BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 38585944)

  • 1. Unraveling the shared genetics of common epilepsies and general cognitive ability.
    Karadag N; Hagen E; Shadrin AA; van der Meer D; O'Connell KS; Rahman Z; Kutrolli G; Parker N; Bahrami S; Fominykh V; Heuser K; Taubøll E; Ueland T; Steen NE; Djurovic S; Dale AM; Frei O; Andreassen OA; Smeland OB
    medRxiv; 2024 Mar; ():. PubMed ID: 38585944
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dissecting the Shared Genetic Architecture of Common Epilepsies With Cortical Brain Morphology.
    Karadag N; Hagen E; Shadrin AA; van der Meer D; O'Connell KS; Rahman Z; Kutrolli G; Parker N; Bahrami S; Fominykh V; Heuser K; Taubøll E; Steen NE; Djurovic S; Dale AM; Frei O; Andreassen OA; Smeland OB
    Neurol Genet; 2024 Jun; 10(3):e200143. PubMed ID: 38817246
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of novel genomic risk loci shared between common epilepsies and psychiatric disorders.
    Karadag N; Shadrin AA; O'Connell KS; Hindley GFL; Rahman Z; Parker N; Bahrami S; Fominykh V; Cheng W; Holen B; Alvestad S; Taubøll E; Steen NE; Djurovic S; Dale AM; Frei O; Andreassen OA; Smeland OB
    Brain; 2023 Aug; 146(8):3392-3403. PubMed ID: 36757824
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
    Delgado-Escueta AV; Medina MT; Serratosa JM; Castroviejo IP; Gee MN; Weissbecker K; Westling BW; Fong CY; Alonso ME; Cordova S; Shah P; Khan S; Sainz J; Rubio-Donnadieu F; Sparkes RS
    Adv Neurol; 1999; 79():351-74. PubMed ID: 10514826
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cognitive Function in Genetic Generalized Epilepsies: Insights From Neuropsychology and Neuroimaging.
    Ratcliffe C; Wandschneider B; Baxendale S; Thompson P; Koepp MJ; Caciagli L
    Front Neurol; 2020; 11():144. PubMed ID: 32210904
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
    ; Leu C; de Kovel CG; Zara F; Striano P; Pezzella M; Robbiano A; Bianchi A; Bisulli F; Coppola A; Giallonardo AT; Beccaria F; Trenité DK; Lindhout D; Gaus V; Schmitz B; Janz D; Weber YG; Becker F; Lerche H; Kleefuss-Lie AA; Hallman K; Kunz WS; Elger CE; Muhle H; Stephani U; Møller RS; Hjalgrim H; Mullen S; Scheffer IE; Berkovic SF; Everett KV; Gardiner MR; Marini C; Guerrini R; Lehesjoki AE; Siren A; Nabbout R; Baulac S; Leguern E; Serratosa JM; Rosenow F; Feucht M; Unterberger I; Covanis A; Suls A; Weckhuysen S; Kaneva R; Caglayan H; Turkdogan D; Baykan B; Bebek N; Ozbek U; Hempelmann A; Schulz H; Rüschendorf F; Trucks H; Nürnberg P; Avanzini G; Koeleman BP; Sander T
    Epilepsia; 2012 Feb; 53(2):308-18. PubMed ID: 22242659
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Involvement of
    Dahawi M; Elmagzoub MS; A Ahmed E; Baldassari S; Achaz G; Elmugadam FA; Abdelgadir WA; Baulac S; Buratti J; Abdalla O; Gamil S; Alzubeir M; Abubaker R; Noé E; Elsayed L; Ahmed AE; Leguern E
    Front Neurol; 2021; 12():738272. PubMed ID: 34744978
    [No Abstract]   [Full Text] [Related]  

  • 8. Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genes.
    Landoulsi Z; Laatar F; Noé E; Mrabet S; Ben Djebara M; Achaz G; Nava C; Baulac S; Kacem I; Gargouri-Berrechid A; Gouider R; Leguern E
    Neurogenetics; 2018 Aug; 19(3):165-178. PubMed ID: 29948376
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians.
    Pathak S; Miller J; Morris EC; Stewart WCL; Greenberg DA
    Epilepsia; 2018 May; 59(5):1011-1019. PubMed ID: 29608786
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trait impulsivity correlates with active myoclonic seizures in genetic generalized epilepsy.
    Syvertsen M; Koht J; Selmer K; Enger U; Pal DK; Smith A
    Epilepsy Behav; 2020 Nov; 112():107260. PubMed ID: 32745958
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Social impairment and stigma in genetic generalized epilepsies.
    Gabriel D; Ventura M; Samões R; Freitas J; Lopes J; Ramalheira J; Martins da Silva A; Chaves J
    Epilepsy Behav; 2020 Mar; 104(Pt A):106886. PubMed ID: 31931462
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of common genetic variation in presumed monogenic epilepsies.
    Campbell C; Leu C; Feng YA; Wolking S; Moreau C; Ellis C; Ganesan S; Martins H; Oliver K; Boothman I; Benson K; Molloy A; Brody L; ; ; Michaud JL; Hamdan FF; Minassian BA; Lerche H; Scheffer IE; Sisodiya S; Girard S; Cosette P; Delanty N; Lal D; Cavalleri GL;
    EBioMedicine; 2022 Jul; 81():104098. PubMed ID: 35679801
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Shared genetics and causality underlying epilepsy and attention-deficit hyperactivity disorder.
    Wu Y; Li Y; Zhu J; Long J
    Psychiatry Res; 2022 Oct; 316():114794. PubMed ID: 35994864
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide analyses reveal shared genetic architecture and novel risk loci between opioid use disorder and general cognitive ability.
    Holen B; Kutrolli G; Shadrin AA; Icick R; Hindley G; Rødevand L; O'Connell KS; Frei O; Parker N; Tesfaye M; Deak JD; Jahołkowski P; Dale AM; Djurovic S; Andreassen OA; Smeland OB
    Drug Alcohol Depend; 2024 Mar; 256():111058. PubMed ID: 38244365
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations.
    Stevelink R; Luykx JJ; Lin BD; Leu C; Lal D; Smith AW; Schijven D; Carpay JA; Rademaker K; Rodrigues Baldez RA; Devinsky O; Braun KPJ; Jansen FE; Smit DJA; Koeleman BPC; ;
    Epilepsia; 2021 Jul; 62(7):1518-1527. PubMed ID: 34002374
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5-6.0 Hz polyspike waves.
    Wight JE; Nguyen VH; Medina MT; Patterson C; Durón RM; Molina Y; Lin YC; Martínez-Juárez IE; Ochoa A; Jara-Prado A; Tanaka M; Bai D; Aftab S; Bailey JN; Delgado-Escueta AV
    Mol Genet Genomic Med; 2016 Mar; 4(2):197-210. PubMed ID: 27066514
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap?
    Taylor I; Marini C; Johnson MR; Turner S; Berkovic SF; Scheffer IE
    Brain; 2004 Aug; 127(Pt 8):1878-86. PubMed ID: 15201194
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Shared genetic loci between depression and cardiometabolic traits.
    Torgersen K; Rahman Z; Bahrami S; Hindley GFL; Parker N; Frei O; Shadrin A; O'Connell KS; Tesli M; Smeland OB; Munkhaugen J; Djurovic S; Dammen T; Andreassen OA
    PLoS Genet; 2022 May; 18(5):e1010161. PubMed ID: 35560157
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.