Classification from cortical folding patterns.

IEEE Transactions on Medical Imaging 2007; 26(4), 553-65.

Duchesnay E, Cachia A, Roche A, Rivère D, Cointepas Y, Papadopoulos-Orfanos D, Zilbovicius M, Martinot JL, Régis J, Mangin JF.

High level group analysis of fMRI data based on dirichlet process mixture models.

Inf Process Med Imaging 2007; 20, 482-94.

Thirion B, Tucholka A, Keller M, Pinel P, Roche A, Mangin JF, Poline JB.

Increased white matter connectivity in euthymic bipolar patients: Diffusion tensor tractography between the subgenual cingulate and the amygdalo-hippocampal complex.

Molecular Psychiatry 2007; 12(11), 1001-10.

Houenou J, Wessa M, Douaud G, Leboyer M, Chanraud S, Perrin M, Poupon C, Martinot JL, Paillère-Martinot ML.

Brain morphometry and cognitive performance in detoxified alcohol-dependent subjects with preserved social functioning.

Neuropsychopharmacology. 2007; 32(2), 429-38.

Chanraud S, Martelli C, Reynaud M, Delain F, Kostogianni N, Douaud G, Aubin HJ, Martinot JL.

Effect Of Deferiprone On Ataxia And Cerebellar Iron Accumulation In Friedreich’s Ataxia : A Pilot Study.

Blood 2007; 110(1), 401-8.

Boddaert N, Le Quan Sang K, Rötig A, Leroy-Willig A, Gallet S, Brunelle F, Sidi D, Thalabard JC, Cabantchik IZ, Munnich A.

Priming magnetic stimulations over Wernicke’s area modulates word detection.

Cerebral Cortex 2008; 18(1), 210-6.

Andoh J, Artiges E, Pallier C, Rivière D, Mangin JF, Paillère-Martinot ML, Martinot JL.

Increased frontal-striatal activation during response inhibition to emotional faces in euthymic bipolar disorder.

American Journal of Psychiatry 2007; 164, 638-46.

Wessa M, Houenou J, Paillère-Martinot ML, Berthoz S, Leboyer M, Martinot JL.

Assessment of 11C-PE2I binding to the neuronal dopamine transporter in humans with the high-spatial-resolution PET scanner HRRT.

J Nucl Med. 2007; 48, 538-46.

Leroy C, Comtat C, Trebossen R, Syrota A, Martinot JL, Ribeiro MJ.

Dopaminergic function in depressed patients with affective flattening or with impulsivity: [18F]fluoro-L-dopa positron emission tomography study with voxel-based analysis.

Psychiatry Res. Neuroimaging 2007; 154, 115-24.

Bragulat V, Paillere-Martinot ML, Artiges E, Frouin V, Poline JB, Martinot JL.

New treatments for cocaine dependence: a focused review.

Int J Neuropsychopharmacol. 2007; 1-14.

Karila L, Gorelick D, Weinstein A, Noble F, Benyamina A, Coscas S, Blecha L, Lowenstein W, Martinot JL, Reynaud M, Lépine JP.

Sensory dysfunction is correlated to cerebellar volume reduction in early schizophrenia.

Schizophrenia Research 2007; 91(1-3), 266-9.

Mouchet-Mages S, Cachia A, Canceil O, Rodrigo S, Oppenheim C, Willard D, Meder JF, Martinot JL, Krebs MO.

Functional imaging of the pancreas: the role of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy.

Endocr Dev. 2007; 12, 55-66.

Ribeiro MJ, Boddaert N, Delzescaux T, Valayannopoulos V, Bellanné-Chantelot C, Jaubert F, Verkarre V, Nihoul-Fékété C, Brunelle F, De Lonlay P.

The added value of [(18)F]fluoro-L: -DOPA PET in the diagnosis of hyperinsulinism of infancy: a retrospective study involving 49 children.

Eur J Nucl Med Mol Imaging 2007; 34(12), 2120-8.

Ribeiro MJ, Boddaert N, Bellanné-Chantelot C, Bourgeois S, Valayannopoulos V, Delzescaux T, Jaubert F, Nihoul-Fékété C, Brunelle F, De Lonlay P.

Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction.

Am J Hum Genet. 200; 80(5), 988-93.

Amiel J, Rio M, de Pontual L, Redon R, Malan V, Boddaert N, Plouin P, Carter NP, Lyonnet S, Munnich A, Colleaux L.

High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations.

J Am Soc Nephrol. 2007; 18(5), 1566-75.

Tory K, Lacoste T, Burglen L, Morinière V, Boddaert N, Macher MA, Llanas B, Nivet H, Bensman A, Niaudet P, Antignac C, Salomon R, Saunier S.

Selective iron chelation in Friedreich ataxia: biologic and clinical implications.

Blood 2007; 110(1), 401-8.

Boddaert N, Le Quan Sang KH, Rötig A, Leroy-Willig A, Gallet S, Brunelle F, Sidi D, Thalabard JC, Munnich A, Cabantchik ZI.

Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis.

Nat Genet. 2007; 39(4), 454-6.

Baala L, Briault S, Etchevers HC, Laumonnier F, Natiq A, Amiel J, Boddaert N, Picard C, Sbiti A, Asermouh A, Attié-Bitach T, Encha-Razavi F, Munnich A, Sefiani A, Lyonnet S.

The Meckel-Gruber Syndrome Gene, MKS3, Is Mutated in Joubert Syndrome.

Am J Hum Genet. 2007; 80(1), 186-94.

Baala L, Romano S, Khaddour R, Saunier S, Smith UM, Audollent S, Ozilou C, Faivre L, Laurent N, Foliguet B, Munnich A, Lyonnet S, Salomon R, Encha-Razavi F, Gubler MC, Boddaert N, Lonlay P, Johnson CA, Vekemans M, Antignac C, Attie-Bitach T.

Coexistence in the same family of both focal and diffuse forms of hyperinsulinism.

Diabetes Care 2007; 30(6), 1590-2.

Valayannopoulos V, Vaxillaire M, Aigrain Y, Jaubert F, Bellanné-Chantelot C, Ribeiro MJ, Brunelle F, Froguel P, Robert JJ, Polak M, Nihoul-Fékété C, de Lonlay P.

Pathogenesis and pharmacology of epilepsy in the lithium-pilocarpine model.

Epilepsia. 2007; 48 Suppl 5, 41-7. erratum in : Epilepsia. 2007; 48(12), 2379.

André V, Dubé C, François J, Leroy C, Rigoulot MA, Roch C, Namer IJ, Nehlig A.