Kejin Zhang

Dr. Kejin Zhang

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2017 in Psychoneuroendocrinology
Verified
Journal Article
Closed access
PGPingyuan Gong
Pingyuan Gong
HFHuiyong Fan
Huiyong Fan
JLJinting Liu
Jinting Liu
XYXing Yang
Xing Yang
KZKejin Zhang
Kejin Zhang
Xiaolin ZhouXiaolin Zhou
Xiaolin Zhou

3 April 2013 in Journal of Gastrointestinal Cancer
Verified
Journal Article
Closed access
PDF file
SWShaogui Wan
Shaogui Wan
YLYinzhi Lai
Yinzhi Lai
RMRonald E. Myers
Ronald E. Myers
BLBingshan Li
Bingshan Li
THTerry Hyslop
Terry Hyslop
HYHushan Yang
Hushan Yang

8 May 2009 in Journal of Molecular Neuroscience
Verified
Journal Article
Closed access
PDF file
PGPingyuan Gong
Pingyuan Gong
AZAnyun Zheng
Anyun Zheng
DCDongmei Chen
Dongmei Chen
WGWanhua Ge
Wanhua Ge
CLChangchao Lv
Changchao Lv
FZFuchang Zhang
Fuchang Zhang

1 January 2014 in World Journal of Gastroenterology
Verified
Journal Article
Open access
KZKejin Zhang
Kejin Zhang
JCJesse Civan
Jesse Civan
SMSushmita Mukherjee
Sushmita Mukherjee
FPFenil Patel
Fenil Patel
HYHushan Yang
Hushan Yang
Colorectal cancer (CRC) has an apparent hereditary component, as evidenced by the well-characterized genetic syndromes and family history associated with the increased risk of this disease. However, in a large fraction of CRC cases, no known genetic syndrome or family history can be identified, suggesting the presence of "missing heritability" in CRC etiology. The genome-wide association study (GWAS) platform has led to the identification of multiple replicable common genetic variants associated with CRC risk. These newly discovered genetic variations might account for a portion of the missing heritability. Here, we summarize the recent GWASs related to newly identified genetic variants associated with CRC risk and clinical outcome. The findings from these studies suggest that there is a lack of understanding of the mechanism of many single nucleotide polymorphisms (SNPs) that are associated with CRC. In addition, the utility of SNPs as prognostic markers of CRC in clinical settings remains to be further assessed. Finally, the currently validated SNPs explain only a small fraction of total heritability in complex-trait diseases like CRC. Thus, the "missing heritability" still needs to be explored further. Future epidemiological and functional investigations of these variants will add to our understanding of CRC pathogenesis, and may ultimately lead to individualized strategies for prevention and treatment of CRC.


1 January 2011 in Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
Verified
Journal Article
Open access
PDF file
PGPingyuan Gong
Pingyuan Gong
JLJing Li
Jing Li
JWJian Wang
Jian Wang
XLXu Lei
Xu Lei
DCDongmei Chen
Dongmei Chen
FZFuchang Zhang
Fuchang Zhang
Background: 5-hydroxytryptamine receptor 2A (5-HT2A) participates in diverse psychiatric disorders by regulating the activity of serotonin. Some previous studies have also suggested that the receptor is involved in cognitive abilities of disease groups. We hypothesize that some functional genetic variants in5-HT2Ahave certain specific influences on cognitive abilities in a normal population.Method: To confirm this hypothesis, two polymorphisms (rs6313 and rs4941573) in5-HT2Awere selected, and a population-based study was performed in a young healthy Chinese Han cohort.Results: The results indicated that the rs6313 and rs4941573 were associated with touching blocks and mental rotation-3D error ratio in males, and the rs4941573 was associated with visuo-spatial working memory in the whole cohort.Conclusion: All the findings suggest that5-HT2Aparticipates in human spatial cognitive abilities and spatial working memory.