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 *

143 related articles for article (PubMed ID: 35123134)

  • 21. Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
    Zhou X; Feliciano P; Shu C; Wang T; Astrovskaya I; Hall JB; Obiajulu JU; Wright JR; Murali SC; Xu SX; Brueggeman L; Thomas TR; Marchenko O; Fleisch C; Barns SD; Snyder LG; Han B; Chang TS; Turner TN; Harvey WT; Nishida A; O'Roak BJ; Geschwind DH; ; Michaelson JJ; Volfovsky N; Eichler EE; Shen Y; Chung WK
    Nat Genet; 2022 Sep; 54(9):1305-1319. PubMed ID: 35982159
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Review on the Role of Genetic Mutations in the Autism Spectrum Disorder.
    Ghafouri-Fard S; Pourtavakoli A; Hussen BM; Taheri M; Ayatollahi SA
    Mol Neurobiol; 2023 Sep; 60(9):5256-5272. PubMed ID: 37278883
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Involvement of endoplasmic reticulum stress and neurite outgrowth in the model mice of autism spectrum disorder.
    Kawada K; Mimori S; Okuma Y; Nomura Y
    Neurochem Int; 2018 Oct; 119():115-119. PubMed ID: 28711654
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
    da Silva Montenegro EM; Costa CS; Campos G; Scliar M; de Almeida TF; Zachi EC; Silva IMW; Chan AJS; Zarrei M; Lourenço NCV; Yamamoto GL; Scherer S; Passos-Bueno MR
    Autism Res; 2020 Feb; 13(2):199-206. PubMed ID: 31696658
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Autism Spectrum Disorder/Intellectual Disability-Associated Mutations in Trio Disrupt Neuroligin 1-Mediated Synaptogenesis.
    Tian C; Paskus JD; Fingleton E; Roche KW; Herring BE
    J Neurosci; 2021 Sep; 41(37):7768-7778. PubMed ID: 34353896
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample.
    Jiao J; Zhang M; Yang P; Huang Y; Hu X; Cai J; Yang C; Situ M; Zhang H; Fu L; Guo K; Huang Y
    J Mol Neurosci; 2020 Feb; 70(2):219-229. PubMed ID: 31838722
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome.
    Darville H; Poulet A; Rodet-Amsellem F; Chatrousse L; Pernelle J; Boissart C; Héron D; Nava C; Perrier A; Jarrige M; Cogé F; Millan MJ; Bourgeron T; Peschanski M; Delorme R; Benchoua A
    EBioMedicine; 2016 Jul; 9():293-305. PubMed ID: 27333044
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder.
    Li SJ; Yu SS; Luo HY; Li X; Rao B; Wang Y; Li ZZ; Liu G; Zou LP; Zhang JS; Feng C; Liu J; Liu JW; Hu N; Chen XQ; Yu SY; Li K; He MW; Yu XG; Wang J; Guo SL; Chen ZY; Zhang L; Ma L
    Clin Chim Acta; 2018 Apr; 479():144-147. PubMed ID: 29366832
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of autism-related
    Wen Z; Cheng TL; Li GZ; Sun SB; Yu SY; Zhang Y; Du YS; Qiu Z
    Mol Autism; 2017; 8():43. PubMed ID: 28785396
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Autism-associated Shank3 mutations alter mGluR expression and mGluR-dependent but not NMDA receptor-dependent long-term depression.
    Lee K; Vyas Y; Garner CC; Montgomery JM
    Synapse; 2019 Aug; 73(8):e22097. PubMed ID: 30868621
    [TBL] [Abstract][Full Text] [Related]  

  • 32. NRXN1α
    Avazzadeh S; Quinlan LR; Reilly J; McDonagh K; Jalali A; Wang Y; McInerney V; Krawczyk J; Ding Y; Fitzgerald J; O'Sullivan M; Forman EB; Lynch SA; Ennis S; Feerick N; Reilly R; Li W; Shen X; Yang G; Lu Y; Peeters H; Dockery P; O'Brien T; Shen S; Gallagher L
    BMC Neurosci; 2021 Sep; 22(1):56. PubMed ID: 34525970
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Idiopathic Autism: Cellular and Molecular Phenotypes in Pluripotent Stem Cell-Derived Neurons.
    Liu X; Campanac E; Cheung HH; Ziats MN; Canterel-Thouennon L; Raygada M; Baxendale V; Pang AL; Yang L; Swedo S; Thurm A; Lee TL; Fung KP; Chan WY; Hoffman DA; Rennert OM
    Mol Neurobiol; 2017 Aug; 54(6):4507-4523. PubMed ID: 27356918
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The Use of Induced Pluripotent Stem Cell Technology to Advance Autism Research and Treatment.
    Acab A; Muotri AR
    Neurotherapeutics; 2015 Jul; 12(3):534-45. PubMed ID: 25851569
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Deletion of TRPC6, an Autism Risk Gene, Induces Hyperexcitability in Cortical Neurons Derived from Human Pluripotent Stem Cells.
    Shin KC; Ali G; Ali Moussa HY; Gupta V; de la Fuente A; Kim HG; Stanton LW; Park Y
    Mol Neurobiol; 2023 Dec; 60(12):7297-7308. PubMed ID: 37552395
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Neural Stem Cells from Shank3-ko Mouse Model Autism Spectrum Disorders.
    Grasselli C; Carbone A; Panelli P; Giambra V; Bossi M; Mazzoccoli G; De Filippis L
    Mol Neurobiol; 2020 Mar; 57(3):1502-1515. PubMed ID: 31773410
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cellular and molecular characterization of multiplex autism in human induced pluripotent stem cell-derived neurons.
    Lewis EMA; Meganathan K; Baldridge D; Gontarz P; Zhang B; Bonni A; Constantino JN; Kroll KL
    Mol Autism; 2019; 10():51. PubMed ID: 31893020
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autism-associated PTEN missense mutation leads to enhanced nuclear localization and neurite outgrowth in an induced pluripotent stem cell line.
    Wong CW; Wang Y; Liu T; Li L; Cheung SKK; Or PM; Cheng AS; Choy KW; Burbach JPH; Feng B; Chang RCC; Chan AM
    FEBS J; 2020 Nov; 287(22):4848-4861. PubMed ID: 32150788
    [TBL] [Abstract][Full Text] [Related]  

  • 39. De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
    Mirzaa GM; Chong JX; Piton A; Popp B; Foss K; Guo H; Harripaul R; Xia K; Scheck J; Aldinger KA; Sajan SA; Tang S; Bonneau D; Beck A; White J; Mahida S; Harris J; Smith-Hicks C; Hoyer J; Zweier C; Reis A; Thiel CT; Jamra RA; Zeid N; Yang A; Farach LS; Walsh L; Payne K; Rohena L; Velinov M; Ziegler A; Schaefer E; Gatinois V; Geneviève D; Simon MEH; Kohler J; Rotenberg J; Wheeler P; Larson A; Ernst ME; Akman CI; Westman R; Blanchet P; Schillaci LA; Vincent-Delorme C; Gripp KW; Mattioli F; Guyader GL; Gerard B; Mathieu-Dramard M; Morin G; Sasanfar R; Ayub M; Vasli N; Yang S; Person R; Monaghan KG; Nickerson DA; van Binsbergen E; Enns GM; Dries AM; Rowe LJ; Tsai ACH; Svihovec S; Friedman J; Agha Z; Qamar R; Rodan LH; Martinez-Agosto J; Ockeloen CW; Vincent M; Sunderland WJ; Bernstein JA; ; Eichler EE; Vincent JB; ; Bamshad MJ
    Genet Med; 2020 Mar; 22(3):538-546. PubMed ID: 31723249
    [TBL] [Abstract][Full Text] [Related]  

  • 40. FoxP1 orchestration of ASD-relevant signaling pathways in the striatum.
    Araujo DJ; Anderson AG; Berto S; Runnels W; Harper M; Ammanuel S; Rieger MA; Huang HC; Rajkovich K; Loerwald KW; Dekker JD; Tucker HO; Dougherty JD; Gibson JR; Konopka G
    Genes Dev; 2015 Oct; 29(20):2081-96. PubMed ID: 26494785
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.