Search Results - Timothy R. Fennell

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  1. 1
    Design and Synthesis of Cannabinoid Receptor 1 Antagonists for Peripheral Selectivity

    Design and Synthesis of Cannabinoid Receptor 1 Antagonists for Peripheral Selectivity by Alan Fulp, Katherine Bortoff, Herbert H. Seltzman, Yanan Zhang, James M. Mathews, Rodney W. Snyder, Timothy R. Fennell, Rangan Maitra

    Published 2012
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  2. 2
    Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries

    Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries by Daniel Aird, Michael Ross, Wei‐Sheng Chen, Maxwell Danielsson, Timothy R. Fennell, Carsten Russ, David B. Jaffe, Chad Nusbaum, Andreas Gnirke

    Published 2011
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  3. 3
    Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts

    Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts by Joshua Z. Levin, Michael F. Berger, Xian Adiconis, Peter Rogov, Alexandre Melnikov, Timothy R. Fennell, Chad Nusbaum, Levi A. Garraway, Andreas Gnirke

    Published 2009
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  4. 4
    RNA-SeQC: RNA-seq metrics for quality control and process optimization

    RNA-SeQC: RNA-seq metrics for quality control and process optimization by David S. DeLuca, Joshua Z. Levin, Andrey Sivachenko, Timothy R. Fennell, Marc-Danie Nazaire, Chris Williams, Michael Reich, Wendy Winckler, Gad Getz

    Published 2012
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  5. 5
    In vitro and in vivo pharmacokinetics and metabolism of synthetic cannabinoids CUMYL-PICA and 5F-CUMYL-PICA

    In vitro and in vivo pharmacokinetics and metabolism of synthetic cannabinoids CUMYL-PICA and 5F-CUMYL-PICA by Richard C. Kevin, Timothy W. Lefever, Rodney W. Snyder, Purvi R. Patel, Timothy R. Fennell, Jenny L. Wiley, Iain S. McGregor, Brian F. Thomas

    Published 2017
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  6. 6
    Comparative analysis of RNA sequencing methods for degraded or low-input samples

    Comparative analysis of RNA sequencing methods for degraded or low-input samples by Xian Adiconis, Diego Borges-Rivera, Rahul Satija, David S. DeLuca, Michele Busby, Aaron M. Berlin, Andrey Sivachenko, Dawn Thompson, Alec Wysoker, Timothy R. Fennell, Andreas Gnirke, Nathalie Pochet, Aviv Regev, Joshua Z. Levin

    Published 2013
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  7. 7
    Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

    Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing by Andreas Gnirke, Alexandre Melnikov, Jared Maguire, Peter Rogov, Emily M LeProust, William W. Brockman, Timothy R. Fennell, Georgia Giannoukos, Sheila Fisher, Carsten Russ, Stacey Gabriel, David B. Jaffe, Eric S. Lander, Chad Nusbaum

    Published 2009
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  8. 8
    The genomic complexity of primary human prostate cancer

    The genomic complexity of primary human prostate cancer by Michael F. Berger, Michael S. Lawrence, Francesca Demichelis, Yotam Drier, Kristian Cibulskis, Andrey Sivachenko, Andrea Sboner, Raquel Esgueva, Dorothee Pflueger, Carrie Sougnez, Robert C. Onofrio, Scott L. Carter, Kyung Park, Lukas Habegger, Lauren Ambrogio, Timothy R. Fennell, Melissa Parkin, Gordon Saksena, Douglas Voet, Alex H. Ramos, Trevor J. Pugh, Jane Wilkinson, Sheila Fisher, Wendy Winckler, Scott Mahan, Kristin Ardlie, Jennifer Baldwin, Jonathan W. Simons, Naoki Kitabayashi, Theresa Y. MacDonald, Philip W. Kantoff, Lynda Chin, Stacey Gabriel, Mark Gerstein, Todd R. Golub, Matthew Meyerson, Ashutosh Tewari, Eric S. Lander, Gad Getz, Mark A. Rubin, Levi A. Garraway

    Published 2011
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  9. 9
    Melanoma genome sequencing reveals frequent PREX2 mutations

    Melanoma genome sequencing reveals frequent PREX2 mutations by Michael F. Berger, Eran Hodis, Timothy P. Heffernan, Yonathan Lissanu Deribe, Michael S. Lawrence, Alexei Protopopov, Elena Ivanova, Ian R. Watson, Elizabeth Nickerson, Papia Ghosh, Hailei Zhang, Rhamy Zeid, Xiaojia Ren, Kristian Cibulskis, Andrey Sivachenko, Nikhil Wagle, Antje Sucker, Carrie Sougnez, Robert C. Onofrio, Lauren Ambrogio, Daniel Auclair, Timothy R. Fennell, Scott L. Carter, Yotam Drier, Petar Stojanov, Meredith A. Singer, Douglas Voet, Rui Jing, Gordon Saksena, Jordi Barretina, Alex H. Ramos, Trevor J. Pugh, Nicolas Stransky, Melissa Parkin, Wendy Winckler, Scott Mahan, Kristin Ardlie, Jennifer Baldwin, Jennifer A. Wargo, Dirk Schadendorf, Matthew Meyerson, Stacey Gabriel, Todd R. Golub, Stephan N. Wagner, Eric S. Lander, Gad Getz, Lynda Chin, Levi A. Garraway

    Published 2012
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  10. 10
    Association of a Low-Frequency Variant in<i>HNF1A</i>With Type 2 Diabetes in a Latino Population

    Association of a Low-Frequency Variant in<i>HNF1A</i>With Type 2 Diabetes in a Latino Population by Karol Estrada, Ingvild Aukrust, Lise Bjørkhaug, Noël P. Burtt, Josep M. Mercader, Humberto Garcia‐Ortíz, Alicia Huerta-Chagoya, Hortensia Moreno-Macías, Geoffrey Walford, Jason Flannick, Amy L. Williams, María José Gómez-Vázquez, Juan Carlos Fernández-López, Angélica Martínez‐Hernández, Federico Centeno-Cruz, Elvia Mendoza‐Caamal, M. Revilla, Sergio Islas‐Andrade, Emilio J. Córdova, Xavier Soberón, María Elena González-Villalpando, Elizabeth Henderson, Lynne R. Wilkens, Loı̈c Le Marchand, Olimpia Arellano‐Campos, María Luisa Ordóñez-Sánchez, M. Rodríguez‐Torres, Rosario Rodríguez-Guillén, Laura Riba, Laeya A. Najmi, Suzanne B.R. Jacobs, Timothy R. Fennell, Stacey Gabriel, Pierre Fontanillas, Craig L. Hanis, Donna M. Lehman, Christopher P. Jenkinson, Hanna E. Abboud, Graeme I. Bell, Maria L. Cortés, Michael Boehnke, Clicerio González‐Villalpando, Lorena Orozco, Christopher A. Haiman, Teresa Tusié‐Luna, Carlos A. Aguilar‐Salinas, David Altshuler, Pål R. Njølstad, José C. Florez, Daniel G. MacArthur

    Published 2014
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  11. 11
    Mutational heterogeneity in cancer and the search for new cancer-associated genes

    Mutational heterogeneity in cancer and the search for new cancer-associated genes by Michael S. Lawrence, Petar Stojanov, Paz Polak, Gregory V. Kryukov, Kristian Cibulskis, Andrey Sivachenko, Scott L. Carter, Chip Stewart, Craig H. Mermel, Steven A. Roberts, Adam Kieżun, Peter S. Hammerman, Aaron McKenna, Yotam Drier, Lihua Zou, Alex H. Ramos, Trevor J. Pugh, Nicolas Stransky, Elena Helman, Jaegil Kim, Carrie Sougnez, Lauren Ambrogio, Elizabeth Nickerson, Erica Shefler, Maria L. Cortés, Daniel Auclair, Gordon Saksena, Douglas Voet, Michael S. Noble, Daniel DiCara, Pei Lin, Lee Lichtenstein, David I. Heiman, Timothy R. Fennell, Marcin Imieliński, Bryan Hernandez, Eran Hodis, Sylvan C. Baca, Austin Dulak, Jens G. Lohr, Dan-Avi Landau, Catherine J. Wu, Jorge Meléndez-Zajgla, Alfredo Hidalgo‐Miranda, Amnon Koren, Steven A. McCarroll, Jaume Mora, Ryan S. Lee, Brian D. Crompton, Robert C. Onofrio, Melissa Parkin, Wendy Winckler, Kristin Ardlie, Stacey Gabriel, Charles W.M. Roberts, Jaclyn A. Biegel, Kimberly Stegmaier, Adam J. Bass, Levi A. Garraway, Matthew Meyerson, Todd R. Golub, Dmitry A. Gordenin, Shamil Sunyaev, Eric S. Lander, Gad Getz

    Published 2013
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  12. 12
    Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

    Loss-of-function mutations in SLC30A8 protect against type 2 diabetes by Jason Flannick, Guðmar Þorleifsson, Nicola L. Beer, Suzanne B.R. Jacobs, Niels Grarup, Noël P. Burtt, Anubha Mahajan, Christian Fuchsberger, Gil Atzmon, Rafn Benediktsson, John Blangero, D. W. Bowden, Ivan Brandslund, Julia Brosnan, Frank Burslem, John C. Chambers, Yoon Shin Cho, Cramer Christensen, Desirée A. Douglas, Ravindranath Duggirala, Zachary Dymek, Yossi Farjoun, Timothy R. Fennell, Pierre Fontanillas, Tom Forsén, Stacey Gabriel, Benjamin Gläser, Daníel F. Guðbjartsson, Craig L. Hanis, Torben Hansen, Ástráður B. Hreiðarsson, Kristian Hveem, Erik Ingelsson, Bo Isomaa, Stefan Johansson, Torben Jørgensen, Marit E. Jørgensen, Sekar Kathiresan, Augustine Kong, Jaspal S. Kooner, Jasmina Kravić, Markku Laakso, Jong‐Young Lee, Lars Lind, Cecilia M. Lindgren, Allan Linneberg, Gísli Másson, Thomas Meitinger, Karen L. Mohlke, Anders Molven, Andrew P. Morris, Shobha Potluri, Rainer Rauramaa, Rasmus Ribel‐Madsen, Ann-Marie Richard, Tim Rolph, Veikko Salomaa, Ayellet V. Segrè, Hanna Skärstrand, Valgerður Steinthórsdóttir, Heather M. Stringham, Patrick Sulem, E Shyong Tai, Yik Ying Teo, Tanya M. Teslovich, Unnur Þorsteinsdóttir, Jeff K. Trimmer, Jaakko Tuomilehto, Jaakko Tuomilehto, Fariba Vaziri‐Sani, Benjamin F. Voight, James G. Wilson, Michael Boehnke, Mark I. McCarthy, Pål R. Njølstad, Oluf Pedersen, Leif Groop, David R. Cox, Kāri Stefánsson, David Altshuler

    Published 2014
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  13. 13
    Analysis of protein-coding genetic variation in 60,706 humans

    Analysis of protein-coding genetic variation in 60,706 humans by Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel, Kaitlin E. Samocha, Eric Banks, Timothy R. Fennell, Anne O’Donnell‐Luria, James S. Ware, Andrew Hill, Beryl B. Cummings, Taru Tukiainen, Daniel P. Birnbaum, Jack A. Kosmicki, Laramie E. Duncan, Karol Estrada, Fengmei Zhao, James Zou, Emma Pierce‐Hoffman, Joanne Berghout, D.N. Cooper, Nicole Deflaux, Mark A. DePristo, Ron Do, Jason Flannick, Menachem Fromer, Laura D. Gauthier, Jackie Goldstein, Namrata Gupta, Daniel P. Howrigan, Adam Kieżun, Mitja Kurki, Ami Levy Moonshine, Pradeep Natarajan, Lorena Orozco, Gina M. Peloso, Ryan Poplin, Manuel A. Rivas, Valentín Ruano-Rubio, Samuel A. Rose, Douglas M. Ruderfer, Khalid Shakir, Peter D. Stenson, Christine Stevens, Brett Thomas, Grace Tiao, Maria T. Tusie-Luna, Ben Weisburd, Hong‐Hee Won, Dongmei Yu, David Altshuler, Diego Ardissino, Michael Boehnke, John Danesh, Stacey Donnelly, Roberto Elosúa, José C. Florez, Stacey Gabriel, Gad Getz, Stephen J. Glatt, Christina M. Hultman, Sekar Kathiresan, Markku Laakso, Steven A. McCarroll, Mark I. McCarthy, Dermot McGovern, Ruth McPherson, Benjamin M. Neale, Aarno Palotie, Shaun Purcell, Danish Saleheen, Jeremiah M. Scharf, Pamela Sklar, Patrick F. Sullivan, Jaakko Tuomilehto, Ming T. Tsuang, Hugh Watkins, James G. Wilson, Mark J. Daly, Daniel G. MacArthur

    Published 2016
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  14. 14
    Analysis of protein-coding genetic variation in 60,706 humans

    Analysis of protein-coding genetic variation in 60,706 humans by Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel, Kaitlin E. Samocha, Eric Banks, Timothy R. Fennell, Anne O’Donnell‐Luria, James S. Ware, Andrew Hill, Beryl B. Cummings, Taru Tukiainen, Daniel P. Birnbaum, Jack A. Kosmicki, Laramie E. Duncan, Karol Estrada, Fengmei Zhao, James Zou, Emma Pierce‐Hoffman, Joanne Berghout, D.N. Cooper, Nicole Deflaux, Mark A. DePristo, Ron Do, Jason Flannick, Menachem Fromer, Laura D. Gauthier, Jackie Goldstein, Namrata Gupta, Daniel P. Howrigan, Adam Kieżun, Mitja Kurki, Ami Levy Moonshine, Pradeep Natarajan, Lorena Orozco, Gina M. Peloso, Ryan Poplin, Manuel A. Rivas, Valentín Ruano-Rubio, Samuel A. Rose, Douglas M. Ruderfer, Khalid Shakir, Peter D. Stenson, Christine Stevens, Brett Thomas, Grace Tiao, Maria T. Tusie-Luna, Ben Weisburd, Hong‐Hee Won, Dongmei Yu, David Altshuler, Diego Ardissino, Michael Boehnke, John Danesh, Stacey Donnelly, Roberto Elosúa, José C. Florez, Stacey Gabriel, Gad Getz, Stephen J. Glatt, Christina M. Hultman, Sekar Kathiresan, Markku Laakso, Steven A. McCarroll, Mark I. McCarthy, Dermot McGovern, Ruth McPherson, Benjamin M. Neale, Aarno Palotie, Shaun Purcell, Danish Saleheen, Jeremiah M. Scharf, Pamela Sklar, Patrick F. Sullivan, Jaakko Tuomilehto, Ming T. Tsuang, Hugh Watkins, James G. Wilson, Mark J. Daly, Daniel G. MacArthur

    Published 2015
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  15. 15
    Analysis of protein-coding genetic variation in 60,706 humans

    Analysis of protein-coding genetic variation in 60,706 humans by Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel, Kaitlin E. Samocha, Eric Banks, Timothy R. Fennell, Anne O’Donnell‐Luria, James S. Ware, Andrew J. Hill, Beryl B. Cummings, Taru Tukiainen, Daniel P. Birnbaum, Jack A. Kosmicki, Laramie E. Duncan, Karol Estrada, Fengmei Zhao, James Zou, Emma Pierce‐Hoffman, Joanne Berghout, D.N. Cooper, Nicole Deflaux, Mark A. DePristo, Ron Do, Jason Flannick, Menachem Fromer, Laura D. Gauthier, Jackie Goldstein, Namrata Gupta, Daniel P. Howrigan, Adam Kieżun, Mitja Kurki, Ami Levy Moonshine, Pradeep Natarajan, Lorena Orozco, Gina M. Peloso, Ryan Poplin, Manuel A. Rivas, Valentín Ruano-Rubio, Samuel A. Rose, Douglas M. Ruderfer, Khalid Shakir, Peter D. Stenson, Christine Stevens, Brett Thomas, Grace Tiao, Maria T. Tusie-Luna, Ben Weisburd, Hong‐Hee Won, Dongmei Yu, David Altshuler, Diego Ardissino, Michael Boehnke, John Danesh, Stacey Donnelly, Roberto Elosúa, José C. Florez, Stacey Gabriel, Gad Getz, Stephen J. Glatt, Christina M. Hultman, Sekar Kathiresan, Markku Laakso, Steven A. McCarroll, Mark I. McCarthy, Dermot McGovern, Ruth McPherson, Benjamin M. Neale, Aarno Palotie, Shaun Purcell, Danish Saleheen, Jeremiah M. Scharf, Pamela Sklar, Patrick F. Sullivan, Jaakko Tuomilehto, Ming T. Tsuang, Hugh Watkins, James G. Wilson, Mark J. Daly, Daniel G. MacArthur, Abboud, Abecasis, Aguilar-Salinas, Arellano-Campos, Atzmon, Aukrust, Barr, Bell, Bergen, Bjørkhaug, Blangero, Bowden, Budman, Burtt, Centeno-Cruz, Chambers, Chambert, Clarke, Collins, Coppola, Córdova

    Published 2016
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  16. 16
    Integrated Genomic Characterization of Papillary Thyroid Carcinoma

    Integrated Genomic Characterization of Papillary Thyroid Carcinoma by Nishant Agrawal, Rehan Akbani, Bülent Arman Aksoy, Adrian Ally, Harindra Arachchi, L. Sylvia, J. Todd Auman, Miruna Balasundaram, Saianand Balu, Stephen B. Baylin, Madhusmita Behera, Brady Bernard, Rameen Beroukhim, Justin A. Bishop, Aaron D. Black, Tom Bodenheimer, Lori Boice, Arnoud Boot, Jay Bowen, Reanne Bowlby, Christopher A. Bristow, Robin Brookens, Denise Brooks, Robert Bryant, Elizabeth Buda, Yaron S.N. Butterfield, Tobias Carling, Rebecca Carlsen, Scott L. Carter, Sally E. Carty, Timothy A. Chan, Amy Y. Chen, Andrew D. Cherniack, Dorothy Cheung, Lynda Chin, Juok Cho, Andy Chu, Eric Chuah, Kristian Cibulskis, Giovanni Ciriello, Amanda Clarke, Gary L. Clayman, Leslie Cope, John A. Copland, Kyle R. Covington, Ludmila Danilova, Tanja M. Davidsen, John A. Demchok, Daniel DiCara, Noreen Dhalla, Rajiv Dhir, Sheliann S. Dookran, Gideon Dresdner, Jonathan Eldridge, Greg Eley, Adel K. El‐Naggar, Stephanie Eng, James A. Fagin, Timothy R. Fennell, Robert L. Ferris, Sheila Fisher, Scott Frazer, Jessica Frick, Stacey Gabriel, Ian Ganly, Jianjiong Gao, Levi A. Garraway, Julie M. Gastier-Foster, Gad Getz, Nils Gehlenborg, Ronald Ghossein, Richard A. Gibbs, Thomas J. Giordano, Karen Gomez-Hernandez, Jonna Grimsby, Benjamin Groß, Ranabir Guin, Angela Hadjipanayis, Hollie A. Harper, D. Neil Hayes, David I. Heiman, James G. Herman, Katherine A. Hoadley, Matan Hofree, Robert A. Holt, Alan P. Hoyle, Franklin W. Huang, Mei Huang, Carolyn M. Hutter, Trey Ideker, Lisa Iype, Anders J. Skanderup, Joshua M. Stuart, Corbin D. Jones, Steven J.M. Jones, L. Sylvia, Electron Kebebew, Fadlo R. Khuri, Jaegil Kim, Roger Kramer

    Published 2014
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  17. 17
    Genomic Classification of Cutaneous Melanoma

    Genomic Classification of Cutaneous Melanoma by Rehan Akbani, Kadir C. Akdemir, Bülent Arman Aksoy, Monique Albert, Adrian Ally, Samirkumar B. Amin, Harindra Arachchi, Arshi Arora, J. Todd Auman, Brenda Ayala, Julien Baboud, Miruna Balasundaram, Saianand Balu, Nandita Barnabas, Thomas John, Pam Bartlett, Boris C. Bastian, Stephen B. Baylin, Madhusmita Behera, D. K. Belyaev, Christopher C. Benz, Brady Bernard, Rameen Beroukhim, Natalie Bir, Aaron D. Black, Tom Bodenheimer, Lori Boice, Genevieve M. Boland, R. Bono, Moiz Bootwalla, Marcus Bosenberg, Jay Bowen, Reanne Bowlby, Christopher A. Bristow, Laura Brockway-Lunardi, Denise Brooks, Jakub Brzezinski, Wiam Bshara, Elizabeth Buda, William R. Burns, Yaron S.N. Butterfield, M. Button, Tiffany L. Calderone, Giancarlo Antonini Cappellini, Candace Carter, Scott L. Carter, Lynn Cherney, Andrew D. Cherniack, Aaron Chevalier, Lynda Chin, Juok Cho, Raymond J. Cho, Yoon‐La Choi, Andy Chu, Sudha Chudamani, Kristian Cibulskis, Giovanni Ciriello, Amanda Clarke, Stephen W. Coons, Leslie Cope, Daniel Crain, Erin Curley, Ludmila Danilova, Stefania D’Atri, Tanja M. Davidsen, Michael A. Davies, Keith A. Delman, John A. Demchok, Qing Deng, Yonathan Lissanu Deribe, Noreen Dhalla, Rajiv Dhir, Daniel DiCara, М С Диникин, Michael Dubina, J. Stephen Ebrom, Sophie Egea, Greg Eley, Jay Engel, Jennifer Eschbacher, Konstantin Fedosenko, Ina Felau, Timothy R. Fennell, Martin L. Ferguson, Sheila Fisher, Keith T. Flaherty, Scott Frazer, Jessica Frick, Victoria Fulidou, Stacey Gabriel, Jianjiong Gao, Johanna Gardner, Levi A. Garraway, Julie M. Gastier-Foster, Carmelo Gaudioso, Nils Gehlenborg, Giannicola Genovese, Mark Gerken, Hui Shen, Gad Getz

    Published 2015
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  18. 18
    Rare variants in <i>PPARG</i> with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

    Rare variants in <i>PPARG</i> with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes by Amit R. Majithia, Jason Flannick, Peter Shahinian, Michael H. Guo, Mark‐Anthony Bray, Pierre Fontanillas, Stacey Gabriel, Evan D. Rosen, David Altshuler, Jason Flannick, Man Li, Christopher Hartl, Vineeta Agarwala, Pierre Fontanillas, Todd J. Green, Eric Banks, Mark A. DePristo, Ryan Poplin, Khalid Shakir, Timothy R. Fennell, Pål R. Njølstad, David Altshuler, Noël P. Burtt, Stacey Gabriel, Christian Fuchsberger, Hun Min Kang, Xueling Sim, Clement Ma, Adam E. Locke, Thomas W. Blackwell, Anne Jackson, Tanya M. Teslovich, Heather M. Stringham, Peter S. Chines, Phoenix Kwan, Jeroen R. Huyghe, Adrian Y. Tan, Goo Jun, Michael L. Stitzel, Richard N. Bergman, Lori L. Bonnycastle, Jaakko Tuomilehto, Francis S. Collins, Laura J. Scott, Karen L. Mohlke, Gonçalo R. Abecasis, Michael Boehnke, Tim M. Strom, Christian Gieger, Martina Müller‐Nurasyid, Harald Grallert, Jennifer Kriebel, Janina S. Ried, Martin Hrabě de Angelis, Cornelia Huth, Christa Meisinger, Annette Peters, Wolfgang Rathmann, Konstantin Strauch, Thomas Meitinger, Jasmina Kravić, Peter Algren, Claes Ladenvall, Tiinamaija Toumi, Bo Isomaa, Leif Groop, Kyle J. Gaulton, Loukas Moutsianas, Manny Rivas, Richard D. Pearson, Anubha Mahajan, Inga Prokopenko, Ashish Kumar, John R. B. Perry, Bryan Howie, Martijn van de Bunt, Kerrin S. Small, Cecilia M. Lindgren, Gerton Lunter, Neil Robertson, W Rayner, Andrew H. Morris, David Buck, Andrew T. Hattersley, Tim D. Spector, Gil McVean, Timothy M. Frayling, Peter Donnelly, Mark I. McCarthy, Namrata Gupta, Herman A. Taylor, Ervin R. Fox, Christopher Newton Cheh, James Wilson, Christopher J. O’Donnell, Sekar Kathiresan, Joel N. Hirschhorn, J G Seidman, Stacey Gabriel, Christine E. Seidman

    Published 2014
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  19. 19
    A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

    A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk by Alisa K. Manning, Heather M. Highland, Jessica A. Gasser, Xueling Sim, Taru Tukiainen, Pierre Fontanillas, Niels Grarup, Manuel A. Rivas, Anubha Mahajan, Adam E. Locke, Pablo Cingolani, Tune H. Pers, Ana Viñuela, Andrew Brown, Ying Wu, Jason Flannick, Christian Fuchsberger, Eric R. Gamazon, Kyle J. Gaulton, Hae Kyung Im, Tanya M. Teslovich, Thomas W. Blackwell, Jette Bork‐Jensen, Noël P. Burtt, Yuhui Chen, Todd J. Green, Christopher Hartl, Hyun Min Kang, Ashish Kumar, Claes Ladenvall, Clement Ma, Loukas Moutsianas, Richard D. Pearson, John R. B. Perry, Nigel W. Rayner, Neil R. Robertson, Laura J. Scott, Martijn van de Bunt, Johan G. Eriksson, Antti Jula, Seppo Koskinen, Terho Lehtimäki, Aarno Palotie, Olli T. Raitakari, Suzanne B.R. Jacobs, Jennifer Wessel, Audrey Y. Chu, Robert A. Scott, Mark O. Goodarzi, Christine Blancher, Gemma Buck, David Buck, Peter S. Chines, Stacey Gabriel, Anette P. Gjesing, Christopher J. Groves, Mette Hollensted, Jeroen R. Huyghe, Anne Jackson, Goo Jun, Johanne Marie Justesen, Massimo Mangino, Jacquelyn Murphy, Matt J. Neville, Robert C. Onofrio, Kerrin S. Small, Heather M. Stringham, Joseph Trakalo, Eric Banks, Jason Carey, Mauricio O. Carneiro, Mark A. DePristo, Yossi Farjoun, Timothy R. Fennell, Jacqueline I. Goldstein, George Grant, Martin Hrabě de Angelis, Jared Maguire, Benjamin M. Neale, Ryan Poplin, Shaun Purcell, Thomas Schwarzmayr, Khalid Shakir, Joshua D. Smith, Tim M. Strom, Thomas Wieland, Jaana Lindström, Ivan Brandslund, Cramer Christensen, Gabriela Surdulescu, Timo A. Lakka, Alex S. F. Doney, Peter M. Nilsson, Nicholas J. Wareham, Claudia Langenberg, Tibor V. Varga, Paul W. Franks, Olov Rolandsson, Anders H. Rosengren, Vidya S. Farook

    Published 2017
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  20. 20
    Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

    Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico by A. L. Williams Amy, S. B R Jacobs Suzanne, Hortensia Moreno-Macías, Alicia Huerta-Chagoya, Claire Churchhouse, Carla Márquez‐Luna, María José Gómez-Vázquez, N. P. Burtt Noël, Carlos A. Aguilar‐Salinas, Clicerio González‐Villalpando, José C. Florez, Lorena Orozco, Teresa Tusié‐Luna, David Altshuler, Stephan Ripke, Alisa K. Manning, Humberto Garcia‐Ortíz, Benjamin M. Neale, David Reich, Daniel O. Stram, Juan Carlos Fernández-López, Sandra Romero‐Hidalgo, Nick Patterson, Christopher A Haiman, Irma Aguilar-Delfín, Angélica Martínez‐Hernández, Federico Centeno-Cruz, Elvia Mendoza‐Caamal, M. Revilla, Sergio Islas‐Andrade, Emilio J. Córdova, Martha Eunice Rodríguez-Arellano, Xavier Soberón, Jobinse Jose, M. A. González-Villalpando María Elena, Brian E. Henderson, Kristine R. Monroe, Lynne R. Wilkens, Laurence N. Kolonel, Loı̈c Le Marchand, Laura Riba, Ma Luisa, Rosario Rodríguez-Guillén, Ivette Cruz‐Bautista, M. Rodríguez‐Torres, Liliana Muñóz-Hernández, Tamara Sáenz, Donají Gómez, Ulices Alvirde, Robert C. Onofrio, Wendy Brodeur, Diane Gage, Jacquelyn Murphy, Jennifer Franklin, Scott Mahan, Kristin Ardlie, Andrew Crenshaw, Wendy Winckler, Kay Prüfer, M.V. Shunkov, Susanna Sawyer, Udo Stenzel, Janet Kelso, Monkol Lek, Sriram Sankararaman, Daniel G. MacArthur, А. П. Деревянко, Svante Pääbo, Suzanne B.R. Jacobs, Shuba Gopal, James A. Grammatikos, Ian C. P. Smith, Kevin Bullock, Amy Deik, Amanda L. Souza, Kerry A. Pierce, Clary B. Clish, Timothy R. Fennell, Yossi Farjoun, Stacey Gabriel, Myron D. Gross, Mark A. Pereira, Mark Seielstad, Woon‐Puay Koh, E. Shyong Tai, Jason Flannick, Pierre Fontanillas, Andrew P. Morris, Tanya M. Teslovich, Gil Atzmon, John Blangero, Donald W. Bowden, John C. Chambers, Yoon Shin Cho, Ravindranath Duggirala, Benjamin Gläser, Craig L. Hanis, Jaspal S. Kooner, Markku Laakso, Jong‐Young Lee

    Published 2013
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