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 *

153 related articles for article (PubMed ID: 39210319)

  • 1. CNVDeep: deep association of copy number variants with neurocognitive disorders.
    Rahaie Z; Rabiee HR; Alinejad-Rokny H
    BMC Bioinformatics; 2024 Aug; 25(1):283. PubMed ID: 39210319
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
    Vysotskiy M; Zhong X; Miller-Fleming TW; Zhou D; ; ; ; Cox NJ; Weiss LA
    Genome Med; 2021 Oct; 13(1):172. PubMed ID: 34715901
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The penetrance of copy number variations for schizophrenia and developmental delay.
    Kirov G; Rees E; Walters JT; Escott-Price V; Georgieva L; Richards AL; Chambert KD; Davies G; Legge SE; Moran JL; McCarroll SA; O'Donovan MC; Owen MJ
    Biol Psychiatry; 2014 Mar; 75(5):378-85. PubMed ID: 23992924
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
    Levinson DF; Duan J; Oh S; Wang K; Sanders AR; Shi J; Zhang N; Mowry BJ; Olincy A; Amin F; Cloninger CR; Silverman JM; Buccola NG; Byerley WF; Black DW; Kendler KS; Freedman R; Dudbridge F; Pe'er I; Hakonarson H; Bergen SE; Fanous AH; Holmans PA; Gejman PV
    Am J Psychiatry; 2011 Mar; 168(3):302-16. PubMed ID: 21285140
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders.
    Yoon J; Mao Y
    Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34071723
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.
    Wolfe K; Strydom A; Morrogh D; Carter J; Cutajar P; Eyeoyibo M; Hassiotis A; McCarthy J; Mukherjee R; Paschos D; Perumal N; Read S; Shankar R; Sharif S; Thirulokachandran S; Thygesen JH; Patch C; Ogilvie C; Flinter F; McQuillin A; Bass N
    Eur J Hum Genet; 2016 Jan; 25(1):66-72. PubMed ID: 27650969
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder.
    Kushima I; Nakatochi M; Aleksic B; Okada T; Kimura H; Kato H; Morikawa M; Inada T; Ishizuka K; Torii Y; Nakamura Y; Tanaka S; Imaeda M; Takahashi N; Yamamoto M; Iwamoto K; Nawa Y; Ogawa N; Iritani S; Hayashi Y; Lo T; Otgonbayar G; Furuta S; Iwata N; Ikeda M; Saito T; Ninomiya K; Okochi T; Hashimoto R; Yamamori H; Yasuda Y; Fujimoto M; Miura K; Itokawa M; Arai M; Miyashita M; Toriumi K; Ohi K; Shioiri T; Kitaichi K; Someya T; Watanabe Y; Egawa J; Takahashi T; Suzuki M; Sasaki T; Tochigi M; Nishimura F; Yamasue H; Kuwabara H; Wakuda T; Kato TA; Kanba S; Horikawa H; Usami M; Kodaira M; Watanabe K; Yoshikawa T; Toyota T; Yokoyama S; Munesue T; Kimura R; Funabiki Y; Kosaka H; Jung M; Kasai K; Ikegame T; Jinde S; Numata S; Kinoshita M; Kato T; Kakiuchi C; Yamakawa K; Suzuki T; Hashimoto N; Ishikawa S; Yamagata B; Nio S; Murai T; Son S; Kunii Y; Yabe H; Inagaki M; Goto YI; Okumura Y; Ito T; Arioka Y; Mori D; Ozaki N
    Biol Psychiatry; 2022 Sep; 92(5):362-374. PubMed ID: 35667888
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
    Bassett AS; Lowther C; Merico D; Costain G; Chow EWC; van Amelsvoort T; McDonald-McGinn D; Gur RE; Swillen A; Van den Bree M; Murphy K; Gothelf D; Bearden CE; Eliez S; Kates W; Philip N; Sashi V; Campbell L; Vorstman J; Cubells J; Repetto GM; Simon T; Boot E; Heung T; Evers R; Vingerhoets C; van Duin E; Zackai E; Vergaelen E; Devriendt K; Vermeesch JR; Owen M; Murphy C; Michaelovosky E; Kushan L; Schneider M; Fremont W; Busa T; Hooper S; McCabe K; Duijff S; Isaev K; Pellecchia G; Wei J; Gazzellone MJ; Scherer SW; Emanuel BS; Guo T; Morrow BE; Marshall CR;
    Am J Psychiatry; 2017 Nov; 174(11):1054-1063. PubMed ID: 28750581
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
    Martin-Brevet S; Rodríguez-Herreros B; Nielsen JA; Moreau C; Modenato C; Maillard AM; Pain A; Richetin S; Jønch AE; Qureshi AY; Zürcher NR; Conus P; ; ; Chung WK; Sherr EH; Spiro JE; Kherif F; Beckmann JS; Hadjikhani N; Reymond A; Buckner RL; Draganski B; Jacquemont S
    Biol Psychiatry; 2018 Aug; 84(4):253-264. PubMed ID: 29778275
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children.
    Fetit R; Price DJ; Lawrie SM; Johnstone M
    Psychiatr Genet; 2020 Oct; 30(5):136-140. PubMed ID: 32732550
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature.
    Lengyel A; Pinti É; Pikó H; Jávorszky E; David D; Tihanyi M; Gönczi É; Kiss E; Tóth Z; Tory K; Fekete G; Haltrich I
    Eur J Med Genet; 2020 Oct; 63(10):104027. PubMed ID: 32758661
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.
    Szatkiewicz JP; Neale BM; O'Dushlaine C; Fromer M; Goldstein JI; Moran JL; Chambert K; Kähler A; Magnusson PK; Hultman CM; Sklar P; Purcell S; McCarroll SA; Sullivan PF
    Mol Psychiatry; 2013 Nov; 18(11):1178-84. PubMed ID: 23938935
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.
    Tropeano M; Ahn JW; Dobson RJ; Breen G; Rucker J; Dixit A; Pal DK; McGuffin P; Farmer A; White PS; Andrieux J; Vassos E; Ogilvie CM; Curran S; Collier DA
    PLoS One; 2013; 8(4):e61365. PubMed ID: 23637818
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
    Degenhardt F; Priebe L; Herms S; Mattheisen M; Mühleisen TW; Meier S; Moebus S; Strohmaier J; Groß M; Breuer R; Lange C; Hoffmann P; Meyer-Lindenberg A; Heinz A; Walter H; Lucae S; Wolf C; Müller-Myhsok B; Holsboer F; Maier W; Rietschel M; Nöthen MM; Cichon S
    Am J Med Genet B Neuropsychiatr Genet; 2012 Apr; 159B(3):263-73. PubMed ID: 22344817
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Refining the Phenotype of Recurrent Rearrangements of Chromosome 16.
    Redaelli S; Maitz S; Crosti F; Sala E; Villa N; Spaccini L; Selicorni A; Rigoldi M; Conconi D; Dalprà L; Roversi G; Bentivegna A
    Int J Mol Sci; 2019 Mar; 20(5):. PubMed ID: 30836598
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
    Glessner JT; Khan ME; Chang X; Liu Y; Otieno FG; Lemma M; Slaby I; Hain H; Mentch F; Li J; Kao C; Sleiman PMA; March ME; Connolly J; Hakonarson H
    J Neurodev Disord; 2023 Apr; 15(1):14. PubMed ID: 37120522
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
    Wolfe K; McQuillin A; Alesi V; Boudry Labis E; Cutajar P; Dallapiccola B; Dentici ML; Dieux-Coeslier A; Duban-Bedu B; Duelund Hjortshøj T; Goel H; Loddo S; Morrogh D; Mosca-Boidron AL; Novelli A; Olivier-Faivre L; Parker J; Parker MJ; Patch C; Pelling AL; Smol T; Tümer Z; Vanakker O; van Haeringen A; Vanlerberghe C; Strydom A; Skuse D; Bass N
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jun; 177(4):397-405. PubMed ID: 29603867
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.