David Malkin
Active 1990–2025
- 161
- Papers
- 30,579
- Citations
- 89
- h-index
- 152
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Medicine55.5%
- Biochemistry, Genetics and Molecular Biology40%
- Immunology and Microbiology1.1%
- Agricultural and Biological Sciences0.8%
- Neuroscience0.8%
- Computer Science0.5%
- Other1.3%
Topics
- Glioma Diagnosis and Treatment7.2%
- Cancer Genomics and Diagnostics5.7%
- Epigenetics and DNA Methylation4.5%
- Cancer-related Molecular Pathways4.4%
- Genetic factors in colorectal cancer2.5%
- Neuroblastoma Research and Treatments2.4%
- Other73.3%
Coauthors
- Adam Shlien21
- Uri Tabori21
- Éric Bouffet20
- Jonathan D. Wasserman17
- Vijay Ramaswamy17
- Anita Villani16
- Cynthia Hawkins16
- Michael D. Taylor14
- Joshua D. Schiffman12
- A. Sorana Morrissy11
- Ana Novokmet11
- Bailey Gallinger11
- David Jones11
- Christian P. Kratz10
- Marc Remke10
- Marcel Kool10
- Paul A. Northcott10
- Stefan M. Pfister10
- Harriet Druker9
- Ledia Brunga9
- Maria Isabel Achatz9
- Melyssa Aronson9
- David Shih8
- Melissa Edwards8
All papers
- Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Authors: Jeremy Schwartzentruber, Andrey Korshunov, Xiao-Yang Liu, David Jones, Elke Pfaff, Karine Jacob, Dominik Sturm, Adam M. Fontebasso, Dong-Anh Khuong Quang, Martje Tönjes, Volker Hovestadt, Steffen Albrecht, Marcel Kool, André Nantel, Carolin Konermann, Anders M. Lindroth, Natalie Jäger, Tobias Rausch, Marina Ryzhova, Jan O. Korbel, Thomas Hielscher, Péter Hauser, Miklós Garami, Álmos Klekner, László Bognár, Martin Ebinger, Martin U. Schuhmann, Wolfram Scheurlen, Arnulf Pekrun, Michael C. Frühwald, Wolfgang Roggendorf, Christoph Kramm, Matthias Dürken, Jeffrey Atkinson, Pierre Lepage, Alexandre Montpetit, Magdalena Zakrzewska, Krzysztof Zakrzewski, Paweł P. Liberski, Zhifeng Dong, Peter M. Siegel, Andreas E. Kulozik, Marc Zapatka, Abhijit Guha, David Malkin, Jörg Felsberg, Guido Reifenberger, Andreas von Deimling, Koichi Ichimura, V. Peter Collins, Hendrik Witt, Till Milde, Olaf Witt, Cindy Zhang, Pedro Castelo‐Branco, Peter Lichter, Damien Faury, Uri Tabori, Christoph Plass, Jacek Majewski, Stefan M. Pfister, Nada Jabado - Nature 2012 cited by 2,711
- Signatures of copy number alterations in human cancer
Authors: Christopher D. Steele, Ammal Abbasi, S. M. Ashiqul Islam, Amy L. Bowes, Azhar Khandekar, Kerstin Haase, Shadi Hames-Fathi, Dolapo Ajayi, Annelien Verfaillie, Pawan Dhami, Alex P. McLatchie, Matt Lechner, Nicholas Light, Adam Shlien, David Malkin, Andrew Feber, Paula Proszek, Tom Lesluyes, Fredrik Mertens, Adrienne M. Flanagan, Maxime Tarabichi, Peter Van Loo, Ludmil B. Alexandrov, Nischalan Pillay - Nature 2022 cited by 516
- Medulloblastoma
Authors: Paul A. Northcott, Giles Robinson, Christian P. Kratz, Donald Mabbott, Scott L. Pomeroy, Steven C. Clifford, Stefan Rutkowski, David W. Ellison, David Malkin, Michael D. Taylor, Amar Gajjar, Stefan M. Pfister - Nature Reviews Disease Primers 2019 cited by 659
- Comprehensive Analysis of Hypermutation in Human Cancer
Authors: Brittany Campbell, Nicholas Light, David Fabrizio, Matthew Zatzman, Fabio Fuligni, Richard de Borja, Scott Davidson, Melissa Edwards, Julia A. Elvin, Karl P. Hodel, Walter J. Zahurancik, Zucai Suo, Tatiana Lipman, Katharina Wimmer, Christian P. Kratz, Daniel C. Bowers, Theodore W. Laetsch, Gavin P. Dunn, Tanner M. Johanns, Matthew Grimmer, Ivan Smirnov, Valérie Larouche, David Samuel, Annika Bronsema, Michael Osborn, Duncan Stearns, Pichai Raman, Kristina A. Cole, Phillip B. Storm, Michal Yalon, Enrico Opocher, Gary Mason, Gregory A. Thomas, Magnus Sabel, Ben George, David S. Ziegler, Scott Lindhorst, Vanan Magimairajan Issai, Shlomi Constantini, Helen Toledano, Ronit Elhasid, Roula Farah, Rina Dvir, Peter B. Dirks, Annie Huang, Melissa A. Galati, Jiil Chung, Vijay Ramaswamy, Meredith S. Irwin, Melyssa Aronson, Carol Durno, Michael D. Taylor, Gideon Rechavi, John M. Maris, Éric Bouffet, Cynthia Hawkins, J Costello, M. Stephen Meyn, Zachary F. Pursell, David Malkin, Uri Tabori, Adam Shlien - Cell 2017 cited by 812
- Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair Deficiency
Authors: Éric Bouffet, Valérie Larouche, Brittany Campbell, Daniele Merico, Richard de Borja, Melyssa Aronson, Carol Durno, Joerg Krueger, Vanja Cabric, Vijay Ramaswamy, Nataliya Zhukova, Gary Mason, Roula Farah, Samina Afzal, Michal Yalon, Gideon Rechavi, Vanan Magimairajan, Michael F. Walsh, Shlomi Constantini, Rina Dvir, Ronit Elhasid, Alyssa Reddy, Michael Osborn, Michael Sullivan, Jordan R. Hansford, Andrew Dodgshun, Nancy Klauber‐DeMore, Lindsay L. Peterson, Sunil J. Patel, Scott Lindhorst, Jeffrey Atkinson, Zane Cohen, Rachel Laframboise, Peter B. Dirks, Michael D. Taylor, David Malkin, Steffen Albrecht, Roy Dudley, Nada Jabado, Cynthia Hawkins, Adam Shlien, Uri Tabori - Journal of Clinical Oncology 2016 cited by 869
- Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer
Authors: Young Seok Ju, Ludmil B. Alexandrov, Moritz Gerstung, Sancha Martin, Serena Nik-Zainal, Manasa Ramakrishna, Helen Davies, Elli Papaemmanuil, Gunes Gundem, Adam Shlien, Niccolò Bolli, Sam Behjati, Patrick Tarpey, Jyoti Nangalia, Charles Massie, Adam P. Butler, Jon W. Teague, George S. Vassiliou, Anthony R. Green, Ming‐Qing Du, Ashwin Unnikrishnan, John E. Pimanda, Bin Tean Teh, Nikhil C. Munshi, Mel Greaves, Paresh Vyas, Adel K. El‐Naggar, Tom Santarius, V. Peter Collins, Richard G. Grundy, Jack A. Taylor, D Neil Hayes, David Malkin, ICGC Breast Cancer Group, ICGC Chronic Myeloid Disorders Group, ICGC Prostate Cancer Group, Christopher S. Foster, Anne Y. Warren, Hayley C. Whitaker, Daniel S. Brewer, Rosalind A. Eeles, Colin Cooper, David E. Neal, Tapio Visakorpi, William B. Isaacs, G. Steven Bova, Adrienne M. Flanagan, P. Andrew Futreal, Andy G. Lynch, Patrick F. Chinnery, Ultan McDermott, Michael R. Stratton, Peter J. Campbell - eLife 2014 cited by 500
- Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations
Authors: Tobias Rausch, David Jones, Marc Zapatka, Adrian M. Stütz, Thomas Zichner, Joachim Weischenfeldt, Natalie Jäger, Marc Remke, David Shih, Paul A. Northcott, Elke Pfaff, Jelena Tica, Qi Wang, Luca Massimi, Hendrik Witt, Sebastian Bender, Sabrina Pleier, Huriye Cin, Cynthia Hawkins, Christian Beck, Andreas von Deimling, Volkmar Hans, Benedikt Brors, Roland Eils, Wolfram Scheurlen, Jonathon Blake, Vladimı́r Beneš, Andreas E. Kulozik, Olaf Witt, Dianna C. Martin, Cindy Zhang, Rinnat M. Porat, Diana M. Merino, Jonathan D. Wasserman, Nada Jabado, Adam M. Fontebasso, Lars Bullinger, Frank G. Rücker, Konstanze Döhner, Hartmut Döhner, Jan Köster, Jan J. Molenaar, Rogier Versteeg, Marcel Kool, Uri Tabori, David Malkin, Andrey Korshunov, Michael D. Taylor, Peter Lichter, Stefan M. Pfister, Jan O. Korbel - Cell 2012 cited by 878
- Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study
Authors: Anita Villani, Ari Shore, Jonathan D. Wasserman, Derek Stephens, Raymond H. Kim, Harriet Druker, Bailey Gallinger, Anne Naumer, Wendy Kohlmann, Ana Novokmet, Uri Tabori, Marta Tijerin, Mary‐Louise C. Greer, Jonathan L. Finlay, Joshua D. Schiffman, David Malkin - The Lancet Oncology 2016 cited by 526
- Childhood cerebellar tumours mirror conserved fetal transcriptional programs
Authors: Maria Vladoiu, Ibrahim El-Hamamy, Laura Donovan, Hamza Farooq, Borja Holgado, Yogi Sundaravadanam, Vijay Ramaswamy, Liam D. Hendrikse, Sachin Kumar, Stephen C. Mack, John J. Y. Lee, Vernon Fong, Kyle Juraschka, David Przelicki, Antony Michealraj, Patryk Skowron, Betty Luu, Hiromichi Suzuki, A. Sorana Morrissy, Florence M.G. Cavalli, Livia Garzia, Craig Daniels, Xiaochong Wu, Maleeha Qazi, Sheila K. Singh, Jennifer A. Chan, Marco A. Marra, David Malkin, Peter B. Dirks, Lawrence E. Heisler, Trevor J. Pugh, Karen Ng, Faiyaz Notta, Eric M. Thompson, Claudia L. Kleinman, Alexandra L. Joyner, Nada Jabado, Lincoln Stein, Michael D. Taylor - Nature 2019 cited by 448
- Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms
Authors: David Malkin, Frederick P. Li, Louise C. Strong, Joseph F. Fraumeni, Camille E. Nelson, David H. Kim, J Kassel, Magdalena A. Gryka, Farideh Z. Bischoff, Michael A. Tainsky, Stephen Friend - Science 1990 cited by 3,786
- Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome
Authors: Christian P. Kratz, Maria Isabel Achatz, Laurence Brugières, Thierry Frébourg, Judy E. Garber, Mary‐Louise C. Greer, Jordan R. Hansford, Katherine A. Janeway, Wendy Kohlmann, Rose B. McGee, Charles G. Mullighan, Kenan Onel, Kristian W. Pajtler, Stefan M. Pfister, Sharon A. Savage, Joshua D. Schiffman, Katherine A. Schneider, Louise C. Strong, D. Gareth Evans, Jonathan D. Wasserman, Anita Villani, David Malkin - Clinical Cancer Research 2017 cited by 521
- Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency
Authors: Anirban Das, Sumedha Sudhaman, Daniel A. Morgenstern, Ailish Coblentz, Jiil Chung, Simone C. Stone, Noor Alsafwani, Zhihui Amy Liu, Ola Abu Al Karsaneh, Shirin Soleimani, Hagay Ladany, David Chen, Matthew Zatzman, Vanja Cabric, Liana Nobre, Vanessa Bianchi, Melissa Edwards, Sambira Nahum Lauren C, Ayse B. Ercan, Arash Nabbi, Shlomi Constantini, Rina Dvir, Michal Yalon-Oren, Gadi Abebe‐Campino, Shani Caspi, Valérie Larouche, Alyssa Reddy, Michael Osborn, Gary Mason, Scott Lindhorst, Annika Bronsema, Vanan Magimairajan, Enrico Opocher, Rebecca Loret De Mola, Magnus Sabel, Charlotta A. Frojd, David Sumerauer, David Samuel, Kristina A. Cole, Stefano Chiaravalli, Maura Massimino, Patrick Tomboc, David S. Ziegler, Ben George, An Van Damme, Nobuko Hijiya, David Gass, Rose B. McGee, Oz Mordechai, Daniel C. Bowers, Theodore W. Laetsch, Alexander Lossos, Deborah T. Blumenthal, Tomasz Sarosiek, Lee Yi Yen, Jeffrey Knipstein, Anne Bendel, Lindsey M. Hoffman, Sandra Luna‐Fineman, Stefanie Zimmermann, Isabelle Scheers, Kim E. Nichols, Michal Zápotocký, Jordan R. Hansford, John M. Maris, Peter B. Dirks, Michael D. Taylor, Abhaya V. Kulkarni, Manohar Shroff, Derek S. Tsang, Anita Villani, Wei Xu, Melyssa Aronson, Carol Durno, Adam Shlien, David Malkin, Gad Getz, Yosef E. Maruvka, Pamela S. Ohashi, Cynthia Hawkins, Trevor J. Pugh, Éric Bouffet, Uri Tabori - Nature Medicine 2022 cited by 144
- The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations
Authors: Anita Villani, Scott Davidson, Nisha Kanwar, Winnie Lo, Yisu Li, Sarah Cohen‐Gogo, Fabio Fuligni, Lisa-Monique Edward, Nicholas Light, Mehdi Layeghifard, Ricardo Harripaul, Larissa Waldman, Bailey Gallinger, Federico Comitani, Ledia Brunga, Reid Hayes, Nathaniel D. Anderson, Arun Ramani, Kyoko E. Yuki, Sasha Blay, Brittney Johnstone, Cara Inglese, Rawan Hammad, Catherine Goudie, Andrew Y. Shuen, Jonathan D. Wasserman, Rosemarie E. Venier, Marianne Eliou, Miranda Lorenti, Carol Ann Ryan, Michael Braga, Meagan Gloven-Brown, Jianan Han, Maria Montero, Famida Spatare, James A. Whitlock, Stephen W. Scherer, Kathy Chun, Martin J. Somerville, Cynthia Hawkins, Mohamed Abdelhaleem, Vijay Ramaswamy, Gino R. Somers, Lianna Kyriakopoulou, Johann Hitzler, Mary Shago, Daniel A. Morgenstern, Uri Tabori, M. Stephen Meyn, Meredith S. Irwin, David Malkin, Adam Shlien - Nature Cancer 2022 cited by 127
- The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute
Authors: Kelvin C. de Andrade, Elaine E. Lee, Elise M. Tookmanian, Chimene Kesserwan, James J. Manfredi, Jessica N. Hatton, Jennifer K. Loukissas, Jiří Zavadil, Lei Zhou, Magali Olivier, Megan N. Frone, Owais Shahzada, William J.R. Longabaugh, Christian P. Kratz, David Malkin, Pierre Hainaut, Sharon A. Savage - Cell Death and Differentiation 2022 cited by 165
- Analysis of the Li-Fraumeni Spectrum Based on an International Germline TP53 Variant Data Set
Authors: Christian P. Kratz, Claire Freyçon, Kara N. Maxwell, Kim E. Nichols, Joshua D. Schiffman, D. Gareth Evans, Maria Isabel Achatz, Sharon A. Savage, Jeffrey N. Weitzel, Judy E. Garber, Pierre Hainaut, David Malkin - JAMA Oncology 2021 cited by 146
- Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
Authors: Adam Shlien, Brittany Campbell, Richard de Borja, Ludmil B. Alexandrov, Daniele Merico, David C. Wedge, Peter Van Loo, Patrick Tarpey, Paul Coupland, Sam Behjati, Aaron Pollett, Tatiana Lipman, Abolfazl Heidari, Shriya Deshmukh, N. Avitzur, Bettina Meier, Moritz Gerstung, Ye Hong, Diana M. Merino, Manasa Ramakrishna, Marc Remke, Roland Arnold, Gagan B. Panigrahi, Neha Thakkar, Karl P. Hodel, Erin E. Henninger, A. Yasemin Göksenin, Doua Bakry, George S. Charames, Harriet Druker, Jordan Lerner‐Ellis, Matthew Mistry, Rina Dvir, Ronald Grant, Ronit Elhasid, Roula Farah, Glenn Taylor, Paul C. Nathan, Sarah Alexander, Shay Ben‐Shachar, Simon C. Ling, Steven Gallinger, Shlomi Constantini, Peter B. Dirks, Annie Huang, Stephen W. Scherer, Richard G. Grundy, Carol Durno, Melyssa Aronson, Anton Gartner, M. Stephen Meyn, Michael D. Taylor, Zachary F. Pursell, Christopher E. Pearson, David Malkin, P. Andrew Futreal, Michael R. Stratton, Éric Bouffet, Cynthia Hawkins, Peter J. Campbell, Uri Tabori - Nature Genetics 2015 cited by 381
- Copy number variations and cancer
Authors: Adam Shlien, David Malkin - Genome Medicine 2009 cited by 403
- Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
Authors: Sebastian M. Waszak, Paul A. Northcott, Ivo Buchhalter, Giles Robinson, Christian Sutter, Susanne N. Groebner, Kerstin Grund, Laurence Brugières, David Jones, Kristian W. Pajtler, A. Sorana Morrissy, Marcel Kool, Dominik Sturm, Lukas Chávez, Aurélie Ernst, Sebastian Brabetz, M. Hain, Thomas Zichner, Maia Segura‐Wang, Joachim Weischenfeldt, Tobias Rausch, Balca R. Mardin, Xin Zhou, Cristina Baciu, Christian Lawerenz, Jennifer A. Chan, Pascale Varlet, Léa Guerrini‐Rousseau, Daniel W. Fults, Wiesława Grajkowska, Péter Hauser, Nada Jabado, Young‐Shin Ra, Karel Zitterbart, Suyash Shringarpure, Francisco M. De La Vega, Carlos D. Bustamante, Ho‐Keung Ng, Arie Perry, Tobey J. MacDonald, Pablo Hernáiz Driever, Anne Bendel, Daniel C. Bowers, Geoffrey McCowage, Murali Chintagumpala, Richard J. Cohn, Tim Hassall, Gudrun Fleischhack, Tone Eggen, Finn Wesenberg, Maria Feychting, Birgitta Lannering, Joachim Schüz, Christoffer Johansen, Tina Veje Andersen, Martin Röösli, Claudia E. Kuehni, Michael A. Grotzer, Kristina Kjærheim, Camelia Maria Monoranu, Tenley C. Archer, Elizabeth S. Duke, Scott L. Pomeroy, Shelagh Redmond, Stephan Frank, David Sumerauer, Wolfram Scheurlen, Marina Ryzhova, Till Milde, Christian P. Kratz, David Samuel, Jinghui Zhang, David A. Solomon, Marco A. Marra, Roland Eils, Claus R. Bartram, Katja von Hoff, Stefan Rutkowski, Vijay Ramaswamy, Richard J. Gilbertson, Andrey Korshunov, Michael D. Taylor, Peter Lichter, David Malkin, Amar Gajjar, Jan O. Korbel, Stefan M. Pfister - The Lancet Oncology 2018 cited by 394
- DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies
Authors: Kris Ann P. Schultz, Gretchen M. Williams, Junne Kamihara, Douglas R. Stewart, Anne K. Harris, Andrew J. Bauer, Joyce Turner, Rachana Shah, Katherine A. Schneider, Kami Wolfe Schneider, Ann G. Carr, Laura A. Harney, Shari Baldinger, A. Lindsay Frazier, Daniel Orbach, Dominik T. Schneider, David Malkin, Louis P. Dehner, Yoav H. Messinger, D. Ashley Hill - Clinical Cancer Research 2018 cited by 373
- Combined Immunotherapy Improves Outcome for Replication-Repair-Deficient (RRD) High-Grade Glioma Failing Anti–PD-1 Monotherapy: A Report from the International RRD Consortium
Authors: Anirban Das, Nicholas R. Fernandez, Adrian Levine, Vanessa Bianchi, Lucie Stengs, Jiil Chung, Logine Negm, Jose Rafael Dimayacyac, Yuan Chang, Liana Nobre, Ayse B. Ercan, Santiago Sánchez‐Ramírez, Sumedha Sudhaman, Melissa Edwards, Valérie Larouche, David Samuel, An Van Damme, David Gass, David S. Ziegler, Stefan Bielack, Carl Koschmann, Shayna Zelcer, Michal Yalon-Oren, Gadi Abede Campino, Tomasz Sarosiek, Kim E. Nichols, Rebecca Loret De Mola, Kevin Bielamowicz, Magnus Sabel, Charlotta A. Frojd, Matthew D. Wood, Jason Glover, Yi‐Yen Lee, Magimairajan Vanan, Jenny Adamski, Sébastien Perreault, Omar Chamdine, Magnus Aasved Hjort, Michal Zápotocký, Fernando Carceller, Erin Wright, Ivana Fedoráková, Alexander Lossos, Ryuma Tanaka, Michael Osborn, Deborah T. Blumenthal, Melyssa Aronson, Ute Bartels, Annie Huang, Vijay Ramaswamy, David Malkin, Adam Shlien, Anita Villani, Peter B. Dirks, Trevor J. Pugh, Gad Getz, Yosef E. Maruvka, Derek S. Tsang, Birgit Ertl‐Wagner, Cynthia Hawkins, Éric Bouffet, Daniel A. Morgenstern, Uri Tabori - Cancer Discovery 2023 cited by 46
- InheritedTP53Mutations and the Li–Fraumeni Syndrome
Authors: Tanya Guha, David Malkin - Cold Spring Harbor Perspectives in Medicine 2017 cited by 254
- Early Cancer Detection in Li–Fraumeni Syndrome with Cell-Free DNA
Authors: Derek Wong, Ping Luo, Leslie E. Oldfield, Haifan Gong, Ledia Brunga, Ron Rabinowicz, Vallijah Subasri, Clarissa Chan, Tiana Downs, Kirsten M. Farncombe, Beatrice Luu, Maia Norman, Julia A. Sobotka, Precious Uju, Jenna Eagles, Stephanie Pedersen, Johanna Wellum, Arnavaz Danesh, Stephenie D. Prokopec, Eric Y. Stutheit-Zhao, Nadia Znassi, Lawrence E. Heisler, Richard Jovelin, Bernard Lam, Beatriz E. Lujan Toro, Kayla Marsh, Yogi Sundaravadanam, Dax Torti, Carina Man, Anna Goldenberg, Wei Xu, Patrick Veit‐Haibach, Andréa S. Doria, David Malkin, Raymond H. Kim, Trevor J. Pugh - Cancer Discovery 2023 cited by 56
- DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells
Authors: Jiil Chung, Yosef E. Maruvka, Sumedha Sudhaman, Jacalyn Kelly, Nicholas J. Haradhvala, Vanessa Bianchi, Melissa Edwards, Victoria J. Forster, Nuno M. Nunes, Melissa A. Galati, Martin Komosa, Shriya Deshmukh, Vanja Cabric, Scott Davidson, Matthew Zatzman, Nicholas Light, Reid Hayes, Ledia Brunga, Nathaniel D. Anderson, Ben Ho, Karl P. Hodel, Robert Siddaway, A. Sorana Morrissy, Daniel C. Bowers, Valérie Larouche, Annika Bronsema, Michael Osborn, Kristina A. Cole, Enrico Opocher, Gary Mason, Gregory A. Thomas, Ben George, David S. Ziegler, Scott Lindhorst, Magimairajan Vanan, Michal Yalon-Oren, Alyssa Reddy, Maura Massimino, Patrick Tomboc, An Van Damme, Alexander Lossos, Carol Durno, Melyssa Aronson, Daniel A. Morgenstern, Éric Bouffet, Annie Huang, Michael D. Taylor, Anita Villani, David Malkin, Cynthia Hawkins, Zachary F. Pursell, Adam Shlien, Thomas A. Kunkel, Gad Getz, Uri Tabori - Cancer Discovery 2020 cited by 86
- Quiescent Sox2+ Cells Drive Hierarchical Growth and Relapse in Sonic Hedgehog Subgroup Medulloblastoma
Authors: Robert J. Vanner, Marc Remke, Marco Gallo, Hayden Selvadurai, Fiona J. Coutinho, Lilian Lee, Michelle Kushida, Renee Head, A. Sorana Morrissy, Xueming Zhu, Tzvi Aviv, Véronique Voisin, Ian D. Clarke, Yisu Li, Andrew J. Mungall, Richard A. Moore, Yussanne Ma, Steven J.M. Jones, Marco A. Marra, David Malkin, Paul A. Northcott, Marcel Kool, Stefan M. Pfister, Gary D. Bader, Konrad Hochedlinger, Andrey Korshunov, Michael D. Taylor, Peter B. Dirks - Cancer Cell 2014 cited by 310
