D. Cohen

发表

Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia

Simon C. Potter, M. Pirinen, P. Donnelly, 2013, Nature Genetics.

Repint of “Reframing autism as a behavioral syndrome and not a specific mental disorder: Implications of genetic and phenotypic heterogeneity”

D. Cohen, N. Coulon, G. Anderson, 2018, Neuroscience & Biobehavioral Reviews.

Biological Insights From 108 Schizophrenia-Associated Genetic Loci

C. Spencer, K. Davis, P. Visscher, 2014, Nature.

Advances in the Research of Melatonin in Autism Spectrum Disorders: Literature Review and New Perspectives

D. Cohen, G. Anderson, S. Tordjman, 2013, International journal of molecular sciences.

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium

C. Spencer, K. Davis, P. Visscher, 2016, bioRxiv.

Analysis of shared heritability in common disorders of the brain

Nick C Fox, Dan J Stein, Janice M. Fullerton, 2018, Science.

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.

P. Visscher, N. Wray, E. Bramon, 2016, JAMA psychiatry.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism

G. Dawson, G. Schellenberg, A. Hardan, 2014, Front. Genet..

Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy

D. Cohen, M. Tanguy, N. Angeard, 2009, European Child & Adolescent Psychiatry.

Narcolepsy and psychosis: A systematic review

D. Levinson, I. Arnulf, D. Cohen, 2021, Acta psychiatrica Scandinavica.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Autism and COVID-19: A Case Series in a Neurodevelopmental Unit

D. Cohen, M. Giannitelli, A. Bleibtreu, 2020, Journal of clinical medicine.

Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders

M. Leboyer, C. Depienne, A. Brice, 2013, European Journal of Human Genetics.

Compressive Garments in Individuals with Autism and Severe Proprioceptive Dysfunction: A Retrospective Exploratory Case Series

D. Cohen, J. Xavier, C. Baeza-Velasco, 2020, Children.

Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self-Injurious Blindness

D. Cohen, J. Xavier, S. Chantot-Bastaraud, 2017, Case reports in psychiatry.

Publisher's Note

D. Cohen, N. Coulon, G. Anderson, 2017, Neuroscience & Biobehavioral Reviews.

Day and nighttime excretion of 6-sulphatoxymelatonin in adolescents and young adults with autistic disorder

D. Cohen, G. Anderson, S. Tordjman, 2012, Psychoneuroendocrinology.

Autism Spectrum and Other Neurodevelopmental Disorders in Children of Immigrants: A Brief Review of Current Evidence and Implications for Clinical Practice

D. Cohen, S. Tordjman, M. Melchior, 2021, Frontiers in Psychiatry.

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia

J. Rapoport, G. Rouleau, C. Laurent, 2018, Molecular Psychiatry.

Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo Mutation

D. Cohen, A. Verloes, I. Gozes, 2019, Journal of Molecular Neuroscience.

Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE

T. Bourgeron, R. Delorme, C. Gillberg, 2012, Translational Psychiatry.

Epilepsy in Simplex Autism Pedigrees is Much Lower Than the Rate in Multiplex Autism Pedigrees

C. Laurent, D. Cohen, S. Tordjman, 2013, Biological Psychiatry.

The Autism Psychodynamic Evaluation of Changes (APEC) scale: A reliability and validity study on a newly developed standardized psychodynamic assessment for youth with Pervasive Developmental Disorders

D. Cohen, S. Tordjman, M. Botbol, 2010, Journal of Physiology-Paris.

Genome-wide association study of multiplex schizophrenia pedigrees.

Jianxin Shi, Stephan Ripke, Pablo V Gejman, 2012, The American journal of psychiatry.

Age at first birth in women is genetically associated with increased risk of schizophrenia

Hoffmann, Hartmann, Roussos, 2017, Scientific Reports.

Gene × Environment Interactions in Autism Spectrum Disorders: Role of Epigenetic Mechanisms

Michel Botbol, Jean Xavier, David Cohen, 2014, Front. Psychiatry.

Epilepsy in Autism is Associated with Intellectual Disability and Gender: Evidence from a Meta-Analysis

M. Baulac, L. Mottron, D. Cohen, 2008, Biological Psychiatry.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Michael F. Green, Max W. Y. Lam, Catherine A. Sugar, 2022, Nature.

Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders

M. Ruberg, V. Guillemot, C. Depienne, 2015, Amino Acids.

Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype

A. Toutain, D. Cohen, A. Verloes, 2012, PloS one.

Specific Genetic Disorders and Autism: Clinical Contribution Towards their Identification

Alain Verloes, David Cohen, D. Cohen, 2005, Journal of autism and developmental disorders.

Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy

D. Cohen, L. Pasquier, S. Tordjman, 2017, International journal of molecular sciences.

Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo Mutation

D. Cohen, A. Verloes, I. Gozes, 2019, Journal of Molecular Neuroscience.

Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients

C. Depienne, A. Afenjar, D. Cohen, 2018, Clinical genetics.

Using medical exome sequencing to identify the causes of neurodevelopmental disorders : experience of two clinical units and 216 patients Running title : Medical exome and NDD

C. Depienne, A. Afenjar, D. Cohen, 2017 .

Acute behavioral crises in psychiatric inpatients with autism spectrum disorder (ASD): recognition of concomitant medical or non-ASD psychiatric conditions predicts enhanced improvement.

D. Cohen, J. Xavier, N. Bodeau, 2015, Research in developmental disabilities.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?

David Cohen, Claudine Laurent, C. Laurent, 2013, Molecular Autism.

Autism as a Disorder of Biological and Behavioral Rhythms: Toward New Therapeutic Perspectives

Michel Botbol, Geraldine Dawson, George M. Anderson, 2015, Front. Pediatr..

Multidisciplinary treatment plan for challenging behaviors in neurodevelopmental disorders.

D. Cohen, V. Guinchat, Cora Cravero, 2020, Handbook of clinical neurology.

1q21.1 microduplication: large verbal–nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number

A. Urban, D. Levinson, Bo Zhou, 2018, npj Genomic Medicine.

An overview of medical risk factors for childhood psychosis: Implications for research and treatment

R. Jardri, D. Levinson, D. Cohen, 2017, Schizophrenia Research.

Autism, Joint Hypermobility-Related Disorders and Pain

D. Cohen, C. Baeza-Velasco, V. Guinchat, 2018, Front. Psychiatry.

MECP2 mutation in a boy with language disorder and schizophrenia.

D. Cohen, D. Heron, P. Couvert, 2002, The American journal of psychiatry.

Risk factors of acute behavioral regression in psychiatrically hospitalized adolescents with autism.

C. Barthélémy, D. Cohen, N. Bodeau, 2010, Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Academie canadienne de psychiatrie de l'enfant et de l'adolescent.

Are There Cultural Differences in Parental Interest in Early Diagnosis and Genetic Risk Assessment for Autism Spectrum Disorder?

D. Cohen, J. Carayol, C. Amiet, 2014, Front. Pediatr..

Reading and spelling impairments in children and adolescents with infantile myotonic dystrophy

D. Cohen, B. Eymard, N. Angeard, 2006, Journal of Neurolinguistics.

Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?

L. Servais, D. Cohen, J. Xavier, 2017, Neuromuscular Disorders.

Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1

L. Vallée, D. Cohen, N. Bodeau, 2012, Developmental medicine and child neurology.

Time perception of simultaneous and sequential events in early-onset schizophrenia

D. Cohen, N. Coulon, S. Tordjman, 2016, Neurocase.

Brief Report: Visual-Spatial Deficit in a 16-year-old Girl with Maternally Derived Duplication of Proximal 15q

L. Cohen, H. Cavé, Anna J. Wilson, 2007, Journal of autism and developmental disorders.

Premigration social adversity and autism spectrum disorder

D. Cohen, J. Xavier, L. Gicquel, 2020, BJPsych Open.

pilepsy in Autism is Associated with Intellectual isability and Gender : Evidence from a Meta-Analysi

M. Baulac, L. Mottron, D. Cohen, 2008 .

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.

John P. Rice, Simon C. Potter, Melissa J. Green, 2018, Cell.

Biological Insights From 108 Schizophrenia-Associated Genetic Loci

C. Spencer, K. Davis, P. Visscher, 2014, Nature.

1q21.1 microduplication: large verbal–nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number

A. Urban, D. Levinson, Bo Zhou, 2018, npj Genomic Medicine.

Gene × Environment Interactions in Autism Spectrum Disorders: Role of Epigenetic Mechanisms

E. Somogyi, D. Cohen, V. Kovess, 2014, Front. Psychiatry.

Advances in the Research of Melatonin in Autism Spectrum Disorders: Literature Review and New Perspectives

D. Cohen, S. Tordjman, M. Botbol, 2013, International journal of molecular sciences.

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.

P. Visscher, E. Bramon, S. Djurovic, 2016, JAMA psychiatry.

[Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].

D. Cohen, D. Heron, C. Pinquier, 2001, L'Encephale.

The Autism Psychodynamic Evaluation of Changes (APEC) scale: A reliability and validity study on a newly developed standardized psychodynamic assessment for youth with Pervasive Developmental Disorders

D. Cohen, S. Tordjman, M. Botbol, 2010, Journal of Physiology-Paris.