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Times Cited: 446
Times Cited
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Similarity
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Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
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CNVs of noncoding cis-regulatory elements in human disease.
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Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
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Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum.
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Partial FMRP expression is sufficient to normalize neuronal hyperactivity in Fragile X neurons.
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CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems.
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FMR1 Reactivating Treatments in Fragile X iPSC-Derived Neural Progenitors In Vitro and In Vivo.
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Targeted Reactivation of FMR1 Transcription in Fragile X Syndrome Embryonic Stem Cells.
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Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons.
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Human Pluripotent Stem Cell-Derived Neural Cells and Brain Organoids Reveal SARS-CoV-2 Neurotropism Predominates in Choroid Plexus Epithelium.
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Molecular Mechanisms Driving mRNA Degradation by m6A Modification.
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Cerebral organoids model human brain development and microcephaly.
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Human cerebral organoids recapitulate gene expression programs of fetal neocortex development.
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Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.