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

nork McGarragle, Kaitlin M., Hare, Crystal, Holter, Spring, Facey, Dorian Anglin, McShane, Kelly, Gallinger, Steven, Hart, Tae L.
Argitaratua izan da Hered Cancer Clin Pract (2019)

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

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

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

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

Clinicopathologic and genetic features of young patients with colorectal cancer

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

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

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

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

nork 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
Argitaratua 2011

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

nork 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
Argitaratua 2009

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

nork 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
Argitaratua izan da Oncologist (2017)

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

nork 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
Argitaratua 2013

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

nork 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
Argitaratua 2010

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

nork 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.
Argitaratua 2013

Identification of germline genomic copy number variation in familial pancreatic cancer

nork 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
Argitaratua 2012

Additional germline findings from a tumor profiling program

nork 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.
Argitaratua izan da BMC Med Genomics (2018)

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

nork 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.
Argitaratua 2011

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

nork 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
Argitaratua izan da 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

nork 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
Argitaratua izan da PLoS Genet (2019)

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

nork 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.
Argitaratua izan da Cancer (2020)

PMS2 monoallelic mutation carriers: the known unknown

nork 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.
Argitaratua izan da Genet Med (2015)

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

nork 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.
Argitaratua izan da Clin Cancer Res (2017)