Colorectal cancer risk in patients with inflammatory bowel disease and Lynch syndrome

Por Aronson, Melyssa, Stempak, Joanne, Silverberg, Mark, Semotiuk, Kara, Gryfe, Robert, Gallinger, Steven
Publicado em 2010

Oncologic surveillance for subjects with biallelic mismatch repair gene mutations-10 year follow-up in a kindred

Por Durno, Carol A, Aronson, Melyssa, Tabori, Uri, Malkin, David, Chan, Helen, Gallinger, Steven
Publicado em 2011

Clinicopathologic and genetic features of young patients with colorectal cancer

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

Lynch syndrome in a predominantly Afrocentric population: a clinicopathological and genetic study

Por Plummer, Joseph M., Chin, Sheray N., Aronson, Melyssa, Graham, Rondell P., Williams, Nadia P., Bapat, Bharati, Wharfe, Gillian, Pollett, Aaron, Gallinger, Steven
Publicado em 2012

HG-80 ISSUES IN THE MANAGEMENT OF CHILDREN WITH BRAIN TUMORS AND BIALLELIC MISMATCH GENE REPAIR DEFICIENCY SYNDROME

Por Farah, Roula, Maalouf, Farid, Abi-Chahine, Nassim, Farhat, Hussein, Campbell, Brittany, Zhukova, Nataliya, Durno, Carol, Aronson, Melyssa, Hawkins, Cynthia, Bouffet, Eric, Tabori, Uri
Publicado no Neuro Oncol (2016)

Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario

Por Choi, Yun-Hee, Cotterchio, Michelle, McKeown-Eyssen, Gail, Neerav, Monga, Bapat, Bharati, Boyd, Kevin, Gallinger, Steven, McLaughlin, John, Aronson, Melyssa, Briollais, Laurent
Publicado em 2009

Development and Validation of an Instrument to Measure the Impact of Genetic Testing on Self-Concept in Lynch Syndrome (LS)

Por Esplen, Mary Jane, Stuckless, Noreen, Wong, Jiahui, Gallinger, Steve, Aronson, Melyssa, Rothenmund, Heidi, Semotiuk, Kara, Stokes, Jackie, Way, Chris, Green, Jane, Butler, Kate, Petersen, Helle Vendel
Publicado em 2011

Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study

Por Esplen, Mary Jane, Cappelli, Mario, Wong, Jiahui, Bottorff, Joan L, Hunter, Jon, Carroll, June, Dorval, Michel, Wilson, Brenda, Allanson, Judith, Semotiuk, Kara, Aronson, Melyssa, Bordeleau, Louise, Charlemagne, Nicole, Meschino, Wendy
Publicado em 2013

Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome

Por Raskin, Leon, Schwenter, Frank, Freytsis, Marina, Tischkowitz, Marc, Wong, Nora, Chong, George, Narod, Steven A., Levine, Douglas A., Bogomolniy, Faina, Aronson, Melyssa, Thibodeau, Stephen N., Hunt, Katherine S., Rennert, Gad, Gallinger, Steven, Gruber, Stephen B., Foulkes, William D.
Publicado no Clin Genet (2010)

GE-09 COMBINED HEREDITARY AND SOMATIC MUTATIONS OF REPLICATION ERROR REPAIR GENES RESULT IN RAPID ONSET OF ULTRA-HYPERMUTATED MALIGNANT BRAIN TUMORS IN CHILDREN

Por Shlien, Adam, Campbell, Brittany B., de Borja, Richard, Alexandrov, Ludmil B., Merino, Diana M., Remke, Marc, Bakry, Doua, Dirks, Peter, Huang, Annie, Grundy, Richard G., Durno, Carol, Aronson, Melyssa, Taylor, Michael D., Pursell, Zachary F., Pearson, Christopher E., Malkin, David, Bouffet, Eric, Hawkins, Cynthia, Campbell, Peter J., Tabori, Uri
Publicado no Neuro Oncol (2015)

Conversion Analysis for Mutation Detection in MLH1 and MSH2 in Patients With Colorectal Cancer

Por Casey, Graham, Lindor, Noralane M., Papadopoulos, Nickolas, Thibodeau, Stephen N., Moskow, John, Steelman, Scott, Buzin, Carolyn H., Sommer, Steve S., Collins, Christine E., Butz, Malinda, Aronson, Melyssa, Gallinger, Steven, Barker, Melissa A., Young, Joanne P., Jass, Jeremy R., Hopper, John L., Diep, Anh, Bapat, Bharati, Salem, Michael, Seminara, Daniela, Haile, Robert
Publicado em 2005

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

Por Rosty, Christophe, Walsh, Michael D., Lindor, Noralane M., Thibodeau, Stephen N., Mundt, Erin, Gallinger, Steven, Aronson, Melyssa, Pollett, Aaron, Baron, John A., Pearson, Sally, Clendenning, Mark, Walters, Rhiannon J., Nagler, Belinda N., Crawford, William J., Young, Joanne P., Winship, Ingrid, Win, Aung Ko, Hopper, John L., Jenkins, Mark A., Buchanan, Daniel D.
Publicado no Fam Cancer (2014)

Multiplicity and Molecular Heterogeneity of Colorectal Carcinomas in Individuals with Serrated Polyposis

Por Rosty, Christophe, Walsh, Michael D., Walters, Rhiannon J, Clendenning, Mark, Pearson, Sally-Ann, Jenkins, Mark A., Win, Aung Ko, Hopper, John L., Sweet, Kevin, Frankel, Wendy L., Aronson, Melyssa, Gallinger, Steve, Goldblatt, Jack, Tucker, Kathy, Greening, Sian, Gattas, Michael R., Woodall, Sonja, Arnold, Julie, Walker, Neal I, Parry, Susan, Young, Joanne P, Buchanan, Daniel D.
Publicado em 2013

Phenotype and Polyp Landscape in Serrated Polyposis Syndrome: A Series of 100 Patients from Genetics Clinics

Por Rosty, Christophe, Buchanan, Daniel D., Walsh, Michael D., Pearson, Sally-Ann, Pavluk, Erika, Walters, Rhiannon J, Clendenning, Mark, Spring, Kevin J., Jenkins, Mark A., Win, Aung K., Hopper, John L., Sweet, Kevin, Frankel, Wendy L., Aronson, Melyssa, Gallinger, Steve, Goldblatt, Jack, Woodall, Sonja, Arnold, Julie, Walker, Neal I, Jass, Jeremy R, Parry, Susan, Young, Joanne P
Publicado em 2012

Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency: Familial Colorectal Cancer Type X

Por Lindor, Noralane M., Rabe, Kari, Petersen, Gloria M., Haile, Robert, Casey, Graham, Baron, John, Gallinger, Steve, Bapat, Bharati, Aronson, Melyssa, Hopper, John, Jass, Jeremy, LeMarchand, Loic, Grove, John, Potter, John, Newcomb, Polly, Terdiman, Jonathan P., Conrad, Peggy, Moslein, Gabriella, Goldberg, Richard, Ziogas, Argyrios, Anton-Culver, Hoda, de Andrade, Mariza, Siegmund, Kim, Thibodeau, Stephen N., Boardman, Lisa A., Seminara, Daniela
Publicado em 2005

PMS2 monoallelic mutation carriers: the known unknown

Por 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.
Publicado no Genet Med (2015)

Cancer risks for relatives of patients with serrated polyposis

Por Win, Aung Ko, Walters, Rhiannon J., Buchanan, Daniel D., Jenkins, Mark A., Sweet, Kevin, Frankel, Wendy L., de la Chapelle, Albert, McKeone, Diane M., Walsh, Michael D., Clendenning, Mark, Pearson, Sally-Ann, Pavluk, Erika, Nagler, Belinda, Hopper, John L., Gattas, Michael R., Goldblatt, Jack, George, Jill, Suthers, Graeme K., Phillips, Kerry D., Woodall, Sonja, Arnold, Julie, Tucker, Kathy, Field, Michael, Greening, Sian, Gallinger, Steve, Aronson, Melyssa, Perrier, Renee, Woods, Michael O., Green, Jane S., Walker, Neal, Rosty, Christophe, Parry, Susan, Young, Joanne P.
Publicado em 2012

HG-53 HYPERMUTATION AND NEOANTIGEN FORMATION PREDICT RESPONSE TO IMMUNE CHECKPOINT INHIBITION IN CHILDHOOD BIALLELIC MISMATCH REPAIR DEFICIENT GLIOBLASTOMA

Por Campbell, Brittany, Bouffet, Eric, Larouche, Valerie, Mason, Gary, Reddy, Alyssa, Osborn, Michael, Magimairan, Vanan, Merico, Daniele, de Borja, Richard, Chung, Brian, Galati, Melissa, Aronson, Melyssa, Durno, Carol, Kruger, Joerg, Cabric, Vanja, Zhukova, Nataliya, Ramaswamy, Vijay, Farah, Roula, Afzal, Samina, Yalon, Michal, Rechavi, Gideon, Walsh, Michael F., Constantini, Shlomi, Dvir, Rina, Elhasid, Ronit, Sullivan, Michael, Hansford, Jordan R., Dodgshun, Andrew, Klauber-Demore, Nancy, Peterson, Lindsay, Patel, Sunil, Lindhorst, Scott, Atkinson, Jeffrey, Laframboise, Rachel, Cohen, Zane, Dirks, Peter, Taylor, Michael, Malkin, David, Albrecht, Steffen, Dudley, Roy, Jabado, Nada, Hawkins, Cynthia, Shlien, Adam, Tabori, Uri
Publicado no Neuro Oncol (2016)

Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers

Por Baglietto, Laura, Lindor, Noralane M., Dowty, James G., White, Darren M., Wagner, Anja, Gomez Garcia, Encarna B., Vriends, Annette H. J. T., Cartwright, Nicola R., Barnetson, Rebecca A., Farrington, Susan M., Tenesa, Albert, Hampel, Heather, Buchanan, Daniel, Arnold, Sven, Young, Joanne, Walsh, Michael D., Jass, Jeremy, Macrae, Finlay, Antill, Yoland, Winship, Ingrid M., Giles, Graham G., Goldblatt, Jack, Parry, Susan, Suthers, Graeme, Leggett, Barbara, Butz, Malinda, Aronson, Melyssa, Poynter, Jenny N., Baron, John A., Le Marchand, Loic, Haile, Robert, Gallinger, Steve, Hopper, John L., Potter, John, de la Chapelle, Albert, Vasen, Hans F., Dunlop, Malcolm G., Thibodeau, Stephen N., Jenkins, Mark A.
Publicado em 2010