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 *

118 related articles for article (PubMed ID: 38123995)

  • 21. Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in
    Fröhlich H; Kollmeyer ML; Linz VC; Stuhlinger M; Groneberg D; Reigl A; Zizer E; Friebe A; Niesler B; Rappold G
    Proc Natl Acad Sci U S A; 2019 Oct; 116(44):22237-22245. PubMed ID: 31611379
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies.
    Meyer R; Begemann M; Demuth S; Kraft F; Dey D; Schüler H; Busse S; Häusler M; Zerres K; Kurth I; Eggermann T; Elbracht M
    Clin Genet; 2020 Oct; 98(4):408-412. PubMed ID: 32720325
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.
    Palumbo O; D'Agruma L; Minenna AF; Palumbo P; Stallone R; Palladino T; Zelante L; Carella M
    Gene; 2013 Mar; 516(1):107-13. PubMed ID: 23287644
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity.
    Araujo DJ; Toriumi K; Escamilla CO; Kulkarni A; Anderson AG; Harper M; Usui N; Ellegood J; Lerch JP; Birnbaum SG; Tucker HO; Powell CM; Konopka G
    J Neurosci; 2017 Nov; 37(45):10917-10931. PubMed ID: 28978667
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene.
    Mutlu-Albayrak H; Karaer K
    Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():179-181. PubMed ID: 30579078
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour.
    Bacon C; Schneider M; Le Magueresse C; Froehlich H; Sticht C; Gluch C; Monyer H; Rappold GA
    Mol Psychiatry; 2015 May; 20(5):632-9. PubMed ID: 25266127
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of a de novo FOXP1 mutation and incidental discovery of inherited genetic variants contributing to a case of autism spectrum disorder and epilepsy.
    Jay K; Mitra A; Harding T; Matthes D; Van Ness B
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00751. PubMed ID: 31111659
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization.
    Fröhlich H; Rafiullah R; Schmitt N; Abele S; Rappold GA
    Hum Mol Genet; 2017 Apr; 26(8):1511-1521. PubMed ID: 28204507
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Development and behaviour in Marshall-Smith syndrome: an exploratory study of cognition, phenotype and autism.
    van Balkom ID; Shaw A; Vuijk PJ; Franssens M; Hoek HW; Hennekam RC
    J Intellect Disabil Res; 2011 Oct; 55(10):973-87. PubMed ID: 21790824
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) With Language Impairment Accompanied by Developmental Disability Caused by Forkhead Box Protein 1 (FOXP1) Exon Deletion: A Case Report.
    Alenezi S; Alyahya A; Aldhalaan H
    Cureus; 2021 Dec; 13(12):e20595. PubMed ID: 35103171
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Severe speech impairment is a distinguishing feature of FOXP1-related disorder.
    Braden RO; Amor DJ; Fisher SE; Mei C; Myers CT; Mefford H; Gill D; Srivastava S; Swanson LC; Goel H; Scheffer IE; Morgan AT
    Dev Med Child Neurol; 2021 Dec; 63(12):1417-1426. PubMed ID: 34109629
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.
    Han L; Chen M; Wang Y; Wu H; Quan Y; Bai T; Li K; Duan G; Gao Y; Hu Z; Xia K; Guo H
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00789. PubMed ID: 31199603
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion.
    Jensen M; Tyryshkina A; Pizzo L; Smolen C; Das M; Huber E; Krishnan A; Girirajan S
    Genome Med; 2021 Oct; 13(1):163. PubMed ID: 34657631
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Case report: Expanding the phenotype of
    Cesaroni CA; Pollazzon M; Mancini C; Rizzi S; Cappelletti C; Pizzi S; Frattini D; Spagnoli C; Caraffi SG; Zuntini R; Trimarchi G; Niceta M; Radio FC; Tartaglia M; Garavelli L; Fusco C
    Front Neurol; 2023; 14():1207176. PubMed ID: 37521304
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome).
    Assia Batzir N; Posey JE; Song X; Akdemir ZC; Rosenfeld JA; Brown CW; Chen E; Holtrop SG; Mizerik E; Nieto Moreno M; Payne K; Raas-Rothschild A; Scott R; Vernon HJ; Zadeh N; ; Lupski JR; Sutton VR
    Am J Med Genet A; 2020 Jan; 182(1):38-52. PubMed ID: 31782611
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families.
    Baldwin I; Shafer RL; Hossain WA; Gunewardena S; Veatch OJ; Mosconi MW; Butler MG
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33562221
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Case report: FOXP1 syndrome caused by a
    Chen M; Sun Y; Qian Y; Chen N; Li H; Wang L; Dong M
    Front Genet; 2022; 13():926070. PubMed ID: 35991577
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pathogenic variants in
    Granadillo JL; P A Stegmann A; Guo H; Xia K; Angle B; Bontempo K; Ranells JD; Newkirk P; Costin C; Viront J; Stumpel CT; Sinnema M; Panis B; Pfundt R; Krapels IPC; Klaassens M; Nicolai J; Li J; Jiang Y; Marco E; Canton A; Latronico AC; Montenegro L; Leheup B; Bonnet C; M Amudhavalli S; Lawson CE; McWalter K; Telegrafi A; Pearson R; Kvarnung M; Wang X; Bi W; Rosenfeld JA; Shinawi M
    J Med Genet; 2020 Oct; 57(10):717-724. PubMed ID: 32152250
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability.
    Zombor M; Kalmár T; Maróti Z; Zimmermann A; Máté A; Bereczki C; Sztriha L
    J Hum Genet; 2018 Nov; 63(11):1189-1193. PubMed ID: 30181650
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The behavioural phenotype of SATB2-associated syndrome: a within-group and cross-syndrome analysis.
    Bissell S; Oliver C; Moss J; Heald M; Waite J; Crawford H; Kothari V; Rumbellow L; Walters G; Richards C
    J Neurodev Disord; 2022 Mar; 14(1):25. PubMed ID: 35350986
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.