Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
Gershon, Elliot
One or more keywords matched the following items that are connected to
Gershon, Elliot
Item Type
Name
Concept
Mutation
Concept
Frameshift Mutation
Concept
INDEL Mutation
Academic Article
Detection of linkage to affective disorders in the catalogued Amish pedigrees: a reply to Pauls et al.
Academic Article
Images in neuroscience. Clinical genetics, VII. From genetics to pathophysiology: positional cloning.
Academic Article
No abnormality in the gene for the G protein stimulatory alpha subunit in patients with bipolar disorder.
Academic Article
Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5).
Academic Article
Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.
Academic Article
Detection of marker associations with a dominant disease gene in genetically complex and heterogeneous diseases.
Academic Article
Accuracy of CNV Detection from GWAS Data.
Academic Article
The detection of major loci by segregation and linkage analysis: a simulation study.
Academic Article
C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families.
Academic Article
Structural change in dopamine D2 receptor gene in a patient with neuroleptic malignant syndrome.
Academic Article
A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain.
Academic Article
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders.
Academic Article
Single-neuron whole genome sequencing identifies increased somatic mutation burden in Alzheimer's disease related genes.
Grant
Fine Genomic Mapping of 13q32 in Bipolar Disorder
Grant
Somatic Mutations in Brain in Alzheimer's Disease
Grant
Genetic Linkage Studies in Bipolar Disorder Families
Grant
The Bipolar Genome Study
Search Criteria
Mutation
detection