publication venue for
- Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample.. 114:598-604. 2002
- Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample.. 105:662-668. 2001
- Department of Veterans Affairs Cooperative Studies Program genetic linkage study of schizophrenia: ascertainment methods and sample description.. 96:342-347. 2000
- Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome).. 80:115-120. 1998
- Substitution of arginine for glycine at position 154 of the alpha 1 chain of type I collagen in a variant of osteogenesis imperfecta: comparison to previous cases with the same mutation.. 61:111-116. 1996
- Substitution of arginine for glycine at position 154 of the 1 chain of type I collagen in a variant of osteogenesis imperfecta: Comparison to previous cases with the same mutation. 61:111-116. 1996
- Somatic cell mosaicism: another source of phenotypic heterogeneity in nuclear families with osteogenesis imperfecta.. 45:246-251. 1993
- Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue.. 34:60-67. 1989
- Osteogenesis imperfecta with unusual skeletal lesions: report of three families.. 21:257-269. 1985
- Contributions of mammalian embryo transfer to developmental genetics.. 18:643-648. 1984
- The shared genetics of trait neuroticism and mood and anxiety disorders 2004
- Fear conditioning and self-report fear ratings: Genetic and environmental sources of covariation 2002