Chromosome abnormalities, mental retardation and the search for genes in bipolar disorder and schizophrenia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Toxicology,General Neuroscience
Link
http://link.springer.com/content/pdf/10.1007/BF03033803.pdf
Reference54 articles.
1. Badner JA and ES Gershon (2002) Meta-analysis of wholegenome linkage scans of bipolar disorder and schizophrenia.Mol. Psychiatry 7, 405–411.
2. Baum AE, N Akula, M Cabanero, I Cardona, W Corona, B Klemens, TG Schulze, S Cichon, M Rietschel, MM Nothen, A Georgi, J Schumacher, M Schwarz, R Abou Jamra, S Hofels, P Propping, J Satagopan, SD Detera-Wadleigh, J Hardy and FJ McMahon (2008) A genome-wide association study implicates diacylglycerol kinase eta(DGKH) and several other genes in the etiology of bipolar disorder.Mol. Psychiatry 13, 197–207.
3. Bennett RL, M Karayiorgou, CA Sobin, TH Norwood and MA Kay (1997) Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophreniasusceptibility locus at 5q21-23.1.Am. J. Hum. Genet. 61, 1450–1454.
4. Blackwood DH, A Fordyce, MT Walker, DM St Clair, DJ Porteous and WJ Muir (2001) Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.Am. J. Hum. Genet. 69, 428–433.
5. Boer H, A Holland, J Whittington, J Butler, T Webb and D Clarke (2002) Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.Lancet 359, 135–136.
Cited by 19 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Review of Neuroreceptors for Clinical and Experimental Neuropharmacology in Central Nervous System Disorders;Current Reviews in Clinical and Experimental Pharmacology;2023-11
2. Whole Genome Sequencing Revealed Inherited Rare Oligogenic Variants Contributing to Schizophrenia and Major Depressive Disorder in Two Families;International Journal of Molecular Sciences;2023-07-21
3. Intellectual Disability, Mental Health and Mental Disorders;Intellectual Disabilities: Health and Social Care Across the Lifespan;2023
4. Involvement of Rare Mutations of SCN9A, DPP4, ABCA13, and SYT14 in Schizophrenia and Bipolar Disorder;International Journal of Molecular Sciences;2021-12-07
5. Identification of a Rare Novel KMT2C Mutation That Presents with Schizophrenia in a Multiplex Family;Journal of Personalized Medicine;2021-11-25
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3