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Extent of magnitude representation deficit and relationship with arithmetic skills in children with 22q11.2DS

Orphanet journal of rare diseases, 2024-07, Vol.19 (1), p.250-9, Article 250

2024

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Dissociation of early and late face-related processes in autism spectrum disorder and Williams syndrome

Orphanet journal of rare diseases, 2022-06, Vol.17 (1), p.1-244, Article 244

2022

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The spatial distribution of eye movements predicts the (false) recognition of emotional facial expressions

PloS one, 2021-01, Vol.16 (1), p.e0245777-e0245777

2021

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Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest?

Journal of autism and developmental disorders, 2018-08, Vol.48 (8), p.2886-2889

2018

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Noninvasive electrical stimulation for psychiatric care in Down syndrome

Brain stimulation, 2022-05, Vol.15 (3), p.678-679

2022

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The Odor Context Facilitates the Perception of Low-Intensity Facial Expressions of Emotion

PloS one, 2015-09, Vol.10 (9), p.e0138656-e0138656

2015

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Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder

International journal of molecular sciences, 2019-07, Vol.20 (14), p.3533

2019

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Psychiatric manifestations of treatable hereditary metabolic disorders in adults

Annals of general psychiatry, 2014-09, Vol.13 (1), p.27-27, Article 27

2014

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An optimized iDISCO+ protocol for tissue clearing and 3D analysis of oxytocin and vasopressin cell network in the developing mouse brain

STAR protocols, 2023-03, Vol.4 (1), p.101968-101968, Article 101968

2023

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Differential fate between oxytocin and vasopressin cells in the developing mouse brain

iScience, 2022-01, Vol.25 (1), p.103655-103655, Article 103655

2022

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Social cognition in Wilson's disease: A new phenotype?

PloS one, 2017-04, Vol.12 (4), p.e0173467

2017

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Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review

BMC psychiatry, 2021-07, Vol.21 (1), p.360-360, Article 360

2021

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From High Intellectual Potential to Asperger Syndrome: Evidence for Differences and a Fundamental Overlap-A Systematic Review

Frontiers in psychology, 2016-10, Vol.7, p.1605-1605

2016

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What do error patterns in processing facial expressions, social interaction scenes and vocal prosody tell us about the way social cognition works in children with 22q11.2DS?

European child & adolescent psychiatry, 2020-03, Vol.29 (3), p.299-313

2020

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Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized controlled trial

BMC psychiatry, 2018-07, Vol.18 (1), p.235-235, Article 235

2018

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An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome

Translational psychiatry, 2019-02, Vol.9 (1), p.67, Article 67

2019

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Behavioral disturbance and treatment strategies in Smith-Magenis syndrome

Orphanet journal of rare diseases, 2015-09, Vol.10 (1), p.111-111, Article 111

2015

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Emotional Modulation of Episodic Memory in School-Age Children and Adults: An Event-Related Potential Study

Brain sciences, 2021-11, Vol.11 (12), p.1598

2021

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Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder

Molecular autism, 2019-08, Vol.10 (1), p.33-33, Article 33

2019

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Organisations & fonctions du comportement verbal de type « backchannels » dans l’interaction clinique avec la personne souffrant de schizophrénie

SHS web of conferences, 2022-05, Vol.138, p.01014

2022

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Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report

BMC medical genetics, 2020-01, Vol.21 (1), p.10-10, Article 10

2020

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Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder

Orphanet journal of rare diseases, 2019-05, Vol.14 (1), p.121-121, Article 121

2019

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Screening of Wilson's disease in a psychiatric population: difficulties and pitfalls. A preliminary study

Annals of general psychiatry, 2017-04, Vol.16 (1), p.19-19, Article 19

2017

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Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype

Frontiers in pediatrics, 2018, Vol.6, p.102-102

2018

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Extent of magnitude representation deficit and relationship with arithmetic skills in children with 22q11.2DS

Dissociation of early and late face-related processes in autism spectrum disorder and Williams syndrome

The spatial distribution of eye movements predicts the (false) recognition of emotional facial expressions

Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest?

Noninvasive electrical stimulation for psychiatric care in Down syndrome

The Odor Context Facilitates the Perception of Low-Intensity Facial Expressions of Emotion

Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder

Psychiatric manifestations of treatable hereditary metabolic disorders in adults

An optimized iDISCO+ protocol for tissue clearing and 3D analysis of oxytocin and vasopressin cell network in the developing mouse brain

Differential fate between oxytocin and vasopressin cells in the developing mouse brain

Social cognition in Wilson's disease: A new phenotype?

Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review

Maternal immune activation during pregnancy is associated with more difficulties in socio-adaptive behaviors in autism spectrum disorder

From High Intellectual Potential to Asperger Syndrome: Evidence for Differences and a Fundamental Overlap-A Systematic Review

What do error patterns in processing facial expressions, social interaction scenes and vocal prosody tell us about the way social cognition works in children with 22q11.2DS?

Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized controlled trial

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome

Behavioral disturbance and treatment strategies in Smith-Magenis syndrome

Emotional Modulation of Episodic Memory in School-Age Children and Adults: An Event-Related Potential Study

Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder

Organisations & fonctions du comportement verbal de type « backchannels » dans l’interaction clinique avec la personne souffrant de schizophrénie

Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report

Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder

Screening of Wilson's disease in a psychiatric population: difficulties and pitfalls. A preliminary study

Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype

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