Identification of DNA methylation changes in newborns related to maternal smoking during pregnancy von Markunas, Christina A, Xu, Zongli, Harlid, Sophia, Wade, Paul A, Lie, Rolv T, Taylor, Jack A, Wilcox, Allen J

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Genomic and epigenetic evidence for oxytocin receptor deficiency in autism von Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A

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Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults von Markunas, Christina A, Wilcox, Allen J, Xu, Zongli, Joubert, Bonnie R, Harlid, Sophia, Panduri, Vijayalakshmi, Håberg, Siri E, Nystad, Wenche, London, Stephanie J, Sandler, Dale P, Lie, Rolv T, Wade, Paul A, Taylor, Jack A

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Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates von Markunas, Christina A, Soldano, Karen, Dunlap, Kaitlyn, Cope, Heidi, Asiimwe, Edgar, Stajich, Jeffrey, Enterline, David, Grant, Gerald, Fuchs, Herbert, Gregory, Simon G, Ashley-Koch, Allison E

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Human Genetics of Addiction: New Insights and Future Directions von Hancock, Dana B., Markunas, Christina A., Bierut, Laura J., Johnson, Eric O.

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Epigenome‐wide analysis uncovers a blood‐based DNA methylation biomarker of lifetime cannabis use von Markunas, Christina A., Hancock, Dana B., Xu, Zongli, Quach, Bryan C., Fang, Fang, Sandler, Dale P., Johnson, Eric O., Taylor, Jack A.

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Genome-wide DNA methylation differences in nucleus accumbens of smokers vs. nonsmokers von Markunas, Christina A., Semick, Stephen A., Quach, Bryan C., Tao, Ran, Deep-Soboslay, Amy, Carnes, Megan U., Bierut, Laura J., Hyde, Thomas M., Kleinman, Joel E., Johnson, Eric O., Jaffe, Andrew E., Hancock, Dana B.

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Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants von Markunas, Christina A., Johnson, Eric O., Hancock, Dana B.

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Developmental effects of maternal smoking during pregnancy on the human frontal cortex transcriptome von Semick, Stephen A., Collado-Torres, Leonardo, Markunas, Christina A., Shin, Joo Heon, Deep-Soboslay, Amy, Tao, Ran, Huestis, Marilyn A., Bierut, Laura J., Maher, Brion S., Johnson, Eric O., Hyde, Thomas M., Weinberger, Daniel R., Hancock, Dana B., Kleinman, Joel E., Jaffe, Andrew E.

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Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis von Connelly, Jessica J, Cherepanova, Olga A, Doss, Jennifer F, Karaoli, Themistoclis, Lillard, Travis S, Markunas, Christina A, Nelson, Sarah, Wang, Tianyuan, Ellis, Peter D, Langford, Cordelia F, Haynes, Carol, Seo, David M, Goldschmidt-Clermont, Pascal J, Shah, Svati H, Kraus, William E, Hauser, Elizabeth R, Gregory, Simon G

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Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association von Xu, Jiayi, Gaddis, Nathan C, Bartz, Traci M, Hou, Ruixue, Manichaikul, Ani W, Pankratz, Nathan, Smith, Albert V, Sun, Fangui, Terzikhan, Natalie, Markunas, Christina A, Patchen, Bonnie K, Schu, Matthew, Beydoun, May A, Brusselle, Guy G, Eiriksdottir, Gudny, Zhou, Xia, Wood, Alexis C, Graff, Mariaelisa, Harris, Tamara B, Ikram, M Arfan, Jacobs, Jr, David R, Launer, Lenore J, Lemaitre, Rozenn N, O'Connor, George T, Oelsner, Elizabeth C, Psaty, Bruce M, Vasan, Ramachandran S, Rohde, Rebecca R, Rich, Stephen S, Rotter, Jerome I, Seshadri, Sudha, Smith, Lewis J, Tiemeier, Henning, Tsai, Michael Y, Uitterlinden, André G, Voruganti, V Saroja, Xu, Hanfei, Zilhão, Nuno R, Fornage, Myriam, Zillikens, M Carola, London, Stephanie J, Barr, R Graham, Dupuis, Josée, Gharib, Sina A, Gudnason, Vilmundur, Lahousse, Lies, North, Kari E, Steffen, Lyn M, Cassano, Patricia A, Hancock, Dana B

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Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation von Lock, Eric F, Soldano, Karen L, Garrett, Melanie E, Cope, Heidi, Markunas, Christina A, Fuchs, Herbert, Grant, Gerald, Dunson, David B, Gregory, Simon G, Ashley-Koch, Allison E

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Genetic Evaluation and Application of Posterior Cranial Fossa Traits as Endophenotypes for Chiari Type I Malformation von Markunas, Christina A., Enterline, David S., Dunlap, Kaitlyn, Soldano, Karen, Cope, Heidi, Stajich, Jeffrey, Grant, Gerald, Fuchs, Herbert, Gregory, Simon G., Ashley‐Koch, Allison E.

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Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics von Markunas, Christina A, Lock, Eric, Soldano, Karen, Cope, Heidi, Ding, Chien-Kuang C, Enterline, David S, Grant, Gerald, Fuchs, Herbert, Ashley-Koch, Allison E, Gregory, Simon G

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Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families von Markunas, Christina A, Quinn, Kaia S, Collins, Ann L, Garrett, Melanie E, Lachiewicz, Ave M, Sommer, Jennifer L, Morrissey-Kane, Erin, Kollins, Scott H, Anastopoulos, Arthur D, Ashley-Koch, Allison E

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The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects von Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, Van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J., Evans, David M., Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund, Steinhausen, Hans Christoph, Taylor, Eric, Faraone, Stephen V., Franke, Barbara, Posthuma, Danielle

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Assessing Candidate Gene nsSNPs for Phenotypic Differences in Double-Strand Break Repair Using Radiation-Induced γH2A.X Foci von Markunas, Christina A., Umbach, David M., Xu, Zongli, Taylor, Jack A.

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Identification of DNA methylation changes in newborns related to maternal smoking during pregnancy von Markunas, Christina A, Xu, Zongli, Harlid, Sophia, Wade, Paul A, Lie, Rolv Terje, Taylor, Jack A, Wilcox, Allen James

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Identification of DNA methylation changes in newborns related to maternal smoking during pregnancy von Markunas, Christina A, Xu, Zongli, Harlid, Sophia, Wade, Paul A, Lie, Rolv T., Taylor, Jack A, Wilcox, Allen J

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Omega-3 fatty acids and genome-wide interaction analyses reveal DPP10-pulmonary function association von Xu, Jiayi, Gaddis, Nathan C, Bartz, Traci M, Hou, Ruixue, Manichaikul, Ani W, Pankratz, Nathan, Smith, Albert V, Sun, Fangui, Terzikhan, Natalie, Markunas, Christina A, Patchen, Bonnie K, Schu, Matthew, Beydoun, May A, Brusselle, Guy, Eiriksdottir, Gudny, Zhou, Xia, Wood, Alexis C, Graff, Mariaelisa, Harris, Tamara B, Ikram, M Arfan, Jacobs, David R, Jr, Launer, Lenore J, Lemaitre, Rozenn N, O'Connor, George T, Oelsner, Elizabeth C, Psaty, Bruce M, Ramachandran, Vasan S, Rohde, Rebecca R, Rich, Sstephen S, Rotter, Jerome I, Seshadri, Sudha, Smith, Lewis J, Tiemeier, Henning, Tsai, Michael Y, Uitterlinden, Andre G, Voruganti, V Saroja, Xu, Hanfei, Zilhão, Nuno R, Fornage, Myriam, Zillikens, M Carola, London, Stephanie J, Barr, R Graham, Dupuis, Josée, Gharib, Sina A, Gudnason, Vilmundur, Lahousse, Lies, North, Kari E, Steffen, Lyn M, Cassano, Patricia A, Hancock, Dana B

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