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Page 1
A Genetic Bridge Between Medicine and Neurodiversity for Autism.
Leblond CS, Rolland T, Barthome E, Mougin Z, Fleury M, Ecker C, Bonnot-Briey S, Cliquet F, Tabet AC, Maruani A, Chaumette B, Green J, Delorme R, Bourgeron T. Leblond CS, et al. Annu Rev Genet. 2024 Nov;58(1):487-512. doi: 10.1146/annurev-genet-111523-102614. Annu Rev Genet. 2024. PMID: 39585908 Free article. Review.
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry.
Bloomfield M, Lautarescu A, Heraty S, Douglas S, Violland P, Plas R, Ghosh A, Van den Bosch K, Eaton E, Absoud M, Battini R, Blázquez Hinojosa A, Bolshakova N, Bölte S, Bonanni P, Borg J, Calderoni S, Calvo Escalona R, Castelo-Branco M, Castro-Fornieles J, Caro P, Cliquet F, Danieli A, Delorme R, Elia M, Hempel M, Leblond CS, Madeira N, McAlonan G, Milone R, Molloy CJ, Mouga S, Montiel V, Pina Rodrigues A, Schaaf CP, Serrano M, Tammimies K, Tye C, Vigevano F, Oliveira G, Mazzone B, O'Neill C, Pender J, Romero V, Tillmann J, Oakley B, Murphy DGM, Gallagher L, Bourgeron T, Chatham C, Charman T. Bloomfield M, et al. Among authors: leblond cs. BMJ Open. 2024 Jun 4;14(6):e080746. doi: 10.1136/bmjopen-2023-080746. BMJ Open. 2024. PMID: 38834317 Free PMC article.
Phenotypic effects of genetic variants associated with autism.
Rolland T, Cliquet F, Anney RJL, Moreau C, Traut N, Mathieu A, Huguet G, Duan J, Warrier V, Portalier S, Dry L, Leblond CS, Douard E, Amsellem F, Malesys S, Maruani A, Toro R, Børglum AD, Grove J, Baron-Cohen S, Packer A, Chung WK, Jacquemont S, Delorme R, Bourgeron T. Rolland T, et al. Among authors: leblond cs. Nat Med. 2023 Jul;29(7):1671-1680. doi: 10.1038/s41591-023-02408-2. Epub 2023 Jun 26. Nat Med. 2023. PMID: 37365347 Free PMC article.
Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism.
Pretzsch CM, Floris DL, Schäfer T, Bletsch A, Gurr C, Lombardo MV, Chatham CH, Tillmann J, Charman T, Arenella M, Jones E, Ambrosino S, Bourgeron T, Dumas G, Cliquet F, Leblond CS, Loth E, Oakley B, Buitelaar JK, Baron-Cohen S, Beckmann CF, Persico AM, Banaschewski T, Durston S, Freitag CM; EU-AIMS/AIMS-2-TRIALS Consortium; Murphy DGM, Ecker C. Pretzsch CM, et al. Among authors: leblond cs. Mol Psychiatry. 2023 May;28(5):2158-2169. doi: 10.1038/s41380-023-02016-z. Epub 2023 Mar 29. Mol Psychiatry. 2023. PMID: 36991132 Free PMC article.
Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome.
Vitrac A, Leblond CS, Rolland T, Cliquet F, Mathieu A, Maruani A, Delorme R, Schön M, Grabrucker AM, van Ravenswaaij-Arts C, Phelan K, Tabet AC, Bourgeron T. Vitrac A, et al. Among authors: leblond cs. Eur J Med Genet. 2023 May;66(5):104732. doi: 10.1016/j.ejmg.2023.104732. Epub 2023 Feb 21. Eur J Med Genet. 2023. PMID: 36822569 Free article. Review.
Stratifying the autistic phenotype using electrophysiological indices of social perception.
Mason L, Moessnang C, Chatham C, Ham L, Tillmann J, Dumas G, Ellis C, Leblond CS, Cliquet F, Bourgeron T, Beckmann C, Charman T, Oakley B, Banaschewski T, Meyer-Lindenberg A, Baron-Cohen S, Bölte S, Buitelaar JK, Durston S, Loth E, Oranje B, Persico A, Dell'Acqua F, Ecker C, Johnson MH, Murphy D, Jones EJH. Mason L, et al. Among authors: leblond cs. Sci Transl Med. 2022 Aug 17;14(658):eabf8987. doi: 10.1126/scitranslmed.abf8987. Epub 2022 Aug 17. Sci Transl Med. 2022. PMID: 35976994 Free article.
Genetic correlates of phenotypic heterogeneity in autism.
Warrier V, Zhang X, Reed P, Havdahl A, Moore TM, Cliquet F, Leblond CS, Rolland T, Rosengren A; EU-AIMS LEAP; iPSYCH-Autism Working Group; Spectrum 10K and APEX Consortia; Rowitch DH, Hurles ME, Geschwind DH, Børglum AD, Robinson EB, Grove J, Martin HC, Bourgeron T, Baron-Cohen S. Warrier V, et al. Among authors: leblond cs. Nat Genet. 2022 Sep;54(9):1293-1304. doi: 10.1038/s41588-022-01072-5. Epub 2022 Jun 2. Nat Genet. 2022. PMID: 35654973 Free PMC article.
Neurobiological Correlates of Change in Adaptive Behavior in Autism.
Pretzsch CM, Schäfer T, Lombardo MV, Warrier V, Mann C, Bletsch A, Chatham CH, Floris DL, Tillmann J, Yousaf A, Jones E, Charman T, Ambrosino S, Bourgeron T, Dumas G, Loth E, Oakley B, Buitelaar JK, Cliquet F, Leblond CS, Baron-Cohen S, Beckmann CF, Banaschewski T, Durston S, Freitag CM; EU-AIMS LEAP Group; Murphy DGM, Ecker C. Pretzsch CM, et al. Among authors: leblond cs. Am J Psychiatry. 2022 May;179(5):336-349. doi: 10.1176/appi.ajp.21070711. Epub 2022 Mar 25. Am J Psychiatry. 2022. PMID: 35331004
Oligogenicity, C9orf72 expansion, and variant severity in ALS.
Ross JP, Leblond CS, Laurent SB, Spiegelman D, Dionne-Laporte A, Camu W, Dupré N, Dion PA, Rouleau GA. Ross JP, et al. Among authors: leblond cs. Neurogenetics. 2020 Jul;21(3):227-242. doi: 10.1007/s10048-020-00612-7. Epub 2020 May 8. Neurogenetics. 2020. PMID: 32385536
51 results