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Page 1
Arguments for the sake of endophenotypes: examining common misconceptions about the use of endophenotypes in psychiatric genetics.
Glahn DC, Knowles EE, McKay DR, Sprooten E, Raventós H, Blangero J, Gottesman II, Almasy L. Glahn DC, et al. Among authors: sprooten e. Am J Med Genet B Neuropsychiatr Genet. 2014 Mar;165B(2):122-30. doi: 10.1002/ajmg.b.32221. Epub 2014 Jan 24. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24464604 Free PMC article. Review.
Shared genetic etiology between ADHD, task-related behavioral measures and brain activation during response inhibition in a youth ADHD case-control study.
Saraçaydın G, Ruisch IH, van Rooij D, Sprooten E, Franke B, Buitelaar JK, Dietrich A, Hoekstra PJ. Saraçaydın G, et al. Among authors: sprooten e. Eur Arch Psychiatry Clin Neurosci. 2024 Feb;274(1):45-58. doi: 10.1007/s00406-023-01632-8. Epub 2023 Jun 28. Eur Arch Psychiatry Clin Neurosci. 2024. PMID: 37378697 Free PMC article.
Genomic patterns linked to gray matter alterations underlying working memory deficits in adults and adolescents with attention-deficit/hyperactivity disorder.
Duan K, Chen J, Calhoun VD, Jiang W, Rootes-Murdy K, Schoenmacker G, Silva RF, Franke B, Buitelaar JK, Hoogman M, Oosterlaan J, Hoekstra PJ, Heslenfeld D, Hartman CA, Sprooten E, Arias-Vasquez A, Turner JA, Liu J. Duan K, et al. Among authors: sprooten e. Transl Psychiatry. 2023 Feb 11;13(1):50. doi: 10.1038/s41398-023-02349-x. Transl Psychiatry. 2023. PMID: 36774336 Free PMC article.
Identification of common variants associated with human hippocampal and intracranial volumes.
Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann Ø, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, Domin M, Grimm O, Hollinshead M, Holmes AJ, Homuth G, Hottenga JJ, Langan C, Lopez LM, Hansell NK, Hwang KS, Kim S, Laje G, Lee PH, Liu X, Loth E, Lourdusamy A, Mattingsdal M, Mohnke S, Maniega SM, Nho K, Nugent AC, O'Brien C, Papmeyer M, Pütz B, Ramasamy A, Rasmussen J, Rijpkema M, Risacher SL, Roddey JC, Rose EJ, Ryten M, Shen L, Sprooten E, Strengman E, Teumer A, Trabzuni D, Turner J, van Eijk K, van Erp TG, van Tol MJ, Wittfeld K, Wolf C, Woudstra S, Aleman A, Alhusaini S, Almasy L, Binder EB, Brohawn DG, Cantor RM, Carless MA, Corvin A, Czisch M, Curran JE, Davies G, de Almeida MA, Delanty N, Depondt C, Duggirala R, Dyer TD, Erk S, Fagerness J, Fox PT, Freimer NB, Gill M, Göring HH, Hagler DJ, Hoehn D, Holsboer F, Hoogman M, Hosten N, Jahanshad N, Johnson MP, Kasperaviciute D, Kent JW Jr, Kochunov P, Lancaster JL, Lawrie SM, Liewald DC, Mandl R, Matarin M, Mattheisen M, Meisenzahl E, Melle I, Moses EK, Mühleisen TW, Nauck M, Nöthen MM, Olvera RL, Pandolfo M, Pike GB, Puls R, Reinvang I, Rentería ME,… See abstract for full author list ➔ Stein JL, et al. Among authors: sprooten e. Nat Genet. 2012 Apr 15;44(5):552-61. doi: 10.1038/ng.2250. Nat Genet. 2012. PMID: 22504417 Free PMC article.
Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Bis JC, DeCarli C, Smith AV, van der Lijn F, Crivello F, Fornage M, Debette S, Shulman JM, Schmidt H, Srikanth V, Schuur M, Yu L, Choi SH, Sigurdsson S, Verhaaren BF, DeStefano AL, Lambert JC, Jack CR Jr, Struchalin M, Stankovich J, Ibrahim-Verbaas CA, Fleischman D, Zijdenbos A, den Heijer T, Mazoyer B, Coker LH, Enzinger C, Danoy P, Amin N, Arfanakis K, van Buchem MA, de Bruijn RF, Beiser A, Dufouil C, Huang J, Cavalieri M, Thomson R, Niessen WJ, Chibnik LB, Gislason GK, Hofman A, Pikula A, Amouyel P, Freeman KB, Phan TG, Oostra BA, Stein JL, Medland SE, Vasquez AA, Hibar DP, Wright MJ, Franke B, Martin NG, Thompson PM; Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium; Nalls MA, Uitterlinden AG, Au R, Elbaz A, Beare RJ, van Swieten JC, Lopez OL, Harris TB, Chouraki V, Breteler MM, De Jager PL, Becker JT, Vernooij MW, Knopman D, Fazekas F, Wolf PA, van der Lugt A, Gudnason V, Longstreth WT Jr, Brown MA, Bennett DA, van Duijn CM, Mosley TH, Schmidt R, Tzourio C, Launer LJ, Ikram MA, Seshadri S; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. Bis JC, et al. Nat Genet. 2012 Apr 15;44(5):545-51. doi: 10.1038/ng.2237. Nat Genet. 2012. PMID: 22504421 Free PMC article.
Polygenic risk and white matter integrity in individuals at high risk of mood disorder.
Whalley HC, Sprooten E, Hackett S, Hall L, Blackwood DH, Glahn DC, Bastin M, Hall J, Lawrie SM, Sussmann JE, McIntosh AM. Whalley HC, et al. Among authors: sprooten e. Biol Psychiatry. 2013 Aug 15;74(4):280-6. doi: 10.1016/j.biopsych.2013.01.027. Epub 2013 Feb 28. Biol Psychiatry. 2013. PMID: 23453289 Free PMC article.
Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA-DTI working group.
Jahanshad N, Kochunov PV, Sprooten E, Mandl RC, Nichols TE, Almasy L, Blangero J, Brouwer RM, Curran JE, de Zubicaray GI, Duggirala R, Fox PT, Hong LE, Landman BA, Martin NG, McMahon KL, Medland SE, Mitchell BD, Olvera RL, Peterson CP, Starr JM, Sussmann JE, Toga AW, Wardlaw JM, Wright MJ, Hulshoff Pol HE, Bastin ME, McIntosh AM, Deary IJ, Thompson PM, Glahn DC. Jahanshad N, et al. Among authors: sprooten e. Neuroimage. 2013 Nov 1;81:455-469. doi: 10.1016/j.neuroimage.2013.04.061. Epub 2013 Apr 28. Neuroimage. 2013. PMID: 23629049 Free PMC article.
Transcriptomics of cortical gray matter thickness decline during normal aging.
Kochunov P, Charlesworth J, Winkler A, Hong LE, Nichols TE, Curran JE, Sprooten E, Jahanshad N, Thompson PM, Johnson MP, Kent JW Jr, Landman BA, Mitchell B, Cole SA, Dyer TD, Moses EK, Goring HH, Almasy L, Duggirala R, Olvera RL, Glahn DC, Blangero J. Kochunov P, et al. Among authors: sprooten e. Neuroimage. 2013 Nov 15;82:273-83. doi: 10.1016/j.neuroimage.2013.05.066. Epub 2013 May 24. Neuroimage. 2013. PMID: 23707588 Free PMC article.
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