Zobrazeno 1 - 10
of 252
pro vyhledávání: '"William Wheeler"'
Autor:
William Wheeler
Publikováno v:
Suomen Antropologi, Vol 48, Iss 1 (2024)
This article explores the story of Sanwar, who fled Bangladesh following persecution for his sexuality, and spent five years struggling for asylum in the UK. Analysing our conversations together with his asylum paperwork, I show how trauma was appreh
Externí odkaz:
https://doaj.org/article/56241fbb380b405599baa442df851a93
Publikováno v:
Batteries, Vol 10, Iss 4, p 119 (2024)
Second-life applications for lithium-ion batteries offer industry opportunities to defer recycling costs, enhance economic value, and reduce environmental impacts. However, cells are affected by numerous aging phenomena which can lead to an accelerat
Externí odkaz:
https://doaj.org/article/4a24b9f0b3774eaabfef605aea244c0e
Publikováno v:
Batteries, Vol 10, Iss 4, p 137 (2024)
Second-life applications for lithium-ion batteries offer the industry opportunities to defer recycling costs, enhance economic value, and reduce environmental impacts. An accurate prognosis of the remaining useful life (RUL) is essential for ensuring
Externí odkaz:
https://doaj.org/article/bc00259b2a314ff78d7f9a34f4caf415
Autor:
Parichoy Pal Choudhury, Paige Maas, Amber Wilcox, William Wheeler, Mark Brook, David Check, Montserrat Garcia-Closas, Nilanjan Chatterjee
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0228198 (2020)
This report describes an R package, called the Individualized Coherent Absolute Risk Estimator (iCARE) tool, that allows researchers to build and evaluate models for absolute risk and apply them to estimate an individual's risk of developing disease
Externí odkaz:
https://doaj.org/article/373fdab1dc954282a9e9ce8251ff0b73
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome
Autor:
Mitchell J. Machiela, Weiyin Zhou, Eric Karlins, Joshua N. Sampson, Neal D. Freedman, Qi Yang, Belynda Hicks, Casey Dagnall, Christopher Hautman, Kevin B. Jacobs, Christian C. Abnet, Melinda C. Aldrich, Christopher Amos, Laufey T. Amundadottir, Alan A. Arslan, Laura E. Beane-Freeman, Sonja I. Berndt, Amanda Black, William J. Blot, Cathryn H. Bock, Paige M. Bracci, Louise A. Brinton, H Bas Bueno-de-Mesquita, Laurie Burdett, Julie E. Buring, Mary A. Butler, Federico Canzian, Tania Carreón, Kari G. Chaffee, I-Shou Chang, Nilanjan Chatterjee, Chu Chen, Constance Chen, Kexin Chen, Charles C. Chung, Linda S. Cook, Marta Crous Bou, Michael Cullen, Faith G. Davis, Immaculata De Vivo, Ti Ding, Jennifer Doherty, Eric J. Duell, Caroline G. Epstein, Jin-Hu Fan, Jonine D. Figueroa, Joseph F. Fraumeni, Christine M. Friedenreich, Charles S. Fuchs, Steven Gallinger, Yu-Tang Gao, Susan M. Gapstur, Montserrat Garcia-Closas, Mia M. Gaudet, J. Michael Gaziano, Graham G. Giles, Elizabeth M. Gillanders, Edward L. Giovannucci, Lynn Goldin, Alisa M. Goldstein, Christopher A. Haiman, Goran Hallmans, Susan E. Hankinson, Curtis C. Harris, Roger Henriksson, Elizabeth A. Holly, Yun-Chul Hong, Robert N. Hoover, Chao A. Hsiung, Nan Hu, Wei Hu, David J. Hunter, Amy Hutchinson, Mazda Jenab, Christoffer Johansen, Kay-Tee Khaw, Hee Nam Kim, Yeul Hong Kim, Young Tae Kim, Alison P. Klein, Robert Klein, Woon-Puay Koh, Laurence N. Kolonel, Charles Kooperberg, Peter Kraft, Vittorio Krogh, Robert C. Kurtz, Andrea LaCroix, Qing Lan, Maria Teresa Landi, Loic Le Marchand, Donghui Li, Xiaolin Liang, Linda M. Liao, Dongxin Lin, Jianjun Liu, Jolanta Lissowska, Lingeng Lu, Anthony M. Magliocco, Nuria Malats, Keitaro Matsuo, Lorna H. McNeill, Robert R. McWilliams, Beatrice S. Melin, Lisa Mirabello, Lee Moore, Sara H. Olson, Irene Orlow, Jae Yong Park, Ana Patiño-Garcia, Beata Peplonska, Ulrike Peters, Gloria M. Petersen, Loreall Pooler, Jennifer Prescott, Ludmila Prokunina-Olsson, Mark P. Purdue, You-Lin Qiao, Preetha Rajaraman, Francisco X. Real, Elio Riboli, Harvey A. Risch, Benjamin Rodriguez-Santiago, Avima M. Ruder, Sharon A. Savage, Fredrick Schumacher, Ann G. Schwartz, Kendra L. Schwartz, Adeline Seow, Veronica Wendy Setiawan, Gianluca Severi, Hongbing Shen, Xin Sheng, Min-Ho Shin, Xiao-Ou Shu, Debra T. Silverman, Margaret R. Spitz, Victoria L. Stevens, Rachael Stolzenberg-Solomon, Daniel Stram, Ze-Zhong Tang, Philip R. Taylor, Lauren R. Teras, Geoffrey S. Tobias, David Van Den Berg, Kala Visvanathan, Sholom Wacholder, Jiu-Cun Wang, Zhaoming Wang, Nicolas Wentzensen, William Wheeler, Emily White, John K. Wiencke, Brian M. Wolpin, Maria Pik Wong, Chen Wu, Tangchun Wu, Xifeng Wu, Yi-Long Wu, Jay S. Wunder, Lucy Xia, Hannah P. Yang, Pan-Chyr Yang, Kai Yu, Krista A. Zanetti, Anne Zeleniuch-Jacquotte, Wei Zheng, Baosen Zhou, Regina G. Ziegler, Luis A. Perez-Jurado, Neil E. Caporaso, Nathaniel Rothman, Margaret Tucker, Michael C. Dean, Meredith Yeager, Stephen J. Chanock
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-9 (2016)
It is unclear how often genetic mosaicism of chromosome X arises. Here, the authors examine women with cancer and cancer-free controls and show that X chromosome mosaicism occurs more frequently than on autosomes, especially on the inactive X chromos
Externí odkaz:
https://doaj.org/article/ff910db139f74f1fb230ff9dacdc3391
Autor:
Jianxin Shi, Ju-Hyun Park, Jubao Duan, Sonja T Berndt, Winton Moy, Kai Yu, Lei Song, William Wheeler, Xing Hua, Debra Silverman, Montserrat Garcia-Closas, Chao Agnes Hsiung, Jonine D Figueroa, Victoria K Cortessis, Núria Malats, Margaret R Karagas, Paolo Vineis, I-Shou Chang, Dongxin Lin, Baosen Zhou, Adeline Seow, Keitaro Matsuo, Yun-Chul Hong, Neil E Caporaso, Brian Wolpin, Eric Jacobs, Gloria M Petersen, Alison P Klein, Donghui Li, Harvey Risch, Alan R Sanders, Li Hsu, Robert E Schoen, Hermann Brenner, MGS (Molecular Genetics of Schizophrenia) GWAS Consortium, GECCO (The Genetics and Epidemiology of Colorectal Cancer Consortium), GAME-ON/TRICL (Transdisciplinary Research in Cancer of the Lung) GWAS Consortium, PRACTICAL (PRostate cancer AssoCiation group To Investigate Cancer Associated aLterations) Consortium, PanScan Consortium, GAME-ON/ELLIPSE Consortium, Rachael Stolzenberg-Solomon, Pablo Gejman, Qing Lan, Nathaniel Rothman, Laufey T Amundadottir, Maria Teresa Landi, Douglas F Levinson, Stephen J Chanock, Nilanjan Chatterjee
Publikováno v:
PLoS Genetics, Vol 12, Iss 12, p e1006493 (2016)
Recent heritability analyses have indicated that genome-wide association studies (GWAS) have the potential to improve genetic risk prediction for complex diseases based on polygenic risk score (PRS), a simple modelling technique that can be implement
Externí odkaz:
https://doaj.org/article/a59b3243ed1d40f794cbb7048b649f62
Autor:
Han Zhang, William Wheeler, Paula L Hyland, Yifan Yang, Jianxin Shi, Nilanjan Chatterjee, Kai Yu
Publikováno v:
PLoS Genetics, Vol 12, Iss 6, p e1006122 (2016)
Meta-analysis of multiple genome-wide association studies (GWAS) has become an effective approach for detecting single nucleotide polymorphism (SNP) associations with complex traits. However, it is difficult to integrate the readily accessible SNP-le
Externí odkaz:
https://doaj.org/article/86c2f2574a9949d3abcf7d942c346138
Autor:
Alina V Brenner, Gila Neta, Erich M Sturgis, Ruth M Pfeiffer, Amy Hutchinson, Meredith Yeager, Li Xu, Cindy Zhou, William Wheeler, Margaret A Tucker, Stephen J Chanock, Alice J Sigurdson
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e57243 (2013)
Accumulating evidence suggests that alterations in immune function may be important in the etiology of papillary thyroid cancer (PTC). To identify genetic markers in immune-related pathways, we evaluated 3,985 tag single nucleotide polymorphisms (SNP
Externí odkaz:
https://doaj.org/article/c495525e47ef4525bf50b5a7208fc635
Autor:
Laura S Burke, Paula L Hyland, Ruth M Pfeiffer, Jennifer Prescott, William Wheeler, Lisa Mirabello, Sharon A Savage, Laurie Burdette, Meredith Yeager, Stephen Chanock, Immaculata De Vivo, Margaret A Tucker, Alisa M Goldstein, Xiaohong R Yang
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e71121 (2013)
INTRODUCTION: Recent evidence suggests a link between constitutional telomere length (TL) and cancer risk. Previous studies have suggested that longer telomeres were associated with an increased risk of melanoma and larger size and number of nevi. Th
Externí odkaz:
https://doaj.org/article/2efd15471e7649819aa2adabed34735c
Autor:
Kai Yu, Sholom Wacholder, William Wheeler, Zhaoming Wang, Neil Caporaso, Maria Teresa Landi, Faming Liang
Publikováno v:
PLoS Genetics, Vol 8, Iss 1, p e1002482 (2012)
An important follow-up step after genetic markers are found to be associated with a disease outcome is a more detailed analysis investigating how the implicated gene or chromosomal region and an established environment risk factor interact to influen
Externí odkaz:
https://doaj.org/article/43b8bae31b7f4ab69bb35f35811baf17