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Year Number of Results
2002 4
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43 results

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Page 1
Pangenomic Classification of Pituitary Neuroendocrine Tumors.
Neou M, Villa C, Armignacco R, Jouinot A, Raffin-Sanson ML, Septier A, Letourneur F, Diry S, Diedisheim M, Izac B, Gaspar C, Perlemoine K, Verjus V, Bernier M, Boulin A, Emile JF, Bertagna X, Jaffrezic F, Laloe D, Baussart B, Bertherat J, Gaillard S, Assié G. Neou M, et al. Among authors: perlemoine k. Cancer Cell. 2020 Jan 13;37(1):123-134.e5. doi: 10.1016/j.ccell.2019.11.002. Epub 2019 Dec 26. Cancer Cell. 2020. PMID: 31883967 Free article.
Whole blood transcriptomic signature of Cushing's syndrome.
Birtolo MF, Armignacco R, Benanteur N, Baussart B, Villa C, De Murat D, Guignat L, Groussin L, Libé R, Zennaro MC, Saidi M, Perlemoine K, Letourneur F, Amar L, Bertherat J, Jouinot A, Assié G. Birtolo MF, et al. Among authors: perlemoine k. Eur J Endocrinol. 2024 Jul 2;191(1):55-63. doi: 10.1093/ejendo/lvae083. Eur J Endocrinol. 2024. PMID: 38970559
Biomarkers Improving Genetic and Metastatic Disease Prediction in Paraganglioma: Insights From a Prospective Study.
Drossart T, Buffet A, Janbain A, Ottolenghi C, Amar L, Libé R, Drui D, Lussey-Lepoutre C, Mancini M, Lounis T, Guénégou-Arnoux A, Méatchi T, Bertherat J, Burnichon N, Favier J, Gimenez-Roqueplo AP; COMETE-TACTIC Study Group. Drossart T, et al. J Clin Endocrinol Metab. 2025 Jul 15;110(8):2193-2204. doi: 10.1210/clinem/dgae797. J Clin Endocrinol Metab. 2025. PMID: 39541377
KDM1A inactivation causes hereditary food-dependent Cushing syndrome.
Vaczlavik A, Bouys L, Violon F, Giannone G, Jouinot A, Armignacco R, Cavalcante IP, Berthon A, Letouzé E, Vaduva P, Barat M, Bonnet F, Perlemoine K, Ribes C, Sibony M, North MO, Espiard S, Emy P, Haissaguerre M, Tauveron I, Guignat L, Groussin L, Dousset B, Reincke M, Fragoso MC, Stratakis CA, Pasmant E, Libé R, Assié G, Ragazzon B, Bertherat J. Vaczlavik A, et al. Among authors: perlemoine k. Genet Med. 2022 Feb;24(2):374-383. doi: 10.1016/j.gim.2021.09.018. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906447 Free article.
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlation.
Bouys L, Vaduva P, Jouinot A, Violon F, Vaczlavik A, Barat M, Charchar H, Chasseloup F, Kamilaris C, Espiard S, Haissaguerre M, Raverot G, Kroiss M, Berthon A, Perlemoine K, Tauveron I, Guignat L, Libé R, Groussin L, Assié G, Pasmant E, Reincke M, Borson-Chazot F, Ferrière A, Vantyghem MC, Stratakis CA, Kamenický P, Fragoso MCBV, Chansavang A, Ragazzon B, Bertherat J. Bouys L, et al. Among authors: perlemoine k. Eur J Endocrinol. 2025 Feb 1;192(2):119-127. doi: 10.1093/ejendo/lvaf016. Eur J Endocrinol. 2025. PMID: 39921449
The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update.
Bouys L, Vaczlavik A, Cavalcante IP, Violon F, Jouinot A, Berthon A, Vaduva P, Espiard S, Perlemoine K, Kamenicky P, Vantyghem MC, Tabarin A, Raverot G, Ronchi CL, Dischinger U, Reincke M, Fragoso MC, Stratakis CA, Chansavang A, Pasmant E, Ragazzon B, Bertherat J; COMETE and ENSAT Networks. Bouys L, et al. Among authors: perlemoine k. Orphanet J Rare Dis. 2025 Feb 5;20(1):51. doi: 10.1186/s13023-025-03554-1. Orphanet J Rare Dis. 2025. PMID: 39910635 Free PMC article. Review.
Integrated genomic characterization of adrenocortical carcinoma.
Assié G, Letouzé E, Fassnacht M, Jouinot A, Luscap W, Barreau O, Omeiri H, Rodriguez S, Perlemoine K, René-Corail F, Elarouci N, Sbiera S, Kroiss M, Allolio B, Waldmann J, Quinkler M, Mannelli M, Mantero F, Papathomas T, De Krijger R, Tabarin A, Kerlan V, Baudin E, Tissier F, Dousset B, Groussin L, Amar L, Clauser E, Bertagna X, Ragazzon B, Beuschlein F, Libé R, de Reyniès A, Bertherat J. Assié G, et al. Among authors: perlemoine k. Nat Genet. 2014 Jun;46(6):607-12. doi: 10.1038/ng.2953. Epub 2014 Apr 20. Nat Genet. 2014. PMID: 24747642
Unexpected discrepancies between steroid intra-tissular content in adrenal tumors and clinical diagnosis of steroid excess.
Bonnet-Serrano F, Thomeret L, Benanteur N, Vaduva P, Violon F, Bouys L, Ragazzon B, Berthon A, Perlemoine K, Wilmot-Roussel H, Zientek C, Nakib S, Gaillard M, Sibony M, Laguillier-Morizot C, Menet MC, Guignat L, Libe R, Groussin L, Guibourdenche J, Jouinot A, Assié G, Bertherat J. Bonnet-Serrano F, et al. Among authors: perlemoine k. Eur J Endocrinol. 2025 Jun 30;193(1):106-116. doi: 10.1093/ejendo/lvaf129. Eur J Endocrinol. 2025. PMID: 40515607
Whole blood methylome-derived features to discriminate endocrine hypertension.
Armignacco R, Reel PS, Reel S, Jouinot A, Septier A, Gaspar C, Perlemoine K, Larsen CK, Bouys L, Braun L, Riester A, Kroiss M, Bonnet-Serrano F, Amar L, Blanchard A, Gimenez-Roqueplo AP, Prejbisz A, Januszewicz A, Dobrowolski P, Davies E, MacKenzie SM, Rossi GP, Lenzini L, Ceccato F, Scaroni C, Mulatero P, Williams TA, Pecori A, Monticone S, Beuschlein F, Reincke M, Zennaro MC, Bertherat J, Jefferson E, Assié G. Armignacco R, et al. Among authors: perlemoine k. Clin Epigenetics. 2022 Nov 3;14(1):142. doi: 10.1186/s13148-022-01347-y. Clin Epigenetics. 2022. PMID: 36329530 Free PMC article.
43 results