Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies a susceptibility locus at PLCE1

Lidong Wang, Fuyou Zhou, Xue-Min Li, +125

Nature Genetics

Genome-wide Association StudyChinese SubjectsEsophageal CancerGeneticsGenetic Epidemiology +7

Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis

Tie‐Lin Yang, Xiang-Ding Chen, Yan Guo, +23

The American Journal of Human Genetics

Genome-wide Association StudyEngineeringMedicineGeneticsGenetic Epidemiology +7

Age-Related Bone Mineral Density, Bone Loss Rate, Prevalence of Osteoporosis, and Reference Database of Women at Multiple Centers in China

Xiaoguang Cheng, Dingzhuo Yang, Qi Zhou, +13

Journal of Clinical Densitometry

Bone HealthBone Loss RateMultiple CentersMenopauseOsteoporosis +5

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

Jian Li, Tie‐Lin Yang, Liang Wang, +9

PLoS ONE

Peripapillary Choroidal Thickness in Both Eyes of Glaucoma Patients With Unilateral Visual Field Loss

Lüe Li, Ailing Bian, Qi Zhou, +1

American Journal of Ophthalmology

Ocular DiseaseOphthalmologyBoth EyesNeurologyGlaucoma +5

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

Shu‐Feng Lei, Tie‐Lin Yang, Lijun Tan, +14

Human Genetics

Genome-wide Association StudyGenome-wide Association ScanGenotype-phenotype AssociationMedicineGenetics +8

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

Yue-Juan Qin, Hui Shen, Qi-Ren Huang, +8

Journal of Bone and Mineral Research

GeneticsGenetic EpidemiologyHuman PolymorphismGynecologyChinese Nuclear Families +17

Posterior displacement of the lamina cribrosa in normal‐tension and high‐tension glaucoma

Lüe Li, Ailing Bian, Gangwei Cheng, +1

Acta Ophthalmologica

Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities.

Zixi Sun, Qi Zhou, Huajin Li, +3

PubMed

Tests of linkage and association of the COL1A2 gene with bone phenotypes’ variation in Chinese nuclear families

Fei‐Yan Deng, M.Y Liu, Miaoxin Li, +5

Bone

Bone DiseaseDevelopmental BiologyMedicineGeneticsMolecular Genetics +5