Ohcanbohtosat - Melissa Parkin

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Aiddostahte ozu
  1. 1
    Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus

    Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Dahkki Robert Graham, Chris Cotsapas, Leela Davies, Rachel Hackett, Christopher J. Lessard, Joanlise M Leon, Noël P. Burtt, Candace Guiducci, Melissa Parkin, Casey Gates, Robert M. Plenge, Timothy W. Behrens, Joan Wither, John D. Rioux, Paul R. Fortin, Deborah Cunninghame Graham, Andrew Wong, Timothy J. Vyse, Mark J. Daly, David Altshuler, Kathy L. Moser, Patrick M. Gaffney

    Almmustuhtton 2008
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  2. 2
    Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion

    Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion Dahkki Adam J. Bass, Michael S. Lawrence, Lear E. Brace, Alex H. Ramos, Yotam Drier, Kristian Cibulskis, Carrie Sougnez, Douglas Voet, Gordon Saksena, Andrey Sivachenko, Rui Jing, Melissa Parkin, Trevor J. Pugh, Roel G.W. Verhaak, Nicolas Stransky, Adam T. Boutin, Jordi Barretina, David B. Solit, Evi Vakiani, Wenlin Shao, Yuji Mishina, Markus Warmuth, José Jiménez, Derek Y. Chiang, Sabina Signoretti, William G. Kaelin, Nicole A. Spardy, William C. Hahn, Yujin Hoshida, Shuji Ogino, Ronald A. DePinho, Lynda Chin, Levi A. Garraway, Charles S. Fuchs, José Baselga, Josep Tabernero, Stacey B. Gabriel, Eric S. Lander, Gad Getz, Matthew Meyerson

    Almmustuhtton 2011
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  3. 3
    The genomic complexity of primary human prostate cancer

    The genomic complexity of primary human prostate cancer Dahkki 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

    Almmustuhtton 2011
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  4. 4
    Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

    Two independent alleles at 6q23 associated with risk of rheumatoid arthritis Dahkki Robert M. Plenge, Chris Cotsapas, Leela Davies, Alkes L. Price, Paul I. W. de Bakker, Julian Maller, Itsik Pe’er, Noël P. Burtt, Brendan Blumenstiel, Matt DeFelice, Melissa Parkin, Rachel Barry, Wendy Winslow, Claire M. Healy, Robert Graham, Benjamin M. Neale, Elena S. Izmailova, Ronenn Roubenoff, Alexander N. Parker, Roberta Glass, Elizabeth W. Karlson, Nancy E. Maher, David A. Hafler, David M. Lee, Michael F. Seldin, Elaine F. Remmers, Annette T. Lee, Leonid Padyukov, Lars Alfredsson, Jonathan Coblyn, Michael E. Weinblatt, Stacey Gabriel, Shaun Purcell, Lars Klareskog, Peter K. Gregersen, Nancy A. Shadick, Mark J. Daly, David Altshuler

    Almmustuhtton 2007
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  5. 5
    The Mutational Landscape of Head and Neck Squamous Cell Carcinoma

    The Mutational Landscape of Head and Neck Squamous Cell Carcinoma Dahkki Nicolas Stransky, Ann Marie Egloff, Aaron D. Tward, Aleksandar D. Kostic, Kristian Cibulskis, Andrey Sivachenko, Gregory V. Kryukov, Michael S. Lawrence, Carrie Sougnez, Aaron McKenna, Erica Shefler, Alex H. Ramos, Petar Stojanov, Scott L. Carter, Douglas Voet, Maria L. Cortés, Daniel Auclair, Michael F. Berger, Gordon Saksena, Candace Guiducci, Robert C. Onofrio, Melissa Parkin, Marjorie Romkes, Joel L. Weissfeld, Raja R. Seethala, Lin Wang, Claudia Rangel‐Escareño, Juan Carlos Fernández-López, Alfredo Hidalgo‐Miranda, Jorge Meléndez-Zajgla, Wendy Winckler, Kristin Ardlie, Stacey Gabriel, Matthew Meyerson, Eric S. Lander, Gad Getz, Todd R. Golub, Levi A. Garraway, Jennifer R. Grandis

    Almmustuhtton 2011
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  6. 6
    Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

    Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing Dahkki Andrew Kirby, Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel, Chun Ye, Daniel Aird, Christine Stevens, James Robinson, Moran N. Cabili, Irit Gat‐Viks, Edward Kelliher, Riza M. Daza, Matthew DeFelice, Helena Hůlková, Jana Sovová, Petr Vyleťal, Corinne Antignac, Mitchell Guttman, Robert E. Handsaker, Danielle Perrin, Scott Steelman, Snævar Sigurðsson, Steven J. Scheinman, Carrie Sougnez, Kristian Cibulskis, Melissa Parkin, Todd J. Green, Elizabeth J. Rossin, Michael C. Zody, Ramnik J. Xavier, Martin R. Pollak, Seth L. Alper, Kerstin Lindblad‐Toh, Stacey B. Gabriel, P. Suzanne Hart, Aviv Regev, Chad Nusbaum, Stanislav Kmoch, Anthony J. Bleyer, Eric S. Lander, Mark J. Daly

    Almmustuhtton 2013
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  7. 7
    Melanoma genome sequencing reveals frequent PREX2 mutations

    Melanoma genome sequencing reveals frequent PREX2 mutations Dahkki 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

    Almmustuhtton 2012
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  8. 8
    Sequence analysis of mutations and translocations across breast cancer subtypes

    Sequence analysis of mutations and translocations across breast cancer subtypes Dahkki Shantanu Banerji, Kristian Cibulskis, Claudia Rangel‐Escareño, Kristin Brown, Scott L. Carter, A. Matsen Frederick, Michael S. Lawrence, Andrey Sivachenko, Carrie Sougnez, Lihua Zou, Maria L. Cortés, Juan Carlos Fernández-López, Shouyong Peng, Kristin Ardlie, Daniel Auclair, Verónica Bautista‐Piña, Fujiko Duke, Joshua M. Francis, Joonil Jung, Antonio Maffuz‐Aziz, Robert C. Onofrio, Melissa Parkin, Nam Pho, Valeria Quintanar‐Jurado, Alex H. Ramos, Rosa Rebollar‐Vega, Sergio Rodrı́guez-Cuevas, Sandra Romero‐Córdoba, Steven E. Schumacher, Nicolas Stransky, Kristin Thompson, Laura Uribe-Figueroa, José Baselga, Rameen Beroukhim, Kornélia Polyák, Dennis C. Sgroi, Andrea L. Richardson, Gerardo Jiménez‐Sánchez, Eric S. Lander, Stacey Gabriel, Levi A. Garraway, Todd R. Golub, Jorge Meléndez-Zajgla, Alex Toker, Gad Getz, Alfredo Hidalgo‐Miranda, Matthew Meyerson

    Almmustuhtton 2012
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  9. 9
    The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits

    The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits Dahkki Benjamin F. Voight, Hyun Min Kang, Jun Ding, Cameron D. Palmer, Carlo Sidore, Peter S. Chines, Noël P. Burtt, Christian Fuchsberger, Yanming Li, Jeanette Erdmann, Timothy M. Frayling, Iris M. Heid, Anne Jackson, Toby Johnson, Tuomas O. Kilpeläinen, Cecilia M. Lindgren, Andrew P. Morris, Inga Prokopenko, Joshua C. Randall, Richa Saxena, Nicole Soranzo, Elizabeth K. Speliotes, Tanya M. Teslovich, Eleanor Wheeler, Jared Maguire, Melissa Parkin, Simon Potter, Nigel W. Rayner, Neil Robertson, Kathleen Stirrups, Wendy Winckler, Serena Sanna, Antonella Mulas, Ramaiah Nagaraja, Francesco Cucca, Inês Barroso, Panos Deloukas, Ruth J. F. Loos, Sekar Kathiresan, Patricia B. Munroe, Christopher Newton‐Cheh, Arne Pfeufer, Nilesh J. Samani, Heribert Schunkert, Joel N. Hirschhorn, David Altshuler, Mark I. McCarthy, Gonçalo R. Abecasis, Michael Boehnke

    Almmustuhtton 2012
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  10. 10
    Correction: The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits

    Correction: The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits Dahkki Benjamin F. Voight, Hyun Min Kang, Jun Ding, Cameron D. Palmer, Carlo Sidore, Peter S. Chines, Noà l P. Burtt, Christian Fuchsberger, Yanming Li, Jeanette Erdmann, Timothy M. Frayling, Iris M. Heid, Anne Jackson, Toby Johnson, Tuomas O. Kilpeläinen, Cecilia M. Lindgren, Andrew P. Morris, Inga Prokopenko, Joshua C. Randall, Richa Saxena, Nicole Soranzo, Elizabeth K. Speliotes, Tanya M. Teslovich, Eleanor Wheeler, Jared Maguire, Melissa Parkin, Simon Potter, Nigel W. Rayner, Neil Robertson, Kathleen Stirrups, Wendy Winckler, Serena Sanna, Antonella Mulas, Ramaiah Nagaraja, Francesco Cucca, Inês Barroso, Panos Deloukas, Ruth J. F. Loos, Sekar Kathiresan, Patricia B. Munroe, Christopher Newton‐Cheh, Arne Pfeufer, Nilesh J. Samani, Heribert Schunkert, Joel N. Hirschhorn, David Altshuler, Mark I. McCarthy, Gonçalo R. Abecasis, Michael Boehnke

    Almmustuhtton 2013
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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 Dahkki 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

    Almmustuhtton 2013
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  12. 12
    Integrating common and rare genetic variation in diverse human populations

    Integrating common and rare genetic variation in diverse human populations Dahkki David Altshuler, Richard A Gibbs, Leena Peltonen, David Altshuler, Richard A Gibbs, Leena Peltonen, Emmanouil T. Dermitzakis, S. F. Schaffner, Fuli Yu, Leena Peltonen, Emmanouil T. Dermitzakis, Penelope E. Bonnen, David Altshuler, Richard A Gibbs, Paul I. W. de Bakker, Panos Deloukas, Stacey B. Gabriel, Rhian Gwilliam, Sarah Hunt, Michael Inouye, Xiaoming Jia, Aarno Palotie, Melissa Parkin, Pamela Whittaker, Fuli Yu, Kyle Chang, Alicia Hawes, Lora Lewis, Yanru Ren, David A. Wheeler, Richard A. Gibbs, Donna M. Muzny, C. Barnes, Katayoon Darvishi, Matthew E. Hurles, Joshua M. Korn, Kati Kristiansson, Charles Lee, Steven A. McCarrol, James Nemesh, Emmanouil T. Dermitzakis, Alon Keinan, Stephen B. Montgomery, Samuela Pollack, Alkes L. Price, Nicole Soranzo, Penelope E. Bonnen, Richard A Gibbs, Claudia Gonzaga‐Jauregui, Alon Keinan, Alkes L. Price, Fuli Yu, Verneri Anttila, Wendy Brodeur, Mark J. Daly, Stephen Leslie, Gil McVean, Loukas Moutsianas, Huy Nguyen, S. F. Schaffner, Qingrun Zhang, Mohammed J. R. Ghori, Ralph McGinnis, William McLaren, Samuela Pollack, Alkes L. Price, S. F. Schaffner, Fumihiko Takeuchi, Sharon R. Grossman, Ilya Shlyakhter, Elizabeth Hostetter, Pardis C. Sabeti, Clement Adebamowo, Morris W. Foster, Deborah R Gordon, Júlio Licinio, María Cristina Manca, Patricia A. Marshall, Ichiro Matsuda, Duncan Ngare, Vivian Ota Wang, Deepa Reddy, Charles N. Rotimi, Charmaine Royal, Richard R. Sharp, Changqing Zeng, Lisa Brooks, Jean E. McEwen

    Almmustuhtton 2010
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  13. 13
    A second generation human haplotype map of over 3.1 million SNPs

    A second generation human haplotype map of over 3.1 million SNPs Dahkki Kelly A. Frazer, Dennis G. Ballinger, David R. Cox, David A. Hinds, Laura L. Stuvé, Richard A. Gibbs, John W. Belmont, Andrew Boudreau, Paul Hardenbol, Suzanne M. Leal, Shiran Pasternak, David A. Wheeler, T. D. Willis, Fuli Yu, Huanming Yang, Changqing Zeng, Yang Gao, Haoran Hu, Weitao Hu, Chaohua Li, Wei Lin, Siqi Liu, Hao Pan, Xiaoli Tang, Jian Wang, Wei Wang, Jun Yu, Bo Zhang, Qingrun Zhang, Hongbin Zhao, Hui Zhao, Jun Zhou, Stacey Gabriel, Rachel Barry, Brendan Blumenstiel, Amy L. Camargo, Matthew DeFelice, Maura Faggart, Mary Goyette, Supriya Gupta, Jamie Moore, Huy Nguyen, Robert C. Onofrio, Melissa Parkin, Jessica Roy, Erich Stahl, Ellen Winchester, Liuda Ziaugra, David Altshuler, Yan Shen, Zhijian Yao, Wei Huang, Xun Chu, Yungang He, Jin Li, Yangfan Liu, Yayun Shen, Weiwei Sun, Haifeng Wang, Yi Wang, Ying Wang, Xiaoyan Xiong, Liang Xu, Mary Miu Yee Waye, Stephen Kwok‐Wing Tsui, Hong Xue, J. Tze‐Fei Wong, Luana Galver, Jian-Bing Fan, Kevin L. Gunderson, Sarah S. Murray, Arnold Oliphant, Mark S. Chee, Alexandre Montpetit, Fanny Chagnon, Vincent Ferretti, Martin Leboeuf, Jean François Olivier, Michael Phillips, Stéphanie Roumy, Clémentine Sallée, Andrei Verner, Thomas J. Hudson, Pui‐Yan Kwok, Dongmei Cai, Daniel C. Koboldt, Raymond D. Miller, Ludmila Pawlikowska, Patricia Taillon‐Miller, Ming Xiao, Lap Chee Tsui, William Mak, You‐Qiang Song, Paul Kwong Hang Tam, Yusuke Nakamura, Takahisa Kawaguchi, Takuya Kitamoto, Takashi Morizono, Atsushi Nagashima, Yozo Ohnishi

    Almmustuhtton 2007
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  14. 14
    Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies

    Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies Dahkki Themistocles L. Assimes, Hilma Hólm, Sekar Kathiresan, Muredach P. Reilly, Guðmar Þorleifsson, Benjamin F. Voight, Jeanette Erdmann, Christina Willenborg, Dhananjay Vaidya, Changchun Xie, C. C. Patterson, Thomas M. Morgan, Mary Susan Burnett, Mingyao Li, Mark A. Hlatky, Joshua W. Knowles, John R. Thompson, Devin Absher, Carlos Iribarren, Alan S. Go, Stephen P. Fortmann, Stephen Sidney, Neil Risch, Hua Tang, Richard M. Myers, Kenneth I. Berger, Monika Stoll, Svati H. Shah, Guðmundur Þorgeirsson, Karl Andersen, Aki S. Havulinna, J. Enrique Herrera, Nauder Faraday, Yoonhee Kim, Brian G. Kral, Rasika A. Mathias, Ingo Ruczinski, Bhoom Suktitipat, Alexander F. Wilson, Lisa R. Yanek, Lewis C. Becker, Patrick Linsel‐Nitschke, Wolfgang Lieb, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Wibke Reinhard, Janina Winogradow, Martina Grassl, Anika Großhennig, Michael Preuß, Stefan Schreiber, H-Erich Wichmann, Christa Meisinger, Jean Yee, Yechiel Friedlander, Ron Do, James B. Meigs, Gordon H. Williams, David M. Nathan, Calum A. MacRae, Liming Qu, Robert L. Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Augusto D. Pichard, Kenneth M. Kent, Lowell F. Satler, Joseph Lindsay, Ron Waksman, Christopher W. Knouff, Dawn Waterworth, Max Walker, Vincent Mooser, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, Nicola Martinelli, Oliviero Olivieri, Elisabetta Trabetti, Giovanni Malerba, Pier Franco Pignatti, Candace Guiducci, Daniel B. Mirel, Melissa Parkin, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Yan V. Sun, Mark J. Daly, Shaun Purcell, Sandra Eifert, Peter S. Braund, Benjamin J. Wright, Anthony J. Balmforth, Stephen G. Ball

    Almmustuhtton 2010
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  15. 15
    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Dahkki Sekar Kathiresan, Benjamin F. Voight, Shaun Purcell, Kiran Musunuru, Diego Ardissino, Pier M Mannucci, Sonia Anand, James C. Engert, Nilesh J Samani, Heribert Schunkert, Jeanette Erdmann, Muredach P. Reilly, Daniel J. Rader, Thomas Morgan, John A. Spertus, Monika Stoll, Domenico Girelli, Pascal McKeown, Chris C Patterson, David S Siscovick, Christopher J O'Donnell, Roberto Elosúa, Leena Peltonen, Veikko Salomaa, Stephen M Schwartz, Olle Melander, David Altshuler, Pier Angelica Merlini, Carlo Berzuini, Luisa Bernardinelli, Flora Peyvandi, Marco Tubaro, Patrizia Celli, Maurizio Ferrario, Raffaela Fetiveau, Nicola Marziliano, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Pietro Zonzin, Alberto Piazza, Jean Yee, Yechiel Friedlander, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, James B Meigs, Gordon Williams, David M Nathan, Calum A. MacRae, Aki S Havulinna, Göran Berglund, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Marta Spreafico, Mark Daly, James Nemesh, Joshua M. Korn, Steven A. McCarroll, Aarti Surti, Candace Guiducci, Lauren Gianniny, Daniel B. Mirel, Melissa Parkin, Noël P. Burtt, Stacey B. Gabriel, John R Thompson, Peter S. Braund, Benjamin J. Wright, Anthony J Balmforth, Stephen G. Ball, Alistair S. Hall, Patrick Linsel‐Nitschke, Wolfgang Lieb, Andreas Ziegler, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Anika Grosshennig, Michael Preuß, H‐Erich Wichmann, Stefan Schreiber, Willem H. Ouwehand, Panos Deloukas, Michael Scholz, Francois Cambien, Mingyao Li, Zhen Chen, Robert Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Joe Devaney, Mary-Susan Burnett

    Almmustuhtton 2009
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  16. 16
    Genome-wide association study of Tourette's syndrome

    Genome-wide association study of Tourette's syndrome Dahkki Jeremiah M. Scharf, Dongmei Yu, Carol A. Mathews, Benjamin M. Neale, S. Evelyn Stewart, Jesen Fagerness, Patrick Evans, Eric R. Gamazon, Christopher K. Edlund, Susan K. Service, А. А. Тихомиров, Lisa Osiecki, Caroline Illmann, Anna Pluzhnikov, Anuar Konkashbaev, Lea K. Davis, Buhm Han, Jacquelyn Crane, Priya Moorjani, Andrew Crenshaw, Melissa Parkin, Victor I. Reus, Trevor Lowe, Martha Rangel‐Lugo, Sylvain Chouinard, Yves Dion, Simon Girard, Daniëlle C. Cath, Jan Smit, Robert A. King, Thomas Fernandez, James F. Leckman, Kenneth K. Kídd, J.R. Kidd, A.J. Pakstis, Matthew W. State, Luis Diego Herrera, Roberto Romero, Eduardo Fournier, Paul Sandor, Cathy L. Barr, N. Phan, Varda Gross‐Tsur, Fortu Benarroch, Yehuda Pollak, Cathy L. Budman, Ruth D. Bruun, Gerald Erenberg, Allan L. Naarden, Paul C. Lee, Noel S. Weiss, Bárbara Kremeyer, Gabriel Bedoya Berrío, Desmond Campbell, Julio César Cardona Silgado, William Cornejo Ochoa, Sandra Catalina Mesa Restrepo, Hans‐Helge Müller, Ana V. Valencia Duarte, Gholson J. Lyon, M. Leppert, J L Morgan, Robert B. Weiss, Marco A. Grados, Kari Anderson, Shekar Davarya, Harvey S. Singer, John T. Walkup, Joseph Jankovic, Jay A. Tischfield, Gary A. Heiman, Donald L. Gilbert, Pieter J. Hoekstra, Mary M. Robertson, Roger Kurlan, Chunyu Liu, J. Raphael Gibbs, Andrew B. Singleton, John Hardy, E Strengman, Roel A. Ophoff, Michael Wagner, R. Moessner, Daniel B. Mirel, Daniëlle Posthuma, C. Sabatti, Eleazar Eskin, D V Conti, James A. Knowles, Andrés Ruiz‐Linares, Guy A. Rouleau, Shaun Purcell, Peter Heutink, Ben A. Oostra, William M. McMahon, Nelson B. Freimer, Nancy J. Cox, David L. Pauls

    Almmustuhtton 2012
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