PubRank

Xiaoping Xing

Author PubWeight™ 20.34‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Very high rates of vitamin D insufficiency in women of child-bearing age living in Beijing and Hong Kong. Br J Nutr 2007 1.00
2 The levels of bone turnover markers in Chinese postmenopausal women: Peking Vertebral Fracture study. Menopause 2011 0.94
3 Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia. PLoS One 2012 0.88
4 Three novel mutations of the PHEX gene in three Chinese families with X-linked dominant hypophosphatemic rickets. Calcif Tissue Int 2007 0.88
5 Germinal mosaicism of GATA3 in a family with HDR syndrome. Am J Med Genet A 2009 0.87
6 Effective detection of the tumors causing osteomalacia using [Tc-99m]-HYNIC-octreotide (99mTc-HYNIC-TOC) whole body scan. Eur J Radiol 2013 0.86
7 Clinical severity of Gitelman syndrome determined by serum magnesium. Am J Nephrol 2014 0.84
8 68Ga DOTATATE PET/CT is an Accurate Imaging Modality in the Detection of Culprit Tumors Causing Osteomalacia. Clin Nucl Med 2015 0.83
9 A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patients. Calcif Tissue Int 2009 0.83
10 Red cell folate and predicted neural tube defect rate in three Asian cities. Asia Pac J Clin Nutr 2007 0.83
11 Novel TRPM6 mutations in familial hypomagnesemia with secondary hypocalcemia. Am J Nephrol 2013 0.82
12 Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism. Eur J Endocrinol 2013 0.82
13 Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients. Bone 2012 0.82
14 Hyperthyroidism caused by an ectopic thyrotropin-secreting tumor of the nasopharynx: a case report and review of the literature. Thyroid 2013 0.81
15 Vildagliptin added to sulfonylurea improves glycemic control without hypoglycemia and weight gain in Chinese patients with type 2 diabetes mellitus. J Diabetes 2014 0.81
16 Association of GALNT3 gene polymorphisms with bone mineral density in Chinese postmenopausal women: the Peking Vertebral Fracture study. Menopause 2014 0.80
17 Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas. PLoS One 2012 0.80
18 China type 2 diabetes treatment status survey of treatment pattern of oral drugs users 2. J Diabetes 2014 0.79
19 FGF23 analysis of a Chinese family with autosomal dominant hypophosphatemic rickets. J Bone Miner Metab 2011 0.79
20 A Mutation in CTSK Gene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin. Calcif Tissue Int 2015 0.79
21 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
22 Laparoscopic enucleation of insulinoma in a patient with annular pancreas: a rare case. J Gastrointest Surg 2014 0.78
23 Milk supplementation and bone health in young adult chinese women. J Womens Health (Larchmt) 2007 0.77
24 NORMOMAGNESEMIC GITELMAN SYNDROME PATIENTS EXHIBIT A STRONGER REACTION TO THIAZIDE THAN HYPOMAGNESEMIC PATIENTS. Endocr Pract 2015 0.77
25 Two novel CAII mutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families. Metab Brain Dis 2015 0.77
26 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
27 EFFECTS OF LONG-TERM ALENDRONATE TREATMENT ON A LARGE SAMPLE OF PEDIATRIC PATIENTS WITH OSTEOGENESIS IMPERFECTA. Endocr Pract 2016 0.75
28 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
29 Clinical and genetic characterization of a Chinese patient with triple A syndrome and novel compound heterozygous mutations in the AAAS gene. J Pediatr Endocrinol Metab 2013 0.75
30 [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
31 Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasia. Hum Genet 2009 0.75
32 Novel human pathological mutations. Gene symbol: CYP19A1. Disease: Aromatase deficiency. Hum Genet 2010 0.75
33 [Electrokinetic chromatographic properties of amphiphilic copolymer poly (styrene-co-methacrylic acid) self-assembled micelle pseudostationary phase]. Se Pu 2015 0.75
34 A haplotype of MATN3 is associated with vertebral fracture in Chinese postmenopausal women: Peking Vertebral Fracture (PK-VF) study. Bone 2012 0.75
35 Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasia. Hum Genet 2009 0.75
36 Novel human pathological mutations. Gene symbol: CYP19A1. Disease: Aromatase deficiency. Hum Genet 2010 0.75
37 [Determination of beta-adrenergic agonists in pig urine and pig fodder using miniaturized capillary electrophoresis with electrochemical detection]. Se Pu 2008 0.75
38 Novel human pathological mutations. Gene symbol: NR0B1. Disease: adrenal hypoplasia. Hum Genet 2009 0.75
39 Successful management of octreotide-insensitive thyrotropin-secreting pituitary adenoma with bromocriptine and surgery: A case report and literature review. Medicine (Baltimore) 2017 0.75
40 Gene identification of potential malignant parathyroid tumors phenotype in Chinese population. Endocr J 2014 0.75
41 [Report of a case with Alstrom syndrome]. Zhonghua Er Ke Za Zhi 2004 0.75