Poisson A - Search Results

1

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.

2

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.

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. 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.

4

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.

5

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

6

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.

7

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

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

[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.

10

Weight loss induced by quetiapine in a 22q11.2DS patient.

Demily C, Poisson A, Thibaut F, Franck N. Demily C, et al. Among authors: poisson a. Mol Genet Metab Rep. 2017 Oct 17;13:95-96. doi: 10.1016/j.ymgmr.2017.10.002. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 29062712 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

85 results

Search Page

Filters