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 *

253 related articles for article (PubMed ID: 33812299)

  • 1. Structural and functional brain alterations revealed by neuroimaging in CNV carriers.
    Moreau CA; Ching CR; Kumar K; Jacquemont S; Bearden CE
    Curr Opin Genet Dev; 2021 Jun; 68():88-98. PubMed ID: 33812299
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
    Sønderby IE; Ching CRK; Thomopoulos SI; van der Meer D; Sun D; Villalon-Reina JE; Agartz I; Amunts K; Arango C; Armstrong NJ; Ayesa-Arriola R; Bakker G; Bassett AS; Boomsma DI; Bülow R; Butcher NJ; Calhoun VD; Caspers S; Chow EWC; Cichon S; Ciufolini S; Craig MC; Crespo-Facorro B; Cunningham AC; Dale AM; Dazzan P; de Zubicaray GI; Djurovic S; Doherty JL; Donohoe G; Draganski B; Durdle CA; Ehrlich S; Emanuel BS; Espeseth T; Fisher SE; Ge T; Glahn DC; Grabe HJ; Gur RE; Gutman BA; Haavik J; Håberg AK; Hansen LA; Hashimoto R; Hibar DP; Holmes AJ; Hottenga JJ; Hulshoff Pol HE; Jalbrzikowski M; Knowles EEM; Kushan L; Linden DEJ; Liu J; Lundervold AJ; Martin-Brevet S; Martínez K; Mather KA; Mathias SR; McDonald-McGinn DM; McRae AF; Medland SE; Moberget T; Modenato C; Monereo Sánchez J; Moreau CA; Mühleisen TW; Paus T; Pausova Z; Prieto C; Ragothaman A; Reinbold CS; Reis Marques T; Repetto GM; Reymond A; Roalf DR; Rodriguez-Herreros B; Rucker JJ; Sachdev PS; Schmitt JE; Schofield PR; Silva AI; Stefansson H; Stein DJ; Tamnes CK; Tordesillas-Gutiérrez D; Ulfarsson MO; Vajdi A; van 't Ent D; van den Bree MBM; Vassos E; Vázquez-Bourgon J; Vila-Rodriguez F; Walters GB; Wen W; Westlye LT; Wittfeld K; Zackai EH; Stefánsson K; Jacquemont S; Thompson PM; Bearden CE; Andreassen OA; ;
    Hum Brain Mapp; 2022 Jan; 43(1):300-328. PubMed ID: 33615640
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies.
    Nakatochi M; Kushima I; Ozaki N
    J Hum Genet; 2021 Jan; 66(1):25-37. PubMed ID: 32958875
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Copy number variation and neuropsychiatric illness.
    Rees E; Kirov G
    Curr Opin Genet Dev; 2021 Jun; 68():57-63. PubMed ID: 33752146
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
    Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
    Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Somatic copy number variants in neuropsychiatric disorders.
    Maury EA; Walsh CA
    Curr Opin Genet Dev; 2021 Jun; 68():9-17. PubMed ID: 33444936
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes.
    Silva AI; Ehrhart F; Ulfarsson MO; Stefansson H; Stefansson K; Wilkinson LS; Hall J; Linden DEJ
    Biol Psychiatry; 2022 Sep; 92(5):341-361. PubMed ID: 35659384
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CNVs: harbingers of a rare variant revolution in psychiatric genetics.
    Malhotra D; Sebat J
    Cell; 2012 Mar; 148(6):1223-41. PubMed ID: 22424231
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry.
    Moreau CA; Harvey A; Kumar K; Huguet G; Urchs SGW; Douard EA; Schultz LM; Sharmarke H; Jizi K; Martin CO; Younis N; Tamer P; Rolland T; Martineau JL; Orban P; Silva AI; Hall J; van den Bree MBM; Owen MJ; Linden DEJ; Labbe A; Lippé S; Bearden CE; Almasy L; Glahn DC; Thompson PM; Bourgeron T; Bellec P; Jacquemont S
    Biol Psychiatry; 2023 Jan; 93(1):45-58. PubMed ID: 36372570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
    Van Den Bossche MJ; Johnstone M; Strazisar M; Pickard BS; Goossens D; Lenaerts AS; De Zutter S; Nordin A; Norrback KF; Mendlewicz J; Souery D; De Rijk P; Sabbe BG; Adolfsson R; Blackwood D; Del-Favero J
    Am J Med Genet B Neuropsychiatr Genet; 2012 Oct; 159B(7):812-22. PubMed ID: 22911887
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.
    Hiroi N; Takahashi T; Hishimoto A; Izumi T; Boku S; Hiramoto T
    Mol Psychiatry; 2013 Nov; 18(11):1153-65. PubMed ID: 23917946
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neuroimaging genomics in psychiatry-a translational approach.
    Mufford MS; Stein DJ; Dalvie S; Groenewold NA; Thompson PM; Jahanshad N
    Genome Med; 2017 Nov; 9(1):102. PubMed ID: 29179742
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CNV biology in neurodevelopmental disorders.
    Takumi T; Tamada K
    Curr Opin Neurobiol; 2018 Feb; 48():183-192. PubMed ID: 29331932
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study.
    Thygesen JH; Presman A; Harju-Seppänen J; Irizar H; Jones R; Kuchenbaecker K; Lin K; Alizadeh BZ; Austin-Zimmerman I; Bartels-Velthuis A; Bhat A; Bruggeman R; Cahn W; Calafato S; Crespo-Facorro B; de Haan L; de Zwarte SMC; Di Forti M; Díez-Revuelta Á; Hall J; Hall MH; Iyegbe C; Jablensky A; Kahn R; Kalaydjieva L; Kravariti E; Lawrie S; Luykx JJ; Mata I; McDonald C; McIntosh AM; McQuillin A; Muir R; Ophoff R; Picchioni M; Prata DP; Ranlund S; Rujescu D; Rutten BPF; Schulze K; Shaikh M; Schirmbeck F; Simons CJP; Toulopoulou T; van Amelsvoort T; van Haren N; van Os J; van Winkel R; Vassos E; Walshe M; Weisbrod M; Zartaloudi E; Bell V; Powell J; Lewis CM; Murray RM; Bramon E
    Mol Psychiatry; 2021 Sep; 26(9):5307-5319. PubMed ID: 32719466
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
    Bergen SE; Ploner A; Howrigan D; ; O'Donovan MC; Smoller JW; Sullivan PF; Sebat J; Neale B; Kendler KS
    Am J Psychiatry; 2019 Jan; 176(1):29-35. PubMed ID: 30392412
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare copy number variants in individuals at clinical high risk for psychosis: Enrichment of synaptic/brain-related functional pathways.
    Jagannath V; Grünblatt E; Theodoridou A; Oneda B; Roth A; Gerstenberg M; Franscini M; Traber-Walker N; Correll CU; Heekeren K; Rössler W; Rauch A; Walitza S
    Am J Med Genet B Neuropsychiatr Genet; 2020 Mar; 183(2):140-151. PubMed ID: 31742845
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Dissecting autism and schizophrenia through neuroimaging genomics.
    Moreau CA; Raznahan A; Bellec P; Chakravarty M; Thompson PM; Jacquemont S
    Brain; 2021 Aug; 144(7):1943-1957. PubMed ID: 33704401
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.