Yujun Shao

Analysis of the RELN gene as a genetic risk factor for autism

J. Sutcliffe, S. Folstein, J. Gilbert, 2005, Molecular Psychiatry.

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2001, American journal of human genetics.

Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism.

R. Jensen, Yi-Ju Li, J. Vance, 2005, Archives of Neurology.

An autosomal genomic screen for dementia in an extended Amish family

J. Haines, M. Pericak-Vance, W. Scott, 2005, Neuroscience Letters.

Fine mapping of autistic disorder to chromosome 15q11‐q13 by use of phenotypic subtypes.

M A Pericak-Vance, J. Gilbert, M. Cuccaro, 2003, American journal of human genetics.

Behavioral Comparisons in Autistic Individuals from Multiplex and Singleton Families

M. Cuccaro, M. Pericak-Vance, R. Abramson, 2003, Journal of autism and developmental disorders.

Genomic screen and follow-up analysis for autistic disorder.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2002, American journal of medical genetics.