Carine Mantoulan

发表

Functional impact of global rare copy number variation in autism spectrum disorders

Gary D Bader, Joseph T. Glessner, Stephen J. Guter, 2010, Nature.

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

Tomi D. Berney, E Maestrini, Stephen J. Guter, 2009, Molecular Psychiatry.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Joseph T. Glessner, Stephen J. Guter, D. Pinto, 2011, Human Genetics.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Stephen J. Guter, D. Pinto, S. Scherer, 2011, Human Genetics.

Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature

C. Mantoulan, P. Barone, V. Laurier, 2019, Orphanet Journal of Rare Diseases.

Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients

C. Mantoulan, B. Rogé, P. Copet, 2011, Orphanet journal of rare diseases.

A study of voice and non-voice processing in Prader-Willi syndrome

C. Mantoulan, P. Barone, V. Laurier, 2020, Orphanet journal of rare diseases.