Demily C - Search Results

1

Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skills.

Babinet MN, Thomas N, Pons L, Schluth-Bolard C, Sanlaville D, Demily C. Babinet MN, et al. Among authors: demily c. Psychiatr Genet. 2023 Oct 1;33(5):202-205. doi: 10.1097/YPG.0000000000000351. Epub 2023 Jul 3. Psychiatr Genet. 2023. PMID: 37706496

2

[No title available]

[No authors listed] [No authors listed] PMID: 37706468

3

Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.

Demily C, Poisson A, Peyroux E, Gatellier V, Nicolas A, Rigard C, Schluth-Bolard C, Sanlaville D, Rossi M. Demily C, et al. BMC Med Genet. 2017 Jan 31;18(1):9. doi: 10.1186/s12881-017-0371-1. BMC Med Genet. 2017. PMID: 28137251 Free PMC article. Review.

4

Eye Direction Detection and Perception as Premises of a Social Brain: A Narrative Review of Behavioral and Neural Data.

Babinet MN, Cublier M, Demily C, Michael GA. Babinet MN, et al. Among authors: demily c. Cogn Affect Behav Neurosci. 2022 Feb;22(1):1-20. doi: 10.3758/s13415-021-00959-w. Epub 2021 Oct 12. Cogn Affect Behav Neurosci. 2022. PMID: 34642895 Review.

5

Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p.

Demily C, Rossi M, Chesnoy-Servanin G, Martin B, Poisson A, Sanlaville D, Edery P. Demily C, et al. BMC Med Genet. 2014 Dec 11;15:132. doi: 10.1186/s12881-014-0132-3. BMC Med Genet. 2014. PMID: 25496186 Free PMC article.

6

16q12.2q21: A new susceptibility locus for schizophrenia?

Poisson A, Schluth Bolard C, Martin B, Babinet MN, Sanlaville D, Demily C. Poisson A, et al. Among authors: demily c. Schizophr Res. 2016 Dec;178(1-3):109-111. doi: 10.1016/j.schres.2016.09.007. Epub 2016 Sep 8. Schizophr Res. 2016. PMID: 27617415 No abstract available.

7

Clinical and molecular cytogenetic characterization of four unrelated patients carrying 2p14 microdeletions.

Mathieu ML, Demily C, Chantot-Bastaraud S, Afenjar A, Mignot C, Andrieux J, Gerard M, Catala-Mora J, Jouk PS, Labalme A, Edery P, Sanlaville D, Rossi M. Mathieu ML, et al. Among authors: demily c. Am J Med Genet A. 2017 Aug;173(8):2268-2274. doi: 10.1002/ajmg.a.38307. Epub 2017 Jun 9. Am J Med Genet A. 2017. PMID: 28599093

8

What do error patterns in processing facial expressions, social interaction scenes and vocal prosody tell us about the way social cognition works in children with 22q11.2DS?

Peyroux E, Babinet MN, Cannarsa C, Madelaine C, Favre E, Demily C, Michael GA. Peyroux E, et al. Among authors: demily c. Eur Child Adolesc Psychiatry. 2020 Mar;29(3):299-313. doi: 10.1007/s00787-019-01345-1. Epub 2019 May 23. Eur Child Adolesc Psychiatry. 2020. PMID: 31123832

9

Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder.

Masson J, Demily C, Chatron N, Labalme A, Rollat-Farnier PA, Schluth-Bolard C, Gilbert-Dussardier B, Giuliano F, Touraine R, Tordjman S, Verloes A, Testa G, Sanlaville D, Edery P, Lesca G, Rossi M. Masson J, et al. Among authors: demily c. Orphanet J Rare Dis. 2019 May 31;14(1):121. doi: 10.1186/s13023-019-1094-5. Orphanet J Rare Dis. 2019. PMID: 31151468 Free PMC article.

10

Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.

Poisson A, Chatron N, Labalme A, Fourneret P, Ville D, Mathieu ML, Sanlaville D, Demily C, Lesca G. Poisson A, et al. Among authors: demily c. BMC Med Genet. 2020 Jan 8;21(1):10. doi: 10.1186/s12881-019-0946-0. BMC Med Genet. 2020. PMID: 31914951 Free PMC article.

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