Research Topics
| L E EsterlingSummaryAffiliation: National Institutes of Health Country: USA Publications
| Collaborators
|
Detail Information
Publications
Serotonin transporter (5-HTT) gene and bipolar affective disorderL E Esterling
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA
Am J Med Genet 81:37-40. 1998..We also refined the location of 5-HTT by radiation hybrid mapping, placing the locus between D17S1294 and SHGC11022 on 17q11.2...
An integrated physical map of 18p11.2: a susceptibility region for bipolar disorderL E Esterling
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA
Mol Psychiatry 2:501-4. 1997..This high resolution integrated map will be an important tool in providing loci for contig construction, and positional candidates for mutation screening...
Multiple transcriptional variants and RNA editing in C18orf1, a novel gene with LDLRA and transmembrane domains on 18p11.2T Yoshikawa
Unit on Gene Mapping and Expression, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892, USA
Genomics 47:246-57. 1998..We also present evidence of RNA editing in the 5'-UTR of beta 2, the first demonstration of this phenomenon in 5'-UTR...
A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2S D Detera-Wadleigh
Clinical Neurogenetics Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA
Proc Natl Acad Sci U S A 96:5604-9. 1999..By comprehensive screening of the entire genome, we detected unreported loci for bipolar disorder, found support for proposed linkages, and gained evidence for the overlap of susceptibility regions for bipolar disorder and schizophrenia...
Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2)T Yoshikawa
Unit on Gene Mapping and Expression, Clinical Neurogenetics Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA
Mol Psychiatry 5:165-71. 2000..By Fisher's exact test the silent mutation showed a trend for association (P = 0.051) with bipolar disorder suggesting that further scrutiny of this gene is warranted...
A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorderT Yoshikawa
Unit on Gene Mapping and Expression, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA
Mol Psychiatry 2:393-7. 1997..2 region. We, therefore, designated this novel gene as IMP.18p. The physical position and possible function suggest that IMP.18p is an important candidate gene for bipolar disorder...
Isolation of chromosome 18-specific brain transcripts as positional candidates for bipolar disorderT Yoshikawa
Clinical Neurogenetics Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892, USA
Am J Med Genet 74:140-9. 1997..The majority of the transcripts were found to cluster to discrete locations on 18p and 18q, previously hypothesized as susceptibility regions for bipolar disorder, identifying them as positional candidate genes...
Assignment of the human gene for smoothelin (SMTN) to chromosome 22q12 by fluorescence in situ hybridization and radiation hybrid mappingJ J Engelen
Department of Molecular Cell Biology and Genetics, University of Maastricht, The Netherlands
Genomics 43:245-7. 1997
Map of candidate genes and STSs on 18p11.2, a bipolar disorder and schizophrenia susceptibility regionG D Reyes
Mol Psychiatry 7:337-9. 2002
