X. Qi

发表

Comparison of the diagnostic value of four scoring systems in primary sjögren's syndrome patients.

X. Qi, Chao Sun, Yu Tian, 2017, Immunology letters.

Upregulated microRNA‐485 suppresses apoptosis of renal tubular epithelial cells in mice with lupus nephritis via regulating the TGF‐β‐MAPK signaling pathway by inhibiting RhoA expression

X. Qi, Chao Sun, Yu Tian, 2018, Journal of cellular biochemistry.

Impaired bone microarchitecture in distal interphalangeal joints in patients with primary hypertrophic osteoarthropathy assessed by high-resolution peripheral quantitative computed tomography

Y. Jiang, L. Qin, Y. Xu, 2020, Osteoporosis International.

Bone Geometry, Density, Microstructure, and Biomechanical Properties in the Distal Tibia in Patients With Primary Hypertrophic Osteoarthropathy Assessed by Second‐Generation High‐Resolution Peripheral Quantitative Computed Tomography

X. Qi, X. Xing, W. Xia, 2021, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Risk factors for the formation of double-contour sign and tophi in gout

X. Qi, Chao Sun, Yu Tian, 2019, Journal of Orthopaedic Surgery and Research.

Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets

X. Qi, X. Xing, W. Xia, 2016, Bone Research.

Associations between Osteocalcin, Calciotropic Hormones, and Energy Metabolism in a Cohort of Chinese Postmenopausal Women: Peking Vertebral Fracture Study

Shuying Liu, X. Qi, X. Xing, 2021, International journal of endocrinology.

Clinical significance of progranulin correlated with serum soluble Oxford 40 ligand in primary Sjögren's syndrome

X. Qi, Chao Sun, Yu Tian, 2020, Medicine.

A Mutation in CTSK Gene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin

X. Qi, X. Xing, W. Xia, 2015, Calcified Tissue International.

Two novel CAII mutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families

X. Qi, X. Xing, W. Xia, 2015, Metabolic Brain Disease.

Familial Early-Onset Paget’s Disease of Bone Associated with a Novel hnRNPA2B1 Mutation

Asan, X. Qi, X. Xing, 2017, Calcified Tissue International.

Calciotropic Hormones and the Prevalence of Vertebral Fractures in Chinese Postmenopausal Women with Vitamin D Insufficiency: Peking Vertebral Fracture Study

X. Qi, X. Xing, W. Xia, 2019, Calcified Tissue International.

Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study.

X. Qi, W. Xia, Yan Jiang, 2018, Bone.

Uncovering potential single nucleotide polymorphisms, copy number variations and related signaling pathways in primary Sjogren’s syndrome

X. Qi, Lixia Gao, Hui-fang Guo, 2021, Bioengineered.

Incident Fracture Risk in Type 2 Diabetic Postmenopausal Women in Mainland China: Peking Vertebral Fracture Study

X. Qi, X. Xing, W. Xia, 2019, Calcified Tissue International.

The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation

L. Qin, X. Qi, X. Xing, 2019, Endocrine connections.

Calciotropic Hormones and the Prevalence of Vertebral Fractures in Chinese Postmenopausal Women with Vitamin D Insufficiency: Peking Vertebral Fracture Study

X. Qi, X. Xing, W. Xia, 2019, Calcified Tissue International.

Importance of baseline musculoskeletal ultrasound findings in the prognosis of rheumatoid arthritis

X. Qi, Chao Sun, Lixia Gao, 2022, Clinical Rheumatology.

A Mutation in CTSK Gene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin

X. Qi, X. Xing, W. Xia, 2015, Calcified Tissue International.