Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Barbara K. Fortini"'
Autor:
Fei Fei, Caitlin Caporale, Lisa Chang, Barbara K. Fortini, Haris Ali, Diana Bell, Anthony Stein, Guido Marcucci, Milhan Telatar, Michelle Afkhami
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 10, p 5183 (2024)
BRAF mutations are rare in myeloid neoplasms and are reported to be associated with poor treatment outcomes. The purpose of our study is to characterize BRAF mutations in myeloid neoplasms using a next-generation sequencing (NGS) panel based on the e
Externí odkaz:
https://doaj.org/article/d07f281057a848bebdb3fa543565c347
Autor:
Katja Butterbach, Julyann Pérez-Mayoral, Douglas F. Easton, Stefanie Brezina, Ben Zhang, Frank J. Manion, Hansong Wang, Sanford D. Markowitz, Liesel M. FitzGerald, Sun Ha Jee, Michelle Cotterchio, Daniel D. Buchanan, Timothy R. Church, Wolfgang Lieb, Xiao-Ou Shu, John L. Hopper, Stephanie A. Bien, Manuela Gago-Dominguez, Jian Gong, Laurence N. Kolonel, Graham G. Giles, Leon Raskin, Yingchang Lu, Kristen Anton, Charles S. Fuchs, Fränzel J.B. van Duijnhoven, Hermann Brenner, Yi Lin, Clicerio Gonzalez-Villalpando, Yong-Bing Xiang, Aaron K. Aragaki, Daniela Seminara, Stephanie M. Gogarten, Gad Rennert, Jose E. Castelao, Rocky Fischer, Antonio J. Molina, Jarmo Virtamo, Tabitha A. Harrison, Volker Arndt, Lee Soo Chin, Michael Hoffmeister, Mark A. Jenkins, Shu Chen Huang, Chris S. Carlson, Stéphane Bézieau, Rebecca D. Jackson, Bhramar Mukherjee, Darin Taverna, Bridget M. Riggs, Christopher K. Edlund, Christopher A. Haiman, Melissa C. Southey, Anna H. Wu, Marilena Melas, Antonia Trichopoulou, Hedy S. Rennert, Gianluca Severi, Stephen B. Gruber, Noralane M. Lindor, Gerhard A. Coetzee, Richard B. Hayes, Sarah J. Plummer, Keitaro Matsuo, Mathieu Lemire, Philipp Hofer, Neil Murphy, José María Huerta, Paul D.P. Pharoah, Erin M. Siegel, Sébastien Küry, Thomas J. Hudson, Annika Lindblom, Marcia Cruz Correa, Michael O. Woods, Sophia Harlid, Tilman Kuehn, David Shibata, Christopher I. Li, Stephen N. Thibodeau, Stephen J. Chanock, Jochen Hampe, Flavio Lejbkowicz, Jeroen R. Huyghe, Suminori Kono, Jenny Chang-Claude, Aung Ko Win, Brent W. Zanke, Alicja Wolk, David V. Conti, Elena M. Gonzalez-Villalpando, Christopher I. Amos, Shuo Jiao, Domenico Palli, Vicente Martín, Jesus P. Paredes Cotoré, Stephanie J. Weinstein, Andrea Gsur, William M. Grady, Koichi Matsuda, Loic Le Marchand, Hanane Omichessan, Marc J. Gunter, Graham Casey, Li Li, Zsofia K. Stadler, Eric J. Jacobs, Kevin McDonnell, Dallas R. English, Demetrius Albanes, Amit Joshi, Wei Zheng, Mariana C. Stern, Cecelia A. Laurie, Jing Ma, Cornelia M. Ulrich, Stephanie L. Schmit, Victor Moreno, John D. Potter, Chenxu Qu, Bette J. Caan, Heinz-Josef Lenz, M. Henar Alonso, Andrea Z. LaCroix, Christoph Mancao, John F. Harju, Yun Ru Liu, Jane C. Figueiredo, Gregory Idos, Kana Wu, Duncan C. Thomas, Motoki Iwasaki, W. James Gauderman, Thomas A. Sellers, David Van Den Berg, Barbara K. Fortini, David N. Levine, James M. Church, Ya Wen Cheng, Edith J. M. Feskens, Edward Giovannucci, Manish Gala, Polly A. Newcomb, Charles Kooperberg, Iona Cheng, David J. Hunter, Martha L. Slattery, Roger L. Milne, Lars G. Fritsche, Niha Zubair, Steven Gallinger, Yi Xin Zeng, Wei Shi, Andrew T. Chan, Fotios Loupakis, Vittorio Krogh, Clemens Schafmayer, Sun-Seog Kweon, Bethany van Guelpan, Amanda Bloomer, Kenneth Offit, Stephanie Tring, Shoichiro Tsugane, David Duggan, Fredrick R. Schumacher, Joseph Vijai, Weihua Jia, Marie-Christine Boutron-Ruault, Joel K. Greenson, Frank Luh, Ulrike Peters, Keith R. Curtis, Juergen Boehm, Robert E. Schoen, Sonja I. Berndt, Elizabeth L. Barry, Sebastian Stintzing, Li Hsu, Emily White, Conghui Qu, Peter T. Campbell, Caroline McNeil, Yun Yen
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Journal of the National Cancer Institute 111 (2019) 2
Journal of the National Cancer Institute, 111(2), 146-157
Schmit, Stephanie L; Edlund, Christopher K; Schumacher, Fredrick R; Gong, Jian; Harrison, Tabitha A; Huyghe, Jeroen R; et al.(2018). Novel Common Genetic Susceptibility Loci for Colorectal Cancer.. Journal of the National Cancer Institute. doi: 10.1093/jnci/djy099. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3bk0g2vk
Universidad de Barcelona
Journal of the National Cancer Institute 111 (2019) 2
Journal of the National Cancer Institute, 111(2), 146-157
Schmit, Stephanie L; Edlund, Christopher K; Schumacher, Fredrick R; Gong, Jian; Harrison, Tabitha A; Huyghe, Jeroen R; et al.(2018). Novel Common Genetic Susceptibility Loci for Colorectal Cancer.. Journal of the National Cancer Institute. doi: 10.1093/jnci/djy099. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3bk0g2vk
Background Previous genome-wide association studies (GWAS) have identified 42 loci (P < 5 × 10−8) associated with risk of colorectal cancer (CRC). Expanded consortium efforts facilitating the discovery of additional susceptibility loci may capture
Autor:
Barbara K Fortini, Stephanie Tring, Sarah J Plummer, Christopher K Edlund, Victor Moreno, Robert S Bresalier, Elizabeth L Barry, Timothy R Church, Jane C Figueiredo, Graham Casey
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e111914 (2014)
Genome-wide association studies (GWAS) of colorectal cancer (CRC) have led to the identification of a number of common variants associated with modest risk. Several risk variants map within the vicinity of TGFβ/BMP signaling pathway genes, including
Externí odkaz:
https://doaj.org/article/ce11f040ecc74e86b4da84901f5e86f9
Autor:
Sarah J. Plummer, Matthew Devall, Mourad Wagdy Ali, Stephanie Tring, Graham Casey, Barbara K. Fortini
Publikováno v:
Human Mutation
Several genome wide association studies of colorectal cancer (CRC) have identified single nucleotide polymorphisms (SNPs) on chromosome 15q13.3 associated with CRC risk. To identify functional variant(s) underlying this association, we investigated S
Autor:
Rosario Rodríguez-Guillén, Christopher K. Edlund, Teresa Tusié-Luna, Ivette Cruz-Bautista, Barbara K. Fortini, Donají Gómez, Linda Liliana Muñoz-Hernandez, Alicia Huerta-Chagoya, Heinz-Josef Lenz, María Elena González-Villalpando, Fredrick R. Schumacher, Peggy Wan, María Luisa Ordóñez-Sánchez, Ulices Alvirde, Carlos A. Aguilar-Salinas, Stephanie L. Schmit, Graham Casey, Jane C. Figueiredo, Olimpia Arellano-Campos, Ugonna Ihenacho, David Van Den Berg, Christopher A. Haiman, David V. Conti, Loic Le Marchand, Hortensia Moreno-Macías, Clicerio González-Villalpando, Maribel Rodríguez-Torres
Publikováno v:
Carcinogenesis
Summary This manuscript describes the first large-scale genome-wide association study of colorectal cancer in Hispanics and Latinos. Our results demonstrate the broad replication of known susceptibility regions and the importance of fine-mapping in e
Autor:
Manish Gala, Stéphane Bézieau, Eric J. Jacobs, Kevin McDonnell, Amit Joshi, Leon Raskin, Shu Chen Huang, W. James Gauderman, Brian E. Henderson, Shoichiro Tsugane, Sonja I. Berndt, Marilena Melas, Jane C. Figueiredo, Christopher P. Fischer, Gregory Idos, Kana Wu, Hermann Brenner, Wei Zheng, Ulrike Peters, Stephen J. Chanock, N. M. Lindor, David J. Hunter, Martha L. Slattery, Charles Kooperberg, Cathy C. Laurie, Ben Zhang, Jing Ma, Cecelia A. Laurie, Rebecca D. Jackson, Gianluca Severi, Graham Casey, Katja Butterbach, David Van Den Berg, Frank J. Manion, Hansong Wang, Daniela Seminara, Christopher S. Carlson, Stephanie M. Gogarten, Karen W. Makar, Duncan C. Thomas, Stephen B. Gruber, David K. Levine, Barbara K. Fortini, Caroline McNeil, Flavio Lejbkowicz, Charles S. Fuchs, Motoki Iwasaki, Robert W. Haile, John D. Potter, Stephanie A. Rosse, Shuo Jiao, Keitaro Matsuo, Wei Hua Jia, Cornelia M. Ulrich, Stephanie L. Schmit, Victor Moreno, Bhramar Mukherjee, Darin Taverna, John L. Hopper, Sun Ha Jee, Dee W. West, Bette J. Caan, Andrea Z. LaCroix, Brent W. Zanke, Robert E. Schoen, Sébastien Küry, Keith R. Curtis, Loic Le Marchand, Aaron K. Aragaki, Steven Gallinger, Gad Rennert, Tabitha A. Harrison, Laurence N. Kolonel, Li Li, David V. Conti, John F. Harju, Polly A. Newcomb, David Duggan, Mathieu Lemire, Christopher K. Edlund, Thomas J. Hudson, Roger C. Green, Wei Shi, Li Hsu, Conghui Qu, Peter T. Campbell, Fredrick R. Schumacher, Mark A. Jenkins, Andrew T. Chan, Yong-Bing Xiang, Richard B. Hayes, Suminori Kono, Jenny Chang-Claude, Gerhard A. Coetzee, Carolyn M. Hutter, Hedy S. Rennert, Emily White, Graham G. Giles, Michael Hoffmeister, Xiao-Ou Shu, Edward Giovannucci
Publikováno v:
Nature Communications. 6
Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Autor:
Piotr Polaczek, Subhash Pokharel, Robert A. Bambara, Barbara K. Fortini, Lata Balakrishnan, Judith L. Campbell
Publikováno v:
Journal of Biological Chemistry. 286:23763-23770
Two processes, DNA replication and DNA damage repair, are key to maintaining genomic fidelity. The Dna2 enzyme lies at the heart of both of these processes, acting in conjunction with flap endonuclease 1 and replication protein A in DNA lagging stran
Autor:
Olivia M. S. Carmo, Julia L. Sun, Barbara K. Fortini, Audrey Chen, Rory D. Spence, Aleah R. Booker, Anastasia E. Ibrahim, Brian Dix, Vanessa N. Gill, Lauren Stanislaw, Jennifer C. Dallego, Helen A. Thomason, Aleena E. Young, Cat N. Ngo, Amanda L. Maheras
Publikováno v:
eNeuro
Visual Abstract
Mild traumatic brain injuries (mTBIs) are one of the most prevalent neurological disorders, and humans are severely limited in their ability to repair and regenerate central nervous system (CNS) tissue postinjury. However, zebraf
Mild traumatic brain injuries (mTBIs) are one of the most prevalent neurological disorders, and humans are severely limited in their ability to repair and regenerate central nervous system (CNS) tissue postinjury. However, zebraf
Autor:
Katja Butterbach, Christopher K. Edlund, Duncan C. Thomas, Gianluca Severi, Motoki Iwasaki, Keith R. Curtis, Emily White, Fredrick R. Schumacher, Wei Shi, Sun Ha Jee, W. James Gauderman, Dee W. West, Robert W. Haile, Wei Hua Jia, Jing Ma, Graham Casey, Mark A. Jenkins, Wei Zheng, Stéphane Bézieau, Mathiew Lemire, Andrea Z. LaCroix, Charles S. Fuchs, David Van Den Berg, Cecelia A. Laurie, Yong-Bing Xiang, Gad Rennert, Tabitha A. Harrison, Karen W. Makar, Marilena Melas, Hermann Brenner, Laurence N. Kolonel, Christopher S. Carlson, Cathy C. Laurie, Barbara K. Fortini, Shoichiro Tsugane, John F. Harju, Bhramar Mukherjee, Steven Gallinger, Darin Taverna, John L. Hopper, John D. Potter, Polly A. Newcomb, Aaron K. Aragaki, Sonja I. Berndt, Keitaro Matsuo, Cornelia M. Ulrich, Stephanie L. Schmit, Jane C. Figueiredo, Li Li, Victor Moreno, Eric J. Jacobs, Gregory Idos, Kana Wu, Stephen B. Gruber, Stephen J. Chanock, Kevin McDonnell, David K. Levine, Amit Joshi, Shuo Jiao, Brian E. Henderson, Thomas J. Hudson, Andrew T. Chan, Daniela Seminara, Stephanie M. Gogarten, Christopher P. Fischer, Roger C. Green, David Duggan, Bette J. Caan, Ulrike Peters, Richard B. Hayes, N. M. Lindor, Rebecca D. Jackson, David J. Hunter, Martha L. Slattery, Loic Le Marchand, Ben Zhang, Edward L. Giocannucci, Brent W. Zanke, Stephanie A. Rosse, David V. Conti, Sebastian Kury, Leon Raskin, Manish Gala, Shu Chen Huang, Frank J. Manion, Hansong Wang, Hedy S. Rennert, Gerhard A. Coetzee, Carolyn M. Hutter, Suminori Kono, Jenny Chang-Claude, Graham G. Giles, Michael Hoffmeister, Xiao-Ou Shu, Caroline McNeil, Flavio Lejbkowicz, Robert E. Schoen, Li Hsu, Conghui Qu, Peter T. Campbell, Charles Kooperberg
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
El document inclou una pàgina final amb una correcció (corrigendum). Aquesta, per si sola, té el següent DOI: 10.1038/ncomms9739 i es va publicar al mateix vol. 6.
Genetic susceptibility to colorectal cancer is caused by rare pathogenic muta
Genetic susceptibility to colorectal cancer is caused by rare pathogenic muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::275954b0a10cab2ecf3c23ec6fa97769
http://hdl.handle.net/2445/124064
http://hdl.handle.net/2445/124064
Autor:
Elizabeth L. Barry, Christopher K. Edlund, Robert S. Bresalier, Graham Casey, Timothy R. Church, Barbara K. Fortini, Sarah J. Plummer, Victor Moreno, Jane C. Figueiredo, Stephanie Tring
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 11, p e111914 (2014)
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS ONE, Vol 9, Iss 11, p e111914 (2014)
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Genome-wide association studies (GWAS) of colorectal cancer (CRC) have led to the identification of a number of common variants associated with modest risk. Several risk variants map within the vicinity of TGFβ/BMP signaling pathway genes, including