Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Eric A. Hungate"'
Autor:
Eric A. Hungate, Sapana R. Vora, Eric R. Gamazon, Takaya Moriyama, Timothy Best, Imge Hulur, Younghee Lee, Tiffany-Jane Evans, Eva Ellinghaus, Martin Stanulla, Jéremie Rudant, Laurent Orsi, Jacqueline Clavel, Elizabeth Milne, Rodney J. Scott, Ching-Hon Pui, Nancy J. Cox, Mignon L. Loh, Jun J. Yang, Andrew D. Skol, Kenan Onel
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
A risk variant located at 9p21.3 is associated with cancer risk in pediatric B-cell precursor acute lymphoblastic leukaemia. Here, the authors show that this variant affects the gene expression of the tumour suppressor gene Cdkn2b.
Externí odkaz:
https://doaj.org/article/3b8c31642c1f4f19aeefef51e4219d06
Autor:
Andrew J. Shih, Tomi Jun, Andrew D. Skol, Riyue Bao, Lei Huang, Sapana Vora, Megan E. McNerney, Eric A. Hungate, Michelle M. Le Beau, Richard A. Larson, Aaron Elliott, Hsiao‐Mei Lu, Robert Huether, Felicia Hernandez, Friedrich Stölzel, James M. Allan, Kenan Onel
Publikováno v:
British journal of haematologyReferences.
Some patients with therapy-related myeloid neoplasms (t-MN) may have unsuspected inherited cancer predisposition syndrome (CPS). We propose a set of clinical criteria to identify t-MN patients with high risk of CPS (HR-CPS). Among 225 t-MN patients w
Autor:
Anne M. Dickinson, Gail Jones, David C. Linch, Clare Lendrem, David Grimwade, Richard A. Larson, Andrew D. Skol, Yaobo Xu, Adam Ivey, Wei-Yu Lin, Manja Meggendorfer, Rosemary E. Gale, Inés Gómez-Seguí, Giovani Marconi, Jean Norden, Jude Fitzgibbon, Mette K. Andersen, M Bornhäuser, Sarah E. Fordham, Amanda F. Gilkes, Heinz Sill, Eric A. Hungate, José Cervera, Friedrich Stölzel, Julia Gaal-Wesinger, Kim Piechocki, Wendy Stock, Theresa Hahn, Konstantin Strauch, David Allsup, Kenan Onel, Claire Elstob, Alyssa I. Clay-Gilmour, Nicola J. Sunter, Jelena D. Milosevic Feenstra, Meyling Cheok, Abrar Alharbi, Ann K. Daly, Sally Jeffries, Lisa Wagenführ, Olaf Heidenreich, Robert Kralovics, Alan K. Burnett, Giovanni Martinelli, Desiree Kunadt, Christian Gieger, Francesco Lo-Coco, Leo Ruhnke, Maria Teresa Voso, Junke Wang, Catherine Park, Nigel H. Russell, Chimène Moreilhon, Robert Kerrin Hills, Claude Preudhomme, Graham Jackson, Daniel Nowak, Maria Chiara Fontana, James M. Allan, Heidi Altmann, Richard S. Houlston, Anne S. Quante, Michelle M. Le Beau, Thahira Rahman, Christoph Röllig, Rebecca Darlay, Sophie Raynaud, Helen Marr, Csaba Bödör, Louise Palm, Thomas Cluzeau, Szilvia Krizsán, Heather J. Cordell, Mathew Collin, Torsten Haferlach, Lara E. Sucheston-Campbell, Wolf-Karsten Hofmann, Kimmo Porkka, Andras Masszi, Hervé Dombret, Miguel A. Sanz, Elisabeth Douglas, Tobias Menne
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Nat. Commun. 12:6233 (2021)
Nature Communications
Nat. Commun. 12:6233 (2021)
Nature Communications
Acute myeloid leukemia (AML) is a hematological malignancy with an undefined heritable risk. Here we perform a meta-analysis of three genome-wide association studies, with replication in a fourth study, incorporating a total of 4018 AML cases and 104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66da5a2f677e98ca34ff7ab5930a5dd3
http://hdl.handle.net/10138/337099
http://hdl.handle.net/10138/337099
Autor:
Michelle M. Le Beau, Thahira Rahman, Yaobo Xu, Wendy Stock, Andrew D. Skol, Abrar Alharbi, David Allsup, Claire Elstob, Lara E. Sucheston-Campbell, Lisa Wagenführ, Olaf Heidenreich, Claude Preudhomme, Tobias Menne, Szilvia Krizsán, Rebecca Darlay, Jelena D. Milosevic Feenstra, David C. Linch, Sophie Raynaud, Helen Marr, Christian Gieger, Francesco Lo-Coco, David Grimwade, Maria Teresa Voso, Junke Wang, Christoph Röllig, Clare Lendrem, Wolf-Karsten Hofmann, Mathew Collin, Manja Meggendorfer, Friedrich Stölzel, Wei-Yu Lin, Ann K. Daly, Theresa Hahn, Torsten Haferlach, Sally Jeffries, Julia Gaal-Wesinger, Konstantin Strauch, Giovani Marconi, Amanda F. Gilkes, Chimène Moreilhon, Giovanni Martinelli, Anne M. Dickinson, Robert Kerrin Hills, Alan K. Burnett, Mette K. Andersen, Leo Ruhnke, Kimmo Porkka, Catherine Park, Desiree Kunadt, Nigel H. Russell, M Bornhäuser, Alyssa I. Clay-Gilmour, Hervé Dombret, Sarah E. Fordham, Eric A. Hungate, Miguel A. Sanz, Inés Gómez-Seguí, Csaba Bödör, Jean Norden, Elisabeth Douglas, Rosemary E. Gale, Heinz Sill, Kim Piechocki, Richard A. Larson, Robert Kralovics, Meyling Cheok, Heidi Altmann, Richard S. Houlston, Andras Masszi, Anne S. Quante, Louise Palm, Thomas Cluzeau, Heather J. Cordell, Nicola J. Sunter, Graham Jackson, Daniel Nowak, Maria Chiara Fontana, James M. Allan, José Cervera, Kenan Onel, Gail Jones, Adam Ivey, Jude Fitzgibbon
Acute myeloid leukemia (AML) is a hematological malignancy with an undefined heritable risk. Here we performed a meta-analysis of three genome-wide association studies, with replication in a fourth study, incorporating a total of 4018 AML cases and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88c65e332ff115796663c5aed53834aa
https://doi.org/10.1101/2021.07.22.21259893
https://doi.org/10.1101/2021.07.22.21259893
Autor:
Mark A. Applebaum, Sharon J. Diskin, Wendy B. London, Eric A. Hungate, Julie R. Park, Arlene Naranjo, Navin Pinto, Samuel L. Volchenboum, Susan L. Cohn, Barbara E. Stranger, Barbara Hero, Andrew D.J. Pearson, Zalman Vaksman, Tara O. Henderson, Sang Mee Lee
Publikováno v:
European Journal of Cancer. 72:177-185
Background: The incidence of second malignant neoplasm (SMN) within the first ten years of diagnosis in high-risk neuroblastoma patients treated with modern, intensive therapy is unknown. Further, the underlying germline genetics that contribute to S
Autor:
Stephen R. Spellman, Ezgi Karaesmen, David Ellinghaus, Lara E. Sucheston-Campbell, Marcelo C. Pasquini, Alyssa I. Clay-Gilmour, David Tritchler, Anne Marie W. Block, Eric A. Hungate, Sheila N.J. Sait, Christopher A. Haiman, Qian Liu, Eva Ellinghaus, Loreall Pooler, Sebastiano Battaglia, Jacqueline Clavel, Theresa Hahn, Laurent Orsi, Qiang Hu, Daniel J. Weisdorf, Philip L. McCarthy, Xiaochun Zhu, Andrew D. Skol, Martin Stanulla, Daniel O. Stram, Kenan Onel, Leah Preus, Abbas Rizvi, Qianqian Zhu, Song Liu, Xin Sheng, Li Yan, Christine B. Ambrosone
Publikováno v:
Blood advances. 1(20)
The incidence and mortality rates of B-cell acute lymphoblastic leukemia (B-ALL) differ by age and sex. To determine if inherited genetic susceptibility contributes to these differences we performed 2 genome-wide association studies (GWAS) by age, se
Publikováno v:
American Society of Clinical Oncology Educational Book. :e57-e67
As the population of cancer survivors has increased and continues to age, the occurrence of second cancers has risen dramatically—from 9% of all cancer diagnoses in 1975–1979 to 19% in 2005–2009. The Childhood Cancer Survivor Study, a cohort of
Autor:
Susan L. Cohn, Barbara E. Stranger, Lee D. McDaniel, Eric A. Hungate, Sharon J. Diskin, Andrew D. Skol, John M. Maris, Maura Diamond, Mark A. Applebaum, Zalman Vaksman, Samuel L. Volchenboum, Kenan Onel
Publikováno v:
Journal of the National Cancer Institute. 109(10)
To investigate genetic predispositions for MYCN-amplified neuroblastoma, we performed a meta-analysis of three genome-wide association studies totaling 615 MYCN-amplified high-risk neuroblastoma cases and 1869 MYCN-nonamplified non-high-risk neurobla
Autor:
Imge Hulur, Laurent Orsi, Eric R. Gamazon, Jérémie Rudant, Mignon L. Loh, Eva Ellinghaus, Eric A. Hungate, Ching-Hon Pui, Martin Stanulla, Andrew D. Skol, Timothy Best, Sapana Vora, Takaya Moriyama, Elizabeth Milne, Younghee Lee, Tiffany-Jane Evans, Jacqueline Clavel, Rodney J. Scott, Nancy J. Cox, Kenan Onel, Jun J. Yang
Publikováno v:
Nature communications, vol 7, iss 1
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
Nature Communications
Nature communications, 7. Nature Publishing Group
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
Nature Communications
Nature communications, 7. Nature Publishing Group
Paediatric B-cell precursor acute lymphoblastic leukaemia (BCP-ALL) is the most common cancer of childhood, yet little is known about BCP-ALL predisposition. In this study, in 2,187 cases of European ancestry and 5,543 controls, we discover and repli
Autor:
Yong Tao, Wenming Zhao, Lingtong Hao, Richard R. Hudson, Qiang Gong, Pei Lin, Chung-I Wu, Ke Chen, Wen-Hsiung Li, Z.F. Yang, Fang Yang, Zheng Hu, Qingjian Chen, Lihua Cao, Dafei Wu, Chunyi Hao, Daniel V.T. Catenacci, Yawei Li, Xiuyun Tian, Lili Dong, Xuemei Lu, Shaoping Ling, Eric A. Hungate, Wenjie Li
The prevailing view that the evolution of cells in a tumor is driven by Darwinian selection has never been rigorously tested. Because selection greatly affects the level of intratumor genetic diversity, it is important to assess whether intratumor ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d91c7b68931c018ffe93a0b17daa7c9
https://europepmc.org/articles/PMC4664355/
https://europepmc.org/articles/PMC4664355/