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Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment
Hum Mutat 40: 2021

Laumonnier F, Bonnet-Brilhault F, Gomot M, Blanc R, David A, Moizard MP, Raynaud M, Ronce N, Lemonnier E, Calvas P, Laudier B, Chelly J, Fryns JP, Ropers HH, Hamel BC, Andres C, Barthelemy C, Moraine C, Briault S (2004)
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
American Journal of Human Genetics 74: 552

Kerjean A, Couvert P, Heams T, Chalas C, Poirier K, Chelly J, Jouannet P, Paldi A, Poirot C (2003)
In vitro follicular growth affects oocyte imprinting establishment in mice
Eur J Hum Genet 11: 493

Francis F, Koulakoff A, Boucher D, Chafey P, Schaar B, Vinet MC, Friocourt G, McDonnell N, Reiner O, Kahn A, McConnell SK, Berwald-Netter Y, Denoulet P, Chelly J (1999)
Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons
Neuron 23: 247

des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakoff A, Carrie A, Gelot A, Dupuis E, Motte J, Berwald-Netter Y, Catala M, Kahn A, Beldjord C, Chelly J (1998)
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
Cell 92: 51

Chelly J, Hamard G, Koulakoff A, Kaplan JC, Kahn A, Berwald-Netter Y (1990)
Dystrophin gene transcribed from different promoters in neuronal and glial cells
Nature 344: 64

Chelly J, Montarras D, Pinset C, Berwald-Netter Y, Kaplan JC, Kahn A (1990)
Quantitative estimation of minor mRNAs by cDNA-polymerase chain reaction. Application to dystrophin mRNA in cultured myogenic and brain cells
European Journal of Biochemistry 187: 691