R. Long

发表

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

A. Caspi, A. Danese, K. Sugden, 2011, Molecular Psychiatry.

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

J. Gécz, A. Addington, J. Rapoport, 2012, Molecular Psychiatry.

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

H. Hakonarson, M. Bayés, J. McCracken, 2010, Molecular Psychiatry.

Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories

P Shaw, J L Rapoport, A. Addington, 2007, Molecular Psychiatry.

Lack of an association between a dopamine-4 receptor polymorphism and attention-deficit/hyperactivity disorder: genetic and brain morphometric analyses

J N Giedd, F X Castellanos, J L Rapoport, 1998, Molecular Psychiatry.

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.

C. Freitag, H. Hakonarson, J. Swanson, 2010, Molecular psychiatry.

Sex chromosome anomalies in childhood onset schizophrenia: an update

A. Addington, J. Rapoport, S. Nelson, 2008, Molecular Psychiatry.

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

N. Gogtay, P. Gochman, G. Rouleau, 2012, Molecular Psychiatry.

Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21.

J. Rapoport, E. Green, S. Kumra, 2000, American journal of medical genetics.

Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

J M Trent, J L Rapoport, J. Rapoport, 1998, American journal of medical genetics.