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科研机构
北京大学 [48]
内容类型
期刊论文 [38]
其他 [10]
发表日期
2017 [9]
2016 [9]
2015 [11]
2014 [8]
2013 [2]
2012 [2]
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共48条,第1-10条
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专题:北京大学
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Genomic analysis of oesophageal squamous-cell carcinoma identifies alcohol drinking-related mutation signature and genomic alterations
其他
2017-01-01
Chang, Jiang
;
Tan, Wenle
;
Ling, Zhiqiang
;
Xi, Ruibin
;
Shao, Mingming
;
Chen, Mengjie
;
Luo, Yingying
;
Zhao, Yanjie
;
Liu, Yun
;
Huang, Xiancong
;
Xia, Yuchao
;
Hu, Jinlin
;
Parker, Joel S.
;
Marron, David
;
Cui, Qionghua
;
Peng, Linna
;
Chu, Jiahui
;
Li, Hongmin
;
Du, Zhongli
;
Han, Yaling
;
Tan, Wen
;
Liu, Zhihua
;
Zhan, Qimin
;
Li, Yun
;
Mao, Weimin
;
Wu, Chen
;
Lin, Dongxin
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2017/12/03
HUMAN CANCERS
LUNG-CANCER
STRUCTURAL VARIATIONS
SUSCEPTIBILITY LOCI
WIDE ASSOCIATION
TUMOR-SUPPRESSOR
PROSTATE-CANCER
POOR-PROGNOSIS
LANDSCAPE
DISCOVERY
Cell Culture System for Analysis of Genetic Heterogeneity Within Hepatocellular Carcinomas and Response to Pharmacologic Agents
其他
2017-01-01
Gao, Qiang
;
Wang, Zhi-Chao
;
Duan, Meng
;
Lin, Yi-Hui
;
Zhou, Xue-Ya
;
Worthley, Daniel L.
;
Wang, Xiao-Ying
;
Niu, Gang
;
Xia, Yuchao
;
Deng, Minghua
;
Liu, Long-Zi
;
Shi, Jie-Yi
;
Yang, Liu-Xiao
;
Zhang, Shu
;
Ding, Zhen-Bin
;
Zhou, Jian
;
Liang, Chun-Min
;
Cao, Ya
;
Xiong, Lei
;
Xi, Ruibin
;
Shi, Yong-Yong
;
Fan, Jia
收藏
  |  
浏览/下载:35/0
  |  
提交时间:2017/12/04
Liver Cancer
Next-Generation Sequencing
Patient-Derived Cell Lines
Targeted Therapy
INTRATUMOR HETEROGENEITY
GENOMIC HETEROGENEITY
TUMOR HETEROGENEITY
DRUG-SENSITIVITY
SEQUENCING DATA
CANCER-CELLS
LIVER-CANCER
MUTATIONS
EVOLUTION
SORAFENIB
Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population
期刊论文
SCIENTIFIC REPORTS, 2017
Wu, Zhiliu
;
Qin, Jian
;
You, Yang
;
Ma, Yuanlin
;
Jia, Meixiang
;
Wang, Linyan
;
Lu, Tianlan
;
Yue, Weihua
;
Ruan, Yanyan
;
Zhang, Dai
;
Li, Jun
;
Wang, Lifang
收藏
  |  
浏览/下载:123/0
  |  
提交时间:2017/12/03
SCAFFOLDING PROTEIN SHANK3
CELL CORPSE ENGULFMENT
COPY NUMBER VARIATION
DE-NOVO MUTATIONS
SPECTRUM DISORDERS
SCHIZOPHRENIA
EXPRESSION
BRAIN
NEUROLIGINS
ASTROCYTES
Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population
期刊论文
MOLECULAR PSYCHIATRY, 2017
Yu, H. G
;
Yan, H. K
;
Li, J. M
;
Li, Z. P
;
Zhang, X. D
;
Ma, Y. C
;
Mei, L. R
;
Liu, C. K
;
Cai, L. T
;
Wang, Q. V
;
Zhang, F. S
;
Iwata, N. D
;
Ikeda, M. E
;
Wang, L. P
;
Lu, T. M
;
Li, M. K
;
Xu, H. R
;
Wu, X. D
;
Liu, B. C
;
Yang, J. I
;
Li, K. R
;
Lv, L. N
;
Ma, X. A
;
Wang, C. T
;
Li, L. P
;
Yang, F. K
;
Jiang, T. L
;
Shi, Y. R
;
Li, T. P
;
Zhang, D. C
;
Yue, W. T
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2017/12/03
GENOME-WIDE ASSOCIATION
GABA(B(1)) RECEPTOR ISOFORMS
JIP1 SCAFFOLD PROTEIN
CONFERRING RISK
HUMAN BRAIN
VRK2
GABA
SUSCEPTIBILITY
METAANALYSIS
REPLICATION
Accurately annotate compound effects of genetic variants using a context-sensitive framework
期刊论文
NUCLEIC ACIDS RESEARCH, 2017
Cheng, Si-Jin
;
Shi, Fang-Yuan
;
Liu, Huan
;
Ding, Yang
;
Jiang, Shuai
;
Liang, Nan
;
Gao, Ge
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2017/12/03
CHARGE-SYNDROME
MUTATION UPDATE
GENOME
PREDICTION
EPISTASIS
HUMANS
Meta-analyses of RELN variants in neuropsychiatric disorders
期刊论文
BEHAVIOURAL BRAIN RESEARCH, 2017
Chen, Na
;
Bao, Yanping
;
Xue, Yanxue
;
Sun, Yan
;
Hu, Die
;
Meng, Shiqiu
;
Lu, Lin
;
Shi, Jie
收藏
  |  
浏览/下载:117/0
  |  
提交时间:2017/12/03
RELN gene
Psychiatric disorders
Single nucleotide polymorphism
Meta-analysis
CHINESE HAN POPULATION
REELIN GENE RELN
BIPOLAR DISORDER
ALZHEIMERS-DISEASE
SPECTRUM DISORDER
MAJOR DEPRESSION
SCHIZOPHRENIA
ASSOCIATION
EXPRESSION
AUTISM
Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer's disease
期刊论文
PLOS GENETICS, 2017
Lu, Qiongshi
;
Powles, Ryan L.
;
Abdallah, Sarah
;
Ou, Derek
;
Wang, Qian
;
Hu, Yiming
;
Lu, Yisi
;
Liu, Wei
;
Li, Boyang
;
Mukherjee, Shubhabrata
;
Crane, Paul K.
;
Zhao, Hongyu
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2017/12/03
WIDE ASSOCIATION SCAN
30 COMPLEX TRAITS
CELL DIFFERENTIATION
SUSCEPTIBILITY LOCI
GENETIC-VARIANTS
INNATE IMMUNITY
METAANALYSIS
EXPRESSION
RISK
ARCHITECTURE
Accurately annotate genetic variants: things we have to do to achieve precision medicine
其他
2017-01-01
高歌
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2017/12/03
遗传变异
生物信息学分析
低成本快速
生物测量
生物功能
things
conceptual
The association between well-being and the COMT gene: Dispositional gratitude and forgiveness as mediators
期刊论文
JOURNAL OF AFFECTIVE DISORDERS, 2017
Liu, Jinting
;
Gong, Pingyuan
;
Gao, Xiaoxue
;
Zhou, Xiaolin
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2017/12/03
COMT
Well-being
Depression
Gratitude
Forgiveness
O-METHYLTRANSFERASE COMT
VAL158MET POLYMORPHISM
LIFE SATISFACTION
DECISION-MAKING
POSITIVE AFFECT
DEPRESSION
HAPPINESS
WOMEN
DIFFERENCE
EMOTIONS
From genetic studies to precision medicine in alcohol dependence
期刊论文
BEHAVIOURAL PHARMACOLOGY, 2016
Sun, Yan
;
Zhang, Yan
;
Wang, Fan
;
Sun, Yankun
;
Shi, Jie
;
Lu, Lin
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2017/12/03
alcohol dependence
environmental factors
genetic candidates
human
precision medicine
therapeutic strategy
OPIOID RECEPTOR GENE
SEROTONIN TRANSPORTER GENE
NEUROTROPHIC-FACTOR BDNF
GENOME-WIDE ASSOCIATION
CATECHOL-O-METHYLTRANSFERASE
RANDOMIZED CONTROLLED-TRIAL
GAMMA-AMINOBUTYRIC-ACID
MONOAMINE-OXIDASE
ALDEHYDE DEHYDROGENASE
USE DISORDERS
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