BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1136 related articles for article (PubMed ID: 35396580)

  • 1. Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
    Trubetskoy V; Pardiñas AF; Qi T; Panagiotaropoulou G; Awasthi S; Bigdeli TB; Bryois J; Chen CY; Dennison CA; Hall LS; Lam M; Watanabe K; Frei O; Ge T; Harwood JC; Koopmans F; Magnusson S; Richards AL; Sidorenko J; Wu Y; Zeng J; Grove J; Kim M; Li Z; Voloudakis G; Zhang W; Adams M; Agartz I; Atkinson EG; Agerbo E; Al Eissa M; Albus M; Alexander M; Alizadeh BZ; Alptekin K; Als TD; Amin F; Arolt V; Arrojo M; Athanasiu L; Azevedo MH; Bacanu SA; Bass NJ; Begemann M; Belliveau RA; Bene J; Benyamin B; Bergen SE; Blasi G; Bobes J; Bonassi S; Braun A; Bressan RA; Bromet EJ; Bruggeman R; Buckley PF; Buckner RL; Bybjerg-Grauholm J; Cahn W; Cairns MJ; Calkins ME; Carr VJ; Castle D; Catts SV; Chambert KD; Chan RCK; Chaumette B; Cheng W; Cheung EFC; Chong SA; Cohen D; Consoli A; Cordeiro Q; Costas J; Curtis C; Davidson M; Davis KL; de Haan L; Degenhardt F; DeLisi LE; Demontis D; Dickerson F; Dikeos D; Dinan T; Djurovic S; Duan J; Ducci G; Dudbridge F; Eriksson JG; Fañanás L; Faraone SV; Fiorentino A; Forstner A; Frank J; Freimer NB; Fromer M; Frustaci A; Gadelha A; Genovese G; Gershon ES; Giannitelli M; Giegling I; Giusti-Rodríguez P; Godard S; Goldstein JI; González Peñas J; González-Pinto A; Gopal S; Gratten J; Green MF; Greenwood TA; Guillin O; Gülöksüz S; Gur RE; Gur RC; Gutiérrez B; Hahn E; Hakonarson H; Haroutunian V; Hartmann AM; Harvey C; Hayward C; Henskens FA; Herms S; Hoffmann P; Howrigan DP; Ikeda M; Iyegbe C; Joa I; Julià A; Kähler AK; Kam-Thong T; Kamatani Y; Karachanak-Yankova S; Kebir O; Keller MC; Kelly BJ; Khrunin A; Kim SW; Klovins J; Kondratiev N; Konte B; Kraft J; Kubo M; Kučinskas V; Kučinskiene ZA; Kusumawardhani A; Kuzelova-Ptackova H; Landi S; Lazzeroni LC; Lee PH; Legge SE; Lehrer DS; Lencer R; Lerer B; Li M; Lieberman J; Light GA; Limborska S; Liu CM; Lönnqvist J; Loughland CM; Lubinski J; Luykx JJ; Lynham A; Macek M; Mackinnon A; Magnusson PKE; Maher BS; Maier W; Malaspina D; Mallet J; Marder SR; Marsal S; Martin AR; Martorell L; Mattheisen M; McCarley RW; McDonald C; McGrath JJ; Medeiros H; Meier S; Melegh B; Melle I; Mesholam-Gately RI; Metspalu A; Michie PT; Milani L; Milanova V; Mitjans M; Molden E; Molina E; Molto MD; Mondelli V; Moreno C; Morley CP; Muntané G; Murphy KC; Myin-Germeys I; Nenadić I; Nestadt G; Nikitina-Zake L; Noto C; Nuechterlein KH; O'Brien NL; O'Neill FA; Oh SY; Olincy A; Ota VK; Pantelis C; Papadimitriou GN; Parellada M; Paunio T; Pellegrino R; Periyasamy S; Perkins DO; Pfuhlmann B; Pietiläinen O; Pimm J; Porteous D; Powell J; Quattrone D; Quested D; Radant AD; Rampino A; Rapaport MH; Rautanen A; Reichenberg A; Roe C; Roffman JL; Roth J; Rothermundt M; Rutten BPF; Saker-Delye S; Salomaa V; Sanjuan J; Santoro ML; Savitz A; Schall U; Scott RJ; Seidman LJ; Sharp SI; Shi J; Siever LJ; Sigurdsson E; Sim K; Skarabis N; Slominsky P; So HC; Sobell JL; Söderman E; Stain HJ; Steen NE; Steixner-Kumar AA; Stögmann E; Stone WS; Straub RE; Streit F; Strengman E; Stroup TS; Subramaniam M; Sugar CA; Suvisaari J; Svrakic DM; Swerdlow NR; Szatkiewicz JP; Ta TMT; Takahashi A; Terao C; Thibaut F; Toncheva D; Tooney PA; Torretta S; Tosato S; Tura GB; Turetsky BI; Üçok A; Vaaler A; van Amelsvoort T; van Winkel R; Veijola J; Waddington J; Walter H; Waterreus A; Webb BT; Weiser M; Williams NM; Witt SH; Wormley BK; Wu JQ; Xu Z; Yolken R; Zai CC; Zhou W; Zhu F; Zimprich F; Atbaşoğlu EC; Ayub M; Benner C; Bertolino A; Black DW; Bray NJ; Breen G; Buccola NG; Byerley WF; Chen WJ; Cloninger CR; Crespo-Facorro B; Donohoe G; Freedman R; Galletly C; Gandal MJ; Gennarelli M; Hougaard DM; Hwu HG; Jablensky AV; McCarroll SA; Moran JL; Mors O; Mortensen PB; Müller-Myhsok B; Neil AL; Nordentoft M; Pato MT; Petryshen TL; Pirinen M; Pulver AE; Schulze TG; Silverman JM; Smoller JW; Stahl EA; Tsuang DW; Vilella E; Wang SH; Xu S; ; ; ; ; Adolfsson R; Arango C; Baune BT; Belangero SI; Børglum AD; Braff D; Bramon E; Buxbaum JD; Campion D; Cervilla JA; Cichon S; Collier DA; Corvin A; Curtis D; Forti MD; Domenici E; Ehrenreich H; Escott-Price V; Esko T; Fanous AH; Gareeva A; Gawlik M; Gejman PV; Gill M; Glatt SJ; Golimbet V; Hong KS; Hultman CM; Hyman SE; Iwata N; Jönsson EG; Kahn RS; Kennedy JL; Khusnutdinova E; Kirov G; Knowles JA; Krebs MO; Laurent-Levinson C; Lee J; Lencz T; Levinson DF; Li QS; Liu J; Malhotra AK; Malhotra D; McIntosh A; McQuillin A; Menezes PR; Morgan VA; Morris DW; Mowry BJ; Murray RM; Nimgaonkar V; Nöthen MM; Ophoff RA; Paciga SA; Palotie A; Pato CN; Qin S; Rietschel M; Riley BP; Rivera M; Rujescu D; Saka MC; Sanders AR; Schwab SG; Serretti A; Sham PC; Shi Y; St Clair D; Stefánsson H; Stefansson K; Tsuang MT; van Os J; Vawter MP; Weinberger DR; Werge T; Wildenauer DB; Yu X; Yue W; Holmans PA; Pocklington AJ; Roussos P; Vassos E; Verhage M; Visscher PM; Yang J; Posthuma D; Andreassen OA; Kendler KS; Owen MJ; Wray NR; Daly MJ; Huang H; Neale BM; Sullivan PF; Ripke S; Walters JTR; O'Donovan MC;
    Nature; 2022 Apr; 604(7906):502-508. PubMed ID: 35396580
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biological insights from 108 schizophrenia-associated genetic loci.
    Schizophrenia Working Group of the Psychiatric Genomics Consortium
    Nature; 2014 Jul; 511(7510):421-7. PubMed ID: 25056061
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel functional variants at the GWAS-implicated loci might confer risk to major depressive disorder, bipolar affective disorder and schizophrenia.
    Bryzgalov LO; Korbolina EE; Brusentsov II; Leberfarb EY; Bondar NP; Merkulova TI
    BMC Neurosci; 2018 Apr; 19(Suppl 1):22. PubMed ID: 29745862
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia.
    Hall LS; Medway CW; Pain O; Pardiñas AF; Rees EG; Escott-Price V; Pocklington A; Bray NJ; Holmans PA; Walters JTR; Owen MJ; O'Donovan MC
    Hum Mol Genet; 2020 Jan; 29(1):159-167. PubMed ID: 31691811
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ultra-rare and common genetic variant analysis converge to implicate negative selection and neuronal processes in the aetiology of schizophrenia.
    Akingbuwa WA; Hammerschlag AR; Bartels M; Nivard MG; Middeldorp CM
    Mol Psychiatry; 2022 Sep; 27(9):3699-3707. PubMed ID: 35665764
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The relationship between case-control differential gene expression from brain tissue and genetic associations in schizophrenia.
    Clifton NE; Schulmann A; ; Holmans PA; O'Donovan MC; Vawter MP
    Am J Med Genet B Neuropsychiatr Genet; 2023; 192(5-6):85-92. PubMed ID: 36652379
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
    Pardiñas AF; Holmans P; Pocklington AJ; Escott-Price V; Ripke S; Carrera N; Legge SE; Bishop S; Cameron D; Hamshere ML; Han J; Hubbard L; Lynham A; Mantripragada K; Rees E; MacCabe JH; McCarroll SA; Baune BT; Breen G; Byrne EM; Dannlowski U; Eley TC; Hayward C; Martin NG; McIntosh AM; Plomin R; Porteous DJ; Wray NR; Caballero A; Geschwind DH; Huckins LM; Ruderfer DM; Santiago E; Sklar P; Stahl EA; Won H; Agerbo E; Als TD; Andreassen OA; Bækvad-Hansen M; Mortensen PB; Pedersen CB; Børglum AD; Bybjerg-Grauholm J; Djurovic S; Durmishi N; Pedersen MG; Golimbet V; Grove J; Hougaard DM; Mattheisen M; Molden E; Mors O; Nordentoft M; Pejovic-Milovancevic M; Sigurdsson E; Silagadze T; Hansen CS; Stefansson K; Stefansson H; Steinberg S; Tosato S; Werge T; ; ; Collier DA; Rujescu D; Kirov G; Owen MJ; O'Donovan MC; Walters JTR
    Nat Genet; 2018 Mar; 50(3):381-389. PubMed ID: 29483656
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia.
    Hook PW; McCallion AS
    Genome Res; 2020 Apr; 30(4):528-539. PubMed ID: 32303558
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rare coding variants in ten genes confer substantial risk for schizophrenia.
    Singh T; Poterba T; Curtis D; Akil H; Al Eissa M; Barchas JD; Bass N; Bigdeli TB; Breen G; Bromet EJ; Buckley PF; Bunney WE; Bybjerg-Grauholm J; Byerley WF; Chapman SB; Chen WJ; Churchhouse C; Craddock N; Cusick CM; DeLisi L; Dodge S; Escamilla MA; Eskelinen S; Fanous AH; Faraone SV; Fiorentino A; Francioli L; Gabriel SB; Gage D; Gagliano Taliun SA; Ganna A; Genovese G; Glahn DC; Grove J; Hall MH; Hämäläinen E; Heyne HO; Holi M; Hougaard DM; Howrigan DP; Huang H; Hwu HG; Kahn RS; Kang HM; Karczewski KJ; Kirov G; Knowles JA; Lee FS; Lehrer DS; Lescai F; Malaspina D; Marder SR; McCarroll SA; McIntosh AM; Medeiros H; Milani L; Morley CP; Morris DW; Mortensen PB; Myers RM; Nordentoft M; O'Brien NL; Olivares AM; Ongur D; Ouwehand WH; Palmer DS; Paunio T; Quested D; Rapaport MH; Rees E; Rollins B; Satterstrom FK; Schatzberg A; Scolnick E; Scott LJ; Sharp SI; Sklar P; Smoller JW; Sobell JL; Solomonson M; Stahl EA; Stevens CR; Suvisaari J; Tiao G; Watson SJ; Watts NA; Blackwood DH; Børglum AD; Cohen BM; Corvin AP; Esko T; Freimer NB; Glatt SJ; Hultman CM; McQuillin A; Palotie A; Pato CN; Pato MT; Pulver AE; St Clair D; Tsuang MT; Vawter MP; Walters JT; Werge TM; Ophoff RA; Sullivan PF; Owen MJ; Boehnke M; O'Donovan MC; Neale BM; Daly MJ
    Nature; 2022 Apr; 604(7906):509-516. PubMed ID: 35396579
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
    Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
    Mol Autism; 2017; 8():21. PubMed ID: 28540026
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
    Brazel DM; Jiang Y; Hughey JM; Turcot V; Zhan X; Gong J; Batini C; Weissenkampen JD; Liu M; ; ; Barnes DR; Bertelsen S; Chou YL; Erzurumluoglu AM; Faul JD; Haessler J; Hammerschlag AR; Hsu C; Kapoor M; Lai D; Le N; de Leeuw CA; Loukola A; Mangino M; Melbourne CA; Pistis G; Qaiser B; Rohde R; Shao Y; Stringham H; Wetherill L; Zhao W; Agrawal A; Bierut L; Chen C; Eaton CB; Goate A; Haiman C; Heath A; Iacono WG; Martin NG; Polderman TJ; Reiner A; Rice J; Schlessinger D; Scholte HS; Smith JA; Tardif JC; Tindle HA; van der Leij AR; Boehnke M; Chang-Claude J; Cucca F; David SP; Foroud T; Howson JMM; Kardia SLR; Kooperberg C; Laakso M; Lettre G; Madden P; McGue M; North K; Posthuma D; Spector T; Stram D; Tobin MD; Weir DR; Kaprio J; Abecasis GR; Liu DJ; Vrieze S
    Biol Psychiatry; 2019 Jun; 85(11):946-955. PubMed ID: 30679032
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-wide identification of the shared genetic basis of cannabis and cigarette smoking and schizophrenia implicates NCAM1 and neuronal abnormality.
    Song W; Lin GN; Yu S; Zhao M
    Psychiatry Res; 2022 Apr; 310():114453. PubMed ID: 35235886
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comprehensive pathway analyses of schizophrenia risk loci point to dysfunctional postsynaptic signaling.
    Schijven D; Kofink D; Tragante V; Verkerke M; Pulit SL; Kahn RS; Veldink JH; Vinkers CH; Boks MP; Luykx JJ
    Schizophr Res; 2018 Sep; 199():195-202. PubMed ID: 29653892
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genomic findings in schizophrenia and their implications.
    Owen MJ; Legge SE; Rees E; Walters JTR; O'Donovan MC
    Mol Psychiatry; 2023 Sep; 28(9):3638-3647. PubMed ID: 37853064
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Schizophrenia Genomics: Convergence on Synaptic Development, Adult Synaptic Plasticity, or Both?
    Hall J; Bray NJ
    Biol Psychiatry; 2022 Apr; 91(8):709-717. PubMed ID: 34974922
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mendelian Randomization Study Using Dopaminergic Neuron-Specific eQTL Identifies Novel Risk Genes for Schizophrenia.
    Dang X; Liu J; Zhang Z; Luo XJ
    Mol Neurobiol; 2023 Mar; 60(3):1537-1546. PubMed ID: 36517655
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic architecture of schizophrenia: a review of major advancements.
    Legge SE; Santoro ML; Periyasamy S; Okewole A; Arsalan A; Kowalec K
    Psychol Med; 2021 Oct; 51(13):2168-2177. PubMed ID: 33550997
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A missense variant in NDUFA6 confers schizophrenia risk by affecting YY1 binding and NAGA expression.
    Li Y; Ma C; Li W; Yang Y; Li X; Liu J; Wang J; Li S; Liu Y; Li K; Li J; Huang D; Chen R; Lv L; Li M; Luo XJ
    Mol Psychiatry; 2021 Nov; 26(11):6896-6911. PubMed ID: 33931730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recent genomic advances in schizophrenia.
    Doherty JL; O'Donovan MC; Owen MJ
    Clin Genet; 2012 Feb; 81(2):103-9. PubMed ID: 21895634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 57.