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

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

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

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

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

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

Clinicopathologic and genetic features of young patients with colorectal cancer

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

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

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

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

av 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
Publicerad 2011

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

av 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
Publicerad 2009

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

av 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
I publikationen Oncologist (2017)

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

av 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
Publicerad 2013

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

av 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
Publicerad 2010

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

av 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.
Publicerad 2013

Identification of germline genomic copy number variation in familial pancreatic cancer

av 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
Publicerad 2012

Additional germline findings from a tumor profiling program

av 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.
I publikationen BMC Med Genomics (2018)

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

av 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.
Publicerad 2011

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

av 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
I publikationen 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

av 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
I publikationen PLoS Genet (2019)

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

av 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.
I publikationen Cancer (2020)

PMS2 monoallelic mutation carriers: the known unknown

av 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.
I publikationen Genet Med (2015)

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

av 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.
I publikationen Clin Cancer Res (2017)