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Recessive mutations in >VPS13D cause childhood onset movement disorders

Annals of neurology, 2018-06, Vol.83 (6), p.1089-1095

2018

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“Bend so you don’t break!” A longitudinal moderated mediation study on human resources management practices, humility, psychological well-being, and job performance

Frontiers in psychology, 2024-10, Vol.15

2024

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SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

Human molecular genetics, 2011-06, Vol.20 (12), p.2297-2307

2011

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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

Human genetics, 2011-10, Vol.130 (4), p.563-573

2011

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De novo variants in sporadic cases of childhood onset schizophrenia

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.944-948

2016

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De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism

Biological psychiatry (1969), 2011-05, Vol.69 (9), p.898-901

2011

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Novel de novo SHANK3 mutation in autistic patients

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2009-04, Vol.150B (3), p.421-424

2009

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SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth

Human molecular genetics, 2014-01, Vol.23 (1), p.90-103

2014

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The effects of artificial intelligence on human resource activities and the roles of the human resource triad: opportunities and challenges

Frontiers in psychology, 2024-06, Vol.15, p.1360401

2024

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Organizational culture and leadership behaviors: is manager’s psychological health the missing piece?

Frontiers in psychology, 2023-09, Vol.14, p.1237775-1237775

2023

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A case of familial transmission of the newly described DNMT3A‐Overgrowth Syndrome

American journal of medical genetics. Part A, 2017-07, Vol.173 (7), p.1887-1890

2017

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Toward a new model of human resource management practices: construction and validation of the High Wellbeing and Performance Work System Scale

Frontiers in psychology, 2023-05, Vol.14, p.1151781-1151781

2023

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Measurement of Bradykinin Formation and Degradation in Blood Plasma: Relevance for Acquired Angioedema Associated With Angiotensin Converting Enzyme Inhibition and for Hereditary Angioedema Due to Factor XII or Plasminogen Gene Variants

Frontiers in medicine, 2020-07, Vol.7, p.358-358

2020

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A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review

American journal of medical genetics. Part A, 2016-05, Vol.170A (5), p.1225-1235

2016

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One down, fifty to go: managers' perceptions of their workload and how they cope with it to maintain their psychological health

Frontiers in psychology, 2024-02, Vol.14, p.1336560-1336560

2024

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De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

Annals of neurology, 2009-06, Vol.65 (6), p.748-753

2009

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A population genetic approach to mapping neurological disorder genes using deep resequencing

PLoS genetics, 2011-02, Vol.7 (2), p.e1001318-e1001318

2011

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Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder

Genome, 2013-10, Vol.56 (10), p.634-640

2013

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P332: A homozygous POU3F2 polyproline tract expansion is associated with severe psychomotor delay, developmental and epileptic encephalopathy, and ichthyosis

Genetics in Medicine Open, 2023, Vol.1 (1), p.100360, Article 100360

2023

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Organization of the basal ganglia: the importance of axonal collateralization

Trends in neurosciences (Regular ed.), 2000-10, Vol.23 (10), p.S20-S27

2000

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Intermittent neurologic decompensation: An underrecognized presentation of tyrosine hydroxylase deficiency

JIMD reports, 2022-09, Vol.63 (5), p.400-406

2022

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Management behaviors during the COVID-19 pandemic: The case of healthcare middle managers

Frontiers in psychology, 2022-11, Vol.13, p.986980-986980

2022

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Erasmus et les langues : entre contradictions, langues cibles et langues de communication

Cahiers internationaux de sociolinguistique, 2021-01, Vol.N° 17 (1), p.75-85

Gauthier, Julie

2021

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Picomolar Sensitivity Analysis of Multiple Bradykinin-Related Peptides in the Blood Plasma of Patients With Hereditary Angioedema in Remission: A Pilot Study

Frontiers in allergy, 2022-02, Vol.3, p.837463-837463

2022

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Does organizational culture play a role in the development of psychological distress?

International journal of human resource management, 2018-07, Vol.29 (12), p.1920-1949

2018

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Recessive mutations in >VPS13D cause childhood onset movement disorders

“Bend so you don’t break!” A longitudinal moderated mediation study on human resources management practices, humility, psychological well-being, and job performance

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

De novo variants in sporadic cases of childhood onset schizophrenia

De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism

Novel de novo SHANK3 mutation in autistic patients

SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth

The effects of artificial intelligence on human resource activities and the roles of the human resource triad: opportunities and challenges

Organizational culture and leadership behaviors: is manager’s psychological health the missing piece?

A case of familial transmission of the newly described DNMT3A‐Overgrowth Syndrome

Toward a new model of human resource management practices: construction and validation of the High Wellbeing and Performance Work System Scale

Measurement of Bradykinin Formation and Degradation in Blood Plasma: Relevance for Acquired Angioedema Associated With Angiotensin Converting Enzyme Inhibition and for Hereditary Angioedema Due to Factor XII or Plasminogen Gene Variants

A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review

One down, fifty to go: managers' perceptions of their workload and how they cope with it to maintain their psychological health

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

A population genetic approach to mapping neurological disorder genes using deep resequencing

Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder

P332: A homozygous POU3F2 polyproline tract expansion is associated with severe psychomotor delay, developmental and epileptic encephalopathy, and ichthyosis

Organization of the basal ganglia: the importance of axonal collateralization

Intermittent neurologic decompensation: An underrecognized presentation of tyrosine hydroxylase deficiency

Management behaviors during the COVID-19 pandemic: The case of healthcare middle managers

Erasmus et les langues : entre contradictions, langues cibles et langues de communication

Picomolar Sensitivity Analysis of Multiple Bradykinin-Related Peptides in the Blood Plasma of Patients With Hereditary Angioedema in Remission: A Pilot Study

Does organizational culture play a role in the development of psychological distress?

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