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 *

158 related articles for article (PubMed ID: 24700553)

  • 1. Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
    Noor A; Lionel AC; Cohen-Woods S; Moghimi N; Rucker J; Fennell A; Thiruvahindrapuram B; Kaufman L; Degagne B; Wei J; Parikh SV; Muglia P; Forte J; Scherer SW; Kennedy JL; Xu W; McGuffin P; Farmer A; Strauss J; Vincent JB
    Am J Med Genet B Neuropsychiatr Genet; 2014 Jun; 165B(4):303-13. PubMed ID: 24700553
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reduced burden of very large and rare CNVs in bipolar affective disorder.
    Grozeva D; Kirov G; Conrad DF; Barnes CP; Hurles M; Owen MJ; O'Donovan MC; Craddock N
    Bipolar Disord; 2013 Dec; 15(8):893-8. PubMed ID: 24127788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders.
    Gerik-Celebi HB; Bolat H; Unsel-Bolat G
    Dev Neurobiol; 2024 Jul; 84(3):158-168. PubMed ID: 38739110
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
    Kirov G; Pocklington AJ; Holmans P; Ivanov D; Ikeda M; Ruderfer D; Moran J; Chambert K; Toncheva D; Georgieva L; Grozeva D; Fjodorova M; Wollerton R; Rees E; Nikolov I; van de Lagemaat LN; Bayés A; Fernandez E; Olason PI; Böttcher Y; Komiyama NH; Collins MO; Choudhary J; Stefansson K; Stefansson H; Grant SG; Purcell S; Sklar P; O'Donovan MC; Owen MJ
    Mol Psychiatry; 2012 Feb; 17(2):142-53. PubMed ID: 22083728
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.
    Nag A; Bochukova EG; Kremeyer B; Campbell DD; Muller H; Valencia-Duarte AV; Cardona J; Rivas IC; Mesa SC; Cuartas M; Garcia J; Bedoya G; Cornejo W; Herrera LD; Romero R; Fournier E; Reus VI; Lowe TL; Farooqi IS; ; Mathews CA; McGrath LM; Yu D; Cook E; Wang K; Scharf JM; Pauls DL; Freimer NB; Plagnol V; Ruiz-Linares A
    PLoS One; 2013; 8(3):e59061. PubMed ID: 23533600
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo CNVs in bipolar affective disorder and schizophrenia.
    Georgieva L; Rees E; Moran JL; Chambert KD; Milanova V; Craddock N; Purcell S; Sklar P; McCarroll S; Holmans P; O'Donovan MC; Owen MJ; Kirov G
    Hum Mol Genet; 2014 Dec; 23(24):6677-83. PubMed ID: 25055870
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A pilot study on commonality and specificity of copy number variants in schizophrenia and bipolar disorder.
    Chen J; Calhoun VD; Perrone-Bizzozero NI; Pearlson GD; Sui J; Du Y; Liu J
    Transl Psychiatry; 2016 May; 6(5):e824. PubMed ID: 27244233
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.
    Charney AW; Stahl EA; Green EK; Chen CY; Moran JL; Chambert K; Belliveau RA; Forty L; Gordon-Smith K; Lee PH; Bromet EJ; Buckley PF; Escamilla MA; Fanous AH; Fochtmann LJ; Lehrer DS; Malaspina D; Marder SR; Morley CP; Nicolini H; Perkins DO; Rakofsky JJ; Rapaport MH; Medeiros H; Sobell JL; Backlund L; Bergen SE; Juréus A; Schalling M; Lichtenstein P; Knowles JA; Burdick KE; Jones I; Jones LA; Hultman CM; Perlis R; Purcell SM; McCarroll SA; Pato CN; Pato MT; Di Florio A; Craddock N; Landén M; Smoller JW; Ruderfer DM; Sklar P
    Biol Psychiatry; 2019 Jul; 86(2):110-119. PubMed ID: 30686506
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
    Priebe L; Degenhardt FA; Herms S; Haenisch B; Mattheisen M; Nieratschker V; Weingarten M; Witt S; Breuer R; Paul T; Alblas M; Moebus S; Lathrop M; Leboyer M; Schreiber S; Grigoroiu-Serbanescu M; Maier W; Propping P; Rietschel M; Nöthen MM; Cichon S; Mühleisen TW
    Mol Psychiatry; 2012 Apr; 17(4):421-32. PubMed ID: 21358712
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1.
    Xu W; Cohen-Woods S; Chen Q; Noor A; Knight J; Hosang G; Parikh SV; De Luca V; Tozzi F; Muglia P; Forte J; McQuillin A; Hu P; Gurling HM; Kennedy JL; McGuffin P; Farmer A; Strauss J; Vincent JB
    BMC Med Genet; 2014 Jan; 15():2. PubMed ID: 24387768
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High frequencies of de novo CNVs in bipolar disorder and schizophrenia.
    Malhotra D; McCarthy S; Michaelson JJ; Vacic V; Burdick KE; Yoon S; Cichon S; Corvin A; Gary S; Gershon ES; Gill M; Karayiorgou M; Kelsoe JR; Krastoshevsky O; Krause V; Leibenluft E; Levy DL; Makarov V; Bhandari A; Malhotra AK; McMahon FJ; Nöthen MM; Potash JB; Rietschel M; Schulze TG; Sebat J
    Neuron; 2011 Dec; 72(6):951-63. PubMed ID: 22196331
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copy number variants in siblings of Mexican origin concordant for schizophrenia or bipolar disorder.
    Vega-Sevey JG; Martínez-Magaña JJ; Genis-Mendoza AD; Escamilla M; Lanzagorta N; Tovilla-Zarate CA; Nicolini H
    Psychiatry Res; 2020 Sep; 291():113018. PubMed ID: 32540681
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.
    Li Z; Chen J; Xu Y; Yi Q; Ji W; Wang P; Shen J; Song Z; Wang M; Yang P; Wang Q; Feng G; Liu B; Sun W; Xu Q; Li B; He L; He G; Li W; Wen Z; Liu K; Huang F; Zhou J; Ji J; Li X; Shi Y
    Biol Psychiatry; 2016 Aug; 80(4):331-337. PubMed ID: 26795442
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Copy number variation in bipolar disorder.
    Green EK; Rees E; Walters JT; Smith KG; Forty L; Grozeva D; Moran JL; Sklar P; Ripke S; Chambert KD; Genovese G; McCarroll SA; Jones I; Jones L; Owen MJ; O'Donovan MC; Craddock N; Kirov G
    Mol Psychiatry; 2016 Jan; 21(1):89-93. PubMed ID: 25560756
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder.
    Kember RL; Georgi B; Bailey-Wilson JE; Stambolian D; Paul SM; Bućan M
    BMC Genet; 2015 Mar; 16():27. PubMed ID: 25887117
    [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. 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]  

  • 19. [Autism spectrum disorder and genes for synaptic proteins].
    Shishido E
    Brain Nerve; 2012 Jan; 64(1):65-70. PubMed ID: 22223503
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disruption of the neurexin 1 gene is associated with schizophrenia.
    Rujescu D; Ingason A; Cichon S; Pietiläinen OP; Barnes MR; Toulopoulou T; Picchioni M; Vassos E; Ettinger U; Bramon E; Murray R; Ruggeri M; Tosato S; Bonetto C; Steinberg S; Sigurdsson E; Sigmundsson T; Petursson H; Gylfason A; Olason PI; Hardarsson G; Jonsdottir GA; Gustafsson O; Fossdal R; Giegling I; Möller HJ; Hartmann AM; Hoffmann P; Crombie C; Fraser G; Walker N; Lonnqvist J; Suvisaari J; Tuulio-Henriksson A; Djurovic S; Melle I; Andreassen OA; Hansen T; Werge T; Kiemeney LA; Franke B; Veltman J; Buizer-Voskamp JE; ; Sabatti C; Ophoff RA; Rietschel M; Nöthen MM; Stefansson K; Peltonen L; St Clair D; Stefansson H; Collier DA
    Hum Mol Genet; 2009 Mar; 18(5):988-96. PubMed ID: 18945720
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.