Chanock, Stephen J.
National Cancer Institute · Division of Cancer Epidemiology and Genetics
72 papers on CoChatORCID 0000-0002-2324-3393
Most cited papers
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Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
The GIANT Consortium, Elks, C. E., Perry, J. R. B., Sulem, P., Chasman, D. I., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., et al. (2010) · Nature Genetics
Hypothalamic control of reproductive hormonesGenetic Associations and Epidemiology
Cited by 504
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A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation
Han, J., Kraft, P., Nan, H., Guo, Q., Chen, C., Qureshi, A., Hankinson, S. E., Hu, F. B., Duffy, D. L., Zhao, Z. Z., et al. (2008) · PLoS Genetics
melanin and skin pigmentationGenetic Associations and Epidemiology
Cited by 499
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Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Rodriguez-Martin, B., Alvarez, E. G., Baez-Ortega, A., Zamora, J., Supek, F., Demeulemeester, J., Santamarina, M., Ju, Y. S., Temes, J., Garcia-Souto, D., et al. (2020) · Nature Genetics
Genomic variations and chromosomal abnormalitiesCancer Genomics and Diagnostics
Cited by 451
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LDlinkR: An R Package for Rapidly Calculating Linkage Disequilibrium Statistics in Diverse Populations
Myers, T. A., Chanock, S. J., & Machiela, M. J. (2020) · Frontiers in Genetics
Genetic Associations and EpidemiologyGenetic diversity and population structure
Cited by 429
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Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
The PRACTICAL Consortium, Day, F. R., kConFab Investigators, AOCS Investigators, Scotland, G., EPIC-InterAct Consortium, Study, L. C., Ruth, K. S., Thompson, D. J., Lunetta, K. L., et al. (2015) · Nature Genetics
Genetic Associations and EpidemiologyBRCA gene mutations in cancer
Cited by 402
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Genome-wide association studies identify loci associated with age at menarche and age at natural menopause
He, C., Kraft, P., Chen, C., Buring, J. E., Paré, G., Hankinson, S. E., Chanock, S. J., Ridker, P. M., Hunter, D. J., & Chasman, D. I. (2009) · Nature Genetics
Genetic Associations and EpidemiologyHypothalamic control of reproductive hormones
Cited by 379
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Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States
Maas, P., Barrdahl, M., Joshi, A. D., Auer, P. L., Gaudet, M. M., Milne, R. L., Schumacher, F. R., Anderson, W. F., Check, D., Chattopadhyay, S., et al. (2016) · JAMA Oncology
Cancer Risks and FactorsBRCA gene mutations in cancer
Cited by 373
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Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita
Alter, B. P., Baerlocher, G. M., Savage, S. A., Chanock, S. J., Weksler, B. B., Willner, J. P., Peters, J. A., Giri, N., & Lansdorp, P. M. (2007) · Blood
Telomeres, Telomerase, and SenescenceBlood disorders and treatments
Cited by 356
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma
NCI DCEG Cancer Sequencing Working Group, Shi, J., Laboratory, N. D. C. G. R., French Familial Melanoma Study Group, Yang, X. R., Ballew, B., Rotunno, M., Calista, D., Fargnoli, M. C., Ghiorzo, P., et al. (2014) · Nature Genetics
Cutaneous Melanoma Detection and ManagementTelomeres, Telomerase, and Senescence
Cited by 331
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Genetic evidence of assortative mating in humans
Robinson, M. R., Kleinman, A., Graff, M., Vinkhuyzen, A. A. E., Couper, D., Miller, M. B., Peyrot, W. J., Abdellaoui, A., Zietsch, B. P., Nolte, I. M., et al. (2017) · Nature Human Behaviour
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 326
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Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome
Yamaguchi, H., Baerlocher, G. M., Lansdorp, P. M., Chanock, S. J., Nunez, O., Sloand, E., & Young, N. S. (2003) · Blood
Telomeres, Telomerase, and SenescenceBlood disorders and treatments
Cited by 301
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Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
Akdemir, K. C., Le, V. T., Chandran, S., Li, Y., Verhaak, R. G., Beroukhim, R., Campbell, P. J., Chin, L., Dixon, J. R., Futreal, P. A., et al. (2020) · Nature Genetics
Genomics and Chromatin DynamicsChromatin Remodeling and Cancer
Cited by 283
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Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants
Park, J.-H., Gail, M. H., Weinberg, C. R., Carroll, R. J., Chung, C. C., Wang, Z., Chanock, S. J., Fraumeni, J. F., & Chatterjee, N. (2011) · Proceedings of the National Academy of Sciences
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 280
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Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Klein, A. P., Wolpin, B. M., Risch, H. A., Stolzenberg-Solomon, R. Z., Mocci, E., Zhang, M., Canzian, F., Childs, E. J., Hoskins, J. W., Jermusyk, A., et al. (2018) · Nature Communications
Pancreatic and Hepatic Oncology ResearchGenetic Associations and Epidemiology
Cited by 268
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A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation
Coviello, A. D., Haring, R., Wellons, M., Vaidya, D., Lehtimäki, T., Keildson, S., Lunetta, K. L., He, C., Fornage, M., Lagou, V., et al. (2012) · PLoS Genetics
Genetic Associations and EpidemiologyHormonal and reproductive studies
Cited by 250
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Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma
Mirabello, L., Zhu, B., Koster, R., Karlins, E., Dean, M., Yeager, M., Gianferante, M., Spector, L. G., Morton, L. M., Karyadi, D., et al. (2020) · JAMA Oncology
Sarcoma Diagnosis and TreatmentBRCA gene mutations in cancer
Cited by 243
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Polymorphisms in GSTT1 , GSTZ1 , and CYP2E1 , Disinfection By-products, and Risk of Bladder Cancer in Spain
Cantor, K. P., Villanueva, C. M., Silverman, D. T., Figueroa, J. D., Real, F. X., Garcia-Closas, M., Malats, N., Chanock, S., Yeager, M., Tardon, A., et al. (2010) · Environmental Health Perspectives
Glutathione Transferases and PolymorphismsWater Treatment and Disinfection
Cited by 238
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Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR) and 15q24 (CYP1A2) As Determinants of Habitual Caffeine Consumption
Cornelis, M. C., Monda, K. L., Yu, K., Paynter, N., Azzato, E. M., Bennett, S. N., Berndt, S. I., Boerwinkle, E., Chanock, S., Chatterjee, N., et al. (2011) · PLoS Genetics
Coffee research and impactsGenetic Associations and Epidemiology
Cited by 228
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Von Hippel-Lindau (VHL) Inactivation in Sporadic Clear Cell Renal Cancer: Associations with Germline VHL Polymorphisms and Etiologic Risk Factors
Moore, L. E., Nickerson, M. L., Brennan, P., Toro, J. R., Jaeger, E., Rinsky, J., Han, S. S., Zaridze, D., Matveev, V., Janout, V., et al. (2011) · PLoS Genetics
Renal cell carcinoma treatmentAdrenal and Paraganglionic Tumors
Cited by 199
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Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors
Middlebrooks, C. D., Banday, A. R., Matsuda, K., Udquim, K.-I., Onabajo, O. O., Paquin, A., Figueroa, J. D., Zhu, B., Koutros, S., Kubo, M., et al. (2016) · Nature Genetics
Cancer Genomics and DiagnosticsEpigenetics and DNA Methylation
Cited by 185
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Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia
Calado, R. T., Regal, J. A., Hills, M., Yewdell, W. T., Dalmazzo, L. F., Zago, M. A., Lansdorp, P. M., Hogge, D., Chanock, S. J., Estey, E. H., et al. (2009) · Proceedings of the National Academy of Sciences
Telomeres, Telomerase, and SenescenceAcute Myeloid Leukemia Research
Cited by 184
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Risk of spontaneous preterm birth is associated with common proinflammatory cytokine polymorphisms
Engel, S. A. M., Erichsen, H. C., Savitz, D. A., Thorp, J., Chanock, S. J., & Olshan, A. F. (2005) · Epidemiology
Preterm Birth and ChorioamnionitisReproductive System and Pregnancy
Cited by 176
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DNA fingerprinting of the NCI-60 cell line panel
Lorenzi, P. L., Reinhold, W. C., Varma, S., Hutchinson, A. A., Pommier, Y., Chanock, S. J., & Weinstein, J. N. (2009) · Molecular Cancer Therapeutics
Cancer Genomics and DiagnosticsGene expression and cancer classification
Cited by 166
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Germline TP53 Variants and Susceptibility to Osteosarcoma
Mirabello, L., Yeager, M., Mai, P. L., Gastier-Foster, J. M., Gorlick, R., Khanna, C., Patiño-Garcia, A., Sierrasesúmaga, L., Lecanda, F., Andrulis, I. L., et al. (2015) · JNCI Journal of the National Cancer Institute
Sarcoma Diagnosis and TreatmentCancer-related Molecular Pathways
Cited by 155
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