Fragile X Syndrome—Diagnosis, Treatment, and Research

Por Suthers, Graeme
Publicado em 1992

Quality standards and samples in genetic testing

Por Ravine, David, Suthers, Graeme
Publicado em 2012

Reply

Por Suthers, Graeme K, Davies, Kay E, Huson, Susan M
Publicado em 1993

Functional characterization of human MutY homolog (hMYH) missense mutation (R231L) that is linked with hMYH-associated polyposis

Por Bai, Haibo, Grist, Scott, Gardner, Justin, Suthers, Graeme, Wilson, Teresa M., Lu, A-Lien
Publicado em 2006

Frequency of the ATM IVS10-6T→G variant in Australian multiple-case breast cancer families

Por Lindeman, Geoffrey J, Hiew, Melody, Visvader, Jane E, Leary, Jennifer, Field, Michael, Gaff, Clara L, Gardner, RJ McKinlay, Trainor, Kevin, Cheetham, Glenice, Suthers, Graeme, Kirk, Judy
Publicado em 2004

Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1

Por Carvalho, Marcelo, Pino, Maria A., Karchin, Rachel, Beddor, Jennifer, Godinho-Netto, Martha, Mesquita, Rafael D., Rodarte, Renato S., Vaz, Danielle C., Monteiro, Viviane A., Manoukian, Siranoush, Colombo, Mara, Ripamonti, Carla B., Rosenquist, Richard, Suthers, Graeme, Borg, Ake, Radice, Paolo, Grist, Scott A., Monteiro, Alvaro N.A., Billack, Blase
Publicado em 2008

Lynch Syndrome-Associated Breast Cancers Do Not Overexpress Chromosome 11 Encoded Mucins

Por Walsh, Michael D, Cummings, Margaret C, Pearson, Sally-Ann, Clendenning, Mark, Walters, Rhiannon J, Nagler, Belinda, Hopper, John L, Jenkins, Mark A, Suthers, Graeme K, Goldblatt, Jack, Tucker, Kathy, Gattas, Michael R, Arnold, Julie, Parry, Susan, Macrae, Finlay A, McGuckin, Michael A, Young, Joanne P, Buchanan, Daniel D
Publicado em 2013

Analysis of Families with Lynch Syndrome Complicated by Advanced Serrated Neoplasia: The Importance of Pathology Review and Pedigree Analysis

Por Walsh, Michael D, Buchanan, Daniel D, Walters, Rhiannon, Roberts, Aedan, Arnold, Sven, McKeone, Diane, Clendenning, Mark, Ruszkiewicz, Andrew R, Jenkins, Mark A, Hopper, John L, Goldblatt, Jack, George, Jillian, Suthers, Graeme K, Phillips, Kerry, Young, Graeme P, Macrae, Finlay, Drini, Musa, Woods, Michael O, Parry, Susan, Jass, Jeremy R, Young, Joanne P
Publicado em 2009

Immunohistochemical Testing of Conventional Adenomas for Loss of Expression of Mismatch Repair proteins in Lynch Syndrome Mutation Carriers: a Case Series from the Australasian Sit...

Por Walsh, Michael D, Buchanan, Daniel D, Pearson, Sally-Ann, Clendenning, Mark, Jenkins, Mark A, Win, Aung Ko, Walters, Rhiannon J, Spring, Kevin, Nagler, Belinda, Pavluk, Erika, Arnold, Sven T, Goldblatt, Jack, George, Jill, Suthers, Graeme, Phillips, Kerry, Hopper, John L, Jass, Jeremy R, Baron, John A, Ahnen, Dennis, Thibodeau, Stephen, Lindor, Noralane, Parry, Susan, Walker, Neal, Rosty, Christophe, Young, Joanne P
Publicado em 2012

Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource

Por Mann, Graham J, Thorne, Heather, Balleine, Rosemary L, Butow, Phyllis N, Clarke, Christine L, Edkins, Edward, Evans, Gerda M, Fereday, Sián, Haan, Eric, Gattas, Michael, Giles, Graham G, Goldblatt, Jack, Hopper, John L, Kirk, Judy, Leary, Jennifer A, Lindeman, Geoffrey, Niedermayr, Eveline, Phillips, Kelly-Anne, Picken, Sandra, Pupo, Gulietta M, Saunders, Christobel, Scott, Clare L, Spurdle, Amanda B, Suthers, Graeme, Tucker, Kathy, Chenevix-Trench, Georgia
Publicado em 2006

Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)

Por Roberts, Aedan, Nancarrow, Derek, Clendenning, Mark, Buchanan, Daniel D., Jenkins, Mark A., Duggan, David, Taverna, Darin, McKeone, Diane, Walters, Rhiannon, Walsh, Michael D., Young, Bruce W., Jass, Jeremy R., Rosty, Christophe, Gattas, Michael, Pelzer, Elise, Hopper, John L., Goldblatt, Jack, George, Jill, Suthers, Graeme K., Phillips, Kerry, Parry, Susan, Woodall, Sonja, Arnold, Julie, Tucker, Kathy, Muir, Amanda, Drini, Musa, Macrae, Finlay, Newcomb, Polly, Potter, John D., Pavluk, Erika, Lindblom, Annika, Young, Joanne P.
Publicado em 2010

Heritable GATA2 Mutations Associated with Familial Myelodysplastic Syndrome and Acute Myeloid Leukemia

Por Hahn, Christopher N., Chong, Chan-Eng, Carmichael, Catherine L., Wilkins, Ella J., Brautigan, Peter J., Li, Xiao-Chun, Babic, Milena, Lin, Ming, Carmagnac, Amandine, Lee, Young K., Kok, Chung H., Gagliardi, Lucia, Friend, Kathryn L., Ekert, Paul G., Butcher, Carolyn M., Brown, Anna L., Lewis, Ian D., To, L. Bik, Timms, Andrew E., Storek, Jan, Moore, Sarah, Altree, Meryl, Escher, Robert, Bardy, Peter G., Suthers, Graeme K., D’Andrea, Richard J., Horwitz, Marshall S., Scott, Hamish S.
Publicado em 2011

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies

Por Lewinsohn, Maya, Brown, Anna L., Weinel, Luke M., Phung, Connie, Rafidi, George, Lee, Ming K., Schreiber, Andreas W., Feng, Jinghua, Babic, Milena, Chong, Chan-Eng, Lee, Young, Yong, Agnes, Suthers, Graeme K., Poplawski, Nicola, Altree, Meryl, Phillips, Kerry, Jaensch, Louise, Fine, Miriam, D’Andrea, Richard J., Lewis, Ian D., Medeiros, Bruno C., Pollyea, Daniel A., King, Mary-Claire, Walsh, Tom, Keel, Siobán, Shimamura, Akiko, Godley, Lucy A., Hahn, Christopher N., Churpek, Jane E., Scott, Hamish S.
Publicado no Blood (2016)

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

Lynch Syndrome-Associated Breast Cancers: Clinicopathological Characteristics of a Case Series from the Colon CFR

Por Walsh, Michael D, Buchanan, Daniel D, Cummings, Margaret C, Pearson, Sally-Ann, Arnold, Sven T, Clendenning, Mark, Walters, Rhiannon, McKeone, Diane M, Spurdle, Amanda B, Hopper, John L, Jenkins, Mark A, Phillips, Kerry D, Suthers, Graeme K, George, Jill, Goldblatt, Jack, Muir, Amanda, Tucker, Kathy, Pelzer, Elise, Gattas, Michael R, Woodall, Sonja, Parry, Susan, Macrae, Finlay A, Haile, Robert W, Baron, John A, Potter, John D, Marchand, Loic Le, Bapat, Bharati, Thibodeau, Stephen N, Lindor, Noralane M, McGuckin, Michael A, Young, Joanne P
Publicado em 2010

Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study

Por Buchanan, Daniel D., Sweet, Kevin, Drini, Musa, Jenkins, Mark A., Win, Aung Ko, Gattas, Michael, Walsh, Michael D., Clendenning, Mark, McKeone, Diane, Walters, Rhiannon, Roberts, Aedan, Young, Alasdair, Hampel, Heather, Hopper, John L., Goldblatt, Jack, George, Jill, Suthers, Graeme K., Phillips, Kerry, Young, Graeme P., Chow, Elizabeth, Parry, Susan, Woodall, Sonja, Tucker, Kathy, Muir, Amanda, Field, Michael, Greening, Sian, Gallinger, Steven, Green, Jane, Woods, Michael O., Spaetgens, Renee, de la Chapelle, Albert, Macrae, Finlay, Walker, Neal I., Jass, Jeremy R., Young, Joanne P.
Publicado em 2010

Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study

Por Buchanan, Daniel D., Sweet, Kevin, Drini, Musa, Jenkins, Mark A., Win, Aung Ko, Gattas, Michael, Walsh, Michael D., Clendenning, Mark, McKeone, Diane, Walters, Rhiannon, Roberts, Aedan, Young, Alasdair, Hampel, Heather, Hopper, John L., Goldblatt, Jack, George, Jill, Suthers, Graeme K., Phillips, Kerry, Young, Graeme P., Chow, Elizabeth, Parry, Susan, Woodall, Sonja, Tucker, Kathy, Muir, Amanda, Field, Michael, Greening, Sian, Gallinger, Steven, Green, Jane, Woods, Michael O., Spaetgens, Renee, de la Chapelle, Albert, Macrae, Finlay, Walker, Neal I., Jass, Jeremy R., Young, Joanne P.
Publicado no Int J Colorectal Dis (2010)

Risk Factors for Colorectal Cancer in Patients with Multiple Serrated Polyps: A Cross-Sectional Case Series from Genetics Clinics

Por Buchanan, Daniel D., Sweet, Kevin, Drini, Musa, Jenkins, Mark A., Win, Aung Ko, English, Dallas R., Walsh, Michael D., Clendenning, Mark, McKeone, Diane M., Walters, Rhiannon J., Roberts, Aedan, Pearson, Sally-Ann, Pavluk, Erika, Hopper, John L., Gattas, Michael R., Goldblatt, Jack, George, Jill, Suthers, Graeme K., Phillips, Kerry D., Woodall, Sonja, Arnold, Julie, Tucker, Kathy, Muir, Amanda, Field, Michael, Greening, Sian, Gallinger, Steven, Perrier, Renee, Baron, John A., Potter, John D., Haile, Robert, Frankel, Wendy, de la Chapelle, Albert, Macrae, Finlay, Rosty, Christophe, Walker, Neal I., Parry, Susan, Young, Joanne P.
Publicado em 2010

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

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

Por Li, Jun, Woods, Susan L., Healey, Sue, Beesley, Jonathan, Chen, Xiaoqing, Lee, Jason S., Sivakumaran, Haran, Wayte, Nicci, Nones, Katia, Waterfall, Joshua J., Pearson, John, Patch, Anne-Marie, Senz, Janine, Ferreira, Manuel A., Kaurah, Pardeep, Mackenzie, Robertson, Heravi-Moussavi, Alireza, Hansford, Samantha, Lannagan, Tamsin R.M., Spurdle, Amanda B., Simpson, Peter T., da Silva, Leonard, Lakhani, Sunil R., Clouston, Andrew D., Bettington, Mark, Grimpen, Florian, Busuttil, Rita A., Di Costanzo, Natasha, Boussioutas, Alex, Jeanjean, Marie, Chong, George, Fabre, Aurélie, Olschwang, Sylviane, Faulkner, Geoffrey J., Bellos, Evangelos, Coin, Lachlan, Rioux, Kevin, Bathe, Oliver F., Wen, Xiaogang, Martin, Hilary C., Neklason, Deborah W., Davis, Sean R., Walker, Robert L., Calzone, Kathleen A., Avital, Itzhak, Heller, Theo, Koh, Christopher, Pineda, Marbin, Rudloff, Udo, Quezado, Martha, Pichurin, Pavel N., Hulick, Peter J., Weissman, Scott M., Newlin, Anna, Rubinstein, Wendy S., Sampson, Jone E., Hamman, Kelly, Goldgar, David, Poplawski, Nicola, Phillips, Kerry, Schofield, Lyn, Armstrong, Jacqueline, Kiraly-Borri, Cathy, Suthers, Graeme K., Huntsman, David G., Foulkes, William D., Carneiro, Fatima, Lindor, Noralane M., Edwards, Stacey L., French, Juliet D., Waddell, Nicola, Meltzer, Paul S., Worthley, Daniel L., Schrader, Kasmintan A., Chenevix-Trench, Georgia
Publicado no Am J Hum Genet (2016)