Identification of rare variants in CADM1 in patients with anorexia nervosa
Author:
Funder
Fondation Maladies Rares
Publisher
Elsevier BV
Subject
Biological Psychiatry,Psychiatry and Mental health
Reference21 articles.
1. Haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005
2. Exome sequencing in a familial form of anorexia nervosa supports multigenic etiology;Bienvenu;J. Neural. Transm.,2019
3. Genetic Nicotinamide N- Methyltransferase (Nnmt) deficiency in male mice improves insulin sensitivity in diet-induced obesity but does not affect glucose tolerance;Brachs;Diabetes,2019
4. Distribution of RA175/TSLC1/SynCAM, a member of the immunoglobulin superfamily, in the developing nervous system;Fujita;Brain Res. Dev. Brain Res.,2005
5. A 2-Mb sequence-ready contig map and a novel immunoglobulin superfamily gene IGSF4 in the LOH region of chromosome 11q23.2;Gomyo;Genomics,1999
Cited by 2 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. Inclusion of the severe and enduring anorexia nervosa phenotype in genetics research: a scoping review;Journal of Eating Disorders;2024-04-29
2. Generalizability of GWA-Identified Genetic Risk Variants for Metabolic Traits to Populations from the Arabian Peninsula;Genes;2021-10-18
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