Poisson A - Search Results

1

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. Among authors: poisson a. BMC Med Genet. 2014 Dec 11;15:132. doi: 10.1186/s12881-014-0132-3. BMC Med Genet. 2014. PMID: 25496186 Free PMC article.

2

12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome.

Poisson A, Lesca G, Chatron N, Favre E, Cottin V, Gamondes D, Sanlaville D, Edery P, Giraud S, Demily C, Dupuis-Girod S. Poisson A, et al. Eur J Med Genet. 2019 Nov;62(11):103565. doi: 10.1016/j.ejmg.2018.10.017. Epub 2018 Oct 30. Eur J Med Genet. 2019. PMID: 30389587

3

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. 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.

4

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. Among authors: poisson a. 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.

5

[Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders].

Poisson A, Nicolas A, Sanlaville D, Cochat P, De Leersnyder H, Rigard C, Franco P, des Portes V, Edery P, Demily C. Poisson A, et al. Arch Pediatr. 2015 Jun;22(6):638-45. doi: 10.1016/j.arcped.2015.03.015. Epub 2015 Apr 28. Arch Pediatr. 2015. PMID: 25934608 French.

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. 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

Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest?

Demily C, Lesca G, Poisson A, Till M, Barcia G, Chatron N, Sanlaville D, Munnich A. Demily C, et al. Among authors: poisson a. J Autism Dev Disord. 2018 Aug;48(8):2886-2889. doi: 10.1007/s10803-018-3552-7. J Autism Dev Disord. 2018. PMID: 29589274

8

Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review.

Gauld C, Poisson A, Reversat J, Peyroux E, Houdayer-Robert F, Rossi M, Lesca G, Sanlaville D, Demily C. Gauld C, et al. Among authors: poisson a. BMC Psychiatry. 2021 Jul 17;21(1):360. doi: 10.1186/s12888-021-03342-8. BMC Psychiatry. 2021. PMID: 34273950 Free PMC article. Review.

9

Regressive Autism Spectrum Disorder Expands the Phenotype of BSCL2/Seipin-Associated Neurodegeneration.

Poisson A, Chatron N, Labalme A, Till M, Broussolle E, Sanlaville D, Demily C, Lesca G. Poisson A, et al. Biol Psychiatry. 2019 Feb 15;85(4):e17-e19. doi: 10.1016/j.biopsych.2018.05.010. Epub 2018 Aug 24. Biol Psychiatry. 2019. PMID: 30150100 No abstract available.

10

Behavioral disturbance and treatment strategies in Smith-Magenis syndrome.

Poisson A, Nicolas A, Cochat P, Sanlaville D, Rigard C, de Leersnyder H, Franco P, Des Portes V, Edery P, Demily C. Poisson A, et al. Orphanet J Rare Dis. 2015 Sep 4;10:111. doi: 10.1186/s13023-015-0330-x. Orphanet J Rare Dis. 2015. PMID: 26336863 Free PMC article.

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