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Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B; 23andMe Research Team; Quantitative Trait Working Group of the GenLang Consortium; Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, Gruen JR, Olson RK, Willcutt EG, DeFries JC, Pennington BF, Smith SD, Wright MJ, Martin NG, Auton A, Bates TC, Fisher SE, Luciano M. Doust C, et al. Among authors: eising e. Nat Genet. 2023 Mar;55(3):520. doi: 10.1038/s41588-023-01336-8. Nat Genet. 2023. PMID: 36823321 Free PMC article. No abstract available.
Despite differential gene expression profiles pediatric MDS derived mesenchymal stromal cells display functionality in vitro.
Calkoen FG, Vervat C, van Pel M, de Haas V, Vijfhuizen LS, Eising E, Kroes WG, 't Hoen PA, van den Heuvel-Eibrink MM, Egeler RM, van Tol MJ, Ball LM. Calkoen FG, et al. Among authors: eising e. Stem Cell Res. 2015 Mar;14(2):198-210. doi: 10.1016/j.scr.2015.01.006. Epub 2015 Jan 28. Stem Cell Res. 2015. PMID: 25679997 Free article.
Involvement of astrocyte and oligodendrocyte gene sets in migraine.
Eising E, de Leeuw C, Min JL, Anttila V, Verheijen MH, Terwindt GM, Dichgans M, Freilinger T, Kubisch C; International Headache Genetics Consortium; Ferrari MD, Smit AB, de Vries B, Palotie A, van den Maagdenberg AM, Posthuma D. Eising E, et al. Cephalalgia. 2016 Jun;36(7):640-7. doi: 10.1177/0333102415618614. Epub 2015 Dec 7. Cephalalgia. 2016. PMID: 26646788
Pearls and pitfalls in genetic studies of migraine.
Eising E, de Vries B, Ferrari MD, Terwindt GM, van den Maagdenberg AM. Eising E, et al. Cephalalgia. 2013 Jun;33(8):614-25. doi: 10.1177/0333102413484988. Cephalalgia. 2013. PMID: 23671257 Review.
Epigenetic mechanisms in migraine: a promising avenue?
Eising E, A Datson N, van den Maagdenberg AM, Ferrari MD. Eising E, et al. BMC Med. 2013 Feb 4;11:26. doi: 10.1186/1741-7015-11-26. BMC Med. 2013. PMID: 23379668 Free PMC article. Review.
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH, Lehtimäki T, Sarin AP, Wedenoja J, Hinds DA, Buring JE, Schürks M, Ridker PM, Hrafnsdottir MG, Stefansson H, Ring SM, Hottenga JJ, Penninx BW, Färkkilä M, Artto V, Kaunisto M, Vepsäläinen S, Malik R, Heath AC, Madden PA, Martin NG, Montgomery GW, Kurki MI, Kals M, Mägi R, Pärn K, Hämäläinen E, Huang H, Byrnes AE, Franke L, Huang J, Stergiakouli E, Lee PH, Sandor C, Webber C, Cader Z, Muller-Myhsok B, Schreiber S, Meitinger T, Eriksson JG, Salomaa V, Heikkilä K, Loehrer E, Uitterlinden AG, Hofman A, van Duijn CM, Cherkas L, Pedersen LM, Stubhaug A, Nielsen CS, Männikkö M, Mihailov E, Milani L, Göbel H, Esserlind AL, Christensen AF, Hansen TF, Werge T; International Headache Genetics Consortium; Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Järvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, Eriksson… See abstract for full author list ➔ Gormley P, et al. Nat Genet. 2016 Aug;48(8):856-66. doi: 10.1038/ng.3598. Epub 2016 Jun 20. Nat Genet. 2016. PMID: 27322543 Free PMC article.
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Eising E, Carrion-Castillo A, Vino A, Strand EA, Jakielski KJ, Scerri TS, Hildebrand MS, Webster R, Ma A, Mazoyer B, Francks C, Bahlo M, Scheffer IE, Morgan AT, Shriberg LD, Fisher SE. Eising E, et al. Mol Psychiatry. 2019 Jul;24(7):1065-1078. doi: 10.1038/s41380-018-0020-x. Epub 2018 Feb 20. Mol Psychiatry. 2019. PMID: 29463886 Free PMC article.
88 results