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Immune transcriptome alterations in the temporal cortex of subjects with autism

Neurobiology of disease, 2008-06, Vol.30 (3), p.303-311

2008

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BRAF Mutations in Melanoma: Biological Aspects, Therapeutic Implications, and Circulating Biomarkers

Cancers, 2023-08, Vol.15 (16), p.4026

2023

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Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families

PloS one, 2022-10, Vol.17 (10), p.e0275988

2022

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Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review

Clinical genetics, 2020-01, Vol.97 (1), p.125-137

2020

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Genome-wide expression studies in Autism spectrum disorder, Rett syndrome, and Down syndrome

Neurobiology of disease, 2012-01, Vol.45 (1), p.57-68

2012

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Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families

PloS one, 2022-10, Vol.17 (10), p.e0275988-e0275988

2022

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Editorial: Epigenetics of Neurodevelopmental, Neuromuscular and Neurodegenerative Disorders

Frontiers in molecular neuroscience, 2022-06, Vol.15, p.948827-948827

2022

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Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer

Genes, 2024-04, Vol.15 (5), p.554

2024

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Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

BMC medicine, 2009-10, Vol.7 (1), p.62-62, Article 62

2009

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Phytochemicals as Immunomodulatory Agents in Melanoma

International journal of molecular sciences, 2023-01, Vol.24 (3), p.2657

2023

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A pathogenic variant in the FLCN gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?

Frontiers in neuroscience, 2024-01, Vol.17, p.1304080-1304080

2024

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Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability

Genes, 2023-06, Vol.14 (7), p.1353

2023

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Melkersson-Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?

Genes, 2023-07, Vol.14 (7), p.1482

2023

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Genetic Dysruption of the Histaminergic Pathways: A Novel Deletion at the 15q21.2 locus Associated with Variable Expressivity of Neuropsychiatric Disorders

Genes, 2022-09, Vol.13 (10), p.1685

2022

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Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations

Genes, 2022-12, Vol.13 (12), p.2266

2022

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Genotype–Phenotype Correlations in Relation to Newly Emerging Monogenic Forms of Autism Spectrum Disorder and Associated Neurodevelopmental Disorders: The Importance of Phenotype Reevaluation after Pangenomic Results

Journal of clinical medicine, 2021-10, Vol.10 (21), p.5060

2021

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Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism

PloS one, 2013-02, Vol.8 (2), p.e56927

2013

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Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders

Genes, 2023-02, Vol.14 (3), p.585

2023

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Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorder

Molecular genetics & genomic medicine, 2023-08, Vol.11 (8), p.e2182-n/a

2023

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Melanoma Cell Resistance to Vemurafenib Modifies Inter-Cellular Communication Signals

Biomedicines, 2021-01, Vol.9 (1), p.79

2021

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Reevaluation of Serum Arylesterase Activity in Neurodevelopmental Disorders

Antioxidants, 2021-01, Vol.10 (2), p.164

2021

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Lack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individuals

PloS one, 2011-02, Vol.6 (2), p.e16609

2011

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Autism genetics： Methodological issues and experimental design

Science China. Life Sciences, 2015-10, Vol.58 (10), p.946-957

2015

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FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

Molecular genetics & genomic medicine, 2020-09, Vol.8 (9), p.e1373-n/a

2020

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Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: A nested case–control study

International journal of cancer, 2006-03, Vol.118 (5), p.1248-1253

2006

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Immune transcriptome alterations in the temporal cortex of subjects with autism

BRAF Mutations in Melanoma: Biological Aspects, Therapeutic Implications, and Circulating Biomarkers

Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families

Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review

Genome-wide expression studies in Autism spectrum disorder, Rett syndrome, and Down syndrome

Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families

Editorial: Epigenetics of Neurodevelopmental, Neuromuscular and Neurodegenerative Disorders

Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Phytochemicals as Immunomodulatory Agents in Melanoma

A pathogenic variant in the FLCN gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?

Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability

Melkersson-Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?

Genetic Dysruption of the Histaminergic Pathways: A Novel Deletion at the 15q21.2 locus Associated with Variable Expressivity of Neuropsychiatric Disorders

Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations

Genotype–Phenotype Correlations in Relation to Newly Emerging Monogenic Forms of Autism Spectrum Disorder and Associated Neurodevelopmental Disorders: The Importance of Phenotype Reevaluation after Pangenomic Results

Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism

Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders

Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorder

Melanoma Cell Resistance to Vemurafenib Modifies Inter-Cellular Communication Signals

Reevaluation of Serum Arylesterase Activity in Neurodevelopmental Disorders

Lack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individuals

Autism genetics： Methodological issues and experimental design

FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: A nested case–control study

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