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2016
Mark Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism
Pilorge, Marion ; Fassier, Coralie ; Le Corronc, Hervé ; Potey, Anaïs ; Bai, Jing ; De Gois, S ; Delaby, Elsa ; Assouline, Brigitte ; Guinchat, Vincent and Devillard, Francoise , et al. (2016) In Molecular Psychiatry 21. p.936-945
- Contribution to journal › Article
2013
Mark Heterozygous FA2H mutations in autism spectrum disorders
Scheid, Isabelle ; Maruani, Anna ; Huguet, Guillaume ; Leblond, Claire S ; Nygren, Gudrun ; Anckarsäter, Henrik ^LU ; Beggiato, Anita ; Råstam, Maria ^LU ; Amsellem, Frédederique and Gillberg, I Carina , et al. (2013) In BMC Medical Genetics 14.
- Contribution to journal › Article
2012
Mark Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Leblond, Claire S. ; Heinrich, Jutta ; Delorme, Richard ; Proepper, Christian ; Betancur, Catalina ; Huguet, Guillaume ; Konyukh, Marina ; Chaste, Pauline ; Ey, Elodie and Råstam, Maria ^LU , et al. (2012) In PLoS Genetics 8(2).
- Contribution to journal › Article
2011
Mark Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations
Konyukh, Marina ; Delorme, Richard ; Chaste, Pauline ; Leblond, Claire ; Lemière, Nathalie ; Nygren, Gudrun ; Anckarsäter, Henrik ^LU ; Råstam, Maria ^LU ; Ståhlberg, Ola and Amsellem, Frederique , et al. (2011) In PLoS ONE 6(3).
- Contribution to journal › Article
Mark Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Chaste, Pauline ; Clement, Nathalie ; Botros, Hany Goubran ; Guillaume, Jean-Luc ; Konyukh, Marina ; Pagan, Cécile ; Scheid, Isabelle ; Nygren, Gudrun ; Anckarsäter, Henrik ^LU and Råstam, Maria ^LU , et al. (2011) In Journal of Pineal Research 51(4). p.394-399
- Contribution to journal › Article
2010
Mark Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
Delorme, Richard ; Scheid, Isabelle ; Anckarsäter, Henrik ^LU ; Chaste, Pauline ; Jamain, Stephane ; Schuroff, Franck ; Nygren, Gudrun ; Herbrecht, Evelyn ; Dumaine, Anne and Mouren, Marie Christine , et al. (2010) In BMC Med Genet 11(1:108).
- Contribution to journal › Article
Mark Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
Chaste, Pauline ; Clement, Nathalie ; Mercati, Oriane ; Guillaume, Jean-Luc ; Delorme, Richard ; Goubran-Botros, Hany ; Pagan, Cécile ; Périvier, Samuel ; Scheid, Isabelle and Nygren, Gudrun , et al. (2010) In PLoS ONE 5(7). p.1-11
- Contribution to journal › Article
2009
Mark Possible association between the androgen receptor gene and autism spectrum disorder
Henningsson, Susanne ; Jonsson, Lina ; Ljunggren, Elin ; Westberg, Lars ; Gillberg, Carina ; Råstam, Maria ^LU ; Anckarsäter, Henrik ^LU ; Nygren, Gudrun ; Landen, Mikael and Thuresson, Kent , et al. (2009) In Psychoneuroendocrinology 34(5). p.752-761
- Contribution to journal › Article
Mark An investigation of ribosomal protein L10 gene in autism spectrum disorders
Gong, Xiaohong ; Delorme, Richard ; Fauchereau, Fabien ; Durand, Christelle M ; Chaste, Pauline ; Betancur, Catalina ; Goubran-Botros, Hany ; Nygren, Gudrun ; Anckarsäter, Henrik ^LU and Råstam, Maria ^LU , et al. (2009) In BMC Medical Genetics 10(7).
- Contribution to journal › Article
Mark Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
Depienne, Christel ; Moreno-De-Luca, Daniel ; Heron, Delphine ; Bouteiller, Delphine ; Gennetier, Aurélie ; Delorme, Richard ; Chaste, Pauline ; Siffroi, Jean-Pierre ; Chantot-Bastaraud, Sandra and Benyahia, Baya , et al. (2009) In Biological Psychiatry 66(4). p.349-359
- Contribution to journal › Article

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