1. Discovery of common and rare genetic risk variants for colorectal cancer. (January 2019) Authors: Huyghe, Jeroen; Bien, Stephanie; Harrison, Tabitha; Kang, Hyun; Chen, Sai; Schmit, Stephanie; Conti, David; Qu, Conghui; Jeon, Jihyoun; Edlund, Christopher; Greenside, Peyton; Wainberg, Michael; Schumacher, Fredrick; Smith, Joshua; Levine, David; Nelson, Sarah; Sinnott-Armstrong, Nasa; Albanes, D... Journal: Nature genetics Issue: Volume 51:Number 1(2019) Page Start: 76 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. UNIT 2.9 Single Nucleotide Polymorphism Genotyping Using BeadChip Microarrays. (July 2013) Authors: Lambert, Gilliam; Tsinajinnie, Darwin; Duggan, David Journal: Current protocols in human genetics Issue: Volume 78(2013) Page Start: 2.9.1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Systematic evaluation of cancer‐specific genetic risk score for 11 types of cancer in The Cancer Genome Atlas and Electronic Medical Records and Genomics cohorts. (9th April 2019) Authors: Shi, Zhuqing; Yu, Hongjie; Wu, Yishuo; Lin, Xiaoling; Bao, Quanwa; Jia, Haifei; Perschon, Chelsea; Duggan, David; Helfand, Brian T.; Zheng, Siqun L.; Xu, Jianfeng Journal: Cancer medicine Issue: Volume 8:Number 6(2019:Jun.) Page Start: 3196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Calibration of polygenic risk scores is required prior to clinical implementation: results of three common cancers in UKB. Issue 3 (21st December 2020) Authors: Wei, Jun; Shi, Zhuqing; Na, Rong; Resurreccion, W Kyle; Wang, Chi-Hsiung; Duggan, David; Zheng, S Lilly; Hulick, Peter J; Helfand, Brian T; Xu, Jianfeng Journal: Journal of medical genetics Issue: Volume 59:Issue 3(2022) Page Start: 243 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Concept and benchmarks for assessing narrow‐sense validity of genetic risk score values. Issue 10 (29th April 2019) Authors: Yu, Hongjie; Shi, Zhuqing; Wu, Yishuo; Wang, Chi‐Hsiung; Lin, Xiaoling; Perschon, Chelsea; Isaacs, William B.; Helfand, Brian T.; Lilly Zheng, S.; Duggan, David; Mo, Zengnan; Lu, Daru; Xu, Jianfeng Journal: Prostate Issue: Volume 79:Issue 10(2019) Page Start: 1099 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic architectures of proximal and distal colorectal cancer are partly distinct. Issue 7 (25th February 2021) Authors: Huyghe, Jeroen R; Harrison, Tabitha A; Bien, Stephanie A; Hampel, Heather; Figueiredo, Jane C; Schmit, Stephanie L; Conti, David V; Chen, Sai; Qu, Conghui; Lin, Yi; Barfield, Richard; Baron, John A; Cross, Amanda J; Diergaarde, Brenda; Duggan, David; Harlid, Sophia; Imaz, Liher; Kang, Hyun Min; L... Journal: Gut Issue: Volume 70:Issue 7(2021) Page Start: 1325 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Novel Common Genetic Susceptibility Loci for Colorectal Cancer. (16th June 2018) Authors: Schmit, Stephanie L; Edlund, Christopher K; Schumacher, Fredrick R; Gong, Jian; Harrison, Tabitha A; Huyghe, Jeroen R; Qu, Chenxu; Melas, Marilena; Van Den Berg, David J; Wang, Hansong; Tring, Stephanie; Plummer, Sarah J; Albanes, Demetrius; Alonso, M Henar; Amos, Christopher I; Anton, Kristen; A... Journal: Journal of the National Cancer Institute Issue: Volume 111:Number 2(2019) Page Start: 146 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials. Issue 9965 (24th January 2015) Authors: Swerdlow, Daniel I; Preiss, David; Kuchenbaecker, Karoline B; Holmes, Michael V; Engmann, Jorgen E L; Shah, Tina; Sofat, Reecha; Stender, Stefan; Johnson, Paul C D; Scott, Robert A; Leusink, Maarten; Verweij, Niek; Sharp, Stephen J; Guo, Yiran; Giambartolomei, Claudia; Chung, Christina; Peasey, A... Journal: Lancet Issue: Volume 385:Issue 9965(2015) Page Start: 351 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Single Nucleotide Polymorphism Genotyping Using BeadChip Microarrays. (1st July 2013) Authors: Lambert, Gilliam; Tsinajinnie, Darwin; Duggan, David Editors: Haines, Jonathan L.; Korf, Bruce R.; Morton, Cynthia C.; Seidman, Christine E.; Seidman, J.G.; Smith, Douglas R. Journal: Current protocols in human genetics Issue: Volume 78(2013) Page Start: 2.9.1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Next generation sequencing and a new era of medicine. Issue 6 (1st May 2012) Authors: Casey, Graham; Conti, David; Haile, Robert; Duggan, David Journal: Gut Issue: Volume 62:Issue 6(2013) Page Start: 920 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗