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1. Content Type:Research Article

     |  29 November 2018

   Genetic associations in community context: a mixed model approach identifies a functional variant in the RBP4 gene associated with HDL-C dyslipidemia

   Authors:Erfan Aref-Eshghi, Oliver Hurley, Guang Sun, Alvin Simms, Marshall Godwin, Pauline Duke, Mehdee Araee, Masoud Mahdavian and Shabnam Asghari
2. Content Type:Research Article

     |  26 November 2018

   A novel mutation in the VHL gene in a Chinese family with von Hippel-Lindau disease

   Authors:Xing Wu, Lanlan Chen, Yixin Zhang, Hainan Xie, Meirong Xue, Yi Wang and Houbin Huang
3. Content Type:Research Article

     |  20 November 2018

   Relationship between transforming growth factor-β1 and type 2 diabetic nephropathy risk in Chinese population

   Authors:Tianbiao Zhou, Hong-Yan Li, Hongzhen Zhong and Zhiqing Zhong
4. Content Type:Research Article

     |  20 November 2018

   Targeted gene panel for genetic testing of south Indian children with steroid resistant nephrotic syndrome

   Authors:Annes Siji, K. N. Karthik, Varsha Chhotusing Pardeshi, P. S. Hari and Anil Vasudevan
5. Content Type:Case Report

     |  20 November 2018

   A novel compound heterozygous mutation in VARS2 in a newborn with mitochondrial cardiomyopathy: a case report of a Chinese family

   Authors:Keze Ma, Mingyu Xie, Xiaoguang He, Guojun Liu, Xiaomei Lu, Qi Peng, Baimao Zhong and Ning Li

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