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 *

332 related articles for article (PubMed ID: 25087078)

  • 1. Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
    International League Against Epilepsy Consortium on Complex Epilepsies. Electronic address: epilepsy-austin@unimelb.edu.au
    Lancet Neurol; 2014 Sep; 13(9):893-903. PubMed ID: 25087078
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
    ; ; Steffens M; Leu C; Ruppert AK; Zara F; Striano P; Robbiano A; Capovilla G; Tinuper P; Gambardella A; Bianchi A; La Neve A; Crichiutti G; de Kovel CG; Kasteleijn-Nolst Trenité D; de Haan GJ; Lindhout D; Gaus V; Schmitz B; Janz D; Weber YG; Becker F; Lerche H; Steinhoff BJ; Kleefuß-Lie AA; Kunz WS; Surges R; Elger CE; Muhle H; von Spiczak S; Ostertag P; Helbig I; Stephani U; Møller RS; Hjalgrim H; Dibbens LM; Bellows S; Oliver K; Mullen S; Scheffer IE; Berkovic SF; Everett KV; Gardiner MR; Marini C; Guerrini R; Lehesjoki AE; Siren A; Guipponi M; Malafosse A; Thomas P; Nabbout R; Baulac S; Leguern E; Guerrero R; Serratosa JM; Reif PS; Rosenow F; Mörzinger M; Feucht M; Zimprich F; Kapser C; Schankin CJ; Suls A; Smets K; De Jonghe P; Jordanova A; Caglayan H; Yapici Z; Yalcin DA; Baykan B; Bebek N; Ozbek U; Gieger C; Wichmann HE; Balschun T; Ellinghaus D; Franke A; Meesters C; Becker T; Wienker TF; Hempelmann A; Schulz H; Rüschendorf F; Leber M; Pauck SM; Trucks H; Toliat MR; Nürnberg P; Avanzini G; Koeleman BP; Sander T
    Hum Mol Genet; 2012 Dec; 21(24):5359-72. PubMed ID: 22949513
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.
    ;
    Lancet Neurol; 2017 Feb; 16(2):135-143. PubMed ID: 28102150
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
    Niestroj LM; Perez-Palma E; Howrigan DP; Zhou Y; Cheng F; Saarentaus E; Nürnberg P; Stevelink R; Daly MJ; Palotie A; Lal D;
    Brain; 2020 Jul; 143(7):2106-2118. PubMed ID: 32568404
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Benchmarking of univariate pleiotropy detection methods applied to epilepsy.
    Adesoji OM; Schulz H; May P; Krause R; Lerche H; Nothnagel M;
    Hum Mutat; 2022 Sep; 43(9):1314-1332. PubMed ID: 35620985
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.
    Pérez-Palma E; Helbig I; Klein KM; Anttila V; Horn H; Reinthaler EM; Gormley P; Ganna A; Byrnes A; Pernhorst K; Toliat MR; Saarentaus E; Howrigan DP; Hoffman P; Miquel JF; De Ferrari GV; Nürnberg P; Lerche H; Zimprich F; Neubauer BA; Becker AJ; Rosenow F; Perucca E; Zara F; Weber YG; Lal D
    J Med Genet; 2017 Sep; 54(9):598-606. PubMed ID: 28756411
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
    Cho MH; McDonald ML; Zhou X; Mattheisen M; Castaldi PJ; Hersh CP; Demeo DL; Sylvia JS; Ziniti J; Laird NM; Lange C; Litonjua AA; Sparrow D; Casaburi R; Barr RG; Regan EA; Make BJ; Hokanson JE; Lutz S; Dudenkov TM; Farzadegan H; Hetmanski JB; Tal-Singer R; Lomas DA; Bakke P; Gulsvik A; Crapo JD; Silverman EK; Beaty TH;
    Lancet Respir Med; 2014 Mar; 2(3):214-25. PubMed ID: 24621683
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Describing the genetic architecture of epilepsy through heritability analysis.
    Speed D; O'Brien TJ; Palotie A; Shkura K; Marson AG; Balding DJ; Johnson MR
    Brain; 2014 Oct; 137(Pt 10):2680-9. PubMed ID: 25063994
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery.
    Oliver KL; Ellis CA; Scheffer IE; Ganesan S; Leu C; Sadleir LG; Heinzen EL; Mefford HC; Bass AJ; Curtis SW; Harris RV; ; Whiteman DC; Helbig I; Ottman R; Epstein MP; Bahlo M; Berkovic SF
    EBioMedicine; 2022 Jul; 81():104079. PubMed ID: 35636315
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
    International League Against Epilepsy Consortium on Complex Epilepsies
    Nat Commun; 2018 Dec; 9(1):5269. PubMed ID: 30531953
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Topiramate versus carbamazepine monotherapy for epilepsy: an individual participant data review.
    Nevitt SJ; Sudell M; Tudur Smith C; Marson AG
    Cochrane Database Syst Rev; 2019 Jun; 6(6):CD012065. PubMed ID: 31233229
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.
    Speed D; Hoggart C; Petrovski S; Tachmazidou I; Coffey A; Jorgensen A; Eleftherohorinou H; De Iorio M; Todaro M; De T; Smith D; Smith PE; Jackson M; Cooper P; Kellett M; Howell S; Newton M; Yerra R; Tan M; French C; Reuber M; Sills GE; Chadwick D; Pirmohamed M; Bentley D; Scheffer I; Berkovic S; Balding D; Palotie A; Marson A; O'Brien TJ; Johnson MR
    Hum Mol Genet; 2014 Jan; 23(1):247-58. PubMed ID: 23962720
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Replication and meta-analysis of previous genome-wide association studies confirm vezatin as the locus with the strongest evidence for association with endometriosis.
    Pagliardini L; Gentilini D; Sanchez AM; Candiani M; Viganò P; Di Blasio AM
    Hum Reprod; 2015 Apr; 30(4):987-93. PubMed ID: 25678572
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Common genetic variation and risk of gallbladder cancer in India: a case-control genome-wide association study.
    Mhatre S; Wang Z; Nagrani R; Badwe R; Chiplunkar S; Mittal B; Yadav S; Zhang H; Chung CC; Patil P; Chanock S; Dikshit R; Chatterjee N; Rajaraman P
    Lancet Oncol; 2017 Apr; 18(4):535-544. PubMed ID: 28274756
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unraveling the genetics of common epilepsies: approaches, platforms, and caveats.
    Petrovski S; Kwan P
    Epilepsy Behav; 2013 Mar; 26(3):229-33. PubMed ID: 23103323
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers.
    Stein MB; Chen CY; Ursano RJ; Cai T; Gelernter J; Heeringa SG; Jain S; Jensen KP; Maihofer AX; Mitchell C; Nievergelt CM; Nock MK; Neale BM; Polimanti R; Ripke S; Sun X; Thomas ML; Wang Q; Ware EB; Borja S; Kessler RC; Smoller JW;
    JAMA Psychiatry; 2016 Jul; 73(7):695-704. PubMed ID: 27167565
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance.
    Ramos YF; Metrustry S; Arden N; Bay-Jensen AC; Beekman M; de Craen AJ; Cupples LA; Esko T; Evangelou E; Felson DT; Hart DJ; Ioannidis JP; Karsdal M; Kloppenburg M; Lafeber F; Metspalu A; Panoutsopoulou K; Slagboom PE; Spector TD; van Spil EW; Uitterlinden AG; Zhu Y; ; ; Valdes AM; van Meurs JB; Meulenbelt I
    J Med Genet; 2014 Sep; 51(9):596-604. PubMed ID: 25057126
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Meta-analysis of genome-wide association studies.
    de Bakker PI; Neale BM; Daly MJ
    Cold Spring Harb Protoc; 2010 Jun; 2010(6):pdb.top81. PubMed ID: 20516189
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.
    ; de Moor MH; van den Berg SM; Verweij KJ; Krueger RF; Luciano M; Arias Vasquez A; Matteson LK; Derringer J; Esko T; Amin N; Gordon SD; Hansell NK; Hart AB; Seppälä I; Huffman JE; Konte B; Lahti J; Lee M; Miller M; Nutile T; Tanaka T; Teumer A; Viktorin A; Wedenoja J; Abecasis GR; Adkins DE; Agrawal A; Allik J; Appel K; Bigdeli TB; Busonero F; Campbell H; Costa PT; Davey Smith G; Davies G; de Wit H; Ding J; Engelhardt BE; Eriksson JG; Fedko IO; Ferrucci L; Franke B; Giegling I; Grucza R; Hartmann AM; Heath AC; Heinonen K; Henders AK; Homuth G; Hottenga JJ; Iacono WG; Janzing J; Jokela M; Karlsson R; Kemp JP; Kirkpatrick MG; Latvala A; Lehtimäki T; Liewald DC; Madden PA; Magri C; Magnusson PK; Marten J; Maschio A; Medland SE; Mihailov E; Milaneschi Y; Montgomery GW; Nauck M; Ouwens KG; Palotie A; Pettersson E; Polasek O; Qian Y; Pulkki-Råback L; Raitakari OT; Realo A; Rose RJ; Ruggiero D; Schmidt CO; Slutske WS; Sorice R; Starr JM; St Pourcain B; Sutin AR; Timpson NJ; Trochet H; Vermeulen S; Vuoksimaa E; Widen E; Wouda J; Wright MJ; Zgaga L; Porteous D; Minelli A; Palmer AA; Rujescu D; Ciullo M; Hayward C; Rudan I; Metspalu A; Kaprio J; Deary IJ; Räikkönen K; Wilson JF; Keltikangas-Järvinen L; Bierut LJ; Hettema JM; Grabe HJ; van Duijn CM; Evans DM; Schlessinger D; Pedersen NL; Terracciano A; McGue M; Penninx BW; Martin NG; Boomsma DI
    JAMA Psychiatry; 2015 Jul; 72(7):642-50. PubMed ID: 25993607
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.