US2011014610A1PendingUtilityA1
Compositions and methods for diagnosing and treating neuropsychiatric disorders
Assignee: UNIV LELAND STANFORD JUNIORPriority: Mar 31, 2005Filed: Feb 5, 2010Published: Jan 20, 2011
Est. expiryMar 31, 2025(expired)· nominal 20-yr term from priority
Inventors:Huda AkilMary AtzWilliam BunneyWilliam ByerleyKathleen CaseyPrabhakara V. ChoudarySimon J. EvansEdward G. JonesJun LiJuan F. LopezRichard M. MyersBrandi RollinsRobert C. ThompsonHiroaki TomitaMarquis VawterStanley Watson
C12Q 2600/136A61P 25/18G01N 2800/302G01N 2500/04A61P 25/24G01N 33/6896G01N 33/573G01N 33/6893G01N 2800/28C12Q 2600/158A61P 25/22C12Q 1/6883G01N 2500/00C12Q 2600/156G01N 2800/304A61P 25/28G01N 2800/30
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Claims
Abstract
The present invention provides methods for diagnosing mental disorders (e.g., psychotic disorders such as schizophrenia and mood disorders such as major depression disorder and bipolar disorder). The invention also provides methods of identifying modulators of such mental disorders as well as methods of using these modulators to treat patients suffering from such mental disorders.
Claims
exact text as granted — not AI-modified1 . A method for determining whether a subject has or is predisposed for a mental disorder, the method comprising the steps of:
(i) obtaining a biological sample from a subject; (ii) contacting the sample with a reagent that selectively associates with a polynucleotide or polypeptide encoded by a nucleic acid that hybridizes under stringent conditions to a nucleotide sequence of Tables 1-14; and (iii) detecting the level of reagent that selectively associates with the sample, thereby determining whether the subject has or is predisposed for a mental disorder.
2 . The method of claim 1 , wherein the reagent is an antibody.
3 . The method of claim 1 , wherein the reagent is a nucleic acid.
4 . The method of claim 1 , wherein the reagent associates with a polynucleotide.
5 . The method of claim 4 , wherein the reagent selectively associates with a polynucleotide comprising at least one of the SNPs listed in Table 6.
6 . The method of claim 1 , wherein the regent associates with a polypeptide.
7 . The method of claim 1 , wherein the level of reagent that associates with the sample is different from a level associated with humans without a mental disorder.
8 . The method of claim 1 , wherein the biological sample is obtained from amniotic fluid.
9 . The method of claim 1 , wherein the mental disorder is a psychotic disorder or a mood disorder.
10 . The method of claim 1 , wherein the sample is derived from brain tissue or lymphocytes.
11 . The method of claim 10 , wherein the sample is derived from brain tissue.
12 . The method of claim 11 , wherein the sample is derived from a brain region selected from the group consisting of the anterior cingulate cortex (AnCg), dorsolateral prefrontal cortex (DLPFC), cerebellar cortex (CB), superior temporal gyrus (STG), parietal cortex (PC), nucleus accumbens (nAcc), and amygdala (amy).
13 . The method of claim 7 , wherein the level of reagent that associates with the sample is higher than a level associated with humans without a mental disorder.
14 . The method of claim 9 , wherein the psychotic disorder is schizophrenia.
15 . The method of claim 9 , wherein the mood disorder is major depression disorder or bipolar disorder.
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