Rachel Miller

CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree

P. Stankiewicz, J. Lupski, S. Cheung, 2014, European Journal of Human Genetics.

A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband

A. Addington, J. Rapoport, M. K. Rudd, 2011, Case reports in genetics.

Adjunctive use of lithium carbonate for the management of neutropenia in clozapine‐treated children

J. Rapoport, N. Gogtay, J. Tossell, 2009, Human psychopharmacology.

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.