1. 11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood. Issue 13 (22nd April 2020) Authors: Fiala, Elise M.; Ortiz, Michael V.; Kennedy, Jennifer A.; Glodzik, Dominik; Fleischut, Megan Harlan; Duffy, Kelly A.; Hathaway, Evan R.; Heaton, Todd; Gerstle, Justin T.; Steinherz, Peter; Shukla, Neerav; McNeer, Nicole; Tkachuk, Kaitlyn; Bouvier, Nancy; Cadoo, Karen; Carlo, Maria I.; Latham, Ali... Journal: Cancer Issue: Volume 126:Issue 13(2020) Page Start: 3114 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Comprehensive Comparison of Early-Onset and Average-Onset Colorectal Cancers. (18th August 2021) Authors: Cercek, Andrea; Chatila, Walid K; Yaeger, Rona; Walch, Henry; Fernandes, Gustavo Dos Santos; Krishnan, Asha; Palmaira, Lerie; Maio, Anna; Kemel, Yelena; Srinivasan, Preethi; Bandlamudi, Chaitanya; Salo-Mullen, Erin; Tejada, Prince R; Belanfanti, Kimeisha; Galle, Jesse; Joseph, Vijai; Segal, Neil;... Journal: Journal of the National Cancer Institute Issue: Volume 113:Number 12(2021) Page Start: 1683 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A counseling framework for moderate-penetrance colorectal cancer susceptibility genes. (November 2018) Authors: Katona, Bryson; Yurgelun, Matthew; Garber, Judy; Offit, Kenneth; Domchek, Susan; Robson, Mark; Stadler, Zsofia Journal: Genetics in medicine Issue: Volume 20:Number 11(2018) Page Start: 1324 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Issue 1 (December 2015) Authors: Blein, Sophie; Bardel, Claire; Danjean, Vincent; McGuffog, Lesley; Healey, Sue; Barrowdale, Daniel; Lee, Andrew; Dennis, Joe; Kuchenbaecker, Karoline; Soucy, Penny; Terry, Mary; Chung, Wendy; Goldgar, David; Buys, Saundra; Janavicius, Ramunas; Tihomirova, Laima; Tung, Nadine; Dorfling, Cecilia; v... Journal: Breast cancer research Issue: Volume 17:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk. (December 2017) Authors: Slavin, Thomas; Maxwell, Kara; Lilyquist, Jenna; Vijai, Joseph; Neuhausen, Susan; Hart, Steve; Ravichandran, Vignesh; Thomas, Tinu; Maria, Ann; Villano, Danylo; Schrader, Kasmintan; Moore, Raymond; Hu, Chunling; Wubbenhorst, Bradley; Wenz, Brandon; D'Andrea, Kurt; Robson, Mark; Peterlongo, Paolo;... Journal: NPJ breast cancer Issue: Volume 3(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry. Issue 10 (3rd July 2019) Authors: Friebel, Tara M.; Andrulis, Irene L.; Balmaña, Judith; Blanco, Amie M.; Couch, Fergus J.; Daly, Mary B.; Domchek, Susan M.; Easton, Douglas F.; Foulkes, William D.; Ganz, Patricia A.; Garber, Judy; Glendon, Gord; Greene, Mark H.; Hulick, Peter J.; Isaacs, Claudine; Jankowitz, Rachel C.; Karlan, B... Journal: Human mutation Issue: Volume 40:Issue 10(2019) Page Start: 1781 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores. (28th July 2021) Authors: Barnes, Daniel R; Silvestri, Valentina; Leslie, Goska; McGuffog, Lesley; Dennis, Joe; Yang, Xin; Adlard, Julian; Agnarsson, Bjarni A; Ahmed, Munaza; Aittomäki, Kristiina; Andrulis, Irene L; Arason, Adalgeir; Arnold, Norbert; Auber, Bernd; Azzollini, Jacopo; Balmaña, Judith; Barkardottir, Rosa B; ... Journal: Journal of the National Cancer Institute Issue: Volume 114:Number 1(2022) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Cascade Testing for Hereditary Cancer Syndromes: Should We Move Toward Direct Relative Contact? A Systematic Review and Meta-Analysis. Issue 35 (10th December 2022) Authors: Frey, Melissa K.; Ahsan, Muhammad Danyal; Bergeron, Hannah; Lin, Jenny; Li, Xuan; Fowlkes, Rana K.; Narayan, Priyanka; Nitecki, Roni; Rauh-Hain, Jose Alejandro; Moss, Haley A.; Baltich Nelson, Becky; Thomas, Charlene; Christos, Paul J.; Hamilton, Jada G.; Chapman-Davis, Eloise; Cantillo, Evelyn; ... Journal: Journal of clinical oncology Issue: Volume 40:Issue 35(2022) Page Start: 4129 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers. (January 2019) Authors: Walker, Logan; Marquart, Louise; Pearson, John; Wiggins, George; O'Mara, Tracy; Parsons, Michael; Barrowdale, Daniel; McGuffog, Lesley; Dennis, Joe; Benitez, Javier; Slavin, Thomas; Radice, Paolo; Frost, Debra; Godwin, Andrew; Meindl, Alfons; Schmutzler, Rita; Isaacs, Claudine; Peshkin, Beth; Cal... Journal: European journal of human genetics Issue: Volume 27:Number 1(2019) Page Start: 167 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. 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) ↗