- Hem
- Om universitetet
- Hitta person
- Gudrun Nygren
Gudrun Nygren
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"The package has been opened”- parents' perspective and social validity of an Early Start Denver Model intervention for young children with
autism
Emilia Carlsson, Gudrun Nygren, Christopher Gillberg, Petra Linnsand
Frontiers in Child and Adolescent Psychiatry - 2024 -
Intervention in autism based on Early Start Denver Model in a multiethnic immigrant setting—experiences of preschool staff involved in its
implementation
Petra Linnsand, Gudrun Nygren, Jonas Hermansson, Christopher Gillberg, Emilia Carlsson
Frontiers in Child and Adolescent Psychiatry - 2024 -
Feeding Problems Including Avoidant Restrictive Food Intake Disorder in Young Children With Autism Spectrum Disorder in a Multiethnic
Population
Gudrun Nygren, Petra Linnsand, J. Hermansson, Lisa Dinkler, Maria Johansson, Christopher Gillberg
Frontiers in Pediatrics - 2021 -
A High Prevalence of Autism Spectrum Disorder in Preschool Children in an Immigrant, Multiethnic Population in Sweden: Challenges for Health
Care
Petra Linnsand, Christopher Gillberg, A. Nilses, Bibbi Hagberg, Gudrun Nygren
Journal of Autism and Developmental Disorders - 2021 -
Experiences Of Immigrant Parents In Sweden Participating In A Community Assessment And Intervention Program For Preschool Children With
Autism
A. Nilses, M. Jingrot, Petra Linnsand, Christopher Gillberg, Gudrun Nygren
Neuropsychiatric Disease and Treatment - 2019 -
Organisation of health care for families with young children with autism in a multiethnic community in Gothenburg,
Sweden
Gudrun Nygren, P. Linnsand, Å Nilses, K. Bondesson, Nanna Gillberg, Elisabeth Fernell, Christopher Gillberg
Läkartidningen - 2017 -
Lokal samverkan positiv vid autism hos små barn i multietnisk
stadsdel
Gudrun Nygren, Petra Linnsand, Åsa Nilses, Karin Bondesson, Nanna Gillberg, Elisabeth Fernell, Christopher Gillberg
Läkartidningen - 2017 -
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in
autism.
M Pilorge, C Fassier, H Le Corronc, A Potey, J Bai, S De Gois, E Delaby, B Assouline, V Guinchat, F Devillard, R Delorme, Gudrun Nygren, Maria Råstam, J C Meier, S Otani, H Cheval, V M James, M Topf, T N Dear, Christopher Gillberg, M Leboyer, B Giros, S Gautron, J Hazan, R J Harvey, P Legendre, C Betancur
Molecular psychiatry - 2016 -
In med uppdaterad medicinsk kunskap när ADHD
handläggs.
Magnus Landgren, Elisabeth Fernell, Svenny Kopp, Mats Johnson, Mats Eriksson, Katarina Lindström, Maria Råstam, Peik Gustafsson, Gudrun Nygren, Ida Lindblad, Leif Svensson, Trygve Lövoll
Läkartidningen - 2015 -
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum
disorder.
Anne-Claude Tabet, Alain Verloes, Marion Pilorge, Elsa Delaby, Richard Delorme, Gudrun Nygren, Françoise Devillard, Marion Gérard, Sandrine Passemard, Delphine Héron, Jean-Pierre Siffroi, Aurelia Jacquette, Andrée Delahaye, Laurence Perrin, Céline Dupont, Azzedine Aboura, Pierre Bitoun, Mary Coleman, Marion Leboyer, Christopher Gillberg, Brigitte Benzacken, Catalina Betancur
Molecular autism - 2015 -
Heterozygous FA2H mutations in autism spectrum
disorders.
Isabelle Scheid, Anna Maruani, Guillaume Huguet, Claire S Leblond, Gudrun Nygren, Henrik Anckarsäter, Anita Beggiato, Maria Rastam, Fréderique Amsellem, I Carina Gillberg, Monique Elmaleh, Marion Leboyer, Christopher Gillberg, Catalina Betancur, Mary Coleman, Hiroko Hama, Edwin H Cook, Thomas Bourgeron, Richard Delorme
BMC medical genetics - 2013 -
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum
disorders.
Claire S Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Rastam, Henrik Anckarsäter, Gudrun Nygren, I Carina Gillberg, Jonas Melke, Roberto Toro, Beatrice 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 A Collier, Patrick Bolton, Andreas 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 F Sequeira, Barbara Oliveira, Astrid Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W Scherer, Diana Zelenika, Marc Delepine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie-Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M Boeckers, Thomas Bourgeron
PLoS Genetics - 2012 -
Individual common variants exert weak effects on the risk for autism spectrum
disorders.
Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick F. Bolton, Thomas Bourgeron, Sean Brennan, Jessica Brian, Jillian Casey, Judith Conroy, Catarina Correia, Christina Corsello, Emily L Crawford, Maretha de Jonge, Richard Delorme, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A Fernandez, Susan E Folstein, Eric Fombonne, John Gilbert, Christopher Gillberg, Joseph T Glessner, Andrew Green, Jonathan Green, Stephen J Guter, Elizabeth A Heron, Richard Holt, Jennifer L Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Suma Jacob, Graham P Kenny, Cecilia Kim, Alexander Kolevzon, Vlad Kustanovich, Clara M Lajonchere, Janine A Lamb, Miriam Law-Smith, Marion Leboyer, Ann Le Couteur, Bennett L Leventhal, Xiao-Qing Liu, Frances Lombard, Catherine Lord, Linda Lotspeich, Sabata C Lund, Tiago R Magalhaes, Carine Mantoulan, Christopher J McDougle, Nadine M Melhem, Alison Merikangas, Nancy J Minshew, Ghazala K Mirza, Jeff Munson, Carolyn Noakes, Gudrun Nygren, Katerina Papanikolaou, Alistair T Pagnamenta, Barbara Parrini, Tara Paton, Andrew Pickles, David J Posey, Fritz Poustka, Jiannis Ragoussis, Regina Regan, Katy Renshaw, Wendy Roberts, Kathryn Roeder, Bernadette Roge, Michael L Rutter, Sabine Schlitt, Naisha Shah, Val C Sheffield, Latha Soorya, Inês Sousa, Vera Stoppioni, Nuala Sykes, Raffaella Tancredi, Ann P Thompson, Susanne Thomson, Ana Tryfon, John Tsiantis, Herman Van Engeland, John B Vincent, Jas Vorstman, Fred Volkmar, Simon Wallace, Kirsty Wing, Shawn Wood, Kerstin Wittemeyer, Danielle Zurawiecki, Lonnie Zwaigenbaum, Anthony J Bailey, Agatino Battaglia, Rita M Cantor, Hilary Coon, Michael L Cuccaro, Geraldine Dawson, Sean Ennis, Christine M Freitag, Daniel H Geschwind, Jonathan L Haines, Sabine M Klauck, William M McMahon, Elena Maestrini, Judith Miller, Anthony P Monaco, Stanley F Nelson, John I Nurnberger, Guiomar Oliveira, Jeremy R Parr, Margaret A Pericak-Vance, Joseph Piven, Gerard D Schellenberg, Stephen W Scherer, Astrid M Vicente, Thomas H Wassink, Ellen M Wijsman, Catalina Betancur, Joseph D Buxbaum, Edwin H Cook, Louise Gallagher, Michael Gill, Joachim Hallmayer, Andrew D Paterson, James S Sutcliffe, Peter Szatmari, Veronica J Vieland, Hakon Hakonarson, Bernie Devlin
Human Molecular Genetics - 2012 -
The prevalence of autism spectrum disorders in toddlers: a population study of 2-year-old Swedish
children.
Gudrun Nygren, Mats Cederlund, Eva Sandberg, Fredrik Gillstedt, Thomas Arvidsson, I Carina Gillberg, Gunilla Westman Andersson, Christopher Gillberg
Journal of Autism and Developmental Disorders - 2012 -
A new screening programme for autism in a general population of Swedish
toddlers.
Gudrun Nygren, Eva Sandberg, Fredrik Gillstedt, Gunnar Ekeroth, Thomas Arvidsson, Christopher Gillberg
Research in Developmental Disabilities - 2012 -
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum
disorder.
Jillian P Casey, Tiago Magalhaes, Judith M Conroy, Regina Regan, Naisha Shah, Richard Anney, Denis C Shields, Brett S Abrahams, Joana Almeida, Elena Bacchelli, Anthony J Bailey, Gillian Baird, Agatino Battaglia, Tom Berney, Nadia Bolshakova, Patrick F. Bolton, Thomas Bourgeron, Sean Brennan, Phil Cali, Catarina Correia, Christina Corsello, Marc Coutanche, Geraldine Dawson, Maretha de Jonge, Richard Delorme, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A Fernandez, Susan E Folstein, Suzanne Foley, Eric Fombonne, Christine M Freitag, John Gilbert, Christopher Gillberg, Joseph T Glessner, Jonathan Green, Stephen J Guter, Hakon Hakonarson, Richard Holt, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M Klauck, Alexander Kolevzon, Janine A Lamb, Marion Leboyer, Ann Le Couteur, Bennett L 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 K Mirza, Jeff Munson, Stanley F Nelson, Gudrun Nygren, Guiomar Oliveira, Alistair T Pagnamenta, Katerina Papanikolaou, Jeremy R Parr, Barbara Parrini, Andrew Pickles, Dalila Pinto, Joseph Piven, David J Posey, Annemarie Poustka, Fritz Poustka, Jiannis Ragoussis, Bernadette Roge, Michael L Rutter, Ana F Sequeira, Latha Soorya, Inês Sousa, Nuala Sykes, Vera Stoppioni, Raffaella Tancredi, Maïté Tauber, Ann P Thompson, Susanne Thomson, John Tsiantis, Herman Van Engeland, John B Vincent, Fred Volkmar, Jacob A S Vorstman, Simon Wallace, Kai Wang, Thomas H Wassink, Kathy White, Kirsty Wing, Kerstin Wittemeyer, Brian L Yaspan, Lonnie Zwaigenbaum, Catalina Betancur, Joseph D Buxbaum, Rita M Cantor, Edwin H Cook, Hilary Coon, Michael L Cuccaro, Daniel H Geschwind, Jonathan L Haines, Joachim Hallmayer, Anthony P Monaco, John I Nurnberger, Margaret A Pericak-Vance, Gerard D Schellenberg, Stephen W Scherer, James S Sutcliffe, Peter Szatmari, Veronica J Vieland, Ellen M Wijsman, Andrew Green, Michael Gill, Louise Gallagher, Astrid Vicente, Sean Ennis
Human Genetics - 2012 -
Screening and Diagnosis of Autism Spectrum
Disorders
Gudrun Nygren
2012 -
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity
disorders.
Pauline Chaste, Nathalie Clement, Hany Goubran Botros, Jean-Luc Guillaume, Marina Konyukh, Cécile Pagan, Isabelle Scheid, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, I Carina Gillberg, Jonas Melke, Richard Delorme, Claire Leblond, Roberto Toro, Guillaume Huguet, Fabien Fauchereau, Christelle Durand, Lydia Boudarene, Emilie Serrano, Nathalie Lemière, Jean Marie Launay, Marion Leboyer, Ralf Jockers, Christopher Gillberg, Thomas Bourgeron
Journal of Pineal Research - 2011 -
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human
populations.
Marina Konyukh, Richard Delorme, Pauline Chaste, Claire Leblond, Nathalie Lemière, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, Frederique Amsellem, I Carina Gillberg, Marie Christine Mouren-Simeoni, Evelyn Herbrecht, Fabien Fauchereau, Roberto Toro, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron
PLoS One - 2011 -
Functional impact of global rare copy number variation in autism spectrum
disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Joana Almeida, Elena Bacchelli, Gary D Bader, Anthony J Bailey, Gillian Baird, Agatino Battaglia, Tom Berney, Nadia Bolshakova, Sven Boelte, Patrick F. Bolton, Thomas Bourgeron, Sean Brennan, Jessica Brian, Susan E Bryson, Andrew R Carson, Guillermo Casallo, Jillian Casey, Brian H Y Chung, Lynne Cochrane, Christina Corsello, Emily L Crawford, Andrew Crossett, Cheryl Cytrynbaum, Geraldine Dawson, Maretha de Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A Fernandez, Susan E Folstein, Eric Fombonne, Christine M Freitag, John Gilbert, Christopher Gillberg, Joseph T Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J Guter, Hakon Hakonarson, Elizabeth A Heron, Matthew Hill, Richard Holt, Jennifer L Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara M Lajonchere, Janine A Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L Leventhal, Anath C Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C Lund, Elena Maestrini, William Mahoney, Carine Mantoulan, Christian R Marshall, Helen McConachie, Christopher J McDougle, Jane McGrath, William M McMahon, Alison Merikangas, Ohsuke Migita, Nancy J Minshew, Ghazala K Mirza, Jeff Munson, Stanley F Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Katerina Papanikolaou, Jeremy R Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge, Joseph Piven, Chris P Ponting, David J Posey, Annemarie Poustka, Fritz Poustka, Aparna Prasad, Jiannis Ragoussis, Katy Renshaw, Jessica Rickaby, Wendy Roberts, Kathryn Roeder, Bernadette Roge, Michael L Rutter, Laura J Bierut, John P Rice, Jeff Salt, Katherine Sansom, Daisuke Sato, Ricardo Segurado, Ana F Sequeira, Lili Senman, Naisha Shah, Val C Sheffield, Latha Soorya, Ines Sousa, Olaf Stein, Nuala Sykes, Vera Stoppioni, Christina Strawbridge, Raffaella Tancredi, Katherine Tansey, Bhooma Thiruvahindrapduram, Ann P Thompson, Susanne Thomson, Ana Tryfon, John Tsiantis, Herman Van Engeland, John B Vincent, Fred Volkmar, Simon Wallace, Kai Wang, Zhouzhi Wang, Thomas H Wassink, Caleb Webber, Rosanna Weksberg, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, J. Wu, Brian L Yaspan, Danielle Zurawiecki, Lonnie Zwaigenbaum, Joseph D Buxbaum, Rita M Cantor, Edwin H Cook, Hilary Coon, Michael L Cuccaro, Bernie Devlin, Sean Ennis, Louise Gallagher, Daniel H Geschwind, Michael Gill, Jonathan L Haines, Joachim Hallmayer, Judith Miller, Anthony P Monaco, John I Nurnberger, Andrew D Paterson, Margaret A Pericak-Vance, Gerard D Schellenberg, Peter Szatmari, Astrid M Vicente, Veronica J Vieland, Ellen M Wijsman, Stephen W Scherer, James S Sutcliffe, Catalina Betancur
Nature - 2010 -
[The unique role of child health services--early recognition of autism. Experiences with new routines in child health care in
Gothenburg].
Gudrun Nygren, Eva Sandberg, Thomas Arvidsson, Christopher Gillberg
Läkartidningen - 2010 -
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and
controls.
Richard Delorme, Catalina Betancur, Isabelle Scheid, Henrik Anckarsäter, Pauline Chaste, Stéphane Jamain, Franck Schuroff, Gudrun Nygren, Evelyn Herbrecht, Anne Dumaine, Marie Christine Mouren-Simeoni, Maria Råstam, Marion Leboyer, Christopher Gillberg, Thomas Bourgeron
BMC Medical Genetics - 2010 -
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general
population.
Pauline Chaste, Nathalie Clement, Oriane Mercati, Jean-Luc Guillaume, Richard Delorme, Hany Goubran Botros, Cécile Pagan, Samuel Périvier, Isabelle Scheid, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, I Carina Gillberg, Emilie Serrano, Nathalie Lemière, Jean Marie Launay, Marie Christine Mouren-Simeoni, Marion Leboyer, Christopher Gillberg, Ralf Jockers, Thomas Bourgeron
PloS One - 2010 -
A genome-wide scan for common alleles affecting risk for
autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Nuala Sykes, Alistair T Pagnamenta, Joana Almeida, Elena Bacchelli, Anthony J Bailey, Gillian Baird, Agatino Battaglia, Tom Berney, Nadia Bolshakova, Sven Bölte, Patrick F. Bolton, Thomas Bourgeron, Sean Brennan, Jessica Brian, Andrew R Carson, Guillermo Casallo, Jillian Casey, Su H Chu, Lynne Cochrane, Christina Corsello, Emily L Crawford, Andrew Crossett, Geraldine Dawson, Maretha de Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A Fernandez, Susan E Folstein, Eric Fombonne, Christine M Freitag, John Gilbert, Christopher Gillberg, Joseph T Glessner, Jeremy Goldberg, Jonathan Green, Stephen J Guter, Hakon Hakonarson, Elizabeth A Heron, Matthew Hill, Richard Holt, Jennifer L Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara M Lajonchere, Janine A Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L Leventhal, Anath C Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C Lund, Elena Maestrini, William Mahoney, Carine Mantoulan, Christian R Marshall, Helen McConachie, Christopher J McDougle, Jane McGrath, William M McMahon, Nadine M Melhem, Alison Merikangas, Ohsuke Migita, Nancy J Minshew, Ghazala K Mirza, Jeff Munson, Stanley F Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Katerina Papanikolaou, Jeremy R Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Joseph Piven, David J Posey, Annemarie Poustka, Fritz Poustka, Aparna Prasad, Jiannis Ragoussis, Katy Renshaw, Jessica Rickaby, Wendy Roberts, Kathryn Roeder, Bernadette Roge, Michael L Rutter, Laura J Bierut, John P Rice, Jeff Salt, Katherine Sansom, Daisuke Sato, Ricardo Segurado, Lili Senman, Naisha Shah, Val C Sheffield, Latha Soorya, Inês Sousa, Vera Stoppioni, Christina Strawbridge, Raffaella Tancredi, Katherine Tansey, Bhooma Thiruvahindrapduram, Ann P Thompson, Susanne Thomson, Ana Tryfon, John Tsiantis, Herman Van Engeland, John B Vincent, Fred Volkmar, Simon Wallace, Kai Wang, Zhouzhi Wang, Thomas H Wassink, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, Brian L Yaspan, Danielle Zurawiecki, Lonnie Zwaigenbaum, Catalina Betancur, Joseph D Buxbaum, Rita M Cantor, Edwin H Cook, Hilary Coon, Michael L Cuccaro, Louise Gallagher, Daniel H Geschwind, Michael Gill, Jonathan L Haines, Judith Miller, Anthony P Monaco, John I Nurnberger, Andrew D Paterson, Margaret A Pericak-Vance, Gerard D Schellenberg, Stephen W Scherer, James S Sutcliffe, Peter Szatmari, Astrid M Vicente, Veronica J Vieland, Ellen M Wijsman, Bernie Devlin, Sean Ennis, Joachim Hallmayer
Human Molecular Genetics - 2010 -
The right hemisphere fails to respond to temporal novelty in autism: evidence from an ERP
study.
Elena V Orekhova, T A Stroganova, A O Prokofiev, Gudrun Nygren, Christopher Gillberg, Mikael Elam
Clinical Neurophysiology - 2009 -
The Swedish version of the Diagnostic Interview for Social and Communication Disorders (DISCO-10). Psychometric
properties.
Gudrun Nygren, Bibbi Hagberg, Eva Billstedt, Åsa Skoglund, Christopher Gillberg, Maria E I Johansson
Journal of Autism and Developmental Disorders - 2009 -
Possible association between the androgen receptor gene and autism spectrum
disorder.
Susanne Henningsson, Lina Jonsson, Elin Ljunggren, Lars Westberg, I Carina Gillberg, Maria Råstam, Henrik Anckarsäter, Gudrun Nygren, Mikael Landén, Kent Thuresson, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Elias Eriksson, Jonas Melke
Psychoneuroendocrinology - 2009 -
An investigation of ribosomal protein L10 gene in autism spectrum
disorders.
Xiaohong Gong, Richard Delorme, Fabien Fauchereau, Christelle M Durand, Pauline Chaste, Catalina Betancur, Hany Goubran-Botros, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, I Carina Gillberg, Svenny Kopp, Marie-Christine Mouren-Simeoni, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron
BMC Medical Genetics - 2009 -
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum
disorders.
Christel Depienne, Daniel Moreno-De-Luca, Delphine Heron, Delphine Bouteiller, Aurélie Gennetier, Richard Delorme, Pauline Chaste, Jean-Pierre Siffroi, Sandra Chantot-Bastaraud, Baya Benyahia, Oriane Trouillard, Gudrun Nygren, Svenny Kopp, Maria E I Johansson, Maria Råstam, Lydie Burglen, Eric Leguern, Alain Verloes, Marion Leboyer, Alexis Brice, Christopher Gillberg, Catalina Betancur
Biological Psychiatry - 2009 -
Sensory gating in young children with autism: relation to age, IQ, and EEG gamma
oscillations.
Elena V Orekhova, Tatiana. A. Stroganova, Andrey. O. Prokofyev, Gudrun Nygren, Christopher Gillberg, Mikael Elam
Neuroscience Letters - 2008 -
Analysis of X chromosome inactivation in autism spectrum
disorders.
Xiaohong Gong, Elena Bacchelli, Francesca Blasi, Claudio Toma, Catalina Betancur, Pauline Chaste, Richard Delorme, Christelle M Durand, Fabien Fauchereau, Hany Goubran Botros, Marion Leboyer, Marie-Christine Mouren-Simeoni, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, I Carina Gillberg, Christopher Gillberg, Daniel Moreno-De-Luca, Simona Carone, Ilona Nummela, Mari Rossi, Agatino Battaglia, Irma Jarvela, Elena Maestrini, Thomas Bourgeron
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics - 2008 -
Abnormal melatonin synthesis in autism spectrum
disorders.
Jonas Melke, Hany Goubran-Botros, Pauline Chaste, Catalina Betancur, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, I Carina Gillberg, Richard Delorme, Nadia Chabane, Marie-Christine Mouren-Simeoni, Fabien Fauchereau, Christelle. M. Durand, Fabien Chevalier, Xavier Drouot, Corinne Collet, Jean-Marie Launay, Marion Leboyer, Christopher Gillberg, Thomas Bourgeron
Molecular Psychiatry - 2008 -
Abnormal EEG lateralization in boys with
autism.
Tatiana A Stroganova, Gudrun Nygren, Marina M Tsetlin, Irina N Posikera, Christopher Gillberg, Mikael Elam, Elena V Orekhova
Clinical Neurophysiology - 2007 -
Excess of high frequency electroencephalogram oscillations in boys with
autism.
Elena V Orekhova, Tatiana A Stroganova, Gudrun Nygren, Marina M Tsetlin, Irina N Posikera, Christopher Gillberg, Mikael Elam
Biological Psychiatry - 2007 -
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum
disorders.
Christelle. M. Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Råstam, I Carina Gillberg, Henrik Anckarsäter, Eili Sponheim, Hany Goubran-Botros, Richard Delorme, Nadia Chabane, Marie-Christine Mouren-Simeoni, Philippe de Mas, Eric Bieth, Bernadette Rogé, Delphine Héron, Lydie Burglen, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron
Nature Genetics - 2007 -
Mutation screening of the ARX gene in patients with
autism.
Pauline Chaste, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Mary Coleman, Marion Leboyer, Christopher Gillberg, Catalina Betancur
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics - 2007 -
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and
macrocephaly.
Joseph. D. Buxbaum, Guiqing Cai, Gudrun Nygren, Pauline Chaste, Richard Delorme, Juliet Goldsmith, Maria Råstam, Jeremy. M. Silverman, Eric Hollander, Christopher Gillberg, Marion Leboyer, Catalina Betancur
BMC Medical Genetics - 2007 -
Mutation screening of the PTEN gene in patients with autism spectrum disorders and
macrocephaly.
Joseph D Buxbaum, Guiqing Cai, Pauline Chaste, Gudrun Nygren, Juliet Goldsmith, Jennifer Reichert, Henrik Anckarsäter, Maria Råstam, Christopher J Smith, Jeremy M Silverman, Eric Hollander, Marion Leboyer, Christopher Gillberg, Alain Verloes, Catalina Betancur
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics - 2007 -
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric
disorders.
Christelle M Durand, Caroline Kappeler, Catalina Betancur, Richard Delorme, Hélène Quach, Hany Goubran-Botros, Jonas Melke, Gudrun Nygren, Nadia Chabane, Franck Bellivier, Andrei Szoke, Franck Schurhoff, Maria Råstam, Henrik Anckarsäter, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication of the International Society of Psychiatric Genetics - 2006 -
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control
subjects.
Richard Delorme, Christelle M Durand, Catalina Betancur, Michael Wagner, Stephan Ruhrmann, Hans-Juergen Grabe, Gudrun Nygren, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron, Philippe Courtet, Fabrice Jollant, Catherine Buresi, Jean-Michel Aubry, Patrick Baud, Guido Bondolfi, Gilles Bertschy, Nader Perroud, Alain Malafosse
Biological Psychiatry - 2006 -
Neuropsychiatric and neurodevelopmental outcome of children at age 6 and 7 years who screened positive for language problems at 30
months.
Carmela Miniscalco, Gudrun Nygren, Bibbi Hagberg, Björn Kadesjö, Christopher Gillberg
Developmental Medicine and Child Neurology - 2006 -
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive
disorder.
Richard Delorme, Catalina Betancur, Michael Wagner, Marie-Odile Krebs, Philip Gorwood, Phillip Pearl, Gudrun Nygren, Christelle M Durand, Friederike Buhtz, P Pickering, Jonas Melke, Stephan Ruhrmann, Henrik Anckarsäter, Nadia Chabane, Amelié Kipman, Claudia Reck, Bruno Millet, Isabelle Roy, Marie-Christine Mouren-Simeoni, Wolgang Maier, Maria Råstam, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron
Molecular Psychiatry - 2005