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 *

134 related articles for article (PubMed ID: 35166138)

  • 1.
    Nuottamo ME; Häppölä P; Artto V; Hautakangas H; Pirinen M; Hiekkalinna T; Ellonen P; Lepistö M; Hämäläinen E; ; Siren A; Lehesjoki AE; Kallela M; Palotie A; Kaunisto MA; Wessman M
    Cephalalgia; 2022 Jun; 42(7):631-644. PubMed ID: 35166138
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3.
    Polvi A; Siren A; Kallela M; Rantala H; Artto V; Sobel EM; Palotie A; Lehesjoki AE; Wessman M
    Neurology; 2012 Jan; 78(3):202-9. PubMed ID: 22218271
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11.
    Oedegaard KJ; Greenwood TA; Lunde A; Fasmer OB; Akiskal HS; Kelsoe JR;
    J Affect Disord; 2010 Apr; 122(1-2):14-26. PubMed ID: 19819557
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity.
    Adewuyi EO; Sapkota Y; International Endogene Consortium Iec ; andMe Research Team ; International Headache Genetics Consortium Ihgc ; Auta A; Yoshihara K; Nyegaard M; Griffiths LR; Montgomery GW; Chasman DI; Nyholt DR
    Genes (Basel); 2020 Feb; 11(3):. PubMed ID: 32121467
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Family studies to find rare high risk variants in migraine.
    Hansen RD; Christensen AF; Olesen J
    J Headache Pain; 2017 Dec; 18(1):32. PubMed ID: 28255817
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Migraine genetics: Status and road forward.
    Harder AVE; Terwindt GM; Nyholt DR; van den Maagdenberg AMJM
    Cephalalgia; 2023 Feb; 43(2):3331024221145962. PubMed ID: 36759319
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants.
    Winsvold BS; Bettella F; Witoelar A; Anttila V; Gormley P; Kurth T; Terwindt GM; Freilinger TM; Frei O; Shadrin A; Wang Y; Dale AM; van den Maagdenberg AMJM; Chasman DI; Nyholt DR; Palotie A; Andreassen OA; Zwart JA;
    PLoS One; 2017; 12(9):e0185663. PubMed ID: 28957430
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.
    Costa C; Prontera P; Sarchielli P; Tonelli A; Bassi MT; Cupini LM; Caproni S; Siliquini S; Donti E; Calabresi P
    Cephalalgia; 2014 Jan; 34(1):68-72. PubMed ID: 23918834
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.
    Norberg A; Forsgren L; Holmberg D; Holmberg M
    Neurosci Lett; 2006 Mar; 396(2):137-42. PubMed ID: 16378686
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics of migraine: Delineation of contemporary understanding of the genetic underpinning of migraine.
    de Boer I; Harder AVE; Ferrari MD; van den Maagdenberg AMJM; Terwindt GM
    Handb Clin Neurol; 2023; 198():85-103. PubMed ID: 38043973
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence for a shared genetic susceptibility to migraine and epilepsy.
    Winawer MR; Connors R;
    Epilepsia; 2013 Feb; 54(2):288-95. PubMed ID: 23294289
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample.
    Esserlind AL; Christensen AF; Steinberg S; Grarup N; Pedersen O; Hansen T; Werge T; Hansen TF; Husemoen LL; Linneberg A; Budtz-Jorgensen E; Westergaard ML; Stefansson H; Olesen J
    Cephalalgia; 2016 Jun; 36(7):615-23. PubMed ID: 25667298
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A cross-tissue transcriptome-wide association study reveals novel susceptibility genes for migraine.
    Gui J; Yang X; Tan C; Wang L; Meng L; Han Z; Liu J; Jiang L
    J Headache Pain; 2024 Jun; 25(1):94. PubMed ID: 38840241
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility.
    Cox HC; Lea RA; Bellis C; Carless M; Dyer TD; Curran J; Charlesworth J; Macgregor S; Nyholt D; Chasman D; Ridker PM; Schürks M; Blangero J; Griffiths LR
    Neurogenetics; 2012 Aug; 13(3):261-6. PubMed ID: 22678113
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate.
    Cox HC; Lea RA; Bellis C; Carless M; Dyer T; Blangero J; Griffiths LR
    J Headache Pain; 2011 Dec; 12(6):603-8. PubMed ID: 22030984
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial analysis reveals rare risk variants for migraine in regulatory regions.
    Techlo TR; Rasmussen AH; Møller PL; Bøttcher M; Winther S; Davidsson OB; Olofsson IA; Chalmer MA; Kogelman LJA; Nyegaard M; Olesen J; Hansen TF
    Neurogenetics; 2020 Jul; 21(3):149-157. PubMed ID: 32076896
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetics of migraine aura: an update.
    de Boer I; Terwindt GM; van den Maagdenberg AMJM
    J Headache Pain; 2020 Jun; 21(1):64. PubMed ID: 32503413
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Future possibilities in migraine genetics.
    Rudkjobing LA; Esserlind AL; Olesen J
    J Headache Pain; 2012 Oct; 13(7):505-11. PubMed ID: 22955452
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic TPH2 variants and the susceptibility for migraine: association of a TPH2 haplotype with migraine without aura.
    Jung A; Huge A; Kuhlenbäumer G; Kempt S; Seehafer T; Evers S; Berger K; Marziniak M
    J Neural Transm (Vienna); 2010 Nov; 117(11):1253-60. PubMed ID: 20740293
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.