Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cecilia A Laurie"'
Autor:
Chani J Hodonsky, Deepti Jain, Ursula M Schick, Jean V Morrison, Lisa Brown, Caitlin P McHugh, Claudia Schurmann, Diane D Chen, Yong Mei Liu, Paul L Auer, Cecilia A Laurie, Kent D Taylor, Brian L Browning, Yun Li, George Papanicolaou, Jerome I Rotter, Ryo Kurita, Yukio Nakamura, Sharon R Browning, Ruth J F Loos, Kari E North, Cathy C Laurie, Timothy A Thornton, Nathan Pankratz, Daniel E Bauer, Tamar Sofer, Alex P Reiner
Publikováno v:
PLoS Genetics, Vol 13, Iss 4, p e1006760 (2017)
Prior GWAS have identified loci associated with red blood cell (RBC) traits in populations of European, African, and Asian ancestry. These studies have not included individuals with an Amerindian ancestral background, such as Hispanics/Latinos, nor e
Externí odkaz:
https://doaj.org/article/d79b27a0384a489caf7bdbe0fd8fe84d
Autor:
JoAnn E. Manson, Yongmei Liu, Daniel Nachun, Russell P. Tracy, Laura M. Raffield, Andrew D. Johnson, Kent D. Taylor, David Van Den Berg, Adolfo Correa, Cecilia A. Laurie, Daniel Levy, Joshua S. Weinstock, Peter Durda, Pradeep Natarajan, Eric A. Whitsel, Sekar Kathiresan, Alexander G. Bick, Joanne M. Murabito, Alexander P. Reiner, Themistocles L. Assimes, Steve Horvath, W. Craig Johnson, Gonçalo R. Abecasis, Stephen S. Rich, George J. Papanicolaou, James G. Wilson, Thomas W. Blackwell, Pinkal Desai, Ake T. Lu, Charles Kooperberg, Siddhartha Jaiswal, Xiuqing Guo, Mindy D. Szeto, Jerome I. Rotter
Publikováno v:
Aging Cell
Clonal hematopoiesis of indeterminate potential (CHIP) is a common precursor state for blood cancers that most frequently occurs due to mutations in the DNA‐methylation modifying enzymes DNMT3A or TET2. We used DNA‐methylation array and whole‐g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3033adac772bfb787ee911947d5320fc
https://pubmed.ncbi.nlm.nih.gov/34050697
https://pubmed.ncbi.nlm.nih.gov/34050697
Autor:
Ethan M. Lange, Matthew P. Conomos, Tamar Sofer, Xiuwen Zheng, Kenneth Rice, O’Connell, J. C. Bis, Stephanie M. Gogarten, Cecilia A. Laurie, Jennifer A. Brody, Bruce M. Psaty, Adam A. Szpiro, Yan Gao, Timothy A. Thornton, L. A. Cupples
SummaryIn modern Whole Genome Sequencing (WGS) epidemiological studies, participant-level data from multiple studies are often pooled and results are obtained from a single analysis. We consider the impact of differential phenotype variances by study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af0c1b16ebd3c63ae6fccf371b2e7d1e
https://doi.org/10.1101/2020.03.03.973420
https://doi.org/10.1101/2020.03.03.973420
Autor:
Steve Buyske, Claudia Schurmann, Andrés Moreno-Estrada, Cathy C. Laurie, Ulrike Peters, Yesha Patel, Eimear E. Kenny, Michael Preuss, Hannah Poisner, Kari E. North, Carlos Bustamante, Christopher A. Haiman, Stephanie A. Bien, Anne E. Justice, Katherine K. Nishimura, Yuqing Li, Loic Le Marchand, Unhee Lim, E Stahl, Christopher R. Gignoux, Alexandra Sockell, Paul Norman, Ewa Deelman, Yingchang Lu, Rebecca D. Jackson, Huckins Lm, Gerardo Heiss, Kimberly F. Doheny, Chani J. Hodonsky, Brenna M. Henn, Benyam Hailu, Genevieve L. Wojcik, Jane Romm, Misa Graff, Loos R, Christy L. Avery, Danyu Lin, José Luis Ambite, Kris Young, Eric Boerwinkle, Kathleen C. Barnes, Gillian M. Belbin, Bridget M Lin, Lindsay Fernández-Rhodes, Cecilia A. Laurie, Christian Caberto, Sung-Hyuk Park, Tara C. Matise, Abhishek Vishnu, Loreall Pooler, Ran Tao, Elena P. Sorokin, Ron Do, Lucia A. Hindorff, Sarah C. Nelson, Heather M. Highland, L R Wilkens, Cheryl A. Winkler, Iona Cheng, Acuna-Alonso, Matthew P. Conomos, Myriam Fornage, Xin Sheng, Girish N. Nadkarni, Christopher S. Carlson, Ruth H. Walker, Janina M. Jeff, Jeffrey Haessler, Daniel O. Stram, Sabati C, Sachiko Yoneyama, Jonathan M. Kocarnik, Christina L. Wassel, Timothy A. Thornton, Charles Kooperberg, Veronica Wendy Setiawan, Yao Hu, Sinead Cullina, Canizales-Quinteroes S, Niha Zubair, Melissa A. Richard, Karan Vahi, Karla Sandoval, Marie Verbanck, Erwin P. Bottinger, Alexander P. Reiner
Summary/AbstractGenome-wide association studies (GWAS) have laid the foundation for investigations into the biology of complex traits, drug development, and clinical guidelines. However, the dominance of European-ancestry populations in GWAS creates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1897152ac6862b7b262354de6a7bac22
Autor:
Deepti Jain, Alex P. Reiner, Kent D. Taylor, Jean Morrison, Timothy A. Thornton, Diane D. Chen, Jerome I. Rotter, Ruth J. F. Loos, Yun Li, Yukio Nakamura, Cecilia A. Laurie, Paul L. Auer, Sharon R. Browning, George Papanicolaou, Kari E. North, Brian L. Browning, Claudia Schurmann, Lisa M. Brown, Tamar Sofer, Chani J. Hodonsky, Caitlin P. McHugh, Cathy C. Laurie, Ursula M. Schick, Ryo Kurita, Nathan Pankratz, Yongmei Liu, Daniel E. Bauer
Publikováno v:
PLoS Genetics, Vol 13, Iss 4, p e1006760 (2017)
PLoS Genetics
PLoS Genetics
Prior GWAS have identified loci associated with red blood cell (RBC) traits in populations of European, African, and Asian ancestry. These studies have not included individuals with an Amerindian ancestral background, such as Hispanics/Latinos, nor e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24cdb6d1f18d66930c747205612125c8
http://europepmc.org/articles/PMC5428979?pdf=render
http://europepmc.org/articles/PMC5428979?pdf=render
Autor:
Chen Wu, Neil E. Caporaso, Daniel B. Mirel, Ann G. Schwartz, Anastasia L. Wise, Loic Le Marchand, Mitchell J. Machiela, Kay-Tee Khaw, Charles Kooperberg, Fredrick R. Schumacher, Tania Carreón, Edward Giovannucci, Kexin Chen, Jiucun Wang, Jolanta Lissowska, Kala Viswanathan, Benjamín Rodríguez-Santiago, Brian M. Wolpin, Annelie Landgren, Krista A. Zanetti, Emily White, Hannah P. Yang, Graham G. Giles, Laura J. Bierut, Baosen Zhou, Luis A. Pérez-Jurado, Beatrice Melin, Cathryn H. Bock, Kathleen C. Barnes, Geoffrey S. Tobias, I. Shou Chang, Harvey A. Risch, Min-Ho Shin, Stephanie J. Weinstein, Jay S. Wunder, Christopher I. Amos, Loreall Pooler, Lynn R. Goldin, Irene Orlow, Louise A. Brinton, Maria Pik Wong, Ana Patiño-García, Xifeng Wu, Qing Lan, Núria Malats, Wei Zheng, Maria Teresa Landi, Susan M. Gapstur, Constance Chen, Mazda Jenab, Adeline Seow, Christoffer Johansen, Mark P. Purdue, Faith G. Davis, Louis R. Pasquale, Lisa Mirabello, Jennifer A. Doherty, Jae H. Kang, Alisa M. Goldstein, Brian E. Henderson, Amy Hutchinson, Roger Henriksson, Laurence N. Kolonel, Jin-Hu Fan, Elio Riboli, Neal D. Freedman, Sholom Wacholder, Laufey T. Amundadottir, Weiyin Zhou, Chu Chen, Hee Nam Kim, John A. Heit, Sara H. Olson, H. Dean Hosgood, David Van Den Berg, Chao A. Hsiung, Janey L. Wiggs, Jianjun Liu, Kendra Schwartz, Christian C. Abnet, Mary L. Marazita, Karl C. Desch, Rachael Z. Stolzenberg-Solomon, Robert R. McWilliams, Victoria L. Stevens, Cecilia A. Laurie, Yi-Long Wu, Kai Yu, Cathy C. Laurie, Lauren R. Teras, Radhai Rastogi, Joshua N. Sampson, Veronica Wendy Setiawan, Caroline G. Epstein, Susan E. Hankinson, Laurie Burdett, Immaculata De Vivo, Beata Peplonska, Paige M. Bracci, Preetha Rajaraman, Eric J. Duell, Kari G. Rabe, Kevin B. Jacobs, Marta Crous Bou, Charles C. Chung, Nan Hu, Montserrat Garcia-Closas, Xiaolin Liang, Young Tae Kim, Debra T. Silverman, Anthony M. Magliocco, Gloria M. Petersen, Pan-Chyr Yang, Jennifer Prescott, Sarah C. Nelson, Xiao-Ou Shu, William L. Lowe, Andrea Z. LaCroix, David Ginsburg, J. Michael Gaziano, Philip R. Taylor, Jae Yong Park, Xin Sheng, Hongbing Shen, Meredith Yeager, Michael Cullen, Robert J. Klein, Lingeng Lu, Yeul Hong Kim, Regina G. Ziegler, Christine M. Friedenreich, Tangchun Wu, Sonja I. Berndt, Charles S. Fuchs, Dongxin Lin, Yun-Chul Hong, Nathaniel Rothman, Gianluca Severi, Ludmila Prokunina-Olsson, Joseph F. Fraumeni, Mariza de Andrade, Lucy Xia, Anne Zeleniuch-Jacquotte, Mads Melbye, Stephen J. Chanock, John K. Wiencke, Daniel O. Stram, Nilanjan Chatterjee, Margaret R. Spitz, Linda S. Cook, William Wheeler, David J. Hunter, Donghui Li, Julie E. Buring, William J. Blot, Lorna H. McNeill, Francisco X. Real, Mark H. Greene, Patricia Hartge, Sharon A. Savage, Kenneth Rice, Linda M. Liao, Robert N. Hoover, Mary Ann Butler, Elizabeth M. Gillanders, You-Lin Qiao, Göran Hallmans, Elizabeth A. Holly, Vittorio Krogh, Michael Dean, Jonine D. Figueroa, Jeffrey C. Murray, Melinda C. Aldrich, Nicolas Wentzensen, Lea Jessop, Zhaoming Wang, Woon-Puay Koh, Peter Kraft, Bjarke Feenstra, Ulrike Peters, Katherine A. McGlynn, Kimberly F. Doheny, Jun Li, Michael B. Cook, Ze Zhong Tang, Amanda Black, Christopher A. Haiman, Margaret A. Tucker, Ti Ding, Avima M. Ruder, Terri H. Beaty, Keitaro Matsuo, Mia M. Gaudet, Robert C. Kurtz, Yu-Tang Gao, Demetrius Albanes, Wei Hu, Curtis C. Harris, Howard D. Sesso
Publikováno v:
Machiela, Mitchell J; Zhou, Weiyin; Sampson, Joshua N; Dean, Michael C; Jacobs, Kevin B; Black, Amanda; et al.(2015). Characterization of large structural genetic mosaicism in human autosomes.. American journal of human genetics, 96(3), 487-497. doi: 10.1016/j.ajhg.2015.01.011. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/1k84j0fp
Recercat. Dipósit de la Recerca de Catalunya
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Recercat. Dipósit de la Recerca de Catalunya
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Analyses of genome-wide association study (GWAS) data have revealed that detectable genetic mosaicism involving large (>2 Mb) structural autosomal alterations occurs in a fraction of individuals. We present results for a set of 24,849 genotyped indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a367258f20dbee8c55b151b8ec74e44
http://www.escholarship.org/uc/item/1k84j0fp
http://www.escholarship.org/uc/item/1k84j0fp