Xuan Qi

发表

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.

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

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

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.

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.

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

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

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.

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.

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.

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

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

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

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

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.

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.

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

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

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.

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.

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.

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

X. Xing, W. Xia, Mei Li, 2015, Metabolic brain disease.

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

Asan, X. Xing, J. Mao, 2017, Calcified Tissue International.

Targeting Metabolomics in Primary Hypertrophic Osteoarthropathy: Uncovering Novel Insights into Disease Pathogenesis.

R. Jiajue, L. Cui, Q. Pang, 2024, The Journal of clinical endocrinology and metabolism.