Lebrun N - Search Results

1

Exome sequencing in a familial form of anorexia nervosa supports multigenic etiology.

Bienvenu T, Lebrun N, Clarke J, Duriez P, Gorwood P, Ramoz N. Bienvenu T, et al. Among authors: lebrun n. J Neural Transm (Vienna). 2019 Nov;126(11):1505-1511. doi: 10.1007/s00702-019-02056-2. Epub 2019 Aug 6. J Neural Transm (Vienna). 2019. PMID: 31388831

2

Identification of rare variants in CADM1 in patients with anorexia nervosa.

Lin Z, Lebrun N, Clarke J, Duriez P, Gorwood P, Ramoz N, Bienvenu T. Lin Z, et al. Among authors: lebrun n. Psychiatry Res. 2020 Sep;291:113191. doi: 10.1016/j.psychres.2020.113191. Epub 2020 Jun 8. Psychiatry Res. 2020. PMID: 32544712

3

Anorexia nervosa is associated with Neuronatin variants.

Lombardi L, Blanchet C, Poirier K, Lebrun N, Ramoz N, Rose Moro M, Gorwood P, Bienvenu T. Lombardi L, et al. Among authors: lebrun n. Psychiatr Genet. 2019 Aug;29(4):103-110. doi: 10.1097/YPG.0000000000000224. Psychiatr Genet. 2019. PMID: 30933048

4

De novo deleterious variants that may alter the dopaminergic reward pathway are associated with anorexia nervosa.

Bienvenu T, Lebrun N, Clarke J, Duriez P, Gorwood P, Ramoz N. Bienvenu T, et al. Among authors: lebrun n. Eat Weight Disord. 2020 Dec;25(6):1643-1650. doi: 10.1007/s40519-019-00802-9. Epub 2019 Oct 29. Eat Weight Disord. 2020. PMID: 31664672

5

Methodological considerations for ghrelin isoforms assay in clinical evaluation in anorexia nervosa.

Tezenas du Montcel C, Duriez P, Lebrun N, Grouselle D, de Grimaudet B, Dardennes R, Epelbaum J, Cuenca M, Viltart O, Gorwood P, Tolle V. Tezenas du Montcel C, et al. Among authors: lebrun n. Compr Psychoneuroendocrinol. 2022 May 20;11:100140. doi: 10.1016/j.cpnec.2022.100140. eCollection 2022 Aug. Compr Psychoneuroendocrinol. 2022. PMID: 35757178 Free PMC article.

6

RNA Sequencing and Pathway Analysis Identify Important Pathways Involved in Hypertrichosis and Intellectual Disability in Patients with Wiedemann-Steiner Syndrome.

Mietton L, Lebrun N, Giurgea I, Goldenberg A, Saintpierre B, Hamroune J, Afenjar A, Billuart P, Bienvenu T. Mietton L, et al. Among authors: lebrun n. Neuromolecular Med. 2018 Sep;20(3):409-417. doi: 10.1007/s12017-018-8502-1. Epub 2018 Jul 16. Neuromolecular Med. 2018. PMID: 30014449

7

Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences.

Lebrun N, Mehler-Jacob C, Poirier K, Zordan C, Lacombe D, Carion N, Billuart P, Bienvenu T. Lebrun N, et al. Gene. 2018 Dec 30;679:305-313. doi: 10.1016/j.gene.2018.09.016. Epub 2018 Sep 12. Gene. 2018. PMID: 30217758

8

MeCP2 is involved in random mono-allelic expression for a subset of human autosomal genes.

Brousseau M, Nectoux J, Saintpierre B, Lebrun N, Cagnard N, Izac B, Olivier E, Letourneur F, Bienvenu T. Brousseau M, et al. Among authors: lebrun n. Biochim Biophys Acta Mol Basis Dis. 2020 Jun 1;1866(6):165730. doi: 10.1016/j.bbadis.2020.165730. Epub 2020 Feb 15. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 32070770 Free article.

9

HDAC inhibitor ameliorates behavioral deficits in Mecp2^308/y mouse model of Rett syndrome.

Lebrun N, Delépine C, Selloum M, Meziane H, Nectoux J, Herault Y, Bienvenu T. Lebrun N, et al. Brain Res. 2021 Dec 1;1772:147670. doi: 10.1016/j.brainres.2021.147670. Epub 2021 Sep 25. Brain Res. 2021. PMID: 34582789

10

Autism spectrum disorder recurrence, resulting of germline mosaicism for a CHD2 gene missense variant.

Lebrun N, Parent P, Gendras J, Billuart P, Poirier K, Bienvenu T. Lebrun N, et al. Clin Genet. 2017 Dec;92(6):669-670. doi: 10.1111/cge.13073. Epub 2017 Sep 28. Clin Genet. 2017. PMID: 28960266

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