PubRank

Weibo Xia

Author PubWeight™ 17.16‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy. Am J Hum Genet 2011 1.22
2 Myostatin regulates glucose metabolism via the AMP-activated protein kinase pathway in skeletal muscle cells. Int J Biochem Cell Biol 2010 0.96
3 The levels of bone turnover markers in Chinese postmenopausal women: Peking Vertebral Fracture study. Menopause 2011 0.94
4 Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia. PLoS One 2012 0.88
5 Germinal mosaicism of GATA3 in a family with HDR syndrome. Am J Med Genet A 2009 0.87
6 A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patients. Calcif Tissue Int 2009 0.83
7 Novel TRPM6 mutations in familial hypomagnesemia with secondary hypocalcemia. Am J Nephrol 2013 0.82
8 Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients. Bone 2012 0.82
9 Association of ESR1 and C6orf97 gene polymorphism with osteoporosis in postmenopausal women. Mol Biol Rep 2014 0.82
10 Hyperthyroidism caused by an ectopic thyrotropin-secreting tumor of the nasopharynx: a case report and review of the literature. Thyroid 2013 0.81
11 Association of GALNT3 gene polymorphisms with bone mineral density in Chinese postmenopausal women: the Peking Vertebral Fracture study. Menopause 2014 0.80
12 Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas. PLoS One 2012 0.80
13 FGF23 analysis of a Chinese family with autosomal dominant hypophosphatemic rickets. J Bone Miner Metab 2011 0.79
14 A Mutation in CTSK Gene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin. Calcif Tissue Int 2015 0.79
15 Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese. Clin Endocrinol (Oxf) 2014 0.78
16 Two novel CAII mutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families. Metab Brain Dis 2015 0.77
17 First report of a novel missense CLDN19 mutations causing familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a Chinese family. Calcif Tissue Int 2015 0.76
18 Longitudinal increase in vitamin D binding protein levels after initiation of tenofovir/lamivudine/efavirenz among individuals with HIV. AIDS 2016 0.75
19 Severe hydronephrosis in nephrogenic diabetes insipidus. Clin Med Res 2009 0.75
20 Osteoporosis knowledge, self-efficacy, and health beliefs among Chinese individuals with HIV. Arch Osteoporos 2014 0.75
21 Bone turnover and bone mineral density in HIV-1 infected Chinese taking highly active antiretroviral therapy -a prospective observational study. BMC Musculoskelet Disord 2013 0.75
22 Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasia. Hum Genet 2009 0.75
23 Gene identification of potential malignant parathyroid tumors phenotype in Chinese population. Endocr J 2014 0.75
24 [Alendronate in postmenopausal women with osteopenia and osteoporosis: effects on bone mineral density during treatment and after withdrawal]. Zhonghua Yi Xue Za Zhi 2002 0.75
25 Novel human pathological mutations. Gene symbol: NR0B1. Disease: adrenal hypoplasia. Hum Genet 2009 0.75
26 Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasia. Hum Genet 2009 0.75
27 Effects of Enhanced Exercise and Combined Vitamin D and Calcium Supplementation on Muscle Strength and Fracture Risk in Postmenopausal Chinese Women. Chin Med Sci J 2017 0.75
28 EFFECTS OF LONG-TERM ALENDRONATE TREATMENT ON A LARGE SAMPLE OF PEDIATRIC PATIENTS WITH OSTEOGENESIS IMPERFECTA. Endocr Pract 2016 0.75
29 A haplotype of MATN3 is associated with vertebral fracture in Chinese postmenopausal women: Peking Vertebral Fracture (PK-VF) study. Bone 2012 0.75