Monsieur
Thierry BIENVENU
Directeur de recherche
Chercheur
ED BioSPC
10-02-2015
07-12-2015
04-04-2017
Available to host a PhD student

Team

Pierre BILLUART
Notre groupe s'intéresse aux causes génétiques de formes non résolues de déficience intellectuelle, et aux causes génétiques de pathologies psychiatriques et neurologiques incluant les ...

Biographie / Publications

1: EndaleAhanda ML, Bienvenu T, Sermet-Gaudelus I, Mazzolini L, Edelman A,Zoorob R, Davezac N. The hsa-miR-125a/hsa-let-7e/hsa-miR-99b cluster ispotentially implicated in Cystic Fibrosis pathogenesis. J Cyst Fibros. 2015 Mar20. pii: S1569-1993(15)00053-3. doi: 10.1016/j.jcf.2015.02.011. [Epub ahead ofprint] PubMed PMID: 25800681.

 

2: Viel M, Hubert D, Burgel PR, Génin E, Honoré I, Martinez B, Gaitch N, Chapron J, Kanaan R, Dusser D, Girodon E, Bienvenu T. DCTN4 as a modifier of chronicPseudomonas aeruginosa infection in cystic fibrosis. Clin Respir J. 2015 Mar 12. doi: 10.1111/crj.12288. [Epub ahead of print] PubMed PMID: 25763772.

 

3: Rousseaud A, Delépine C, Nectoux J, Billuart P, Bienvenu T. DifferentialExpression and Regulation of Brain-Derived Neurotrophic Factor (BDNF) mRNAIsoforms in Brain Cells from Mecp2(308/y) Mouse Model. J MolNeurosci.2015 Jan30. [Epub ahead of print] PubMed PMID: 25634725.

 

4: Bonini J, Varilh J, Raynal C, Thèze C, Beyne E, Audrezet MP, Ferec C, BienvenuT, Girodon E, Tuffery-Giraud S, Des Georges M, Claustres M, Taulan-Cadars M.Small-scale high-throughput sequencing-based identification of new therapeutictools in cystic fibrosis. Genet Med. 2015 Jan 8. doi: 10.1038/gim.2014.194. [Epubahead of print] PubMed PMID: 25569440.

 

5: Mignot C, Lambert L, Pasquier L, Bienvenu T, Delahaye-Duriez A, Keren B,Lefranc J, Saunier A, Allou L, Roth V, Valduga M, Moustaïne A, Auvin S, Barrey C,Chantot-Bastaraud S, Lebrun N, Moutard ML, Nougues MC, Vermersch AI, Héron B,Pipiras E, Héron D, Olivier-Faivre L, Guéant JL, Jonveaux P, Philippe C.WWOX-related encephalopathies: delineation of the phenotypical spectrum andemerging genotype-phenotype correlation. J Med Genet. 2015 Jan;52(1):61-70. doi: 10.1136/jmedgenet-2014-102748. Epub 2014 Nov 19. PubMed PMID: 25411445.

 

6: Puéchal X, Génin E, Bienvenu T, Le Jeunne C, Dusser DJ. Poor survival inrheumatoid arthritis associated with bronchiectasis: a family-based cohort study.PLoS One. 2014 Oct 13;9(10):e110066. doi: 10.1371/journal.pone.0110066.eCollection 2014. PubMed PMID: 25310716; PubMed Central PMCID: PMC4195708.

 

7: Terrone G, Bienvenu T, Germanaud D, Barthez-Carpentier MA, Diebold B, DelanoeC, Passemard S, Auvin S. A case of Lennox-Gastaut syndrome in a patient withFOXG1-related disorder.Epilepsia. 2014 Nov;55(11):e116-9. doi:10.1111/epi.12800. Epub 2014 Sep 29. PubMed PMID: 25266269.

 

8: Diebold B, Délepine C, Nectoux J, Bahi-Buisson N, Parent P, Bienvenu T.Somatic mosaicism for a FOXG1 mutation: diagnostic implication. Clin Genet. 2014 Jun;85(6):589-91. doi: 10.1111/cge.12212. Epub 2013 Jun 24. PubMed PMID:24766421.

 

9: Balloy V, Thévenot G, Bienvenu T, Morand P, Corvol H, Clement A, Ramphal R,Hubert D, Chignard M. Flagellin concentrations in expectorations from cysticfibrosis patients. BMC Pulm Med. 2014 Jun 9;14:100. doi:10.1186/1471-2466-14-100. PubMed PMID: 24909229; PubMed Central PMCID:PMC4060841.

10: Curie A, Nazir T, Brun A, Paulignan Y, Reboul A, Delange K, CheylusA,Bertrand S, Rochefort F, Bussy G, Marignier S, Lacombe D, Chiron C, CosséeM,Leheup B, Philippe C, Laugel V, De Saint Martin A, Sacco S, Poirier K, BienvenuT, Souville I, Gilbert-Dussardier B, Bieth E, Kauffmann D, Briot P, deFréminville B, Prieur F, Till M, Rooryck-Thambo C, MortemousqueI,Bobillier-Chaumont I, Toutain A, Touraine R, Sanlaville D, Chelly J, Freeman S,Kong J, Hadjikhani N, Gollub RL, Roy A, des Portes V. The c.429_452 duplicationof the ARX gene: a unique developmental-model of limb kinetic apraxia. Orphanet JRare Dis. 2014 Feb 14;9:25. doi: 10.1186/1750-1172-9-25. PubMed PMID: 24528893;PubMed Central PMCID: PMC4016261.

 

11: Martinez B, Heller M, Gaitch N, Hubert D, Burgel PR, Levy P, Girodon E,Bienvenu T. p.Arg75Gln, a CFTR variant involved in the risk of CFTR-relateddisorders? J Hum Genet. 2014 Apr;59(4):206-10. doi: 10.1038/jhg.2014.2. Epub 2014Jan 23. PubMed PMID: 24451227.

 

12: Bakouh N, Bienvenu T, Thomas A, Ehrenfeld J, Liote H, Roussel D, Duquesnoy P,Farman N, Viel M, Cherif-Zahar B, Amselem S, Taam RA, Edelman A, Planelles G,Sermet-Gaudelus I. Characterization of SLC26A9 in patients with CF-like lungdisease. Hum Mutat. 2013 Oct;34(10):1404-14. doi: 10.1002/humu.22382. Epub 2013Aug 13. PubMed PMID: 24272871.

 

13: Diebold B, Delépine C, Gataullina S, Delahaye A, Nectoux J, Bienvenu T.Mutations in the C-terminus of CDKL5: proceed with caution. Eur J Hum Genet. 2014Feb;22(2):270-2. doi: 10.1038/ejhg.2013.133. Epub 2013 Jun 12. PubMed PMID:23756444; PubMed Central PMCID: PMC3895649.

 

14: Dirami T, Rode B, Jollivet M, Da Silva N, Escalier D, Gaitch N, Norez C,Tuffery P, Wolf JP, Becq F, Ray PF, Dulioust E, Gacon G, Bienvenu T, Touré A.Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, areassociated with human asthenozoospermia. Am J Hum Genet. 2013 May 2;92(5):760-6. doi: 10.1016/j.ajhg.2013.03.016. Epub 2013 Apr 11. PubMed PMID: 23582645; PubMed Central PMCID: PMC3644633.

 

15: Thauvin-Robinet C, Munck A, Huet F, de Becdelièvre A, Jimenez C, Lalau G,Gautier E, Rollet J, Flori J, Nové-Josserand R, Soufir JC, Haloun A, Hubert D,Houssin E, Bellis G, Rault G, David A, Janny L, Chiron R, Rives N, Hairion D,Collignon P, Valeri A, Karsenty G, Rossi A, Audrézet MP, Férec C, Leclerc J,Georges Md, Claustres M, Bienvenu T, Gérard B, Boisseau P, Cabet-Bey F, CheillanD, Feldmann D, Clavel C, Bieth E, Iron A, Simon-Bouy B, Izard V, Steffann J,Viville S, Costa C, Drouineaud V, Fauque P, Binquet C, Bonithon-Kopp C, MorrisMA, Faivre L, Goossens M, Roussey M, Girodon E; collaborating working group onp.Arg117His. CFTR p.Arg117His associated with CBAVD and other CFTR-relateddisorders. J Med Genet. 2013 Apr;50(4):220-7. doi: 10.1136/jmedgenet-2012-101427.Epub 2013 Feb 1. PubMed PMID: 23378603.

 

16: Vasson A, Leroux C, Orhant L, Boimard M, Toussaint A, Leroy C, Commere V,Ghiotti T, Deburgrave N, Saillour Y, Atlan I, Fouveaut C, Beldjord C, Valleix S, Leturcq F, Dodé C, Bienvenu T, Chelly J, Cossée M. Custom oligonucleotidearray-based CGH: a reliable diagnostic tool for detection of exonic copy-numberchanges in multiple targeted genes. Eur J Hum Genet. 2013 Sep;21(9):977-87. doi: 10.1038/ejhg.2012.279. Epub 2013 Jan 23. PubMed PMID: 23340513; PubMed CentralPMCID: PMC3746255.

 

17: El-Seedy A, Pasquet MC, Bienvenu T, Bieth E, Audrezet MP, Kitzis A, LadevezeV. Consequences of partial duplications of the human CFTR gene on cf diagnosis:mutations or ectopic variations. J Cyst Fibros. 2013 Jul;12(4):407-10. doi:10.1016/j.jcf.2012.11.006. Epub 2012 Dec 21. PubMed PMID: 23261175.

 

18: Delépine C, Nectoux J, Bahi-Buisson N, Chelly J, Bienvenu T. MeCP2 deficiencyis associated with impaired microtubule stability. FEBS Lett. 2013 Jan16;587(2):245-53. doi: 10.1016/j.febslet.2012.11.033. Epub 2012 Dec 10. PubMedPMID: 23238081.

 

19: Raymond L, Diebold B, Leroux C, Maurey H, Drouin-Garraud V, Delahaye A, DulacO, Metreau J, Melikishvili G, Toutain A, Rivier F, Bahi-Buisson N, Bienvenu T.Validation of high-resolution DNA melting analysis for mutation scanning of theCDKL5 gene: identification of novel mutations. Gene. 2013 Jan 1;512(1):70-5. doi:10.1016/j.gene.2012.09.056. Epub 2012 Oct 11. PubMed PMID: 23064044.

 

20: Bienvenu T, Diebold B, Chelly J, Isidor B. Refining the phenotype associated with MEF2C point mutations. Neurogenetics. 2013 Feb;14(1):71-5. doi:10.1007/s10048-012-0344-7. Epub 2012 Sep 23. PubMed PMID: 23001426.

 

23: Bahi-Buisson N, Villeneuve N, Caietta E, Jacquette A, Maurey H, Matthijs G,Van Esch H, Delahaye A, Moncla A, Milh M, Zufferey F, Diebold B, Bienvenu T.Recurrent mutations in the CDKL5 gene: genotype-phenotype relationships. Am J MedGenet A. 2012 Jul;158A(7):1612-9. doi: 10.1002/ajmg.a.35401. Epub 2012 Jun 7.PubMed PMID: 22678952.

 

24: El-Seedy A, Girodon E, Norez C, Pajaud J, Pasquet MC, de Becdelièvre A,Bienvenu T, des Georges M, Cabet F, Lalau G, Bieth E, Blayau M, Becq F, Kitzis A,Fanen P, Ladeveze V. CFTR mutation combinations producing frequent complexalleles with different clinical and functional outcomes. Hum Mutat. 2012Nov;33(11):1557-65. doi: 10.1002/humu.22129. Epub 2012 Jul 2. PubMed PMID:22678879.

 

25: Florian C, Bahi-Buisson N, Bienvenu T. FOXG1-Related Disorders: From ClinicalDescription to Molecular Genetics. MolSyndromol. 2012 Apr;2(3-5):153-163. Epub2011 Apr 29. PubMed PMID: 22670136; PubMed Central PMCID: PMC3366704.

 

26: Bahi-Buisson N, Bienvenu T. CDKL5-Related Disorders: From ClinicalDescription to Molecular Genetics. MolSyndromol. 2012 Apr;2(3-5):137-152. Epub2011 Sep 13. PubMed PMID: 22670135; PubMed Central PMCID: PMC3366705.

 

27: Lambert L, Bienvenu T, Allou L, Valduga M, Echenne B, Diebold B, Mignot C,Héron D, Roth V, Saunier A, Moustaïne A, Jonveaux P, Philippe C. MEF2C mutations are a rare cause of Rett or severe Rett-like encephalopathies. Clin Genet. 2012Nov;82(5):499-501. doi: 10.1111/j.1399-0004.2012.01861.x. Epub 2012 Mar 26.PubMed PMID: 22449245.

28: Grillo E, Villard L, Clarke A, Ben Zeev B, Pineda M, Bahi-Buisson N,Hryniewiecka-Jaworska A, Bienvenu T, Armstrong J, Roche-Martinez A, Mari F,Veneselli E, Russo S, Vignoli A, Pini G, Djuric M, Bisgaard AM, MejaškiBošnjakV, Polgár N, Cogliati F, Ravn K, Pintaudi M, Melegh B, Craiu D, Djukic A, RenieriA. Rett networked database: an integrated clinical and genetic network of Rettsyndrome databases. Hum Mutat. 2012 Jul;33(7):1031-6. doi: 10.1002/humu.22072.Epub 2012 Apr 13. PubMed PMID: 22415763.

 

29: Nectoux J, Florian C, Delepine C, Bahi-Buisson N, Khelfaoui M, Reibel S,Chelly J, Bienvenu T. Altered microtubule dynamics in Mecp2-deficient astrocytes.J Neurosci Res. 2012 May;90(5):990-8. doi: 10.1002/jnr.23001. Epub 2012 Jan 18.PubMed PMID: 22252744.

 

30: Bertin C, Pelletier AL, Vullierme MP, Bienvenu T, Rebours V, Hentic O, MaireF, Hammel P, Vilgrain V, Ruszniewski P, Lévy P. Pancreas divisum is not a causeof pancreatitis by itself but acts as a partner of genetic mutations. Am JGastroenterol. 2012 Feb;107(2):311-7. doi: 10.1038/ajg.2011.424. Epub 2011 Dec13. PubMed PMID: 22158025.

 

31: Rode B, Dirami T, Bakouh N, Rizk-Rabin M, Norez C, Lhuillier P, Lorès P,Jollivet M, Melin P, Zvetkova I, Bienvenu T, Becq F, Planelles G, Edelman A,Gacon G, Touré A. The testis anion transporter TAT1 (SLC26A8) physically andfunctionally interacts with the cystic fibrosis transmembrane conductanceregulator channel: a potential role during sperm capacitation. Hum Mol Genet.2012 Mar 15;21(6):1287-98. doi: 10.1093/hmg/ddr558. Epub 2011 Nov 25. PubMedPMID: 22121115.

 

32: Méneret A, Mignot C, An I, Habert MO, Jacquette A, Vidailhet M, Bienvenu T,Roze E. Generalized dystonia, athetosis, and parkinsonism associated with FOXG1mutation. MovDisord. 2012 Jan;27(1):160-1. doi: 10.1002/mds.23956. Epub 2011 Sep23. PubMed PMID: 21953941.

 

33: Rosas-Vargas H, Martínez-Ezquerro JD, Bienvenu T. Brain-derived neurotrophicfactor, food intake regulation, and obesity. Arch Med Res. 2011 Aug;42(6):482-94.doi: 10.1016/j.arcmed.2011.09.005. Epub 2011 Sep 22. Review. PubMed PMID:21945389.

 

34: Klein KM, Yendle SC, Harvey AS, Antony JH, Wallace G, Bienvenu T, SchefferIE. A distinctive seizure type in patients with CDKL5 mutations:Hypermotor-tonic-spasms sequence. Neurology. 2011 Apr 19;76(16):1436-8. doi:10.1212/WNL.0b013e3182166e58. PubMed PMID: 21502606.

 

36: Le Guen T, Fichou Y, Nectoux J, Bahi-Buisson N, Rivier F, Boddaert N, DieboldB, Héron D, Chelly J, Bienvenu T. A missense mutation within the fork-head domainof the forkhead box G1 Gene (FOXG1) affects its nuclear localization. Hum Mutat. 2011 Feb;32(2):E2026-35. doi: 10.1002/humu.21422. Epub 2010 Dec 7. PubMed PMID:21280142.

 

37: Puéchal X, Bienvenu T, Génin E, Berthelot JM, Sibilia J, Gaudin P, MarcelliC, Lasbleiz S, Michou L, Cornélis F, Kahan A, Dusser DJ. Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoidarthritis. Ann Rheum Dis. 2011 Apr;70(4):653-9. doi: 10.1136/ard.2010.142760.Epub 2010 Dec 3. PubMed PMID: 21131649.

 

38: Fichou Y, Nectoux J, Bahi-Buisson N, Chelly J, Bienvenu T. An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremelyhigh sequence conservation, is specifically expressed in brain. J Hum Genet. 2011Jan;56(1):52-7. doi: 10.1038/jhg.2010.143. Epub 2010 Dec 2. PubMed PMID:21124335.

 

39: Nectoux J, Fichou Y, Cagnard N, Bahi-Buisson N, Nusbaum P, Letourneur F,Chelly J, Bienvenu T. Cell cloning-based transcriptome analysis incyclin-dependent kinase-like 5 mutation patients with severe epilepticencephalopathy. J Mol Med (Berl). 2011 Feb;89(2):193-202. doi:10.1007/s00109-010-0699-x. Epub 2010 Nov 24. PubMed PMID: 21107515.

 

40: Le Guen T, Bahi-Buisson N, Nectoux J, Boddaert N, Fichou Y, Diebold B,Desguerre I, Raqbi F, Daire VC, Chelly J, Bienvenu T. A FOXG1 mutation in a boywithcongenital variant of Rett syndrome. Neurogenetics. 2011 Feb;12(1):1-8. doi:10.1007/s10048-010-0255-4. Epub 2010 Aug 24. Review. PubMed PMID: 20734096.

 

41: René C, Paulet D, Girodon E, Costa C, Lalau G, Leclerc J, Cabet-Bey F,Bienvenu T, Blayau M, Iron A, Mittre H, Feldmann D, Guittard C, Claustres M,Georges Md. p.Ser1235Arg should no longer be considered as a cystic fibrosismutation: results from a large collaborative study. Eur J Hum Genet. 2011Jan;19(1):36-42. doi: 10.1038/ejhg.2010.137. Epub 2010 Aug 18. PubMed PMID:20717170; PubMed Central PMCID: PMC3039504.

 

42: Masliah-Plachon J, Auvin S, Nectoux J, Fichou Y, Chelly J, Bienvenu T.Somatic mosaicism for a CDKL5 mutation as an epileptic encephalopathy in males.Am J Med Genet A. 2010 Aug;152A(8):2110-1. doi: 10.1002/ajmg.a.33037. PubMedPMID: 20602487.

 

43: Nectoux J, Fichou Y, Rosas-Vargas H, Cagnard N, Bahi-Buisson N, Nusbaum P,Letourneur F, Chelly J, Bienvenu T. Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes. J Cell Mol Med. 2010 Jul;14(7):1962-74. doi:10.1111/j.1582-4934.2010.01107.x. Epub 2010 Jun 21. PubMed PMID: 20569274; PubMedCentral PMCID: PMC3823278.

 

44: Sermet-Gaudelus I, Munck A, Rota M, Roussey M, Feldmann D, Nguyen-Khoa T;Groupe de travail "Dépistage néonatal" de la Fédération des centres de ressourceset de compétences de la mucoviscidose. [French guidelines for sweat test practiceand interpretation for cystic fibrosis neonatal screening]. Arch Pediatr. 2010Sep;17(9):1349-58. doi: 10.1016/j.arcped.2010.06.021. Epub 2010 Aug 16. French.

 

45: Sermet-Gaudelus I, Girodon E, Sands D, Stremmler N, Vavrova V, Deneuville E, Reix P, Bui S, Huet F, Lebourgeois M, Munck A, Iron A, Skalicka V, Bienvenu T,Roussel D, Lenoir G, Bellon G, Sarles J, Macek M, Roussey M, Fajac I, Edelman A. Clinical phenotype and genotype of children with borderline sweat test andabnormal nasal epithelial chloride transport. Am J RespirCrit Care Med. 2010 Oct1;182(7):929-36. doi: 10.1164/rccm.201003-0382OC. Epub 2010 Jun 10. PubMed PMID: 20538955.

 

46: Pelletier AL, Bienvenu T, Rebours V, O'Toole D, Hentic O, Maire F, Hammel P, Ruszniewski P, Lévy P. CFTR gene mutation in patients with apparently idiopathic pancreatitis: lack of phenotype-genotype correlation. Pancreatology.2010;10(2-3):158-64. doi: 10.1159/000231976. Epub 2010 May 12. PubMed PMID:20460946.

 

47: White R, Ho G, Schmidt S, Scheffer IE, Fischer A, Yendle SC, Bienvenu T,Nectoux J, Ellaway CJ, Darmanian A, Tong X, Cloosterman D, Bennetts B, Kalra V,Fullston T, Gecz J, Cox TC, Christodoulou J. Cyclin-dependent kinase-like 5(CDKL5) mutation screening in Rett syndrome and related disorders. Twin Res HumGenet. 2010 Apr;13(2):168-78. doi: 10.1375/twin.13.2.168. PubMed PMID: 20397747.

 

48: Bienvenu T, Sermet-Gaudelus I, Burgel PR, Hubert D, Crestani B, Bassinet L,Dusser D, Fajac I. Cystic fibrosis transmembrane conductance regulator channeldysfunction in non-cystic fibrosis bronchiectasis. Am J RespirCrit Care Med.2010 May 15;181(10):1078-84. doi: 10.1164/rccm.200909-1434OC. Epub 2010 Feb 18.PubMed PMID: 20167849.

 

49: Quemener S, Chen JM, Chuzhanova N, Bénech C, Casals T, Macek M Jr, BienvenuT, McDevitt T, Farrell PM, Loumi O, Messaoud T, Cuppens H, Cutting GR, StensonPD, Giteau K, Audrézet MP, Cooper DN, Férec C. Complete ascertainment ofintragenic copy number mutations (CNMs) in the CFTR gene and its implications forCNM formation at other autosomal loci. Hum Mutat. 2010 Apr;31(4):421-8. doi:10.1002/humu.21196. PubMed PMID: 20052766; PubMed Central PMCID: PMC2855493.

 

50: Burgel PR, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D,Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M,Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser D.Non-classic cystic fibrosis associated with D1152H CFTR mutation. Clin Genet.2010 Apr;77(4):355-64. doi: 10.1111/j.1399-0004.2009.01294.x. Epub 2009 Oct 15.PubMed PMID: 19843100.

 

51: Bahi-Buisson N, Nectoux J, Girard B, Van Esch H, De Ravel T, Boddaert N,Plouin P, Rio M, Fichou Y, Chelly J, Bienvenu T. Revisiting the phenotypeassociated with FOXG1 mutations: two novel cases of congenital Rett variant.Neurogenetics. 2010 May;11(2):241-9. doi: 10.1007/s10048-009-0220-2. Epub 2009Oct 6. PubMed PMID: 19806373.

 

52: Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R,Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B,Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F,Renieri A. Novel FOXG1 mutations associated with the congenital variant of Rettsyndrome. J Med Genet. 2010 Jan;47(1):49-53. doi: 10.1136/jmg.2009.067884. Epub2009 Jul 2. PubMed PMID: 19578037.

 

53: Bahi-Buisson N, Girard B, Gautier A, Nectoux J, Fichou Y, Saillour Y, PoirierK, Chelly J, Bienvenu T. Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 gene. Am J Med GenetB Neuropsychiatr Genet. 2010 Jan 5;153B(1):202-7. doi: 10.1002/ajmg.b.30974.PubMed PMID: 19455595.

 

54: Patrat C, Bienvenu T, Janny L, Faure AK, Fauque P, Aknin-Seifer I, Davy C,Thiounn N, Jouannet P, Lévy R. Clinical data and parenthood of 63 infertile andY-microdeleted men. FertilSteril. 2010 Feb;93(3):822-32. doi:10.1016/j.fertnstert.2008.10.033. Epub 2008 Dec 4. PubMed PMID: 19062004.

 

Facteur H (au 17 Juillet 2015) (Web of Science)

Results found:     245

Sum of the Times Cited [?] :            5316

Sum of Times Cited without self-citations [?] :           5026

Citing Articles [?] :              3902

Citing Articles without self-citations [?] :       3762

Average Citations per Item [?] :      21.70

h-index [?] :         33