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本文引用的文献

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Strategies for Advancing Disease Definition Using Biomarkers and Genetics: The Bipolar and Schizophrenia Network for Intermediate Phenotypes.利用生物标志物和遗传学推进疾病定义的策略:双相情感障碍和精神分裂症中间表型网络。
Biol Psychiatry Cogn Neurosci Neuroimaging. 2017 Jan;2(1):20-27. doi: 10.1016/j.bpsc.2016.07.005. Epub 2016 Aug 2.
2
Irving I. Gottesman (1930-2016): the multifactorial threshold model of complex phenotypes mediated by endophenotype strategies.欧文·I·戈特斯曼(1930 - 2016):以内表型策略介导的复杂表型的多因素阈值模型。
Genes Brain Behav. 2016 Nov;15(8):775-776. doi: 10.1111/gbb.12345.
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Epigenetic Mechanisms in Psychiatric Diseases and Epigenetic Therapy.精神疾病中的表观遗传机制与表观遗传治疗
Drug Dev Res. 2016 Nov;77(7):407-413. doi: 10.1002/ddr.21340. Epub 2016 Sep 4.
4
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation.精神分裂症的综合遗传-表观遗传分析:遗传关联与DNA甲基化差异共定位的证据
Genome Biol. 2016 Aug 30;17(1):176. doi: 10.1186/s13059-016-1041-x.
5
Reviewing the epigenetics of schizophrenia.精神分裂症的表观遗传学研究综述。
J Ment Health. 2019 Feb;28(1):71-79. doi: 10.1080/09638237.2016.1207229. Epub 2016 Aug 25.
6
Sensorimotor gating of the startle reflex: what we said 25 years ago, what has happened since then, and what comes next.惊吓反射的感觉运动门控:我们25年前所说的,从那时起发生了什么,以及接下来会怎样。
J Psychopharmacol. 2016 Nov;30(11):1072-1081. doi: 10.1177/0269881116661075. Epub 2016 Aug 18.
7
Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study.一项全基因组关联研究中DNA甲基化差异与精神分裂症的关联
JAMA Psychiatry. 2016 May 1;73(5):506-14. doi: 10.1001/jamapsychiatry.2016.0144.
8
Identification of Distinct Psychosis Biotypes Using Brain-Based Biomarkers.利用基于脑的生物标志物识别不同的精神病生物型
Am J Psychiatry. 2016 Apr 1;173(4):373-84. doi: 10.1176/appi.ajp.2015.14091200. Epub 2015 Dec 7.
9
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内表型、表观遗传学、多基因性等等:欧文·戈特斯曼的动态遗产。

Endophenotypes, Epigenetics, Polygenicity and More: Irv Gottesman's Dynamic Legacy.

作者信息

Braff David L, Tamminga Carol A

机构信息

Department of Psychiatry, University of California, San Diego, La Jolla, CA;

Department of Psychiatry, UT Southwestern Medical School, Dallas, TX.

出版信息

Schizophr Bull. 2017 Jan;43(1):10-16. doi: 10.1093/schbul/sbw157. Epub 2016 Nov 21.

DOI:10.1093/schbul/sbw157
PMID:27872267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5216869/
Abstract

First, we describe the hallmark contributions of Irv Gottesman's pioneering scholarship for schizophrenia research including concepts of polygenicity, gene × environment interactions, epigenetics and the endophenotype concept. Gottesman and colleagues' twin studies showed that genes, not social factors, mediate schizophrenia risk. He then showed that schizophrenia is highly polygenic. Next, he introduced the concept of epigenetics into schizophrenia research. Gottesman then introduced the quantitative endophenotype concept. Endophenotypes are laboratory-based measures that show deficits in schizophrenia patients and lesser deficits in their first degree "unaffected" relatives and are viewed as being more proximal to genes and having a simpler genetic architecture than are "fuzzy" qualitative diagnostic disorders. Endophenotypes offer an exciting path to gene discovery, neural circuits, genetic architecture and new treatment pathways of schizophrenia and related psychotic disorders. Second, we were asked to discuss 2 of many endophenotype Consortia and related studies, in order to illustrate the impact of Gottesman's work. We describe the Consortium on the Genetics of Schizophrenia (COGS) exploring neurocognitive and neurophysiological endophenotypes in family and case-control studies. Association, linkage, sequencing and epigenetic studies are described. The Bipolar and Schizophrenia Network for Intermediate Phenotypes (BSNIP) uses an array of endophenotypes including brain imaging in studies across the psychosis dimension, allowing for dimensional analyses. BSNIP results have led to the concept of biotypes, advancing the field. Irv Gottesman was imaginatively prescient in generating novel insights and predicting many major issues which challenge schizophrenia researchers who still use his concepts to guide current research approaches.

摘要

首先,我们阐述欧文·戈特斯曼开创性学术研究对精神分裂症研究的标志性贡献,包括多基因性、基因×环境相互作用、表观遗传学和内表型概念。戈特斯曼及其同事的双生子研究表明,介导精神分裂症风险的是基因,而非社会因素。随后他证明精神分裂症具有高度多基因性。接着,他将表观遗传学概念引入精神分裂症研究。戈特斯曼随后引入了定量内表型概念。内表型是基于实验室的测量指标,在精神分裂症患者中表现出缺陷,在其一级“未患病”亲属中缺陷程度较轻,并且被视为比“模糊”的定性诊断疾病更接近基因且遗传结构更简单。内表型为精神分裂症及相关精神障碍的基因发现、神经回路、遗传结构和新治疗途径提供了一条令人兴奋的道路。其次,我们受邀讨论众多内表型联盟及相关研究中的两项,以阐明戈特斯曼工作的影响。我们描述了精神分裂症遗传学联盟(COGS),该联盟在家庭研究和病例对照研究中探索神经认知和神经生理内表型。文中介绍了关联研究、连锁研究、测序研究和表观遗传学研究。双相情感障碍和精神分裂症中间表型网络(BSNIP)在整个精神病维度的研究中使用一系列内表型,包括脑成像,从而能够进行维度分析。BSNIP的研究结果催生了生物型的概念,推动了该领域的发展。欧文·戈特斯曼极具想象力和先见之明,提出了新颖的见解并预测了许多重大问题,这些问题至今仍困扰着精神分裂症研究者,他们仍在使用他的概念来指导当前的研究方法。