探索精神疾病遗传学中的替代表型。 - Suppr

Suppr

超能文献

Searching for alternative phenotypes in psychiatric genetics.

作者信息

Leboyer Marion

机构信息

Service de psychiatrie (Pr Rouillon), Hôpital Albert Chenevier, 94010 Creitel, France.

出版信息

Methods Mol Med. 2003;77:145-61. doi: 10.1385/1-59259-348-8:145.

DOI:10.1385/1-59259-348-8:145

PMID:12298368

Abstract

摘要

相似文献

Searching for alternative phenotypes in psychiatric genetics.

Methods Mol Med. 2003;77:145-61. doi: 10.1385/1-59259-348-8:145.

Genetic markers in psychiatric genetics.

Methods Mol Med. 2003;77:63-98. doi: 10.1385/1-59259-348-8:63.

Psychiatric genetics. Future and prospects.

Methods Mol Med. 2003;77:251-65. doi: 10.1385/1-59259-348-8:251.

Psychopharmacogenetics and psychiatric genetics: similar methodological challenges.

J Psychiatry Neurosci. 1999 May;24(3):211-4.

Psychiatric genetics: back to the future.

Mol Psychiatry. 2000 Jan;5(1):22-31. doi: 10.1038/sj.mp.4000702.

Analytical methods applied to psychiatric genetics.

Methods Mol Med. 2003;77:23-61. doi: 10.1385/1-59259-348-8:23.

Psychiatric genetics. Overview on achievements, problems, perspectives.

Methods Mol Med. 2003;77:3-20.

[The concept of environment in human genetics and psychiatry].

Fortschr Neurol Psychiatr Grenzgeb. 1972 Oct;40(10):554-64.

Psychiatric genetics in Israel.

Psychiatr Genet. 1999 Jun;9(2):53-7. doi: 10.1097/00041444-199906000-00001.

[Biological studies in psychiatry].

Neuropsihijatrija. 1970;18(1):19-27.

引用本文的文献

Executive functions as a potential neurocognitive endophenotype in anxiety disorders: A systematic review considering DSM-IV and DSM-5 diagnostic criteria classification.

Dement Neuropsychol. 2015 Jul-Sep;9(3):285-294. doi: 10.1590/1980-57642015DN93000012.

Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):542-548. doi: 10.1002/ajmg.b.31016.

Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):424-33. doi: 10.1002/ajmg.b.30612.

Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder.

Eur Psychiatry. 2007 Jan;22(1):32-8. doi: 10.1016/j.eurpsy.2006.05.002. Epub 2006 Nov 28.

Familial resemblance for executive functions in families of schizophrenic and bipolar patients.

Psychiatry Res. 2006 Nov 15;144(2-3):131-8. doi: 10.1016/j.psychres.2005.11.013. Epub 2006 Oct 2.

Lack of influence of COMT and NET genes variants on executive functions in schizophrenic and bipolar patients, their first-degree relatives and controls.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 5;141B(5):504-12. doi: 10.1002/ajmg.b.30352.

Endophenotypes in the personality disorders.

Dialogues Clin Neurosci. 2005;7(2):139-51. doi: 10.31887/DCNS.2005.7.2/lsiever.

Platelet serotonergic markers as endophenotypes for obsessive-compulsive disorder.

Neuropsychopharmacology. 2005 Aug;30(8):1539-47. doi: 10.1038/sj.npp.1300752.

Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia.

Neurotox Res. 2004;6(1):35-41. doi: 10.1007/BF03033294.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验