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Excess protein synthesis in Drosophila Fragile X mutants impairs long-term memory

Nature neuroscience, 2008-10, Vol.11 (10), p.1143-1145

2008

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Leveraging Knowledge Graphs and Natural Language Processing for Automated Web Resource Labeling and Knowledge Mobilization in Neurodevelopmental Disorders: Development and Usability Study

Journal of medical Internet research, 2023-04, Vol.25 (1), p.e45268-e45268

2023

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Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile X model

Molecular psychiatry, 2017-08, Vol.22 (8), p.1140-1148

2017

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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

American journal of human genetics, 2016-05, Vol.98 (5), p.1038-1046

2016

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Deciphering the Diversity of Mental Models in Neurodevelopmental Disorders: Knowledge Graph Representation of Public Data Using Natural Language Processing

Journal of medical Internet research, 2022-08, Vol.24 (8), p.e39888-e39888

2022

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How Knowledge Mapping Can Bridge the Communication Gap Between Caregivers and Health Professionals Supporting Individuals With Complex Medical Needs: A Study in Fragile X Syndrome

Frontiers in psychiatry, 2021-11, Vol.12, p.731011-731011

2021

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Phenotypic Trade-Offs: Deciphering the Impact of Neurodiversity on Drug Development in Fragile X Syndrome

Frontiers in psychiatry, 2021-10, Vol.12, p.730987

2021

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Prenatal fruit juice exposure enhances memory consolidation in male post-weanling Sprague-Dawley rats

PloS one, 2020-01, Vol.15 (1), p.e0227938-e0227938

2020

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Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype

Human genetics, 2017-03, Vol.136 (3), p.297-305

2017

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Longitudinal follow-up of metformin treatment in Fragile X Syndrome

Frontiers in psychology, 2024-06, Vol.15, p.1305597

2024

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Developing a cluster-based approach for deciphering complexity in individuals with neurodevelopmental differences

Frontiers in pediatrics, 2023-09, Vol.11, p.1171920-1171920

2023

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Drosophila model for Angelman syndrome

Proceedings of the National Academy of Sciences - PNAS, 2008-08, Vol.105 (34), p.12399-12404

2008

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Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms

Human molecular genetics, 2016-03, Vol.25 (6), p.1088-1099

2016

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TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype

Annals of neurology, 2015-12, Vol.78 (6), p.982-994

2015

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Long-term Memory Testing in Children With Typical Development and Neurodevelopmental Disorders: Remote Web-based Image Task Feasibility Study

JMIR pediatrics and parenting, 2023-05, Vol.6, p.e39720-e39720

2023

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Stress Odorant Sensory Response Dysfunction in Drosophila Fragile X Syndrome Mutants

Frontiers in molecular neuroscience, 2018-08, Vol.11, p.242-242

2018

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From Learning to Memory: What Flies Can Tell Us about Intellectual Disability Treatment

Frontiers in psychiatry, 2015-06, Vol.6, p.85-85

2015

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Sex difference contributes to phenotypic diversity in individuals with neurodevelopmental disorders

Frontiers in pediatrics, 2023-08, Vol.11, p.1172154-1172154

2023

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Intercorrelation of Molecular Biomarkers and Clinical Phenotype Measures in Fragile X Syndrome

Cells (Basel, Switzerland), 2023-07, Vol.12 (14), p.1920

2023

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Insulin signaling is acutely required for long-term memory in Drosophila

Frontiers in neural circuits, 2015-03, Vol.9, p.8

2015

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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

American journal of human genetics, 2016-06, Vol.98 (6), p.1271-1271

2016

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Analyzing the Quality of Life in Individuals with Fragile X Syndrome in Relation to Sleep and Mental Health

Journal of autism and developmental disorders, 2024-04

2024

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Fruit flies and intellectual disability

Fly (Austin, Tex.), 2009-01, Vol.3 (1), p.91-104

2009

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Rearrangement of Chromosome 14q with Associated White Matter Disease

Pediatric neurology, 2011-08, Vol.45 (2), p.117-120

2011

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G.P.216

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.881-882

2014

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Excess protein synthesis in Drosophila Fragile X mutants impairs long-term memory

Leveraging Knowledge Graphs and Natural Language Processing for Automated Web Resource Labeling and Knowledge Mobilization in Neurodevelopmental Disorders: Development and Usability Study

Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile X model

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Deciphering the Diversity of Mental Models in Neurodevelopmental Disorders: Knowledge Graph Representation of Public Data Using Natural Language Processing

How Knowledge Mapping Can Bridge the Communication Gap Between Caregivers and Health Professionals Supporting Individuals With Complex Medical Needs: A Study in Fragile X Syndrome

Phenotypic Trade-Offs: Deciphering the Impact of Neurodiversity on Drug Development in Fragile X Syndrome

Prenatal fruit juice exposure enhances memory consolidation in male post-weanling Sprague-Dawley rats

Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype

Longitudinal follow-up of metformin treatment in Fragile X Syndrome

Developing a cluster-based approach for deciphering complexity in individuals with neurodevelopmental differences

Drosophila model for Angelman syndrome

Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms

TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype

Long-term Memory Testing in Children With Typical Development and Neurodevelopmental Disorders: Remote Web-based Image Task Feasibility Study

Stress Odorant Sensory Response Dysfunction in Drosophila Fragile X Syndrome Mutants

From Learning to Memory: What Flies Can Tell Us about Intellectual Disability Treatment

Sex difference contributes to phenotypic diversity in individuals with neurodevelopmental disorders

Intercorrelation of Molecular Biomarkers and Clinical Phenotype Measures in Fragile X Syndrome

Insulin signaling is acutely required for long-term memory in Drosophila

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Analyzing the Quality of Life in Individuals with Fragile X Syndrome in Relation to Sleep and Mental Health

Fruit flies and intellectual disability

Rearrangement of Chromosome 14q with Associated White Matter Disease

G.P.216

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