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 *

174 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. 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
    Seizure; 2024 Nov; 122():105-112. PubMed ID: 39388989
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.