Current status of genome-wide association studies in cancerCHUNG, Charles C; CHANOCK, Stephen J.Human genetics. 2011, Vol 130, Num 1, pp 59-78, issn 0340-6717, 20 p.Article

Detectable Clonal Mosaicism in the Human Genome : Next-Generation Sequencing in Hematologic CancersMACHIELA, Mitchell J; CHANOCK, Stephen J.Seminars in hematology. 2013, Vol 50, Num 4, pp 348-359, issn 0037-1963, 12 p.Article

Personalized medicine: new genomics, old lessonsOFFIT, Kenneth.Human genetics. 2011, Vol 130, Num 1, pp 3-14, issn 0340-6717, 12 p.Article

Special Issue on Personalized MedicineCHANOCK, Stephen J; BIANKIN, Andrew V.Human genetics. 2011, Vol 130, Num 1, issn 0340-6717, 167 p.Serial Issue

Direct-to-consumer testing: if consumers are not anxious, why are policymakers?CAULFIELD, Timothy.Human genetics. 2011, Vol 130, Num 1, pp 23-25, issn 0340-6717, 3 p.Article

Using germ-line genetic variation to investigate and treat cancerSAVAGE, Sharon A; CHANOCK, Stephen J.Drug discovery today. 2004, Vol 9, Num 14, pp 610-618, issn 1359-6446, 9 p.Article

Genetic counselling for personalised medicineCLARKE, Angus; THIRLAWAY, Katie.Human genetics. 2011, Vol 130, Num 1, pp 27-31, issn 0340-6717, 5 p.Article

Translating genomics into improved population screening: hype or hope?PASHAYAN, Nora; PHAROAH, Paul.Human genetics. 2011, Vol 130, Num 1, pp 19-21, issn 0340-6717, 3 p.Article

Genomic markers to tailor treatments: waiting or initiating?TAJIK, Parvin; BOSSUYT, Patrick M.Human genetics. 2011, Vol 130, Num 1, pp 15-18, issn 0340-6717, 4 p.Article

Somatic variation and cancer: therapies lost in the mixBIANKIN, Andrew V; HUDSON, Thomas J.Human genetics. 2011, Vol 130, Num 1, pp 79-91, issn 0340-6717, 13 p.Article

Genome-wide association studies in cancer—current and future directionsCHUNG, Charles C; MAGALHAES, Wagner C. S; GONZALEZ-BOSQUET, Jesus et al.Carcinogenesis (New York. Print). 2010, Vol 31, Num 1, pp 111-120, issn 0143-3334, 10 p.Article

Association of common haplotypes of surfactant protein A1 and A2 (SFTPA1 and SFTPA2) genes with severity of lung disease in cystic fibrosisEUN HWA CHOI; EHRMANTRAUT, Mary; FOSTER, Charles B et al.Pediatric pulmonology. 2006, Vol 41, Num 3, pp 255-262, issn 8755-6863, 8 p.Article

Inflammation-related gene polymorphisms and colorectal adenomaGUNTER, Marc J; CANZIAN, Federico; LANDI, Stefano et al.Cancer epidemiology, biomarkers & prevention. 2006, Vol 15, Num 6, pp 1126-1131, issn 1055-9965, 6 p.Article

A common haplotype of interleukin-4 gene IL4 is associated with severe respiratory syncytial virus disease in Korean childrenEUN HWA CHOI; HOAN JONG LEE; TAIWOO YOO et al.The Journal of infectious diseases. 2002, Vol 186, Num 9, pp 1207-1211, issn 0022-1899, 5 p.Article

Genomic medicine and neurological diseaseBOONE, Philip M; WISZNIEWSKI, Wojciech; LUPSKI, James R et al.Human genetics. 2011, Vol 130, Num 1, pp 103-121, issn 0340-6717, 19 p.Article

Invasive candidiasis stimulates hepatocyte and monocyte production of active transforming growth factor βLETTERIO, John J; LEHRNBECHER, Thomas; POLLACK, Greg et al.Infection and immunity. 2001, Vol 69, Num 8, pp 5115-5120, issn 0019-9567Article

Comprehensive screen of genetic variation in DNA repair pathway genes and postmenopausal breast cancer riskMONSEES, Genevieve M; KRAFT, Peter; CHANOCK, Stephen J et al.Breast cancer research and treatment. 2011, Vol 125, Num 1, pp 207-214, issn 0167-6806, 8 p.Article

Electronic medical records and personalized medicineHOFFMAN, Mark A; WILLIAMS, Marc S.Human genetics. 2011, Vol 130, Num 1, pp 33-39, issn 0340-6717, 7 p.Article

Type 2 diabetes and obesity: genomics and the clinicTRAVERS, Mary E; MCCARTHY, Mark I.Human genetics. 2011, Vol 130, Num 1, pp 41-58, issn 0340-6717, 18 p.Article

Risk factors for autism: translating genomic discoveries into diagnosticsSCHERER, Stephen W; DAWSON, Geraldine.Human genetics. 2011, Vol 130, Num 1, pp 123-148, issn 0340-6717, 26 p.Article

Insulin-like Growth Factor Pathway Genetic Polymorphisms, Circulating IGF1 and IGFBP3, and Prostate Cancer SurvivalYIN CAO; LINDSTRÖM, Sara; CHANOCK, Stephen J et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 5, issn 0027-8874, dju085.1-dju085.10Article

Obesity and Risk of Esophageal Adenocarcinoma and Barrett's Esophagus: A Mendelian Randomization StudyTHRIFT, Aaron P; SHAHEEN, Nicholas J; CORLEY, Douglas A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 11, issn 0027-8874, 252.1-252.8Article

Genetic Predictors of Circulating 25-Hydroxyvitamin D and Risk of Colorectal CancerHIRAKI, Linda T; CONGHUI QU; CHANOCK, Stephen J et al.Cancer epidemiology, biomarkers & prevention. 2013, Vol 22, Num 11, pp 2037-2046, issn 1055-9965, 10 p.Article

Known glioma risk loci are associated with glioma with a family history of brain tumours—A case―control gene association studyMELIN, Beatrice; DAHLIN, Anna M; KITAHARA, Cari M et al.International journal of cancer (Print). 2013, Vol 132, Num 10, pp 2464-2468, issn 0020-7136, 5 p.Article

PRRC2A and BCL2Ll1 gene variants influence risk of non-Hodgkin lymphoma: results from the InterLymph consortiumNIETERS, Alexandra; CONDE, Lucia; SHANAFELT, Tait D et al.Blood. 2012, Vol 120, Num 23, pp 4645-4648, issn 0006-4971, 4 p.Article