Publications

Research Articles: (Google Scholar)

*: co-first author；†: corresponding author, IF: impact factor on published year 

First/Corresponding Author: 

1. Cai LR and Wang Y† (2024) Automated Identification of Moderate-Severe Traumatic Brain Injury Lesions, The International Brain Tumor Segmentation (BraTS) challenge, Medical Image Computing and Computer-Assisted Intervention–MICCAI 2024: 27th International Conference (In print) 

2. Wang Y, Starovoytov A. Murad A.M., Hunker K.; Brunham L., Li J. Saw J. Ganesh S.K† (2022), Increased burden of rare genetic variants in spontaneous coronary-artery dissection with high-risk features , JAMA Cardiology 7(10), 1045-1055 (PMID: 36103205, IF: 30.2) 

3. Wang Y., Richer, J. Ganesh, S. K.(2022) Letter to the Editor Regarding Lavanya et al. A patient with a novel pathogenic variant in COL5A1 exhibiting prominent vascular and cardiac features, Am J Med Genet A. 188(9), 2832-2833. (PMID: 35762247, IF: 2.0) 

4. Coleman, D. M.*, Wang, Y*., Yang, M. L., Hunker, K. L., Birt, I., Bergin, I. L., Li, J. Z., Stanley, J. C. and Ganesh, S. K. (2022) ’Molecular genetic evaluation of Pediatric Renovascular hypertension due to renal artery stenosis and abdominal aortic Coarctation in Neurofibromatosis type 1’, Hum Mol Genet. 31(3), pp. 334-346. (PMID: 34476477, IF: 5.1) 

5. Richer, J.*, Hill, H. L.*, Wang, Y.*, Yang, M. L., Hunker, K. L., Lane, J., Blackburn, S., Coleman, D. M., Eliason, J., Sillon, G., D’Agostino, M. D., Jetty, P., Mongeon, F. P., Laberge, A. M., Ryan, S. E., Fendrikova Mahlay, N., Coutinho, T., Mathis, M. R., Zawistowski, M., Hazen, S. L., Katz, A. E., Gornik, H. L., Brummett, C. M., Abecasis, G., Bergin, I. L., Stanley, J. C., Li, J. Z. and Ganesh, S. K. (2020) ’A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia’, Arterioscler Thromb Vasc Biol, 40(11), pp. 2686-2699. (PMID: 32938213, IF: 10.5) 

6. Tao, Y*., Ruan, J.*, Yeh, S. H*., Lu, X*., Wang, Y*., Zhai, W*., Cai, J*., Ling, S., Gong, Q., Chong, Z., Qu, Z., Li, Q., Liu, J., Yang, J., Zheng, C., Zeng, C., Wang, H. Y., Zhang, J., Wang, S. H., Hao, L., Dong, L., Li, W., Sun, M., Zou, W., Yu, C., Li, C., Liu, G., Jiang, L., Xu, J., Huang, H., Mi, S., Zhang, B., Chen, B., Zhao, W., Hu, S., Zhuang, S. M., Shen, Y., Shi, S., Brown, C., White, K. P., Chen, D. S., Chen, P. J. and Wu, C. I. (2011) ’Rapid growth of a hepatocellular carcinoma and the driving mutations revealed by cell-population genetic analysis of whole-genome data’, Proc Natl Acad Sci USA, 108(29), pp. 12042-7. (PMID: 21730188, IF: 9.7) 

Non-First Author: 

1. DK Atchison, CL O’Connor, K. Converso-Baran, IL Bergin, H. Zhang, Wang Y, JR Hartman, W. Ju, AV Smrcka, SK Ganesh , M. Bitzer (2022),Phospholipase Cff insufficiency causes ascending aortic aneurysm and dissection, Am J Phys - Heart and Circ Phys, 323(6), H1376-H1387 (PMID: 36367690, IF: 4.8) 

2. Murad, A. M., Hill, H. L., Wang, Y., Ghannam, M., Yang, M. L., Pugh, N. L., Asch, F. M., Hornsby, W., Driscoll, A., McNamara, J., Willer, C. J., Regalado, E. S., Milewicz, D. M., Eagle, K. A. and Ganesh, S. K. (2022) ’Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility’, Am J Med Genet A. 188(5), 1448-1456. (PMID: 35092149, IF: 2.0) 

3. Georges, A., Albuisson, J., Berrandou, T., Dupré, D., Lorthioir, A., D’Escamard, V., Di Narzo, A. F., Kadian Dodov, D., Olin, J. W., Warchol-Celinska, E., Prejbisz, A., Januszewicz, A., Bruneval, P., Baranowska, A. A., Webb, T. R., Hamby, S. E., Samani, N. J., Adlam, D., Fendrikova-Mahlay, N., Hazen, S., Wang, Y., Yang, M. L., Hunker, K., Combaret, N., Motreff, P., Chédid, A., Fiquet, B., Plouin, P. F., Mousseaux, E., Azarine, A., Amar, L., Azizi, M., Gornik, H. L., Ganesh, S. K., Kovacic, J. C., Jeunemaitre, X. and Bouatia-Naji, N. (2021) ’Rare Loss-of-function Mutations of PTGIR are enriched in Fibromuscular Dysplasia’, Cardiovasc Res, 117(4), pp. 1154-1165. (PMID: 32531060, IF: 13.1)

4. Wang, D., Niu, X., Wang, Z., Song, C. L., Huang, Z., Chen, K. N., Duan, J., Bai, H., Xu, J., Zhao, J., Wang, Y., Zhuo, M., Xie, X. S., Kang, X., Tian, Y., Cai, L., Han, J. F., An, T., Sun, Y., Gao, S., Ying, J., Wang, L., He, J. and Wang, J. (2019) ’Multiregion Sequencing Reveals the Genetic Heterogeneity and Evolutionary History of Osteosarcoma and Matched Pulmonary Metastases’, Cancer Res, 79(1), pp. 7-20. (PMID: 30389703, IF: 9.7) 

5. Yuan, W., Liu, Z., Wang, Y., Liu, M., Pan, Y., Lei, W., Yang, H., Xu, R., Zhang, L., Cai, H., Li, J. and Ke, Y. (2019) ’Clonal evolution of esophageal squamous cell carcinoma from normal mucosa to primary tumor and metastases’, Carcinogenesis, 40(12), pp. 1445-1451. (PMID: 29050228, IF: 4.6) 

6. Yuan, W., Liu, Z., Lei, W., Sun, L., Yang, H., Wang, Y., Ramdas, S., Dong, X., Xu, R., Cai, H., Li, J. Z. and Ke, Y. (2017) ’Mutation landscape and intra-tumor heterogeneity of two MANECs of the esophagus revealed by multi-region sequencing’, Oncotarget, 8(41), pp. 69610-69621. (PMID: 31570939, IF: 5.1) 

7. Li, C., Liu, Z., Yang, F., Liu, W., Wang, D., Dong, E., Wang, Y., Wu, C. I. and Lu, X. (2015) ’siRNAs with decreased off-target effect facilitate the identification of essential genes in cancer cells’, Oncotarget, 6(25), pp. 21603-13. (PMID: 26057633, IF: 5.0) 

8. He, Z., Zhai, W., Wen, H., Tang, T., Wang, Y., Lu, X., Greenberg, A. J., Hudson, R. R., Wu, C. I. and Shi, S. (2011) ’Two evolutionary histories in the genome of rice: the roles of domestication genes’, PLoS Genet, 7(6), pp. e1002100. (PMID: 21695282, IF: 8.7) 

9. Zhou, Y., Lu, C., Wu, Q. J., Wang, Y., Sun, Z. T., Deng, J. C. and Zhang, Y. (2008) ’GISSD: Group I Intron Sequence and Structure Database’, Nucleic Acids Res, 36(Database issue), pp. D31-7. (PMID: 17942415, IF: 7.8) 


Non-peer Reviewed:


Dissertation: 


Meeting Abstract: