Výsledky vyhledávání - Stan F. Nelson

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  1. 1
    High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene

    High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene Autor Samuel P. Strom, Jennifer Stone, Jason Bosch, Barry Merriman, Rita M. Cantor, Daniel H. Geschwind, Stan F. Nelson

    Vydáno 2009
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  2. 2
    Analysis of oncogenic signaling networks in glioblastoma identifies <i>ASPM</i> as a molecular target

    Analysis of oncogenic signaling networks in glioblastoma identifies <i>ASPM</i> as a molecular target Autor Steve Horvath, B. Zhang, Marc Carlson, Kan Lu, Shoutian Zhu, Ramon M. Felciano, Megan Laurance, Wenqi Zhao, Songyan Qi, Z. Chen, Y. Lee, Adrienne C. Scheck, Linda M. Liau, Hung‐Yi Wu, Daniel H. Geschwind, Philip G. Febbo, Harley I. Kornblum, Timothy F. Cloughesy, Stan F. Nelson, Paul S. Mischel

    Vydáno 2006
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  3. 3
    Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma

    Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma Autor Rameen Beroukhim, Gad Getz, Leia Nghiemphu, Jordi Barretina, Teli Hsueh, David Linhart, Igor Vivanco, Jeffrey C. Lee, Julie H. Huang, Sethu Alexander, Jinyan Du, Tweeny R. Kau, Roman K. Thomas, Kinjal Shah, Horacio Soto, Sven Perner, John R. Prensner, Ralph DeBiasi, Francesca Demichelis, Charlie Hatton, Mark A. Rubin, Levi A. Garraway, Stan F. Nelson, Linda M. Liau, Paul S. Mischel, Tim Cloughesy, Matthew Meyerson, Todd Golub, Eric S. Lander, Ingo K. Mellinghoff, William R. Sellers

    Vydáno 2007
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  4. 4
    Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes

    Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes Autor Naomi Lowe, Aiveen Kirley, Ziarih Hawi, Pak C. Sham, Harvey Wickham, Christopher J. Kratochvil, Shelley D. Smith, Saretta Y. Lee, Florence Lévy, Lindsey Kent, Fiona Middle, Luís Augusto Rohde, Tatiana Roman, Eda Tahir Turanlı, Y. Yazgan, Philip Asherson, Jonathan Mill, Anita Thapar, Antony Payton, Richard D. Todd, Timothy G. Stephens, Richard P. Ebstein, Iris Manor, Cathy L. Barr, Karen G. Wigg, Richard J. Sinke, Jan K. Buitelaar, Susan L. Smalley, Stan F. Nelson, Joseph Biederman, Stephen V. Faraone, Michael Gill

    Vydáno 2004
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  5. 5
    Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

    Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder Autor Benjamin M. Neale, Sarah E. Medland, Stephan Ripke, Philip Asherson, Barbara Franke, Klaus‐Peter Lesch, Stephen V. Faraone, Thuy Trang Nguyen, H. Schäfer, Peter Holmans, Mark J. Daly, Hans‐Christoph Steinhausen, Christine M. Freitag, Andreas Reif, Tobias Renner, Marcel Romanos, Jasmin Romanos, Susanne Walitza, Andreas Warnke, Jobst Meyer, Haukur Pálmason, Jan K. Buitelaar, Alejandro Arias Vásquez, Nanda Lambregts-Rommelse, Michael Gill, Richard Anney, Kate Langely, Michael O’Donovan, Nigel Williams, Michael J. Owen, Anita Thapar, Lindsey Kent, Joseph A. Sergeant, Herbert Roeyers, Eric Mick, Joseph Biederman, Alysa E. Doyle, Susan L. Smalley, Sandra K. Loo, Hákon Hákonarson, Josephine Elia, Alexandre A. Todorov, Ana Miranda, Fernando Mulas, Richard P. Ebstein, Aribert Rothenberger, Tobias Banaschewski, Robert D. Oades, Edmund Sonuga‐Barke, James J. McGough, Laura Nisenbaum, Frank A. Middleton, Xiaolan Hu, Stan F. Nelson

    Vydáno 2010
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  6. 6
    Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients

    Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients Autor Laura Bryant, Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson, Kevin A. Janssen, Pearl Lee, Michael March, Divya Nair, Elliott H. Sherr, Brieana Fregeau, Klaas J. Wierenga, Alexandrea Wadley, Grazia M.S. Mancini, Nina Powell‐Hamilton, Jiddeke van de Kamp, Theresa A. Grebe, John Dean, Alison Ross, Heather P. Crawford, Zöe Powis, Megan T. Cho, Marcia Willing, Linda Manwaring, Rachel Schot, Caroline Nava, Alexandra Afenjar, Davor Lessel, Matias Wagner, Thomas Klopstock, Juliane Winkelmann, Claudia B. Catarino, Kyle Retterer, Jane L. Schuette, Jeffrey W. Innis, Amy Pizzino, Sabine Lüttgen, Jonas Denecke, Tim M. Strom, Kristin G. Monaghan, Zuo‐Fei Yuan, Holly Dubbs, Renee Bend, Jennifer A. Lee, Michael J. Lyons, Julia Hoefele, Roman Günthner, Heiko Reutter, Boris Keren, Kelly Radtke, Omar Sherbini, Cameron Mrokse, Katherine L. Helbig, Sylvie Odent, Benjamin Cogné, Sandra Mercier, Stéphane Bézieau, Thomas Besnard, Sébastien Küry, Richard Redon, Karit Reinson, Monica H. Wojcik, Katrin Õunap, Pilvi Ilves, A. Micheil Innes, Kristin D. Kernohan, Gregory Costain, M. Stephen Meyn, David Chitayat, Elaine H. Zackai, Anna Lehman, Hilary Kitson, Martin G. Martin, Julián A. Martínez-Agosto, Stan F. Nelson, Christina G.S. Palmer, Jeanette C. Papp, Neil H. Parker, Janet S. Sinsheimer, Éric Vilain, Jijun Wan, Amanda J. Yoon, Allison Zheng, Elise Brimble, Giovanni Battista Ferrero, Francesca Clementina Radio, Diana Carli, Sabina Barresi, Alfredo Brusco, Marco Tartaglia, Jennifer Muncy Thomas, Luis A. Umaña, Marjan M. Weiss, Garrett Gotway, Kyra E. Stuurman, Michelle L. Thompson, Kirsty McWalter, Constance T. R. M. Stumpel, Servi J.C. Stevens

    Vydáno 2020
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  7. 7
    Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Mapping autism risk loci using genetic linkage and chromosomal rearrangements Autor Peter Szatmari, Andrew D. Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiaoqing Liu, John B. Vincent, Jennifer Skaug, Ann Thompson, Lili Senman, Lars Feuk, Qian Cheng, Susan E. Bryson, Marshall B. Jones, Christian R. Marshall, Stephen W. Scherer, Veronica J. Vieland, Christopher W. Bartlett, La Vonne Mangin, Rhinda Goedken, Alberto M. Segre, Margaret A. Pericak‐Vance, Michael L. Cuccaro, John R. Gilbert, Harry H. Wright, Ruth K. Abramson, Catalina Betancur, Thomas Bourgeron, Christopher Gillberg, Marion Leboyer, Joseph D. Buxbaum, Kenneth L. Davis, Eric Hollander, Jeremy M. Silverman, Joachim Hallmayer, Linda Lotspeich, James S. Sutcliffe, Jonathan L. Haines, Susan E. Folstein, Joseph Piven, Thomas H. Wassink, Val C. Sheffield, Daniel H. Geschwind, Maja Bućan, W. Ted Brown, Rita M. Cantor, John N. Constantino, T. Conrad Gilliam, Martha R. Herbert, Clara Lajonchere, David H. Ledbetter, Christa Lese‐Martin, Janet Miller, Stan F. Nelson, Carol A Samango-Sprouse, Sarah Spence, Matthew W. State, Rudolph E. Tanzi, Hilary Coon, Géraldine Dawson, Bernie Devlin, Annette Estes, Pamela Flodman, Lambertus Klei, William M. McMahon, Nancy J. Minshew, Jeff Munson, Elena Korvatska, Patricia M. Rodier, Gerard D. Schellenberg, Moyra Smith, M. Anne Spence, Chris Stodgell, Ping G. Tepper, Ellen M. Wijsman, Chang-En Yu, Bernadette Rogé, Carine Mantoulan, Kerstin Wittemeyer, Annemarie Poustka, Bärbel Felder, Sabine M. Klauck, Claudia Schuster, Fritz Poustka, Sven Bölte, Sabine Feineis-Matthews, Evelyn Herbrecht, Gabi Schmötzer, John Tsiantis, Κaterina Papanikolaou, Elena Maestrini, Elena Bacchelli, Francesca Blasi, Simona Carone, Claudio Toma, Hermán van Engeland, Maretha Jonge, Chantal Kemner, Frederieke Koop, Frederike Koop

    Vydáno 2007
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