Qi Zhou

发表

A Novel Variant of the FZD4 Gene in a Chinese Family Causes Autosomal Dominant Familial Exudative Vitreoretinopathy

Jingliang Cheng, Junjiang Fu, Lisha Yang, 2018, Cellular Physiology and Biochemistry.

A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree

Jingliang Cheng, Junjiang Fu, M. Khan, 2019, Journal of cellular and molecular medicine.

Effective inhibition of human cytomegalovirus gene expression by DNA-based external guide sequences.

Yi Zou, Hongjian Li, Qi Zhou, 2009, Acta biochimica et biophysica Sinica.

A heterozygous mutation in RPGR associated with X‐linked retinitis pigmentosa in a patient with Turner syndrome mosaicism (45,X/46,XX)

Rui Chen, R. Sui, Hui Li, 2018, American journal of medical genetics. Part A.

Lack of association between the HindIII RFLP of the osteocalcin (BGP) gene and bone mineral density (BMD) in healthy pre- and postmenopausal Chinese women

H. Deng, Qi Zhou, Yuan-yuan Zhang, 2003, Journal of Bone and Mineral Metabolism.

Estrogen receptor alpha gene polymorphisms and peak bone density in Chinese nuclear families.

Hui Shen, R. Recker, H. Deng, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[Association of Apa I polymorphism of vitamin D receptor gene with bone mass in men].

Qi Zhou, Zhenlin Zhang, Jin-wei He, 2003, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.

Association of estrogen receptor-alpha and vitamin D receptor genotypes with therapeutic response to calcium in postmenopausal Chinese women.

Qi Zhou, Zhenlin Zhang, Jin-wei He, 2004, Acta pharmacologica Sinica.

The regulation-of-autophagy pathway may influence Chinese stature variation: evidence from elder adults

Xue-zhen Zhu, H. Deng, Xiao-gang Liu, 2010, Journal of Human Genetics.

Types and viral load of human papillomavirus, and vaginal microbiota in vaginal intraepithelial neoplasia: a cross-sectional study

K. Hua, Jingxin Ding, Qi Zhou, 2020, Annals of translational medicine.

Parathyroid hormone gene with bone phenotypes in Chinese.

S. Lei, Yao-Zhong Liu, H. Deng, 2003, Biochemical and biophysical research communications.

Whole Genome Distribution and Ethnic Differentiation of Copy Number Variation in Caucasian and Asian Populations

S. Levy, R. Recker, H. Deng, 2009, PloS one.

Polymorphisms of four bone mineral density candidate genes in Chinese populations and comparison with other populations of different ethnicity

Hui Shen, Xiangding Chen, S. Lei, 2003, Journal of Bone and Mineral Metabolism.

Mutations/polymorphisms in the 55 kDa subunit of DNA polymerase epsilon in human colorectal cancer.

H. Pospiech, Y. Collan, J. Syväoja, 2009, Cancer genomics & proteomics.

Five novel mutations of SRD5A2 found in eight Chinese patients with 46,XY disorders of sex development.

M. Nie, Xueyan Wu, J. Mao, 2011, Molecular human reproduction.

Genomic changes of the 55 kDa subunit of DNA polymerase epsilon in human breast cancer.

H. Pospiech, Y. Collan, J. Syväoja, 2008, Cancer Genomics & Proteomics.

Novel compound heterozygous missense variants (c.G955A and c.A1822C) of CACNA2D4 likely causing autosomal recessive retinitis pigmentosa in a Chinese patient

Jingliang Cheng, Jiewen Fu, Chunli Wei, 2021, 3 Biotech.

Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA

Jingliang Cheng, Jiewen Fu, Qi Zhou, 2020, Molecular medicine reports.

A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa

Jingliang Cheng, Jiewen Fu, Chunli Wei, 2019, Bioscience reports.

Identification of a Novel Heterozygous Missense Mutation in the CACNA1F Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing

Jingliang Cheng, Rui Chen, Junjiang Fu, 2015, BioMed research international.

Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci

Xiangding Chen, S. Lei, Yao-Zhong Liu, 2009, Human Genetics.

DNA repair gene polymorphism associated with sensitivity of lung cancer to therapy

Yu Liu, Qi Zhou, Qi-ying Li, 2012, Medical Oncology.

Genetic and phenotypic characteristics of three Mainland Chinese families with choroideremia

I. MacDonald, Y. Sergeev, R. Sui, 2012, Molecular vision.

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis.

Yan Guo, Tie-Lin Yang, Meng Li, 2008, American journal of human genetics.

A genome wide association study between copy number variation (CNV) and human height in Chinese population.

Xiangding Chen, S. Lei, Yao-Zhong Liu, 2010, Journal of genetics and genomics = Yi chuan xue bao.

Genome-Wide Association Study Identifies ALDH7A1 as a Novel Susceptibility Gene for Osteoporosis

Meng Li, Xiangding Chen, S. Lei, 2010, PLoS genetics.

Genomic analysis of the 55 kDa subunit of DNA polymerase epsilon in human intracranial neoplasms.

H. Pospiech, Y. Collan, K. Huoponen, 2010, Cancer genomics & proteomics.

CLINICAL CHARACTERISTICS AND MOLECULAR GENETIC ANALYSIS OF A COHORT OF CHINESE PATIENTS WITH CHOROIDEREMIA.

R. Sui, Shijing Wu, Hui Li, 2020, Retina.

Rep1 copy number variation is an important genetic cause of choroideremia in Chinese patients

R. Sui, Lizhu Yang, Hui Li, 2017, Experimental eye research.

Novel homozygous p.R454C mutation in the CYP11B1 gene leads to 11β-hydroxylase deficiency in a Chinese patient.

Chaoming Wu, Qi Zhou, Chao Zheng, 2011, Fertility and sterility.

Protein expression profile of the mouse metaphase-II oocyte.

Liu Wang, Qing-zhang Li, Xuejiang Guo, 2008, Journal of proteome research.

Genomic Changes of the 55 kDa Subunit of DNA Polymerase ε in Human Breast Cancer

H. Pospiech, Y. Collan, J. Syväoja, 2008 .

Genomic Analysis of the 55 kDa Subunit of DNA Polymerase ϵ in Human Intracranial Neoplasms

H. Pospiech, Y. Collan, K. Huoponen, 2010 .

Estrogen Receptor α Gene Polymorphisms and Peak Bone Density in Chinese Nuclear Families

Hui Shen, R. Recker, H. Deng, 2003 .

No major effect of the insulin-like growth factor I gene on bone mineral density in premenopausal Chinese women.

Hui Shen, H. Deng, Qi Zhou, 2005, Bone.

Mutations/Polymorphisms in the 55 kDa Subunit of DNA Polymerase ϵ in Human Colorectal Cancer

H. Pospiech, Y. Collan, J. Syväoja, 2009 .

Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I

I. MacDonald, W. Kimberling, O. Lehmann, 2012, Molecular vision.

Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the CDH23 Gene Causing Usher Syndrome Type ID in a Chinese Patient

Jiewen Fu, Qi Zhou, H. Lv, 2020, Frontiers in Genetics.

Mutational analysis of androgen receptor gene in four Chinese patients with male pseudohermaphroditism.

M. Nie, Xueyan Wu, J. Mao, 2010, Fertility and sterility.