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Overview: Research on the Genetic Architecture of the Developing Cerebral Cortex in Norms and Diseases

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2794, p.1

Momoi, Mariko Y

2024

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Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder

PloS one, 2012-12, Vol.7 (12), p.e51155

2012

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Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (8), p.3117-3122

2008

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LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome

PloS one, 2014-03, Vol.9 (3), p.e92695

2014

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Comment on: Risk of neuropsychiatric adverse events associated with the use of oseltamivir: a nationwide population-based case-crossover study

Journal of antimicrobial chemotherapy, 2019-06, Vol.74 (6), p.1762-1764

2019

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CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder‐related mutation

Journal of neurochemistry, 2015-08, Vol.134 (4), p.783-793

2015

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Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity

PloS one, 2012-01, Vol.7 (1), p.e30151-e30151

2012

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Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS

Clinical neurophysiology, 2012-06, Vol.123 (6), p.1147-1157

2012

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Impairment of social and emotional behaviors in Cadm1-knockout mice

Biochemical and biophysical research communications, 2010-06, Vol.396 (3), p.703-708

2010

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A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum

Journal of neurochemistry, 2012-12, Vol.123 (5), p.886-894

2012

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Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders

Journal of neurochemistry, 2016-10, Vol.139 (2), p.245-255

2016

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Mutations in the gene encoding CADM1 are associated with autism spectrum disorder

Biochemical and biophysical research communications, 2008-12, Vol.377 (3), p.926-929

2008

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MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus

Brain & development (Tokyo. 1979), 2014-01, Vol.36 (1), p.64-69

2014

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Association of moderately abnormal behavior and administered neuraminidase inhibitors

Drug Discoveries & Therapeutics, 2020/02/29, Vol.14(1), pp.50-53

2020

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Severe abnormal behavior incidence after administration of neuraminidase inhibitors using the national database of medical claims

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2018-03, Vol.24 (3), p.177-181

2018

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Cytokine profiles of seventeen cytokines, growth factors and chemokines in cord blood and its relation to perinatal clinical findings

Cytokine (Philadelphia, Pa.), 2010-03, Vol.49 (3), p.331-337

2010

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Life-Threatening Abnormal Behavior Incidence in 10-19 Year Old Patients Administered Neuraminidase Inhibitors

PloS one, 2015-07, Vol.10 (7), p.e0129712-e0129712

2015

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Role of an adaptor protein Lin‐7B in brain development: possible involvement in autism spectrum disorders

Journal of neurochemistry, 2015-01, Vol.132 (1), p.61-69

2015

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Inquiry into some gap among oseltamivir use and severe abnormal behavior in Japanese children and adolescents with influenza

Drug Discoveries & Therapeutics, 2018/12/31, Vol.12(6), pp.381-383

2018

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Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder

Neuroscience letters, 2012-01, Vol.506 (2), p.277-280

2012

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Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case

Neuropathology, 2013-06, Vol.33 (3), p.292-298

2013

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The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis

Molecular autism, 2015-03, Vol.6 (1), p.17-17, Article 17

2015

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Th2 cells predominate in idiopathic steroid-sensitive nephrotic syndrome

Clinical and experimental nephrology, 2010-12, Vol.14 (6), p.578-583

2010

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Association of severe abnormal behavior and acetaminophen with/without neuraminidase inhibitors

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2019-06, Vol.25 (6), p.423-426

2019

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Right prefrontal activation as a neuro-functional biomarker for monitoring acute effects of methylphenidate in ADHD children: An fNIRS study

NeuroImage clinical, 2012-01, Vol.1 (1), p.131-140

2012

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Overview: Research on the Genetic Architecture of the Developing Cerebral Cortex in Norms and Diseases

Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder

Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome

Comment on: Risk of neuropsychiatric adverse events associated with the use of oseltamivir: a nationwide population-based case-crossover study

CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder‐related mutation

Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity

Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS

Impairment of social and emotional behaviors in Cadm1-knockout mice

A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum

Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders

Mutations in the gene encoding CADM1 are associated with autism spectrum disorder

MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus

Association of moderately abnormal behavior and administered neuraminidase inhibitors

Severe abnormal behavior incidence after administration of neuraminidase inhibitors using the national database of medical claims

Cytokine profiles of seventeen cytokines, growth factors and chemokines in cord blood and its relation to perinatal clinical findings

Life-Threatening Abnormal Behavior Incidence in 10-19 Year Old Patients Administered Neuraminidase Inhibitors

Role of an adaptor protein Lin‐7B in brain development: possible involvement in autism spectrum disorders

Inquiry into some gap among oseltamivir use and severe abnormal behavior in Japanese children and adolescents with influenza

Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder

Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case

The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis

Th2 cells predominate in idiopathic steroid-sensitive nephrotic syndrome

Association of severe abnormal behavior and acetaminophen with/without neuraminidase inhibitors

Right prefrontal activation as a neuro-functional biomarker for monitoring acute effects of methylphenidate in ADHD children: An fNIRS study

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