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Academic Journal

Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature.

Subjects: MICROCEPHALY; GENETIC variation; SEX chromosomesBRAZIL

  • Source: Journal of Autism & Developmental Disorders. Mar2024, Vol. 54 Issue 3, p1181-1212. 32p.

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Academic Journal

Development of the gut microbiota in the first 14 years of life and its relations to internalizing and externalizing difficulties and social anxiety during puberty.

Subjects: BODY composition; RESEARCH; SEQUENCE analysis

  • Source: European Child & Adolescent Psychiatry. Mar2024, Vol. 33 Issue 3, p847-860. 14p.

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Academic Journal

Single-locus and Haplotype Associations of GRIN2B Gene with Autism Spectrum Disorders and the Demographic and Clinical Characteristics of Patients in Guilan, Iran.

Subjects: GENETIC mutation; CHILD development; DNA demethylationIRAN

  • Source: Journal of Autism & Developmental Disorders. Feb2024, Vol. 54 Issue 2, p607-614. 8p.

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Periodical

Lucky Genes.

Subjects: GENES; PLANT genes

  • Source: Scientific American. Jun2024, Vol. 330 Issue 6, p14-14. 2/3p. 1 Color Photograph.

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Periodical

Gene Thief.

Subjects: HORIZONTAL gene transfer; HELMINTHS; GENES

  • Source: Scientific American. Jan2024, Vol. 330 Issue 1, p16-17. 2p. 1 Color Photograph.

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Academic Journal

Williams syndrome: reduced orienting to other's eyes in a hypersocial phenotype.

Subjects: SOCIALIZATION; SOCIAL perception; AROUSAL (Physiology)

  • Source: Journal of Autism & Developmental Disorders. Jul2023, Vol. 53 Issue 7, p2786-2797. 12p. 1 Color Photograph, 4 Charts, 2 Graphs.

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Academic Journal

A pilot study on identifying gene signatures as markers for predicting patient response to antiseizure medications.

Subjects: EPILEPSY; GENE expression profiling; GENE ontology

  • Source: Neurological Sciences. Jun2023, Vol. 44 Issue 6, p2137-2148. 12p. 2 Diagrams, 4 Charts, 3 Graphs.

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Academic Journal

Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.

Subjects: ESSENTIAL tremor; GENETIC variation; GENE expressionCHINA

  • Source: Neurological Sciences. Jun2023, Vol. 44 Issue 6, p2003-2015. 13p. 1 Black and White Photograph, 1 Diagram, 2 Charts, 1 Graph.

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Academic Journal

Case Report: A Disease Phenotype of Rett Syndrome and Neurofibromatosis Resulting from A Bilocus Variant Combination.

Subjects: BRAIN physiology; DIAGNOSIS of autism; GENETICS of autism

  • Source: Journal of Autism & Developmental Disorders. May2023, Vol. 53 Issue 5, p2138-2142. 5p.

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Academic Journal

A case report of infantile parkinsonism-dystonia-2 caused by homozygous mutation in the SLC18A2 gene.

Subjects: MONOAMINE transporters; MOVEMENT disorders; GENETIC mutation

  • Source: International Journal of Neuroscience. May2023, Vol. 133 Issue 5, p574-577. 4p.

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  • 1-10 of  4,945 results for ""Genes""