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[1] Xiang R#,*（通讯作者，第一作者）, Fan L L#, Huang H#, Chen Y Q#, He W X, Guo S, Li J J, Jin J Y, Du R, Yan R Q, Xia K. Increased RTN3 Leads to Obesity and Hypertriglyceridemia by Interacting with HSPA5[J]. Circulation, 2018, online.
[2] Guo S, Fan X F, Jin J Y, Fan L L, Zhou Z B, Xiang R*（共同通讯作者）, Tang J Y*. A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel’s deformity[J]. Molecular cytogenetics, 2018, 11(1): 8.
[4] Ding D B, Fan L L, Xiao Z, Huang H, Chen Y Q, Guo S, Liu Z H, Xiang R*（通讯作者）. A novel mutation of dipeptidyl aminopeptidase-like protein-6 in a family with suspicious idiopathic ventricular fibrillation[J]. QJM: An International Journal of Medicine, 2018, 111(6): 373-377.
[5] Huang H, Ding D B, Fan L L, Jin J Y, Li J J, Guo S, Chen Y Q, Xiang R*（通讯作者）. Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmia[J]. Cardiology in the young, 2018, 28(5): 688-691.
[6] Li J J, Chen Y Q, Fan L L, Jin J Y, Guo S, Xiang R*（通讯作者）. Microduplication of 10q26. 3 in a Chinese hypertriglyceridemia patient[J]. Molecular and cellular probes, 2018, 37: 28-31.
[7] Fan L L, Huang H, Jin J Y, Li J J, Chen Y Q, Zhao S P, Xiang R*（通讯作者）. Whole exome sequencing identifies a novel mutation (c. 333+ 2T> C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease[J]. Gene, 2018, 648: 63-67.
[8] Huang H, Chen Y Q, Fan L L, Guo S, Li J J, Jin J Y, Xiang R*（通讯作者）. Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death[J]. Journal of cellular and molecular medicine, 2018, 22(2): 1350-1354.
[9] Xiang R*（第一作者，共同通讯作者）, Fan L L, Lin M J, Li J J, Shi X Y, Jin J Y, Liu Y X, Chen Y Q, Xia K*, Zhao S P*.The genetic spectrum of familial hypercholesterolemia in the central south region of China[J]. Atherosclerosis, 2017, 258: 84-88.
[10] Liu J S, Fan L L, Li J J, Xiang R*（通讯作者）. Whole-exome sequencing identifies a novel mutation of desmocollin 2 in a Chinese family with arrhythmogenic right ventricular cardiomyopathy[J]. The American journal of cardiology, 2017, 119(9): 1485-1489.
[11] Liu J S, Fan L L, Zhang H, Liu X, Huang H, Tao L J, Xia K, Xiang R*（通讯作者）. Whole-exome sequencing identifies two novel TTN mutations in Chinese families with dilated cardiomyopathy[J]. Cardiology, 2017, 136(1): 10-14.
[12] Xiang R*（第一作者，通讯作者）, Du R, Guo S, Jin J Y, Fan L L, Tang J Y, Zhou Z B. Microduplications of 10q24 Detected in Two Chinese Patients with Split-hand/foot Malformation Type 3[J]. Annals of Clinical & Laboratory Science, 2017, 47(6): 754-757.
[13] Xiang R（第一作者）, Fan L L, Huang H, Zhao S P, Chen Y Q. Whole-exome sequencing identifies a novel mutation of DSG2 (Y198C) in a Chinese arrhythmogenic right ventricular cardiomyopathy patient[J]. International journal of cardiology, 2016, 214: 1-3.
[14] Wu P F, Guo S, Fan X F, Fan L L, Jin J Y, Tang J Y, Xiang R*（通讯作者）. A novel ZRS mutation in a Chinese patient with Preaxial Polydactyly and Triphalangeal thumb[J]. Cytogenetic and genome research, 2016, 149(3): 171-175.
[15] Du RF, Huang H, Fan L L, Li X P, Xia K*, Xiang R*（共同通讯作者）. A Novel Mutation of FOXC1 (R127L) in an Axenfeld–Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases[J]. Ophthalmic genetics, 2016, 37(1): 111-115.
[16] Chen Y, Wu Z, Zhao S, Xiang R. Chemical chaperones reduce ER stress and adipose tissue inflammation in high fat diet-induced mouse model of obesity[J]. Scientific reports, 2016, 6: 27486.
[17] Fan L L, Lin M J, Chen Y Q, Huang H, Peng D Q, Xia K*, Zhao S P*, Xiang R*（共同通讯作者）. Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia[J]. Applied biochemistry and biotechnology, 2015, 176(1): 101-109.
[18] Yu B L, Xiang R, Hu D, Peng D Q. A novel MYH7 mutation in a family with cardiomyopathy presenting with restrictive physiology and varying degrees of left ventricle hypertrophy[J]. European heart journal, 2014, 36(3): 178-178.
[19] Shi Q, Ge Y, Sharoar M G, He W, Xiang R, Zhang Z, Hu X, Yan R. Impact of RTN3 deficiency on expression of BACE1 and amyloid deposition[J]. Journal of Neuroscience, 2014, 34(42): 13954-13962.
[20] Xiang R（第一作者）, Fan L L, Huang H, Cao B B, Li X P, Peng D Q*, Xia K*. A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis[J]. Gene, 2014, 534(2): 320-323.
[21] Chen Y, Xiang R, Zhao S. The potential role of RTN3 in monocyte recruitment and atherosclerosis[J]. Molecular and cellular biochemistry, 2012, 361(1-2): 67-70.
[22] Chen Y, Zhao S, Xiang R*（通讯作者）. RTN3 and RTN4: candidate modulators in vascular cell apoptosis and atherosclerosis[J]. Journal of cellular biochemistry, 2010, 111(4): 797-800.
[23] Xing Y, Zhao S, Xiang R*（通讯作者）. Alzheimer’s disease and atherosclerosis: Passers-by or brothers?[J]. Medical hypotheses, 2009, 73(2): 138-139.
[24] Xiang R, Zhao S. RTN3 inducing apoptosis is modulated by an adhesion protein CRELD1[J]. Molecular and cellular biochemistry, 2009, 331(1-2): 225.
[25] Zhu L, Xiang R（并列）, Dong W, et al. Anti‐apoptotic activity of Bcl‐2 is enhanced by its interaction with RTN3[J].Cell biology international, 2007, 31(8): 825-830.
[26] Xiang R, Liu Y, Zhu L, et al. Adaptor FADD is recruited by RTN3/HAP in ER-bound signaling complexes[J]. Apoptosis, 2006, 11(11): 1923-1932.
[27] Liu Y, Dong W, Chen L, Xiang R, Xiao H, De G, Wang Z, Qi Y. BCL10 mediates lipopolysaccharide/toll-like receptor-4 signaling through interaction with Pellino2[J]. Journal of Biological Chemistry, 2004, 279(36): 37436-37444.
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