Publications en rapport avec les thèmes de recherche de l’EA3808

Freyssin A, Page G, Fauconneau B*, Rioux Bilan A* (*Co-last authors). Natural polyphenols effects on protein aggregates in Alzheimer’s and Parkinson’s prion-like diseases. Neural Regeneration Research 2018; Invited review, 13(6):955-961. doi: 10.4103/1673-5374.233432. [IF: 3.171]

Hanon O, Vidal JS, Lehmann S, Bombois S, Allinquant B, Tréluyer JM, Gelé P, Delmaire C, Blanc F, Mangin JF, Buée L, Touchon J, Hugon J, Vellas B, Galbrun E, Benetos A, Berrut G, Paillaud E, Wallon D, Castelnovo G, Volpe-Gillot L, Paccalin M, Robert PH, Godefroy O, Dantoine T, Camus V, Belmin J, Vandel P, Novella JL, Duron E, Rigaud AS, Schraen-Maschke S, Gabelle A; BALTAZAR study group. Plasma amyloid levels within the Alzheimer’s process and correlations with central biomarkers. Alzheimers Dement. 2018 Feb 16. pii: S1552-5260(18)30021-9. [IF: 9.478]

Julian A, Rioux Bilan A, Ragot S, Krolak-Salmon P, Berrut G, Dantoine T, Hommet C, Hanon O, Page G*, Paccalin M* (*Co-last authors). Blood inflammatory mediators and cognitive decline in Alzheimer’s disease: a two years longitudinal study. Journal of Alzheimer’s Disease.  2018;63(1):87-92. doi: 10.3233/JAD-171131.  [IF: 3.731]

Mulhern MS, Stumpel C, Stong N, Brunner HG, Bier L, Lippa N, Riviello J, Rouhl RPW, Kempers M, Pfundt R, Stegmann APA, Kukolich MK, Telegrafi A, Lehman A; CAUSES study, Lopez-Rangel E, Houcinat N, Barth M, den Hollander N, Hoffer MJV, Weckhuysen S; EuroEPINOMICS-RES-MAE working group, Roovers J, Djemie T, Barca D, Ceulemans B, Craiu D, Lemke JR, Korff C, Mefford HC, Meyers CT, Siegler Z, Hiatt SM, Cooper GM, Bebin EM, Snijders Blok L, Veenstra-Knol HE, Baugh EH, Brilstra EH, Volker-Touw CML, van Binsbergen E, Revah-Politi A, Pereira E, McBrian D, Pacault M, Isidor B, Le Caignec C, Gilbert-Dussardier B, Bilan F, Heinzen EL, Goldstein DB, Stevens SJC, Sands TT. NBEA: Developmental disease gene with early generalized epilepsy phenotypes. Ann Neurol. 2018 Nov;84(5):788-795. doi: 10.1002/ana.25350.  [IF: 10.244]

Vérité J, Janet T, Chassaing D, Fauconneau B, Rabeony H, Page G. Longitudinal chemokine profile expression in a blood brain barrier model from Alzheimer transgenic versus wild-type mice. Journal of Neuroinflammation, Jun 13;15(1):182. doi: 10.1186/s12974-018-1220-7.  [IF: 5.102]

Vérité J, Page G, Paccalin M, Julian A*, Janet T*, §Differential chemokine expression under the control of peripheral blood mononuclear cells issued from Alzheimer’s patients in a human blood brain barrier model. PLoS ONE, 2018 Aug 9;13(8):e0201232. doi: 10.1371/journal.pone.0201232. eCollection 2018. * Co-last authors, § Corresponding author [IF: 2.766]

Vion E, Page G, Bourdeaud E, Paccalin M, Guillard J, Rioux Bilan A. Trans ε‑viniferin is an amyloid-β disaggregating and anti-inflammatory drug in a mouse primary cellular model of Alzheimer’s disease. Molecular and Cellular Neuroscience, 2018 Apr;88:1-6. doi: 10.1016/j.mcn.2017.12.003. Epub 2017 Dec 7.  [IF: 3.084]

Autres publications

Bémer P, Léger J, Milin S, Plouzeau C, Valentin AS, Stock N, Jolivet-Gougeon A, Moreau A, Corvec S, Quintin-Roue I, Tandé D, Héry-Arnaud G, Rousselet MC, Lemarié C, Kempf M, Michenet P, Bret L, de Pinieux G, Burucoa C; CRIOGO (Centre de Référence des Infections Ostéo-articulaires du Grand Ouest) Study Team. Histopathological Diagnosis of Prosthetic Joint Infection: Does a Threshold of 23 Neutrophils Do Better than Classification of the Periprosthetic Membrane in a Prospective Multicenter Study? J Clin Microbiol. 2018 Aug 27;56(9). pii: e00536-18. doi: 10.1128/JCM.00536-18. Print 2018 Sep. PubMed PMID: 29976593; PubMed Central PMCID: PMC6113493.

Guichet PO, Masliantsev K, Tachon G, Petropoulos C, Godet J, Larrieu D, Milin  S, Wager M, Karayan-Tapon L. Fatal correlation between YAP1 expression and glioma aggressiveness: clinical and molecular evidence. J Pathol. 2018 Oct;246(2):205-216. doi: 10.1002/path.5133. Epub 2018 Aug 28. PubMed PMID: 30009411.

Ingrand I, Paccalin M, Liuu E, Gil R, Ingrand P. Positive perception of aging is a key predictor of quality-of-life in aging people. PLoS One. 2018 Oct 3;13(10):e0204044. doi: 10.1371/journal.pone.0204044. eCollection 2018. PubMed PMID: 30281672; PubMed Central PMCID: PMC6169874.

Martellosio JP, Landron C, Milin S, Sarfati R, Arrivé F, Beuvon C, Roblot P. [Surgical treatment of an auto-immune hemolytic anemia]. Rev Med Interne. 2018 Jun;39(6):435-438. doi: 10.1016/j.revmed.2018.03.018. Epub 2018 Apr 9. French. PubMed PMID: 29650300.

Meester JAN, Sukalo M, Schröder KC, Schanze D, Baynam G, Borck G, Bramswig NC, Duman D, Gilbert-Dussardier B, Holder-Espinasse M, Itin P, Johnson DS, Joss S, Koillinen H, McKenzie F, Morton J, Nelle H, Reardon W, Roll C, Salih MA, Savarirayan R, Scurr I, Splitt M, Thompson E, Titheradge H, Travers CP, Van Maldergem L, Whiteford M, Wieczorek D, Vandeweyer G, Trembath R, Van Laer L, Loeys BL, Zenker M, Southgate L, Wuyts W. Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort. Hum Mutat. 2018 Sep;39(9):1246-1261. doi: 10.1002/humu.23567. Epub 2018 Jul 4. PubMed PMID: 29924900; PubMed Central PMCID: PMC6175364.

Michot C, Le Goff C, Blair E, Blanchet P, Capri Y, Gilbert-Dussardier B, Goldenberg A, Henderson A, Isidor B, Kayserili H, Kinning E, Le Merrer M, Lyonnet S, Odent S, Simsek-Kiper PO, Quelin C, Savarirayan R, Simon M, Splitt M, Verhagen JMA, Verloes A, Munnich A, Baujat G, Cormier-Daire V. Expanding the phenotypic spectrum of variants in PDE4D/PRKAR1A: from acrodysostosis to acroscyphodysplasia. Eur J Hum Genet. 2018 Nov;26(11):1611-1622. doi: 10.1038/s41431-018-0135-1. Epub 2018 Jul 13. PubMed PMID: 30006632; PubMed Central PMCID: PMC6189044.

Miguet M, Faivre L, Amiel J, Nizon M, Touraine R, Prieur F, Pasquier L, Lefebvre M, Thevenon J, Dubourg C, Julia S, Sarret C, Remerand G, Francannet C, Laffargue F, Boespflug-Tanguy O, David A, Isidor B, Vigneron J, Leheup B, Lambert L, Philippe C, Béri-Dexheimer M, Cuisset JM, Andrieux J, Plessis G, Toutain A, Guibaud L, Cormier-Daire V, Rio M, Bonnefont JP, Echenne B, Journel H, Burglen L, Chantot-Bastaraud S, Bienvenu T, Baumann C, Perrin L, Drunat S, Jouk PS, Dieterich K, Devillard F, Lacombe D, Philip N, Sigaudy S, Moncla A, Missirian C, Badens C, Perreton N, Thauvin-Robinet C, AChro-Puce R, Pedespan JM, Rooryck C, Goizet C, Vincent-Delorme C, Duban-Bedu B, Bahi-Buisson N, Afenjar A, Maincent K, Héron D, Alessandri JL, Martin-Coignard D, Lesca G, Rossi M, Raynaud M, Callier P, Mosca-Boidron AL, Marle N, Coutton C, Satre V, Caignec CL, Malan V, Romana S,  Keren B, Tabet AC, Kremer V, Scheidecker S, Vigouroux A, Lackmy-Port-Lis M, Sanlaville D, Till M, Carneiro M, Gilbert-Dussardier B, Willems M, Van Esch H, Portes VD, El Chehadeh S. Further delineation of the MECP2 duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features. J Med Genet. 2018 Jun;55(6):359-371. doi: 10.1136/jmedgenet-2017-104956. Epub 2018 Apr 4. PubMed PMID: 29618507.

Mulhern MS, Stumpel C, Stong N, Brunner HG, Bier L, Lippa N, Riviello J, Rouhl RPW, Kempers M, Pfundt R, Stegmann APA, Kukolich MK, Telegrafi A, Lehman A; CAUSES study, Lopez-Rangel E, Houcinat N, Barth M, den Hollander N, Hoffer MJV, Weckhuysen S; EuroEPINOMICS-RES-MAE working group, Roovers J, Djemie T, Barca D, Ceulemans B, Craiu D, Lemke JR, Korff C, Mefford HC, Meyers CT, Siegler Z, Hiatt SM, Cooper GM, Bebin EM, Snijders Blok L, Veenstra-Knol HE, Baugh EH, Brilstra EH, Volker-Touw CML, van Binsbergen E, Revah-Politi A, Pereira E, McBrian D, Pacault M, Isidor B, Le Caignec C, Gilbert-Dussardier B, Bilan F, Heinzen EL, Goldstein DB, Stevens SJC, Sands TT. NBEA: Developmental disease gene with early generalized epilepsy phenotypes. Ann Neurol. 2018 Nov;84(5):788-795. doi: 10.1002/ana.25350. Epub 2018 Oct 25. PubMed PMID: 30269351; PubMed Central PMCID: PMC6249120.

Pilotto A, Veronese N, Daragjati J, Cruz-Jentoft AJ, Polidori MC, Mattace-Raso F, Paccalin M, Topinkova E, Siri G, Greco A, Mangoni AA, Maggi S, Ferrucci L; MPI_AGE Investigators. Using the Multidimensional Prognostic Index to Predict Clinical Outcomes of Hospitalized Older Persons: a Prospective, Multicentre, International Study. J Gerontol A Biol Sci Med Sci. 2018 Oct 17. doi: 10.1093/gerona/gly239. [Epub ahead of print] PubMed PMID: 30329033.

Roussille P, Tachon G, Villalva C, Milin S, Frouin E, Godet J, Berger A, Emambux S, Petropoulos C, Wager M, Karayan-Tapon L, Tougeron D. Pathological and  Molecular Characteristics of Colorectal Cancer with Brain Metastases. Cancers (Basel). 2018 Dec 10;10(12). pii: E504. doi: 10.3390/cancers10120504. PubMed PMID: 30544743; PubMed Central PMCID: PMC6316286.

Vuillaume ML, Jeanne M, Blesson S, Denommé-Pichon AS, Alirol S, Brulard C , Bonneau D, Isidor B, Gilbert-Dussardier B, Odent S, Parent P, Donnart A, Redon R, Bézieau S, Laumonnier F, Toutain A.  A novel GABBR2 mutation identified by whole exome sequencing highlights the involvement of GABAB receptors in severe intellectual disability Ann Neurol. 2018 Jan 25. doi: 10.1002/ana.25155   [IF: 9.890]

Vuillaume ML, Jeanne M, Xue L, Blesson S, Denommé-Pichon AS, Alirol S, Brulard C, Colin E, Isidor B, Gilbert-Dussardier B, Odent S, Parent P, Donnart A, Redon R, Bézieau S, Rondard P, Laumonnier F, Toutain A. A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett-like phenotype. Ann Neurol. 2018 Feb;83(2):437-439. doi: 10.1002/ana.25155. Epub 2018 Feb 7. PubMed PMID: 29369404.

Xavier J, Zhou B, Bilan F, Zhang X, Gilbert-Dussardier B, Viaux-Savelon S, Pattni R, Ho SS, Cohen D, Levinson DF, Urban AE, Laurent-Levinson C. 1q21.1 microduplication: large verbal-nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number. NPJ Genom Med. 2018 Aug 22;3:24. doi: 10.1038/s41525-018-0059-2. eCollection 2018.  [IF: 3.467]