Kejin Zhang

发表

Revisiting the impact of OXTR rs53576 on empathy: A population-based study and a meta-analysis

Xiaolin Zhou, Jinting Liu, Pingyuan Gong, 2017, Psychoneuroendocrinology.

Revisiting the relationships of 2D:4D with androgen receptor (AR) gene and current testosterone levels: Replication study and meta‐analyses

J. Zhao, Pingyuan Gong, R. Pan, 2020, Journal of neuroscience research.

Association between the ABCA1 (R219K) polymorphism and lipid profiles: a meta-analysis

Kejin Zhang, Xiuxia Hu, Zhangyan Shi, 2020, Scientific Reports.

The c.553G>T Genetic Variant of the APOA5 Gene and Altered Triglyceride Levels in the Asian Population: A Meta-Analysis of Case-Control Studies.

Hongjuan He, Lei Lei, Kejin Zhang, 2016, Genetic testing and molecular biomarkers.

Integrative Networks by BRWD3 Regulates Cytoskeleton Organization and Cell Motility

Xiao-cai Gao, Kejin Zhang, Kefan Ding, 2020 .

Association Analysis of TPH2, 5-HT2A, and 5-HT6 With Executive Function in a Young Chinese Han Population

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2011, Journal of neurogenetics.

Genetic variants of SLC12A3 modulate serum lipid profiles in a group of Mongolian pedigree population

X. Su, Kejin Zhang, Junqing Liang, 2018, Lipids in Health and Disease.

Genetic Polymorphism of GABRR2 Modulates Individuals’ General Cognitive Ability in Healthy Chinese Han People

Fuchang Zhang, Xiao-cai Gao, Kejin Zhang, 2016, Cellular and Molecular Neurobiology.

No Observable Relationship Between the 12 Genes of Nervous System and Reasoning Skill in a Young Chinese Han Population

Xiaodong Wu, Pingyuan Gong, Wenjiang Zhang, 2011, Cellular and Molecular Neurobiology.

Correlation between novel compound heterozygous ADAMTSL4 variants and primary phenotypes of ectopia lentis et pupillae.

Kejin Zhang, Junlin Li, Lijun Shang, 2022, Experimental eye research.

Kidney ion handling genes and their interaction in blood pressure control

Junjing Zhang, Kejin Zhang, C. An, 2022, Bioscience reports.

A Family-based Association Study of DIO2 and children mental retardation in the Qinba region of China

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2011, Journal of Human Genetics.

Genetic variants of SLC12A3 modulate serum lipid profiles in a group of Mongolian pedigree population

X. Su, Kejin Zhang, Junqing Liang, 2018, Lipids in Health and Disease.

Polymorphisms in the SLC12A3 Gene Encoding Sodium-Chloride Cotransporter are Associated with Hypertension: A Family-Based Study in the Mongolian Population

X. Su, Kejin Zhang, Junqing Liang, 2016, Kidney and Blood Pressure Research.

Gender Differences in Cognitive Ability Associated with Genetic Variants of NLGN4

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2010, Neuropsychobiology.

SLC12A3 variants modulate LDL cholesterol levels in the Mongolian population

X. Su, Kejin Zhang, C. An, 2017, Lipids in Health and Disease.

Genetic diversity and gentiopicroside content of four Gentiana species in China revealed by ISSR and HPLC methods

P. Zheng, Zhe-zhi Wang, Kejin Zhang, 2011 .

Independent self-construal mediates the association between CYP19A1 gene variant and subjective well-being

Rongjun Yu, G. Shen, Pingyuan Gong, 2017, Consciousness and Cognition.

Positive association of neuroligin-4 gene with nonspecific mental retardation in the Qinba Mountains Region of China

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2009, Psychiatric genetics.

Genetic variants of the type-3 metabotropic glutamate receptor gene associated with human spatial localization ability

Xiao-cai Gao, Jing Zhang, Kejin Zhang, 2021 .

Mutations of ARX and non-syndromic intellectual disability in Chinese population

Xiaofen Liu, Fuchang Zhang, Xiao-cai Gao, 2018, Genes & Genomics.

EP300 and CREBBP histone acetyltransferases modulate individuals’ episodic memory

Fuchang Zhang, Xiao-cai Gao, Kejin Zhang, 2020, Biologia.

An Association Study of the Genetic Polymorphisms in 13 Neural Plasticity-Related Genes with Semantic and Episodic Memories

Xiaodong Wu, Pingyuan Gong, Fuchang Zhang, 2011, Journal of Molecular Neuroscience.

Prediction of Alzheimer’s disease with serum lipid levels in Asian individuals: a meta-analysis

Kejin Zhang, Yufei Wu, Junlin Li, 2019, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.

A study on the correlation between IL1RAPL1 and human cognitive ability

Hui He, Fuchang Zhang, Xiao-cai Gao, 2008, Neuroscience Letters.

An Association Study on the Polymorphisms of Dopaminergic Genes with Working Memory in a Healthy Chinese Han Population

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2012, Cellular and molecular neurobiology.

A family-based association study of dopamine receptor D4 and mental retardation in Qinba region of China

Hongjuan He, Fuchang Zhang, Xiao-cai Gao, 2012, Neuroscience Letters.

Variants in COMT and DBH Influence on Response Inhibition Ability in Chinese Han Females

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2011, Cellular and Molecular Neurobiology.

Variations in 5-HT2A Influence Spatial Cognitive Abilities and Working Memory

Pingyuan Gong, Wenjiang Zhang, Fuchang Zhang, 2011, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Variations in 5-HT 2 A Influence Spatial Cognitive Abilities and Working Memory

Pingyuan Gong, Wenjiang Zhang, Fuchang Zhang, 2022 .

Integrative bioinformatic analyses of genome-wide association studies for understanding the genetic bases of human height

Tingxue Wang, Kejin Zhang, Tingxue Wang, 2020, Biologia.

Integrative bioinformatic analyses of genome-wide association studies for understanding the genetic bases of human height

Tingxue Wang, Kejin Zhang, Rao Jiang, 2020, Biologia.

An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2007, Neuroscience Letters.

Positive association between POU1F1 and mental retardation in young females in the Chinese Han population.

Lin He, Yongyong Shi, Wei Tang, 2006, Human molecular genetics.

Positive association between POU 1 F 1 and mental retardation in young females in the Chinese Han population

Lin He, Yongyong Shi, Yonglan Zheng, 2006 .

SLC12A3 variants modulate LDL cholesterol levels in the Mongolian population

X. Su, Kejin Zhang, C. An, 2017, Lipids in Health and Disease.

Polymorphic variation in CHAT gene modulates general cognitive ability: An association study with random student cohort

Xu Liu, Pingyuan Gong, Fuchang Zhang, 2016, Neuroscience Letters.

Association Analysis Between 12 Genetic Variants of Ten Genes and Personality Traits in a Young Chinese Han Population

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2010, Journal of Molecular Neuroscience.

Effect of BDNF Val66Met Polymorphism on Digital Working Memory and Spatial Localization in a Healthy Chinese Han Population

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2009, Journal of Molecular Neuroscience.

Genetic Variations in FTSJ1 Influence Cognitive Ability in Young Males in the Chinese Han Population

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2008, Journal of neurogenetics.

Positive association of the FTSJ1 gene polymorphisms with nonsyndromic X-linked mental retardation in young Chinese male subjects

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2008, Journal of Human Genetics.

Types of milk consumed and risk of essential hypertension: A 2-sample Mendelian randomization analysis.

Kejin Zhang, Zhangyan Shi, C. An, 2023, Journal of dairy science.

Non-syndromic Mental Retardation is not expressed in RAC1 Gene Polymorphisms

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2008, Neuroscience Letters.

An Association Study of the Genetic Polymorphisms in 13 Neural Plasticity-Related Genes with Semantic and Episodic Memories

Xiaodong Wu, Pingyuan Gong, Fuchang Zhang, 2012, Journal of Molecular Neuroscience.

Mental retardation and Xq12–Xq23: candidate loci for nonspecific mental retardation in the male population of the QinBa region

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2009, Psychiatric genetics.

Genetic Variants of the MTMR9 Gene Are Associated with NonSpecific Intellectual Disability: A Family-Based Association Study.

Xiaofen Liu, Fuchang Zhang, Xiao-cai Gao, 2020, Genetic testing and molecular biomarkers.

A New Role for LOC101928437 in Non-Syndromic Intellectual Disability: Findings from a Family-Based Association Test

Xingli Guo, Lin Gao, Pingyuan Gong, 2015, PloS one.

A family-based association study of dopamine receptor D4 and mental retardation in Qinba region of China

Hongjuan He, Fuchang Zhang, Xiao-cai Gao, 2012, Neuroscience Letters.

Polymorphisms in the DLG3 Gene is not Associated with Non-Syndromic Mental Retardation in the Chinese Han Population of Qin-Ba Mountain

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2011, Cellular and Molecular Neurobiology.

Genetic variations of FACL4 have no obvious influence on cognitive ability in young Chinese children

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2010, Psychiatry Research.

Mutations of ARX and non-syndromic intellectual disability in Chinese population

Xiaofen Liu, Fuchang Zhang, Xiao-cai Gao, 2018, Genes & Genomics.

Genetic Variations in FTSJ1 Influence Cognitive Ability in Young Males in the Chinese Han Population

Pingyuan Gong, Fuchang Zhang, Xiao-cai Gao, 2008, Journal of neurogenetics.

Possible Relationship between the COMT Gene Vel158Met Polymorphism and Psychometric IQ in Girls of the Qinba Region in China

Fuchang Zhang, Xiao-cai Gao, Zi-jian Zheng, 2008, Neuropsychobiology.