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Year Number of Results
1997 1
2010 2
2011 3
2012 4
2013 2
2014 2
2016 1
2024 0

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Page 1
Lung disease modifier genes in cystic fibrosis.
Guillot L, Beucher J, Tabary O, Le Rouzic P, Clement A, Corvol H. Guillot L, et al. Among authors: beucher j. Int J Biochem Cell Biol. 2014 Jul;52:83-93. doi: 10.1016/j.biocel.2014.02.011. Epub 2014 Feb 22. Int J Biochem Cell Biol. 2014. PMID: 24569122 Review.
[Genetics and modifier genes, atypical and rare forms].
Férec C, Scotet V, Beucher J, Corvol H. Férec C, et al. Among authors: beucher j. Arch Pediatr. 2012 May;19 Suppl 1:S3-7. doi: 10.1016/S0929-693X(12)71099-0. Arch Pediatr. 2012. PMID: 22682487 Review. French.
Tufted angioma with Kasabach-Merritt syndrome mistaken for child abuse.
Bouvet R, Pierre M, Toutain F, Beucher J, Dabadie A, Le Gall F, François-Chervet C, Pladys P, Bruneau B, Le Gueut M. Bouvet R, et al. Among authors: beucher j. Forensic Sci Int. 2014 Dec;245:e15-7. doi: 10.1016/j.forsciint.2014.10.003. Epub 2014 Oct 14. Forensic Sci Int. 2014. PMID: 25459275
Indication of electron neutrino appearance from an accelerator-produced off-axis muon neutrino beam.
Abe K, Abgrall N, Ajima Y, Aihara H, Albert JB, Andreopoulos C, Andrieu B, Aoki S, Araoka O, Argyriades J, Ariga A, Ariga T, Assylbekov S, Autiero D, Badertscher A, Barbi M, Barker GJ, Barr G, Bass M, Bay F, Bentham S, Berardi V, Berger BE, Bertram I, Besnier M, Beucher J, Beznosko D, Bhadra S, Blaszczyk Fd, Blondel A, Bojechko C, Bouchez J, Boyd SB, Bravar A, Bronner C, Brook-Roberge DG, Buchanan N, Budd H, Calvet D, Cartwright SL, Carver A, Castillo R, Catanesi MG, Cazes A, Cervera A, Chavez C, Choi S, Christodoulou G, Coleman J, Coleman W, Collazuol G, Connolly K, Curioni A, Dabrowska A, Danko I, Das R, Davies GS, Davis S, Day M, De Rosa G, de André JP, de Perio P, Delbart A, Densham C, Di Lodovico F, Di Luise S, Dinh Tran P, Dobson J, Dore U, Drapier O, Dufour F, Dumarchez J, Dytman S, Dziewiecki M, Dziomba M, Emery S, Ereditato A, Escudero L, Esposito LS, Fechner M, Ferrero A, Finch AJ, Frank E, Fujii Y, Fukuda Y, Galymov V, Gannaway FC, Gaudin A, Gendotti A, George MA, Giffin S, Giganti C, Gilje K, Golan T, Goldhaber M, Gomez-Cadenas JJ, Gonin M, Grant N, Grant A, Gumplinger P, Guzowski P, Haesler A, Haigh MD, Hamano K, Hansen C, Hansen D, Hara T, Harrison PF, Hartfie… See abstract for full author list ➔ Abe K, et al. Among authors: beucher j. Phys Rev Lett. 2011 Jul 22;107(4):041801. doi: 10.1103/PhysRevLett.107.041801. Epub 2011 Jul 18. Phys Rev Lett. 2011. PMID: 21866992 Free article.
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.
Kott E, Legendre M, Copin B, Papon JF, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, Just J, Nathan N, Tamalet A, Collot N, Jeanson L, Le Gouez M, Vallette B, Vojtek AM, Epaud R, Coste A, Clement A, Housset B, Louis B, Escudier E, Amselem S. Kott E, et al. Among authors: beucher j. Am J Hum Genet. 2013 Sep 5;93(3):561-70. doi: 10.1016/j.ajhg.2013.07.013. Epub 2013 Aug 29. Am J Hum Genet. 2013. PMID: 23993197 Free PMC article.
13 results