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 *

197 related articles for article (PubMed ID: 37872557)

  • 1. Genome-wide analyses identify NEAT1 as genetic modifier of age at onset of amyotrophic lateral sclerosis.
    Li C; Wei Q; Hou Y; Lin J; Ou R; Zhang L; Jiang Q; Xiao Y; Liu K; Chen X; Yang T; Song W; Zhao B; Wu Y; Shang H
    Mol Neurodegener; 2023 Oct; 18(1):77. PubMed ID: 37872557
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic Modifiers of Age at Onset for Amyotrophic Lateral Sclerosis: A Genome-Wide Association Study.
    Li C; Lin J; Jiang Q; Yang T; Xiao Y; Huang J; Hou Y; Wei Q; Cui Y; Wang S; Zheng X; Ou R; Liu K; Chen X; Song W; Zhao B; Shang H
    Ann Neurol; 2023 Nov; 94(5):933-941. PubMed ID: 37528491
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study.
    Li C; Ou R; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Hou Y; Liu K; Chen X; Song W; Zhao B; Wu Y; Li T; Dong X; Shang H
    Mov Disord; 2021 Sep; 36(9):2077-2084. PubMed ID: 33884653
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An association study between SCFD1 rs10139154 variant and amyotrophic lateral sclerosis in a Chinese cohort.
    Chen Y; Zhou Q; Gu X; Wei Q; Cao B; Liu H; Hou Y; Shang H
    Amyotroph Lateral Scler Frontotemporal Degener; 2018 Aug; 19(5-6):413-418. PubMed ID: 29260601
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Genome-wide Expression Association Analysis Identifies Genes and Pathways Associated with Amyotrophic Lateral Sclerosis.
    Du Y; Wen Y; Guo X; Hao J; Wang W; He A; Fan Q; Li P; Liu L; Liang X; Zhang F
    Cell Mol Neurobiol; 2018 Apr; 38(3):635-639. PubMed ID: 28639078
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lack of an association between SCFD1 rs10139154 polymorphism and amyotrophic lateral sclerosis.
    Siokas V; Aloizou AM; Liampas I; Bakirtzis C; Nasios G; Paterakis K; Sgantzos M; Bogdanos DP; Spandidos DA; Tsatsakis A; Mitsias PD; Dardiotis E
    Mol Med Rep; 2022 Apr; 25(4):. PubMed ID: 35234271
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identifying novel genes for amyotrophic lateral sclerosis by integrating human brain proteomes with genome-wide association data.
    Gu XJ; Su WM; Dou M; Jiang Z; Duan QQ; Wang H; Ren YL; Cao B; Wang Y; Chen YP
    J Neurol; 2023 Aug; 270(8):4013-4023. PubMed ID: 37148340
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis.
    McLaughlin RL; Kenna KP; Vajda A; Bede P; Elamin M; Cronin S; Donaghy CG; Bradley DG; Hardiman O
    Neurobiol Aging; 2015 Feb; 36(2):1221.e7-13. PubMed ID: 25442119
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1.
    Restuadi R; Steyn FJ; Kabashi E; Ngo ST; Cheng FF; Nabais MF; Thompson MJ; Qi T; Wu Y; Henders AK; Wallace L; Bye CR; Turner BJ; Ziser L; Mathers S; McCombe PA; Needham M; Schultz D; Kiernan MC; van Rheenen W; van den Berg LH; Veldink JH; Ophoff R; Gusev A; Zaitlen N; McRae AF; Henderson RD; Wray NR; Giacomotto J; Garton FC
    Genome Med; 2022 Jan; 14(1):7. PubMed ID: 35042540
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
    Fogh I; Lin K; Tiloca C; Rooney J; Gellera C; Diekstra FP; Ratti A; Shatunov A; van Es MA; Proitsi P; Jones A; Sproviero W; Chiò A; McLaughlin RL; Sorarù G; Corrado L; Stahl D; Del Bo R; Cereda C; Castellotti B; Glass JD; Newhouse S; Dobson R; Smith BN; Topp S; van Rheenen W; Meininger V; Melki J; Morrison KE; Shaw PJ; Leigh PN; Andersen PM; Comi GP; Ticozzi N; Mazzini L; D'Alfonso S; Traynor BJ; Van Damme P; Robberecht W; Brown RH; Landers JE; Hardiman O; Lewis CM; van den Berg LH; Shaw CE; Veldink JH; Silani V; Al-Chalabi A; Powell J
    JAMA Neurol; 2016 Jul; 73(7):812-20. PubMed ID: 27244217
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide association analysis reveals potential genetic correlation and causality between circulating inflammatory proteins and amyotrophic lateral sclerosis.
    Shen J; Gu X; Xiao C; Yan H; Feng Y; Li X
    Aging (Albany NY); 2024 May; 16(11):9470-9484. PubMed ID: 38819224
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Bidirectional Mendelian randomization to explore the causal relationships between Sleep traits, Parkinson's disease and Amyotrophic lateral sclerosis.
    Di H; Zhu Y; Xia W; Meng X; Zhang M; Xu M; Feng J; Tian Q; He Y; Cao S; Lu Z
    Sleep Med; 2022 Aug; 96():42-49. PubMed ID: 35594779
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide analysis of the heritability of amyotrophic lateral sclerosis.
    Keller MF; Ferrucci L; Singleton AB; Tienari PJ; Laaksovirta H; Restagno G; Chiò A; Traynor BJ; Nalls MA
    JAMA Neurol; 2014 Sep; 71(9):1123-34. PubMed ID: 25023141
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
    Ahmeti KB; Ajroud-Driss S; Al-Chalabi A; Andersen PM; Armstrong J; Birve A; Blauw HM; Brown RH; Bruijn L; Chen W; Chio A; Comeau MC; Cronin S; Diekstra FP; Soraya Gkazi A; Glass JD; Grab JD; Groen EJ; Haines JL; Hardiman O; Heller S; Huang J; Hung WY; ; Jaworski JM; Jones A; Khan H; Landers JE; Langefeld CD; Leigh PN; Marion MC; McLaughlin RL; Meininger V; Melki J; Miller JW; Mora G; Pericak-Vance MA; Rampersaud E; Robberecht W; Russell LP; Salachas F; Saris CG; Shatunov A; Shaw CE; Siddique N; Siddique T; Smith BN; Sufit R; Topp S; Traynor BJ; Vance C; van Damme P; van den Berg LH; van Es MA; van Vught PW; Veldink JH; Yang Y; Zheng JG;
    Neurobiol Aging; 2013 Jan; 34(1):357.e7-19. PubMed ID: 22959728
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis.
    Bandres-Ciga S; Noyce AJ; Hemani G; Nicolas A; Calvo A; Mora G; ; ; Tienari PJ; Stone DJ; Nalls MA; Singleton AB; Chiò A; Traynor BJ
    Ann Neurol; 2019 Apr; 85(4):470-481. PubMed ID: 30723964
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium.
    Grover S; Kumar Sreelatha AA; Pihlstrom L; Domenighetti C; Schulte C; Sugier PE; Radivojkov-Blagojevic M; Lichtner P; Mohamed O; Portugal B; Landoulsi Z; May P; Bobbili D; Edsall C; Bartusch F; Hanussek M; Krüger J; Hernandez DG; Blauwendraat C; Mellick GD; Zimprich A; Pirker W; Tan M; Rogaeva E; Lang A; Koks S; Taba P; Lesage S; Brice A; Corvol JC; Chartier-Harlin MC; Mutez E; Brockmann K; Deutschländer AB; Hadjigeorgiou GM; Dardiotis E; Stefanis L; Simitsi AM; Valente EM; Petrucci S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G; Quattrone A; Gagliardi M; Burbulla LF; Matsuo H; Kawamura Y; Hattori N; Nishioka K; Chung SJ; Kim YJ; Pavelka L; van de Warrenburg BPC; Bloem BR; Singleton AB; Aasly J; Toft M; Guedes LC; Ferreira JJ; Bardien S; Carr J; Tolosa E; Ezquerra M; Pastor P; Diez-Fairen M; Wirdefeldt K; Pedersen NL; Ran C; Belin AC; Puschmann A; Hellberg C; Clarke CE; Morrison KE; Krainc D; Farrer MJ; Kruger R; Elbaz A; Gasser T; Sharma M;
    Neurology; 2022 Aug; 99(7):e698-e710. PubMed ID: 35970579
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
    Laaksovirta H; Peuralinna T; Schymick JC; Scholz SW; Lai SL; Myllykangas L; Sulkava R; Jansson L; Hernandez DG; Gibbs JR; Nalls MA; Heckerman D; Tienari PJ; Traynor BJ
    Lancet Neurol; 2010 Oct; 9(10):978-85. PubMed ID: 20801718
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Causal association of type 2 diabetes with amyotrophic lateral sclerosis: new evidence from Mendelian randomization using GWAS summary statistics.
    Zeng P; Wang T; Zheng J; Zhou X
    BMC Med; 2019 Dec; 17(1):225. PubMed ID: 31796040
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Associations of the circulating levels of cytokines with risk of amyotrophic lateral sclerosis: a Mendelian randomization study.
    Liu B; Lyu L; Zhou W; Song J; Ye D; Mao Y; Chen GB; Sun X
    BMC Med; 2023 Feb; 21(1):39. PubMed ID: 36737740
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
    van Rheenen W; van der Spek RAA; Bakker MK; van Vugt JJFA; Hop PJ; Zwamborn RAJ; de Klein N; Westra HJ; Bakker OB; Deelen P; Shireby G; Hannon E; Moisse M; Baird D; Restuadi R; Dolzhenko E; Dekker AM; Gawor K; Westeneng HJ; Tazelaar GHP; van Eijk KR; Kooyman M; Byrne RP; Doherty M; Heverin M; Al Khleifat A; Iacoangeli A; Shatunov A; Ticozzi N; Cooper-Knock J; Smith BN; Gromicho M; Chandran S; Pal S; Morrison KE; Shaw PJ; Hardy J; Orrell RW; Sendtner M; Meyer T; Başak N; van der Kooi AJ; Ratti A; Fogh I; Gellera C; Lauria G; Corti S; Cereda C; Sproviero D; D'Alfonso S; Sorarù G; Siciliano G; Filosto M; Padovani A; Chiò A; Calvo A; Moglia C; Brunetti M; Canosa A; Grassano M; Beghi E; Pupillo E; Logroscino G; Nefussy B; Osmanovic A; Nordin A; Lerner Y; Zabari M; Gotkine M; Baloh RH; Bell S; Vourc'h P; Corcia P; Couratier P; Millecamps S; Meininger V; Salachas F; Mora Pardina JS; Assialioui A; Rojas-García R; Dion PA; Ross JP; Ludolph AC; Weishaupt JH; Brenner D; Freischmidt A; Bensimon G; Brice A; Durr A; Payan CAM; Saker-Delye S; Wood NW; Topp S; Rademakers R; Tittmann L; Lieb W; Franke A; Ripke S; Braun A; Kraft J; Whiteman DC; Olsen CM; Uitterlinden AG; Hofman A; Rietschel M; Cichon S; Nöthen MM; Amouyel P; ; ; ; ; Traynor BJ; Singleton AB; Mitne Neto M; Cauchi RJ; Ophoff RA; Wiedau-Pazos M; Lomen-Hoerth C; van Deerlin VM; Grosskreutz J; Roediger A; Gaur N; Jörk A; Barthel T; Theele E; Ilse B; Stubendorff B; Witte OW; Steinbach R; Hübner CA; Graff C; Brylev L; Fominykh V; Demeshonok V; Ataulina A; Rogelj B; Koritnik B; Zidar J; Ravnik-Glavač M; Glavač D; Stević Z; Drory V; Povedano M; Blair IP; Kiernan MC; Benyamin B; Henderson RD; Furlong S; Mathers S; McCombe PA; Needham M; Ngo ST; Nicholson GA; Pamphlett R; Rowe DB; Steyn FJ; Williams KL; Mather KA; Sachdev PS; Henders AK; Wallace L; de Carvalho M; Pinto S; Petri S; Weber M; Rouleau GA; Silani V; Curtis CJ; Breen G; Glass JD; Brown RH; Landers JE; Shaw CE; Andersen PM; Groen EJN; van Es MA; Pasterkamp RJ; Fan D; Garton FC; McRae AF; Davey Smith G; Gaunt TR; Eberle MA; Mill J; McLaughlin RL; Hardiman O; Kenna KP; Wray NR; Tsai E; Runz H; Franke L; Al-Chalabi A; Van Damme P; van den Berg LH; Veldink JH
    Nat Genet; 2021 Dec; 53(12):1636-1648. PubMed ID: 34873335
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.