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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1998 1
1999 1
2001 4
2004 1
2005 2
2008 1
2009 2
2010 2
2012 2
2013 5
2014 5
2015 7
2016 3
2017 2
2018 4
2019 3
2020 4
2021 4
2022 4
2023 4
2024 2

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55 results

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Page 1
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.
Poirier K, Lebrun N, Broix L, Tian G, Saillour Y, Boscheron C, Parrini E, Valence S, Pierre BS, Oger M, Lacombe D, Geneviève D, Fontana E, Darra F, Cances C, Barth M, Bonneau D, Bernadina BD, N'guyen S, Gitiaux C, Parent P, des Portes V, Pedespan JM, Legrez V, Castelnau-Ptakine L, Nitschke P, Hieu T, Masson C, Zelenika D, Andrieux A, Francis F, Guerrini R, Cowan NJ, Bahi-Buisson N, Chelly J. Poirier K, et al. Among authors: lebrun n. Nat Genet. 2013 Jun;45(6):639-47. doi: 10.1038/ng.2613. Epub 2013 Apr 21. Nat Genet. 2013. PMID: 23603762 Free PMC article.
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
Hu H, Haas SA, Chelly J, Van Esch H, Raynaud M, de Brouwer AP, Weinert S, Froyen G, Frints SG, Laumonnier F, Zemojtel T, Love MI, Richard H, Emde AK, Bienek M, Jensen C, Hambrock M, Fischer U, Langnick C, Feldkamp M, Wissink-Lindhout W, Lebrun N, Castelnau L, Rucci J, Montjean R, Dorseuil O, Billuart P, Stuhlmann T, Shaw M, Corbett MA, Gardner A, Willis-Owen S, Tan C, Friend KL, Belet S, van Roozendaal KE, Jimenez-Pocquet M, Moizard MP, Ronce N, Sun R, O'Keeffe S, Chenna R, van Bömmel A, Göke J, Hackett A, Field M, Christie L, Boyle J, Haan E, Nelson J, Turner G, Baynam G, Gillessen-Kaesbach G, Müller U, Steinberger D, Budny B, Badura-Stronka M, Latos-Bieleńska A, Ousager LB, Wieacker P, Rodríguez Criado G, Bondeson ML, Annerén G, Dufke A, Cohen M, Van Maldergem L, Vincent-Delorme C, Echenne B, Simon-Bouy B, Kleefstra T, Willemsen M, Fryns JP, Devriendt K, Ullmann R, Vingron M, Wrogemann K, Wienker TF, Tzschach A, van Bokhoven H, Gecz J, Jentsch TJ, Chen W, Ropers HH, Kalscheuer VM. Hu H, et al. Among authors: lebrun n. Mol Psychiatry. 2016 Jan;21(1):133-48. doi: 10.1038/mp.2014.193. Epub 2015 Feb 3. Mol Psychiatry. 2016. PMID: 25644381 Free PMC article.
The role of dysregulated ghrelin/LEAP-2 balance in anorexia nervosa.
Tezenas du Montcel C, Duriez P, Cao J, Lebrun N, Ramoz N, Viltart O, Gorwood P, Tolle V. Tezenas du Montcel C, et al. Among authors: lebrun n. iScience. 2023 Sep 22;26(11):107996. doi: 10.1016/j.isci.2023.107996. eCollection 2023 Nov 17. iScience. 2023. PMID: 37867951 Free PMC article.
Bacterial sensors of oxygen.
Green J, Crack JC, Thomson AJ, LeBrun NE. Green J, et al. Among authors: lebrun ne. Curr Opin Microbiol. 2009 Apr;12(2):145-51. doi: 10.1016/j.mib.2009.01.008. Epub 2009 Feb 24. Curr Opin Microbiol. 2009. PMID: 19246238 Review.
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
Variants in CUL4B are associated with cerebral malformations.
Vulto-van Silfhout AT, Nakagawa T, Bahi-Buisson N, Haas SA, Hu H, Bienek M, Vissers LE, Gilissen C, Tzschach A, Busche A, Müsebeck J, Rump P, Mathijssen IB, Avela K, Somer M, Doagu F, Philips AK, Rauch A, Baumer A, Voesenek K, Poirier K, Vigneron J, Amram D, Odent S, Nawara M, Obersztyn E, Lenart J, Charzewska A, Lebrun N, Fischer U, Nillesen WM, Yntema HG, Järvelä I, Ropers HH, de Vries BB, Brunner HG, van Bokhoven H, Raymond FL, Willemsen MA, Chelly J, Xiong Y, Barkovich AJ, Kalscheuer VM, Kleefstra T, de Brouwer AP. Vulto-van Silfhout AT, et al. Among authors: lebrun n. Hum Mutat. 2015 Jan;36(1):106-17. doi: 10.1002/humu.22718. Hum Mutat. 2015. PMID: 25385192 Free PMC article.
Ghrelin Gene Deletion Alters Pulsatile Growth Hormone Secretion in Adult Female Mice.
Hassouna R, Fernandez G, Lebrun N, Fiquet O, Roelfsema F, Labarthe A, Zizzari P, Tomasetto C, Epelbaum J, Viltart O, Chauveau C, Perello M, Tolle V. Hassouna R, et al. Among authors: lebrun n. Front Endocrinol (Lausanne). 2021 Oct 13;12:754522. doi: 10.3389/fendo.2021.754522. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34721302 Free PMC article.
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.
55 results