BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 38798629)

  • 1. 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]  

  • 2. Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort.
    Alexander-Bloch A; Huguet G; Schultz LM; Huffnagle N; Jacquemont S; Seidlitz J; Saci Z; Moore TM; Bethlehem RAI; Mollon J; Knowles EK; Raznahan A; Merikangas A; Chaiyachati BH; Raman H; Schmitt JE; Barzilay R; Calkins ME; Shinohara RT; Satterthwaite TD; Gur RC; Glahn DC; Almasy L; Gur RE; Hakonarson H; Glessner J
    JAMA Psychiatry; 2022 Jul; 79(7):699-709. PubMed ID: 35544191
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Copy number variations and cognitive phenotypes in unselected populations.
    Männik K; Mägi R; Macé A; Cole B; Guyatt AL; Shihab HA; Maillard AM; Alavere H; Kolk A; Reigo A; Mihailov E; Leitsalu L; Ferreira AM; Nõukas M; Teumer A; Salvi E; Cusi D; McGue M; Iacono WG; Gaunt TR; Beckmann JS; Jacquemont S; Kutalik Z; Pankratz N; Timpson N; Metspalu A; Reymond A
    JAMA; 2015 May; 313(20):2044-54. PubMed ID: 26010633
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Impact of Copy Number Variants and Polygenic Risk Scores on Psychopathology in the UK Biobank.
    Mollon J; Schultz LM; Huguet G; Knowles EEM; Mathias SR; Rodrigue A; Alexander-Bloch A; Saci Z; Jean-Louis M; Kumar K; Douard E; Almasy L; Jacquemont S; Glahn DC
    Biol Psychiatry; 2023 Oct; 94(7):591-600. PubMed ID: 36764568
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.
    Calle Sánchez X; Helenius D; Bybjerg-Grauholm J; Pedersen C; Hougaard DM; Børglum AD; Nordentoft M; Mors O; Mortensen PB; Geschwind DH; Montalbano S; Raznahan A; Thompson WK; Ingason A; Werge T
    JAMA Psychiatry; 2022 Jan; 79(1):59-69. PubMed ID: 34817560
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
    Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
    JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder.
    Mosca SJ; Langevin LM; Dewey D; Innes AM; Lionel AC; Marshall CC; Scherer SW; Parboosingh JS; Bernier FP
    J Med Genet; 2016 Dec; 53(12):812-819. PubMed ID: 27489308
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
    Martin CL; Wain KE; Oetjens MT; Tolwinski K; Palen E; Hare-Harris A; Habegger L; Maxwell EK; Reid JG; Walsh LK; Myers SM; Ledbetter DH
    JAMA Psychiatry; 2020 Dec; 77(12):1276-1285. PubMed ID: 32697297
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases.
    Yamasaki M; Makino T; Khor SS; Toyoda H; Miyagawa T; Liu X; Kuwabara H; Kano Y; Shimada T; Sugiyama T; Nishida H; Sugaya N; Tochigi M; Otowa T; Okazaki Y; Kaiya H; Kawamura Y; Miyashita A; Kuwano R; Kasai K; Tanii H; Sasaki T; Honda M; Tokunaga K
    BMC Med Genomics; 2020 Mar; 13(1):55. PubMed ID: 32223758
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
    Jarick I; Volckmar AL; Pütter C; Pechlivanis S; Nguyen TT; Dauvermann MR; Beck S; Albayrak Ö; Scherag S; Gilsbach S; Cichon S; Hoffmann P; Degenhardt F; Nöthen MM; Schreiber S; Wichmann HE; Jöckel KH; Heinrich J; Tiesler CM; Faraone SV; Walitza S; Sinzig J; Freitag C; Meyer J; Herpertz-Dahlmann B; Lehmkuhl G; Renner TJ; Warnke A; Romanos M; Lesch KP; Reif A; Schimmelmann BG; Hebebrand J; Scherag A; Hinney A
    Mol Psychiatry; 2014 Jan; 19(1):115-21. PubMed ID: 23164820
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
    Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A
    Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.
    Kendall KM; Bracher-Smith M; Fitzpatrick H; Lynham A; Rees E; Escott-Price V; Owen MJ; O'Donovan MC; Walters JTR; Kirov G
    Br J Psychiatry; 2019 May; 214(5):297-304. PubMed ID: 30767844
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.