SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Bulletin de l'Academie Nationale de Medecine

Volumn 193, Issue 2, 2009, Pages 299-305

Autism: MMore evidence of a genetic cause;Autisme, la piste génétique se confirme

(3) Bourgeron, Thomas a Leboyer, Marion b Delorme, Richard c

a INSTITUT PASTEUR (France)

b INSERM (France)

c HÔPITAL ROBERT DEBRÉ (France)

Author keywords

Autistic disorder; Mgnetic resonance imaging; Positron emission tomography

Indexed keywords

EID: 69249127043 PISSN: 00014079 EISSN: None Source Type: Journal
DOI: 10.1016/s0001-4079(19)32583-x Document Type: Article

Times cited : (8)

References (8)

1
- 40349096250
- Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
- DOI 10.1073/pnas.0711555105
- JAMAIN S., RADYUSHKIN K., HAMMERSCHMIDT K., GRANON S., BORETIUS S., VAROQUEAUX F. et al. - Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism. Proc Natl Acad. Sci. U S A, 2008, 105, 1710-1715. (Pubitemid 351346579)
- (2008) Proceedings of the National Academy of Sciences of the United States of America , vol.105 , Issue.5 , pp. 1710-1715
- Jamain, S.¹ Radyushkin, K.² Hammerschmidt, K.³ Granon, S.⁴ Boretius, S.⁵ Varoqueaux, F.⁶ Ramanantsoa, N.⁷ Gallego, J.⁸ Ronnenberg, A.⁹ Winter, D.¹⁰ Frahm, J.¹¹ Fischer, J.¹² Bourgeron, T.¹³ Ehrenreich, H.¹⁴ Brose, N.¹⁵

2
- 35148858044
- A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice
- DOI 10.1126/science.1146221
- TABUCHI K., BLUNDELL J., ETHERTON MR., HAMMER RE., LIU X., POWELL CM. et al. - A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice. Science, 2007, 318, 71-76. (Pubitemid 47538032)
- (2007) Science , vol.318 , Issue.5847 , pp. 71-76
- Tabuchi, K.¹ Blundell, J.² Etherton, M.R.³ Hammer, R.E.⁴ Liu, X.⁵ Powell, C.M.⁶ Sudhof, T.C.⁷

3
- 0037656313
- Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
- DOI 10.1038/ng1136
- JAMAIN S., QUACH H., BETANCUR C, RASTAM M, COLINEAUX C, GILLBERG IC. et al. - Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat. Genet., 2003, 34, 27-29. (Pubitemid 36548785)
- (2003) Nature Genetics , vol.34 , Issue.1 , pp. 27-29
- Jamain, S.¹ Quach, H.² Betancur, C.³ Rastam, M.⁴ Colineaux, C.⁵ Gillberg, C.⁶ Soderstrom, H.⁷ Giros, B.⁸ Leboyer, M.⁹ Gillberg, C.¹⁰ Bourgeron, T.¹¹ Nyden, A.¹² Philippe, A.¹³ Cohen, D.¹⁴ Chabane, N.¹⁵ Mouren-Simeoni, M.-C.¹⁶ Brice, A.¹⁷ Sponheim, E.¹⁸ Spurkland, I.¹⁹ Skjeldal, O.H.²⁰ more..

4
- 33845889998
- Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
- DOI 10.1038/ng1933, PII NG1933
- DURAND CM., BETANCUR C, BOECKERS TM., BOCKMANN J., CHASTE P., FAUCHEREAU F. et al. - Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat. Genet., 2007 ; 39, 25-27. (Pubitemid 46026497)
- (2007) Nature Genetics , vol.39 , Issue.1 , pp. 25-27
- Durand, C.M.¹ Betancur, C.² Boeckers, T.M.³ Bockmann, J.⁴ Chaste, P.⁵ Fauchereau, F.⁶ Nygren, G.⁷ Rastam, M.⁸ Gillberg, I.C.⁹ Anckarsater, H.¹⁰ Sponheim, E.¹¹ Goubran-Botros, H.¹² Delorme, R.¹³ Chabane, N.¹⁴ Mouren-Simeoni, M.-C.¹⁵ De Mas, P.¹⁶ Bieth, E.¹⁷ Roge, B.¹⁸ Heron, D.¹⁹ Burglen, L.²⁰ more..

5
- 12144291350
- X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
- DOI 10.1086/382137
- LAUMMONNIER F, BONNET-BRILHAULT F., GOMOT M., BLANC R., DAVID., MOIZARD MP. et al. - X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. Am. J. Hum. Genet., 2004, 74, 552-557. (Pubitemid 38325925)
- (2004) American Journal of Human Genetics , vol.74 , Issue.3 , pp. 552-557
- Laumonnier, F.¹ Bonnet-Brilhault, F.² Gomot, M.³ Blanc, R.⁴ David, A.⁵ Moizard, M.-P.⁶ Raynaud, M.⁷ Ronce, N.⁸ Lemonnier, E.⁹ Calvas, P.¹⁰ Laudier, B.¹¹ Chelly, J.¹² Fryns, J.-P.¹³ Ropers, H.-H.¹⁴ Hamel, B.C.J.¹⁵ Andres, C.¹⁶ Barthelemy, C.¹⁷ Moraine, C.¹⁸ Briault, S.¹⁹

6
- 33847327313
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements
- DOI 10.1038/ng1985, PII NG1985
- SZATMARI P., PATERSON AD., ZWAIGENBAUM L., ROBERTS W., BRIAN J., LIU XQ. et al. - Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat. Genet., 2007, 39, 319-328. (Pubitemid 46328498)
- (2007) Nature Genetics , vol.39 , Issue.3 , pp. 319-328
- Szatmari, P.¹ Paterson, A.D.² Zwaigenbaum, L.³ Roberts, W.⁴ Brian, J.⁵ Liu, X.-Q.⁶

7

8
- 36849011564
- A randomized, placebo-controlled trial of controlled release melatonin treatment of delayed sleep phase syndrome and impaired sleep maintenance in children with neurodevelopmental disabilities
- DOI 10.1111/j.1600-079X.2007.00528.x
- WASDELL MB., JAN JE., BOMBEN MM., FREEMAN RD., RIETVELD W., TAI J. et al. - A randomized, placebo-controlled trial of controlled release melatonin treatment of delayed sleep phase syndrome and impaired sleep maintenance in children with neurodevelopmental disabilities. Journal of pineal research, 2008, 44, 57-64. (Pubitemid 350231110)
- (2008) Journal of Pineal Research , vol.44 , Issue.1 , pp. 57-64
- Wasdell, M.B.¹ Jan, J.E.² Bomben, M.M.³ Freeman, R.D.⁴ Rietveld, W.J.⁵ Tai, J.⁶ Hamilton, D.⁷ Weiss, M.D.⁸

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.