These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 39123267)

  • 21. Graph Node Classification to Predict Autism Risk in Genes.
    Bandara D; Riccardi K
    Genes (Basel); 2024 Apr; 15(4):. PubMed ID: 38674382
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders.
    Ashitha SNM; Ramachandra NB
    Neuroscience; 2020 Jul; 438():25-40. PubMed ID: 32407977
    [TBL] [Abstract][Full Text] [Related]  

  • 23. PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder.
    Pijuan J; Ortigoza-Escobar JD; Ortiz J; Alcalá A; Calvo MJ; Cubells M; Hernando-Davalillo C; Palau F; Hoenicka J
    Autism Res; 2021 Jun; 14(6):1088-1100. PubMed ID: 33749153
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies.
    Murtaza N; Cheng AA; Brown CO; Meka DP; Hong S; Uy JA; El-Hajjar J; Pipko N; Unda BK; Schwanke B; Xing S; Thiruvahindrapuram B; Engchuan W; Trost B; Deneault E; Calderon de Anda F; Doble BW; Ellis J; Anagnostou E; Bader GD; Scherer SW; Lu Y; Singh KK
    Cell Rep; 2022 Nov; 41(8):111678. PubMed ID: 36417873
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.
    Zhou WZ; Zhang J; Li Z; Lin X; Li J; Wang S; Yang C; Wu Q; Ye AY; Wang M; Wang D; Pu TZ; Wu YY; Wei L
    Hum Mutat; 2019 Jun; 40(6):801-815. PubMed ID: 30763456
    [TBL] [Abstract][Full Text] [Related]  

  • 26. De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types.
    Chen S; Wang J; Cicek E; Roeder K; Yu H; Devlin B
    Mol Autism; 2020 Oct; 11(1):76. PubMed ID: 33032641
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Copy number variations independently induce autism spectrum disorder.
    Yingjun X; Haiming Y; Mingbang W; Liangying Z; Jiaxiu Z; Bing S; Qibin Y; Xiaofang S
    Biosci Rep; 2017 Aug; 37(4):. PubMed ID: 28533427
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gene Regulation Analysis Reveals Perturbations of Autism Spectrum Disorder during Neural System Development.
    Li D; Xu J; Yang MQ
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946850
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.
    Menashe I; Larsen EC; Banerjee-Basu S
    PLoS One; 2013; 8(6):e66707. PubMed ID: 23825557
    [TBL] [Abstract][Full Text] [Related]  

  • 30. AutDB: a gene reference resource for autism research.
    Basu SN; Kollu R; Banerjee-Basu S
    Nucleic Acids Res; 2009 Jan; 37(Database issue):D832-6. PubMed ID: 19015121
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex.
    Golovina E; Fadason T; Lints TJ; Walker C; Vickers MH; O'Sullivan JM
    Sci Rep; 2021 Aug; 11(1):15867. PubMed ID: 34354167
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association of genes with phenotype in autism spectrum disorder.
    Nisar S; Hashem S; Bhat AA; Syed N; Yadav S; Azeem MW; Uddin S; Bagga P; Reddy R; Haris M
    Aging (Albany NY); 2019 Nov; 11(22):10742-10770. PubMed ID: 31744938
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
    Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
    Mol Autism; 2017; 8():14. PubMed ID: 28344757
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study.
    Abdi M; Aliyev E; Trost B; Kohailan M; Aamer W; Syed N; Shaath R; Gandhi GD; Engchuan W; Howe J; Thiruvahindrapuram B; Geng M; Whitney J; Syed A; Lakshmi J; Hussein S; Albashir N; Hussein A; Poggiolini I; Elhag SF; Palaniswamy S; Kambouris M; de Fatima Janjua M; Tahir MOE; Nazeer A; Shahwar D; Azeem MW; Mokrab Y; Aati NA; Akil A; Scherer SW; Kamal M; Fakhro KA
    Genome Med; 2023 Oct; 15(1):81. PubMed ID: 37805537
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clustering Analysis Supports the Detection of Biological Processes Related to Autism Spectrum Disorder.
    Emberti Gialloreti L; Enea R; Di Micco V; Di Giovanni D; Curatolo P
    Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33316975
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.
    Alibutud R; Hansali S; Cao X; Zhou A; Mahaganapathy V; Azaro M; Gwin C; Wilson S; Buyske S; Bartlett CW; Flax JF; Brzustowicz LM; Xing J
    Int J Mol Sci; 2023 Aug; 24(17):. PubMed ID: 37686052
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Screening and Bioinformatics Analysis of Differential Genes in Autism Spectrum Disorder Based on GEO Database.
    Zhu J; Meng H; Li Y
    Stud Health Technol Inform; 2023 Nov; 308():280-288. PubMed ID: 38007751
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The mTOR Signaling Pathway Activity and Vitamin D Availability Control the Expression of Most Autism Predisposition Genes.
    Trifonova EA; Klimenko AI; Mustafin ZS; Lashin SA; Kochetov AV
    Int J Mol Sci; 2019 Dec; 20(24):. PubMed ID: 31847491
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.
    Cosemans N; Maljaars J; Vogels A; Holvoet M; Devriendt K; Steyaert J; Van Den Bogaert K; Noens I; Peeters H
    Neurogenetics; 2021 Jul; 22(3):207-213. PubMed ID: 33683518
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.