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Genomic Structural Equation Modeling Reveals Latent Phenotypes in the Human Cortex with Distinct Genetic Architecture.
Morey R, Zheng Y, Sun D, Garrett M, Gasperi M, Maihofer A, Baird CL, Grasby K, Huggins A, Haswell C, Thompson P, Medland S, Gustavson D, Panizzon M, Kremen W, Nievergelt C, Ashley-Koch A, Logue L. Morey R, et al. Among authors: medland s. Res Sq [Preprint]. 2023 Oct 3:rs.3.rs-3253035. doi: 10.21203/rs.3.rs-3253035/v1. Res Sq. 2023. PMID: 37886496 Free PMC article. Preprint.
ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide.
Thompson PM, Andreassen OA, Arias-Vasquez A, Bearden CE, Boedhoe PS, Brouwer RM, Buckner RL, Buitelaar JK, Bulayeva KB, Cannon DM, Cohen RA, Conrod PJ, Dale AM, Deary IJ, Dennis EL, de Reus MA, Desrivieres S, Dima D, Donohoe G, Fisher SE, Fouche JP, Francks C, Frangou S, Franke B, Ganjgahi H, Garavan H, Glahn DC, Grabe HJ, Guadalupe T, Gutman BA, Hashimoto R, Hibar DP, Holland D, Hoogman M, Hulshoff Pol HE, Hosten N, Jahanshad N, Kelly S, Kochunov P, Kremen WS, Lee PH, Mackey S, Martin NG, Mazoyer B, McDonald C, Medland SE, Morey RA, Nichols TE, Paus T, Pausova Z, Schmaal L, Schumann G, Shen L, Sisodiya SM, Smit DJA, Smoller JW, Stein DJ, Stein JL, Toro R, Turner JA, van den Heuvel MP, van den Heuvel OL, van Erp TGM, van Rooij D, Veltman DJ, Walter H, Wang Y, Wardlaw JM, Whelan CD, Wright MJ, Ye J; ENIGMA Consortium. Thompson PM, et al. Among authors: medland se. Neuroimage. 2017 Jan 15;145(Pt B):389-408. doi: 10.1016/j.neuroimage.2015.11.057. Epub 2015 Dec 4. Neuroimage. 2017. PMID: 26658930 Free PMC article. Review.
Estimating Heritability from Twin Studies.
Grasby KL, Verweij KJH, Mosing MA, Zietsch BP, Medland SE. Grasby KL, et al. Methods Mol Biol. 2017;1666:171-194. doi: 10.1007/978-1-4939-7274-6_9. Methods Mol Biol. 2017. PMID: 28980246
Heritability and GWAS Analyses of Acne in Australian Adolescent Twins.
Mina-Vargas A, Colodro-Conde L, Grasby K, Zhu G, Gordon S, Medland SE, Martin NG. Mina-Vargas A, et al. Among authors: medland se. Twin Res Hum Genet. 2017 Dec;20(6):541-549. doi: 10.1017/thg.2017.58. Epub 2017 Nov 7. Twin Res Hum Genet. 2017. PMID: 29110752
Significant concordance of genetic variation that increases both the risk for obsessive-compulsive disorder and the volumes of the nucleus accumbens and putamen.
Hibar DP, Cheung JW, Medland SE, Mufford MS, Jahanshad N, Dalvie S, Ramesar R, Stewart E, van den Heuvel OA, Pauls DL, Knowles JA, Stein DJ, Thompson PM; Enhancing Neuro Imaging Genetics through Meta Analysis (ENIGMA) Consortium and International Obsessive Compulsive Disorder Foundation Genetics Collaborative (IOCDF-GC). Hibar DP, et al. Among authors: medland se. Br J Psychiatry. 2018 Jul;213(1):430-436. doi: 10.1192/bjp.2018.62. Br J Psychiatry. 2018. PMID: 29947313 Free PMC article.
Genomic kinship construction to enhance genetic analyses in the human connectome project data.
Kochunov P, Donohue B, Mitchell BD, Ganjgahi H, Adhikari B, Ryan M, Medland SE, Jahanshad N, Thompson PM, Blangero J, Fieremans E, Novikov DS, Marcus D, Van Essen DC, Glahn DC, Elliot Hong L, Nichols TE. Kochunov P, et al. Among authors: medland se. Hum Brain Mapp. 2019 Apr 1;40(5):1677-1688. doi: 10.1002/hbm.24479. Epub 2018 Nov 29. Hum Brain Mapp. 2019. PMID: 30496643 Free PMC article.
472 results