Search Results - Nuala Sykes
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1
Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT by Gabrielle Barnby, Aaron Abbott, Nuala Sykes, Andrew P. Morris, Daniel E. Weeks, Richard Mott, Janine A. Lamb, Anthony Bailey, Anthony P. Monaco
Published 2005Artigo -
2
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection by Nuala Sykes, Claudio Toma, Natalie Wilson, Emanuela V. Volpi, Inês Sousa, Alistair T. Pagnamenta, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini, Anthony Bailey, Anthony P. Monaco
Published 2009Artigo -
3
MET and autism susceptibility: family and case–control studies by Inês Sousa, Taane G. Clark, Claudio Toma, Kazuhiro Kobayashi, Maja K. Choma, Richard Holt, Nuala Sykes, Janine A. Lamb, Anthony Bailey, Agatino Battaglia, Elena Maestrini, Anthony P. Monaco
Published 2008Artigo -
4
Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits by Kay MacDermot, Elena Bonora, Nuala Sykes, Anne-Marie Coupe, Cecilia Lai, Sonja C. Vernes, Faraneh Vargha‐Khadem, Fiona McKenzie, Robert L. Smith, Anthony P. Monaco, Simon E. Fisher
Published 2005Artigo -
5
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility by Elena Maestrini, Alistair T. Pagnamenta, Janine A. Lamb, Elena Bacchelli, Nuala Sykes, Inês Sousa, Claudio Toma, Gabrielle Barnby, Helen Butler, Laura Winchester, Thomas Scerri, Fiorella Minopoli, Jennifer Reichert, Guiqing Cai, Joseph D. Buxbaum, Olena Korvatska, Gerry Schellenberg, Géraldine Dawson, Annelies de Bildt, Ruud B. Minderaa, E Mulder, Andrew P. Morris, Anthony Bailey, Anthony P. Monaco
Published 2009Artigo -
6
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q by Elena Bonora, Janine A. Lamb, Gabrielle Barnby, Nuala Sykes, Thomas Moberly, Kim S. Beyer, Sabine M. Klauck, F. Poustka, Elena Bacchelli, Francesca Blasi, Elena Maestrini, Agatino Battaglia, Demetrios Haracopos, Lennart Pedersen, Torben Isager, Gunna Eriksen, Birgitte Viskum, Ester-Ulsted Sorensen, Karen Brøndum‐Nielsen, R. M. J. Cotterill, Herman von Engeland, Maretha Jonge, Chantal Kemner, Karlijn Steggehuis, Margret Scherpenisse, Michael Rutter, Patrick Bolton, Jeremy Parr, Annemarie Poustka, Anthony Bailey, Anthony P. Monaco
Published 2004Artigo -
7
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder by Jillian P. Casey, Tiago R. Magalhães, Judith Conroy, Regina Regan, Naisha Shah, Richard Anney, Denis C. Shields, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Patrick Bolton, Thomas Bourgeron, S. Brennan, Phil Cali, Catarina Correia, Christina Corsello, Marc N. Coutanche, Géraldine Dawson, Maretha Jonge, Richard Delorme, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, S. Foley, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jonathan Green, Stephen J. Guter, Hákon Hákonarson, Richard Holt, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, Alexander Kolevzon, Janine A. Lamb, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Catherine Lord, Sabata C. Lund, Elena Maestrini, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Judith Miller, Fiorella Minopoli, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Gudrun Nygren, Guiomar Oliveira, Alistair T. Pagnamenta, Katerina Papanikolaou, Jeremy Parr, Barbara Parrini, Andrew Pickles, Dalila Pinto, Joseph Piven, David J. Posey, Annemarie Poustka, Fritz Poustka, Jiannis Ragoussis, Bernadette Rogé, Michael Rutter, Ana Filipa Sequeira, Latha Soorya, Inês Sousa, Nuala Sykes, Vera Stoppioni, Raffaella Tancredi, M. Tauber, Ann Thompson, Susanne Thomson, John Tsiantis, Herman Van Engeland, John B. Vincent, Fred Volkmar, Jacob Vorstman, Simon Wallace, Kai Wang, Thomas H. Wassink, Kathy White, Kirsty Wing
Published 2011Artigo -
8
Individual common variants exert weak effects on the risk for autism spectrum disorders by Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, Jillian P. Casey, Judith Conroy, Catarina Correia, Christina Corsello, Emily L. Crawford, Maretha Jonge, Richard Delorme, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Andrew Green, Jonathan Green, Stephen J. Guter, Elizabeth A. Heron, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Suma Jacob, Graham P. Kenny, Cecilia Kim, Alexander Kolevzon, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Miriam Law-Smith, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Xiaoqing Liu, Frances Lombard, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Tiago R. Magalhães, Carine Mantoulan, Christopher J. McDougle, Nadine Melhem, Alison Merikangas, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Carolyn Noakes, Gudrun Nygren, Κaterina Papanikolaou, Alistair T. Pagnamenta, Barbara Parrini, Tara Paton, Andrew Pickles, David J. Posey, Fritz Poustka, Jiannis Ragoussis, Regina Regan, Wendy Roberts, Kathryn Roeder, Bernadette Rogé, Michael Rutter, Sabine Schlitt, Naisha Shah, Val C. Sheffield, Latha Soorya, Inês Sousa, Vera Stoppioni, Nuala Sykes, Raffaella Tancredi, Ann Thompson, Susanne Thomson, Ana Tryfon, John Tsiantis, Hermán van Engeland, John B. Vincent, Fred R. Volkmar, JAS Vorstman, Simon Wallace, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, Danielle Zurawiecki, Lonnie Zwaigenbaum, Anthony Bailey
Published 2012Artigo
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Autism
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Copy-number variation
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Genome-wide association study
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