Stephen Chanock

Stephen Jacob Chanock (born April 15, 1956) is an American physician and geneticist. He currently serves as Director of the Division of Cancer Epidemiology and Genetics at the U.S. National Cancer Institute (NCI).[1]

Dr. Stephen Chanock, 2014

Biography

Stephen Chanock is the son of NIH scientist Robert M. Chanock, discoverer of human respiratory syncytial virus.

Chanock completed undergraduate studies at Princeton University in 1978, and his medical training at Harvard Medical School in 1983. He completed clinical training in pediatrics, pediatric infectious diseases, and pediatric hematology/oncology at Boston Children’s Hospital and the Dana–Farber Cancer Institute, Boston, MA. He has held multiple positions, both in research and scientific leadership over his career at the NCI.[1] He has received numerous awards for his work in the discovery and characterization of cancer susceptibility regions in the human genome. These include the Niehaus, Southorth, Weissenbach Award in Clinical Cancer Genetics and the NIH Directors Award. Chanock is an elected member of Association of American Physicians, the American Epidemiology Society, the Society for Pediatric Research and the American Association of Cancer Research. He is the author of over 1200 publications and dozens of book chapters.

Since 1995, Chanock has served as the Medical Director for Camp Fantastic, a week-long recreational camp for pediatric cancer patients.

Research activities

Chanock co-leads several international consortial studies to identify and characterize the genetics of cancer susceptibility including BRCA Challenge, Game-On, and the NCI Cohort Consortium. His work focuses specifically on efforts to clarify the genetic architecture of cancer susceptibility,[2][3] the scope of genetic mosaicism and its contribution to cancer risk,[4][5] and how germline variation informs our understanding of somatic alterations in cancer[6][7] and investigation of how ionizing radiation causes thyroid cancer in children exposed to the Chornobyl accident and the lack of evidence for a transgenerational effect in cleanup workers following the Chornobyl accident.[8][9]

Awards
  • NIH Directors Award (2008, 2013, 2019, 2022)
  • The Niehaus, Southorth, Weissenbach Award in Clinical Cancer Genetics, Memorial Sloan Kettering Cancer Center, New York, NY (2010)
  • NCI Directors Award (2014, 2015, 2018, 2020, 2021, 2022)
  • Society for Pediatric Research (elected 1998)
  • Association of American Physicians (elected 2013)
  • American Epidemiology Society (elected 2013)
  • Randy Schools Light of Love Award, Special Love, Inc (2022)
  • Fellow of the Academy of American Association of Cancer Research (2023)

References
  1. "Stephen J. Chanock, M.D." Division of Cancer Epidemiology and Genetics – National Cancer Institute. January 1980. Retrieved 2016-09-21.
  2. Cerhan, James R.; Berndt, Sonja I.; Vijai, Joseph; Ghesquières, Hervé; McKay, James; Wang, Sophia S.; Wang, Zhaoming; Yeager, Meredith; Conde, Lucia (2014-11-01). "Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma". Nature Genetics. 46 (11): 1233–1238. doi:10.1038/ng.3105. ISSN 1546-1718. PMC 4213349. PMID 25261932.
  3. Wu, Chen; Wang, Zhaoming; Song, Xin; Feng, Xiao-Shan; Abnet, Christian C.; He, Jie; Hu, Nan; Zuo, Xian-Bo; Tan, Wen (2014-09-01). "Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations". Nature Genetics. 46 (9): 1001–1006. doi:10.1038/ng.3064. ISSN 1546-1718. PMC 4212832. PMID 25129146.
  4. Jacobs, Kevin B.; Yeager, Meredith; Zhou, Weiyin; Wacholder, Sholom; Wang, Zhaoming; Rodriguez-Santiago, Benjamin; Hutchinson, Amy; Deng, Xiang; Liu, Chenwei (2012-06-01). "Detectable clonal mosaicism and its relationship to aging and cancer". Nature Genetics. 44 (6): 651–658. doi:10.1038/ng.2270. ISSN 1546-1718. PMC 3372921. PMID 22561519.
  5. Zhou, Weiyin; Machiela, Mitchell J.; Freedman, Neal D.; Rothman, Nathaniel; Malats, Nuria; Dagnall, Casey; Caporaso, Neil; Teras, Lauren T.; Gaudet, Mia M. (2016-05-01). "Mosaic loss of chromosome Y is associated with common variation near TCL1A". Nature Genetics. 48 (5): 563–568. doi:10.1038/ng.3545. ISSN 1546-1718. PMC 4848121. PMID 27064253.
  6. Machiela, Mitchell J.; Ho, Brian M.; Fisher, Victoria A.; Hua, Xing; Chanock, Stephen J. (2015-01-01). "Limited evidence that cancer susceptibility regions are preferential targets for somatic mutation". Genome Biology. 16 (1): 193. doi:10.1186/s13059-015-0755-5. ISSN 1474-7596. PMC 4571124. PMID 26374197.
  7. Wang, Zhaoming; Rajaraman, Preetha; Melin, Beatrice S.; Chung, Charles C.; Zhang, Weijia; McKean-Cowdin, Roberta; Michaud, Dominique; Yeager, Meredith; Ahlbom, Anders (2015-07-01). "Further Confirmation of Germline Glioma Risk Variant rs78378222 in TP53 and Its Implication in Tumor Tissues via Integrative Analysis of TCGA Data". Human Mutation. 36 (7): 684–688. doi:10.1002/humu.22799. ISSN 1059-7794. PMC 4750473. PMID 25907361.
  8. Morton, Lindsay M.; Karyadi, Danielle M.; Stewart, Chip; Bogdanova, Tetiana I.; Dawson, Eric T.; Steinberg, Mia K.; Dai, Jieqiong; Hartley, Stephen W.; Schonfeld, Sara J.; Sampson, Joshua N.; Maruvka, Yosef E.; Kapoor, Vidushi; Ramsden, Dale A.; Carvajal-Garcia, Juan; Perou, Charles M. (2021-05-14). "Radiation-related genomic profile of papillary thyroid carcinoma after the Chernobyl accident". Science. 372 (6543): eabg2538. doi:10.1126/science.abg2538. ISSN 1095-9203. PMC 9022889. PMID 33888599.
  9. Yeager, Meredith; Machiela, Mitchell J.; Kothiyal, Prachi; Dean, Michael; Bodelon, Clara; Suman, Shalabh; Wang, Mingyi; Mirabello, Lisa; Nelson, Chase W.; Zhou, Weiyin; Palmer, Cameron; Ballew, Bari; Colli, Leandro M.; Freedman, Neal D.; Dagnall, Casey (2021-05-14). "Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident". Science. 372 (6543): 725–729. doi:10.1126/science.abg2365. ISSN 1095-9203. PMC 9398532. PMID 33888597.
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