Výsledky vyhledávání - Sarah Curran

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  1. 1
    Treatment-resistant schizophrenia: current insights on the pharmacogenomics of antipsychotics

    Treatment-resistant schizophrenia: current insights on the pharmacogenomics of antipsychotics Autor John Lally, Fiona Gaughran, Philip Timms, Sarah Curran

    Vydáno 2016
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  2. 2
    A systematic review of the effect of foot orthoses and shoe characteristics on balance in healthy older subjects

    A systematic review of the effect of foot orthoses and shoe characteristics on balance in healthy older subjects Autor Atefeh Aboutorabi, Mahmood Bahramizadeh, Mokhtar Arazpour, Reza Fadayevatan, Farzam Farahmand, Sarah Curran, Stephen W Hutchins

    Vydáno 2015
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  3. 3
    Behavioral signatures related to genetic disorders in autism

    Behavioral signatures related to genetic disorders in autism Autor Hilgo Bruining, Marinus J.C. Eijkemans, Martien J. Kas, Sarah Curran, Jacob Vorstman, Patrick Bolton

    Vydáno 2014
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  4. 4
    Process evaluation of a store-based environmental obesity intervention on two American Indian Reservations

    Process evaluation of a store-based environmental obesity intervention on two American Indian Reservations Autor Sarah Curran, Joel Gittelsohn, Jean Anliker, Becky Ethelbah, Kelly D. Blake, Sangita Sharma, Benjamı́n Caballero

    Vydáno 2005
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  5. 5
    Methyl‐CpG‐binding protein 2 polymorphisms and vulnerability to autism

    Methyl‐CpG‐binding protein 2 polymorphisms and vulnerability to autism Autor Caroline S. Loat, Sarah Curran, Cathryn M. Lewis, Jacqueline A. Duvall, Daniel H. Geschwind, Patrick Bolton, Ian Craig

    Vydáno 2008
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  6. 6
    The dopamine transporter gene is associated with attention deficit hyperactivity disorder in a Taiwanese sample

    The dopamine transporter gene is associated with attention deficit hyperactivity disorder in a Taiwanese sample Autor C.-K. CHEN, S-L Chen, Jonathan Mill, Y-S Huang, S-K Lin, Sarah Curran, S Purcell, Pak C. Sham, Philip Asherson

    Vydáno 2003
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  7. 7
    The utility of patient specific induced pluripotent stem cells for the modelling of Autistic Spectrum Disorders

    The utility of patient specific induced pluripotent stem cells for the modelling of Autistic Spectrum Disorders Autor Graham Cocks, Sarah Curran, Priya Gami‐Patel, Dafe Uwanogho, Aaron R. Jeffries, Annie Kathuria, Walter Lucchesi, Victoria Wood, Rosemary Dixon, Caroline Mackie Ogilvie, Thomas Steckler, Jack Price

    Vydáno 2013
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  8. 8
    Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample

    Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample Autor Emma Colvert, Beata Tick, Fiona McEwen, Catherine Stewart, Sarah Curran, Emma Woodhouse, Nicola Gillan, Victoria Hallett, Stephanie Lietz, Tracy Garnett, Angelica Ronald, Robert Plomin, Frühling Rijsdijk, Francesca Happé, Patrick Bolton

    Vydáno 2015
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  9. 9
    Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders

    Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders Autor Maria Tropeano, Joo Wook Ahn, Richard Dobson, Gerome Breen, James Rucker, Abhishek Dixit, Deb K. Pal, Peter McGuffin, Anne Farmer, Peter S. White, Joris Andrieux, Evangelos Vassos, Caroline Mackie Ogilvie, Sarah Curran, David Collier

    Vydáno 2013
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  10. 10
    Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples

    Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples Autor Sarah Curran, Jonathan Mill, Eda Tahir Turanlı, Lindsey Kent, Stephen J. Richards, Alison L. Gould, L Huckett, Julie D. Sharp, Carrie Batten, S Fernando, Fatih Ozbay, Yankı Yazgan, Emily Simonoff, Miles D. Thompson, Eric Taylor, Philip Asherson

    Vydáno 2001
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  11. 11
    <i>Tbx1</i> haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome

    <i>Tbx1</i> haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome Autor Richard Paylor, Beate Glaser, Annalisa Mupo, Paris Ataliotis, Corinne M. Spencer, Angela Sobotka, Chelsey Sparks, Chul-Hee Choi, John S. Oghalai, Sarah Curran, Kieran C. Murphy, Stephen Monks, Nigel Williams, Michael O’Donovan, Michael J. Owen, Peter Scambler, Elizabeth Lindsay

    Vydáno 2006
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  12. 12
    Microdeletions of<i>ELP4</i>Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

    Microdeletions of<i>ELP4</i>Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation Autor Laura Addis, Joo Wook Ahn, Richard Dobson, Abhishek Dixit, Caroline Mackie Ogilvie, Dalila Pinto, Andrea K. Vaags, Hilary Coon, Pauline Chaste, Scott G. Wilson, Jeremy Parr, Joris Andrieux, Bruno Lenne, Zeynep Tümer, Vincenzo Leuzzi, Kristina Aubell, Hannele Koillinen, Sarah Curran, Christian R. Marshall, Stephen W. Scherer, Lisa J. Strug, David Collier, Deb K. Pal

    Vydáno 2015
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  13. 13
    Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder

    Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder Autor Andrea K. Vaags, Anath C. Lionel, Daisuke Sato, McKinsey L. Goodenberger, Quinn Stein, Sarah Curran, Caroline Mackie Ogilvie, Joo Wook Ahn, Irene Drmic, Lili Senman, Christina Chrysler, Ann Thompson, Carolyn Russell, Aparna Prasad, Susan Walker, Dalila Pinto, Christian R. Marshall, Dimitri J. Stavropoulos, Lonnie Zwaigenbaum, Bridget A. Fernandez, Éric Fombonne, Patrick Bolton, David Collier, Jennelle C. Hodge, Wendy Roberts, Peter Szatmari, Stephen W. Scherer

    Vydáno 2011
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  14. 14
    A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

    A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants Autor Samuel J. R. A. Chawner, Joanne Doherty, Richard Anney, Kevin M. Antshel, Carrie E. Bearden, Raphael Bernier, Wendy K. Chung, Caitlin C. Clements, Sarah Curran, Goran Čuturilo, Ania Fiksinski, Louise Gallagher, Robin P. Goin‐Kochel, Raquel E. Gur, Ellen Hanson, Sébastien Jacquemont, Wendy R. Kates, Leila Kushan, Anne Maillard, Donna M. McDonald‐McGinn, Marina Mihaljević, Judith S. Miller, Hayley Moss, Milica Pejović-Milovančević, Robert T. Schultz, LeeAnne Green‐Snyder, Jacob Vorstman, Tara Wenger, Jérémy Hall, Michael J. Owen, Marianne B. M. van den Bree

    Vydáno 2021
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  15. 15
    Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

    Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders Autor Claire S. Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Råstam, Henrik Anckarsäter, Gudrun Nygren, I. Carina Gillberg, Jonas Melke, Roberto Toro, Béatrice Regnault, Fabien Fauchereau, Oriane Mercati, Nathalie Lemière, David Skuse, Martin Poot, Richard Holt, Anthony P. Monaco, Irma Järvelä, Katri Kantojärvi, Raija Vanhala, Sarah Curran, David Collier, Patrick Bolton, Andreas G. Chiocchetti, Sabine M. Klauck, Fritz Poustka, Christine M. Freitag, Regina Waltes, Marnie Kopp, Eftichia Duketis, Elena Bacchelli, Fiorella Minopoli, Liliana Ruta, Agatino Battaglia, Luigi Mazzone, Elena Maestrini, Ana Filipa Sequeira, Bárbara Oliveira, Astrid M. Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W. Scherer, Diana Zélénika, Marc Delépine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie–Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M. Boeckers, Thomas Bourgeron

    Vydáno 2012
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  16. 16
    Psychosocial risk factors for suicidality in children and adolescents

    Psychosocial risk factors for suicidality in children and adolescents Autor Juan J. Carballo, C. Llorente, L. Kehrmann, Itziar Flamarique, Alessandro Zuddas, Diane Purper‐Ouakil, P. J. Hoekstra, David Coghill, Ulrike Schulze, Regina Dittmann, Jan K. Buitelaar, Josefina Castro‐Fornieles, Kate Lievesley, Paramala Santosh, Celso Arango, Alastair Sutcliffe, Sarah Curran, Laura Selema, Robert J. Flanagan, Ian Craig, Nathan Parnell, Keren Yeboah, Regina Sala, Jatinder Singh, Federico Fiori, Florence Pupier, Loes Vinkenvleugel, Jeffrey Glennon, Mireille J. Bakker, Cora Drent, Elly Bloem, Mark‐Peter Steenhuis, Ruth Berg, Alexander Häge, Mahmud Ben Dau, Konstantin Mechler, Sylke Rauscher, Sonja Aslan, Simon Schlanser, Ferdinand Keller, Alexander Schneider, Paul L. Plener, Jörg M. Fegert, Jacqui Paton, M. G. Macey, Noha Iessa, Kolozsvari Alfred, Furse Helen, P. Lao-Kaim Nick, Claire Baillon, Hugo Peyre, Doron Cohen, Olivier Bonnot, Julie Brunelle, Nathalie Franc, Pierre Raysse, Véronique Humbertclaude, Alberto Rodríguez-Quiroga, Covadonga M. Díaz‐Caneja, Ana Espliego, Jessica Merchán‐Naranjo, Cecilia Tapia, Immaculada Baeza, Soledad Romero, Amalia La Fuente, Ana E. Ortiz, Manuela Pintor, Franca Ligas, Francesca Micol, Roberta Frongia, Bruno Falissard, Ameli Schwalber, Juliane Dittrich, Andrea Wohner, Katrin Zimmermann, Andrea Schwalber, Katherine J. Aitchison

    Vydáno 2019
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  17. 17
    Synaptic, transcriptional and chromatin genes disrupted in autism

    Synaptic, transcriptional and chromatin genes disrupted in autism Autor Silvia De Rubeis, Xin He, Arthur P. Goldberg, Christopher S. Poultney, Kaitlin E. Samocha, A. Ercüment Çiçek, Yan Kou, Li Liu, Menachem Fromer, Susan L. Walker, Tarjinder Singh, Lambertus Klei, Jack A. Kosmicki, Shih‐Chen Fu, Branko Aleksić, Monica Biscaldi, Patrick Bolton, Jessica M. Brownfeld, Jinlu Cai, Nicholas G. Campbell, Ángel Carracedo, Maria H. Chahrour, Andreas G. Chiocchetti, Hilary Coon, Emily L. Crawford, Lucy Crooks, Sarah Curran, Géraldine Dawson, Eftichia Duketis, Bridget A. Fernandez, Louise Gallagher, Evan Geller, Stephen J. Guter, R. Sean Hill, Iuliana Ionita‐Laza, Patricia González, Helena Kilpinen, Sabine M. Klauck, Alexander Kolevzon, Irene Lee, Jing Lei, Terho Lehtimäki, Chiao‐Feng Lin, Avi Ma’ayan, Christian R. Marshall, Alison McInnes, Benjamin M. Neale, Michael J. Owen, Norio Ozaki, Mara Parellada, Jeremy Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Max Sachse, Stephan Sanders, Chad Schafer, Martin Schulte‐Rüther, David Skuse, Christine Stevens, Peter Szatmari, Kristiina Tammimies, Otto Valladares, Annette Voran, Li‐San Wang, Lauren A. Weiss, A. Jeremy Willsey, Timothy W. Yu, Ryan K. C. Yuen, Edwin H. Cook, Christine M. Freitag, Michael Gill, Christina M. Hultman, Thomas Lehner, Aarno Palotie, Gerard D. Schellenberg, Pamela Sklar, Matthew W. State, James S. Sutcliffe, Christopher A. Walsh, Stephen W. Scherer, Michael E. Zwick, Jeffrey C. Barrett, David J. Cutler, Kathryn Roeder, Bernie Devlin, Mark J. Daly, Joseph D. Buxbaum

    Vydáno 2014
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  18. 18
    A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

    A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans Autor Nicholas J. Timpson, Klaudia Walter, Josine L. Min, Ioanna Tachmazidou, Giovanni Malerba, So–Youn Shin, Lu Chen, Marta Futema, Lorraine Southam, Valentina Iotchkova, Massimiliano Cocca, Jie Huang, Yasin Memari, Shane McCarthy, Petr Danecek, Dawn Muddyman, Massimo Mangino, Cristina Menni, John R. B. Perry, Susan M. Ring, Amadou Gaye, George Dedoussis, Aliki‐Eleni Farmaki, Paul R. Burton, Philippa J. Talmud, Giovanni Gambaro, Tim D. Spector, George Davey Smith, Richard Durbin, J. Brent Richards, Steve E. Humphries, Eleftheria Zeggini, Nicole Soranzo, Saeed Al Turki, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Balasubramaniam, Jeffrey C. Barrett, Inês Barroso, Phil Beales, Jamie Bentham, Shoumo Bhattacharya, Ewan Birney, Douglas Blackwood, Martin Bobrow, Elena G. Bochukova, Patrick Bolton, Rebecca Bounds, Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebhattin Cirak, Peter Clapham, Gail Clement, Guy Coates, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Petr Danecek, George Davey Smith, Aaron Day-Williams, Ian N.M. Day, Thomas A. Down, Yuanping Du, Ian Dunham, Richard Durbin, Sarah Edkins, Peter Ellis, David M. Evans, Sadaf Faroogi, Ghazaleh Fatemifar, David Fitzpatrick, Paul Flicek, James Flyod, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Tom R. Gaunt, Matthias Geihs, Daniel Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xueqin Guo, Xiaosen Guo, Hugh Gurling, Deborah Hart

    Vydáno 2014
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  19. 19
    Common variant at 16p11.2 conferring risk of psychosis

    Common variant at 16p11.2 conferring risk of psychosis Autor Stacy Steinberg, Simone de Jong, Manuel Mattheisen, Javier Costas, Ditte Demontis, Stéphane Jamain, Olli Pietiläinen, Kuang Lin, Sergi Papiol, Johanna Huttenlocher, Engilbert Sigurðsson, Evangelos Vassos, Ina Giegling, René Breuer, G. T. Fraser, Nicholas Walker, Ingrid Melle, Srdjan Djurovic, Ingrid Agartz, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Line Olsen, Thomas Hansen, Andrés Ingason, Matti Pirinen, E Strengman, David M. Hougaard, Torben Ørntoft, Michael Didriksen, Mads V. Hollegaard, Merete Nordentoft, Л. И. Абрамова, В. Г. Каледа, Manuel Arrojo, Julio Sanjuán, Celso Arango, Bruno Étain, Frank Bellivier, A. Méary, Franck Schürhoff, Andreı̈ Szöke, Michele Ribolsi, Valentina Magni, Alberto Siracusano, Swetlana Sperling, Moritz J. Rossner, Claus Christiansen, Lambertus A. Kiemeney, Barbara Franke, Leonard H. van den Berg, Jan H. Veldink, Sarah Curran, Patrick Bolton, Martin Poot, Wouter Staal, Karola Rehnström, Helena Kilpinen, Christine M. Freitag, Jobst Meyer, Patrik K. E. Magnusson, Evald Sæmundsen, Igor Martsenkovsky, I Bikshaieva, I.I. Martsenkovska, O.S. Vashchenko, Marija Raleva, K Paketchieva, Branislav Stefanovski, Naser Durmishi, Milica Pejović-Milovančević, Dušica Lečić Toševski, Teimuraz Silagadze, N Naneishvili, Nina Mikeladze, Simon Surguladze, John B. Vincent, Anne Farmer, Philip B. Mitchell, A. Jordan Wright, Peter R. Schofield, Janice M. Fullerton, Grant W. Montgomery, Nicholas G. Martin, I. Alex Rubino, Ruud van Winkel, Günter Kenis, Marc D. Binder, János Réthelyi, István Bitter, Lars Terenius, Erik G. Jönsson, S C Bakker, Jim van Os, Assen Jablensky, Marion Leboyer, Elvira Bramon, John Powell, Robin Murray

    Vydáno 2012
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  20. 20
    Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

    Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel Autor Jie Huang, Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min, Petr Danecek, Giovanni Malerba, Elisabetta Trabetti, Hou‐Feng Zheng, Saeed Al Turki, Antoinette Amuzu, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Bala, Jeffrey C. Barrett, Inês Barroso, Phil Beales, Marianne Benn, Jamie Bentham, Shoumo Bhattacharya, Ewan Birney, Douglas Blackwood, Martin Bobrow, Elena G. Bochukova, Patrick Bolton, Rebecca Bounds, Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Juan P. Casas, John C. Chambers, Ruth Charlton, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebahattin Çırak, Peter Clapham, Gail Clement, Guy Coates, Massimiliano Cocca, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Ian N.M. Day, Aaron Day-Williams, George Dedoussis, Thomas A. Down, Yuanping Du, Cornelia M. van Duijn, Ian Dunham, Sarah Edkins, Rosemary Ekong, Peter Ellis, David M. Evans, I. Sadaf Farooqi, David Fitzpatrick, Paul Flicek, James Floyd, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Paolo Gasparini, Tom R. Gaunt, Matthias Geihs, Daniel H. Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xiaosen Guo, Xueqin Guo, Hugh Gurling, Deborah Hart, Audrey E. Hendricks, Peter Holmans, Jie Huang, Tim Hubbard, Steve E. Humphries, Matthew E. Hurles, Pirro G. Hysi, Valentina Iotchkova, Aaron Isaacs, David K. Jackson, Yalda Jamshidi, Jon Johnson, Christopher Joyce, Konrad J. Karczewski, Jane Kaye, Thomas Keane, John P. Kemp

    Vydáno 2015
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