Zobrazeno 1 - 10
of 384
pro vyhledávání: '"Margaret A, Tucker"'
Autor:
Alisa M. Goldstein, PhD, Richard Qin, BS, Emily Y. Chu, MD, PhD, David E. Elder, MBChB, Daniela Massi, MD, PhD, David J. Adams, PhD, Paul W. Harms, MD, PhD, Carla Daniela Robles-Espinoza, PhD, Julia A. Newton-Bishop, MD, PhD, D. Timothy Bishop, PhD, Mark Harland, PhD, Elizabeth A. Holland, BSc, Anne E. Cust, PhD, Helen Schmid, MPH, Graham J. Mann, MBBS, PhD, Susana Puig, MD, PhD, Miriam Potrony, PhD, Llucia Alos, MD, PhD, Eduardo Nagore, MD, PhD, David Millán-Esteban, PhD, Nicholas K. Hayward, PhD, Natasa Broit, PhD, Jane M. Palmer, RN, Vaishnavi Nathan, PhD, Elizabeth G. Berry, MD, Esteban Astiazaran-Symonds, MD, Xiaohong R. Yang, PhD, Margaret A. Tucker, MD, Maria Teresa Landi, MD, PhD, Ruth M. Pfeiffer, PhD, Michael R. Sargen, MD
Publikováno v:
JAAD International, Vol 11, Iss , Pp 43-51 (2023)
Background: Spitzoid morphology in familial melanoma has been associated with germline variants in POT1, a telomere maintenance gene (TMG), suggesting a link between telomere biology and spitzoid differentiation. Objective: To assess if familial mela
Externí odkaz:
https://doaj.org/article/b6d3451b882d49dc952ed23a5da93142
Autor:
Megan M. Herr, Sara J. Schonfeld, Graça M. Dores, Eric A. Engels, Margaret A. Tucker, Rochelle E. Curtis, Lindsay M. Morton
Publikováno v:
Blood Advances, Vol 3, Iss 13, Pp 1961-1969 (2019)
Abstract: Infectious agents have been identified in the etiology of certain non-Hodgkin lymphoma (NHL) subtypes and solid tumors. The impact of this shared etiology on risk for second cancers in NHL survivors has not been comprehensively studied. We
Externí odkaz:
https://doaj.org/article/5740ab443da74f24bcc622eba33ee568
Autor:
Jung Kim, Wen Luo, Mingyi Wang, Talia Wegman-Ostrosky, Megan N. Frone, Jennifer J. Johnston, Michael L. Nickerson, Melissa Rotunno, Shengchao A. Li, Maria I. Achatz, Seth A. Brodie, Michael Dean, Kelvin C. de Andrade, Fernanda P. Fortes, Matthew Gianferante, Payal Khincha, Mary L. McMaster, Lisa J. McReynolds, Alexander Pemov, Maisa Pinheiro, Karina M. Santiago, Blanche P. Alter, Neil E. Caporaso, Shahinaz M. Gadalla, Lynn R. Goldin, Mark H. Greene, Jennifer Loud, Xiaohong R. Yang, Neal D. Freedman, Susan M. Gapstur, Mia M. Gaudet, Donato Calista, Paola Ghiorzo, Maria Concetta Fargnoli, Eduardo Nagore, Ketty Peris, Susana Puig, Maria Teresa Landi, Belynda Hicks, Bin Zhu, Jia Liu, Joshua N. Sampson, Stephen J. Chanock, Lisa J. Mirabello, Lindsay M. Morton, Leslie G. Biesecker, Margaret A. Tucker, Sharon A. Savage, Alisa M. Goldstein, Douglas R. Stewart
Publikováno v:
Genome Medicine, Vol 10, Iss 1, Pp 1-9 (2018)
Abstract Background Prior research has established that the prevalence of pathogenic/likely pathogenic (P/LP) variants across all of the American College of Medical Genetics (ACMG) Secondary Findings (SF) genes is approximately 0.8–5%. We investiga
Externí odkaz:
https://doaj.org/article/f8d664b0a6b34bb18931cda5ffb1397c
Autor:
Shu-Hong Lin, Joshua N Sampson, Thomas G P Grünewald, Didier Surdez, Stephanie Reynaud, Olivier Mirabeau, Eric Karlins, Rebeca Alba Rubio, Sakina Zaidi, Sandrine Grossetête-Lalami, Stelly Ballet, Eve Lapouble, Valérie Laurence, Jean Michon, Gaelle Pierron, Heinrich Kovar, Udo Kontny, Anna González-Neira, Javier Alonso, Ana Patino-Garcia, Nadège Corradini, Perrine Marec Bérard, Jeremy Miller, Neal D Freedman, Nathaniel Rothman, Brian D Carter, Casey L Dagnall, Laurie Burdett, Kristine Jones, Michelle Manning, Kathleen Wyatt, Weiyin Zhou, Meredith Yeager, David G Cox, Robert N Hoover, Javed Khan, Gregory T Armstrong, Wendy M Leisenring, Smita Bhatia, Leslie L Robison, Andreas E Kulozik, Jennifer Kriebel, Thomas Meitinger, Markus Metzler, Manuela Krumbholz, Wolfgang Hartmann, Konstantin Strauch, Thomas Kirchner, Uta Dirksen, Lisa Mirabello, Margaret A Tucker, Franck Tirode, Lindsay M Morton, Stephen J Chanock, Olivier Delattre, Mitchell J Machiela
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0237792 (2020)
BackgroundEwing sarcoma (EwS) is a rare, aggressive solid tumor of childhood, adolescence and young adulthood associated with pathognomonic EWSR1-ETS fusion oncoproteins altering transcriptional regulation. Genome-wide association studies (GWAS) have
Externí odkaz:
https://doaj.org/article/f21a3cae3175421296c803674a427eeb
Autor:
Mitchell J. Machiela, Thomas G. P. Grünewald, Didier Surdez, Stephanie Reynaud, Olivier Mirabeau, Eric Karlins, Rebeca Alba Rubio, Sakina Zaidi, Sandrine Grossetete-Lalami, Stelly Ballet, Eve Lapouble, Valérie Laurence, Jean Michon, Gaelle Pierron, Heinrich Kovar, Nathalie Gaspar, Udo Kontny, Anna González-Neira, Piero Picci, Javier Alonso, Ana Patino-Garcia, Nadège Corradini, Perrine Marec Bérard, Neal D. Freedman, Nathaniel Rothman, Casey L. Dagnall, Laurie Burdett, Kristine Jones, Michelle Manning, Kathleen Wyatt, Weiyin Zhou, Meredith Yeager, David G. Cox, Robert N. Hoover, Javed Khan, Gregory T. Armstrong, Wendy M. Leisenring, Smita Bhatia, Leslie L. Robison, Andreas E. Kulozik, Jennifer Kriebel, Thomas Meitinger, Markus Metzler, Wolfgang Hartmann, Konstantin Strauch, Thomas Kirchner, Uta Dirksen, Lindsay M. Morton, Lisa Mirabello, Margaret A. Tucker, Franck Tirode, Stephen J. Chanock, Olivier Delattre
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-8 (2018)
Ewing sarcoma (EWS) is a rare pediatric bone cancer typically involving the EWSR1-FLI1 fusion. Here the authors perform a genome-wide association study and report three new EWS risk loci that reside near GGAA repeat sequences, and identify candidate
Externí odkaz:
https://doaj.org/article/0ac8edbb89d948f498acb3404c1156e8
Autor:
Casey L. Dagnall, Lindsay M. Morton, Belynda D. Hicks, Shengchao Li, Weiyin Zhou, Eric Karlins, Kedest Teshome, Salma Chowdhury, Kerrie S. Lashley, Joshua N. Sampson, Leslie L. Robison, Gregory T. Armstrong, Smita Bhatia, Gretchen A. Radloff, Stella M. Davies, Margaret A. Tucker, Meredith Yeager, Stephen J. Chanock
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background The recommended genomic DNA input requirements for whole genome single nucleotide polymorphism microarrays can limit the scope of molecular epidemiological studies. We performed a large-scale evaluation of whole genome amplified D
Externí odkaz:
https://doaj.org/article/371d8d142e9f4e97baedf052bf07d0ac
Autor:
Xin Song, Wen-Qing Li, Nan Hu, Xue Ke Zhao, Zhaoming Wang, Paula L. Hyland, Tao Jiang, Guo Qiang Kong, Hua Su, Chaoyu Wang, Lemin Wang, Li Sun, Zong Min Fan, Hui Meng, Tang Juan Zhang, Ling Fen Ji, Shou Jia Hu, Wei Li Han, Min Jie Wu, Peng Yuan Zheng, Shuang Lv, Xue Min Li, Fu You Zhou, Laurie Burdett, Ti Ding, You-Lin Qiao, Jin-Hu Fan, Xiao-You Han, Carol Giffen, Margaret A. Tucker, Sanford M. Dawsey, Neal D. Freedman, Stephen J. Chanock, Christian C. Abnet, Philip R. Taylor, Li-Dong Wang, Alisa M. Goldstein
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract Based on our initial genome-wide association study (GWAS) on esophageal squamous cell carcinoma (ESCC) in Han Chinese, we conducted a follow-up study to examine the single nucleotide polymorphisms (SNPs) associated with family history (FH) o
Externí odkaz:
https://doaj.org/article/ee819a9753a54ca2a0f945426e94214d
Autor:
Elizabeth K. Cahoon, Margaret A. Tucker, Martha S. Linet, Bruce H. Alexander, Mark P. Little, Michael R. Sargen, Cari M. Kitahara, Jim Z. Mai
Although NSAIDs have been associated with both reduced and increased cutaneous melanoma risk, few studies have examined these associations by ultraviolet radiation (UVR) or personal sun-sensitivity. We examined the associations between NSAID use and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::165917a1aae364922b9a4e5d64efa344
https://doi.org/10.1158/1940-6207.c.6547055.v1
https://doi.org/10.1158/1940-6207.c.6547055.v1
Autor:
Lindsay M. Morton, Amy Berrington de Gonzalez, Joshua N. Sampson, Joanne Elena, Rochelle E. Curtis, Anne Zeleniuch-Jacquotte, James R. Cerhan, Robert N. Hoover, Margaret A. Tucker, Patricia Hartge, Joseph F. Fraumeni, Mark P. Purdue, Gabriella Andreotti, Laura E. Beane Freeman, Stephanie J. Weinstein, Demetrius Albanes, Kim Robien, Yikyung Park, Meredith S. Shiels, Todd M. Gibson, Amanda Black
Background: With over 13 million cancer survivors in the United States today, second cancers are of rapidly growing importance. However, data on nontreatment risk factors for second cancers are sparse. We explored the feasibility of pooling data from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60aa3eb6daa940bb56dd92732f18d6d9
https://doi.org/10.1158/1055-9965.c.6515146
https://doi.org/10.1158/1055-9965.c.6515146
Autor:
Ena Wang, Lisa M. McShane, Neil E. Caporaso, Angela C. Pesatori, Pier Alberto Bertazzi, Margaret A. Tucker, Francesco M. Marincola, Ilona Linnoila, Alisa M. Goldstein, Maurizia Rubagotti, Andrew W. Bergen, Hui Liu, Jill Koshiol, Melissa Rotunno, Yingdong Zhao, Maria Teresa Landi
Purpose: The molecular drivers that determine histology in lung cancer are largely unknown. We investigated whether microRNA (miR) expression profiles can differentiate histologic subtypes and predict survival for non–small cell lung cancer.Experim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5baf5005a396fc6e582a88805c463093
https://doi.org/10.1158/1078-0432.c.6517893.v1
https://doi.org/10.1158/1078-0432.c.6517893.v1