BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

438 related articles for article (PubMed ID: 33338084)

  • 1. Coupling of autism genes to tissue-wide expression and dysfunction of synapse, calcium signalling and transcriptional regulation.
    Reilly J; Gallagher L; Leader G; Shen S
    PLoS One; 2020; 15(12):e0242773. PubMed ID: 33338084
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pathway Network Analyses for Autism Reveal Multisystem Involvement, Major Overlaps with Other Diseases and Convergence upon MAPK and Calcium Signaling.
    Wen Y; Alshikho MJ; Herbert MR
    PLoS One; 2016; 11(4):e0153329. PubMed ID: 27055244
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.
    Larsen E; Menashe I; Ziats MN; Pereanu W; Packer A; Banerjee-Basu S
    Mol Autism; 2016; 7():44. PubMed ID: 27790361
    [TBL] [Abstract][Full Text] [Related]  

  • 4. First glimpses of the neurobiology of autism spectrum disorder.
    Sanders SJ
    Curr Opin Genet Dev; 2015 Aug; 33():80-92. PubMed ID: 26547130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Integrative analysis of transcriptome-wide association study and mRNA expression profiles identifies candidate genes associated with autism spectrum disorders.
    Huang H; Cheng S; Ding M; Wen Y; Ma M; Zhang L; Li P; Cheng B; Liang X; Liu L; Du Y; Zhao Y; Kafle OP; Han B; Zhang F
    Autism Res; 2019 Jan; 12(1):33-38. PubMed ID: 30561910
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.
    Casanova EL; Sharp JL; Chakraborty H; Sumi NS; Casanova MF
    Mol Autism; 2016; 7():18. PubMed ID: 26985359
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Salivary miRNA profiles identify children with autism spectrum disorder, correlate with adaptive behavior, and implicate ASD candidate genes involved in neurodevelopment.
    Hicks SD; Ignacio C; Gentile K; Middleton FA
    BMC Pediatr; 2016 Apr; 16():52. PubMed ID: 27105825
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An autism spectrum disorder-related de novo mutation hotspot discovered in the GEF1 domain of Trio.
    Sadybekov A; Tian C; Arnesano C; Katritch V; Herring BE
    Nat Commun; 2017 Sep; 8(1):601. PubMed ID: 28928363
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SFARI genes and where to find them; modelling Autism Spectrum Disorder specific gene expression dysregulation with RNA-seq data.
    Arpi MNT; Simpson TI
    Sci Rep; 2022 Jun; 12(1):10158. PubMed ID: 35710789
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exploring key genes and pathways associated with sex differences in autism spectrum disorder: integrated bioinformatic analysis.
    Nautiyal H; Jaiswar A; Jha PK; Dwivedi S
    Mamm Genome; 2024 Jun; 35(2):280-295. PubMed ID: 38594551
    [TBL] [Abstract][Full Text] [Related]  

  • 11. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
    Gilbert J; O'Connor M; Templet S; Moghaddam M; Di Via Ioschpe A; Sinclair A; Zhu LQ; Xu W; Man HY
    J Neurosci; 2020 Jan; 40(1):237-254. PubMed ID: 31704787
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of amygdala-expressed genes associated with autism spectrum disorder.
    Herrero MJ; Velmeshev D; Hernandez-Pineda D; Sethi S; Sorrells S; Banerjee P; Sullivan C; Gupta AR; Kriegstein AR; Corbin JG
    Mol Autism; 2020 May; 11(1):39. PubMed ID: 32460837
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hierarchical cortical transcriptome disorganization in autism.
    Lombardo MV; Courchesne E; Lewis NE; Pramparo T
    Mol Autism; 2017; 8():29. PubMed ID: 28649314
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiplex gene and phenotype network to characterize shared genetic pathways of epilepsy and autism.
    Peng J; Zhou Y; Wang K
    Sci Rep; 2021 Jan; 11(1):952. PubMed ID: 33441621
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and genetic analysis of children with a dual diagnosis of Tourette syndrome and autism spectrum disorder.
    Carias KV; Wevrick R
    J Psychiatr Res; 2019 Apr; 111():145-153. PubMed ID: 30771620
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Common mechanisms of excitatory and inhibitory imbalance in schizophrenia and autism spectrum disorders.
    Gao R; Penzes P
    Curr Mol Med; 2015; 15(2):146-67. PubMed ID: 25732149
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epigenetic regulation of RELN and GAD1 in the frontal cortex (FC) of autism spectrum disorder (ASD) subjects.
    Zhubi A; Chen Y; Guidotti A; Grayson DR
    Int J Dev Neurosci; 2017 Nov; 62():63-72. PubMed ID: 28229923
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cell cycle networks link gene expression dysregulation, mutation, and brain maldevelopment in autistic toddlers.
    Pramparo T; Lombardo MV; Campbell K; Barnes CC; Marinero S; Solso S; Young J; Mayo M; Dale A; Ahrens-Barbeau C; Murray SS; Lopez L; Lewis N; Pierce K; Courchesne E
    Mol Syst Biol; 2015 Dec; 11(12):841. PubMed ID: 26668231
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism-Epilepsy Phenotype with Macrocephaly.
    Marchese M; Valvo G; Moro F; Sicca F; Santorelli FM
    Neuromolecular Med; 2016 Mar; 18(1):69-80. PubMed ID: 26537360
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cell-Type-Specific Analysis of Molecular Pathology in Autism Identifies Common Genes and Pathways Affected Across Neocortical Regions.
    Velmeshev D; Magistri M; Mazza EMC; Lally P; Khoury N; D'Elia ER; Bicciato S; Faghihi MA
    Mol Neurobiol; 2020 May; 57(5):2279-2289. PubMed ID: 32008165
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.