BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 38890284)

  • 1. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs).
    Hall JH; Chawner SJRA; ; Wolstencroft J; Skuse D; Hall J; Holmans P; Owen MJ; van den Bree MBM
    Transl Psychiatry; 2024 Jun; 14(1):259. PubMed ID: 38890284
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs).
    Hall JH; Chawner SJRA; ; Wolstencroft J; Skuse D; Holmans P; Owen MJ; van den Bree MBM
    medRxiv; 2023 Dec; ():. PubMed ID: 38106165
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Coordination difficulties, IQ and psychopathology in children with high-risk copy number variants.
    Cunningham AC; Hall J; Owen MJ; van den Bree MBM
    Psychol Med; 2021 Jan; 51(2):290-299. PubMed ID: 31739810
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
    Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM
    Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs.
    Cunningham AC; Hall J; Einfeld S; Owen MJ; ; van den Bree MBM
    Psychol Med; 2022 Feb; 52(3):574-586. PubMed ID: 32643597
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
    Huguet G; Schramm C; Douard E; Jiang L; Labbe A; Tihy F; Mathonnet G; Nizard S; Lemyre E; Mathieu A; Poline JB; Loth E; Toro R; Schumann G; Conrod P; Pausova Z; Greenwood C; Paus T; Bourgeron T; Jacquemont S;
    JAMA Psychiatry; 2018 May; 75(5):447-457. PubMed ID: 29562078
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of copy number variation across the genome with neuropsychiatric traits in the general population.
    Guyatt AL; Stergiakouli E; Martin J; Walters J; O'Donovan M; Owen M; Thapar A; Kirov G; Rodriguez S; Rai D; Zammit S; Gaunt TR
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jul; 177(5):489-502. PubMed ID: 29687944
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of Rare Copy Number Variants With Risk of Depression.
    Kendall KM; Rees E; Bracher-Smith M; Legge S; Riglin L; Zammit S; O'Donovan MC; Owen MJ; Jones I; Kirov G; Walters JTR
    JAMA Psychiatry; 2019 Aug; 76(8):818-825. PubMed ID: 30994872
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A review of the cognitive impact of neurodevelopmental and neuropsychiatric associated copy number variants.
    Molloy CJ; Quigley C; McNicholas Á; Lisanti L; Gallagher L
    Transl Psychiatry; 2023 Apr; 13(1):116. PubMed ID: 37031194
    [TBL] [Abstract][Full Text] [Related]  

  • 10. How does genetic variation modify ND-CNV phenotypes?
    Dinneen TJ; Ghrálaigh FN; Walsh R; Lopez LM; Gallagher L
    Trends Genet; 2022 Feb; 38(2):140-151. PubMed ID: 34364706
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An assessment of sex bias in neurodevelopmental disorders.
    Polyak A; Rosenfeld JA; Girirajan S
    Genome Med; 2015 Aug; 7(1):94. PubMed ID: 26307204
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome.
    Douard E; Zeribi A; Schramm C; Tamer P; Loum MA; Nowak S; Saci Z; Lord MP; Rodríguez-Herreros B; Jean-Louis M; Moreau C; Loth E; Schumann G; Pausova Z; Elsabbagh M; Almasy L; Glahn DC; Bourgeron T; Labbe A; Paus T; Mottron L; Greenwood CMT; Huguet G; Jacquemont S
    Am J Psychiatry; 2021 Jan; 178(1):87-98. PubMed ID: 32911998
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
    Lowther C; Merico D; Costain G; Waserman J; Boyd K; Noor A; Speevak M; Stavropoulos DJ; Wei J; Lionel AC; Marshall CR; Scherer SW; Bassett AS
    Genome Med; 2017 Nov; 9(1):105. PubMed ID: 29187259
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The psychiatric phenotypes of 1q21 distal deletion and duplication.
    Linden SC; Watson CJ; Smith J; Chawner SJRA; Lancaster TM; Evans F; Williams N; Skuse D; Raymond FL; Hall J; Owen MJ; Linden DEJ; Green-Snyder L; Chung WK; Maillard AM; Jacquemont S; van den Bree MBM
    Transl Psychiatry; 2021 Feb; 11(1):105. PubMed ID: 33542195
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
    Moreno-De-Luca A; Evans DW; Boomer KB; Hanson E; Bernier R; Goin-Kochel RP; Myers SM; Challman TD; Moreno-De-Luca D; Slane MM; Hare AE; Chung WK; Spiro JE; Faucett WA; Martin CL; Ledbetter DH
    JAMA Psychiatry; 2015 Feb; 72(2):119-26. PubMed ID: 25493922
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank.
    Birnbaum R; Mahjani B; Loos RJF; Sharp AJ
    JAMA Psychiatry; 2022 Mar; 79(3):250-259. PubMed ID: 35080590
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.
    Klaassen P; Duijff S; Swanenburg de Veye H; Beemer F; Sinnema G; Breetvelt E; Schappin R; Vorstman J
    Am J Med Genet B Neuropsychiatr Genet; 2016 Sep; 171(6):790-6. PubMed ID: 26953189
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.
    Stamouli S; Anderlid BM; Willfors C; Thiruvahindrapuram B; Wei J; Berggren S; Nordgren A; Scherer SW; Lichtenstein P; Tammimies K; Bölte S
    Twin Res Hum Genet; 2018 Feb; 21(1):1-11. PubMed ID: 29307321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The copy number variant architecture of psychopathology and cognitive development in the ABCD
    Sha Z; Sun KY; Jung B; Barzilay R; Moore TM; Almasy L; Forsyth JK; Prem S; Gandal MJ; Seidlitz J; Glessner JT; Alexander-Bloch AF
    medRxiv; 2024 May; ():. PubMed ID: 38798629
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders.
    Krgovic D; Kokalj Vokac N; Zagorac A; Gregoric Kumperscak H
    Sci Rep; 2018 Jun; 8(1):9449. PubMed ID: 29930340
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.