Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study

by McGarragle, Kaitlin M., Hare, Crystal, Holter, Spring, Facey, Dorian Anglin, McShane, Kelly, Gallinger, Steven, Hart, Tae L.
Published in Hered Cancer Clin Pract (2019)

Regulation of Tissue Inhibitor of Metalloproteinase-1 by Astrocytes: Links to HIV-1 Dementia

by SURYADEVARA, RADHIKA, HOLTER, SPRING, BORGMANN, KATHLEEN, PERSIDSKY, RAISA, LABENZ-ZINK, CHRISTINE, PERSIDSKY, YURI, GENDELMAN, HOWARD E., WU, LI, GHORPADE, ANUJA
Published 2003

Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome

by McGarragle, Kaitlin M., Aronson, Melyssa, Semotiuk, Kara, Holter, Spring, Hare, Crystal J., Ferguson, Sarah E., Cohen, Zane, Hart, Tae L.
Published in Hered Cancer Clin Pract (2019)

Clinicopathologic and genetic features of young patients with colorectal cancer

by Aronson, Melyssa, Gallinger, Steve, Rothenmund, Heidi, Semotiuk, Kara, Holter, Spring, Berk, Terri, Pollett, Aaron, Cohen, Zane, Bapat, Bharati, Kim, Hyeja, Gryfe, Robert
Published 2010

Prevalence of Germline Mutations in Cancer Predisposition Genes in Patients with Pancreatic Cancer

by Grant, Robert C., Selander, Iris, Connor, Ashton A., Selvarajah, Shamini, Borgida, Ayelet, Briollais, Laurent, Petersen, Gloria M., Lerner-Ellis, Jordan, Holter, Spring, Gallinger, Steven
Published in Gastroenterology (2014)

Disclosing genetic research results: experiences of the Colon Cancer Family Registry

by Keogh, Louise, Fisher, Douglass, Schully, Sheri, Lowery, Jan, Ahnen, Dennis, Maskiell, Judi, Lindor, Noralane, Hopper, John, Burnett, Terrilea, Holter, Spring, Gorin, Sheri Sheinfeld, Sinicrope, Pam
Published 2011

Analysis of the Gene Coding for the BRCA2-Interacting Protein PALB2 in Familial and Sporadic Pancreatic Cancer

by Tischkowitz, Marc D., Sabbaghian, Nelly, Hamel, Nancy, Borgida, Ayelet, Rosner, Chaim, Taherian, Nassim, Srivastava, Archana, Holter, Spring, Rothenmund, Heidi, Ghadirian, Parviz, Foulkes, William D., Gallinger, Steven
Published 2009

Overall Survival and Clinical Characteristics of BRCA‐Associated Cholangiocarcinoma: A Multicenter Retrospective Study

by Golan, Talia, Raitses‐Gurevich, Maria, Kelley, Robin K., Bocobo, Andrea G., Borgida, Ayelet, Shroff, Rachna T., Holter, Spring, Gallinger, Steven, Ahn, Daniel H., Aderka, Dan, Apurva, Jain, Bekaii‐Saab, Tanois, Friedman, Eitan, Javle, Milind
Published in Oncologist (2017)

Exome sequencing identifies nonsegregating nonsense ATM and PALB2 variants in familial pancreatic cancer

by Grant, Robert C, Al-Sukhni, Wigdan, Borgida, Ayelet E, Holter, Spring, Kanji, Zaheer S, McPherson, Treasa, Whelan, Emily, Serra, Stefano, Trinh, Quang M, Peltekova, Vanya, Stein, Lincoln D, McPherson, John D, Gallinger, Steven
Published 2013

The PREMM(1,2,6) Model Predicts Risk of MLH1, MSH2, and MSH6 Germline Mutations Based on Cancer History

by Kastrinos, Fay, Steyerberg, Ewout W., Mercado, Rowena, Balmaña, Judith, Holter, Spring, Gallinger, Steven, Siegmund, Kimberly D., Church, James M., Jenkins, Mark A., Lindor, Noralane M., Thibodeau, Stephen N., Burbidge, Lynn Anne, Wenstrup, Richard J., Syngal, Sapna
Published 2010

How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry

by Keogh, Louise A., Fisher, Douglass, Sheinfeld Gorin, Sherri, Schully, Sheri D., Lowery, Jan T., Ahnen, Dennis J., Maskiell, Judith A., Lindor, Noralane M., Hopper, John L., Burnett, Terrilea, Holter, Spring, Arnold, Julie L., Gallinger, Steven, Laurino, Mercy, Esplen, Mary-Jane, Sinicrope, Pamela S.
Published 2013

Identification of germline genomic copy number variation in familial pancreatic cancer

by Al-Sukhni, Wigdan, Joe, Sarah, Lionel, Anath C., Zwingerman, Nora, Zogopoulos, George, Marshall, Christian R., Borgida, Ayelet, Holter, Spring, Gropper, Aaron, Moore, Sara, Bondy, Melissa, Klein, Alison P., Petersen, Gloria M., Rabe, Kari G., Schwartz, Ann G., Syngal, Sapna, Scherer, Stephen W., Gallinger, Steven
Published 2012

Additional germline findings from a tumor profiling program

by Stjepanovic, Neda, Stockley, Tracy L., Bedard, Philippe L., McCuaig, Jeanna M., Aronson, Melyssa, Holter, Spring, Semotiuk, Kara, Leighl, Natasha B., Jang, Raymond, Krzyzanowska, Monika K., Oza, Amit M., Gupta, Abha, Elser, Christine, Ahmed, Lailah, Wang, Lisa, Kamel-Reid, Suzanne, Siu, Lillian L., Kim, Raymond H.
Published in BMC Med Genomics (2018)

Frequency of Deletions of EPCAM (TACSTD1) in MSH2-Associated Lynch Syndrome Cases

by Rumilla, Kandelaria, Schowalter, Karen V., Lindor, Noralane M., Thomas, Brittany C., Mensink, Kara A., Gallinger, Steven, Holter, Spring, Newcomb, Polly A., Potter, John D., Jenkins, Mark A., Hopper, John L., Long, Tiffany I., Weisenberger, Daniel J., Haile, Robert W., Casey, Graham, Laird, Peter W., Le Marchand, Loic, Thibodeau, Stephen N.
Published 2011

Candidate DNA Repair Susceptibility Genes Identified by Exome Sequencing in High-Risk Pancreatic Cancer

by Smith, Alyssa L., Alirezaie, Najmeh, Connor, Ashton, Chan-Seng-Yue, Michelle, Grant, Robert, Selander, Iris, Bascuñana, Claire, Borgida, Ayelet, Hall, Anita, Whelan, Thomas, Holter, Spring, McPherson, Treasa, Cleary, Sean, Petersen, Gloria M., Omeroglu, Atilla, Saloustros, Emmanouil, McPherson, John, Stein, Lincoln D., Foulkes, William D., Majewski, Jacek, Gallinger, Steven, Zogopoulos, George
Published in Cancer Lett (2015)

A region-based gene association study combined with a leave-one-out sensitivity analysis identifies SMG1 as a pancreatic cancer susceptibility gene

by Wong, Cavin, Chen, Fei, Alirezaie, Najmeh, Wang, Yifan, Cuggia, Adeline, Borgida, Ayelet, Holter, Spring, Lenko, Tatiana, Domecq, Celine, Petersen, Gloria M., Syngal, Sapna, Brand, Randall, Rustgi, Anil K., Cote, Michele L., Stoffel, Elena, Olson, Sara H., Roberts, Nicholas J., Akbari, Mohammad R., Majewski, Jacek, Klein, Alison P., Greenwood, Celia M. T., Gallinger, Steven, Zogopoulos, George
Published in PLoS Genet (2019)

Performance characteristics of screening strategies to identify Lynch syndrome in women with ovarian cancer

by Kim, Soyoun Rachel, Tone, Alicia, Kim, Raymond H., Cesari, Matthew, Clarke, Blaise A., Eiriksson, Lua, Hart, Tae, Aronson, Melyssa, Holter, Spring, Lytwyn, Alice, Maganti, Manjula, Oldfield, Leslie, Gallinger, Steven, Bernardini, Marcus Q., Oza, Amit M., Djordjevic, Bojana, Lerner‐Ellis, Jordan, Van de Laar, Emily, Vicus, Danielle, Pugh, Trevor J., Pollett, Aaron, Ferguson, Sarah E.
Published in Cancer (2020)

PMS2 monoallelic mutation carriers: the known unknown

by Goodenberger, McKinsey L., Thomas, Brittany C., Riegert-Johnson, Douglas, Boland, C. Richard, Plon, Sharon E., Clendenning, Mark, Ko Win, Aung, Senter, Leigha, Lipkin, Steven M., Stadler, Zsofia K., Macrae, Finlay A., Lynch, Henry T., Weitzel, Jeffrey N., de la Chapelle, Albert, Syngal, Sapna, Lynch, Patrick, Parry, Susan, Jenkins, Mark A., Gallinger, Steven, Holter, Spring, Aronson, Melyssa, Newcomb, Polly A., Burnett, Terrilea, Le Marchand, Loïc, Pichurin, Pavel, Hampel, Heather, Terdiman, Jonathan P., Lu, Karen H., Thibodeau, Stephen, Lindor, Noralane M.
Published in Genet Med (2015)

Genomics-Driven Precision Medicine for Advanced Pancreatic Cancer: Early Results from the COMPASS Trial

by Aung, Kyaw L., Fischer, Sandra E., Denroche, Robert E., Jang, Gun-Ho, Dodd, Anna, Creighton, Sean, Southwood, Bernadette, Liang, Sheng-Ben, Chadwick, Dianne, Zhang, Amy, O’Kane, Grainne M., Albaba, Hamzeh, Moura, Shari, Grant, Robert C., Miller, Jessica K., Mbabaali, Faridah, Pasternack, Danielle, Lungu, Ilinca M., Bartlett, John M.S., Ghai, Sangeet, Lemire, Mathieu, Holter, Spring, Connor, Ashton A., Moffitt, Richard A., Yeh, Jen Jen, Timms, Lee, Krzyzanowski, Paul M., Dhani, Neesha, Hedley, David, Notta, Faiyaz, Wilson, Julie M., Moore, Malcolm J., Gallinger, Steven, Knox, Jennifer J.
Published in Clin Cancer Res (2017)