Concepedia

Carine Mantoulan

CM

Statistics

Publications

11

Citations

3.4K

H-Index

10

Active since

2010

Affiliations

Inserm(Current)

Centre National de la Recherche Scientifique

University of Manchester

University of Oxford

Goethe University Frankfurt

Carine Mantoulan is an author at Inserm specializing in neurodevelopmental disorders, autism spectrum disorders, and human genetics.

Publications per year

2010–2020

11

Publications

11

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

Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei et al. · Nature · 2010 · 2K citations · Full text

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

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2010 · 588 citations · Full text

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

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2012 · 378 citations · Full text

, , +17

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

Jillian P. Casey, Tiago R. Magalhães, Judith Conroy et al. · Human Genetics · 2011 · 203 citations · Full text

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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

M. Tauber, Carine Mantoulan, P. Copet et al. · Orphanet Journal of Rare Diseases · 2011 · 113 citations · Full text

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