Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Anne, Sturcke"'
Autor:
Adam S, Gordon, Holly K, Tabor, Andrew D, Johnson, Beverly M, Snively, Themistocles L, Assimes, Paul L, Auer, John P A, Ioannidis, Ulrike, Peters, Jennifer G, Robinson, Lara E, Sucheston, Danxin, Wang, Nona, Sotoodehnia, Jerome I, Rotter, Bruce M, Psaty, Rebecca D, Jackson, David M, Herrington, Christopher J, O'Donnell, Alexander P, Reiner, Stephen S, Rich, Mark J, Rieder, Michael J, Bamshad, Deborah A, Nickerson, Anne, Sturcke
Publikováno v:
Human Molecular Genetics. 23:1957-1963
The study of genetic influences on drug response and efficacy (‘pharmacogenetics’) has existed for over 50 years. Yet, we still lack a complete picture of how genetic variation, both common and rare, affects each individual's responses to medicat
Autor:
Zhen Y Wang, Kimberly A Tryka, Luning Hao, Yumi Jin, Lora Ziyabari, Moira Lee, Masato Kimura, Nataliya Sharopova, Natalia Popova, Michael Feolo, Anne Sturcke
Publikováno v:
Nucleic Acids Research
The Database of Genotypes and Phenotypes (dbGap, http://www.ncbi.nlm.nih.gov/gap) is a National Institutes of Health-sponsored repository charged to archive, curate and distribute information produced by studies investigating the interaction of genot
Autor:
Nadine, Norton, Duanxiang, Li, Evadnie, Rampersaud, Ana, Morales, Eden R, Martin, Stephan, Zuchner, Shengru, Guo, Michael, Gonzalez, Dale J, Hedges, Peggy D, Robertson, Niklas, Krumm, Deborah A, Nickerson, Ray E, Hershberger, Anne, Sturcke
Publikováno v:
Circulation: Cardiovascular Genetics. 6:144-153
Background— Familial dilated cardiomyopathy (DCM) is a genetically heterogeneous disease with >30 known genes. TTN truncating variants were recently implicated in a candidate gene study to cause 25% of familial and 18% of sporadic DCM cases. Method
Autor:
Roby Joehanes, Daniel Levy, Quang Tri Nguyen, Poching Liu, Peter J. Munson, Xiaoling Zhang, Andrew D. Johnson, Josée Dupuis, Nataliya Sharopova, Kahraman Tanriverdi, Michael Feolo, Jane E. Freedman, Nancy L. Heard-Costa, Han Chen, Alejandro A. Schäffer, Richard J. Wang, Saixia Ying, Kimberly Woodhouse, Tianxiao Huan, Anne Sturcke, Chen Yao, Christopher J. O'Donnell, Nalini Raghavachari, Cumhur Y Demirkale
Publikováno v:
Genome Biology
Background Identification of single nucleotide polymorphisms (SNPs) associated with gene expression levels, known as expression quantitative trait loci (eQTLs), may improve understanding of the functional role of phenotype-associated SNPs in genome-w
Autor:
Anne Sturcke, Christopher J. O'Donnell, Zeng Y Wang, Lora Ziyabari, Stephen S. Rich, Bruce M. Psaty, Kenneth Rice, Mike Feolo, Joshua C. Bis
Publikováno v:
Nature Genetics. 48:702-703
Rapid evaluation of phenotypes, SNPs and results through the dbGaP CHARGE Summary Results site
Autor:
Leslie A. Lange, Youna Hu, He Zhang, Chenyi Xue, Ellen M. Schmidt, Zheng-Zheng Tang, Chris Bizon, Ethan M. Lange, Joshua D. Smith, Emily H. Turner, Goo Jun, Hyun Min Kang, Gina Peloso, Paul Auer, Kuo-ping Li, Jason Flannick, Ji Zhang, Christian Fuchsberger, Kyle Gaulton, Cecilia Lindgren, Adam Locke, Alisa Manning, Xueling Sim, Manuel A. Rivas, Oddgeir L. Holmen, Omri Gottesman, Yingchang Lu, Douglas Ruderfer, Eli A. Stahl, Qing Duan, Yun Li, Peter Durda, Shuo Jiao, Aaron Isaacs, Albert Hofman, Joshua C. Bis, Adolfo Correa, Michael E. Griswold, Johanna Jakobsdottir, Albert V. Smith, Pamela J. Schreiner, Mary F. Feitosa, Qunyuan Zhang, Jennifer E. Huffman, Jacy Crosby, Christina L. Wassel, Ron Do, Nora Franceschini, Lisa W. Martin, Jennifer G. Robinson, Themistocles L. Assimes, David R. Crosslin, Elisabeth A. Rosenthal, Michael Tsai, Mark J. Rieder, Deborah N. Farlow, Aaron R. Folsom, Thomas Lumley, Ervin R. Fox, Christopher S. Carlson, Ulrike Peters, Rebecca D. Jackson, Cornelia M. van Duijn, André G. Uitterlinden, Daniel Levy, Jerome I. Rotter, Herman A. Taylor, Vilmundur Gudnason, David S. Siscovick, Myriam Fornage, Ingrid B. Borecki, Caroline Hayward, Igor Rudan, Y. Eugene Chen, Erwin P. Bottinger, Ruth J.F. Loos, Pål Sætrom, Kristian Hveem, Michael Boehnke, Leif Groop, Mark McCarthy, Thomas Meitinger, Christie M. Ballantyne, Stacey B. Gabriel, Christopher J. O’Donnell, Wendy S. Post, Kari E. North, Alexander P. Reiner, Eric Boerwinkle, Bruce M. Psaty, David Altshuler, Sekar Kathiresan, Dan-Yu Lin, Gail P. Jarvik, L. Adrienne Cupples, Charles Kooperberg, James G. Wilson, Deborah A. Nickerson, Goncalo R. Abecasis, Stephen S. Rich, Russell P. Tracy, Cristen J. Willer, David M. Altshuler, Gonçalo R. Abecasis, Hooman Allayee, Sharon Cresci, Mark J. Daly, Paul I.W. de Bakker, Mark A. DePristo, Peter Donnelly, Tim Fennell, Kiran Garimella, Stanley L. Hazen, Daniel M. Jordan, Adam Kiezun, Guillaume Lettre, Bingshan Li, Mingyao Li, Christopher H. Newton-Cheh, Sandosh Padmanabhan, Sara Pulit, Daniel J. Rader, David Reich, Muredach P. Reilly, Steve Schwartz, Laura Scott, John A. Spertus, Nathaniel O. Stitziel, Nina Stoletzki, Shamil R. Sunyaev, Benjamin F. Voight, Ermeg Akylbekova, Larry D. Atwood, Maja Barbalic, R. Graham Barr, Emelia J. Benjamin, Joshua Bis, Donald W. Bowden, Jennifer Brody, Matthew Budoff, Greg Burke, Sarah Buxbaum, Jeff Carr, Donna T. Chen, Ida Y. Chen, Wei-Min Chen, Pat Concannon, Ralph D’Agostino, Anita L. DeStefano, Albert Dreisbach, Josée Dupuis, J. Peter Durda, Jaclyn Ellis, Caroline S. Fox, Ervin Fox, Vincent Funari, Santhi K. Ganesh, Julius Gardin, David Goff, Ora Gordon, Wayne Grody, Myron Gross, Xiuqing Guo, Ira M. Hall, Nancy L. Heard-Costa, Susan R. Heckbert, Nicholas Heintz, David M. Herrington, DeMarc Hickson, Jie Huang, Shih-Jen Hwang, David R. Jacobs, Nancy S. Jenny, Andrew D. Johnson, Craig W. Johnson, Steven Kawut, Richard Kronmal, Raluca Kurz, Martin G. Larson, Mark Lawson, Cora E. Lewis, Dalin Li, Honghuang Lin, Chunyu Liu, Jiankang Liu, Kiang Liu, Xiaoming Liu, Yongmei Liu, William T. Longstreth, Cay Loria, Kathryn Lunetta, Aaron J. Mackey, Rachel Mackey, Ani Manichaikul, Taylor Maxwell, Barbara McKnight, James B. Meigs, Alanna C. Morrison, Solomon K. Musani, Josyf C. Mychaleckyj, Jennifer A. Nettleton, Kari North, Daniel O’Leary, Frank Ong, Walter Palmas, James S. Pankow, Nathan D. Pankratz, Shom Paul, Marco Perez, Sharina D. Person, Joseph Polak, Aaron R. Quinlan, Leslie J. Raffel, Vasan S. Ramachandran, Kenneth Rice, Jill P. Sanders, Pamela Schreiner, Sudha Seshadri, Steve Shea, Stephen Sidney, Kevin Silverstein, Nicholas L. Smith, Nona Sotoodehnia, Asoke Srinivasan, Kent Taylor, Fridtjof Thomas, Michael Y. Tsai, Kelly A. Volcik, Chrstina L. Wassel, Karol Watson, Gina Wei, Wendy White, Kerri L. Wiggins, Jemma B. Wilk, O. Dale Williams, Gregory Wilson, Phillip Wolf, Neil A. Zakai, John Hardy, James F. Meschia, Michael Nalls, Andrew Singleton, Brad Worrall, Michael J. Bamshad, Kathleen C. Barnes, Ibrahim Abdulhamid, Frank Accurso, Ran Anbar, Terri Beaty, Abigail Bigham, Phillip Black, Eugene Bleecker, Kati Buckingham, Anne Marie Cairns, Daniel Caplan, Barbara Chatfield, Aaron Chidekel, Michael Cho, David C. Christiani, James D. Crapo, Julia Crouch, Denise Daley, Anthony Dang, Hong Dang, Alicia De Paula, Joan DeCelie-Germana, Allen DozorMitch Drumm, Maynard Dyson, Julia Emerson, Mary J. Emond, Thomas Ferkol, Robert Fink, Cassandra Foster, Deborah Froh, Li Gao, William Gershan, Ronald L. Gibson, Elizabeth Godwin, Magdalen Gondor, Hector Gutierrez, Nadia N. Hansel, Paul M. Hassoun, Peter Hiatt, John E. Hokanson, Michelle Howenstine, Laura K. Hummer, Jamshed Kanga, Yoonhee Kim, Michael R. Knowles, Michael Konstan, Thomas Lahiri, Nan Laird, Christoph Lange, Lin Lin, Xihong Lin, Tin L. Louie, David Lynch, Barry Make, Thomas R. Martin, Steve C. Mathai, Rasika A. Mathias, John McNamara, Sharon McNamara, Deborah Meyers, Susan Millard, Peter Mogayzel, Richard Moss, Tanda Murray, Dennis Nielson, Blakeslee Noyes, Wanda O’Neal, David Orenstein, Brian O’Sullivan, Rhonda Pace, Peter Pare, H. Worth Parker, Mary Ann Passero, Elizabeth Perkett, Adrienne Prestridge, Nicholas M. Rafaels, Bonnie Ramsey, Elizabeth Regan, Clement Ren, George Retsch-Bogart, Michael Rock, Antony Rosen, Margaret Rosenfeld, Ingo Ruczinski, Andrew Sanford, David Schaeffer, Cindy Sell, Daniel Sheehan, Edwin K. Silverman, Don Sin, Terry Spencer, Jackie Stonebraker, Holly K. Tabor, Laurie Varlotta, Candelaria I. Vergara, Robert Weiss, Fred Wigley, Robert A. Wise, Fred A. Wright, Mark M. Wurfel, Robert Zanni, Fei Zou, Phil Green, Jay Shendure, Joshua M. Akey, Carlos D. Bustamante, Evan E. Eichler, P. Keolu Fox, Wenqing Fu, Adam Gordon, Simon Gravel, Jill M. Johnsen, Mengyuan Kan, Eimear E. Kenny, Jeffrey M. Kidd, Fremiet Lara-Garduno, Suzanne M. Leal, Dajiang J. Liu, Sean McGee, Timothy D. O’Connor, Bryan Paeper, Peggy D. Robertson, Jeffrey C. Staples, Jacob A. Tennessen, Gao Wang, Qian Yi, Rebecca Jackson, Garnet Anderson, Hoda Anton-Culver, Paul L. Auer, Shirley Beresford, Henry Black, Robert Brunner, Robert Brzyski, Dale Burwen, Bette Caan, Cara L. Carty, Rowan Chlebowski, Steven Cummings, J. David Curb, Charles B. Eaton, Leslie Ford, Stephanie M. Fullerton, Margery Gass, Nancy Geller, Gerardo Heiss, Barbara V. Howard, Li Hsu, Carolyn M. Hutter, John Ioannidis, Karen C. Johnson, Lewis Kuller, Andrea LaCroix, Kamakshi Lakshminarayan, Dorothy Lane, Norman Lasser, Erin LeBlanc, Kuo-Ping Li, Marian Limacher, Benjamin A. Logsdon, Shari Ludlam, JoAnn E. Manson, Karen Margolis, Lisa Martin, Joan McGowan, Keri L. Monda, Jane Morley Kotchen, Lauren Nathan, Judith Ockene, Mary Jo O’Sullivan, Lawrence S. Phillips, Ross L. Prentice, John Robbins, Jacques E. Rossouw, Haleh Sangi-Haghpeykar, Gloria E. Sarto, Sally Shumaker, Michael S. Simon, Marcia L. Stefanick, Evan Stein, Hua Tang, Kira C. Taylor, Cynthia A. Thomson, Timothy A. Thornton, Linda Van Horn, Mara Vitolins, Jean Wactawski-Wende, Robert Wallace, Sylvia Wassertheil-Smoller, Donglin Zeng, Deborah Applebaum-Bowden, Michael Feolo, Weiniu Gan, Dina N. Paltoo, Phyliss Sholinsky, Anne Sturcke
Publikováno v:
American Journal of Human Genetics, 94(2), 233-245. Cell Press
American Journal of Human Genetics, 94(2), 233-45. Cell Press
American Journal of Human Genetics, 94(2), 233-45. Cell Press
Elevated low-density lipoprotein cholesterol (LDL-C) is a treatable, heritable risk factor for cardiovascular disease. Genome-wide association studies (GWASs) have identified 157 variants associated with lipid levels but are not well suited to assess
Autor:
Mark S. Guyer, Mark I. McCarthy, Assya Abdallah, Bree Berghuis, Fernando U. Garcia, Manolis Kellis, Robin Burges, Karna Robinson, Jeffery P. Struewing, Daphne Koller, John T. Lonsdale, Leslie Derr, Roger Little, Bryan Gillard, Edmund Lo, Penelope Williams, Sara Mostafavi, Deborah C. Mash, Gary Walters, Johnelle Fleming, Alexander Thomson, David S. DeLuca, Norma Diaz-Mayoral, Timothée Flutre, Kevin Groch, MacArthur Daniel MacArthur, Zhidong Tu, Jean Monlong, Eric R. Gamazon, Steve Buia, Gary F. Temple, Susan E. Koester, Manual Rivas, Matthew Stevens, Saboor Shad, Wendy Winckler, Patrick Bender, Charles Shive, Harold Magazine, Ellen Gelfand, Helen F. Moore, Mike Moser, Nancy Young, Dan Maxim, Ivan Rusyn, Nataliya Sharopova, Andrew B. Nobel, Anuar Konkashbaev, Richard Hasz, David Tabor, Thomas R. Insel, Leslie H. Sobin, Jun Liu, Eric D. Green, Deborah Colantuoni, Xiaoquan Wen, Kenyon Erickson, Mike Feolo, Mike Salvatore, George B. Grant, Kim Valentino, Eddie Cortadillo, Yvonne Marcus, Julian Maller, Sreenath Nampally, Anne Sturcke, John Syron, Jimmie B. Vaught, Jun Zhu, Hae Kyung Im, Liqun Qi, Mark Cosentino, Heather M. Traino, Thomas Lehner, Jason Bridge, Carolyn C. Compton, Barbara A. Foster, Michael Sammeth, Nicole C. Lockhart, Alexis Battle, Kimberley Ramsey, Laura A. Siminoff, Gad Getz, Joanne P. Demchok, Mary Kennedy, Justin Paschal, Angela Zimmerman, Kristin Feenstra, Ellen Karasik, Laura Barker, Jonathan K. Pritchard, Elizabeth J. Thomson, Deborah Bradbury, Molly Donovan, Yin Yao, Kristin G. Ardlie, Philip Harbach, Daniel C. Rohrer, Eric Hudson, James A. Robb, Roderic Guigó, Taylor Young, Elizabeth L. Wilder, Rebecca Phillips, Nancy J. Cox, Andrey A. Shabalin, Phillip Branton, Susan L. Sullivan, James M. Anderson, Fred A. Wright, Simona Volpi, Joy T. Boyer, Cathy Ng, Emmanouil T. Dermitzakis, Tuuli Lappalainen, Margaret J. Basile, Maghboeba Mosavel, Jeffrey Thomas, Scott D. Jewell, Yan Meng, Dana Filkins, Dan L. Nicolae, Lisa Turner, Sherilyn Sawyer, Anna M. Smith, Greg E. Korzeniewski, Theresa Engel
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2013, 45 (6), pp.580-5. ⟨10.1038/ng.2653⟩
PMC
Nature Genetics, Nature Publishing Group, 2013, 45 (6), pp.580-585. ⟨10.1038/ng.2653⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature Genetics 6 (45), 580-5. (2013)
Nature Genetics, Nature Publishing Group, 2013, 45 (6), pp.580-5. ⟨10.1038/ng.2653⟩
PMC
Nature Genetics, Nature Publishing Group, 2013, 45 (6), pp.580-585. ⟨10.1038/ng.2653⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature Genetics 6 (45), 580-5. (2013)
Genome-wide association studies have identified thousands of loci for common diseases, but, for the majority of these, the mechanisms underlying disease susceptibility remain unknown. Most associated variants are not correlated with protein-coding ch
Autor:
MÓNIKA, NOGEL1
Publikováno v:
Information Society / Információs Társadalom (InfTars). 2022, Vol. 22 Issue 3, p39-60. 22p.
Autor:
Hardy, Dale S.1 (AUTHOR) Shardy30@aol.com, Racette, Susan B.2 (AUTHOR), Garvin, Jane T.3 (AUTHOR), Gebrekristos, Hirut T.1 (AUTHOR), Mersha, Tesfaye B.4 (AUTHOR)
Publikováno v:
BMC Medical Genomics. 5/1/2021, Vol. 14 Issue 1, p1-20. 20p.
Autor:
Rosenthal, Elisabeth A., Shirts, Brian H., Amendola, Laura M., Horike-Pyne, Martha, Robertson, Peggy D., Hisama, Fuki M., Bennett, Robin L., Dorschner, Michael O., Nickerson, Deborah A., Stanaway, Ian B., Nassir, Rami, Vickers, Kathy T., Li, Christopher, Grady, William M., Peters, Ulrike, Jarvik, Gail P., NHLBI GO Exome Sequencing Project
Publikováno v:
Human Genetics; Oct2018, Vol. 137 Issue 10, p795-806, 12p