Jia-lun Chen

发表

Prevalence and control of diabetes in Chinese adults.

Jiang He, Meng Dai, Yong Jiang, 2013, JAMA.

Estrogen receptor gene polymorphisms and bone mineral density in Chinese postmenopausal women.

M. Dai, Jian-min Liu, Han-min Zhu, 2003, Chinese medical journal.

Osteoporotic fractures in Asia: risk factors and strategies for prevention

G. Ning, Jian-min Liu, Jia-lun Chen, 2006, Journal of Bone and Mineral Metabolism.

The influence of Lys3Asn polymorphism in the osteoprotegerin gene on bone mineral density in Chinese postmenopausal women

A. Uitterlinden, G. Ning, Jian-min Liu, 2005, Osteoporosis International.

Interleukin-18 enhances glucose uptake in 3T3-L1 adipocytes

G. Ning, Xiao-ying Li, Yifei Zhang, 2007, Endocrine.

Relationship between body composition and bone mineral density in healthy young and premenopausal Chinese women

G. Ning, Jian-min Liu, Li-hao Sun, 2004, Osteoporosis International.

The effects of bisphenol A (BPA) exposure on fat mass and serum leptin concentrations have no impact on bone mineral densities in non-obese premenopausal women.

Lin Zhao, Weiqing Wang, G. Ning, 2012, Clinical biochemistry.

An independent positive relationship between the serum total osteocalcin level and fat-free mass in healthy premenopausal women.

Lin Zhao, Weiqing Wang, G. Ning, 2013, The Journal of clinical endocrinology and metabolism.

Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.

L. Liang, Zhu Chen, G. Ning, 2013, Human molecular genetics.

RobustevidenceforfivenewGraves ’ diseaserisk loci from a staged genome-wide association analysis

L. Liang, Zhu Chen, G. Ning, 2013 .

Efficacy and safety of 2 g/day of strontium ranelate in Asian women with postmenopausal osteoporosis.

Jian-min Liu, Ling Xu, Zhenlin Zhang, 2009, Bone.

A complex heterozygous mutation of His373Leu and Asp487–Ser488–Phe489 deletion in human cytochrome P450c17 causes 17α-hydroxylase/17,20-lyase deficiency in three Chinese sisters

Huai-Dong Song, Yong-de Peng, R. Hu, 2003, Molecular and Cellular Endocrinology.

The mimecan gene expressed in human pituitary and regulated by pituitary transcription factor-1 as a marker for diagnosing pituitary tumors.

Feng Li, Huai-Dong Song, Hui-min Yu, 2005, The Journal of clinical endocrinology and metabolism.

A novel, complex heterozygous mutation within Gsα gene in patient with McCune-albright syndrome

Huai-Dong Song, R. Hu, Jia-lun Chen, 2002, Endocrine.

A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditism

Bing-Li Liu, Huai-Dong Song, Ying Ru, 2009, Human mutation.

A genome-wide association study identifies two new risk loci for Graves' disease

L. Liang, X. Chu, Zhu Chen, 2011, Nature Genetics.

Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.

W. Liu, G. Ning, Wei Huang, 2014, Human molecular genetics.

IGF-1 as an early marker for low bone mass or osteoporosis in premenopausal and postmenopausal women

G. Ning, Jian-min Liu, Li-hao Sun, 2008, Journal of Bone and Mineral Metabolism.

A Refined Study of FCRL Genes from a Genome-Wide Association Study for Graves’ Disease

L. Liang, Chang-gui Li, G. Gao, 2013, PloS one.

Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults

H. Tian, G. Gao, Bing-Li Liu, 2019, JAMA network open.

Association of the CTLA4 Gene with Graves' Disease in the Chinese Han Population

Jiajun Zhao, G. Gao, Jing-yi Shi, 2010, PloS one.

Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.

X. Chu, Li Jin, Zhi Liu, 2009, Human molecular genetics.

Identification of steroid biosynthetic defects in genotype‐proven heterozygous individuals for 17α‐hydroxylase/17,20‐lyase deficiency

Bing-Li Liu, Huai-Dong Song, Yan Gu, 2010, Clinical endocrinology.

Phenotype-genotype correlation in eight Chinese 17alpha-hydroxylase/17,20 lyase-deficiency patients with five novel mutations of CYP17A1 gene.

G. Ning, Y. Bi, Siyuan Zheng, 2006, The Journal of clinical endocrinology and metabolism.

Structure and functional analysis of unclassified genes strongly expressed in human visceral adipose tissue

G. Ning, Xiao-ying Li, Huai-Dong Song, 2005, Endocrine.

Chromosome localization analysis of genes strongly expressed in human visceral adipose tissue

Ze-Guang Han, Huai-Dong Song, R. Hu, 2002, Endocrine.

The gene expression profiling of human visceral adipose tissue and its secretory functions.

Ze-Guang Han, Huai-Dong Song, R. Hu, 2003, Biochemical and biophysical research communications.

Two unusual cases of intractable hyperthyroidism responsive to octreotide: Munchausen syndrome or not?

Lin Zhao, Weiqing Wang, G. Ning, 2011, Clinica chimica acta; international journal of clinical chemistry.

Genetic Heterogeneity of Susceptibility Gene in Different Ethnic Populations: Refining Association Study of PTPN22 for Graves’ Disease in a Chinese Han Population

W. Liu, Chang-gui Li, G. Gao, 2013, PloS one.

Effect of short-term and long-term fasting on transcriptional regulation of metabolic genes in rat tissues.

Zhi Liu, H. Xiao, Huai-Dong Song, 2006, Biochemical and biophysical research communications.

[Novel full-length cDNA cloning from normal adrenal gland and pheochromocytoma and functional prediction].

Zeguang Han, Yongde Peng, Huaidong Song, 2002, Zhonghua yi xue za zhi.

[Association of calcitonin receptor gene polymorphism with bone mineral density in Shanghai women].

G. Ning, M. Dai, Jian-min Liu, 2003, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.

Relationships between insulin-like growth factor-I (IGF-I) and OPG, RANKL, bone mineral density in healthy Chinese women

G. Ning, Yuhong Chen, Li-hao Sun, 2008, Osteoporosis International.