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Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. SCI-41 - SCI-41
Abstract RASopathies are a group of rare congenital diseases in which dysregulated signaling through the RAS-MAPK signaling cases is the critical pathogenetic... 
Journal Article
by Jacobs, Kevin B and Yeager, Meredith and Zhou, Weiyin and Wacholder, Sholom and Wang, Zhaoming and Rodriguez-Santiago, Benjamin and Hutchinson, Amy and Deng, Xiang and Liu, Chenwei and Horner, Marie-Josephe and Cullen, Michael and Epstein, Caroline G and Burdett, Laurie and Dean, Michael C and Chatterjee, Nilanjan and Sampson, Joshua and Chung, Charles C and Kovaks, Joseph and Gapstur, Susan M and Stevens, Victoria L and Teras, Lauren T and Gaudet, Mia M and Albanes, Demetrius and Weinstein, Stephanie J and Virtamo, Jarmo and Taylor, Philip R and Freedman, Neal D and Abnet, Christian C and Goldstein, Alisa M and Hu, Nan and Yu, Kai and Yuan, Jian-Min and Liao, Linda and Ding, Ti and Qiao, You-Lin and Gao, Yu-Tang and Koh, Woon-Puay and Xiang, Yong-Bing and Tang, Ze-Zhong and Fan, Jin-Hu and Aldrich, Melinda C and Amos, Christopher and Blot, William J and Bock, Cathryn H and Gillanders, Elizabeth M and Harris, Curtis C and Haiman, Christopher A and Henderson, Brian E and Kolonel, Laurence N and Le Marchand, Loic and McNeill, Lorna H and Rybicki, Benjamin A and Schwartz, Ann G and Signorello, Lisa B and Spitz, Margaret R and Wiencke, John K and Wrensch, Margaret and Wu, Xifeng and Zanetti, Krista A and Ziegler, Regina G and Figueroa, Jonine D and Garcia-Closas, Montserrat and Malats, Nuria and Marenne, Gaelle and Prokunina-Olsson, Ludmila and Baris, Dalsu and Schwenn, Molly and Johnson, Alison and Landi, Maria Teresa and Goldin, Lynn and Consonni, Dario and Bertazzi, Pier Alberto and Rotunno, Melissa and Rajaraman, Preetha and Andersson, Ulrika and Freeman, Laura E. Beane and Berg, Christine D and Buring, Julie E and Butler, Mary A and Carreon, Tania and Feychting, Maria and Ahlbom, Anders and Gaziano, J Michael and Giles, Graham G and Hallmans, Goran and Hankinson, Susan E and Hartge, Patricia and Henriksson, Roger and Inskip, Peter D and Johansen, Christoffer and Landgren, Annelie and McKean-Cowdin, Roberta and Michaud, Dominique S and Melin, Beatrice S and Peters, Ulrike and Ruder, Avima M and Sesso, Howard D and Severi, Gianluca and Shu, Xiao-Ou and Visvanathan, Kala and ... and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Institutionen för strålningsvetenskaper and Näringsforskning and Onkologi and Umeå universitet
Nature Genetics, ISSN 1061-4036, 06/2012, Volume 44, Issue 6, pp. 651 - 658
Journal Article
by Gröbner, Susanne N and Worst, Barbara C and Weischenfeldt, Joachim and Buchhalter, Ivo and Kleinheinz, Kortine and Rudneva, Vasilisa A and Johann, Pascal D and Balasubramanian, Gnana Prakash and Segura-Wang, Maia and Brabetz, Sebastian and Bender, Sebastian and Hutter, Barbara and Sturm, Dominik and Pfaff, Elke and Hübschmann, Daniel and Zipprich, Gideon and Heinold, Michael and Eils, Jürgen and Lawerenz, Christian and Erkek, Serap and Lambo, Sander and Waszak, Sebastian and Blattmann, Claudia and Borkhardt, Arndt and Kuhlen, Michaela and Eggert, Angelika and Fulda, Simone and Gessler, Manfred and Wegert, Jenny and Kappler, Roland and Baumhoer, Daniel and Burdach, Stefan and Kirschner-Schwabe, Renate and Kontny, Udo and Kulozik, Andreas E and Lohmann, Dietmar and Hettmer, Simone and Eckert, Cornelia and Bielack, Stefan and Nathrath, Michaela and Niemeyer, Charlotte and Richter, Günther H and Schulte, Johannes and Siebert, Reiner and Westermann, Frank and Molenaar, Jan J and Vassal, Gilles and Witt, Hendrik and Zapatka, Marc and Burkhardt, Birgit and Kratz, Christian P and Witt, Olaf and Tilburg, Cornelis M. Van and Kramm, Christof M and Fleischhack, Gudrun and Dirksen, Uta and Rutkowski, Stefan and Frühwald, Michael and Hoff, Katja Von and Wolf, Stephan and Klingebiel, Thomas and Koscielniak, Ewa and Landgraf, Pablo and Koster, Jan and Resnick, Adam C and Zhang, Jinghui and Liu, Yanling and Zhou, Xin and Waanders, Angela J and Zwijnenburg, Danny A and Raman, Pichai and Brors, Benedikt and Weber, Ursula D and Northcott, Paul A and Pajtler, Kristian W and Kool, Marcel and Piro, Rosario M and Korbel, Jan O and Schlesner, Matthias and Eils, Roland and Jones, David T. W and Lichter, Peter and Chavez, Lukas and Pfister, Stefan M and ICGC PedBrain-Seq Project ICGC and ICGC MMML-Seq Project and ICGC PedBrain-Seq Project
Nature, ISSN 0028-0836, 03/2018, Volume 555, Issue 7696, pp. 321 - 327
Journal Article
by Waszak, Sebastian M and Northcott, Paul A and Buchhalter, Ivo and Robinson, Giles W and Sutter, Christian and Groebner, Susanne and Grund, Kerstin B and Brugières, Laurence and Jones, David T W and Pajtler, Kristian W and Morrissy, A Sorana and Kool, Marcel and Sturm, Dominik and Chavez, Lukas and Ernst, Aurelie and Brabetz, Sebastian and Hain, Michael and Zichner, Thomas and Segura-Wang, Maia and Weischenfeldt, Joachim and Rausch, Tobias and Mardin, Balca R and Zhou, Xin and Baciu, Cristina and Lawerenz, Christian and Chan, Jennifer A and Varlet, Pascale and Guerrini-Rousseau, Lea and Fults, Daniel W and Grajkowska, Wiesława and Hauser, Peter and Jabado, Nada and Ra, Young-Shin and Zitterbart, Karel and Shringarpure, Suyash S and De La Vega, Francisco M and Bustamante, Carlos D and Ng, Ho-Keung and Perry, Arie and MacDonald, Tobey J and Hernáiz Driever, Pablo and Bendel, Anne E and Bowers, Daniel C and McCowage, Geoffrey and Chintagumpala, Murali M and Cohn, Richard and Hassall, Timothy and Fleischhack, Gudrun and Eggen, Tone and Wesenberg, Finn and Feychting, Maria and Lannering, Birgitta and Schüz, Joachim and Johansen, Christoffer and Andersen, Tina V and Röösli, Martin and Kuehni, Claudia E and Grotzer, Michael and Kjaerheim, Kristina and Monoranu, Camelia M and Archer, Tenley C and Duke, Elizabeth and Pomeroy, Scott L and Shelagh, Redmond and Frank, Stephan and Sumerauer, David and Scheurlen, Wolfram and Ryzhova, Marina V and Milde, Till and Kratz, Christian P and Samuel, David and Zhang, Jinghui and Solomon, David A and Marra, Marco and Eils, Roland and Bartram, Claus R and von Hoff, Katja and Rutkowski, Stefan and Ramaswamy, Vijay and Gilbertson, Richard J and Korshunov, Andrey and Taylor, Michael D and Lichter, Peter and Malkin, David and Gajjar, Amar and Korbel, Jan O and Pfister, Stefan M and Sahlgrenska akademin and Institute of Clinical Sciences, Department of Pediatrics and Göteborgs universitet and Gothenburg University and Institutionen för kliniska vetenskaper, Avdelningen för pediatrik and Sahlgrenska Academy
The Lancet Oncology, ISSN 1470-2045, 06/2018, Volume 19, Issue 6, pp. 785 - 798
Medulloblastoma is associated with rare hereditary cancer predisposition syndromes; however, consensus medulloblastoma predisposition genes have not been... 
BREAST-CANCER | CHILDHOOD-CANCER | ONCOLOGY | LANDSCAPE | TP53 MUTATION | SUBGROUPS | FANCONI-ANEMIA | PALB2 | SOMATIC MUTATIONS | BRAIN-TUMORS | CHILDREN | Medicine, Experimental | Genetic research | Clinical trials | Medical research | Medulloblastoma | fanconi-anemia | Oncology | breast-cancer | tp53 | somatic mutations | mutation | subgroups | palb2 | brain-tumors | children | childhood-cancer | Cancer and Oncology | landscape | Cancer och onkologi
Journal Article
by Campbell, Brittany B and Light, Nicholas and Fabrizio, David and Zatzman, Matthew and Fuligni, Fabio and de Borja, Richard and Davidson, Scott and Edwards, Melissa and Elvin, Julia A and Hodel, Karl P and Zahurancik, Walter J and Suo, Zucai and Lipman, Tatiana and Wimmer, Katharina and Kratz, Christian P and Bowers, Daniel C and Laetsch, Theodore W and Dunn, Gavin P and Johanns, Tanner M and Grimmer, Matthew R and Smirnov, Ivan V and Larouche, Valérie and Samuel, David and Bronsema, Annika and Osborn, Michael and Stearns, Duncan and Raman, Pichai and Cole, Kristina A and Storm, Phillip B and Yalon, Michal and Opocher, Enrico and Mason, Gary and Thomas, Gregory A and Sabel, Magnus and George, Ben and Ziegler, David S and Lindhorst, Scott and Issai, Vanan Magimairajan and Constantini, Shlomi and Toledano, Helen and Elhasid, Ronit and Farah, Roula and Dvir, Rina and Dirks, Peter and Huang, Annie and Galati, Melissa A and Chung, Jiil and Ramaswamy, Vijay and Irwin, Meredith S and Aronson, Melyssa and Durno, Carol and Taylor, Michael D and Rechavi, Gideon and Maris, John M and Bouffet, Eric and Hawkins, Cynthia and Costello, Joseph F and Meyn, M. Stephen and Pursell, Zachary F and Malkin, David and Tabori, Uri and Shlien, Adam and Sahlgrenska akademin and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Pediatrics and Göteborgs universitet and Gothenburg University and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för pediatrik and Sahlgrenska Academy
Cell, ISSN 0092-8674, 11/2017, Volume 171, Issue 5, pp. 1042 - 1056.e10
Journal Article
Cancer Research, ISSN 0008-5472, 04/2011, Volume 71, Issue 8 Supplement, pp. 871 - 871
Journal Article
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 11, pp. e32 - e37
Replication proofreading is crucial to avoid mutation accumulation in dividing cells. In humans, proofreading and replication repair is maintained by the... 
HEREDITARY | ONCOLOGY | MICROSATELLITE INSTABILITY | GERMLINE MUTATIONS | EARLY-ONSET | FOLLOW-UP | LYNCH SYNDROME | EUROPEAN CONSORTIUM CARE | CANCER | POLE | CHILDREN | Microsatellite Instability | Neoplastic Syndromes, Hereditary - pathology | Colorectal Neoplasms - genetics | Humans | Brain Neoplasms - pathology | Germ-Line Mutation - genetics | MutL Protein Homolog 1 - deficiency | Colorectal Neoplasms - diagnosis | DNA-Binding Proteins - deficiency | Neoplastic Syndromes, Hereditary - epidemiology | MutS Homolog 2 Protein - deficiency | Neoplastic Syndromes, Hereditary - genetics | Child | Mismatch Repair Endonuclease PMS2 - deficiency | Colorectal Neoplasms - epidemiology | Early Detection of Cancer | Brain Neoplasms - diagnosis | Brain Neoplasms - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | MutL Protein Homolog 1 - genetics | Colorectal Neoplasms - pathology | Mismatch Repair Endonuclease PMS2 - genetics | Brain Neoplasms - epidemiology | Yeast | MLH1 protein | Therapeutic applications | Genes | Organs | MSH2 protein | Disorders | Health risks | MSH6 protein | Exonuclease | Surveillance | Proofreading | Mismatch repair | Replication | Diagnostic systems | Mutation | Children | Genetic recombination | Repair | DNA-directed DNA polymerase | Deoxyribonucleic acid--DNA | Cancer
Journal Article
by Wang, Zhaoming and Zhu, Bin and Zhang, Mingfeng and Parikh, Hemang and Jia, Jinping and Chung, Charles C and Sampson, Joshua N and Hoskins, Jason W and Hutchinson, Amy and Burdette, Laurie and Ibrahim, Abdisamad and Hautman, Christopher and Raj, Preethi S and Abnet, Christian C and Adjei, Andrew A and Ahlbom, Anders and Albanes, Demetrius and Allen, Naomi E and Ambrosone, Christine B and Aldrich, Melinda and Amiano, Pilar and Amos, Christopher and Andersson, Ulrika and Gerald Andriole, G.A and Andrulis, Irene L and Arici, Cecilia and Arslan, Alan A and Austin, Melissa A and Baris, Dalsu and Barkauskas, Donald A and Bassig, Bryan A and Freeman, Laura E. Beane and Berg, Christine D and Berndt, Sonja I and Bertazzi, Pier Alberto and Biritwum, Richard B and Black, Amanda and Blot, William and Boeing, Heiner and Boffetta, Paolo and Bolton, Kelly and Boutron-Ruault, Marie-Christine and Bracci, Paige M and Brennan, Paul and Brinton, Louise A and Brotzman, Michelle and Bueno-de-Mesquita, H. Bas and Buring, Julie E and Butler, Mary Ann and Cai, Qiuyin and Cancel-Tassin, Geraldine and Canzian, Federico and Cao, Guangwen and Caporaso, Neil E and Carrato, Alfredo and Carreon, Tania and Carta, Angela and Chang, Gee-Chen and Chang, I-Shou and Chang-Claude, Jenny and Che, Xu and Chen, Chien-Jen and Chen, Chih-Yi and Chen, Chung-Hsing and Chen, Constance and Chen, Kuan-Yu and Chen, Yuh-Min and Chokkalingam, Anand P and Chu, Lisa W and Clavel-Chapelon, Francoise and Colditz, Graham A and Colt, Joanne S and Conti, David and Cook, Michael B and Cortessis, Victoria K and Crawford, E. David and Cussenot, Olivier and Davis, Faith G and De Vivo, Immaculata and Deng, Xiang and Ding, Ti and Dinney, Colin P and Di Stefano, Anna Luisa and Diver, W. Ryan and Duell, Eric J and Elena, Joanne W and Fan, Jin-Hu and Feigelson, Heather Spencer and Feychting, Maria and Figueroa, Jonine D and Flanagan, Adrienne M and Fraumeni, Joseph F and Freedman, Neal D and Fridley, Brooke L and Fuchs, Charles S and Gago-Dominguez, Manuela and Gallinger, Steven and Gao, Yu-Tang and Gapstur, Susan M and Garcia-Closas, Montserrat and ... and Medicinska fakulteten and Institutionen för strålningsvetenskaper and Umeå universitet and Institutionen för folkhälsa och klinisk medicin and Urologi och andrologi and Enheten för biobanksforskning and Kirurgi and Näringsforskning and Institutionen för kirurgisk och perioperativ vetenskap and Onkologi
Human Molecular Genetics, ISSN 0964-6906, 11/2014, Volume 23, Issue 24, pp. 6616 - 6633
Journal Article