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| Exome-wide Association Study Identifies CLEC3B Missense Variant p.S106G as Being Associated With Extreme Longevity in East Asian Populations 期刊论文
Journals of Gerontology: Biological Sciences, 2017, 卷号: 72, 期号: 3, 页码: 309–318
作者: Tanisawa K; Arai Y; Hirose N; Shimokata H; Yamada Y
  收藏 | 浏览/下载：61/0 | 提交时间：2016/05/13
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| Transcriptome Profile Reveals that Pu-Erh Tea Represses the Expression of Vitellogenin Family to Reduce Fat Accumulation in Caenorhabditis elegans 期刊论文
Molecules, 2016, 卷号: 21, 期号: X, 页码: E1379
作者: Xiao RY; Hao JJ; Liang B[*]; Ding YH; Che YY
收藏 | 浏览/下载：19/0 | 提交时间：2016/10/24
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| A comprehensive meta-analysis of ZNF804A SNPs in the risk of schizophrenia among Asian populations 期刊论文
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2016, 卷号: 171, 期号: 3, 页码: 437-446
作者: Huang L; Ohi K; Yue WH; Zhang D; Gao L[*]
收藏 | 浏览/下载：24/0 | 提交时间：2016/07/20
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| The impact of CACNA1C allelic variation on regional gray matter volume in Chinese population 期刊论文
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2016, 卷号: 171, 期号: 3, 页码: 396-401
作者: Huang L; Mo Y; Sun XJ; Yu HL; Li H
收藏 | 浏览/下载：13/0 | 提交时间：2016/01/14
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| GWAS-identified schizophrenia risk SNPs at TSPAN18 are highly diverged between Europeans and East Asians. 期刊论文
AMERICAN JOURNAL OF MEDICAL GENETICS PART B Neuropsychiatric Genetics, 2016, 卷号: 171, 期号: 8, 页码: 1032–1040
作者: Liu JW; Li M[*]; Su B[*]
收藏 | 浏览/下载：11/0 | 提交时间：2016/06/20
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| No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects 期刊论文
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2016, 卷号: 171, 期号: 2, 页码: 160-168
作者: Li M; Huang L; Wang J; Su B[*]; Luo XJ[*]
收藏 | 浏览/下载：21/0 | 提交时间：2015/10/12
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| Genetic variant in NDUFS1 gene is associated with schizophrenia and negative symptoms in Han Chinese 期刊论文
JOURNAL OF HUMAN GENETICS, 2015, 卷号: 60, 期号: 1, 页码: 11-16;
作者: Zhu YL; Wang ZL; Ni JL; Zhang Y; Chen MJ
收藏 | 浏览/下载：14/0 | 提交时间：2015/03/06 |
| The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies 期刊论文
JOURNAL OF HUMAN GENETICS, 2014, 卷号: 59, 期号: 2, 页码: 66-77
作者: Bandelt HJ[*]; Kloss-Brandstatter A; Richards MB; Yao YG; Logan I
收藏 | 浏览/下载：14/0 | 提交时间：2014/04/04
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| IDH1 p.R132 mutations may not be actively involved in the carcinogenesis of hepatocellular carcinoma 期刊论文
MEDICAL SCIENCE MONITOR, 2014, 卷号: 20, 期号: X, 页码: 247-254
作者: Lu J; Zou Y; Xu L; Yang RX; Fan Y
收藏 | 浏览/下载：16/0 | 提交时间：2014/10/16
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| Meta-analysis of differentially expressed genes in osteosarcoma based on gene expression data 期刊论文
BMC MEDICAL GENETICS, 2014, 卷号: 15, 期号: X, 页码: e80
作者: Yang ZZ[*]; Chen YB; Fu Y; Yang YH; Zhang Y
收藏 | 浏览/下载：17/0 | 提交时间：2014/10/10
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