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 *

123 related articles for article (PubMed ID: 33720513)

  • 1. A novel microduplication in INPP5A segregates with schizophrenia spectrum disorder in the family of a patient with both childhood onset schizophrenia and autism spectrum disorder.
    Fernandez A; Drozd M; Thümmler S; Bardoni B; Askenazy F; Capovilla M
    Am J Med Genet A; 2021 Jun; 185(6):1841-1847. PubMed ID: 33720513
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Risk of Psychiatric and Neurodevelopmental Disorders Among Siblings of Probands With Autism Spectrum Disorders.
    Jokiranta-Olkoniemi E; Cheslack-Postava K; Sucksdorff D; Suominen A; Gyllenberg D; Chudal R; Leivonen S; Gissler M; Brown AS; Sourander A
    JAMA Psychiatry; 2016 Jun; 73(6):622-9. PubMed ID: 27145529
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High rate of disease-related copy number variations in childhood onset schizophrenia.
    Ahn K; Gotay N; Andersen TM; Anvari AA; Gochman P; Lee Y; Sanders S; Guha S; Darvasi A; Glessner JT; Hakonarson H; Lencz T; State MW; Shugart YY; Rapoport JL
    Mol Psychiatry; 2014 May; 19(5):568-72. PubMed ID: 23689535
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.
    Addington AM; Gauthier J; Piton A; Hamdan FF; Raymond A; Gogtay N; Miller R; Tossell J; Bakalar J; Inoff-Germain G; Gochman P; Long R; Rapoport JL; Rouleau GA
    Mol Psychiatry; 2011 Mar; 16(3):238-9. PubMed ID: 20479756
    [No Abstract]   [Full Text] [Related]  

  • 5. Exploration and characterisation of the phenotypic and genetic profiles of patients with early onset schizophrenia associated with autism spectrum disorder and their first-degree relatives: a French multicentre case series study protocol (GenAuDiss).
    Fernandez A; Dor E; Maurin T; Laure G; Menard ML; Drozd M; Poinso F; Bardoni B; Askenazy F; Thümmler S
    BMJ Open; 2018 Jul; 8(7):e023330. PubMed ID: 29980548
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Triad of Childhood-Onset Schizophrenia, Autism Spectrum Disorder, and Catatonia: A Case Report.
    Leslie AC; O'Sullivan M
    Schizophr Bull; 2023 Mar; 49(2):239-243. PubMed ID: 36719136
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?
    Sporn AL; Addington AM; Gogtay N; Ordoñez AE; Gornick M; Clasen L; Greenstein D; Tossell JW; Gochman P; Lenane M; Sharp WS; Straub RE; Rapoport JL
    Biol Psychiatry; 2004 May; 55(10):989-94. PubMed ID: 15121482
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Common polygenic variation and risk for childhood-onset schizophrenia.
    Ahn K; An SS; Shugart YY; Rapoport JL
    Mol Psychiatry; 2016 Jan; 21(1):94-6. PubMed ID: 25510512
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Neurodevelopmental Disorders, Psychiatric Comorbidities and Associated Pathologies in Patients with Childhood-Onset Schizophrenia and Premorbid Autistic Symptoms.].
    Fernandez A; Pasquet-Levy M; Laure G; Thümmler S; Askenazy F
    Can J Psychiatry; 2021 Dec; 66(12):1042-1050. PubMed ID: 33563032
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 15q13.3 duplication in two patients with childhood-onset schizophrenia.
    Zhou D; Gochman P; Broadnax DD; Rapoport JL; Ahn K
    Am J Med Genet B Neuropsychiatr Genet; 2016 Sep; 171(6):777-83. PubMed ID: 26968334
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Psychotic symptoms in 16p11.2 copy-number variant carriers.
    Jutla A; Turner JB; Green Snyder L; Chung WK; Veenstra-VanderWeele J
    Autism Res; 2020 Feb; 13(2):187-198. PubMed ID: 31724820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Advancing the understanding of autism disease mechanisms through genetics.
    de la Torre-Ubieta L; Won H; Stein JL; Geschwind DH
    Nat Med; 2016 Apr; 22(4):345-61. PubMed ID: 27050589
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increased burden of deleterious variants in essential genes in autism spectrum disorder.
    Ji X; Kember RL; Brown CD; Bućan M
    Proc Natl Acad Sci U S A; 2016 Dec; 113(52):15054-15059. PubMed ID: 27956632
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
    J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay.
    Wiśniowiecka-Kowalnik B; Nesteruk M; Peters SU; Xia Z; Cooper ML; Savage S; Amato RS; Bader P; Browning MF; Haun CL; Duda AW; Cheung SW; Stankiewicz P
    Am J Med Genet B Neuropsychiatr Genet; 2010 Jul; 153B(5):983-93. PubMed ID: 20162629
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Advances in understanding the pathophysiology of autism spectrum disorders.
    Yenkoyan K; Grigoryan A; Fereshetyan K; Yepremyan D
    Behav Brain Res; 2017 Jul; 331():92-101. PubMed ID: 28499914
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
    Woodbury-Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Anagnostou E; Scherer SW; Vieland VJ; Szatmari P
    Am J Med Genet B Neuropsychiatr Genet; 2020 Jul; 183(5):268-276. PubMed ID: 32372567
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q26.32 microdeletion syndrome.
    Riehmer V; Erger F; Herkenrath P; Seland S; Jackels M; Wiater A; Heller R; Beck BB; Netzer C
    Am J Med Genet A; 2017 Aug; 173(8):2132-2138. PubMed ID: 28574232
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder.
    Chen CP; Lin SP; Lee CL; Chern SR; Wu PS; Chen YN; Chen SW; Wang W
    Taiwan J Obstet Gynecol; 2017 Feb; 56(1):98-101. PubMed ID: 28254236
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited.
    Rapoport J; Chavez A; Greenstein D; Addington A; Gogtay N
    J Am Acad Child Adolesc Psychiatry; 2009 Jan; 48(1):10-8. PubMed ID: 19218893
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.