Assessing Candidate Gene nsSNPs for Phenotypic Differences in Double-Strand Break Repair Using Radiation-Induced γH2A.X Foci

od Markunas, Christina A., Umbach, David M., Xu, Zongli, Taylor, Jack A.
Izdano 2008

Human Genetics of Addiction: New Insights and Future Directions

od Hancock, Dana B., Markunas, Christina A., Bierut, Laura J., Johnson, Eric O.
izdano v Curr Psychiatry Rep (2018)

Identification of DNA Methylation Changes in Newborns Related to Maternal Smoking during Pregnancy

od Markunas, Christina A., Xu, Zongli, Harlid, Sophia, Wade, Paul A., Lie, Rolv T., Taylor, Jack A., Wilcox, Allen J.
Izdano 2014

Epigenome-wide analysis uncovers a blood-based DNA methylation biomarker of lifetime cannabis use.

od Markunas, Christina A., Hancock, Dana B., Xu, Zongli, Quach, Bryan C., Fang, Fang, Sandler, Dale P., Johnson, Eric O., Taylor, Jack A.
izdano v Am J Med Genet B Neuropsychiatr Genet (2020)

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations

od Markunas, Christina A., Tubbs, R. Shane, Moftakhar, Roham, Ashley-Koch, Allison E., Gregory, Simon G., Oakes, W. Jerry, Speer, Marcy C., Iskandar, Bermans J.
Izdano 2012

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari Type I Malformation

od 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.
Izdano 2013

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

od 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.
Izdano 2013

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics

od 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
Izdano 2014

Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation

od 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
izdano v BMC Genomics (2015)

Genetic variants in SLC9A9 are associated with measures of Attention-deficit/hyperactivity disorder symptoms in families

od 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.
Izdano 2010

Maternal Age at Delivery Is Associated with an Epigenetic Signature in Both Newborns and Adults

od 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.
izdano v PLoS One (2016)

Genome-wide DNA methylation differences in nucleus accumbens of smokers vs. nonsmokers

od 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.
izdano v Neuropsychopharmacology (2020)

Developmental effects of maternal smoking during pregnancy on the human frontal cortex transcriptome

od Semick, Stephen A., Collado-Torres, Leonardo, Markunas, Christina A., Shin, Joo Heon, Deep-Soboslay, Amy, Tao, Ran, Huestis, Marilyn, Bierut, Laura J., Maher, Brion S., Johnson, Eric O., Hyde, Thomas M., Weinberger, Daniel R., Hancock, Dana B., Kleinman, Joel E., Jaffe, Andrew E.
izdano v Mol Psychiatry (2018)

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

od Worley Gordon, Langford Cordelia F, Ellis Peter, Wright Harry H, Abramson Ruth K, Lintas Carla, Markunas Christina A, Biscocho Dhani, Johnson Jessica, Towers Aaron J, Connelly Jessica J, Gregory Simon G, Delong G Robert, Murphy Susan K, Cuccaro Michael L, Persico Antonello, Pericak-Vance Margaret A
Izdano 2009-10-01

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

od 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
Izdano 2009

Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis

od 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.
Izdano 2013

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

od Hancock, Dana B., Guo, Yuelong, Reginsson, Gunnar W., Gaddis, Nathan C., Lutz, Sharon M., Sherva, Richard, Loukola, Anu, Minica, Camelia, Markunas, Christina A., Han, Younghun, Young, Kendra A., Gudbjartsson, Daniel F., Gu, Fangyi, McNeil, Daniel W., Qaiser, Beenish, Glasheen, Cristie, Olson, Sean, Landi, Maria Teresa, Madden, Pamela A. F., Farrer, Lindsay A., Vink, Jacqueline, Saccone, Nancy L., Neale, Michael C., Kranzler, Henry R., McKay, James, Hung, Rayjean J., Amos, Christopher I., Marazita, Mary L., Boomsma, Dorret I., Baker, Timothy B., Gelernter, Joel, Kaprio, Jaakko, Caporaso, Neil E., Thorgeirsson, Thorgeir E., Hokanson, John E., Bierut, Laura J., Stefansson, Kari, Johnson, Eric O.
izdano v Mol Psychiatry (2017)

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

od 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
Izdano 2011

Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits

od Quach, Bryan C., Bray, Michael J., Gaddis, Nathan C., Liu, Mengzhen, Palviainen, Teemu, Minica, Camelia C., Zellers, Stephanie, Sherva, Richard, Aliev, Fazil, Nothnagel, Michael, Young, Kendra A., Marks, Jesse A., Young, Hannah, Carnes, Megan U., Guo, Yuelong, Waldrop, Alex, Sey, Nancy Y. A., Landi, Maria T., McNeil, Daniel W., Drichel, Dmitriy, Farrer, Lindsay A., Markunas, Christina A., Vink, Jacqueline M., Hottenga, Jouke-Jan, Iacono, William G., Kranzler, Henry R., Saccone, Nancy L., Neale, Michael C., Madden, Pamela, Rietschel, Marcella, Marazita, Mary L., McGue, Matthew, Won, Hyejung, Winterer, Georg, Grucza, Richard, Dick, Danielle M., Gelernter, Joel, Caporaso, Neil E., Baker, Timothy B., Boomsma, Dorret I., Kaprio, Jaakko, Hokanson, John E., Vrieze, Scott, Bierut, Laura J., Johnson, Eric O., Hancock, Dana B.
izdano v Nat Commun (2020)

Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10–Pulmonary Function Association

od 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, 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.
izdano v Am J Respir Crit Care Med (2019)