Peng-Chieh Chen

Personal profile

Education

2006 PhD, Department of Biological Chemistry, School of Medicine, University of California, Irvine

Experience

2018-present Associate Professor Institute of Clinical Medicine, National Cheng Kung University
2012-2018 Assistant Professor Institute of Clinical Medicine, National Cheng Kung University
2007-2012 Research Follow Harvard Medical School
2007-2012 Post-doctoral Fellow Brigham & Women's Hospital

Research Interests

Molecular Genetics
Genomic Medicine
Personalized Medicine

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22 Similar Profiles

Mutation Medicine & Life Sciences

DNA Mismatch Repair Medicine & Life Sciences

Neoplasms Medicine & Life Sciences

Exome Medicine & Life Sciences

Noonan Syndrome Medicine & Life Sciences

Colorectal Neoplasms Medicine & Life Sciences

Genes Medicine & Life Sciences

Glioblastoma Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

努南式症的治療:疾病模式與表現形之研究

Chen, P.

17-08-01 → 18-07-31

Project: Research project

努南式症的治療:疾病模式與表現形之研究

Chen, P.

16-08-01 → 17-07-31

Project: Research project

新穎努南式症致病機制及治療之探討

Chen, P.

15-08-01 → 16-07-31

Project: Research project

新穎努南式症致病機制及治療之探討

Chen, P.

14-08-01 → 15-07-31

Project: Research project

新穎努南式症致病機制及治療之探討

Chen, P.

13-08-01 → 14-07-31

Project: Research project

Research Output 2004 2018

14226 Citations
12 h-Index
15 Article

2 Citations (Scopus)

A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing

Liao, C. Y., Yu, H. W., Cheng, C-N., Chen, C-H., Lin, C-W., Chen, P-C. & Shieh, C-C., 2018 Jan 1, (Accepted/In press) In : Journal of Microbiology, Immunology and Infection.

Research output: Contribution to journal › Article

Interleukin-7 Receptors

Exome

Severe Combined Immunodeficiency

Newborn Infant

Mutation

2 Citations (Scopus)

Rare compound heterozygous frameshift mutations in ALMS1 gene identified through exome sequencing in a Taiwanese patient with Alström syndrome

Tsai, M-C., Yu, H. W., Liu, T., Chou, Y-Y., Chiou, Y-Y. & Chen, P-C., 2018 Apr 18, In : Frontiers in Genetics. 9, APR, 110.

Research output: Contribution to journal › Article

Exome

Frameshift Mutation

Mutation

Genes

Insulin Resistance

1868 Citations (Scopus)

Comprehensive molecular profiling of lung adenocarcinoma: The cancer genome atlas research network

Collisson, E. A., Campbell, J. D., Brooks, A. N., Berger, A. H., Lee, W., Chmielecki, J., Beer, D. G., Cope, L., Creighton, C. J., Danilova, L., Ding, L., Getz, G., Hammerman, P. S., Hayes, D. N., Hernandez, B., Herman, J. G., Heymach, J. V., Jurisica, I., Kucherlapati, R., Kwiatkowski, D. & 290 others, Ladanyi, M., Robertson, G., Schultz, N., Shen, R., Sinha, R., Sougnez, C., Tsao, M. S., Travis, W. D., Weinstein, J. N., Wigle, D. A., Wilkerson, M. D., Chu, A., Cherniack, A. D., Hadjipanayis, A., Rosenberg, M., Weisenberger, D. J., Laird, P. W., Radenbaugh, A., Ma, S., Stuart, J. M., Byers, L. A., Baylin, S. B., Govindan, R., Meyerson, M., Gabriel, S. B., Cibulskis, K., Kim, J., Stewart, C., Lichtenstein, L., Lander, E. S., Lawrence, M. S., Getz, E., Fulton, R., Fulton, L. L., McLellan, M. D., Wilson, R. K., Ye, K., Fronick, C. C., Maher, C. A., Miller, C. A., Wendl, M. C., Cabanski, C., Mardis, E., Wheeler, D., Balasundaram, M., Butterfield, Y. S. N., Carlsen, R., Chuah, E., Dhalla, N., Guin, R., Hirst, C., Lee, D., Li, H. I., Mayo, M., Moore, R. A., Mungall, A. J., Schein, J. E., Sipahimalani, P., Tam, A., Varhol, R., Robertson, A. G., Wye, N., Thiessen, N., Holt, R. A., Jones, S. J. M., Marra, M. A., Imielinski, M., Onofrio, R. C., Hodis, E., Zack, T., Helman, E., Pedamallu, C. S., Mesirov, J., Saksena, G., Schumacher, S. E., Carter, S. L., Garraway, L., Beroukhim, R., Lee, S., Mahadeshwar, H. S., Pantazi, A., Protopopov, A., Ren, X., Seth, S., Song, X., Tang, J., Yang, L., Zhang, J., Chen, P. C., Parfenov, M., Xu, A. W., Santoso, N., Chin, L., Park, P. J., Hoadley, K. A., Auman, J. T., Meng, S., Shi, Y., Buda, E., Waring, S., Veluvolu, U., Tan, D., Mieczkowski, P. A., Jones, C. D., Simons, J. V., Soloway, M. G., Bodenheimer, T., Jefferys, S. R., Roach, J., Hoyle, A. P., Wu, J., Balu, S., Singh, D., Prins, J. F., Marron, J. S., Parker, J. S., Perou, C. M., Liu, J., Maglinte, D. T., Lai, P. H., Bootwalla, M. S., Van Den Berg, D. J., Triche, T., Cho, J., DiCara, D., Heiman, D., Lin, P., Mallard, W., Voet, D., Zhang, H., Zou, L., Noble, M. S., Gehlenborg, N., Thorvaldsdottir, H., Nazaire, M. D., Robinson, J., Aksoy, B. A., Ciriello, G., Taylor, B. S., Dresdner, G., Gao, J., Gross, B., Seshan, V. E., Reva, B., Sumer, S. O., Weinhold, N., Sander, C., Ng, S., Zhu, J., Benz, C. C., Yau, C., Haussler, D., Spellman, P. T., Kimes, P. K., Broom, B. M., Wang, J., Lu, Y., Ng, P. K. S., Diao, L., Liu, W., Amos, C. I., Akbani, R., Mills, G. B., Curley, E., Paulauskis, J., Lau, K., Morris, S., Shelton, T., Mallery, D., Gardner, J., Penny, R., Saller, C., Tarvin, K., Richards, W. G., Cerfolio, R., Bryant, A., Raymond, D. P., Pennell, N. A., Farver, C., Czerwinski, C., Huelsenbeck-Dill, L., Iacocca, M., Petrelli, N., Rabeno, B., Brown, J., Bauer, T., Dolzhanskiy, C. O., Potapova, O., Rotin, D., Voronina, O., Nemirovich-Danchenko, E., Fedosenko, K. V., Gal, A., Behera, M., Ramalingam, S. S., Sica, G., Flieder, D., Boyd, J., Weaver, J. E., Kohl, B., Thinh, D. H. Q., Sandusky, G., Juhl, H., Duhig, E., Illei, P., Gabrielson, E., Shin, J., Lee, B., Rogers, K., Trusty, D., Brock, M. V., Williamson, C., Burks, E., Rieger-Christ, K., Holway, A., Sullivan, T., Asiedu, M. K., Kosari, F., Rekhtman, N., Zakowski, M., Rusch, V. W., Zippile, P., Suh, J., Pass, H., Goparaju, C., Owusu-Sarpong, Y., Bartlett, J. M. S., Kodeeswaran, S., Parfitt, J., Sekhon, H., Albert, M., Eckman, J., Myers, J. B., Morrison, C., Gaudioso, C., Borgia, J. A., Bonomi, P., Pool, M., Liptay, M. J., Moiseenko, F., Zaytseva, I., Dienemann, H., Meister, M., Schnabel, P. A., Muley, T. R., Peifer, M., Gomez-Fernandez, C., Herbert, L., Egea, S., Huang, M., Thorne, L. B., Boice, L., Salazar, A. H., Funkhouser, W. K., Rathmell, W. K., Dhir, R., Yousem, S. A., Dacic, S., Schneider, F., Siegfried, J. M., Hajek, R., Watson, M. A., McDonald, S., Meyers, B., Clarke, B., Yang, I. A., Fong, K. M., Hunter, L., Windsor, M., Bowman, R. V., Peters, S., Letovanec, I., Khan, K. Z., Jensen, M. A., Snyder, E. E., Srinivasan, D., Kahn, A. B., Baboud, J., Pot, D. A., Shaw, K. R. M., Sheth, M., Davidsen, T., Demchok, J. A., Yang, L., Wang, Z., Tarnuzzer, R., Zenklusen, J. C., Ozenberger, B. A., Sofia, H. J. & Cheney, R., 2014 Jan 1, In : Nature. 511, 7511, p. 543-550 8 p.

Research output: Contribution to journal › Article

Atlases

Genome

Mutation

Research

Neoplasms

81 Citations (Scopus)

Next-generation sequencing identifies rare variants associated with Noonan syndrome

Chen, P. C., Yin, J., Yu, H. W., Yuan, T., Fernandez, M., Yung, C. K., Trinh, Q. M., Peltekova, V. D., Reid, J. G., Tworog-Dube, E., Morgan, M. B., Muzny, D. M., Stein, L., McPherson, J. D., Roberts, A. E., Gibbs, R. A., Neel, B. G. & Kucherlapati, R., 2014 Aug 5, In : Proceedings of the National Academy of Sciences of the United States of America. 111, 31, p. 11473-11478 6 p.

Research output: Contribution to journal › Article

Noonan Syndrome

Nonsense Codon

Alleles

Coffin-Lowry Syndrome

MAP Kinase Kinase 1

1695 Citations (Scopus)

The somatic genomic landscape of glioblastoma

TCGA Research Network, 2013 Oct 10, In : Cell. 155, 2, 1 p.

Research output: Contribution to journal › Article

Glioblastoma

Tumors

Telomerase

Biomarkers

Neoplasms

Thesis

Regulatory role of RASIP1 in cardiovascular cell differentiation

Author: 惟政, 孫., 2018 Sep 4

Supervisor: Chen, P. (Supervisor)

Student thesis: Master's Thesis