検索結果 - Deborah Farlow

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  1. 1
    MAP Kinase Pathway Alterations in <i>BRAF</i>-Mutant Melanoma Patients with Acquired Resistance to Combined RAF/MEK Inhibition

    MAP Kinase Pathway Alterations in <i>BRAF</i>-Mutant Melanoma Patients with Acquired Resistance to Combined RAF/MEK Inhibition 著者: Nikhil Wagle, Eliezer M. Van Allen, Daniel J. Treacy, Dennie T. Frederick, Zachary A. Cooper, Amaro Taylor‐Weiner, Mara Rosenberg, Eva M. Goetz, Ryan J. Sullivan, Deborah Farlow, Dennis C. Friedrich, Kristin Anderka, Danielle Perrin, Cory M. Johannessen, Aaron McKenna, Kristian Cibulskis, Gregory V. Kryukov, Eran Hodis, Donald P. Lawrence, Sheila Fisher, Gad Getz, Stacey Gabriel, Scott L. Carter, Keith T. Flaherty, Jennifer A. Wargo, Levi A. Garraway

    出版事項 2013
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    Artigo
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  2. 2
    The Genetic Landscape of Clinical Resistance to RAF Inhibition in Metastatic Melanoma

    The Genetic Landscape of Clinical Resistance to RAF Inhibition in Metastatic Melanoma 著者: Eliezer M. Van Allen, Nikhil Wagle, Antje Sucker, Daniel J. Treacy, Cory M. Johannessen, Eva M. Goetz, Chelsea S. Place, Amaro Taylor‐Weiner, Steven R. Whittaker, Gregory V. Kryukov, Eran Hodis, Mara Rosenberg, Aaron McKenna, Kristian Cibulskis, Deborah Farlow, Lisa Zimmer, Uwe Hillen, Ralf Gutzmer, Simone M. Goldinger, Selma Ugurel, Helen Gogas, Friederike Egberts, Carola Berking, Uwe Trefzer, Carmen Loquai, Benjamin Weide, Jessica C. Hassel, Stacey Gabriel, Scott L. Carter, Gad Getz, Levi A. Garraway, Dirk Schadendorf

    出版事項 2013
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    Artigo
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  3. 3
    Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine

    Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine 著者: Eliezer M. Van Allen, Nikhil Wagle, Petar Stojanov, Danielle Perrin, Kristian Cibulskis, Sara Marlow, Judit Jané‐Valbuena, Dennis C. Friedrich, Gregory V. Kryukov, Scott L. Carter, Aaron McKenna, Andrey Sivachenko, Mara Rosenberg, Adam Kieżun, Douglas Voet, Michael S. Lawrence, Lee Lichtenstein, Jeff Gentry, Franklin W. Huang, Jennifer Fostel, Deborah Farlow, David A. Barbie, Leena Gandhi, Eric S. Lander, Stacy W. Gray, Steven Joffe, Pasi A. Jänne, Judy E. Garber, Laura E. MacConaill, Neal I. Lindeman, Barrett J. Rollins, Philip W. Kantoff, Sheila Fisher, Stacey Gabriel, Gad Getz, Levi A. Garraway

    出版事項 2014
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    Artigo
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  4. 4
    Candidate Gene Association Resource (CARe)

    Candidate Gene Association Resource (CARe) 著者: Yan V. Sun, Guillaume Lettre, Taylor Young, Deborah Farlow, James P. Pirruccello, Kenechi G. Ejebe, Brendan J. Keating, Qiong Yang, Ming‐Huei Chen, Nina Lapchyk, Andrew Crenshaw, Liuda Ziaugra, Anthony Rachupka, Emelia J. Benjamin, L. Adrienne Cupples, Myriam Fornage, Ervin R. Fox, Susan R. Heckbert, Joel N. Hirschhorn, Christopher Newton‐Cheh, Marcia M. Nizzari, Dina N. Paltoo, George Papanicolaou, Sanjay R. Patel, Bruce M. Psaty, Daniel J. Rader, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Herman A. Taylor, Russell P. Tracy, Ramachandran S. Vasan, James G. Wilson, Sekar Kathiresan, Richard R. Fabsitz, Eric Boerwinkle, Stacey Gabriel

    出版事項 2010
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    Artigo
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  5. 5
    Somatic <i>ERCC2</i> Mutations Correlate with Cisplatin Sensitivity in Muscle-Invasive Urothelial Carcinoma

    Somatic <i>ERCC2</i> Mutations Correlate with Cisplatin Sensitivity in Muscle-Invasive Urothelial Carcinoma 著者: Eliezer M. Van Allen, Kent W. Mouw, Philip Kim, Gopa Iyer, Nikhil Wagle, Hikmat Al‐Ahmadie, Cong Zhu, Irina Ostrovnaya, Gregory V. Kryukov, Kevin W. O’Connor, John P. Sfakianos, Ilana Garcia-Grossman, Jaegil Kim, Elizabeth A. Guancial, Richard Bambury, Samira Bahl, Namrata Gupta, Deborah Farlow, Angela Qu, Sabina Signoretti, Justine A. Barletta, Victor E. Reuter, Jesse S. Boehm, Michael S. Lawrence, Gad Getz, Philip W. Kantoff, Bernard H. Bochner, Toni K. Choueiri, Dean F. Bajorin, David B. Solit, Stacey Gabriel, Alan D. D’Andrea, Levi A. Garraway, Jonathan E. Rosenberg

    出版事項 2014
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    Artigo
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  6. 6
    Large-Scale Candidate Gene Analysis in Whites and African Americans Identifies <i>IL6R</i> Polymorphism in Relation to Atrial Fibrillation

    Large-Scale Candidate Gene Analysis in Whites and African Americans Identifies <i>IL6R</i> Polymorphism in Relation to Atrial Fibrillation 著者: Renate B. Schnabel, Kathleen F. Kerr, Steven A. Lubitz, Ermeg L. Alkylbekova, Gregory M. Marcus, Moritz F. Sinner, Jared W. Magnani, Philip A. Wolf, Rajat Deo, Donald M. Lloyd‐Jones, Kathryn L. Lunetta, Reena Mehra, Daniel Levy, Ervin R. Fox, Dan E. Arking, Thomas H. Mosley, Martina Müller‐Nurasyid, Taylor Young, H.‐Erich Wichmann, Sudha Seshadri, Deborah Farlow, Jerome I. Rotter, Elsayed Z. Soliman, Nicole L. Glazer, James G. Wilson, Monique M.B. Breteler, Nona Sotoodehnia, Christopher Newton‐Cheh, Stefan Kääb, Patrick T. Ellinor, Álvaro Alonso, Emelia J. Benjamin, Susan R. Heckbert

    出版事項 2011
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    Artigo
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  7. 7
    Genome-Wide Association Study of Cardiac Structure and Systolic Function in African Americans

    Genome-Wide Association Study of Cardiac Structure and Systolic Function in African Americans 著者: Ervin R. Fox, Solomon K. Musani, Maja Barbalić, Honghuang Lin, Bing Yu, Kofo O. Ogunyankin, Nicholas L. Smith, Abdullah Kutlar, Nicole L. Glazer, Wendy S. Post, Dina N. Paltoo, Daniel L. Dries, Deborah Farlow, Christine W. Duarte, Sharon L. R. Kardia, Kristin J. Meyers, Yan V. Sun, Donna K. Arnett, Amit Patki, Jin Sha, Xiangqin Cui, Tandaw E. Samdarshi, Alan D. Penman, Kirsten Bibbins‐Domingo, Petra Bůžková, Emelia J. Benjamin, David A. Bluemke, Alanna C. Morrison, Gerardo Heiss, J. Jeffrey Carr, Russell P. Tracy, Thomas H. Mosley, Herman A. Taylor, Bruce M. Psaty, Susan R. Heckbert, Thomas P. Cappola, Ramachandran S. Vasan

    出版事項 2012
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    Artigo
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  8. 8
    Exome Sequencing in Suspected Monogenic Dyslipidemias

    Exome Sequencing in Suspected Monogenic Dyslipidemias 著者: Nathan O. Stitziel, Gina M. Peloso, Marianne Abifadel, Angelo B. Cefalù, Sigrid W. Fouchier, Mohammad Mahdi Motazacker, Hayato Tada, Daniel B. Larach, Zuhier Awan, Jorge F. Haller, Clive R. Pullinger, Mathilde Varret, Jean‐Pierre Rabès, Davide Noto, Patrizia Tarugi, Masa-aki Kawashiri, Atsushi Nohara, Masakazu Yamagishi, Marjorie Risman, Rahul C. Deo, Isabelle L. Ruel, Jay Shendure, Deborah A. Nickerson, James G. Wilson, Stephen S. Rich, Namrata Gupta, Deborah Farlow, Benjamin M. Neale, Mark Daly, John P. Kane, Mason W. Freeman, Jacques Genest, Daniel J. Rader, Hiroshi Mabuchi, John J.P. Kastelein, G. Kees Hovingh, Maurizio Averna, Stacey Gabriel, Cathérine Boileau, Sekar Kathiresan

    出版事項 2015
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    Artigo
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  9. 9
    Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies

    Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies 著者: Brendan J. Keating, Sam E. Tischfield, Sarah S. Murray, Tushar Bhangale, Thomas S. Price, Joseph Glessner, Luana Galver, Jeffrey C. Barrett, Struan F.A. Grant, Deborah Farlow, Hareesh Chandrupatla, Thomas Hansen, Saad Ajmal, George Papanicolaou, Yiran Guo, Mingyao Li, Stephanie DerOhannessian, Paul I. W. de Bakker, Swneke D. Bailey, Alexandre Montpetit, Andrew C. Edmondson, Kent D. Taylor, Xiaowu Gai, Susanna S. Wang, Myriam Fornage, Tamim H. Shaikh, Per‐Henrik Groop, Michael Boehnke, Alistair S. Hall, Andrew T. Hattersley, Edward C. Frackelton, Nick Patterson, Charleston W. K. Chiang, Cecelia E. Kim, Richard R. Fabsitz, Willem H. Ouwehand, Alkes L. Price, Patricia B. Munroe, Mark J. Caulfield, Thomas A. Drake, Eric Boerwinkle, David Reich, A.S. Whitehead, Thomas P. Cappola, Nilesh J. Samani, Aldons J. Lusis, Eric E. Schadt, James G. Wilson, Wolfgang Köenig, Mark I. McCarthy, Sekar Kathiresan, Stacey B. Gabriel, Hákon Hákonarson, Sonia S. Anand, Muredach P. Reilly, James C. Engert, Deborah A. Nickerson, Daniel J. Rader, Joel N. Hirschhorn, Garret A. FitzGerald

    出版事項 2008
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    Artigo
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  10. 10
    Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project

    Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project 著者: Guillaume Lettre, Cameron D. Palmer, Taylor Young, Kenechi G. Ejebe, Hooman Allayee, Emelia J. Benjamin, Franklyn I. Bennett, Donald W. Bowden, Aravinda Chakravarti, Al Dreisbach, Deborah Farlow, Aaron R. Folsom, Myriam Fornage, Terrence Forrester, Ervin R. Fox, Christopher A. Haiman, Jaana Hartiala, Tamara B. Harris, Stanley L. Hazen, Susan R. Heckbert, Brian E. Henderson, Joel N. Hirschhorn, Brendan J. Keating, Stephen B. Kritchevsky, Emma K. Larkin, Mingyao Li, Megan E. Rudock, Colin A. McKenzie, James B. Meigs, Yang A. Meng, Tom Mosley, Anne B. Newman, Christopher Newton‐Cheh, Dina N. Paltoo, George Papanicolaou, Hon‐Cheong So, Wendy S. Post, Bruce M. Psaty, Atif Qasim, Liming Qu, Daniel J. Rader, Susan Redline, Muredach P. Reilly, Alexander P. Reiner, Stephen S. Rich, Jerome I. Rotter, Yongmei Liu, Peter Shrader, David S. Siscovick, W.H. Wilson Tang, Herman A. Taylor, Russell P. Tracy, Ramachandran S. Vasan, Kevin Waters, Rainford Wilks, James G. Wilson, Richard R. Fabsitz, Stacey Gabriel, Sekar Kathiresan, Eric Boerwinkle

    出版事項 2011
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    Artigo
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  11. 11
    Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

    Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction 著者: Ron Do, Nathan O. Stitziel, Hong‐Hee Won, Anders Berg Jørgensen, Stefano Duga, Pier Angelica Merlini, Adam Kieżun, Martin Farrall, Anuj Goel, Or Zuk, I. Guella, Rosanna Asselta, Leslie A. Lange, Gina M. Peloso, Paul L. Auer, Domenico Girelli, Nicola Martinelli, Deborah Farlow, Mark A. DePristo, Robert Roberts, Alexandre F.R. Stewart, Danish Saleheen, John Danesh, Stephen E. Epstein, Suthesh Sivapalaratnam, G. Kees Hovingh, John J.P. Kastelein, Nilesh J. Samani, Heribert Schunkert, Jeanette Erdmann, Svati H. Shah, William E. Kraus, R. W. Davies, Majid Nikpay, Christopher T. Johansen, Jian Wang, Robert A. Hegele, Eliana Hechter, Winfried März, Marcus E. Kleber, Jie Huang, Andrew D. Johnson, Mingyao Li, Greg Burke, Myron D. Gross, Yongmei Liu, Themistocles L. Assimes, Gerardo Heiss, Ethan M. Lange, Aaron R. Folsom, Herman A. Taylor, Oliviero Olivieri, Anders Hamsten, Robert Clarke, Dermot F. Reilly, Yin Wu, Manuel A. Rivas, Peter Donnelly, Jacques E. Rossouw, Bruce M. Psaty, David M. Herrington, James G. Wilson, Stephen S. Rich, Michael J. Bamshad, Russell P. Tracy, L. Adrienne Cupples, Daniel J. Rader, Muredach P. Reilly, John A. Spertus, Sharon Cresci, Jaana Hartiala, W.H. Wilson Tang, Stanley L. Hazen, Hooman Allayee, Alex P. Reiner, Christopher S. Carlson, Charles Kooperberg, Rebecca D. Jackson, Eric Boerwinkle, Eric S. Lander, Stephen M. Schwartz, David S. Siscovick, Ruth McPherson, Anne Tybjærg‐Hansen, Gonçalo R. Abecasis, Hugh Watkins, Deborah A. Nickerson, Diego Ardissino, Shamil Sunyaev, Christopher J. O’Donnell, David Altshuler, Stacey Gabriel, Sekar Kathiresan

    出版事項 2014
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    Artigo
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  12. 12
    Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

    Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study 著者: Ervin R. Fox, J. Hunter Young, Yali Li, Albert W. Dreisbach, Brendan J. Keating, Solomon K. Musani, Kiang Liu, Alanna C. Morrison, Santhi K. Ganesh, Abdullah Kutlar, Ramachandran S. Vasan, Josef F. Polak, Richard R. Fabsitz, Daniel L. Dries, Deborah Farlow, Susan Redline, Adebowale Adeyemo, Joel N. Hirschorn, Yan V. Sun, Sharon B. Wyatt, Alan D. Penman, Walter Palmas, Jerome I. Rotter, Raymond R. Townsend, Ayo P. Doumatey, Bamidele O. Tayo, Thomas H. Mosley, Helen N. Lyon, Sun Jung Kang, Charles N. Rotimi, Stephen S. Rich, Nora Franceschini, J. David Curb, Lisa W. Martin, Charles B. Eaton, Sharon L. R. Kardia, Herman A. Taylor, Mark J. Caulfield, Georg Ehret, Toby Johnson, Patricia B. Munroe, Kenneth Rice, Murielle Bochud, Andrew D. Johnson, Daniel I. Chasman, Albert V. Smith, Martin D. Tobin, Germaine C. Verwoert, Shih‐Jen Hwang, Vasyl Pihur, Péter Vollenweider, Paul F. O’Reilly, Najaf Amin, Jennifer L. Bragg‐Gresham, Alexander Teumer, Nicole L. Glazer, Lenore J. Launer, Jing Zhao, Yurii S. Aulchenko, Simon Heath, Siim Sõber, Afshin Parsa, Jian’an Luan, Pankaj Arora, Abbas Dehghan, Feng Zhang, Gavin Lucas, Andrew A. Hicks, Anne Jackson, John F. Peden, Toshiko Tanaka, Philipp S. Wild, Igor Rudan, Wilmar Igl, Yuri Milaneschi, Alex Parker, Cristiano Fava, John C. Chambers, Meena Kumari, Min JinGo, Pim van der Harst, Wen Hong Linda Kao, Marketa Sjögren, D. G. Vinay, M Alexander, Yasuharu Tabara, Sue Shaw‐Hawkins, Peter H. Whincup, Yongmei Liu, Gang Shi, Johanna Kuusisto, Mark Seielstad, Xueling Sim, Khanh‐Dung H. Nguyen, Terho Lehtimäki, Giuseppe Matullo, Ying Wu, Tom R. Gaunt, N. Charlotte Onland‐Moret, Matthew N. Cooper

    出版事項 2011
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    Revisão
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  13. 13
    Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

    Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol 著者: 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 M. Peloso, Paul L. Auer, Kuo-ping Li, Jason Flannick, Ji Zhang, Christian Fuchsberger, Kyle J. Gaulton, Cecilia M. Lindgren, Adam E. Locke, Alisa K. Manning, Xueling Sim, Manuel A. Rivas, Oddgeir L. Holmen, Omri Gottesman, Yingchang Lu, Douglas M. Ruderfer, Eli A. Stahl, Qing Duan, Yun Li, Peter Durda, Shuo Jiao, Aaron Isaacs, Albert Hofman, Joshua C. Bis, Adolfo Correa, Michael Griswold, Jóhanna Jakobsdóttir, Albert V. Smith, Pamela J. Schreiner, Mary F. Feitosa, Qunyuan Zhang, Jennifer E. Huffman, Jacy R. Crosby, Christina L. Wassel, Ron Do, Nora Franceschini, Lisa W. Martin, Jennifer G. Robinson, Themistocles L. Assimes, David R. Crosslin, Elisabeth A. Rosenthal, Michael Y. Tsai, Mark J. Rieder, Deborah 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 Guðnason, David S. Siscovick, Myriam Fornage, Ingrid B. Borecki, Caroline Hayward, Igor Rudan, Y. Eugene Chen, Erwin P. Böttinger, Ruth J. F. Loos, Pål Sætrom, Kristian Hveem, Michael Boehnke, Leif Groop, Mark I. McCarthy, Thomas Meitinger, Christie M. Ballantyne, Stacey 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, Gonçalo R. Abecasis, Stephen S. Rich

    出版事項 2014
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    Artigo
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