BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 35536379)

  • 1. Social and emotional characteristics of girls and young women with DDX3X-associated intellectual disability: a descriptive and comparative study.
    Ng-Cordell E; Kolesnik-Taylor A; O'Brien S; Astle D; Scerif G; Baker K
    J Autism Dev Disord; 2023 Aug; 53(8):3208-3219. PubMed ID: 35536379
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo DDX3X missense variants in males appear viable and contribute to syndromic intellectual disability.
    Nicola P; Blackburn PR; Rasmussen KJ; Bertsch NL; Klee EW; Hasadsri L; Pichurin PN; Rankin J; Raymond FL; ; Clayton-Smith J
    Am J Med Genet A; 2019 Apr; 179(4):570-578. PubMed ID: 30734472
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
    Snijders Blok L; Madsen E; Juusola J; Gilissen C; Baralle D; Reijnders MR; Venselaar H; Helsmoortel C; Cho MT; Hoischen A; Vissers LE; Koemans TS; Wissink-Lindhout W; Eichler EE; Romano C; Van Esch H; Stumpel C; Vreeburg M; Smeets E; Oberndorff K; van Bon BW; Shaw M; Gecz J; Haan E; Bienek M; Jensen C; Loeys BL; Van Dijck A; Innes AM; Racher H; Vermeer S; Di Donato N; Rump A; Tatton-Brown K; Parker MJ; Henderson A; Lynch SA; Fryer A; Ross A; Vasudevan P; Kini U; Newbury-Ecob R; Chandler K; Male A; ; Dijkstra S; Schieving J; Giltay J; van Gassen KL; Schuurs-Hoeijmakers J; Tan PL; Pediaditakis I; Haas SA; Retterer K; Reed P; Monaghan KG; Haverfield E; Natowicz M; Myers A; Kruer MC; Stein Q; Strauss KA; Brigatti KW; Keating K; Burton BK; Kim KH; Charrow J; Norman J; Foster-Barber A; Kline AD; Kimball A; Zackai E; Harr M; Fox J; McLaughlin J; Lindstrom K; Haude KM; van Roozendaal K; Brunner H; Chung WK; Kooy RF; Pfundt R; Kalscheuer V; Mehta SG; Katsanis N; Kleefstra T
    Am J Hum Genet; 2015 Aug; 97(2):343-52. PubMed ID: 26235985
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prospective and detailed behavioral phenotyping in DDX3X syndrome.
    Tang L; Levy T; Guillory S; Halpern D; Zweifach J; Giserman-Kiss I; Foss-Feig JH; Frank Y; Lozano R; Belani P; Layton C; Lerman B; Frowner E; Breen MS; De Rubeis S; Kostic A; Kolevzon A; Buxbaum JD; Siper PM; Grice DE
    Mol Autism; 2021 May; 12(1):36. PubMed ID: 33993884
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features.
    Kellaris G; Khan K; Baig SM; Tsai IC; Zamora FM; Ruggieri P; Natowicz MR; Katsanis N
    Hum Genomics; 2018 Mar; 12(1):11. PubMed ID: 29490693
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DDX3X Syndrome: Summary of Findings and Recommendations for Evaluation and Care.
    Levy T; Siper PM; Lerman B; Halpern D; Zweifach J; Belani P; Thurm A; Kleefstra T; Berry-Kravis E; Buxbaum JD; Grice DE
    Pediatr Neurol; 2023 Jan; 138():87-94. PubMed ID: 36434914
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability: a case report.
    Moresco G; Costanza J; Santaniello C; Rondinone O; Grilli F; Prada E; Orcesi S; Coro I; Pichiecchio A; Marchisio P; Miozzo M; Fontana L; Milani D
    Ital J Pediatr; 2021 Mar; 47(1):81. PubMed ID: 33789733
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females.
    Scala M; Torella A; Severino M; Morana G; Castello R; Accogli A; Verrico A; Vari MS; Cappuccio G; Pinelli M; Vitiello G; Terrone G; D'Amico A; ; Nigro V; Capra V
    Eur J Hum Genet; 2019 Aug; 27(8):1254-1259. PubMed ID: 30936465
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expansion of Clinical and Genetic Spectrum of
    Dai Y; Yang Z; Guo J; Li H; Gong J; Xie Y; Xiao B; Wang H; Long L
    Front Mol Neurosci; 2022; 15():793001. PubMed ID: 35392274
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic and phenotypic findings in 34 novel Spanish patients with DDX3X neurodevelopmental disorder.
    Parra A; Pascual P; Cazalla M; Arias P; Gallego-Zazo N; San-Martín EA; Silván C; Santos-Simarro F; ; Nevado J; Tenorio-Castano J; Lapunzina P
    Clin Genet; 2024 Feb; 105(2):140-149. PubMed ID: 37904618
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.
    Dikow N; Granzow M; Graul-Neumann LM; Karch S; Hinderhofer K; Paramasivam N; Behl LJ; Kaufmann L; Fischer C; Evers C; Schlesner M; Eils R; Borck G; Zweier C; Bartram CR; Carey JC; Moog U
    Am J Med Genet A; 2017 May; 173(5):1369-1373. PubMed ID: 28371085
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gene functional networks and autism spectrum characteristics in young people with intellectual disability: a dimensional phenotyping study.
    Brkić D; Ng-Cordell E; O'Brien S; Scerif G; Astle D; Baker K
    Mol Autism; 2020 Dec; 11(1):98. PubMed ID: 33308299
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Aberrant cortical development is driven by impaired cell cycle and translational control in a
    Hoye ML; Calviello L; Poff AJ; Ejimogu NE; Newman CR; Montgomery MD; Ou J; Floor SN; Silver DL
    Elife; 2022 Jun; 11():. PubMed ID: 35762573
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development.
    Lennox AL; Hoye ML; Jiang R; Johnson-Kerner BL; Suit LA; Venkataramanan S; Sheehan CJ; Alsina FC; Fregeau B; Aldinger KA; Moey C; Lobach I; Afenjar A; Babovic-Vuksanovic D; Bézieau S; Blackburn PR; Bunt J; Burglen L; Campeau PM; Charles P; Chung BHY; Cogné B; Curry C; D'Agostino MD; Di Donato N; Faivre L; Héron D; Innes AM; Isidor B; Keren B; Kimball A; Klee EW; Kuentz P; Küry S; Martin-Coignard D; Mirzaa G; Mignot C; Miyake N; Matsumoto N; Fujita A; Nava C; Nizon M; Rodriguez D; Blok LS; Thauvin-Robinet C; Thevenon J; Vincent M; Ziegler A; Dobyns W; Richards LJ; Barkovich AJ; Floor SN; Silver DL; Sherr EH
    Neuron; 2020 May; 106(3):404-420.e8. PubMed ID: 32135084
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Risk factors and topographies for self-injurious behaviour in a sample of adults with intellectual developmental disorders.
    Folch A; Cortés MJ; Salvador-Carulla L; Vicens P; Irazábal M; Muñoz S; Rovira L; Orejuela C; Haro JM; Vilella E; Martínez-Leal R
    J Intellect Disabil Res; 2018 Dec; 62(12):1018-1029. PubMed ID: 29607562
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DDX3X Syndrome Behavioral Manifestations with Particular Emphasis on Psycho-Pathological Symptoms-A Review.
    Stefaniak U; Malak R; Kaczmarek A; Samborski W; Mojs E
    Biomedicines; 2023 Nov; 11(11):. PubMed ID: 38002045
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome.
    Boitnott A; Garcia-Forn M; Ung DC; Niblo K; Mendonca D; Park Y; Flores M; Maxwell S; Ellegood J; Qiu LR; Grice DE; Lerch JP; Rasin MR; Buxbaum JD; Drapeau E; De Rubeis S
    Biol Psychiatry; 2021 Dec; 90(11):742-755. PubMed ID: 34344536
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The role of intellectual disability and emotional regulation in the autism-depression relationship.
    Sáez-Suanes GP; García-Villamisar D; Del Pozo Armentia A
    Autism; 2023 Oct; 27(7):1960-1967. PubMed ID: 36967538
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A comprehensive review on DDX3X liquid phase condensation in health and neurodevelopmental disorders.
    Rosa E Silva I; Smetana JHC; de Oliveira JF
    Int J Biol Macromol; 2024 Feb; 259(Pt 2):129330. PubMed ID: 38218270
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The gap between IQ and adaptive functioning in autism spectrum disorder: Disentangling diagnostic and sex differences.
    McQuaid GA; Pelphrey KA; Bookheimer SY; Dapretto M; Webb SJ; Bernier RA; McPartland JC; Van Horn JD; Wallace GL
    Autism; 2021 Aug; 25(6):1565-1579. PubMed ID: 33715473
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.