneity through use of population substructure: an example from a population of African American families with sarcoidosisCheryl L Thompson, Benjamin A Rybicki, Michael C Iannuzzi, et al.American Journal of Human Genetics|September 9, 2006
CRYBA4, a novel human cataract gene, is also involved in microphthalmiaGail Billingsley, Sathiyavedu T Santhiya, Andrew D Paterson, et al.American Journal of Human Genetics|September 9, 2006
A genomewide search finds major susceptibility loci for nicotine dependence on chromosome 10 in African AmericansMing D Li, Thomas J Payne, Jennie Z Ma, et al.American Journal of Human Genetics|May 11, 2006
Total-genome analysis of BRCA1/2-related invasive carcinomas of the breast identifies tumor stroma as potential landscaper for neoplastic initiationFrank Weber, Lei Shen, Koichi Fukino, et al.American Journal of Human Genetics|May 11, 2006
Cathepsin D deficiency is associated with a human neurodegenerative disorderRobert Steinfeld, Konstanze Reinhardt, Kathrin Schreiber, et al.American Journal of Human Genetics|May 11, 2006
Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genesLude Franke, Harm van Bakel, Like Fokkens, et al.American Journal of Human Genetics|May 11, 2006
Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.American Journal of Human Genetics|May 11, 2006
Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genesCapucine Delnatte, Damien Sanlaville, Jean-Francois Mougenot, et al.American Journal of Human Genetics|May 11, 2006
Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndromeVishwanathan Hucthagowder, Nina Sausgruber, Katherine H Kim, et al.Pageof 979