recent publications
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academic article
- Chen, C. H., Schork, A. J., Lo, M. T., Fan, C. C., Wang, Y., Desikan, R. S., Bettella, F., Hagler, D. J., Pediatric Imaging, Neurocognition, Alzheimer's Disease Neuroimaging Initiative, Westlye, L. T., Kremen, W. S. Large-scale genomics unveil polygenic architecture of human cortical surface area Nature Communications 2015 6:7549 DOI:10.1038/ncomms8549 PMID:26189703 PMCID:PMC4518289
- Akshoomoff, N., Newman, E., Thompson, W. K., McCabe, C., Bloss, C. S., Chang, L., Amaral, D. G., Casey, B. J., Ernst, T. M., Frazier, J. A., Gruen, J. R., Kaufmann, W. E., et al. The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING) Neuropsychology 2014 28:1-10 DOI:10.1037/neu0000001 PMID:24219608 PMCID:PMC3925365
- Eicher, J. D., Powers, N. R., Miller, L. L., Akshoomoff, N., Amaral, D. G., Bloss, C. S., Libiger, O., Schork, N. J., Darst, B. F., Casey, B. J., Chang, L., Ernst, T., et al. Genome-wide association study of shared components of reading disability and language impairment Genes Brain and Behavior 2013 12:792-801 DOI:10.1111/gbb.12085 PMID:24024963 PMCID:PMC3904347
- Schork, A. J., Thompson, W. K., Pham, P., Torkamani, A., Roddey, J. C., Sullivan, P. F., Kelsoe, J. R., O'Donovan, M. C., Furberg, H., The Tobacco & Genetics Consortium, The Bipolar Disorder Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics Consortium, et al. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs PLoS Genetics 2013 9:e1003449 DOI:10.1371/journal.pgen.1003449 PMID:23637621 PMCID:PMC3636284
- Walhovd, K. B., Fjell, A. M., Brown, T. T., Kuperman, J. M., Chung, Y. H., Hagler, D. J., Roddey, J. C., Erhart, M., McCabe, C., Akshoomoff, N., Amaral, D. G., Bloss, C. S., et al. Long-term influence of normal variation in neonatal characteristics on human brain development Proceedings of the National Academy of Sciences of the United States of America 2012 109:20089-20094 DOI:10.1073/pnas.1208180109 PMID:23169628 PMCID:PMC3523836
- Fjell, A. M., Walhovd, K. B., Brown, T. T., Kuperman, J. M., Chung, Y., Hagler, D. J., Venkatraman, V., Roddey, J. C., Erhart, M., McCabe, C., Akshoomoff, N., Amaral, D. G., et al. Multimodal imaging of the self-regulating developing brain Proceedings of the National Academy of Sciences of the United States of America 2012 109:19620-19625 DOI:10.1073/pnas.1208243109 PMID:23150548 PMCID:PMC3511748
- Brown, T. T., Kuperman, J. M., Chung, Y. H., Erhart, M., McCabe, C., Hagler, D. J., Venkatraman, V. K., Akshoomoff, N., Amaral, D. G., Bloss, C. S., Casey, B. J., Chang, L., et al. Neuroanatomical assessment of biological maturity Current Biology 2012 22:1693-1698 DOI:10.1016/j.cub.2012.07.002 PMID:22902750 PMCID:PMC3461087
- Bakken, T. E., Roddey, J. C., Djurovic, S., Akshoomoff, N., Amaral, D. G., Bloss, C. S., Casey, B. J., Chang, L., Ernst, T. M., Gruen, J. R., Jernigan, T. L., Kaufmann, W. E., et al. Association of common genetic variants in gpcpd1 with scaling of visual cortical surface area in humans Proceedings of the National Academy of Sciences of the United States of America 2012 109:3985-3990 DOI:10.1073/pnas.1105829109 PMID:22343285 PMCID:PMC3309762
- Bakken, T. E., Dale, A. M., Schork, N. J., Alzheimer's Dis Neuroimaging, Initi A geographic cline of skull and brain morphology among individuals of european ancestry Human Heredity 2011 72:35-44 DOI:10.1159/000330168 PMID:21849792 PMCID:PMC3171282
- Bakken, T. E., Bloss, C. S., Roddey, J. C., Joyner, A. H., Rimol, L. M., Djurovic, S., Melle, I., Sundet, K., Agartz, I., Andreassen, O. A., Dale, A. M., Schork, N. J. Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia Archives of General Psychiatry 2011 68:781-790 DOI:10.1001/archgenpsychiatry.2011.81 PMID:21810643 PMCID:PMC3375053
- Rimol, L. M., Agartz, I., Djurovic, S., Brown, A. A., Roddey, J. C., Kahler, A. K., Mattingsdal, M., Athanasiu, L., Joyner, A. H., Schork, N. J., Halgren, E., Sundet, K., et al. Sex-dependent association of common variants of microcephaly genes with brain structure Proceedings of the National Academy of Sciences of the United States of America 2010 107:384-388 DOI:10.1073/pnas.0908454107 PMID:20080800 PMCID:PMC2806758
- Joyner, A. H., Roddey, J. C., Bloss, C. S., Bakken, T. E., Rimol, L. M., Melle, I., Agartz, I., Djurovic, S., Topol, E. J., Schork, N. J., Andreassen, O. A., Dale, A. M. A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations Proceedings of the National Academy of Sciences of the United States of America 2009 106:15483-15488 DOI:10.1073/pnas.0901866106 PMID:19717458 PMCID:PMC2741277