3 results match your criteria: "and Harvard Partners Center for Genetics and Genomics[Affiliation]"
Schizophr Res
October 2006
Department of Psychiatry Research, The Zucker Hillside Hospital, North Shore-Long Island Jewish Health System, 75-59 263rd Street, Glen Oaks, NY 11004, and Harvard Partners Center for Genetics and Genomics, Boston, MA, United States.
Inconsistencies in the relation between COMT variation and schizophrenia may be clarified by careful delineation of a target phenotype. The present study reports a significant association between a COMT haplotype and the severity of manic symptoms in 162 patients with schizophrenia or schizoaffective disorder (SZ). These data suggest that the effect of COMT variation may be associated with comorbid manic symptoms in SZ.
View Article and Find Full Text PDFArch Pathol Lab Med
March 2005
Department of Pathology, Massachusetts General Hospital and Harvard Partners Center for Genetics and Genomics, Boston, Mass, USA.
Context: The College of American Pathologists (CAP) provides proficiency testing (PT) surveys to laboratories around the world.
Objectives: To compare diagnostic assay methods for serum/plasma cortisol and immunoglobulin (Ig) E in terms of their bias and precision, to determine how well CAP PT specimens simulate human serum, and to reassess proficiency test grading criteria in light of these findings.
Design: A participant-blinded, prospective trial.
Proc Natl Acad Sci U S A
July 2002
Department of Medicine and Harvard Partners Center for Genetics and Genomics, Harvard Medical School, Boston, MA 02115, USA.
Flap endonuclease (Fen1) is required for DNA replication and repair, and defects in the gene encoding Fen1 cause increased accumulation of mutations and genome rearrangements. Because mutations in some genes involved in these processes cause cancer predisposition, we investigated the possibility that Fen1 may function in tumorigenesis of the gastrointestinal tract. Using gene knockout approaches, we introduced a null mutation into murine Fen1.
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