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 *

504 related articles for article (PubMed ID: 27957625)

  • 1. A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.
    Bacchelli E; Cainazzo MM; Cameli C; Guerzoni S; Martinelli A; Zoli M; Maestrini E; Pini LA
    J Headache Pain; 2016 Dec; 17(1):114. PubMed ID: 27957625
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort.
    Ran C; Fourier C; Michalska JM; Steinberg A; Sjöstrand C; Waldenlind E; Belin AC
    J Headache Pain; 2017 Aug; 18(1):88. PubMed ID: 28831700
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A genome-wide scan and HCRTR2 candidate gene analysis in a European cluster headache cohort.
    Baumber L; Sjöstrand C; Leone M; Harty H; Bussone G; Hillert J; Trembath RC; Russell MB
    Neurology; 2006 Jun; 66(12):1888-93. PubMed ID: 16801656
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic association of HCRTR2, ADH4 and CLOCK genes with cluster headache: a Chinese population-based case-control study.
    Fan Z; Hou L; Wan D; Ao R; Zhao D; Yu S
    J Headache Pain; 2018 Jan; 19(1):1. PubMed ID: 29318394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome-Wide Association Study Identifies Risk Loci for Cluster Headache.
    O'Connor E; Fourier C; Ran C; Sivakumar P; Liesecke F; Southgate L; Harder AVE; Vijfhuizen LS; Yip J; Giffin N; Silver N; Ahmed F; Hostettler IC; Davies B; Cader MZ; Simpson BS; Sullivan R; Efthymiou S; Adebimpe J; Quinn O; Campbell C; Cavalleri GL; Vikelis M; Kelderman T; Paemeleire K; Kilbride E; Grangeon L; Lagrata S; Danno D; Trembath R; Wood NW; Kockum I; Winsvold BS; Steinberg A; Sjöstrand C; Waldenlind E; Vandrovcova J; Houlden H; Matharu M; Belin AC
    Ann Neurol; 2021 Aug; 90(2):193-202. PubMed ID: 34184781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cluster headache is associated with the G1246A polymorphism in the hypocretin receptor 2 gene.
    Schürks M; Kurth T; Geissler I; Tessmann G; Diener HC; Rosskopf D
    Neurology; 2006 Jun; 66(12):1917-9. PubMed ID: 16554494
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Implications for the migraine SNP rs1835740 in a Swedish cluster headache population.
    Ran C; Fourier C; Zinnegger M; Steinberg A; Sjöstrand C; Waldenlind E; Belin AC
    J Headache Pain; 2018 Nov; 19(1):100. PubMed ID: 30382894
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene polymorphism association studies in cluster headache: A field synopsis and systematic meta-analyses.
    Cargnin S; Sances G; Shin JI; Tassorelli C; Terrazzino S
    Headache; 2021 Jul; 61(7):1060-1076. PubMed ID: 34309832
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Genetics of cluster headache.
    Gibson KF; Santos AD; Lund N; Jensen R; Stylianou IM
    Cephalalgia; 2019 Sep; 39(10):1298-1312. PubMed ID: 30917683
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden.
    Fourier C; Ran C; Steinberg A; Sjöstrand C; Waldenlind E; Belin AC
    Headache; 2019 Mar; 59(3):410-417. PubMed ID: 30652302
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache.
    Harder AVE; Winsvold BS; Noordam R; Vijfhuizen LS; Børte S; Kogelman LJA; de Boer I; Tronvik E; Rosendaal FR; Willems van Dijk K; O'Connor E; Fourier C; Thomas LF; Kristoffersen ES; ; Fronczek R; Pozo-Rosich P; Jensen RH; Ferrari MD; Hansen TF; Zwart JA; Terwindt GM; van den Maagdenberg AMJM
    Ann Neurol; 2021 Aug; 90(2):203-216. PubMed ID: 34180076
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide-associated variants in migraine susceptibility: a replication study from North India.
    Ghosh J; Pradhan S; Mittal B
    Headache; 2013; 53(10):1583-94. PubMed ID: 24266335
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Test for association of common variants in GRM7 with alcohol consumption.
    Melroy-Greif WE; Vadasz C; Kamens HM; McQueen MB; Corley RP; Stallings MC; Hopfer CJ; Krauter KS; Brown SA; Hewitt JK; Ehringer MA
    Alcohol; 2016 Sep; 55():43-50. PubMed ID: 27788777
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Endometrial vezatin and its association with endometriosis risk.
    Holdsworth-Carson SJ; Fung JN; Luong HT; Sapkota Y; Bowdler LM; Wallace L; Teh WT; Powell JE; Girling JE; Healey M; Montgomery GW; Rogers PA
    Hum Reprod; 2016 May; 31(5):999-1013. PubMed ID: 27005890
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular analysis of cluster headache.
    Zarrilli F; Tomaiuolo R; Ceglia C; Lombardo B; Izzo B; Castaldo G; Pastore L; De Simone R
    Clin J Pain; 2015 Jan; 31(1):52-7. PubMed ID: 24469609
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cluster headache is associated with the alcohol dehydrogenase 4 (ADH4) gene.
    Rainero I; Rubino E; Gallone S; Fenoglio P; Negro E; De Martino P; Savi L; Pinessi L
    Headache; 2010 Jan; 50(1):92-8. PubMed ID: 19925625
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Family-based exome-wide assessment of maternal genetic effects on susceptibility to childhood B-cell acute lymphoblastic leukemia in hispanics.
    Archer NP; Perez-Andreu V; Scheurer ME; Rabin KR; Peckham-Gregory EC; Plon SE; Zabriskie RC; De Alarcon PA; Fernandez KS; Najera CR; Yang JJ; Antillon-Klussmann F; Lupo PJ
    Cancer; 2016 Dec; 122(23):3697-3704. PubMed ID: 27529658
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A genetic variant near GATA3 implicated in inherited susceptibility and etiology of benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS).
    Na R; Helfand BT; Chen H; Conran CA; Crawford SE; Hayward SW; Tammela TLJ; Hoffman-Bolton J; Zheng SL; Walsh PC; Schleutker J; Platz EA; Isaacs WB; Xu J
    Prostate; 2017 Aug; 77(11):1213-1220. PubMed ID: 28656603
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Circadian pathway genetic variation and cancer risk: evidence from genome-wide association studies.
    Mocellin S; Tropea S; Benna C; Rossi CR
    BMC Med; 2018 Feb; 16(1):20. PubMed ID: 29455641
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.